---
_id: '331'
abstract:
- lang: eng
text: We report a procedure to prepare highly monodisperse copper telluride nanocubes,
nanoplates, and nanorods. The procedure is based on the reaction of a copper salt
with trioctylphosphine telluride in the presence of lithium bis(trimethylsilyl)amide
and oleylamine. CuTe nanocrystals display a strong near-infrared optical absorption
associated with localized surface plasmon resonances. We exploit this plasmon
resonance for the design of surface-enhanced Raman scattering sensors for unconventional
optical probes. Furthermore, we also report here our preliminary analysis of the
use of CuTe nanocrystals as cytotoxic and photothermal agents.
article_processing_charge: No
article_type: original
author:
- first_name: Wenhua
full_name: Li, Wenhua
last_name: Li
- first_name: Reza
full_name: Zamani, Reza
last_name: Zamani
- first_name: Pilar
full_name: Rivera Gil, Pilar
last_name: Rivera Gil
- first_name: Beatriz
full_name: Pelaz, Beatriz
last_name: Pelaz
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Ramon
full_name: Alvarez Puebla, Ramon
last_name: Alvarez Puebla
- first_name: Wolfgang
full_name: Parak, Wolfgang
last_name: Parak
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: 'Li W, Zamani R, Rivera Gil P, et al. CuTe nanocrystals: Shape and size control,
plasmonic properties, and use as SERS probes and photothermal agents. Journal
of the American Chemical Society. 2013;135(19):7098-7101. doi:10.1021/ja401428e'
apa: 'Li, W., Zamani, R., Rivera Gil, P., Pelaz, B., Ibáñez, M., Cadavid, D., …
Cabot, A. (2013). CuTe nanocrystals: Shape and size control, plasmonic properties,
and use as SERS probes and photothermal agents. Journal of the American Chemical
Society. ACS. https://doi.org/10.1021/ja401428e'
chicago: 'Li, Wenhua, Reza Zamani, Pilar Rivera Gil, Beatriz Pelaz, Maria Ibáñez,
Doris Cadavid, Alexey Shavel, et al. “CuTe Nanocrystals: Shape and Size Control,
Plasmonic Properties, and Use as SERS Probes and Photothermal Agents.” Journal
of the American Chemical Society. ACS, 2013. https://doi.org/10.1021/ja401428e.'
ieee: 'W. Li et al., “CuTe nanocrystals: Shape and size control, plasmonic
properties, and use as SERS probes and photothermal agents,” Journal of the
American Chemical Society, vol. 135, no. 19. ACS, pp. 7098–7101, 2013.'
ista: 'Li W, Zamani R, Rivera Gil P, Pelaz B, Ibáñez M, Cadavid D, Shavel A, Alvarez
Puebla R, Parak W, Arbiol J, Cabot A. 2013. CuTe nanocrystals: Shape and size
control, plasmonic properties, and use as SERS probes and photothermal agents.
Journal of the American Chemical Society. 135(19), 7098–7101.'
mla: 'Li, Wenhua, et al. “CuTe Nanocrystals: Shape and Size Control, Plasmonic Properties,
and Use as SERS Probes and Photothermal Agents.” Journal of the American Chemical
Society, vol. 135, no. 19, ACS, 2013, pp. 7098–101, doi:10.1021/ja401428e.'
short: W. Li, R. Zamani, P. Rivera Gil, B. Pelaz, M. Ibáñez, D. Cadavid, A. Shavel,
R. Alvarez Puebla, W. Parak, J. Arbiol, A. Cabot, Journal of the American Chemical
Society 135 (2013) 7098–7101.
date_created: 2018-12-11T11:45:51Z
date_published: 2013-04-30T00:00:00Z
date_updated: 2021-01-12T07:42:33Z
day: '30'
doi: 10.1021/ja401428e
extern: '1'
intvolume: ' 135'
issue: '19'
language:
- iso: eng
month: '04'
oa_version: None
page: 7098 - 7101
publication: Journal of the American Chemical Society
publication_status: published
publisher: ACS
publist_id: '7521'
quality_controlled: '1'
status: public
title: 'CuTe nanocrystals: Shape and size control, plasmonic properties, and use as
SERS probes and photothermal agents'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 135
year: '2013'
...
---
_id: '3321'
author:
- first_name: Novi
full_name: Quadrianto, Novi
last_name: Quadrianto
- first_name: Christoph
full_name: Lampert, Christoph
id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
last_name: Lampert
orcid: 0000-0001-8622-7887
citation:
ama: 'Quadrianto N, Lampert C. Kernel based learning. In: Dubitzky W, Wolkenhauer
O, Cho K, Yokota H, eds. Encyclopedia of Systems Biology. Vol 3. Springer;
2013:1069-1069. doi:10.1007/978-1-4419-9863-7_604'
apa: Quadrianto, N., & Lampert, C. (2013). Kernel based learning. In W. Dubitzky,
O. Wolkenhauer, K. Cho, & H. Yokota (Eds.), Encyclopedia of Systems Biology
(Vol. 3, pp. 1069–1069). Springer. https://doi.org/10.1007/978-1-4419-9863-7_604
chicago: Quadrianto, Novi, and Christoph Lampert. “Kernel Based Learning.” In Encyclopedia
of Systems Biology, edited by Werner Dubitzky, Olaf Wolkenhauer, Kwang Cho,
and Hiroki Yokota, 3:1069–1069. Springer, 2013. https://doi.org/10.1007/978-1-4419-9863-7_604.
ieee: N. Quadrianto and C. Lampert, “Kernel based learning,” in Encyclopedia
of Systems Biology, vol. 3, W. Dubitzky, O. Wolkenhauer, K. Cho, and H. Yokota,
Eds. Springer, 2013, pp. 1069–1069.
ista: 'Quadrianto N, Lampert C. 2013.Kernel based learning. In: Encyclopedia of
Systems Biology. vol. 3, 1069–1069.'
mla: Quadrianto, Novi, and Christoph Lampert. “Kernel Based Learning.” Encyclopedia
of Systems Biology, edited by Werner Dubitzky et al., vol. 3, Springer, 2013,
pp. 1069–1069, doi:10.1007/978-1-4419-9863-7_604.
short: N. Quadrianto, C. Lampert, in:, W. Dubitzky, O. Wolkenhauer, K. Cho, H. Yokota
(Eds.), Encyclopedia of Systems Biology, Springer, 2013, pp. 1069–1069.
date_created: 2018-12-11T12:02:39Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2021-01-12T07:42:38Z
day: '01'
department:
- _id: ChLa
doi: 10.1007/978-1-4419-9863-7_604
editor:
- first_name: Werner
full_name: Dubitzky, Werner
last_name: Dubitzky
- first_name: Olaf
full_name: Wolkenhauer, Olaf
last_name: Wolkenhauer
- first_name: Kwang
full_name: Cho, Kwang
last_name: Cho
- first_name: Hiroki
full_name: Yokota, Hiroki
last_name: Yokota
intvolume: ' 3'
language:
- iso: eng
month: '01'
oa_version: None
page: 1069 - 1069
publication: Encyclopedia of Systems Biology
publication_status: published
publisher: Springer
publist_id: '3314'
quality_controlled: '1'
status: public
title: Kernel based learning
type: encyclopedia_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2013'
...
---
_id: '10749'
abstract:
- lang: eng
text: Fluxoid quantization provides a direct means to study phase coherence. In
cuprate superconductors, there have been observations which suggest that phase
coherent superconducting fluctuations may persist at temperatures significantly
above Tc. The focus of this work is to study the vortex states in mesoscopic cuprate
superconducting samples to directly probe phase coherence over a wide range of
temperatures. We present cantilever torque susceptometry measurements of micron
and sub-micron size Bi2212 rings and disks. The high sensitivity of this technique
allowed observation of transitions between different fluxoid states of a single
ring, and the discrete vortex states of micron size disks. The dependence of magnetic
susceptibility on diameter and wall thickness of the ring was investigated. Measurements
were made at different values of the in-plane magnetic field, and over a wide
range of temperatures.
acknowledgement: This work was supported by the Center for Emergent Superconductivity,
an Energy Frontier Research Center funded by the US DOE, Office of Science.
alternative_title:
- Bulletin of the American Physical Society
article_number: N36.00001
article_processing_charge: No
author:
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
- first_name: Raffi
full_name: Budakian, Raffi
last_name: Budakian
- first_name: Genda
full_name: Gu, Genda
last_name: Gu
citation:
ama: 'Polshyn H, Budakian R, Gu G. Cantilever micro-susceptometry of mesoscopic
Bi2212 samples. In: APS March Meeting 2013. Vol 58. American Physical Society;
2013.'
apa: 'Polshyn, H., Budakian, R., & Gu, G. (2013). Cantilever micro-susceptometry
of mesoscopic Bi2212 samples. In APS March Meeting 2013 (Vol. 58). Baltimore,
MD, United States: American Physical Society.'
chicago: Polshyn, Hryhoriy, Raffi Budakian, and Genda Gu. “Cantilever Micro-Susceptometry
of Mesoscopic Bi2212 Samples.” In APS March Meeting 2013, Vol. 58. American
Physical Society, 2013.
ieee: H. Polshyn, R. Budakian, and G. Gu, “Cantilever micro-susceptometry of mesoscopic
Bi2212 samples,” in APS March Meeting 2013, Baltimore, MD, United States,
2013, vol. 58, no. 1.
ista: 'Polshyn H, Budakian R, Gu G. 2013. Cantilever micro-susceptometry of mesoscopic
Bi2212 samples. APS March Meeting 2013. APS: American Physical Society, Bulletin
of the American Physical Society, vol. 58, N36.00001.'
mla: Polshyn, Hryhoriy, et al. “Cantilever Micro-Susceptometry of Mesoscopic Bi2212
Samples.” APS March Meeting 2013, vol. 58, no. 1, N36.00001, American Physical
Society, 2013.
short: H. Polshyn, R. Budakian, G. Gu, in:, APS March Meeting 2013, American Physical
Society, 2013.
conference:
end_date: 2013-03-22
location: Baltimore, MD, United States
name: 'APS: American Physical Society'
start_date: 2013-03-18
date_created: 2022-02-08T10:34:29Z
date_published: 2013-03-01T00:00:00Z
date_updated: 2022-02-08T10:48:06Z
day: '01'
extern: '1'
intvolume: ' 58'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://meetings.aps.org/Meeting/MAR13/Event/186873
month: '03'
oa: 1
oa_version: Published Version
publication: APS March Meeting 2013
publication_identifier:
issn:
- 0003-0503
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
status: public
title: Cantilever micro-susceptometry of mesoscopic Bi2212 samples
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 58
year: '2013'
...
