---
_id: '12208'
abstract:
- lang: eng
text: The inadequate understanding of the mechanisms that reversibly convert molecular
sulfur (S) into lithium sulfide (Li2S) via soluble polysulfides
(PSs) formation impedes the development of high-performance lithium-sulfur (Li-S)
batteries with non-aqueous electrolyte solutions. Here, we use operando small
and wide angle X-ray scattering and operando small angle neutron scattering (SANS)
measurements to track the nucleation, growth and dissolution of solid deposits
from atomic to sub-micron scales during real-time Li-S cell operation. In particular,
stochastic modelling based on the SANS data allows quantifying the nanoscale phase
evolution during battery cycling. We show that next to nano-crystalline Li2S
the deposit comprises solid short-chain PSs particles. The analysis of the experimental
data suggests that initially, Li2S2
precipitates from the solution and then is partially converted via solid-state
electroreduction to Li2S. We further demonstrate that mass
transport, rather than electron transport through a thin passivating film, limits
the discharge capacity and rate performance in Li-S cells.
acknowledgement: "This project has received funding from the European Union’s Horizon
2020 research and innovation program under the Marie Skłodowska-Curie grant NanoEvolution,
grant agreement No 894042. The authors acknowledge the CERIC-ERIC Consortium for
the access to the Austrian SAXS beamline and TU Graz for support through the Lead
Project LP-03.\r\nLikewise, the use of SOMAPP Lab, a core facility supported by
the Austrian Federal Ministry of Education, Science and Research, the Graz University
of Technology, the University of Graz, and Anton Paar GmbH is acknowledged. In addition,
the authors acknowledge access to the D-22SANS beamline at the ILL neutron source.
Electron microscopy measurements were performed at the Scientific Scenter for Optical
and Electron Microscopy (ScopeM) of the Swiss Federal Institute of Technology. C.P.
and J.M.M. thank A. Senol for her support with the SANS\r\nbeamtime preparation.
S.D.T, A.V. and R.D. acknowledge the financial support by the Slovenian Research
Agency (ARRS) research core funding P2-0393 and P2-0423. Furthermore, A.V. acknowledge
the funding from the Slovenian Research Agency, research project Z2−1863.\r\nS.A.F.
is indebted to IST Austria for support. "
article_number: '6326'
article_processing_charge: No
article_type: original
author:
- first_name: Christian
full_name: Prehal, Christian
last_name: Prehal
- first_name: Jean-Marc
full_name: von Mentlen, Jean-Marc
last_name: von Mentlen
- first_name: Sara
full_name: Drvarič Talian, Sara
last_name: Drvarič Talian
- first_name: Alen
full_name: Vizintin, Alen
last_name: Vizintin
- first_name: Robert
full_name: Dominko, Robert
last_name: Dominko
- first_name: Heinz
full_name: Amenitsch, Heinz
last_name: Amenitsch
- first_name: Lionel
full_name: Porcar, Lionel
last_name: Porcar
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
- first_name: Vanessa
full_name: Wood, Vanessa
last_name: Wood
citation:
ama: Prehal C, von Mentlen J-M, Drvarič Talian S, et al. On the nanoscale structural
evolution of solid discharge products in lithium-sulfur batteries using operando
scattering. Nature Communications. 2022;13. doi:10.1038/s41467-022-33931-4
apa: Prehal, C., von Mentlen, J.-M., Drvarič Talian, S., Vizintin, A., Dominko,
R., Amenitsch, H., … Wood, V. (2022). On the nanoscale structural evolution of
solid discharge products in lithium-sulfur batteries using operando scattering.
Nature Communications. Springer Nature. https://doi.org/10.1038/s41467-022-33931-4
chicago: Prehal, Christian, Jean-Marc von Mentlen, Sara Drvarič Talian, Alen Vizintin,
Robert Dominko, Heinz Amenitsch, Lionel Porcar, Stefan Alexander Freunberger,
and Vanessa Wood. “On the Nanoscale Structural Evolution of Solid Discharge Products
in Lithium-Sulfur Batteries Using Operando Scattering.” Nature Communications.
Springer Nature, 2022. https://doi.org/10.1038/s41467-022-33931-4.
ieee: C. Prehal et al., “On the nanoscale structural evolution of solid discharge
products in lithium-sulfur batteries using operando scattering,” Nature Communications,
vol. 13. Springer Nature, 2022.
ista: Prehal C, von Mentlen J-M, Drvarič Talian S, Vizintin A, Dominko R, Amenitsch
H, Porcar L, Freunberger SA, Wood V. 2022. On the nanoscale structural evolution
of solid discharge products in lithium-sulfur batteries using operando scattering.
Nature Communications. 13, 6326.
mla: Prehal, Christian, et al. “On the Nanoscale Structural Evolution of Solid Discharge
Products in Lithium-Sulfur Batteries Using Operando Scattering.” Nature Communications,
vol. 13, 6326, Springer Nature, 2022, doi:10.1038/s41467-022-33931-4.
short: C. Prehal, J.-M. von Mentlen, S. Drvarič Talian, A. Vizintin, R. Dominko,
H. Amenitsch, L. Porcar, S.A. Freunberger, V. Wood, Nature Communications 13 (2022).
date_created: 2023-01-16T09:45:09Z
date_published: 2022-10-24T00:00:00Z
date_updated: 2023-08-04T09:15:31Z
day: '24'
ddc:
- '540'
department:
- _id: StFr
doi: 10.1038/s41467-022-33931-4
external_id:
isi:
- '000871563700006'
pmid:
- '36280671'
file:
- access_level: open_access
checksum: 5034336dbf0f860030ef745c08df9e0e
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T07:19:11Z
date_updated: 2023-01-27T07:19:11Z
file_id: '12411'
file_name: 2022_NatureCommunications_Prehal.pdf
file_size: 4216931
relation: main_file
success: 1
file_date_updated: 2023-01-27T07:19:11Z
has_accepted_license: '1'
intvolume: ' 13'
isi: 1
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
- Multidisciplinary
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the nanoscale structural evolution of solid discharge products in lithium-sulfur
batteries using operando scattering
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 13
year: '2022'
...
---
_id: '12209'
abstract:
- lang: eng
text: Embryo development requires biochemical signalling to generate patterns of
cell fates and active mechanical forces to drive tissue shape changes. However,
how these processes are coordinated, and how tissue patterning is preserved despite
the cellular flows occurring during morphogenesis, remains poorly understood.
Gastrulation is a crucial embryonic stage that involves both patterning and internalization
of the mesendoderm germ layer tissue. Here we show that, in zebrafish embryos,
a gradient in Nodal signalling orchestrates pattern-preserving internalization
movements by triggering a motility-driven unjamming transition. In addition to
its role as a morphogen determining embryo patterning, graded Nodal signalling
mechanically subdivides the mesendoderm into a small fraction of highly protrusive
leader cells, able to autonomously internalize via local unjamming, and less protrusive
followers, which need to be pulled inwards by the leaders. The Nodal gradient
further enforces a code of preferential adhesion coupling leaders to their immediate
followers, resulting in a collective and ordered mode of internalization that
preserves mesendoderm patterning. Integrating this dual mechanical role of Nodal
signalling into minimal active particle simulations quantitatively predicts both
physiological and experimentally perturbed internalization movements. This provides
a quantitative framework for how a morphogen-encoded unjamming transition can
bidirectionally couple tissue mechanics with patterning during complex three-dimensional
morphogenesis.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
acknowledgement: "We thank K. Sampath, A. Pauli and Y. Bellaїche for feedback on the
manuscript. We also thank the members of the Heisenberg group, in particular A.
Schauer and F. Nur Arslan, for help, technical advice and discussions, and the Bioimaging
and Life Science facilities at IST\r\nAustria for continuous support. We thank C.
Flandoli for the artwork in the figures. This work was supported by postdoctoral
fellowships from EMBO (LTF-850-2017) and HFSP (LT000429/2018-L2) to D.P. and the
European Union (European Research Council starting grant 851288 to É.H. and European
Research Council advanced grant 742573 to C.-P.H.)."
article_processing_charge: No
article_type: original
author:
- first_name: Diana C
full_name: Nunes Pinheiro, Diana C
id: 2E839F16-F248-11E8-B48F-1D18A9856A87
last_name: Nunes Pinheiro
orcid: 0000-0003-4333-7503
- first_name: Roland
full_name: Kardos, Roland
id: 4039350E-F248-11E8-B48F-1D18A9856A87
last_name: Kardos
- first_name: Edouard B
full_name: Hannezo, Edouard B
id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
last_name: Hannezo
orcid: 0000-0001-6005-1561
- first_name: Carl-Philipp J
full_name: Heisenberg, Carl-Philipp J
id: 39427864-F248-11E8-B48F-1D18A9856A87
last_name: Heisenberg
orcid: 0000-0002-0912-4566
citation:
ama: Nunes Pinheiro DC, Kardos R, Hannezo EB, Heisenberg C-PJ. Morphogen gradient
orchestrates pattern-preserving tissue morphogenesis via motility-driven unjamming.
Nature Physics. 2022;18(12):1482-1493. doi:10.1038/s41567-022-01787-6
apa: Nunes Pinheiro, D. C., Kardos, R., Hannezo, E. B., & Heisenberg, C.-P.
J. (2022). Morphogen gradient orchestrates pattern-preserving tissue morphogenesis
via motility-driven unjamming. Nature Physics. Springer Nature. https://doi.org/10.1038/s41567-022-01787-6
chicago: Nunes Pinheiro, Diana C, Roland Kardos, Edouard B Hannezo, and Carl-Philipp
J Heisenberg. “Morphogen Gradient Orchestrates Pattern-Preserving Tissue Morphogenesis
via Motility-Driven Unjamming.” Nature Physics. Springer Nature, 2022.
https://doi.org/10.1038/s41567-022-01787-6.
ieee: D. C. Nunes Pinheiro, R. Kardos, E. B. Hannezo, and C.-P. J. Heisenberg, “Morphogen
gradient orchestrates pattern-preserving tissue morphogenesis via motility-driven
unjamming,” Nature Physics, vol. 18, no. 12. Springer Nature, pp. 1482–1493,
2022.
ista: Nunes Pinheiro DC, Kardos R, Hannezo EB, Heisenberg C-PJ. 2022. Morphogen
gradient orchestrates pattern-preserving tissue morphogenesis via motility-driven
unjamming. Nature Physics. 18(12), 1482–1493.
mla: Nunes Pinheiro, Diana C., et al. “Morphogen Gradient Orchestrates Pattern-Preserving
Tissue Morphogenesis via Motility-Driven Unjamming.” Nature Physics, vol.
18, no. 12, Springer Nature, 2022, pp. 1482–93, doi:10.1038/s41567-022-01787-6.
short: D.C. Nunes Pinheiro, R. Kardos, E.B. Hannezo, C.-P.J. Heisenberg, Nature
Physics 18 (2022) 1482–1493.
date_created: 2023-01-16T09:45:19Z
date_published: 2022-12-01T00:00:00Z
date_updated: 2023-08-04T09:15:58Z
day: '01'
ddc:
- '570'
department:
- _id: CaHe
- _id: EdHa
doi: 10.1038/s41567-022-01787-6
ec_funded: 1
external_id:
isi:
- '000871319900002'
file:
- access_level: open_access
checksum: c86a8e8d80d1bfc46d56a01e88a2526a
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T07:32:01Z
date_updated: 2023-01-27T07:32:01Z
file_id: '12412'
file_name: 2022_NaturePhysics_Pinheiro.pdf
file_size: 36703569
relation: main_file
success: 1
file_date_updated: 2023-01-27T07:32:01Z
has_accepted_license: '1'
intvolume: ' 18'
isi: 1
issue: '12'
keyword:
- General Physics and Astronomy
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 1482-1493
project:
- _id: 26520D1E-B435-11E9-9278-68D0E5697425
grant_number: ALTF 850-2017
name: Coordination of mesendoderm cell fate specification and internalization during
zebrafish gastrulation
- _id: 26520D1E-B435-11E9-9278-68D0E5697425
grant_number: ALTF 850-2017
name: Coordination of mesendoderm cell fate specification and internalization during
zebrafish gastrulation
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
call_identifier: H2020
grant_number: '851288'
name: Design Principles of Branching Morphogenesis
- _id: 260F1432-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '742573'
name: Interaction and feedback between cell mechanics and fate specification in
vertebrate gastrulation
publication: Nature Physics
publication_identifier:
eissn:
- 1745-2481
issn:
- 1745-2473
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Morphogen gradient orchestrates pattern-preserving tissue morphogenesis via
motility-driven unjamming
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 18
year: '2022'
...
---
_id: '12210'
abstract:
- lang: eng
text: "The aim of this paper is to find new estimates for the norms of functions
of a (minus) distinguished Laplace operator L on the ‘ax+b’ groups. The central
part is devoted to spectrally localized wave propagators, that is, functions of
the type ψ(L−−√)exp(itL−−√), with ψ∈C0(R). We show that for t→+∞, the convolution
kernel kt of this operator satisfies\r\n∥kt∥1≍t,∥kt∥∞≍1,\r\nso that the upper
estimates of D. Müller and C. Thiele (Studia Math., 2007) are sharp. As a necessary
component, we recall the Plancherel density of L and spend certain time presenting
and comparing different approaches to its calculation. Using its explicit form,
we estimate uniform norms of several functions of the shifted Laplace-Beltrami
operator Δ~, closely related to L. The functions include in particular exp(−tΔ~γ),
t>0,γ>0, and (Δ~−z)s, with complex z, s."
acknowledgement: "Yu. K. thanks Professor Waldemar Hebisch for valuable discussions
on the general context of multipliers on Lie groups. This work was started during
an ICL-CNRS fellowship of the second\r\nnamed author at the Imperial College London.