---
_id: '10895'
abstract:
- lang: eng
text: 'Due to their sessile lifestyles, plants need to deal with the limitations
and stresses imposed by the changing environment. Plants cope with these by a
remarkable developmental flexibility, which is embedded in their strategy to survive.
Plants can adjust their size, shape and number of organs, bend according to gravity
and light, and regenerate tissues that were damaged, utilizing a coordinating,
intercellular signal, the plant hormone, auxin. Another versatile signal is the
cation, Ca2+, which is a crucial second messenger for many rapid cellular processes
during responses to a wide range of endogenous and environmental signals, such
as hormones, light, drought stress and others. Auxin is a good candidate for one
of these Ca2+-activating signals. However, the role of auxin-induced Ca2+ signaling
is poorly understood. Here, we will provide an overview of possible developmental
and physiological roles, as well as mechanisms underlying the interconnection
of Ca2+ and auxin signaling. '
article_processing_charge: No
article_type: original
author:
- first_name: Steffen
full_name: Vanneste, Steffen
last_name: Vanneste
- first_name: Jiří
full_name: Friml, Jiří
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: 'Vanneste S, Friml J. Calcium: The missing link in auxin action. Plants.
2013;2(4):650-675. doi:10.3390/plants2040650'
apa: 'Vanneste, S., & Friml, J. (2013). Calcium: The missing link in auxin action.
Plants. MDPI. https://doi.org/10.3390/plants2040650'
chicago: 'Vanneste, Steffen, and Jiří Friml. “Calcium: The Missing Link in Auxin
Action.” Plants. MDPI, 2013. https://doi.org/10.3390/plants2040650.'
ieee: 'S. Vanneste and J. Friml, “Calcium: The missing link in auxin action,” Plants,
vol. 2, no. 4. MDPI, pp. 650–675, 2013.'
ista: 'Vanneste S, Friml J. 2013. Calcium: The missing link in auxin action. Plants.
2(4), 650–675.'
mla: 'Vanneste, Steffen, and Jiří Friml. “Calcium: The Missing Link in Auxin Action.”
Plants, vol. 2, no. 4, MDPI, 2013, pp. 650–75, doi:10.3390/plants2040650.'
short: S. Vanneste, J. Friml, Plants 2 (2013) 650–675.
date_created: 2022-03-21T07:13:49Z
date_published: 2013-10-21T00:00:00Z
date_updated: 2022-03-21T12:15:29Z
day: '21'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.3390/plants2040650
external_id:
pmid:
- '27137397'
file:
- access_level: open_access
checksum: fb4ff2e820e344e253c9197544610be6
content_type: application/pdf
creator: dernst
date_created: 2022-03-21T12:12:56Z
date_updated: 2022-03-21T12:12:56Z
file_id: '10916'
file_name: 2013_Plants_Vanneste.pdf
file_size: 670188
relation: main_file
success: 1
file_date_updated: 2022-03-21T12:12:56Z
has_accepted_license: '1'
intvolume: ' 2'
issue: '4'
keyword:
- Plant Science
- Ecology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
license: https://creativecommons.org/licenses/by/3.0/
month: '10'
oa: 1
oa_version: Published Version
page: 650-675
pmid: 1
publication: Plants
publication_identifier:
issn:
- 2223-7747
publication_status: published
publisher: MDPI
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Calcium: The missing link in auxin action'
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/3.0/legalcode
name: Creative Commons Attribution 3.0 Unported (CC BY 3.0)
short: CC BY (3.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2
year: '2013'
...
---
_id: '10897'
abstract:
- lang: eng
text: Taking images is an efficient way to collect data about the physical world.
It can be done fast and in exquisite detail. By definition, image processing is
the field that concerns itself with the computation aimed at harnessing the information
contained in images [10]. This talk is concerned with topological information.
Our main thesis is that persistent homology [5] is a useful method to quantify
and summarize topological information, building a bridge that connects algebraic
topology with applications. We provide supporting evidence for this thesis by
touching upon four technical developments in the overlap between persistent homology
and image processing.
acknowledgement: This research is partially supported by the European Science Foundation
(ESF) under the Research Network Programme, the European Union under the Toposys
Project FP7-ICT-318493-STREP, the Russian Government under the Mega Project 11.G34.31.0053.
article_processing_charge: No
author:
- first_name: Herbert
full_name: Edelsbrunner, Herbert
id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
last_name: Edelsbrunner
orcid: 0000-0002-9823-6833
citation:
ama: 'Edelsbrunner H. Persistent homology in image processing. In: Graph-Based
Representations in Pattern Recognition. Vol 7877. LNCS. Berlin, Heidelberg:
Springer Nature; 2013:182-183. doi:10.1007/978-3-642-38221-5_19'
apa: 'Edelsbrunner, H. (2013). Persistent homology in image processing. In Graph-Based
Representations in Pattern Recognition (Vol. 7877, pp. 182–183). Berlin, Heidelberg:
Springer Nature. https://doi.org/10.1007/978-3-642-38221-5_19'
chicago: 'Edelsbrunner, Herbert. “Persistent Homology in Image Processing.” In Graph-Based
Representations in Pattern Recognition, 7877:182–83. LNCS. Berlin, Heidelberg:
Springer Nature, 2013. https://doi.org/10.1007/978-3-642-38221-5_19.'
ieee: H. Edelsbrunner, “Persistent homology in image processing,” in Graph-Based
Representations in Pattern Recognition, Vienna, Austria, 2013, vol. 7877,
pp. 182–183.
ista: 'Edelsbrunner H. 2013. Persistent homology in image processing. Graph-Based
Representations in Pattern Recognition. GbRPR: Graph-based Representations in
Pattern RecognitionLNCS vol. 7877, 182–183.'
mla: Edelsbrunner, Herbert. “Persistent Homology in Image Processing.” Graph-Based
Representations in Pattern Recognition, vol. 7877, Springer Nature, 2013,
pp. 182–83, doi:10.1007/978-3-642-38221-5_19.
short: H. Edelsbrunner, in:, Graph-Based Representations in Pattern Recognition,
Springer Nature, Berlin, Heidelberg, 2013, pp. 182–183.
conference:
end_date: 2013-05-17
location: Vienna, Austria
name: 'GbRPR: Graph-based Representations in Pattern Recognition'
start_date: 2013-05-15
date_created: 2022-03-21T07:30:33Z
date_published: 2013-06-01T00:00:00Z
date_updated: 2023-09-05T15:10:20Z
day: '01'
department:
- _id: HeEd
doi: 10.1007/978-3-642-38221-5_19
ec_funded: 1
intvolume: ' 7877'
language:
- iso: eng
month: '06'
oa_version: None
page: 182-183
place: Berlin, Heidelberg
project:
- _id: 255D761E-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '318493'
name: Topological Complex Systems
publication: Graph-Based Representations in Pattern Recognition
publication_identifier:
eisbn:
- '9783642382215'
eissn:
- 1611-3349
isbn:
- '9783642382208'
issn:
- 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
series_title: LNCS
status: public
title: Persistent homology in image processing
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 7877
year: '2013'
...
---
_id: '10898'
abstract:
- lang: eng
text: A prominent remedy to multicore scalability issues in concurrent data structure
implementations is to relax the sequential specification of the data structure.
We present distributed queues (DQ), a new family of relaxed concurrent queue implementations.
DQs implement relaxed queues with linearizable emptiness check and either configurable
or bounded out-of-order behavior or pool behavior. Our experiments show that DQs
outperform and outscale in micro- and macrobenchmarks all strict and relaxed queue
as well as pool implementations that we considered.
article_number: '17'
article_processing_charge: No
author:
- first_name: Andreas
full_name: Haas, Andreas
last_name: Haas
- first_name: Michael
full_name: Lippautz, Michael
last_name: Lippautz
- first_name: Thomas A
full_name: Henzinger, Thomas A
id: 40876CD8-F248-11E8-B48F-1D18A9856A87
last_name: Henzinger
orcid: 0000-0002-2985-7724
- first_name: Hannes
full_name: Payer, Hannes
last_name: Payer
- first_name: Ana
full_name: Sokolova, Ana
last_name: Sokolova
- first_name: Christoph M.
full_name: Kirsch, Christoph M.
last_name: Kirsch
- first_name: Ali
full_name: Sezgin, Ali
id: 4C7638DA-F248-11E8-B48F-1D18A9856A87
last_name: Sezgin
citation:
ama: 'Haas A, Lippautz M, Henzinger TA, et al. Distributed queues in shared memory:
Multicore performance and scalability through quantitative relaxation. In: Proceedings
of the ACM International Conference on Computing Frontiers - CF ’13. ACM Press;
2013. doi:10.1145/2482767.2482789'
apa: 'Haas, A., Lippautz, M., Henzinger, T. A., Payer, H., Sokolova, A., Kirsch,
C. M., & Sezgin, A. (2013). Distributed queues in shared memory: Multicore
performance and scalability through quantitative relaxation. In Proceedings
of the ACM International Conference on Computing Frontiers - CF ’13. Ischia,
Italy: ACM Press. https://doi.org/10.1145/2482767.2482789'
chicago: 'Haas, Andreas, Michael Lippautz, Thomas A Henzinger, Hannes Payer, Ana
Sokolova, Christoph M. Kirsch, and Ali Sezgin. “Distributed Queues in Shared Memory:
Multicore Performance and Scalability through Quantitative Relaxation.” In Proceedings
of the ACM International Conference on Computing Frontiers - CF ’13. ACM Press,
2013. https://doi.org/10.1145/2482767.2482789.'
ieee: 'A. Haas et al., “Distributed queues in shared memory: Multicore performance
and scalability through quantitative relaxation,” in Proceedings of the ACM
International Conference on Computing Frontiers - CF ’13, Ischia, Italy, 2013,
no. 5.'
ista: 'Haas A, Lippautz M, Henzinger TA, Payer H, Sokolova A, Kirsch CM, Sezgin
A. 2013. Distributed queues in shared memory: Multicore performance and scalability
through quantitative relaxation. Proceedings of the ACM International Conference
on Computing Frontiers - CF ’13. CF: Conference on Computing Frontiers, 17.'
mla: 'Haas, Andreas, et al. “Distributed Queues in Shared Memory: Multicore Performance
and Scalability through Quantitative Relaxation.” Proceedings of the ACM International
Conference on Computing Frontiers - CF ’13, no. 5, 17, ACM Press, 2013, doi:10.1145/2482767.2482789.'
short: A. Haas, M. Lippautz, T.A. Henzinger, H. Payer, A. Sokolova, C.M. Kirsch,
A. Sezgin, in:, Proceedings of the ACM International Conference on Computing Frontiers
- CF ’13, ACM Press, 2013.
conference:
end_date: 2013-05-16
location: Ischia, Italy
name: 'CF: Conference on Computing Frontiers'
start_date: 2013-05-14
date_created: 2022-03-21T07:33:22Z
date_published: 2013-05-01T00:00:00Z
date_updated: 2022-06-21T08:01:19Z
day: '01'
department:
- _id: ToHe
doi: 10.1145/2482767.2482789
issue: '5'
language:
- iso: eng
month: '05'
oa_version: None
publication: Proceedings of the ACM International Conference on Computing Frontiers
- CF '13
publication_identifier:
isbn:
- 978-145032053-5
publication_status: published
publisher: ACM Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Distributed queues in shared memory: Multicore performance and scalability
through quantitative relaxation'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2013'
...
---
_id: '10899'
article_processing_charge: No
author:
- first_name: Nicholas H
full_name: Barton, Nicholas H
id: 4880FE40-F248-11E8-B48F-1D18A9856A87
last_name: Barton
orcid: 0000-0002-8548-5240
citation:
ama: 'Barton NH. Differentiation. In: Encyclopedia of Biodiversity. 2nd ed.
Elsevier; 2013:508-515. doi:10.1016/b978-0-12-384719-5.00031-9'
apa: Barton, N. H. (2013). Differentiation. In Encyclopedia of Biodiversity
(2nd ed., pp. 508–515). Elsevier. https://doi.org/10.1016/b978-0-12-384719-5.00031-9
chicago: Barton, Nicholas H. “Differentiation.” In Encyclopedia of Biodiversity,
2nd ed., 508–15. Elsevier, 2013. https://doi.org/10.1016/b978-0-12-384719-5.00031-9.
ieee: N. H. Barton, “Differentiation,” in Encyclopedia of Biodiversity, 2nd
ed., Elsevier, 2013, pp. 508–515.
ista: 'Barton NH. 2013.Differentiation. In: Encyclopedia of Biodiversity. , 508–515.'
mla: Barton, Nicholas H. “Differentiation.” Encyclopedia of Biodiversity,
2nd ed., Elsevier, 2013, pp. 508–15, doi:10.1016/b978-0-12-384719-5.00031-9.
short: N.H. Barton, in:, Encyclopedia of Biodiversity, 2nd ed., Elsevier, 2013,
pp. 508–515.
date_created: 2022-03-21T07:46:22Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2022-06-20T09:18:06Z
day: '01'
department:
- _id: NiBa
doi: 10.1016/b978-0-12-384719-5.00031-9
edition: '2'
keyword:
- Adaptive landscape
- Cline
- Coalescent process
- Gene flow
- Hybrid zone
- Local adaptation
- Natural selection
- Neutral theory
- Population structure
- Speciation
language:
- iso: eng
month: '01'
oa_version: None
page: 508-515
publication: Encyclopedia of Biodiversity
publication_identifier:
isbn:
- 978-0-12-384720-1
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Differentiation
type: book_chapter
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2013'
...
---
_id: '10900'
abstract:
- lang: eng
text: Leukocyte migration through the interstitial space is crucial for the maintenance
of tolerance and immunity. The main cues for leukocyte trafficking are chemokines
thought to directionally guide these cells towards their targets. However, model
systems that facilitate quantification of chemokine-guided leukocyte migration
in vivo are uncommon. Here we describe an ex vivo crawl-in assay using explanted
mouse ears that allows the visualization of chemokine-dependent dendritic cell
(DC) motility in the dermal interstitium in real time. We present methods for
the preparation of mouse ear sheets and their use in multidimensional confocal
imaging experiments to monitor and analyze the directional migration of fluorescently
labelled DCs through the dermis and into afferent lymphatic vessels. The assay
provides a more physiological approach to study leukocyte migration than in vitro
three-dimensional (3D) or 2-dimensional (2D) migration assays such as collagen
gels and transwell assays.
acknowledgement: We would like to thank Alexander Eichner and Ingrid de Vries for
discussion and critical reading of the manuscript, and Mary Frank for assistance
with the recording of videos and images in Fig. 1. M.S. is supported through funding
from the German Research Foundation (DFG). M.W. acknowledges the Alexander von Humboldt
Foundation for funding.
alternative_title:
- Methods in Molecular Biology
article_processing_charge: No
author:
- first_name: Michele
full_name: Weber, Michele
id: 3A3FC708-F248-11E8-B48F-1D18A9856A87
last_name: Weber
- first_name: Michael K
full_name: Sixt, Michael K
id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
last_name: Sixt
orcid: 0000-0002-6620-9179
citation:
ama: 'Weber M, Sixt MK. Live Cell Imaging of Chemotactic Dendritic Cell Migration
in Explanted Mouse Ear Preparations. In: Cardona A, Ubogu E, eds. Chemokines.
Vol 1013. MIMB. Totowa, NJ: Humana Press; 2013:215-226. doi:10.1007/978-1-62703-426-5_14'
apa: 'Weber, M., & Sixt, M. K. (2013). Live Cell Imaging of Chemotactic Dendritic
Cell Migration in Explanted Mouse Ear Preparations. In A. Cardona & E. Ubogu
(Eds.), Chemokines (Vol. 1013, pp. 215–226). Totowa, NJ: Humana Press.
https://doi.org/10.1007/978-1-62703-426-5_14'
chicago: 'Weber, Michele, and Michael K Sixt. “Live Cell Imaging of Chemotactic
Dendritic Cell Migration in Explanted Mouse Ear Preparations.” In Chemokines,
edited by Astrid Cardona and Eroboghene Ubogu, 1013:215–26. MIMB. Totowa, NJ:
Humana Press, 2013. https://doi.org/10.1007/978-1-62703-426-5_14.'
ieee: 'M. Weber and M. K. Sixt, “Live Cell Imaging of Chemotactic Dendritic Cell
Migration in Explanted Mouse Ear Preparations,” in Chemokines, vol. 1013,
A. Cardona and E. Ubogu, Eds. Totowa, NJ: Humana Press, 2013, pp. 215–226.'
ista: 'Weber M, Sixt MK. 2013.Live Cell Imaging of Chemotactic Dendritic Cell Migration
in Explanted Mouse Ear Preparations. In: Chemokines. Methods in Molecular Biology,
vol. 1013, 215–226.'
mla: Weber, Michele, and Michael K. Sixt. “Live Cell Imaging of Chemotactic Dendritic
Cell Migration in Explanted Mouse Ear Preparations.” Chemokines, edited
by Astrid Cardona and Eroboghene Ubogu, vol. 1013, Humana Press, 2013, pp. 215–26,
doi:10.1007/978-1-62703-426-5_14.
short: M. Weber, M.K. Sixt, in:, A. Cardona, E. Ubogu (Eds.), Chemokines, Humana
Press, Totowa, NJ, 2013, pp. 215–226.
date_created: 2022-03-21T07:47:41Z
date_published: 2013-04-03T00:00:00Z
date_updated: 2023-09-05T13:15:33Z
day: '03'
department:
- _id: MiSi
doi: 10.1007/978-1-62703-426-5_14
editor:
- first_name: Astrid
full_name: Cardona, Astrid
last_name: Cardona
- first_name: Eroboghene
full_name: Ubogu, Eroboghene
last_name: Ubogu
external_id:
pmid:
- '23625502'
intvolume: ' 1013'
language:
- iso: eng
month: '04'
oa_version: None
page: 215-226
place: Totowa, NJ
pmid: 1
publication: Chemokines
publication_identifier:
eisbn:
- '9781627034265'
eissn:
- 1940-6029
isbn:
- '9781627034258'
issn:
- 1064-3745
publication_status: published
publisher: Humana Press
quality_controlled: '1'
scopus_import: '1'
series_title: MIMB
status: public
title: Live Cell Imaging of Chemotactic Dendritic Cell Migration in Explanted Mouse
Ear Preparations
type: book_chapter
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 1013
year: '2013'
...