Yu. K. is supported by the ANR-19-CE40-0002 grant of the French National Research
Agency (ANR). H. Z. is supported by the European Union’s Horizon 2020 research and
innovation programme under the Marie Skłodowska-Curie grant agreement No. 754411
and the Lise Meitner fellowship, Austrian Science Fund (FWF) M3337. R. A. was supported
by the EPSRC grant EP/R003025. M. R. is supported by the EPSRC grant EP/R003025/2
and by the FWO Odysseus 1 grant G.0H94.18N: Analysis and Partial Differential Equations."
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Rauan
full_name: Akylzhanov, Rauan
last_name: Akylzhanov
- first_name: Yulia
full_name: Kuznetsova, Yulia
last_name: Kuznetsova
- first_name: Michael
full_name: Ruzhansky, Michael
last_name: Ruzhansky
- first_name: Haonan
full_name: Zhang, Haonan
id: D8F41E38-9E66-11E9-A9E2-65C2E5697425
last_name: Zhang
citation:
ama: Akylzhanov R, Kuznetsova Y, Ruzhansky M, Zhang H. Norms of certain functions
of a distinguished Laplacian on the ax + b groups. Mathematische Zeitschrift.
2022;302(4):2327-2352. doi:10.1007/s00209-022-03143-z
apa: Akylzhanov, R., Kuznetsova, Y., Ruzhansky, M., & Zhang, H. (2022). Norms
of certain functions of a distinguished Laplacian on the ax + b groups. Mathematische
Zeitschrift. Springer Nature. https://doi.org/10.1007/s00209-022-03143-z
chicago: Akylzhanov, Rauan, Yulia Kuznetsova, Michael Ruzhansky, and Haonan Zhang.
“Norms of Certain Functions of a Distinguished Laplacian on the Ax + b Groups.”
Mathematische Zeitschrift. Springer Nature, 2022. https://doi.org/10.1007/s00209-022-03143-z.
ieee: R. Akylzhanov, Y. Kuznetsova, M. Ruzhansky, and H. Zhang, “Norms of certain
functions of a distinguished Laplacian on the ax + b groups,” Mathematische
Zeitschrift, vol. 302, no. 4. Springer Nature, pp. 2327–2352, 2022.
ista: Akylzhanov R, Kuznetsova Y, Ruzhansky M, Zhang H. 2022. Norms of certain functions
of a distinguished Laplacian on the ax + b groups. Mathematische Zeitschrift.
302(4), 2327–2352.
mla: Akylzhanov, Rauan, et al. “Norms of Certain Functions of a Distinguished Laplacian
on the Ax + b Groups.” Mathematische Zeitschrift, vol. 302, no. 4, Springer
Nature, 2022, pp. 2327–52, doi:10.1007/s00209-022-03143-z.
short: R. Akylzhanov, Y. Kuznetsova, M. Ruzhansky, H. Zhang, Mathematische Zeitschrift
302 (2022) 2327–2352.
date_created: 2023-01-16T09:45:31Z
date_published: 2022-12-01T00:00:00Z
date_updated: 2023-08-04T09:22:14Z
day: '01'
department:
- _id: JaMa
doi: 10.1007/s00209-022-03143-z
ec_funded: 1
external_id:
arxiv:
- '2101.00584'
isi:
- '000859680700001'
intvolume: ' 302'
isi: 1
issue: '4'
keyword:
- General Mathematics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/2101.00584
month: '12'
oa: 1
oa_version: Preprint
page: 2327-2352
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
- _id: eb958bca-77a9-11ec-83b8-c565cb50d8d6
grant_number: M03337
name: Curvature-dimension in noncommutative analysis
publication: Mathematische Zeitschrift
publication_identifier:
eissn:
- 1432-1823
issn:
- 0025-5874
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Norms of certain functions of a distinguished Laplacian on the ax + b groups
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 302
year: '2022'
...
---
_id: '12212'
abstract:
- lang: eng
text: Alzheimer’s disease (AD) is characterized by a reorganization of brain activity
determining network hyperexcitability and loss of synaptic plasticity. Precisely,
a dysfunction in metabotropic GABAB receptor signalling through G protein-gated
inwardly rectifying K+ (GIRK or Kir3) channels on the hippocampus has been postulated.
Thus, we determined the impact of amyloid-β (Aβ) pathology in GIRK channel density,
subcellular distribution, and its association with GABAB receptors in hippocampal
CA1 pyramidal neurons from the APP/PS1 mouse model using quantitative SDS-digested
freeze-fracture replica labelling (SDS-FRL) and proximity ligation in situ assay
(P-LISA). In wild type mice, single SDS-FRL detection revealed a similar dendritic
gradient for GIRK1 and GIRK2 in CA1 pyramidal cells, with higher densities in
spines, and GIRK3 showed a lower and uniform distribution. Double SDS-FRL showed
a co-clustering of GIRK2 and GIRK1 in post- and presynaptic compartments, but
not for GIRK2 and GIRK3. Likewise, double GABAB1 and GIRK2 SDS-FRL detection displayed
a high degree of co-clustering in nanodomains (40–50 nm) mostly in spines and
axon terminals. In APP/PS1 mice, the density of GIRK2 and GIRK1, but not for GIRK3,
was significantly reduced along the neuronal surface of CA1 pyramidal cells and
in axon terminals contacting them. Importantly, GABAB1 and GIRK2 co-clustering
was not present in APP/PS1 mice. Similarly, P-LISA experiments revealed a significant
reduction in GABAB1 and GIRK2 interaction on the hippocampus of this animal model.
Overall, our results provide compelling evidence showing a significant reduction
on the cell surface density of pre- and postsynaptic GIRK1 and GIRK2, but not
GIRK3, and a decline in GABAB receptors and GIRK2 channels co-clustering in hippocampal
pyramidal neurons from APP/PS1 mice, thus suggesting that a disruption in the
GABAB receptor–GIRK channel membrane assembly causes dysregulation in the GABAB
signalling via GIRK channels in this AD animal model.
acknowledgement: "We thank Ms. Diane Latawiec for the English revision of the manuscript.
Funding sources were the Spanish Ministerio de Economía y Competitividad, Junta
de Comunidades de Castilla-La Mancha (Spain), and Life Science Innovation Center
at University of Fukui. We thank Centres de Recerca de Catalunya (CERCA) Programme/Generalitat
de Catalunya for IDIBELL institutional support. We thank Hitoshi Takagi and Takako
Maegawa at the University of Fukui for their technical assistance on SDS-FRL experiments.\r\nThis
work was supported by grants from the Spanish Ministerio de Economía y Competitividad
(BFU2015-63769-R, RTI2018-095812-B-I00, and PID2021-125875OB-I00) and Junta de Comunidades
de Castilla-La Mancha (SBPLY/17/180501/000229 and SBPLY/21/180501/000064) to RL,
Life Science Innovation Center at University of Fukui and JSPS KAKENHI (Grant Numbers
16H04662, 19H03323, and 20H05058) to YF, and Margarita Salas fellowship from Ministerio
de Universidades and Universidad de Castilla-La Mancha to AMB."
article_number: '136'
article_processing_charge: No
article_type: original
author:
- first_name: Alejandro
full_name: Martín-Belmonte, Alejandro
last_name: Martín-Belmonte
- first_name: Carolina
full_name: Aguado, Carolina
last_name: Aguado
- first_name: Rocío
full_name: Alfaro-Ruiz, Rocío
last_name: Alfaro-Ruiz
- first_name: Ana Esther
full_name: Moreno-Martínez, Ana Esther
last_name: Moreno-Martínez
- first_name: Luis
full_name: de la Ossa, Luis
last_name: de la Ossa
- first_name: Ester
full_name: Aso, Ester
last_name: Aso
- first_name: Laura
full_name: Gómez-Acero, Laura
last_name: Gómez-Acero
- first_name: Ryuichi
full_name: Shigemoto, Ryuichi
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Yugo
full_name: Fukazawa, Yugo
last_name: Fukazawa
- first_name: Francisco
full_name: Ciruela, Francisco
last_name: Ciruela
- first_name: Rafael
full_name: Luján, Rafael
last_name: Luján
citation:
ama: Martín-Belmonte A, Aguado C, Alfaro-Ruiz R, et al. Nanoscale alterations in
GABAB receptors and GIRK channel organization on the hippocampus of APP/PS1 mice.
Alzheimer’s Research & Therapy. 2022;14. doi:10.1186/s13195-022-01078-5
apa: Martín-Belmonte, A., Aguado, C., Alfaro-Ruiz, R., Moreno-Martínez, A. E., de
la Ossa, L., Aso, E., … Luján, R. (2022). Nanoscale alterations in GABAB receptors
and GIRK channel organization on the hippocampus of APP/PS1 mice. Alzheimer’s
Research & Therapy. Springer Nature. https://doi.org/10.1186/s13195-022-01078-5
chicago: Martín-Belmonte, Alejandro, Carolina Aguado, Rocío Alfaro-Ruiz, Ana Esther
Moreno-Martínez, Luis de la Ossa, Ester Aso, Laura Gómez-Acero, et al. “Nanoscale
Alterations in GABAB Receptors and GIRK Channel Organization on the Hippocampus
of APP/PS1 Mice.” Alzheimer’s Research & Therapy. Springer Nature,
2022. https://doi.org/10.1186/s13195-022-01078-5.
ieee: A. Martín-Belmonte et al., “Nanoscale alterations in GABAB receptors
and GIRK channel organization on the hippocampus of APP/PS1 mice,” Alzheimer’s
Research & Therapy, vol. 14. Springer Nature, 2022.
ista: Martín-Belmonte A, Aguado C, Alfaro-Ruiz R, Moreno-Martínez AE, de la Ossa
L, Aso E, Gómez-Acero L, Shigemoto R, Fukazawa Y, Ciruela F, Luján R. 2022. Nanoscale
alterations in GABAB receptors and GIRK channel organization on the hippocampus
of APP/PS1 mice. Alzheimer’s Research & Therapy. 14, 136.
mla: Martín-Belmonte, Alejandro, et al. “Nanoscale Alterations in GABAB Receptors
and GIRK Channel Organization on the Hippocampus of APP/PS1 Mice.” Alzheimer’s
Research & Therapy, vol. 14, 136, Springer Nature, 2022, doi:10.1186/s13195-022-01078-5.
short: A. Martín-Belmonte, C. Aguado, R. Alfaro-Ruiz, A.E. Moreno-Martínez, L. de
la Ossa, E. Aso, L. Gómez-Acero, R. Shigemoto, Y. Fukazawa, F. Ciruela, R. Luján,
Alzheimer’s Research & Therapy 14 (2022).
date_created: 2023-01-16T09:45:51Z
date_published: 2022-09-21T00:00:00Z
date_updated: 2023-08-04T09:23:10Z
day: '21'
ddc:
- '570'
department:
- _id: RySh
doi: 10.1186/s13195-022-01078-5
external_id:
isi:
- '000857985500001'
file:
- access_level: open_access
checksum: 88e49715ad6a1abf0fdb27efd65368dc
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T07:53:18Z
date_updated: 2023-01-27T07:53:18Z
file_id: '12413'
file_name: 2022_AlzheimersResearch_MartinBelmont.pdf
file_size: 11013325
relation: main_file
success: 1
file_date_updated: 2023-01-27T07:53:18Z
has_accepted_license: '1'
intvolume: ' 14'
isi: 1
keyword:
- Cognitive Neuroscience
- Neurology (clinical)
- Neurology
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
publication: Alzheimer's Research & Therapy
publication_identifier:
issn:
- 1758-9193
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nanoscale alterations in GABAB receptors and GIRK channel organization on the
hippocampus of APP/PS1 mice
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 14
year: '2022'
...