---
_id: '10902'
abstract:
- lang: eng
text: We consider how to edit strings from a source language so that the edited
strings belong to a target language, where the languages are given as deterministic
finite automata. Non-streaming (or offline) transducers perform edits given the
whole source string. We show that the class of deterministic one-pass transducers
with registers along with increment and min operation suffices for computing optimal
edit distance, whereas the same class of transducers without the min operation
is not sufficient. Streaming (or online) transducers perform edits as the letters
of the source string are received. We present a polynomial time algorithm for
the partial-repair problem that given a bound α asks for the construction of a
deterministic streaming transducer (if one exists) that ensures that the ‘maximum
fraction’ η of the strings of the source language are edited, within cost α, to
the target language.
acknowledgement: 'The research was supported by Austrian Science Fund (FWF) Grant
No P 23499-N23, FWF NFN Grant No S11407-N23 (RiSE), ERC Start grant (279307: Graph
Games), and Microsoft faculty fellows award. Thanks to Gabriele Puppis for suggesting
the problem of identifying a deterministic transducer to compute the optimal cost,
and to Martin Chmelik for his comments on the introduction.'
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Siddhesh
full_name: Chaubal, Siddhesh
last_name: Chaubal
- first_name: Sasha
full_name: Rubin, Sasha
id: 2EC51194-F248-11E8-B48F-1D18A9856A87
last_name: Rubin
citation:
ama: 'Chatterjee K, Chaubal S, Rubin S. How to travel between languages. In: 7th
International Conference on Language and Automata Theory and Applications.
Vol 7810. LNCS. Berlin, Heidelberg: Springer Nature; 2013:214-225. doi:10.1007/978-3-642-37064-9_20'
apa: 'Chatterjee, K., Chaubal, S., & Rubin, S. (2013). How to travel between
languages. In 7th International Conference on Language and Automata Theory
and Applications (Vol. 7810, pp. 214–225). Berlin, Heidelberg: Springer Nature.
https://doi.org/10.1007/978-3-642-37064-9_20'
chicago: 'Chatterjee, Krishnendu, Siddhesh Chaubal, and Sasha Rubin. “How to Travel
between Languages.” In 7th International Conference on Language and Automata
Theory and Applications, 7810:214–25. LNCS. Berlin, Heidelberg: Springer Nature,
2013. https://doi.org/10.1007/978-3-642-37064-9_20.'
ieee: K. Chatterjee, S. Chaubal, and S. Rubin, “How to travel between languages,”
in 7th International Conference on Language and Automata Theory and Applications,
Bilbao, Spain, 2013, vol. 7810, pp. 214–225.
ista: 'Chatterjee K, Chaubal S, Rubin S. 2013. How to travel between languages.
7th International Conference on Language and Automata Theory and Applications.
LATA: Conference on Language and Automata Theory and ApplicationsLNCS, LNCS, vol.
7810, 214–225.'
mla: Chatterjee, Krishnendu, et al. “How to Travel between Languages.” 7th International
Conference on Language and Automata Theory and Applications, vol. 7810, Springer
Nature, 2013, pp. 214–25, doi:10.1007/978-3-642-37064-9_20.
short: K. Chatterjee, S. Chaubal, S. Rubin, in:, 7th International Conference on
Language and Automata Theory and Applications, Springer Nature, Berlin, Heidelberg,
2013, pp. 214–225.
conference:
end_date: 2013-04-05
location: Bilbao, Spain
name: 'LATA: Conference on Language and Automata Theory and Applications'
start_date: 2013-04-02
date_created: 2022-03-21T07:56:21Z
date_published: 2013-04-15T00:00:00Z
date_updated: 2023-09-05T15:10:38Z
day: '15'
department:
- _id: KrCh
doi: 10.1007/978-3-642-37064-9_20
ec_funded: 1
intvolume: ' 7810'
language:
- iso: eng
month: '04'
oa_version: None
page: 214-225
place: Berlin, Heidelberg
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P 23499-N23
name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S11407
name: Game Theory
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
name: Microsoft Research Faculty Fellowship
publication: 7th International Conference on Language and Automata Theory and Applications
publication_identifier:
eisbn:
- '9783642370649'
eissn:
- 1611-3349
isbn:
- '9783642370632'
issn:
- 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
series_title: LNCS
status: public
title: How to travel between languages
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 7810
year: '2013'
...
---
_id: '11083'
abstract:
- lang: eng
text: Nuclear pore complex (NPC) proteins are known for their critical roles in
regulating nucleocytoplasmic traffic of macromolecules across the nuclear envelope.
However, recent findings suggest that some nucleoporins (Nups), including Nup98,
have additional functions in developmental gene regulation. Nup98, which exhibits
transcription-dependent mobility at the NPC but can also bind chromatin away from
the nuclear envelope, is frequently involved in chromosomal translocations in
a subset of patients suffering from acute myeloid leukemia (AML). A common paradigm
suggests that Nup98 translocations cause aberrant transcription when they are
recuited to aberrant genomic loci. Importantly, this model fails to account for
the potential loss of wild type (WT) Nup98 function in the presence of Nup98 translocation
mutants. Here we examine how the cell might regulate Nup98 nucleoplasmic protein
levels to control transcription in healthy cells. In addition, we discuss the
possibility that dominant negative Nup98 fusion proteins disrupt the transcriptional
activity of WT Nup98 in the nucleoplasm to drive AML.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Tobias M.
full_name: Franks, Tobias M.
last_name: Franks
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Franks TM, Hetzer M. The role of Nup98 in transcription regulation in healthy
and diseased cells. Trends in Cell Biology. 2013;23(3):112-117. doi:10.1016/j.tcb.2012.10.013
apa: Franks, T. M., & Hetzer, M. (2013). The role of Nup98 in transcription
regulation in healthy and diseased cells. Trends in Cell Biology. Elsevier.
https://doi.org/10.1016/j.tcb.2012.10.013
chicago: Franks, Tobias M., and Martin Hetzer. “The Role of Nup98 in Transcription
Regulation in Healthy and Diseased Cells.” Trends in Cell Biology. Elsevier,
2013. https://doi.org/10.1016/j.tcb.2012.10.013.
ieee: T. M. Franks and M. Hetzer, “The role of Nup98 in transcription regulation
in healthy and diseased cells,” Trends in Cell Biology, vol. 23, no. 3.
Elsevier, pp. 112–117, 2013.
ista: Franks TM, Hetzer M. 2013. The role of Nup98 in transcription regulation in
healthy and diseased cells. Trends in Cell Biology. 23(3), 112–117.
mla: Franks, Tobias M., and Martin Hetzer. “The Role of Nup98 in Transcription Regulation
in Healthy and Diseased Cells.” Trends in Cell Biology, vol. 23, no. 3,
Elsevier, 2013, pp. 112–17, doi:10.1016/j.tcb.2012.10.013.
short: T.M. Franks, M. Hetzer, Trends in Cell Biology 23 (2013) 112–117.
date_created: 2022-04-07T07:50:33Z
date_published: 2013-03-01T00:00:00Z
date_updated: 2022-07-18T08:45:34Z
day: '01'
doi: 10.1016/j.tcb.2012.10.013
extern: '1'
external_id:
pmid:
- '23246429'
intvolume: ' 23'
issue: '3'
keyword:
- Cell Biology
language:
- iso: eng
month: '03'
oa_version: None
page: 112-117
pmid: 1
publication: Trends in Cell Biology
publication_identifier:
issn:
- 0962-8924
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: The role of Nup98 in transcription regulation in healthy and diseased cells
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 23
year: '2013'
...
---
_id: '11084'
abstract:
- lang: eng
text: Protein turnover is an effective way of maintaining a functional proteome,
as old and potentially damaged polypeptides are destroyed and replaced by newly
synthesized copies. An increasing number of intracellular proteins, however, have
been identified that evade this turnover process and instead are maintained over
a cell's lifetime. This diverse group of long-lived proteins might be particularly
prone to accumulation of damage and thus have a crucial role in the functional
deterioration of key regulatory processes during ageing.
article_processing_charge: No
article_type: original
author:
- first_name: Brandon H.
full_name: Toyama, Brandon H.
last_name: Toyama
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: 'Toyama BH, Hetzer M. Protein homeostasis: Live long, won’t prosper. Nature
Reviews Molecular Cell Biology. 2013;14:55-61. doi:10.1038/nrm3496'
apa: 'Toyama, B. H., & Hetzer, M. (2013). Protein homeostasis: Live long, won’t
prosper. Nature Reviews Molecular Cell Biology. Springer Nature. https://doi.org/10.1038/nrm3496'
chicago: 'Toyama, Brandon H., and Martin Hetzer. “Protein Homeostasis: Live Long,
Won’t Prosper.” Nature Reviews Molecular Cell Biology. Springer Nature,
2013. https://doi.org/10.1038/nrm3496.'
ieee: 'B. H. Toyama and M. Hetzer, “Protein homeostasis: Live long, won’t prosper,”
Nature Reviews Molecular Cell Biology, vol. 14. Springer Nature, pp. 55–61,
2013.'
ista: 'Toyama BH, Hetzer M. 2013. Protein homeostasis: Live long, won’t prosper.