---
_id: '12213'
abstract:
- lang: eng
text: 'Motivated by properties-controlling potential of the strain, we investigate
strain dependence of structure, electronic, and magnetic properties of Sr2IrO4
using complementary theoretical tools: ab-initio calculations, analytical approaches
(rigid octahedra picture, Slater-Koster integrals), and extended t−J model. We
find that strain affects both Ir-Ir distance and Ir-O-Ir angle, and the rigid
octahedra picture is not relevant. Second, we find fundamentally different behavior
for compressive and tensile strain. One remarkable feature is the formation of
two subsets of bond- and orbital-dependent carriers, a compass-like model, under
compression. This originates from the strain-induced renormalization of the Ir-O-Ir
superexchange and O on-site energy. We also show that under compressive (tensile)
strain, Fermi surface becomes highly dispersive (relatively flat). Already at
a tensile strain of 1.5%, we observe spectral weight redistribution, with the
low-energy band acquiring almost purely singlet character. These results can be
directly compared with future experiments.'
acknowledgement: E.M.P. thanks Eugenio Paris, Thorsten Schmitt, Krzysztof Wohlfeld,
and other coauthors for an inspiring previous collaboration23, and is grateful to
Gang Cao, Ambrose Seo, and Jungho Kim for insightful discussions. R.R. acknowledges
helpful discussion with Sanjeev Kumar and Manuel Richter. This project has received
funding from the European Union’s Horizon 2020 research and innovation program under
the Marie Sklodowska-Curie grant agreement No 754411. C.C.C. acknowledges support
from the U.S. National Science Foundation Award No. DMR-2142801.
article_number: '90'
article_processing_charge: No
article_type: original
author:
- first_name: Ekaterina
full_name: Paerschke, Ekaterina
id: 8275014E-6063-11E9-9B7F-6338E6697425
last_name: Paerschke
orcid: 0000-0003-0853-8182
- first_name: Wei-Chih
full_name: Chen, Wei-Chih
last_name: Chen
- first_name: Rajyavardhan
full_name: Ray, Rajyavardhan
last_name: Ray
- first_name: Cheng-Chien
full_name: Chen, Cheng-Chien
last_name: Chen
citation:
ama: Paerschke E, Chen W-C, Ray R, Chen C-C. Evolution of electronic and magnetic
properties of Sr₂IrO₄ under strain. npj Quantum Materials. 2022;7. doi:10.1038/s41535-022-00496-w
apa: Paerschke, E., Chen, W.-C., Ray, R., & Chen, C.-C. (2022). Evolution of
electronic and magnetic properties of Sr₂IrO₄ under strain. Npj Quantum Materials.
Springer Nature. https://doi.org/10.1038/s41535-022-00496-w
chicago: Paerschke, Ekaterina, Wei-Chih Chen, Rajyavardhan Ray, and Cheng-Chien
Chen. “Evolution of Electronic and Magnetic Properties of Sr₂IrO₄ under Strain.”
Npj Quantum Materials. Springer Nature, 2022. https://doi.org/10.1038/s41535-022-00496-w.
ieee: E. Paerschke, W.-C. Chen, R. Ray, and C.-C. Chen, “Evolution of electronic
and magnetic properties of Sr₂IrO₄ under strain,” npj Quantum Materials,
vol. 7. Springer Nature, 2022.
ista: Paerschke E, Chen W-C, Ray R, Chen C-C. 2022. Evolution of electronic and
magnetic properties of Sr₂IrO₄ under strain. npj Quantum Materials. 7, 90.
mla: Paerschke, Ekaterina, et al. “Evolution of Electronic and Magnetic Properties
of Sr₂IrO₄ under Strain.” Npj Quantum Materials, vol. 7, 90, Springer Nature,
2022, doi:10.1038/s41535-022-00496-w.
short: E. Paerschke, W.-C. Chen, R. Ray, C.-C. Chen, Npj Quantum Materials 7 (2022).
date_created: 2023-01-16T09:46:01Z
date_published: 2022-09-10T00:00:00Z
date_updated: 2023-08-04T09:23:43Z
day: '10'
ddc:
- '530'
department:
- _id: MiLe
doi: 10.1038/s41535-022-00496-w
ec_funded: 1
external_id:
isi:
- '000852381200003'
file:
- access_level: open_access
checksum: d93b477b5b95c0d1b8f9fef90a81f565
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T07:59:27Z
date_updated: 2023-01-27T07:59:27Z
file_id: '12414'
file_name: 2022_NPJ_Paerschke.pdf
file_size: 1852598
relation: main_file
success: 1
file_date_updated: 2023-01-27T07:59:27Z
has_accepted_license: '1'
intvolume: ' 7'
isi: 1
keyword:
- Condensed Matter Physics
- Electronic
- Optical and Magnetic Materials
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: npj Quantum Materials
publication_identifier:
eissn:
- 2397-4648
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
link:
- relation: erratum
url: https://doi.org/10.1038/s41535-022-00510-1
scopus_import: '1'
status: public
title: Evolution of electronic and magnetic properties of Sr₂IrO₄ under strain
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 7
year: '2022'
...
---
_id: '12214'
abstract:
- lang: eng
text: 'Motivated by Kloeckner’s result on the isometry group of the quadratic Wasserstein
space W2(Rn), we describe the isometry group Isom(Wp(E)) for all parameters 0
< p < ∞ and for all separable real Hilbert spaces E. In particular, we show that
Wp(X) is isometrically rigid for all Polish space X whenever 0 < p < 1. This is
a consequence of our more general result: we prove that W1(X) is isometrically
rigid if X is a complete separable metric space that satisfies the strict triangle
inequality. Furthermore, we show that this latter rigidity result does not generalise
to parameters p > 1, by solving Kloeckner’s problem affirmatively on the existence
of mass-splitting isometries. '
acknowledgement: "Geher was supported by the Leverhulme Trust Early Career Fellowship
(ECF-2018-125), and also by the Hungarian National Research, Development and Innovation
Office - NKFIH (grant no. K115383 and K134944).\r\nTitkos was supported by the Hungarian
National Research, Development and Innovation Office - NKFIH (grant no. PD128374,
grant no. K115383 and K134944), by the J´anos Bolyai Research Scholarship of the
Hungarian Academy of Sciences, and by the UNKP-20-5-BGE-1 New National Excellence
Program of the ´Ministry of Innovation and Technology.\r\nVirosztek was supported
by the European Union’s Horizon 2020 research and innovation program under the Marie
Sklodowska-Curie Grant Agreement No. 846294, by the Momentum program of the Hungarian
Academy of Sciences under grant agreement no. LP2021-15/2021, and partially supported
by the Hungarian National Research, Development and Innovation Office - NKFIH (grants
no. K124152 and no. KH129601). "
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: György Pál
full_name: Gehér, György Pál
last_name: Gehér
- first_name: Tamás
full_name: Titkos, Tamás
last_name: Titkos
- first_name: Daniel
full_name: Virosztek, Daniel
id: 48DB45DA-F248-11E8-B48F-1D18A9856A87
last_name: Virosztek
orcid: 0000-0003-1109-5511
citation:
ama: 'Gehér GP, Titkos T, Virosztek D. The isometry group of Wasserstein spaces:
The Hilbertian case. Journal of the London Mathematical Society. 2022;106(4):3865-3894.
doi:10.1112/jlms.12676'
apa: 'Gehér, G. P., Titkos, T., & Virosztek, D. (2022). The isometry group of
Wasserstein spaces: The Hilbertian case. Journal of the London Mathematical
Society. Wiley. https://doi.org/10.1112/jlms.12676'
chicago: 'Gehér, György Pál, Tamás Titkos, and Daniel Virosztek. “The Isometry Group
of Wasserstein Spaces: The Hilbertian Case.” Journal of the London Mathematical
Society. Wiley, 2022. https://doi.org/10.1112/jlms.12676.'
ieee: 'G. P. Gehér, T. Titkos, and D. Virosztek, “The isometry group of Wasserstein
spaces: The Hilbertian case,” Journal of the London Mathematical Society,
vol. 106, no. 4. Wiley, pp. 3865–3894, 2022.'
ista: 'Gehér GP, Titkos T, Virosztek D. 2022. The isometry group of Wasserstein
spaces: The Hilbertian case. Journal of the London Mathematical Society. 106(4),
3865–3894.'
mla: 'Gehér, György Pál, et al. “The Isometry Group of Wasserstein Spaces: The Hilbertian
Case.” Journal of the London Mathematical Society, vol. 106, no. 4, Wiley,
2022, pp. 3865–94, doi:10.1112/jlms.12676.'
short: G.P. Gehér, T. Titkos, D. Virosztek, Journal of the London Mathematical Society
106 (2022) 3865–3894.
date_created: 2023-01-16T09:46:13Z
date_published: 2022-09-18T00:00:00Z
date_updated: 2023-08-04T09:24:17Z
day: '18'
department:
- _id: LaEr
doi: 10.1112/jlms.12676
ec_funded: 1
external_id:
arxiv:
- '2102.02037'
isi:
- '000854878500001'
intvolume: ' 106'
isi: 1
issue: '4'
keyword:
- General Mathematics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.48550/arXiv.2102.02037
month: '09'
oa: 1
oa_version: Preprint
page: 3865-3894
project:
- _id: 26A455A6-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '846294'
name: Geometric study of Wasserstein spaces and free probability
publication: Journal of the London Mathematical Society
publication_identifier:
eissn:
- 1469-7750
issn:
- 0024-6107
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'The isometry group of Wasserstein spaces: The Hilbertian case'
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 106
year: '2022'
...
---
_id: '12216'
abstract:
- lang: eng
text: Many trace inequalities can be expressed either as concavity/convexity theorems
or as monotonicity theorems. A classic example is the joint convexity of the quantum
relative entropy which is equivalent to the Data Processing Inequality. The latter
says that quantum operations can never increase the relative entropy. The monotonicity
versions often have many advantages, and often have direct physical application,
as in the example just mentioned. Moreover, the monotonicity results are often
valid for a larger class of maps than, say, quantum operations (which are completely
positive). In this paper we prove several new monotonicity results, the first
of which is a monotonicity theorem that has as a simple corollary a celebrated
concavity theorem of Epstein. Our starting points are the monotonicity versions
of the Lieb Concavity and the Lieb Convexity Theorems. We also give two new proofs
of these in their general forms using interpolation. We then prove our new monotonicity
theorems by several duality arguments.
acknowledgement: Work partially supported by the Lise Meitner fellowship, Austrian
Science Fund (FWF) M3337.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Eric A.
full_name: Carlen, Eric A.
last_name: Carlen
- first_name: Haonan
full_name: Zhang, Haonan
id: D8F41E38-9E66-11E9-A9E2-65C2E5697425
last_name: Zhang
citation:
ama: Carlen EA, Zhang H. Monotonicity versions of Epstein’s concavity theorem and
related inequalities. Linear Algebra and its Applications. 2022;654:289-310.
doi:10.1016/j.laa.2022.09.001
apa: Carlen, E. A., & Zhang, H. (2022). Monotonicity versions of Epstein’s concavity
theorem and related inequalities. Linear Algebra and Its Applications.
Elsevier. https://doi.org/10.1016/j.laa.2022.09.001
chicago: Carlen, Eric A., and Haonan Zhang. “Monotonicity Versions of Epstein’s
Concavity Theorem and Related Inequalities.” Linear Algebra and Its Applications.
Elsevier, 2022. https://doi.org/10.1016/j.laa.2022.09.001.
ieee: E. A. Carlen and H. Zhang, “Monotonicity versions of Epstein’s concavity theorem
and related inequalities,” Linear Algebra and its Applications, vol. 654.
Elsevier, pp. 289–310, 2022.
ista: Carlen EA, Zhang H. 2022. Monotonicity versions of Epstein’s concavity theorem
and related inequalities. Linear Algebra and its Applications. 654, 289–310.
mla: Carlen, Eric A., and Haonan Zhang. “Monotonicity Versions of Epstein’s Concavity
Theorem and Related Inequalities.” Linear Algebra and Its Applications,
vol. 654, Elsevier, 2022, pp. 289–310, doi:10.1016/j.laa.2022.09.001.
short: E.A. Carlen, H. Zhang, Linear Algebra and Its Applications 654 (2022) 289–310.
date_created: 2023-01-16T09:46:38Z
date_published: 2022-12-01T00:00:00Z
date_updated: 2023-08-04T09:24:51Z
day: '01'
ddc:
- '510'
department:
- _id: JaMa
doi: 10.1016/j.laa.2022.09.001
external_id:
isi:
- '000860689600014'
file:
- access_level: open_access
checksum: cf3cb7e7e34baa967849f01d8f0c1ae4
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T08:08:39Z
date_updated: 2023-01-27T08:08:39Z
file_id: '12415'
file_name: 2022_LinearAlgebra_Carlen.pdf
file_size: 441184
relation: main_file
success: 1
file_date_updated: 2023-01-27T08:08:39Z
has_accepted_license: '1'
intvolume: ' 654'
isi: 1
keyword:
- Discrete Mathematics and Combinatorics
- Geometry and Topology
- Numerical Analysis
- Algebra and Number Theory
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 289-310
project:
- _id: eb958bca-77a9-11ec-83b8-c565cb50d8d6
grant_number: M03337
name: Curvature-dimension in noncommutative analysis
publication: Linear Algebra and its Applications
publication_identifier:
issn:
- 0024-3795
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Monotonicity versions of Epstein's concavity theorem and related inequalities
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 654
year: '2022'
...
---
_id: '12217'
abstract:
- lang: eng
text: The development dynamics and self-organization of glandular branched epithelia
is of utmost importance for our understanding of diverse processes ranging from
normal tissue growth to the growth of cancerous tissues. Using single primary
murine pancreatic ductal adenocarcinoma (PDAC) cells embedded in a collagen matrix
and adapted media supplementation, we generate organoids that self-organize into
highly branched structures displaying a seamless lumen connecting terminal end
buds, replicating in vivo PDAC architecture. We identify distinct morphogenesis
phases, each characterized by a unique pattern of cell invasion, matrix deformation,
protein expression, and respective molecular dependencies. We propose a minimal
theoretical model of a branching and proliferating tissue, capturing the dynamics
of the first phases. Observing the interaction of morphogenesis, mechanical environment
and gene expression in vitro sets a benchmark for the understanding of self-organization
processes governing complex organoid structure formation processes and branching
morphogenesis.
acknowledgement: "A.R.B. acknowledges the financial support of the European Research
Council (ERC) through the funding of the grant Principles of Integrin Mechanics
and Adhesion (PoINT) and the German Research Foundation (DFG, SFB 1032, project
ID 201269156). E.H. was supported by the European Union (European Research Council
Starting Grant 851288). D.S., M.R., and R.R. acknowledge the support by the German
Research Foundation (DFG, SFB1321 Modeling and Targeting Pancreatic Cancer, Project
S01, project ID 329628492). C.S. and M.R. acknowledge the support by the German
Research Foundation (DFG, SFB1321 Modeling and Targeting Pancreatic Cancer, Project
12, project ID 329628492). M.R. was supported by the German Research Foundation
(DFG RE 3723/4-1). A.P. and M.R. were supported by the German Cancer Aid (Max-Eder
Program 111273 and 70114328).\r\nOpen Access funding enabled and organized by Projekt
DEAL."
article_number: '5219'
article_processing_charge: No
article_type: original
author:
- first_name: S.
full_name: Randriamanantsoa, S.
last_name: Randriamanantsoa
- first_name: A.
full_name: Papargyriou, A.
last_name: Papargyriou
- first_name: H. C.
full_name: Maurer, H. C.
last_name: Maurer
- first_name: K.
full_name: Peschke, K.
last_name: Peschke
- first_name: M.
full_name: Schuster, M.
last_name: Schuster
- first_name: G.
full_name: Zecchin, G.
last_name: Zecchin
- first_name: K.
full_name: Steiger, K.
last_name: Steiger
- first_name: R.
full_name: Öllinger, R.
last_name: Öllinger
- first_name: D.
full_name: Saur, D.
last_name: Saur
- first_name: C.
full_name: Scheel, C.
last_name: Scheel
- first_name: R.
full_name: Rad, R.
last_name: Rad
- first_name: Edouard B
full_name: Hannezo, Edouard B
id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
last_name: Hannezo
orcid: 0000-0001-6005-1561
- first_name: M.
full_name: Reichert, M.
last_name: Reichert
- first_name: A. R.
full_name: Bausch, A. R.
last_name: Bausch
citation:
ama: Randriamanantsoa S, Papargyriou A, Maurer HC, et al. Spatiotemporal dynamics
of self-organized branching in pancreas-derived organoids. Nature Communications.
2022;13. doi:10.1038/s41467-022-32806-y
apa: Randriamanantsoa, S., Papargyriou, A., Maurer, H. C., Peschke, K., Schuster,
M., Zecchin, G., … Bausch, A. R. (2022). Spatiotemporal dynamics of self-organized
branching in pancreas-derived organoids. Nature Communications. Springer
Nature. https://doi.org/10.1038/s41467-022-32806-y
chicago: Randriamanantsoa, S., A. Papargyriou, H. C. Maurer, K. Peschke, M. Schuster,
G. Zecchin, K. Steiger, et al. “Spatiotemporal Dynamics of Self-Organized Branching
in Pancreas-Derived Organoids.” Nature Communications. Springer Nature,
2022. https://doi.org/10.1038/s41467-022-32806-y.
ieee: S. Randriamanantsoa et al., “Spatiotemporal dynamics of self-organized
branching in pancreas-derived organoids,” Nature Communications, vol. 13.
Springer Nature, 2022.
ista: Randriamanantsoa S, Papargyriou A, Maurer HC, Peschke K, Schuster M, Zecchin
G, Steiger K, Öllinger R, Saur D, Scheel C, Rad R, Hannezo EB, Reichert M, Bausch
AR. 2022. Spatiotemporal dynamics of self-organized branching in pancreas-derived
organoids. Nature Communications. 13, 5219.
mla: Randriamanantsoa, S., et al. “Spatiotemporal Dynamics of Self-Organized Branching
in Pancreas-Derived Organoids.” Nature Communications, vol. 13, 5219, Springer
Nature, 2022, doi:10.1038/s41467-022-32806-y.
short: S. Randriamanantsoa, A. Papargyriou, H.C. Maurer, K. Peschke, M. Schuster,
G. Zecchin, K. Steiger, R. Öllinger, D. Saur, C. Scheel, R. Rad, E.B. Hannezo,
M. Reichert, A.R. Bausch, Nature Communications 13 (2022).
date_created: 2023-01-16T09:46:53Z
date_published: 2022-09-05T00:00:00Z
date_updated: 2023-08-04T09:25:23Z
day: '05'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1038/s41467-022-32806-y
ec_funded: 1
external_id:
isi:
- '000850348400025'
file:
- access_level: open_access
checksum: 295261b5172274fd5b8f85a6a6058828
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T08:14:48Z
date_updated: 2023-01-27T08:14:48Z
file_id: '12416'
file_name: 2022_NatureCommunications_Randriamanantsoa.pdf
file_size: 22645149
relation: main_file
success: 1
file_date_updated: 2023-01-27T08:14:48Z
has_accepted_license: '1'
intvolume: ' 13'
isi: 1
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
- Multidisciplinary
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
call_identifier: H2020
grant_number: '851288'
name: Design Principles of Branching Morphogenesis
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
record:
- id: '13068'
relation: research_data
status: public
scopus_import: '1'
status: public
title: Spatiotemporal dynamics of self-organized branching in pancreas-derived organoids
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 13
year: '2022'
...
---
_id: '12224'
abstract:
- lang: eng
text: Muskelin (Mkln1) is implicated in neuronal function, regulating plasma membrane
receptor trafficking. However, its influence on intrinsic brain activity and corresponding
behavioral processes remains unclear. Here we show that murine Mkln1
knockout causes non-habituating locomotor activity, increased exploratory drive,
and decreased locomotor response to amphetamine. Muskelin deficiency impairs social
novelty detection while promoting the retention of spatial reference memory and
fear extinction recall. This is strongly mirrored in either weaker or stronger
resting-state functional connectivity between critical circuits mediating locomotor
exploration and cognition. We show that Mkln1 deletion
alters dendrite branching and spine structure, coinciding with enhanced AMPAR-mediated
synaptic transmission but selective impairment in synaptic potentiation maintenance.
We identify muskelin at excitatory synapses and highlight its role in regulating
dendritic spine actin stability. Our findings point to aberrant spine actin modulation
and changes in glutamatergic synaptic function as critical mechanisms that contribute
to the neurobehavioral phenotype arising from Mkln1
ablation.
acknowledgement: "The authors are grateful to the UKE Animal Facilities (Hamburg)
for animal husbandry and Dr. Bastian Tiemann for his veterinary expertise and supervision
of animal care. We thank Dr. Franco Lombino for critically reading the manuscript
and for helpful discussion. This work was supported by grants from the Deutsche
Forschungsgemeinschaft (DFG) (FOR2419-KN556/11-1, FOR2419-KN556/11-2, KN556/12-1)
and the Landesforschungsförderung Hamburg (LFF-FV76) to M.K.\r\nOpen Access funding
enabled and organized by Projekt DEAL."
article_number: '589'
article_processing_charge: No
article_type: original
author:
- first_name: Mary W
full_name: Muhia, Mary W
id: ab7ed20f-09f7-11eb-909c-d5d0b443ee9d
last_name: Muhia
- first_name: PingAn
full_name: YuanXiang, PingAn
last_name: YuanXiang
- first_name: Jan
full_name: Sedlacik, Jan
last_name: Sedlacik
- first_name: Jürgen R.
full_name: Schwarz, Jürgen R.
last_name: Schwarz
- first_name: Frank F.
full_name: Heisler, Frank F.
last_name: Heisler
- first_name: Kira V.
full_name: Gromova, Kira V.
last_name: Gromova
- first_name: Edda
full_name: Thies, Edda
last_name: Thies
- first_name: Petra
full_name: Breiden, Petra
last_name: Breiden
- first_name: Yvonne
full_name: Pechmann, Yvonne
last_name: Pechmann
- first_name: Michael R.
full_name: Kreutz, Michael R.
last_name: Kreutz
- first_name: Matthias
full_name: Kneussel, Matthias
last_name: Kneussel
citation:
ama: Muhia MW, YuanXiang P, Sedlacik J, et al. Muskelin regulates actin-dependent
synaptic changes and intrinsic brain activity relevant to behavioral and cognitive
processes. Communications Biology. 2022;5. doi:10.1038/s42003-022-03446-1
apa: Muhia, M. W., YuanXiang, P., Sedlacik, J., Schwarz, J. R., Heisler, F. F.,
Gromova, K. V., … Kneussel, M. (2022). Muskelin regulates actin-dependent synaptic
changes and intrinsic brain activity relevant to behavioral and cognitive processes.
Communications Biology. Springer Nature. https://doi.org/10.1038/s42003-022-03446-1
chicago: Muhia, Mary W, PingAn YuanXiang, Jan Sedlacik, Jürgen R. Schwarz, Frank
F. Heisler, Kira V. Gromova, Edda Thies, et al. “Muskelin Regulates Actin-Dependent
Synaptic Changes and Intrinsic Brain Activity Relevant to Behavioral and Cognitive
Processes.” Communications Biology. Springer Nature, 2022. https://doi.org/10.1038/s42003-022-03446-1.
ieee: M. W. Muhia et al., “Muskelin regulates actin-dependent synaptic changes
and intrinsic brain activity relevant to behavioral and cognitive processes,”
Communications Biology, vol. 5. Springer Nature, 2022.
ista: Muhia MW, YuanXiang P, Sedlacik J, Schwarz JR, Heisler FF, Gromova KV, Thies
E, Breiden P, Pechmann Y, Kreutz MR, Kneussel M. 2022. Muskelin regulates actin-dependent
synaptic changes and intrinsic brain activity relevant to behavioral and cognitive
processes. Communications Biology. 5, 589.
mla: Muhia, Mary W., et al. “Muskelin Regulates Actin-Dependent Synaptic Changes
and Intrinsic Brain Activity Relevant to Behavioral and Cognitive Processes.”
Communications Biology, vol. 5, 589, Springer Nature, 2022, doi:10.1038/s42003-022-03446-1.
short: M.W. Muhia, P. YuanXiang, J. Sedlacik, J.R. Schwarz, F.F. Heisler, K.V. Gromova,
E. Thies, P. Breiden, Y. Pechmann, M.R. Kreutz, M. Kneussel, Communications Biology
5 (2022).
date_created: 2023-01-16T09:48:19Z
date_published: 2022-06-15T00:00:00Z
date_updated: 2023-08-04T09:25:59Z
day: '15'
ddc:
- '570'
department:
- _id: PreCl
doi: 10.1038/s42003-022-03446-1
external_id:
isi:
- '000811777900003'
file:
- access_level: open_access
checksum: bd95be1e77090208b79bc45ea8785d0b
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T08:23:46Z
date_updated: 2023-01-27T08:23:46Z
file_id: '12417'
file_name: 2022_CommBiology_Muhia.pdf
file_size: 3968356
relation: main_file
success: 1
file_date_updated: 2023-01-27T08:23:46Z
has_accepted_license: '1'
intvolume: ' 5'
isi: 1
keyword:
- General Agricultural and Biological Sciences
- General Biochemistry
- Genetics and Molecular Biology
- Medicine (miscellaneous)
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: Communications Biology
publication_identifier:
issn:
- 2399-3642
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Muskelin regulates actin-dependent synaptic changes and intrinsic brain activity
relevant to behavioral and cognitive processes
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 5
year: '2022'
...
---
_id: '12225'
abstract:
- lang: eng
text: In social networks, users often engage with like-minded peers. This selective
exposure to opinions might result in echo chambers, i.e., political fragmentation
and social polarization of user interactions. When echo chambers form, opinions
have a bimodal distribution with two peaks on opposite sides. In certain issues,
where either extreme positions contain a degree of misinformation, neutral consensus
is preferable for promoting discourse. In this paper, we use an opinion dynamics
model that naturally forms echo chambers in order to find a feedback mechanism
that bridges these communities and leads to a neutral consensus. We introduce the
random dynamical nudge (RDN), which presents each agent
with input from a random selection of other agents’ opinions and does not require
surveillance of every person’s opinions. Our computational results in two different
models suggest that the RDN leads to a unimodal distribution of opinions centered
around the neutral consensus. Furthermore, the RDN is effective both for preventing
the formation of echo chambers and also for depolarizing existing echo chambers.