Nature Reviews Molecular Cell Biology. 14, 55–61.'
mla: 'Toyama, Brandon H., and Martin Hetzer. “Protein Homeostasis: Live Long, Won’t
Prosper.” Nature Reviews Molecular Cell Biology, vol. 14, Springer Nature,
2013, pp. 55–61, doi:10.1038/nrm3496.'
short: B.H. Toyama, M. Hetzer, Nature Reviews Molecular Cell Biology 14 (2013) 55–61.
date_created: 2022-04-07T07:50:43Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2022-07-18T08:37:53Z
day: '01'
doi: 10.1038/nrm3496
extern: '1'
external_id:
pmid:
- '23258296'
intvolume: ' 14'
keyword:
- Cell Biology
- Molecular Biology
language:
- iso: eng
month: '01'
oa_version: None
page: 55-61
pmid: 1
publication: Nature Reviews Molecular Cell Biology
publication_identifier:
issn:
- 1471-0072
- 1471-0080
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Protein homeostasis: Live long, won''t prosper'
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 14
year: '2013'
...
---
_id: '11085'
abstract:
- lang: eng
text: During mitotic exit, missegregated chromosomes can recruit their own nuclear
envelope (NE) to form micronuclei (MN). MN have reduced functioning compared to
primary nuclei in the same cell, although the two compartments appear to be structurally
comparable. Here we show that over 60% of MN undergo an irreversible loss of compartmentalization
during interphase due to NE collapse. This disruption of the MN, which is induced
by defects in nuclear lamina assembly, drastically reduces nuclear functions and
can trigger massive DNA damage. MN disruption is associated with chromatin compaction
and invasion of endoplasmic reticulum (ER) tubules into the chromatin. We identified
disrupted MN in both major subtypes of human non-small-cell lung cancer, suggesting
that disrupted MN could be a useful objective biomarker for genomic instability
in solid tumors. Our study shows that NE collapse is a key event underlying MN
dysfunction and establishes a link between aberrant NE organization and aneuploidy.
article_processing_charge: No
article_type: original
author:
- first_name: Emily M.
full_name: Hatch, Emily M.
last_name: Hatch
- first_name: Andrew H.
full_name: Fischer, Andrew H.
last_name: Fischer
- first_name: Thomas J.
full_name: Deerinck, Thomas J.
last_name: Deerinck
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Hatch EM, Fischer AH, Deerinck TJ, Hetzer M. Catastrophic nuclear envelope
collapse in cancer cell micronuclei. Cell. 2013;154(1):47-60. doi:10.1016/j.cell.2013.06.007
apa: Hatch, E. M., Fischer, A. H., Deerinck, T. J., & Hetzer, M. (2013). Catastrophic
nuclear envelope collapse in cancer cell micronuclei. Cell. Elsevier. https://doi.org/10.1016/j.cell.2013.06.007
chicago: Hatch, Emily M., Andrew H. Fischer, Thomas J. Deerinck, and Martin Hetzer.
“Catastrophic Nuclear Envelope Collapse in Cancer Cell Micronuclei.” Cell.
Elsevier, 2013. https://doi.org/10.1016/j.cell.2013.06.007.
ieee: E. M. Hatch, A. H. Fischer, T. J. Deerinck, and M. Hetzer, “Catastrophic nuclear
envelope collapse in cancer cell micronuclei,” Cell, vol. 154, no. 1. Elsevier,
pp. 47–60, 2013.
ista: Hatch EM, Fischer AH, Deerinck TJ, Hetzer M. 2013. Catastrophic nuclear envelope
collapse in cancer cell micronuclei. Cell. 154(1), 47–60.
mla: Hatch, Emily M., et al. “Catastrophic Nuclear Envelope Collapse in Cancer Cell
Micronuclei.” Cell, vol. 154, no. 1, Elsevier, 2013, pp. 47–60, doi:10.1016/j.cell.2013.06.007.
short: E.M. Hatch, A.H. Fischer, T.J. Deerinck, M. Hetzer, Cell 154 (2013) 47–60.
date_created: 2022-04-07T07:50:51Z
date_published: 2013-07-03T00:00:00Z
date_updated: 2022-07-18T08:45:47Z
day: '03'
doi: 10.1016/j.cell.2013.06.007
extern: '1'
external_id:
pmid:
- '23827674'
intvolume: ' 154'
issue: '1'
keyword:
- General Biochemistry
- Genetics and Molecular Biology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.cell.2013.06.007
month: '07'
oa: 1
oa_version: Published Version
page: 47-60
pmid: 1
publication: Cell
publication_identifier:
issn:
- 0092-8674
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Catastrophic nuclear envelope collapse in cancer cell micronuclei
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 154
year: '2013'
...
---
_id: '11086'
abstract:
- lang: eng
text: Faithful execution of developmental gene expression programs occurs at multiple
levels and involves many different components such as transcription factors, histone-modification
enzymes, and mRNA processing proteins. Recent evidence suggests that nucleoporins,
well known components that control nucleo-cytoplasmic trafficking, have wide-ranging
functions in developmental gene regulation that potentially extend beyond their
role in nuclear transport. Whether the unexpected role of nuclear pore proteins
in transcription regulation, which initially has been described in fungi and flies,
also applies to human cells is unknown. Here we show at a genome-wide level that
the nuclear pore protein NUP98 associates with developmentally regulated genes
active during human embryonic stem cell differentiation. Overexpression of a dominant
negative fragment of NUP98 levels decreases expression levels of NUP98-bound genes.
In addition, we identify two modes of developmental gene regulation by NUP98 that
are differentiated by the spatial localization of NUP98 target genes. Genes in
the initial stage of developmental induction can associate with NUP98 that is
embedded in the nuclear pores at the nuclear periphery. Alternatively, genes that
are highly induced can interact with NUP98 in the nuclear interior, away from
the nuclear pores. This work demonstrates for the first time that NUP98 dynamically
associates with the human genome during differentiation, revealing a role of a
nuclear pore protein in regulating developmental gene expression programs.
article_number: e1003308
article_processing_charge: No
article_type: original
author:
- first_name: Yun
full_name: Liang, Yun
last_name: Liang
- first_name: Tobias M.
full_name: Franks, Tobias M.
last_name: Franks
- first_name: Maria C.
full_name: Marchetto, Maria C.
last_name: Marchetto
- first_name: Fred H.
full_name: Gage, Fred H.
last_name: Gage
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Liang Y, Franks TM, Marchetto MC, Gage FH, Hetzer M. Dynamic association of
NUP98 with the human genome. PLoS Genetics. 2013;9(2). doi:10.1371/journal.pgen.1003308
apa: Liang, Y., Franks, T. M., Marchetto, M. C., Gage, F. H., & Hetzer, M. (2013).
Dynamic association of NUP98 with the human genome. PLoS Genetics. Public
Library of Science. https://doi.org/10.1371/journal.pgen.1003308
chicago: Liang, Yun, Tobias M. Franks, Maria C. Marchetto, Fred H. Gage, and Martin
Hetzer. “Dynamic Association of NUP98 with the Human Genome.” PLoS Genetics.
Public Library of Science, 2013. https://doi.org/10.1371/journal.pgen.1003308.
ieee: Y. Liang, T. M. Franks, M. C. Marchetto, F. H. Gage, and M. Hetzer, “Dynamic
association of NUP98 with the human genome,” PLoS Genetics, vol. 9, no.
2. Public Library of Science, 2013.
ista: Liang Y, Franks TM, Marchetto MC, Gage FH, Hetzer M. 2013. Dynamic association
of NUP98 with the human genome. PLoS Genetics. 9(2), e1003308.
mla: Liang, Yun, et al. “Dynamic Association of NUP98 with the Human Genome.” PLoS
Genetics, vol. 9, no. 2, e1003308, Public Library of Science, 2013, doi:10.1371/journal.pgen.1003308.
short: Y. Liang, T.M. Franks, M.C. Marchetto, F.H. Gage, M. Hetzer, PLoS Genetics
9 (2013).
date_created: 2022-04-07T07:50:59Z
date_published: 2013-02-28T00:00:00Z
date_updated: 2022-07-18T08:45:58Z
day: '28'
doi: 10.1371/journal.pgen.1003308
extern: '1'
external_id:
pmid:
- '23468646'
intvolume: ' 9'
issue: '2'
keyword:
- Cancer Research
- Genetics (clinical)
- Genetics
- Molecular Biology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1371/journal.pgen.1003308
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLoS Genetics
publication_identifier:
issn:
- 1553-7404
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dynamic association of NUP98 with the human genome
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 9
year: '2013'
...
---
_id: '11087'
abstract:
- lang: eng
text: Intracellular proteins with long lifespans have recently been linked to age-dependent
defects, ranging from decreased fertility to the functional decline of neurons.
Why long-lived proteins exist in metabolically active cellular environments and
how they are maintained over time remains poorly understood. Here, we provide
a system-wide identification of proteins with exceptional lifespans in the rat
brain. These proteins are inefficiently replenished despite being translated robustly
throughout adulthood. Using nucleoporins as a paradigm for long-term protein persistence,
we found that nuclear pore complexes (NPCs) are maintained over a cell’s life
through slow but finite exchange of even its most stable subcomplexes. This maintenance
is limited, however, as some nucleoporin levels decrease during aging, providing
a rationale for the previously observed age-dependent deterioration of NPC function.