Due to the simple and robust nature of the RDN, social media networks might be
able to implement a version of this self-feedback mechanism, when appropriate,
to prevent the segregation of online communities on complex social issues.
acknowledgement: CBC and AKN would like to thank Neuromatch Academy https://www.neuromatchacademy.org
for introducing the authors to each other. We thank Dr. Krešimir Josic (University
of Houston) , Fabian Baumann (Humboldt University) and Dr. Igor M. Sokolov (Humboldt
University) for carefully reading the early versions of the manuscript and providing
constructive feedback. CBC is supported by the German Deutscher Akademischer Austauschdienst
(DAAD, https://daad.de), the South African National Research Foundation (NRF, https://nrf.ac.za),
the University of Cape Town (UCT, https://uct.ac.za), and the NOMIS Foundation through
the NOMIS Fellowships at IST Austria program (https://nomisfoundation.ch). SVV appreciate
the generosity of Tecnológico de Monterrey for covering the publication fee.
article_number: '9234'
article_processing_charge: No
article_type: original
author:
- first_name: Christopher
full_name: Currin, Christopher
id: e8321fc5-3091-11eb-8a53-83f309a11ac9
last_name: Currin
orcid: 0000-0002-4809-5059
- first_name: Sebastián Vallejo
full_name: Vera, Sebastián Vallejo
last_name: Vera
- first_name: Ali
full_name: Khaledi-Nasab, Ali
last_name: Khaledi-Nasab
citation:
ama: Currin C, Vera SV, Khaledi-Nasab A. Depolarization of echo chambers by random
dynamical nudge. Scientific Reports. 2022;12. doi:10.1038/s41598-022-12494-w
apa: Currin, C., Vera, S. V., & Khaledi-Nasab, A. (2022). Depolarization of
echo chambers by random dynamical nudge. Scientific Reports. Springer Nature.
https://doi.org/10.1038/s41598-022-12494-w
chicago: Currin, Christopher, Sebastián Vallejo Vera, and Ali Khaledi-Nasab. “Depolarization
of Echo Chambers by Random Dynamical Nudge.” Scientific Reports. Springer
Nature, 2022. https://doi.org/10.1038/s41598-022-12494-w.
ieee: C. Currin, S. V. Vera, and A. Khaledi-Nasab, “Depolarization of echo chambers
by random dynamical nudge,” Scientific Reports, vol. 12. Springer Nature,
2022.
ista: Currin C, Vera SV, Khaledi-Nasab A. 2022. Depolarization of echo chambers
by random dynamical nudge. Scientific Reports. 12, 9234.
mla: Currin, Christopher, et al. “Depolarization of Echo Chambers by Random Dynamical
Nudge.” Scientific Reports, vol. 12, 9234, Springer Nature, 2022, doi:10.1038/s41598-022-12494-w.
short: C. Currin, S.V. Vera, A. Khaledi-Nasab, Scientific Reports 12 (2022).
date_created: 2023-01-16T09:48:30Z
date_published: 2022-06-02T00:00:00Z
date_updated: 2023-08-04T09:26:30Z
day: '02'
ddc:
- '570'
department:
- _id: TiVo
doi: 10.1038/s41598-022-12494-w
external_id:
isi:
- '000805561200024'
pmid:
- '35654942'
file:
- access_level: open_access
checksum: e024a75f14ce5667795a31e44a259c52
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T08:56:18Z
date_updated: 2023-01-27T08:56:18Z
file_id: '12418'
file_name: 2022_ScientificReports_Currin.pdf
file_size: 3625627
relation: main_file
success: 1
file_date_updated: 2023-01-27T08:56:18Z
has_accepted_license: '1'
intvolume: ' 12'
isi: 1
keyword:
- Multidisciplinary
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: Scientific Reports
publication_identifier:
issn:
- 2045-2322
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Depolarization of echo chambers by random dynamical nudge
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 12
year: '2022'
...
---
_id: '12226'
abstract:
- lang: eng
text: "Background: Biases of DNA repair can shape the nucleotide landscape of genomes
at evolutionary timescales. The molecular mechanisms of those biases are still
poorly understood because it is difficult to isolate the contributions of DNA
repair from those of DNA damage.\r\n\r\nResults: Here, we develop a genome-wide
assay whereby the same DNA lesion is repaired in different genomic contexts. We
insert thousands of barcoded transposons carrying a reporter of DNA mismatch repair
in the genome of mouse embryonic stem cells. Upon inducing a double-strand break
between tandem repeats, a mismatch is generated if the break is repaired through
single-strand annealing. The resolution of the mismatch showed a 60–80% bias in
favor of the strand with the longest 3′ flap. The location of the lesion in the
genome and the type of mismatch had little influence on the bias. Instead, we
observe a complete reversal of the bias when the longest 3′ flap is moved to the
opposite strand by changing the position of the double-strand break in the reporter.\r\n\r\nConclusions:
These results suggest that the processing of the double-strand break has a major
influence on the repair of mismatches during single-strand annealing."
acknowledgement: We acknowledge the financial support of the Natural Sciences and
Engineering Research Council of Canada (NSERC RGPIN-2020-06377), the Spanish Ministry
of Economy, Industry and Competitiveness (“Centro de Excelencia Severo Ochoa 2013-2017”,
Plan Estatal PGC2018-099807-B-I00), of the CERCA Programme/Generalitat de Catalunya,
and of the European Research Council (Synergy Grant 609989). VOP was supported by
the European Union’s Horizon 2020 research and innovation program under the Marie
Skłodowska-Curie programme (665385). We also acknowledge the support of the Spanish
Ministry of Economy and Competitiveness (MEIC) to the EMBL partnership.
article_number: '93'
article_processing_charge: No
article_type: original
author:
- first_name: Victoria
full_name: Pokusaeva, Victoria
id: 3184041C-F248-11E8-B48F-1D18A9856A87
last_name: Pokusaeva
orcid: 0000-0001-7660-444X
- first_name: Aránzazu Rosado
full_name: Diez, Aránzazu Rosado
last_name: Diez
- first_name: Lorena
full_name: Espinar, Lorena
last_name: Espinar
- first_name: Albert Torelló
full_name: Pérez, Albert Torelló
last_name: Pérez
- first_name: Guillaume J.
full_name: Filion, Guillaume J.
last_name: Filion
citation:
ama: Pokusaeva V, Diez AR, Espinar L, Pérez AT, Filion GJ. Strand asymmetry influences
mismatch resolution during single-strand annealing. Genome Biology. 2022;23.
doi:10.1186/s13059-022-02665-3
apa: Pokusaeva, V., Diez, A. R., Espinar, L., Pérez, A. T., & Filion, G. J.
(2022). Strand asymmetry influences mismatch resolution during single-strand annealing.
Genome Biology. Springer Nature. https://doi.org/10.1186/s13059-022-02665-3
chicago: Pokusaeva, Victoria, Aránzazu Rosado Diez, Lorena Espinar, Albert Torelló
Pérez, and Guillaume J. Filion. “Strand Asymmetry Influences Mismatch Resolution
during Single-Strand Annealing.” Genome Biology. Springer Nature, 2022.
https://doi.org/10.1186/s13059-022-02665-3.
ieee: V. Pokusaeva, A. R. Diez, L. Espinar, A. T. Pérez, and G. J. Filion, “Strand
asymmetry influences mismatch resolution during single-strand annealing,” Genome
Biology, vol. 23. Springer Nature, 2022.
ista: Pokusaeva V, Diez AR, Espinar L, Pérez AT, Filion GJ. 2022. Strand asymmetry
influences mismatch resolution during single-strand annealing. Genome Biology.
23, 93.
mla: Pokusaeva, Victoria, et al. “Strand Asymmetry Influences Mismatch Resolution
during Single-Strand Annealing.” Genome Biology, vol. 23, 93, Springer
Nature, 2022, doi:10.1186/s13059-022-02665-3.
short: V. Pokusaeva, A.R. Diez, L. Espinar, A.T. Pérez, G.J. Filion, Genome Biology
23 (2022).
date_created: 2023-01-16T09:48:44Z
date_published: 2022-04-12T00:00:00Z
date_updated: 2023-08-04T09:27:00Z
day: '12'
ddc:
- '570'
department:
- _id: MaJö
doi: 10.1186/s13059-022-02665-3
ec_funded: 1
external_id:
isi:
- '000781953800001'
pmid:
- '35414014'
file:
- access_level: open_access
checksum: 17bb091fec04d82ba20a3458c4cfd2bd
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T09:01:40Z
date_updated: 2023-01-27T09:01:40Z
file_id: '12419'
file_name: 2022_GenomeBiology_Pokusaeva.pdf
file_size: 4939342
relation: main_file
success: 1
file_date_updated: 2023-01-27T09:01:40Z
has_accepted_license: '1'
intvolume: ' 23'
isi: 1
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
publication: Genome Biology
publication_identifier:
issn:
- 1474-760X
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
link:
- relation: software
url: 'https://github.com/cellcomplexitylab/strand_asymmetry '
- relation: software
url: https://hub.docker.com/r/gui11aume/strand_asymmetry
scopus_import: '1'
status: public
title: Strand asymmetry influences mismatch resolution during single-strand annealing
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 23
year: '2022'
...
---
_id: '12227'
abstract:
- lang: eng
text: Polydicyclopentadiene (pDCPD), a thermoset with excellent mechanical properties,
has enormous potential as a lightweight, tough, and stable matrix material owing
to its highly cross-linked macromolecular network. This work describes generating
pDCPD-based foams and hierarchically porous carbons derived therefrom by combining
ring-opening metathesis polymerization (ROMP) of DCPD, high internal phase emulsions
(HIPEs) as structural templates, and subsequent carbonization. The structure and
function of the carbon foams were characterized and discussed in detail using
scanning electron, transmission electron, or atomic force microscopy (SEM, TEM,
AFM), electron energy-loss spectroscopy (TEM-EELS), N2 sorption, and analyses
of electrical conductivity as well as mechanical properties. The resulting materials
exhibited uniform, shape-retaining shrinkage of only ∼1/3 after carbonization.
No structural failure was observed even when the pDCPD precursor foams were heated
to 1400 °C. Instead, the high porosity, void size, and 3D interconnectivity were
fully preserved, and the void diameters could be adjusted between 87 and 2.5 μm.
Moreover, foams have a carbon content >97%, an electronic conductivity of up to
2800 S·m–1, a Young’s modulus of up to 2.1 GPa, and a specific surface area of
up to 1200 m2·g–1. Surprisingly, the pDCPD foams were carbonized into shapes other
than monoliths, such as 10’s of micron thick membranes or foamy coatings adhered
to a metal foil or grid substrate. The latter coatings even adhere upon bending.
Finally, as a use case, carbonized foams were applied as porous cathodes for Li–O2
batteries where the foams show a favorable combination of porosity, active surface
area, and pore size for outstanding capacity.
acknowledgement: S.K. acknowledges the financial support from the Slovenian Research
Agency (grants P1-0021, P2-0150). Support by Graz University of Technology (LP-03
– Porous Materials@Work) and from VARTA Innovation GmbH is kindly acknowledged.
We thank Umicore for providing the initiator and Matjaž Mazaj (National Institute
of Chemistry, Ljubljana) and Karel Jerabek (Czech Academy of Sciences) for measurements
and fruitful discussions. S.A.F. is indebted to the Austrian Federal Ministry of
Science, Research and Economy; the Austrian Research Promotion Agency (Grant No.
845364); and ISTA for support.
article_processing_charge: No
article_type: original
author:
- first_name: Sebastijan
full_name: Kovačič, Sebastijan
last_name: Kovačič
- first_name: Bettina
full_name: Schafzahl, Bettina
last_name: Schafzahl
- first_name: Nadejda B.
full_name: Matsko, Nadejda B.
last_name: Matsko
- first_name: Katharina
full_name: Gruber, Katharina
last_name: Gruber
- first_name: Martin
full_name: Schmuck, Martin
last_name: Schmuck
- first_name: Stefan
full_name: Koller, Stefan
last_name: Koller
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
- first_name: Christian
full_name: Slugovc, Christian
last_name: Slugovc
citation:
ama: 'Kovačič S, Schafzahl B, Matsko NB, et al. Carbon foams via ring-opening metathesis
polymerization of emulsion templates: A facile method to make carbon current collectors
for battery applications. ACS Applied Energy Materials. 2022;5(11):14381-14390.
doi:10.1021/acsaem.2c02787'
apa: 'Kovačič, S., Schafzahl, B., Matsko, N. B., Gruber, K., Schmuck, M., Koller,
S., … Slugovc, C. (2022). Carbon foams via ring-opening metathesis polymerization
of emulsion templates: A facile method to make carbon current collectors for battery
applications. ACS Applied Energy Materials. American Chemical Society.
https://doi.org/10.1021/acsaem.2c02787'
chicago: 'Kovačič, Sebastijan, Bettina Schafzahl, Nadejda B. Matsko, Katharina Gruber,
Martin Schmuck, Stefan Koller, Stefan Alexander Freunberger, and Christian Slugovc.
“Carbon Foams via Ring-Opening Metathesis Polymerization of Emulsion Templates:
A Facile Method to Make Carbon Current Collectors for Battery Applications.” ACS
Applied Energy Materials. American Chemical Society, 2022. https://doi.org/10.1021/acsaem.2c02787.'
ieee: 'S. Kovačič et al., “Carbon foams via ring-opening metathesis polymerization
of emulsion templates: A facile method to make carbon current collectors for battery
applications,” ACS Applied Energy Materials, vol. 5, no. 11. American Chemical
Society, pp. 14381–14390, 2022.'
ista: 'Kovačič S, Schafzahl B, Matsko NB, Gruber K, Schmuck M, Koller S, Freunberger
SA, Slugovc C. 2022. Carbon foams via ring-opening metathesis polymerization of
emulsion templates: A facile method to make carbon current collectors for battery
applications. ACS Applied Energy Materials. 5(11), 14381–14390.'
mla: 'Kovačič, Sebastijan, et al. “Carbon Foams via Ring-Opening Metathesis Polymerization
of Emulsion Templates: A Facile Method to Make Carbon Current Collectors for Battery
Applications.” ACS Applied Energy Materials, vol. 5, no. 11, American Chemical
Society, 2022, pp. 14381–90, doi:10.1021/acsaem.2c02787.'
short: S. Kovačič, B. Schafzahl, N.B. Matsko, K. Gruber, M. Schmuck, S. Koller,
S.A. Freunberger, C. Slugovc, ACS Applied Energy Materials 5 (2022) 14381–14390.
date_created: 2023-01-16T09:48:53Z
date_published: 2022-10-16T00:00:00Z
date_updated: 2023-08-04T09:27:32Z
day: '16'
ddc:
- '540'
department:
- _id: StFr
doi: 10.1021/acsaem.2c02787
external_id:
isi:
- '000875635900001'
file:
- access_level: open_access
checksum: 572d15c250ab83d44f4e2c3aeb5f7388
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T09:09:15Z
date_updated: 2023-01-27T09:09:15Z
file_id: '12420'
file_name: 2022_AppliedEnergyMaterials_Kovacic.pdf
file_size: 13105589
relation: main_file
success: 1
file_date_updated: 2023-01-27T09:09:15Z
has_accepted_license: '1'
intvolume: ' 5'
isi: 1
issue: '11'
keyword:
- Electrical and Electronic Engineering
- Materials Chemistry
- Electrochemistry
- Energy Engineering and Power Technology
- Chemical Engineering (miscellaneous)
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 14381-14390
publication: ACS Applied Energy Materials
publication_identifier:
issn:
- 2574-0962
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Carbon foams via ring-opening metathesis polymerization of emulsion templates:
A facile method to make carbon current collectors for battery applications'
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 5
year: '2022'
...
---
_id: '12228'
abstract:
- lang: eng
text: The question of how RNA, as the principal carrier of genetic information evolved
is fundamentally important for our understanding of the origin of life. The RNA
molecule is far too complex to have formed in one evolutionary step, suggesting
that ancestral proto-RNAs (first ancestor of RNA) may have existed, which evolved
over time into the RNA of today. Here we show that isoxazole nucleosides, which
are quickly formed from hydroxylamine, cyanoacetylene, urea and ribose, are plausible
precursors for RNA. The isoxazole nucleoside can rearrange within an RNA-strand
to give cytidine, which leads to an increase of pairing stability. If the proto-RNA
contains a canonical seed-nucleoside with defined stereochemistry, the seed-nucleoside
can control the configuration of the anomeric center that forms during the in-RNA
transformation. The results demonstrate that RNA could have emerged from evolutionarily
primitive precursor isoxazole ribosides after strand formation.
acknowledgement: We thank Stefan Wiedemann for the synthesis of reference compounds
and Pia Heinrichs for assistance in the NMR measurements of the oligonucleotides.
We also thank Dr. Luis Escobar and Jonas Feldmann for valued discussions. This work
was supported by the German Research Foundation (DFG) for financial support via
CRC1309 (Project ID 325871075, A04), CRC1361 (Project ID 893547839, P02) and CRC1032
(Project ID 201269156, A5). This project has received funding from the European
Research Council (ERC) under the European Union's Horizon 2020 research and innovation
program under grant agreement No 741912 (EpiR). We are grateful for additional funding
from the Volkswagen Foundation (EvoRib). Open Access funding enabled and organized
by Projekt DEAL.
article_number: e202211945
article_processing_charge: No
article_type: original
author:
- first_name: Felix
full_name: Xu, Felix
last_name: Xu
- first_name: Antony
full_name: Crisp, Antony
last_name: Crisp
- first_name: Thea
full_name: Schinkel, Thea
last_name: Schinkel
- first_name: Romeo C. A.
full_name: Dubini, Romeo C. A.
last_name: Dubini
- first_name: Sarah
full_name: Hübner, Sarah
last_name: Hübner
- first_name: Sidney
full_name: Becker, Sidney
last_name: Becker
- first_name: Florian
full_name: Schelter, Florian
last_name: Schelter
- first_name: Petra
full_name: Rovo, Petra
id: c316e53f-b965-11eb-b128-bb26acc59c00
last_name: Rovo
orcid: 0000-0001-8729-7326
- first_name: Thomas
full_name: Carell, Thomas
last_name: Carell
citation:
ama: Xu F, Crisp A, Schinkel T, et al. Isoxazole nucleosides as building blocks
for a plausible proto‐RNA. Angewandte Chemie International Edition. 2022;61(45).
doi:10.1002/anie.202211945
apa: Xu, F., Crisp, A., Schinkel, T., Dubini, R. C. A., Hübner, S., Becker, S.,
… Carell, T. (2022). Isoxazole nucleosides as building blocks for a plausible
proto‐RNA. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202211945
chicago: Xu, Felix, Antony Crisp, Thea Schinkel, Romeo C. A. Dubini, Sarah Hübner,
Sidney Becker, Florian Schelter, Petra Rovo, and Thomas Carell. “Isoxazole Nucleosides
as Building Blocks for a Plausible Proto‐RNA.” Angewandte Chemie International
Edition. Wiley, 2022. https://doi.org/10.1002/anie.202211945.
ieee: F. Xu et al., “Isoxazole nucleosides as building blocks for a plausible
proto‐RNA,” Angewandte Chemie International Edition, vol. 61, no. 45. Wiley,
2022.
ista: Xu F, Crisp A, Schinkel T, Dubini RCA, Hübner S, Becker S, Schelter F, Rovo
P, Carell T. 2022. Isoxazole nucleosides as building blocks for a plausible proto‐RNA.
Angewandte Chemie International Edition. 61(45), e202211945.
mla: Xu, Felix, et al. “Isoxazole Nucleosides as Building Blocks for a Plausible
Proto‐RNA.” Angewandte Chemie International Edition, vol. 61, no. 45, e202211945,
Wiley, 2022, doi:10.1002/anie.202211945.
short: F. Xu, A. Crisp, T. Schinkel, R.C.A. Dubini, S. Hübner, S. Becker, F. Schelter,
P. Rovo, T. Carell, Angewandte Chemie International Edition 61 (2022).
date_created: 2023-01-16T09:49:05Z
date_published: 2022-11-07T00:00:00Z
date_updated: 2023-08-04T09:32:42Z
day: '07'
ddc:
- '540'
department:
- _id: NMR
doi: 10.1002/anie.202211945
external_id:
isi:
- '000866428500001'
file:
- access_level: open_access
checksum: 4e8152454d12025d13f6e6e9ca06b5d0
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T10:28:45Z
date_updated: 2023-01-27T10:28:45Z
file_id: '12422'
file_name: 2022_AngewandteChemieInternat_Xu.pdf
file_size: 1076715
relation: main_file
success: 1
file_date_updated: 2023-01-27T10:28:45Z
has_accepted_license: '1'
intvolume: ' 61'
isi: 1
issue: '45'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Isoxazole nucleosides as building blocks for a plausible proto‐RNA
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 61
year: '2022'
...
---
_id: '12229'
abstract:
- lang: eng
text: "We present Bullshark, the first directed acyclic graph (DAG) based asynchronous
Byzantine Atomic Broadcast protocol that is optimized for the common synchronous
case. Like previous DAG-based BFT protocols [19, 25], Bullshark requires no extra
communication to achieve consensus on top of building the DAG. That is, parties
can totally order the vertices of the DAG by interpreting their local view of
the DAG edges. Unlike other asynchronous DAG-based protocols, Bullshark provides
a practical low latency fast-path that exploits synchronous periods and deprecates
the need for notoriously complex view-change and view-synchronization mechanisms.
Bullshark achieves this while maintaining all the desired properties of its predecessor
DAG-Rider [25]. Namely, it has optimal amortized communication complexity, it
provides fairness and asynchronous liveness, and safety is guaranteed even under
a quantum adversary.\r\n\r\nIn order to show the practicality and simplicity of
our approach, we also introduce a standalone partially synchronous version of
Bullshark, which we evaluate against the state of the art. The implemented protocol
is embarrassingly simple (200 LOC on top of an existing DAG-based mempool implementation).
It is highly efficient, achieving for example, 125,000 transactions per second
with a 2 seconds latency for a deployment of 50 parties. In the same setting,
the state of the art pays a steep 50% latency increase as it optimizes for asynchrony."
article_processing_charge: No
arxiv: 1
author:
- first_name: Alexander
full_name: Spiegelman, Alexander
last_name: Spiegelman
- first_name: Neil
full_name: Giridharan, Neil
last_name: Giridharan
- first_name: Alberto
full_name: Sonnino, Alberto
last_name: Sonnino
- first_name: Eleftherios
full_name: Kokoris Kogias, Eleftherios
id: f5983044-d7ef-11ea-ac6d-fd1430a26d30
last_name: Kokoris Kogias
citation:
ama: 'Spiegelman A, Giridharan N, Sonnino A, Kokoris Kogias E. Bullshark: DAG BFT
protocols made practical. In: Proceedings of the 2022 ACM SIGSAC Conference
on Computer and Communications Security. Association for Computing Machinery;
2022:2705–2718. doi:10.1145/3548606.3559361'
apa: 'Spiegelman, A., Giridharan, N., Sonnino, A., & Kokoris Kogias, E. (2022).
Bullshark: DAG BFT protocols made practical. In Proceedings of the 2022 ACM
SIGSAC Conference on Computer and Communications Security (pp. 2705–2718).
Los Angeles, CA, United States: Association for Computing Machinery. https://doi.org/10.1145/3548606.3559361'
chicago: 'Spiegelman, Alexander, Neil Giridharan, Alberto Sonnino, and Eleftherios
Kokoris Kogias. “Bullshark: DAG BFT Protocols Made Practical.” In Proceedings
of the 2022 ACM SIGSAC Conference on Computer and Communications Security,
2705–2718. Association for Computing Machinery, 2022. https://doi.org/10.1145/3548606.3559361.'
ieee: 'A. Spiegelman, N. Giridharan, A. Sonnino, and E. Kokoris Kogias, “Bullshark:
DAG BFT protocols made practical,” in Proceedings of the 2022 ACM SIGSAC Conference
on Computer and Communications Security, Los Angeles, CA, United States, 2022,
pp. 2705–2718.'
ista: 'Spiegelman A, Giridharan N, Sonnino A, Kokoris Kogias E. 2022. Bullshark:
DAG BFT protocols made practical. Proceedings of the 2022 ACM SIGSAC Conference
on Computer and Communications Security. CCS: CConference on Computer and Communications
Security, 2705–2718.'
mla: 'Spiegelman, Alexander, et al. “Bullshark: DAG BFT Protocols Made Practical.”
Proceedings of the 2022 ACM SIGSAC Conference on Computer and Communications
Security, Association for Computing Machinery, 2022, pp. 2705–2718, doi:10.1145/3548606.3559361.'
short: A. Spiegelman, N. Giridharan, A. Sonnino, E. Kokoris Kogias, in:, Proceedings
of the 2022 ACM SIGSAC Conference on Computer and Communications Security, Association
for Computing Machinery, 2022, pp. 2705–2718.
conference:
end_date: 2022-11-11
location: Los Angeles, CA, United States
name: 'CCS: CConference on Computer and Communications Security'
start_date: 2022-11-07
date_created: 2023-01-16T09:49:48Z
date_published: 2022-11-01T00:00:00Z
date_updated: 2023-01-27T10:33:17Z
day: '01'
department:
- _id: ElKo
doi: 10.1145/3548606.3559361
external_id:
arxiv:
- '2201.05677'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.48550/arXiv.2201.05677
month: '11'
oa: 1
oa_version: Preprint
page: 2705–2718
publication: Proceedings of the 2022 ACM SIGSAC Conference on Computer and Communications
Security
publication_identifier:
isbn:
- '9781450394505'
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Bullshark: DAG BFT protocols made practical'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '12231'
abstract:
- lang: eng
text: Ventral tail bending, which is transient but pronounced, is found in many
chordate embryos and constitutes an interesting model of how tissue interactions
control embryo shape. Here, we identify one key upstream regulator of ventral
tail bending in embryos of the ascidian Ciona. We show that during the early tailbud
stages, ventral epidermal cells exhibit a boat-shaped morphology (boat cell) with
a narrow apical surface where phosphorylated myosin light chain (pMLC) accumulates.