Our identification of a long-lived proteome reveals cellular components that are
at increased risk for damage accumulation, linking long-term protein persistence
to the cellular aging process.
article_processing_charge: No
article_type: original
author:
- first_name: Brandon H.
full_name: Toyama, Brandon H.
last_name: Toyama
- first_name: Jeffrey N.
full_name: Savas, Jeffrey N.
last_name: Savas
- first_name: Sung Kyu
full_name: Park, Sung Kyu
last_name: Park
- first_name: Michael S.
full_name: Harris, Michael S.
last_name: Harris
- first_name: Nicholas T.
full_name: Ingolia, Nicholas T.
last_name: Ingolia
- first_name: John R.
full_name: Yates, John R.
last_name: Yates
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Toyama BH, Savas JN, Park SK, et al. Identification of long-lived proteins
reveals exceptional stability of essential cellular structures. Cell. 2013;154(5):971-982.
doi:10.1016/j.cell.2013.07.037
apa: Toyama, B. H., Savas, J. N., Park, S. K., Harris, M. S., Ingolia, N. T., Yates,
J. R., & Hetzer, M. (2013). Identification of long-lived proteins reveals
exceptional stability of essential cellular structures. Cell. Elsevier.
https://doi.org/10.1016/j.cell.2013.07.037
chicago: Toyama, Brandon H., Jeffrey N. Savas, Sung Kyu Park, Michael S. Harris,
Nicholas T. Ingolia, John R. Yates, and Martin Hetzer. “Identification of Long-Lived
Proteins Reveals Exceptional Stability of Essential Cellular Structures.” Cell.
Elsevier, 2013. https://doi.org/10.1016/j.cell.2013.07.037.
ieee: B. H. Toyama et al., “Identification of long-lived proteins reveals
exceptional stability of essential cellular structures,” Cell, vol. 154,
no. 5. Elsevier, pp. 971–982, 2013.
ista: Toyama BH, Savas JN, Park SK, Harris MS, Ingolia NT, Yates JR, Hetzer M. 2013.
Identification of long-lived proteins reveals exceptional stability of essential
cellular structures. Cell. 154(5), 971–982.
mla: Toyama, Brandon H., et al. “Identification of Long-Lived Proteins Reveals Exceptional
Stability of Essential Cellular Structures.” Cell, vol. 154, no. 5, Elsevier,
2013, pp. 971–82, doi:10.1016/j.cell.2013.07.037.
short: B.H. Toyama, J.N. Savas, S.K. Park, M.S. Harris, N.T. Ingolia, J.R. Yates,
M. Hetzer, Cell 154 (2013) 971–982.
date_created: 2022-04-07T07:51:08Z
date_published: 2013-08-29T00:00:00Z
date_updated: 2022-07-18T08:50:47Z
day: '29'
doi: 10.1016/j.cell.2013.07.037
extern: '1'
external_id:
pmid:
- '23993091'
intvolume: ' 154'
issue: '5'
keyword:
- General Biochemistry
- Genetics and Molecular Biology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.cell.2013.07.037
month: '08'
oa: 1
oa_version: Published Version
page: 971-982
pmid: 1
publication: Cell
publication_identifier:
issn:
- 0092-8674
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Identification of long-lived proteins reveals exceptional stability of essential
cellular structures
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 154
year: '2013'
...
---
_id: '11088'
abstract:
- lang: eng
text: 'The crowded intracellular environment poses a formidable challenge to experimental
and theoretical analyses of intracellular transport mechanisms. Our measurements
of single-particle trajectories in cytoplasm and their random-walk interpretations
elucidate two of these mechanisms: molecular diffusion in crowded environments
and cytoskeletal transport along microtubules. We employed acousto-optic deflector
microscopy to map out the three-dimensional trajectories of microspheres migrating
in the cytosolic fraction of a cellular extract. Classical Brownian motion (BM),
continuous time random walk, and fractional BM were alternatively used to represent
these trajectories. The comparison of the experimental and numerical data demonstrates
that cytoskeletal transport along microtubules and diffusion in the cytosolic
fraction exhibit anomalous (nonFickian) behavior and posses statistically distinct
signatures. Among the three random-walk models used, continuous time random walk
provides the best representation of diffusion, whereas microtubular transport
is accurately modeled with fractional BM.'
article_processing_charge: No
article_type: original
author:
- first_name: Benjamin M.
full_name: Regner, Benjamin M.
last_name: Regner
- first_name: Dejan
full_name: Vučinić, Dejan
last_name: Vučinić
- first_name: Cristina
full_name: Domnisoru, Cristina
last_name: Domnisoru
- first_name: Thomas M.
full_name: Bartol, Thomas M.
last_name: Bartol
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Daniel M.
full_name: Tartakovsky, Daniel M.
last_name: Tartakovsky
- first_name: Terrence J.
full_name: Sejnowski, Terrence J.
last_name: Sejnowski
citation:
ama: Regner BM, Vučinić D, Domnisoru C, et al. Anomalous diffusion of single particles
in cytoplasm. Biophysical Journal. 2013;104(8):1652-1660. doi:10.1016/j.bpj.2013.01.049
apa: Regner, B. M., Vučinić, D., Domnisoru, C., Bartol, T. M., Hetzer, M., Tartakovsky,
D. M., & Sejnowski, T. J. (2013). Anomalous diffusion of single particles
in cytoplasm. Biophysical Journal. Elsevier. https://doi.org/10.1016/j.bpj.2013.01.049
chicago: Regner, Benjamin M., Dejan Vučinić, Cristina Domnisoru, Thomas M. Bartol,
Martin Hetzer, Daniel M. Tartakovsky, and Terrence J. Sejnowski. “Anomalous Diffusion
of Single Particles in Cytoplasm.” Biophysical Journal. Elsevier, 2013.
https://doi.org/10.1016/j.bpj.2013.01.049.
ieee: B. M. Regner et al., “Anomalous diffusion of single particles in cytoplasm,”
Biophysical Journal, vol. 104, no. 8. Elsevier, pp. 1652–1660, 2013.
ista: Regner BM, Vučinić D, Domnisoru C, Bartol TM, Hetzer M, Tartakovsky DM, Sejnowski
TJ. 2013. Anomalous diffusion of single particles in cytoplasm. Biophysical Journal.
104(8), 1652–1660.
mla: Regner, Benjamin M., et al. “Anomalous Diffusion of Single Particles in Cytoplasm.”
Biophysical Journal, vol. 104, no. 8, Elsevier, 2013, pp. 1652–60, doi:10.1016/j.bpj.2013.01.049.
short: B.M. Regner, D. Vučinić, C. Domnisoru, T.M. Bartol, M. Hetzer, D.M. Tartakovsky,
T.J. Sejnowski, Biophysical Journal 104 (2013) 1652–1660.
date_created: 2022-04-07T07:51:26Z
date_published: 2013-04-16T00:00:00Z
date_updated: 2022-07-18T08:51:01Z
day: '16'
doi: 10.1016/j.bpj.2013.01.049
extern: '1'
external_id:
pmid:
- '23601312'
intvolume: ' 104'
issue: '8'
keyword:
- Biophysics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.bpj.2013.01.049
month: '04'
oa: 1
oa_version: Published Version
page: 1652-1660
pmid: 1
publication: Biophysical Journal
publication_identifier:
issn:
- 0006-3495
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Anomalous diffusion of single particles in cytoplasm
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 104
year: '2013'
...
---
_id: '115'
abstract:
- lang: eng
text: We present the design and performance characterization of a new experimental
technique for measuring individual particle charges in large ensembles of macroscopic
grains. The measurement principle is qualitatively similar to that used in determining
the elementary charge by Millikan in that it follows individual particle trajectories.
However, by taking advantage of new technology we are able to work with macroscopic
grains and achieve several orders of magnitude better resolution in charge to
mass ratios. By observing freely falling grains accelerated in a horizontal electric
field with a co-falling, high-speed video camera, we dramatically increase particle
tracking time and measurement precision. Keeping the granular medium under vacuum,
we eliminate air drag, leaving the electrostatic force as the primary source of
particle accelerations in the co-moving frame. Because the technique is based
on direct imaging, we can distinguish between different particle types during
the experiment, opening up the possibility of studying charge transfer processes
between different particle species. For the ∼300 μm diameter grains reported here,
we achieve an average acceleration resolution of ∼0.008 m/s2, a force resolution
of ∼500 pN, and a median charge resolution ∼6× 104 elementary charges per grain
(corresponding to surface charge densities ∼1 elementary charges per μm2). The
primary source of error is indeterminacy in the grain mass, but with higher resolution
cameras and better optics this can be further improved. The high degree of resolution
and the ability to visually identify particles of different species or sizes with
direct imaging make this a powerful new tool to characterize charging processes
in granular media.
acknowledgement: This work was supported financially by the National Science Foundation
(NSF) through its Materials Research Science and Engineering Center (MRSEC) program
(DMR-0820054) and by the US Army Research Office through Grant No. W911NF-12-1-0182.
S.R.W. acknowledges support from a University of Chicago Millikan Fellowship.
article_number: '025104'
author:
- first_name: Scott R
full_name: Waitukaitis, Scott R
id: 3A1FFC16-F248-11E8-B48F-1D18A9856A87
last_name: Waitukaitis
orcid: 0000-0002-2299-3176
- first_name: Heinrich
full_name: Jaeger, Heinrich
last_name: Jaeger
citation:
ama: Waitukaitis SR, Jaeger H. In situ granular charge measurement by free-fall
videography. Review of Scientific Instruments. 2013;84(2). doi:10.1063/1.4789496
apa: Waitukaitis, S. R., & Jaeger, H. (2013). In situ granular charge measurement
by free-fall videography. Review of Scientific Instruments. AIP. https://doi.org/10.1063/1.4789496
chicago: Waitukaitis, Scott R, and Heinrich Jaeger. “In Situ Granular Charge Measurement
by Free-Fall Videography.” Review of Scientific Instruments. AIP, 2013.
https://doi.org/10.1063/1.4789496.
ieee: S. R. Waitukaitis and H. Jaeger, “In situ granular charge measurement by free-fall
videography,” Review of Scientific Instruments, vol. 84, no. 2. AIP, 2013.
ista: Waitukaitis SR, Jaeger H. 2013. In situ granular charge measurement by free-fall
videography. Review of Scientific Instruments. 84(2), 025104.
mla: Waitukaitis, Scott R., and Heinrich Jaeger. “In Situ Granular Charge Measurement
by Free-Fall Videography.” Review of Scientific Instruments, vol. 84, no.
2, 025104, AIP, 2013, doi:10.1063/1.4789496.
short: S.R. Waitukaitis, H. Jaeger, Review of Scientific Instruments 84 (2013).
date_created: 2018-12-11T11:44:42Z
date_published: 2013-02-07T00:00:00Z
date_updated: 2021-01-12T06:48:39Z
day: '07'
doi: 10.1063/1.4789496
extern: '1'
intvolume: ' 84'
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
publication: Review of Scientific Instruments
publication_status: published
publisher: AIP
publist_id: '7939'
quality_controlled: '1'
status: public
title: In situ granular charge measurement by free-fall videography
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 84
year: '2013'
...
---
_id: '11520'
abstract:
- lang: eng
text: We present the spatially resolved Hα dynamics of 16 star-forming galaxies
at z ∼ 0.81 using the new KMOS multi-object integral field spectrograph on the
ESO Very Large Telescope. These galaxies, selected using 1.18 μm narrowband imaging
from the 10 deg2 CFHT-HiZELS survey of the SA 22 hr field, are found in a ∼4 Mpc
overdensity of Hα emitters and likely reside in a group/intermediate environment,
but not a cluster. We confirm and identify a rich group of star-forming galaxies
at z = 0.813 ± 0.003, with 13 galaxies within 1000 km s−1 of each other, and seven
within a diameter of 3 Mpc. All of our galaxies are “typical” star-forming galaxies
at their redshift, 0.8 ± 0.4 SFR$^*_{z = 0.8}$, spanning a range of specific star
formation rates (sSFRs) of 0.2–1.1 Gyr−1 and have a median metallicity very close
to solar of 12 + log(O/H) = 8.62 ± 0.06. We measure the spatially resolved Hα
dynamics of the galaxies in our sample and show that 13 out of 16 galaxies can
be described by rotating disks and use the data to derive inclination corrected
rotation speeds of 50–275 km s−1. The fraction of disks within our sample is 75%
± 8%, consistent with previous results based on Hubble Space Telescope morphologies
of Hα-selected galaxies at z ∼ 1 and confirming that disks dominate the SFR density
at z ∼ 1. Our Hα galaxies are well fitted by the z ∼ 1–2 Tully–Fisher (TF) relation,
confirming the evolution seen in the zero point. Apart from having, on average,
higher stellar masses and lower sSFRs, our group galaxies at z = 0.81 present
the same mass–metallicity and TF relation as z ∼ 1 field galaxies and are all
disk galaxies.
acknowledgement: 'We thank the referee for many helpful comments and suggestions which
greatly improved the clarity and quality of this work. D.S. acknowledges financial
support from the Netherlands Organisation for Scientific research (NWO) through
a Veni fellowship and also funding from the European Community Seventh Framework
Programme (FP7/2007-2013) under grant agreement number RG226604 (OPTICON) which
allowed access to CFHT time (proposals: 11BO29 & 12AO19). A.M.S. gratefully acknowledges
an STFC Advanced Fellowship through grant number ST/H005234/1. I.R.S., J.P.S., and
R.G.B. acknowledge support from the UK Science and Technology Facilities Council
(STFC) under ST/I001573/1. I.R.S. acknowledges STFC (ST/J001422/1), the ERC Advanced
Investigator program DUSTYGAL and a Royal Society/Wolfson Merit Award. P.N.B. acknowledges
support from STFC. R.M.S. acknowledges support from the grant ST/1001573/1. The
data presented here are based on observations with the KMOS spectrograph on the
ESO/VLT under program 60.A-9460 and can be accessed through the ESO data archive.
The authors also wish to acknowledge the help from Michael Hilker in preparing the
KMOS observations.'
article_number: '139'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: D.
full_name: Sobral, D.
last_name: Sobral
- first_name: A. M.
full_name: Swinbank, A. M.
last_name: Swinbank
- first_name: J. P.
full_name: Stott, J. P.
last_name: Stott
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: R. G.
full_name: Bower, R. G.
last_name: Bower
- first_name: Ian
full_name: Smail, Ian
last_name: Smail
- first_name: P.
full_name: Best, P.
last_name: Best
- first_name: J. E.
full_name: Geach, J. E.
last_name: Geach
- first_name: R. M.
full_name: Sharples, R. M.
last_name: Sharples
citation:
ama: Sobral D, Swinbank AM, Stott JP, et al. The dynamics of z=0.8 H-alpha-selected
star-forming galaxies from KMOS/CF-HiZELS. The Astrophysical Journal. 2013;779(2).
doi:10.1088/0004-637x/779/2/139
apa: Sobral, D., Swinbank, A. M., Stott, J. P., Matthee, J. J., Bower, R. G., Smail,
I., … Sharples, R. M. (2013). The dynamics of z=0.8 H-alpha-selected star-forming
galaxies from KMOS/CF-HiZELS. The Astrophysical Journal. IOP Publishing.
https://doi.org/10.1088/0004-637x/779/2/139
chicago: Sobral, D., A. M. Swinbank, J. P. Stott, Jorryt J Matthee, R. G. Bower,
Ian Smail, P. Best, J. E. Geach, and R. M. Sharples. “The Dynamics of Z=0.8 H-Alpha-Selected
Star-Forming Galaxies from KMOS/CF-HiZELS.” The Astrophysical Journal.
IOP Publishing, 2013. https://doi.org/10.1088/0004-637x/779/2/139.
ieee: D. Sobral et al., “The dynamics of z=0.8 H-alpha-selected star-forming
galaxies from KMOS/CF-HiZELS,” The Astrophysical Journal, vol. 779, no.
2. IOP Publishing, 2013.
ista: Sobral D, Swinbank AM, Stott JP, Matthee JJ, Bower RG, Smail I, Best P, Geach
JE, Sharples RM. 2013. The dynamics of z=0.8 H-alpha-selected star-forming galaxies
from KMOS/CF-HiZELS. The Astrophysical Journal. 779(2), 139.
mla: Sobral, D., et al. “The Dynamics of Z=0.8 H-Alpha-Selected Star-Forming Galaxies
from KMOS/CF-HiZELS.” The Astrophysical Journal, vol. 779, no. 2, 139,
IOP Publishing, 2013, doi:10.1088/0004-637x/779/2/139.
short: D. Sobral, A.M. Swinbank, J.P. Stott, J.J. Matthee, R.G. Bower, I. Smail,
P. Best, J.E. Geach, R.M. Sharples, The Astrophysical Journal 779 (2013).
date_created: 2022-07-07T09:14:48Z
date_published: 2013-12-03T00:00:00Z
date_updated: 2022-08-18T10:43:07Z
day: '03'
doi: 10.1088/0004-637x/779/2/139
extern: '1'
external_id:
arxiv:
- '1310.3822'
intvolume: ' 779'
issue: '2'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: evolution – galaxies'
- high-redshift – galaxies
- starburst
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1310.3822
month: '12'
oa: 1
oa_version: Preprint
publication: The Astrophysical Journal
publication_identifier:
eissn:
- 1538-4357
issn:
- 0004-637X
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: The dynamics of z=0.8 H-alpha-selected star-forming galaxies from KMOS/CF-HiZELS
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 779
year: '2013'
...
---
_id: '116'
abstract:
- lang: eng
text: 'We describe a model experiment for dynamic jamming: a two-dimensional collection
of initially unjammed disks that are forced into the jammed state by uniaxial
compression via a rake. This leads to a stable densification front that travels
ahead of the rake, leaving regions behind it jammed. Using disk conservation in
conjunction with an upper limit to the packing fraction at jamming onset, we predict
the front speed as a function of packing fraction and rake speed. However, we
find that the jamming front has a finite width, a feature that cannot be explained
by disk conservation alone. This width appears to diverge on approach to jamming,
which suggests that it may be related to growing lengthscales encountered in other
jamming studies.'
acknowledgement: This work was supported by the National Science Foundation (NSF)
through its Materials Research Science and Engineering program (DMR-0820054). SRW
was supported by the U.S. Department of Energy, Office of Basic Energy Sciences,
Division of Materials Sciences and Engineering under Award DE-FG02-03ER46088. LKR
acknowledges support through the NSF Research Experience for Undergraduates program.
article_number: '44001'
author:
- first_name: Scott R
full_name: Waitukaitis, Scott R
id: 3A1FFC16-F248-11E8-B48F-1D18A9856A87
last_name: Waitukaitis
orcid: 0000-0002-2299-3176
- first_name: Leah
full_name: Roth, Leah
last_name: Roth
- first_name: Vincenzo
full_name: Vitelli, Vincenzo
last_name: Vitelli
- first_name: Heinrich
full_name: Jaeger, Heinrich
last_name: Jaeger
citation:
ama: Waitukaitis SR, Roth L, Vitelli V, Jaeger H. Dynamic jamming fronts. EPL.
2013;102(4). doi:10.1209/0295-5075/102/44001
apa: Waitukaitis, S. R., Roth, L., Vitelli, V., & Jaeger, H. (2013). Dynamic
jamming fronts. EPL. Elsevier. https://doi.org/10.1209/0295-5075/102/44001
chicago: Waitukaitis, Scott R, Leah Roth, Vincenzo Vitelli, and Heinrich Jaeger.