We further show that interfering with the function of the BMP ligand Admp led
to pMLC localizing to the basal instead of the apical side of ventral epidermal
cells and a reduced number of boat cells. Finally, we show that cutting ventral
epidermal midline cells at their apex using an ultraviolet laser relaxed ventral
tail bending. Based on these results, we propose a previously unreported function
for Admp in localizing pMLC to the apical side of ventral epidermal cells, which
causes the tail to bend ventrally by resisting antero-posterior notochord extension
at the ventral side of the tail.
acknowledgement: "iona intestinalis adults were provided by Dr Yutaka Satou (Kyoto
University) and Dr Manabu Yoshida (the University of Tokyo) with support from the
National Bio-Resource Project of AMED, Japan. We thank Dr Hidehiko Hashimoto and
Dr Yuji Mizotani for technical information about 1P-myosin antibody staining. We
thank Dr Kaoru Imai and Dr Yutaka Satou for valuable discussion about Admp and for
the DNA construct of Bmp2/4 under the Dlx.b upstream sequence. We thank Ms Maki
Kogure for constructing the FUSION360 of the intercalating epidermal cell.\r\nThis
work was supported by funding from the Japan Society for the Promotion of Science
(JP16H01451, JP21H00440). Open Access funding provided by Keio University: Keio
Gijuku Daigaku."
article_number: dev200215
article_processing_charge: No
article_type: original
author:
- first_name: Yuki S.
full_name: Kogure, Yuki S.
last_name: Kogure
- first_name: Hiromochi
full_name: Muraoka, Hiromochi
last_name: Muraoka
- first_name: Wataru C.
full_name: Koizumi, Wataru C.
last_name: Koizumi
- first_name: Raphaël
full_name: Gelin-alessi, Raphaël
last_name: Gelin-alessi
- first_name: Benoit G
full_name: Godard, Benoit G
id: 3263621A-F248-11E8-B48F-1D18A9856A87
last_name: Godard
- first_name: Kotaro
full_name: Oka, Kotaro
last_name: Oka
- first_name: Carl-Philipp J
full_name: Heisenberg, Carl-Philipp J
id: 39427864-F248-11E8-B48F-1D18A9856A87
last_name: Heisenberg
orcid: 0000-0002-0912-4566
- first_name: Kohji
full_name: Hotta, Kohji
last_name: Hotta
citation:
ama: Kogure YS, Muraoka H, Koizumi WC, et al. Admp regulates tail bending by controlling
ventral epidermal cell polarity via phosphorylated myosin localization in Ciona.
Development. 2022;149(21). doi:10.1242/dev.200215
apa: Kogure, Y. S., Muraoka, H., Koizumi, W. C., Gelin-alessi, R., Godard, B. G.,
Oka, K., … Hotta, K. (2022). Admp regulates tail bending by controlling ventral
epidermal cell polarity via phosphorylated myosin localization in Ciona. Development.
The Company of Biologists. https://doi.org/10.1242/dev.200215
chicago: Kogure, Yuki S., Hiromochi Muraoka, Wataru C. Koizumi, Raphaël Gelin-alessi,
Benoit G Godard, Kotaro Oka, Carl-Philipp J Heisenberg, and Kohji Hotta. “Admp
Regulates Tail Bending by Controlling Ventral Epidermal Cell Polarity via Phosphorylated
Myosin Localization in Ciona.” Development. The Company of Biologists,
2022. https://doi.org/10.1242/dev.200215.
ieee: Y. S. Kogure et al., “Admp regulates tail bending by controlling ventral
epidermal cell polarity via phosphorylated myosin localization in Ciona,” Development,
vol. 149, no. 21. The Company of Biologists, 2022.
ista: Kogure YS, Muraoka H, Koizumi WC, Gelin-alessi R, Godard BG, Oka K, Heisenberg
C-PJ, Hotta K. 2022. Admp regulates tail bending by controlling ventral epidermal
cell polarity via phosphorylated myosin localization in Ciona. Development. 149(21),
dev200215.
mla: Kogure, Yuki S., et al. “Admp Regulates Tail Bending by Controlling Ventral
Epidermal Cell Polarity via Phosphorylated Myosin Localization in Ciona.” Development,
vol. 149, no. 21, dev200215, The Company of Biologists, 2022, doi:10.1242/dev.200215.
short: Y.S. Kogure, H. Muraoka, W.C. Koizumi, R. Gelin-alessi, B.G. Godard, K. Oka,
C.-P.J. Heisenberg, K. Hotta, Development 149 (2022).
date_created: 2023-01-16T09:50:12Z
date_published: 2022-11-01T00:00:00Z
date_updated: 2023-08-04T09:33:24Z
day: '01'
ddc:
- '570'
department:
- _id: CaHe
doi: 10.1242/dev.200215
external_id:
isi:
- '000903991700002'
pmid:
- '36227591'
file:
- access_level: open_access
checksum: 871b9c58eb79b9e60752de25a46938d6
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T10:36:50Z
date_updated: 2023-01-27T10:36:50Z
file_id: '12423'
file_name: 2022_Development_Kogure.pdf
file_size: 9160451
relation: main_file
success: 1
file_date_updated: 2023-01-27T10:36:50Z
has_accepted_license: '1'
intvolume: ' 149'
isi: 1
issue: '21'
keyword:
- Developmental Biology
- Molecular Biology
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
pmid: 1
publication: Development
publication_identifier:
eissn:
- 1477-9129
issn:
- 0950-1991
publication_status: published
publisher: The Company of Biologists
quality_controlled: '1'
scopus_import: '1'
status: public
title: Admp regulates tail bending by controlling ventral epidermal cell polarity
via phosphorylated myosin localization in Ciona
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 149
year: '2022'
...
---
_id: '12232'
abstract:
- lang: eng
text: We derive a precise asymptotic formula for the density of the small singular
values of the real Ginibre matrix ensemble shifted by a complex parameter z as
the dimension tends to infinity. For z away from the real axis the formula coincides
with that for the complex Ginibre ensemble we derived earlier in Cipolloni et
al. (Prob Math Phys 1:101–146, 2020). On the level of the one-point function of
the low lying singular values we thus confirm the transition from real to complex
Ginibre ensembles as the shift parameter z becomes genuinely complex; the analogous
phenomenon has been well known for eigenvalues. We use the superbosonization formula
(Littelmann et al. in Comm Math Phys 283:343–395, 2008) in a regime where the
main contribution comes from a three dimensional saddle manifold.
acknowledgement: Open access funding provided by Swiss Federal Institute of Technology
Zurich. Supported by Dr. Max Rössler, the Walter Haefner Foundation and the ETH
Zürich Foundation.
article_processing_charge: No
article_type: original
author:
- first_name: Giorgio
full_name: Cipolloni, Giorgio
id: 42198EFA-F248-11E8-B48F-1D18A9856A87
last_name: Cipolloni
orcid: 0000-0002-4901-7992
- first_name: László
full_name: Erdös, László
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
- first_name: Dominik J
full_name: Schröder, Dominik J
id: 408ED176-F248-11E8-B48F-1D18A9856A87
last_name: Schröder
orcid: 0000-0002-2904-1856
citation:
ama: Cipolloni G, Erdös L, Schröder DJ. Density of small singular values of the
shifted real Ginibre ensemble. Annales Henri Poincaré. 2022;23(11):3981-4002.
doi:10.1007/s00023-022-01188-8
apa: Cipolloni, G., Erdös, L., & Schröder, D. J. (2022). Density of small singular
values of the shifted real Ginibre ensemble. Annales Henri Poincaré. Springer
Nature. https://doi.org/10.1007/s00023-022-01188-8
chicago: Cipolloni, Giorgio, László Erdös, and Dominik J Schröder. “Density of Small
Singular Values of the Shifted Real Ginibre Ensemble.” Annales Henri Poincaré.
Springer Nature, 2022. https://doi.org/10.1007/s00023-022-01188-8.
ieee: G. Cipolloni, L. Erdös, and D. J. Schröder, “Density of small singular values
of the shifted real Ginibre ensemble,” Annales Henri Poincaré, vol. 23,
no. 11. Springer Nature, pp. 3981–4002, 2022.
ista: Cipolloni G, Erdös L, Schröder DJ. 2022. Density of small singular values
of the shifted real Ginibre ensemble. Annales Henri Poincaré. 23(11), 3981–4002.
mla: Cipolloni, Giorgio, et al. “Density of Small Singular Values of the Shifted
Real Ginibre Ensemble.” Annales Henri Poincaré, vol. 23, no. 11, Springer
Nature, 2022, pp. 3981–4002, doi:10.1007/s00023-022-01188-8.
short: G. Cipolloni, L. Erdös, D.J. Schröder, Annales Henri Poincaré 23 (2022) 3981–4002.
date_created: 2023-01-16T09:50:26Z
date_published: 2022-11-01T00:00:00Z
date_updated: 2023-08-04T09:33:52Z
day: '01'
ddc:
- '510'
department:
- _id: LaEr
doi: 10.1007/s00023-022-01188-8
external_id:
isi:
- '000796323500001'
file:
- access_level: open_access
checksum: 5582f059feeb2f63e2eb68197a34d7dc
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T11:06:47Z
date_updated: 2023-01-27T11:06:47Z
file_id: '12424'
file_name: 2022_AnnalesHenriP_Cipolloni.pdf
file_size: 1333638
relation: main_file
success: 1
file_date_updated: 2023-01-27T11:06:47Z
has_accepted_license: '1'
intvolume: ' 23'
isi: 1
issue: '11'
keyword:
- Mathematical Physics
- Nuclear and High Energy Physics
- Statistical and Nonlinear Physics
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 3981-4002
publication: Annales Henri Poincaré
publication_identifier:
eissn:
- 1424-0661
issn:
- 1424-0637
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Density of small singular values of the shifted real Ginibre ensemble
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 23
year: '2022'
...
---
_id: '12233'
abstract:
- lang: eng
text: A novel recursive list decoding (RLD) algorithm for Reed-Muller (RM) codes
based on successive permutations (SP) of the codeword is presented. A low-complexity
SP scheme applied to a subset of the symmetry group of RM codes is first proposed
to carefully select a good codeword permutation on the fly. Then, the proposed
SP technique is integrated into an improved RLD algorithm that initializes different
decoding paths with random codeword permutations, which are sampled from the full
symmetry group of RM codes. Finally, efficient latency and complexity reduction
schemes are introduced that virtually preserve the error-correction performance
of the proposed decoder. Simulation results demonstrate that at the target frame
error rate of 10−3 for the RM code of length 256 with 163 information bits, the
proposed decoder reduces 6% of the computational complexity and 22% of the decoding
latency of the state-of-the-art semi-parallel simplified successive-cancellation
decoder with fast Hadamard transform (SSC-FHT) that uses 96 permutations from
the full symmetry group of RM codes, while relatively maintaining the error-correction
performance and memory consumption of the semi-parallel permuted SSC-FHT decoder.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Nghia
full_name: Doan, Nghia
last_name: Doan
- first_name: Seyyed Ali
full_name: Hashemi, Seyyed Ali
last_name: Hashemi
- first_name: Marco
full_name: Mondelli, Marco
id: 27EB676C-8706-11E9-9510-7717E6697425
last_name: Mondelli
orcid: 0000-0002-3242-7020
- first_name: Warren J.
full_name: Gross, Warren J.
last_name: Gross
citation:
ama: Doan N, Hashemi SA, Mondelli M, Gross WJ. Decoding Reed-Muller codes with successive
codeword permutations. IEEE Transactions on Communications. 2022;70(11):7134-7145.
doi:10.1109/tcomm.2022.3211101
apa: Doan, N., Hashemi, S. A., Mondelli, M., & Gross, W. J. (2022). Decoding
Reed-Muller codes with successive codeword permutations. IEEE Transactions
on Communications. Institute of Electrical and Electronics Engineers. https://doi.org/10.1109/tcomm.2022.3211101
chicago: Doan, Nghia, Seyyed Ali Hashemi, Marco Mondelli, and Warren J. Gross. “Decoding
Reed-Muller Codes with Successive Codeword Permutations.” IEEE Transactions
on Communications. Institute of Electrical and Electronics Engineers, 2022.
https://doi.org/10.1109/tcomm.2022.3211101.
ieee: N. Doan, S. A. Hashemi, M. Mondelli, and W. J. Gross, “Decoding Reed-Muller
codes with successive codeword permutations,” IEEE Transactions on Communications,
vol. 70, no. 11. Institute of Electrical and Electronics Engineers, pp. 7134–7145,
2022.
ista: Doan N, Hashemi SA, Mondelli M, Gross WJ. 2022. Decoding Reed-Muller codes
with successive codeword permutations. IEEE Transactions on Communications. 70(11),
7134–7145.
mla: Doan, Nghia, et al. “Decoding Reed-Muller Codes with Successive Codeword Permutations.”
IEEE Transactions on Communications, vol. 70, no. 11, Institute of Electrical
and Electronics Engineers, 2022, pp. 7134–45, doi:10.1109/tcomm.2022.3211101.
short: N. Doan, S.A. Hashemi, M. Mondelli, W.J. Gross, IEEE Transactions on Communications
70 (2022) 7134–7145.
date_created: 2023-01-16T09:50:38Z
date_published: 2022-11-01T00:00:00Z
date_updated: 2023-08-04T09:34:43Z
day: '01'
department:
- _id: MaMo
doi: 10.1109/tcomm.2022.3211101
external_id:
arxiv:
- '2109.02122'
isi:
- '000937284600006'
intvolume: ' 70'
isi: 1
issue: '11'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: ' https://doi.org/10.48550/arXiv.2109.02122'
month: '11'
oa: 1
oa_version: Preprint
page: 7134-7145
publication: IEEE Transactions on Communications
publication_identifier:
eissn:
- 1558-0857
issn:
- 0090-6778
publication_status: published
publisher: Institute of Electrical and Electronics Engineers
quality_controlled: '1'
scopus_import: '1'
status: public
title: Decoding Reed-Muller codes with successive codeword permutations
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 70
year: '2022'
...