“Dynamic Jamming Fronts.” EPL. Elsevier, 2013. https://doi.org/10.1209/0295-5075/102/44001.
ieee: S. R. Waitukaitis, L. Roth, V. Vitelli, and H. Jaeger, “Dynamic jamming fronts,”
EPL, vol. 102, no. 4. Elsevier, 2013.
ista: Waitukaitis SR, Roth L, Vitelli V, Jaeger H. 2013. Dynamic jamming fronts.
EPL. 102(4), 44001.
mla: Waitukaitis, Scott R., et al. “Dynamic Jamming Fronts.” EPL, vol. 102,
no. 4, 44001, Elsevier, 2013, doi:10.1209/0295-5075/102/44001.
short: S.R. Waitukaitis, L. Roth, V. Vitelli, H. Jaeger, EPL 102 (2013).
date_created: 2018-12-11T11:44:43Z
date_published: 2013-05-24T00:00:00Z
date_updated: 2021-01-12T06:48:44Z
day: '24'
doi: 10.1209/0295-5075/102/44001
extern: '1'
intvolume: ' 102'
issue: '4'
language:
- iso: eng
month: '05'
oa_version: None
publication: EPL
publication_status: published
publisher: Elsevier
publist_id: '7938'
quality_controlled: '1'
status: public
title: Dynamic jamming fronts
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 102
year: '2013'
...
---
_id: '11671'
abstract:
- lang: eng
text: "Given only the URL of a Web page, can we identify its language? In this article
we examine this question. URL-based language classification is useful when the
content of the Web page is not available or downloading the content is a waste
of bandwidth and time.\r\nWe built URL-based language classifiers for English,
German, French, Spanish, and Italian by applying a variety of algorithms and features.
As algorithms we used machine learning algorithms which are widely applied for
text classification and state-of-art algorithms for language identification of
text. As features we used words, various sized n-grams, and custom-made features
(our novel feature set). We compared our approaches with two baseline methods,
namely classification by country code top-level domains and classification by
IP addresses of the hosting Web servers.\r\n\r\nWe trained and tested our classifiers
in a 10-fold cross-validation setup on a dataset obtained from the Open Directory
Project and from querying a commercial search engine. We obtained the lowest F1-measure
for English (94) and the highest F1-measure for German (98) with the best performing
classifiers.\r\n\r\nWe also evaluated the performance of our methods: (i) on a
set of Web pages written in Adobe Flash and (ii) as part of a language-focused
crawler. In the first case, the content of the Web page is hard to extract and
in the second page downloading pages of the “wrong” language constitutes a waste
of bandwidth. In both settings the best classifiers have a high accuracy with
an F1-measure between 95 (for English) and 98 (for Italian) for the Adobe Flash
pages and a precision between 90 (for Italian) and 97 (for French) for the language-focused
crawler."
article_number: '3'
article_processing_charge: No
article_type: original
author:
- first_name: Eda
full_name: Baykan, Eda
last_name: Baykan
- first_name: Ingmar
full_name: Weber, Ingmar
last_name: Weber
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
citation:
ama: Baykan E, Weber I, Henzinger MH. A comprehensive study of techniques for URL-based
web page language classification. ACM Transactions on the Web. 2013;7(1).
doi:10.1145/2435215.2435218
apa: Baykan, E., Weber, I., & Henzinger, M. H. (2013). A comprehensive study
of techniques for URL-based web page language classification. ACM Transactions
on the Web. Association for Computing Machinery. https://doi.org/10.1145/2435215.2435218
chicago: Baykan, Eda, Ingmar Weber, and Monika H Henzinger. “A Comprehensive Study
of Techniques for URL-Based Web Page Language Classification.” ACM Transactions
on the Web. Association for Computing Machinery, 2013. https://doi.org/10.1145/2435215.2435218.
ieee: E. Baykan, I. Weber, and M. H. Henzinger, “A comprehensive study of techniques
for URL-based web page language classification,” ACM Transactions on the Web,
vol. 7, no. 1. Association for Computing Machinery, 2013.
ista: Baykan E, Weber I, Henzinger MH. 2013. A comprehensive study of techniques
for URL-based web page language classification. ACM Transactions on the Web. 7(1),
3.
mla: Baykan, Eda, et al. “A Comprehensive Study of Techniques for URL-Based Web
Page Language Classification.” ACM Transactions on the Web, vol. 7, no.
1, 3, Association for Computing Machinery, 2013, doi:10.1145/2435215.2435218.
short: E. Baykan, I. Weber, M.H. Henzinger, ACM Transactions on the Web 7 (2013).
date_created: 2022-07-27T12:50:18Z
date_published: 2013-03-01T00:00:00Z
date_updated: 2022-09-12T08:51:57Z
day: '01'
doi: 10.1145/2435215.2435218
extern: '1'
intvolume: ' 7'
issue: '1'
keyword:
- Computer Networks and Communications
language:
- iso: eng
month: '03'
oa_version: None
publication: ACM Transactions on the Web
publication_identifier:
eissn:
- 1559-114X
issn:
- 1559-1131
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
scopus_import: '1'
status: public
title: A comprehensive study of techniques for URL-based web page language classification
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2013'
...
---
_id: '117'
abstract:
- lang: eng
text: The packing arrangement of individual particles inside a granular material
and the resulting response to applied stresses depend critically on particle-particle
interactions. One aspect that recently received attention are nanoscale surface
features of particles, which play an important role in determining the strength
of cohesive van der Waals and capillary interactions and also affect tribo-charging
of grains. We describe experiments on freely falling granular streams that can
detect the contributions from all three of these forces. We show that it is possible
to measure the charge of individual grains and build up distributions that are
detailed enough to provide stringent tests of tribo-charging models currently
available. A second aspect concerns particle shape. In this case steric interactions
become important and new types of aggregate behavior can be expected when non-convex
particle shapes are considered that can interlock or entangle. However, a general
connection between the mechanical response of a granular material and the constituents\'
shape remains unknown. This has made it infeasible to tackle the "inverse
packing problem", namely to start from a given, desired behavior for the
aggregate as a whole and then find the particle shape the produces it. We discuss
a new approach, using concepts rooted in artificial evolution that provides a
way to solve this inverse problem. This approach facilitates exploring the role
of arbitrary particle geometry in jammed systems and invites the discovery and
design of granular matter with optimized properties.
acknowledgement: This work was supported by the NSF MRSEC program under DMR-0820054.
Additional support came from the US Army Research Office through W911NF-12-1-0182.
author:
- first_name: Heinrich
full_name: Jaeger, Heinrich
last_name: Jaeger
- first_name: Marc
full_name: Miskin, Marc
last_name: Miskin
- first_name: Scott R
full_name: Waitukaitis, Scott R
id: 3A1FFC16-F248-11E8-B48F-1D18A9856A87
last_name: Waitukaitis
orcid: 0000-0002-2299-3176
citation:
ama: 'Jaeger H, Miskin M, Waitukaitis SR. From nanoscale cohesion to macroscale
entanglement: opportunities for designing granular aggregate behaviour by tailoring
grain shape and interactions. In: AIP Conference Proceedings. Vol 1542.
AIP; 2013:3-6. doi:10.1063/1.4811858'
apa: 'Jaeger, H., Miskin, M., & Waitukaitis, S. R. (2013). From nanoscale cohesion
to macroscale entanglement: opportunities for designing granular aggregate behaviour
by tailoring grain shape and interactions. In AIP Conference Proceedings
(Vol. 1542, pp. 3–6). Sydney, Australia: AIP. https://doi.org/10.1063/1.4811858'
chicago: 'Jaeger, Heinrich, Marc Miskin, and Scott R Waitukaitis. “From Nanoscale
Cohesion to Macroscale Entanglement: Opportunities for Designing Granular Aggregate
Behaviour by Tailoring Grain Shape and Interactions.” In AIP Conference Proceedings,
1542:3–6. AIP, 2013. https://doi.org/10.1063/1.4811858.'
ieee: 'H. Jaeger, M. Miskin, and S. R. Waitukaitis, “From nanoscale cohesion to
macroscale entanglement: opportunities for designing granular aggregate behaviour
by tailoring grain shape and interactions,” in AIP Conference Proceedings,
Sydney, Australia, 2013, vol. 1542, pp. 3–6.'
ista: 'Jaeger H, Miskin M, Waitukaitis SR. 2013. From nanoscale cohesion to macroscale
entanglement: opportunities for designing granular aggregate behaviour by tailoring
grain shape and interactions. AIP Conference Proceedings. Powders and Grains
vol. 1542, 3–6.'
mla: 'Jaeger, Heinrich, et al. “From Nanoscale Cohesion to Macroscale Entanglement:
Opportunities for Designing Granular Aggregate Behaviour by Tailoring Grain Shape
and Interactions.” AIP Conference Proceedings, vol. 1542, AIP, 2013, pp.
3–6, doi:10.1063/1.4811858.'
short: H. Jaeger, M. Miskin, S.R. Waitukaitis, in:, AIP Conference Proceedings,
AIP, 2013, pp. 3–6.
conference:
end_date: 2013-07-12
location: Sydney, Australia
name: Powders and Grains
start_date: 2013-07-08
date_created: 2018-12-11T11:44:43Z
date_published: 2013-06-01T00:00:00Z
date_updated: 2021-01-12T06:48:49Z
day: '01'
doi: 10.1063/1.4811858
extern: '1'
intvolume: ' 1542'
language:
- iso: eng
month: '06'
oa_version: None
page: 3 - 6
publication: ' AIP Conference Proceedings'
publication_status: published
publisher: AIP
publist_id: '7937'
quality_controlled: '1'
status: public
title: 'From nanoscale cohesion to macroscale entanglement: opportunities for designing
granular aggregate behaviour by tailoring grain shape and interactions'
type: conference
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 1542
year: '2013'
...