---
_id: '12234'
abstract:
- lang: eng
text: Hybrid speciation—the origin of new species resulting from the hybridization
of genetically divergent lineages—was once considered rare, but genomic data suggest
that it may occur more often than once thought. In this study, Noguerales and
Ortego found genomic evidence supporting the hybrid origin of a grasshopper that
is able to exploit a broader range of host plants than either of its putative
parents.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Sean
full_name: Stankowski, Sean
id: 43161670-5719-11EA-8025-FABC3DDC885E
last_name: Stankowski
citation:
ama: 'Stankowski S. Digest: On the origin of a possible hybrid species. Evolution.
2022;76(11):2784-2785. doi:10.1111/evo.14632'
apa: 'Stankowski, S. (2022). Digest: On the origin of a possible hybrid species.
Evolution. Wiley. https://doi.org/10.1111/evo.14632'
chicago: 'Stankowski, Sean. “Digest: On the Origin of a Possible Hybrid Species.”
Evolution. Wiley, 2022. https://doi.org/10.1111/evo.14632.'
ieee: 'S. Stankowski, “Digest: On the origin of a possible hybrid species,” Evolution,
vol. 76, no. 11. Wiley, pp. 2784–2785, 2022.'
ista: 'Stankowski S. 2022. Digest: On the origin of a possible hybrid species. Evolution.
76(11), 2784–2785.'
mla: 'Stankowski, Sean. “Digest: On the Origin of a Possible Hybrid Species.” Evolution,
vol. 76, no. 11, Wiley, 2022, pp. 2784–85, doi:10.1111/evo.14632.'
short: S. Stankowski, Evolution 76 (2022) 2784–2785.
date_created: 2023-01-16T09:50:48Z
date_published: 2022-11-01T00:00:00Z
date_updated: 2023-08-04T09:35:48Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/evo.14632
external_id:
isi:
- '000855751600001'
file:
- access_level: open_access
checksum: 4c0f05083b414ac0323a1b9ee1abc275
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T11:28:38Z
date_updated: 2023-01-27T11:28:38Z
file_id: '12425'
file_name: 2022_Evolution_Stankowski.pdf
file_size: 287282
relation: main_file
success: 1
file_date_updated: 2023-01-27T11:28:38Z
has_accepted_license: '1'
intvolume: ' 76'
isi: 1
issue: '11'
keyword:
- General Agricultural and Biological Sciences
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 2784-2785
publication: Evolution
publication_identifier:
eissn:
- 1558-5646
issn:
- 0014-3820
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Digest: On the origin of a possible hybrid species'
tmp:
image: /images/cc_by_nc_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
(CC BY-NC-ND 4.0)
short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 76
year: '2022'
...
---
_id: '12235'
abstract:
- lang: eng
text: "Background: About 800 women die every day worldwide from pregnancy-related
complications, including excessive blood loss, infections and high-blood pressure
(World Health Organization, 2019). To improve screening for high-risk pregnancies,
we set out to identify patterns of maternal hematological changes associated with
future pregnancy complications.\r\n\r\nMethods: Using mixed effects models, we
established changes in 14 complete blood count (CBC) parameters for 1710 healthy
pregnancies and compared them to measurements from 98 pregnancy-induced hypertension,
106 gestational diabetes and 339 postpartum hemorrhage cases.\r\n\r\nResults:
Results show interindividual variations, but good individual repeatability in
CBC values during physiological pregnancies, allowing the identification of specific
alterations in women with obstetric complications. For example, in women with
uncomplicated pregnancies, haemoglobin count decreases of 0.12 g/L (95% CI −0.16,
−0.09) significantly per gestation week (p value <.001). Interestingly, this decrease
is three times more pronounced in women who will develop pregnancy-induced hypertension,
with an additional decrease of 0.39 g/L (95% CI −0.51, −0.26). We also confirm
that obstetric complications and white CBC predict the likelihood of giving birth
earlier during pregnancy.\r\n\r\nConclusion: We provide a comprehensive description
of the associations between haematological changes through pregnancy and three
major obstetric complications to support strategies for prevention, early-diagnosis
and maternal care."
acknowledgement: This project was funded by an SNSF Eccellenza Grant to MRR (PCEGP3-181181),
and by core funding from the Institute of Science and Technology Austria. We would
like to thank the participants of the study and all the midwives and doctors involved
for the computerized obstetrical data from the CHUV Maternity Hospital. Open access
funding provided by Universite de Lausanne.
article_processing_charge: No
article_type: original
author:
- first_name: Marion
full_name: Patxot, Marion
last_name: Patxot
- first_name: Miloš
full_name: Stojanov, Miloš
last_name: Stojanov
- first_name: Sven Erik
full_name: Ojavee, Sven Erik
last_name: Ojavee
- first_name: Rosanna Pescini
full_name: Gobert, Rosanna Pescini
last_name: Gobert
- first_name: Zoltán
full_name: Kutalik, Zoltán
last_name: Kutalik
- first_name: Mathilde
full_name: Gavillet, Mathilde
last_name: Gavillet
- first_name: David
full_name: Baud, David
last_name: Baud
- first_name: Matthew Richard
full_name: Robinson, Matthew Richard
id: E5D42276-F5DA-11E9-8E24-6303E6697425
last_name: Robinson
orcid: 0000-0001-8982-8813
citation:
ama: 'Patxot M, Stojanov M, Ojavee SE, et al. Haematological changes from conception
to childbirth: An indicator of major pregnancy complications. European Journal
of Haematology. 2022;109(5):566-575. doi:10.1111/ejh.13844'
apa: 'Patxot, M., Stojanov, M., Ojavee, S. E., Gobert, R. P., Kutalik, Z., Gavillet,
M., … Robinson, M. R. (2022). Haematological changes from conception to childbirth:
An indicator of major pregnancy complications. European Journal of Haematology.
Wiley. https://doi.org/10.1111/ejh.13844'
chicago: 'Patxot, Marion, Miloš Stojanov, Sven Erik Ojavee, Rosanna Pescini Gobert,
Zoltán Kutalik, Mathilde Gavillet, David Baud, and Matthew Richard Robinson. “Haematological
Changes from Conception to Childbirth: An Indicator of Major Pregnancy Complications.”
European Journal of Haematology. Wiley, 2022. https://doi.org/10.1111/ejh.13844.'
ieee: 'M. Patxot et al., “Haematological changes from conception to childbirth:
An indicator of major pregnancy complications,” European Journal of Haematology,
vol. 109, no. 5. Wiley, pp. 566–575, 2022.'
ista: 'Patxot M, Stojanov M, Ojavee SE, Gobert RP, Kutalik Z, Gavillet M, Baud D,
Robinson MR. 2022. Haematological changes from conception to childbirth: An indicator
of major pregnancy complications. European Journal of Haematology. 109(5), 566–575.'
mla: 'Patxot, Marion, et al. “Haematological Changes from Conception to Childbirth:
An Indicator of Major Pregnancy Complications.” European Journal of Haematology,
vol. 109, no. 5, Wiley, 2022, pp. 566–75, doi:10.1111/ejh.13844.'
short: M. Patxot, M. Stojanov, S.E. Ojavee, R.P. Gobert, Z. Kutalik, M. Gavillet,
D. Baud, M.R. Robinson, European Journal of Haematology 109 (2022) 566–575.
date_created: 2023-01-16T09:50:58Z
date_published: 2022-11-01T00:00:00Z
date_updated: 2023-08-04T09:36:21Z
day: '01'
ddc:
- '570'
- '610'
department:
- _id: MaRo
doi: 10.1111/ejh.13844
external_id:
isi:
- '000849690500001'
pmid:
- '36059200'
file:
- access_level: open_access
checksum: a676d732f67c2990197e34f96b219370
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T11:42:43Z
date_updated: 2023-01-27T11:42:43Z
file_id: '12426'
file_name: 2022_EuropJourHaematology_Patxot.pdf
file_size: 1225073
relation: main_file
success: 1
file_date_updated: 2023-01-27T11:42:43Z
has_accepted_license: '1'
intvolume: ' 109'
isi: 1
issue: '5'
keyword:
- Hematology
- General Medicine
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 566-575
pmid: 1
publication: European Journal of Haematology
publication_identifier:
eissn:
- 1600-0609
issn:
- 0902-4441
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Haematological changes from conception to childbirth: An indicator of major
pregnancy complications'
tmp:
image: /images/cc_by_nc_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
(CC BY-NC-ND 4.0)
short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 109
year: '2022'
...
---
_id: '12236'
abstract:
- lang: eng
text: High-entropy materials offer numerous advantages as catalysts, including a
flexible composition to tune the catalytic activity and selectivity and a large
variety of adsorption/reaction sites for multistep or multiple reactions. Herein,
we report on the synthesis, properties, and electrocatalytic performance of an
amorphous high-entropy boride based on abundant transition metals, CoFeNiMnZnB.
This metal boride provides excellent performance toward the oxygen evolution reaction
(OER), including a low overpotential of 261 mV at 10 mA cm–2, a reduced Tafel
slope of 56.8 mV dec–1, and very high stability. The outstanding OER performance
of CoFeNiMnZnB is attributed to the synergistic interactions between the different
metals, the leaching of Zn ions, the generation of oxygen vacancies, and the in
situ formation of an amorphous oxyhydroxide at the CoFeNiMnZnB surface during
the OER.
acknowledgement: This work was supported by the Spanish MCIN project COMBENERGY (PID2019-105490RB-C32).
X.W. and L.Y. thank the China Scholarship Council (CSC) for the scholarship support.
article_processing_charge: No
article_type: original
author:
- first_name: Xiang
full_name: Wang, Xiang
last_name: Wang
- first_name: Yong
full_name: Zuo, Yong
last_name: Zuo
- first_name: Sharona
full_name: Horta, Sharona
id: 03a7e858-01b1-11ec-8b71-99ae6c4a05bc
last_name: Horta
- first_name: Ren
full_name: He, Ren
last_name: He
- first_name: Linlin
full_name: Yang, Linlin
last_name: Yang
- first_name: Ahmad
full_name: Ostovari Moghaddam, Ahmad
last_name: Ostovari Moghaddam
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Xueqiang
full_name: Qi, Xueqiang
last_name: Qi
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Wang X, Zuo Y, Horta S, et al. CoFeNiMnZnB as a high-entropy metal boride to
boost the oxygen evolution reaction. ACS Applied Materials & Interfaces.
2022;14(42):48212-48219. doi:10.1021/acsami.2c11627
apa: Wang, X., Zuo, Y., Horta, S., He, R., Yang, L., Ostovari Moghaddam, A., … Cabot,
A. (2022). CoFeNiMnZnB as a high-entropy metal boride to boost the oxygen evolution
reaction. ACS Applied Materials & Interfaces. American Chemical Society.
https://doi.org/10.1021/acsami.2c11627
chicago: Wang, Xiang, Yong Zuo, Sharona Horta, Ren He, Linlin Yang, Ahmad Ostovari
Moghaddam, Maria Ibáñez, Xueqiang Qi, and Andreu Cabot. “CoFeNiMnZnB as a High-Entropy
Metal Boride to Boost the Oxygen Evolution Reaction.” ACS Applied Materials
& Interfaces. American Chemical Society, 2022. https://doi.org/10.1021/acsami.2c11627.
ieee: X. Wang et al., “CoFeNiMnZnB as a high-entropy metal boride to boost
the oxygen evolution reaction,” ACS Applied Materials & Interfaces,
vol. 14, no. 42. American Chemical Society, pp. 48212–48219, 2022.
ista: Wang X, Zuo Y, Horta S, He R, Yang L, Ostovari Moghaddam A, Ibáñez M, Qi X,
Cabot A. 2022. CoFeNiMnZnB as a high-entropy metal boride to boost the oxygen
evolution reaction. ACS Applied Materials & Interfaces. 14(42), 48212–48219.
mla: Wang, Xiang, et al. “CoFeNiMnZnB as a High-Entropy Metal Boride to Boost the
Oxygen Evolution Reaction.” ACS Applied Materials & Interfaces, vol.
14, no. 42, American Chemical Society, 2022, pp. 48212–19, doi:10.1021/acsami.2c11627.
short: X. Wang, Y. Zuo, S. Horta, R. He, L. Yang, A. Ostovari Moghaddam, M. Ibáñez,
X. Qi, A. Cabot, ACS Applied Materials & Interfaces 14 (2022) 48212–48219.
date_created: 2023-01-16T09:51:10Z
date_published: 2022-10-14T00:00:00Z
date_updated: 2023-10-04T08:28:14Z
day: '14'
department:
- _id: MaIb
doi: 10.1021/acsami.2c11627
external_id:
isi:
- '000873782700001'
pmid:
- '36239982'
intvolume: ' 14'
isi: 1
issue: '42'
keyword:
- General Materials Science
language:
- iso: eng
month: '10'
oa_version: None
page: 48212-48219
pmid: 1
publication: ACS Applied Materials & Interfaces
publication_identifier:
eissn:
- 1944-8252
issn:
- 1944-8244
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: CoFeNiMnZnB as a high-entropy metal boride to boost the oxygen evolution reaction
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 14
year: '2022'
...