---
_id: '2958'
abstract:
- lang: eng
text: 'The activity of hippocampal pyramidal cells reflects both the current position
of the animal and information related to its current behavior. Here we investigated
whether single hippocampal neurons can encode several independent features defining
trials during a memory task. We also tested whether task-related information is
represented by partial remapping of the place cell population or, instead, via
firing rate modulation of spatially stable place cells. To address these two questions,
the activity of hippocampal neurons was recorded in rats performing a conditional
discrimination task on a modified T-maze in which the identity of a food reward
guided behavior. When the rat was on the central arm of the maze, the firing rate
of pyramidal cells changed depending on two independent factors: (1) the identity
of the food reward given to the animal and (2) the previous location of the animal
on the maze. Importantly, some pyramidal cells encoded information relative to
both factors. This trial-type specific and retrospective coding did not interfere
with the spatial representation of the maze: hippocampal cells had stable place
fields and their theta-phase precession profiles were unaltered during the task,
indicating that trial-related information was encoded via rate remapping. During
error trials, encoding of both trial-related information and spatial location
was impaired. Finally, we found that pyramidal cells also encode trial-related
information via rate remapping during the continuous version of the rewarded alternation
task without delays. These results suggest that hippocampal neurons can encode
several task-related cognitive aspects via rate remapping.'
acknowledgement: J.C. was supported by a MRC Intramural Programme Grant (U138197111)
and a European Research Council Starter Grant (281511). K.A. held a Wellcome Trust
PhD studentship and a Humboldt Research Fellowship for Postdoctoral Researchers.
D.M.B. was supported by Wellcome Trust Senior Fellowships (074385 and 087736).
author:
- first_name: Kevin
full_name: Allen, Kevin
last_name: Allen
- first_name: J Nick
full_name: Rawlins, J Nick
last_name: Rawlins
- first_name: David
full_name: Bannerman, David
last_name: Bannerman
- first_name: Jozsef L
full_name: Csicsvari, Jozsef L
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
citation:
ama: Allen K, Rawlins JN, Bannerman D, Csicsvari JL. Hippocampal place cells can
encode multiple trial-dependent features through rate remapping. Journal of
Neuroscience. 2012;32(42):14752-14766. doi:10.1523/JNEUROSCI.6175-11.2012
apa: Allen, K., Rawlins, J. N., Bannerman, D., & Csicsvari, J. L. (2012). Hippocampal
place cells can encode multiple trial-dependent features through rate remapping.
Journal of Neuroscience. Society for Neuroscience. https://doi.org/10.1523/JNEUROSCI.6175-11.2012
chicago: Allen, Kevin, J Nick Rawlins, David Bannerman, and Jozsef L Csicsvari.
“Hippocampal Place Cells Can Encode Multiple Trial-Dependent Features through
Rate Remapping.” Journal of Neuroscience. Society for Neuroscience, 2012.
https://doi.org/10.1523/JNEUROSCI.6175-11.2012.
ieee: K. Allen, J. N. Rawlins, D. Bannerman, and J. L. Csicsvari, “Hippocampal place
cells can encode multiple trial-dependent features through rate remapping,” Journal
of Neuroscience, vol. 32, no. 42. Society for Neuroscience, pp. 14752–14766,
2012.
ista: Allen K, Rawlins JN, Bannerman D, Csicsvari JL. 2012. Hippocampal place cells
can encode multiple trial-dependent features through rate remapping. Journal of
Neuroscience. 32(42), 14752–14766.
mla: Allen, Kevin, et al. “Hippocampal Place Cells Can Encode Multiple Trial-Dependent
Features through Rate Remapping.” Journal of Neuroscience, vol. 32, no.
42, Society for Neuroscience, 2012, pp. 14752–66, doi:10.1523/JNEUROSCI.6175-11.2012.
short: K. Allen, J.N. Rawlins, D. Bannerman, J.L. Csicsvari, Journal of Neuroscience
32 (2012) 14752–14766.
date_created: 2018-12-11T12:00:33Z
date_published: 2012-10-17T00:00:00Z
date_updated: 2021-01-12T07:40:03Z
day: '17'
department:
- _id: JoCs
doi: 10.1523/JNEUROSCI.6175-11.2012
ec_funded: 1
external_id:
pmid:
- '23077060'
intvolume: ' 32'
issue: '42'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531717/
month: '10'
oa: 1
oa_version: Submitted Version
page: 14752 - 14766
pmid: 1
project:
- _id: 257A4776-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '281511'
name: Memory-related information processing in neuronal circuits of the hippocampus
and entorhinal cortex
publication: Journal of Neuroscience
publication_status: published
publisher: Society for Neuroscience
publist_id: '3768'
quality_controlled: '1'
scopus_import: 1
status: public
title: Hippocampal place cells can encode multiple trial-dependent features through
rate remapping
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2012'
...
---
_id: '2959'
abstract:
- lang: eng
text: We study maximum likelihood estimation in Gaussian graphical models from a
geometric point of view. An algebraic elimination criterion allows us to find
exact lower bounds on the number of observations needed to ensure that the maximum
likelihood estimator (MLE) exists with probability one. This is applied to bipartite
graphs, grids and colored graphs. We also study the ML degree, and we present
the first instance of a graph for which the MLE exists with probability one, even
when the number of observations equals the treewidth.
acknowledgement: "I wish to thank Bernd Sturmfels for many helpful discus- sions and
Steffen Lauritzen for introducing me to the problem of the existence of the MLE
in Gaussian graphical models. I would also like to thank two referees who provided
helpful comments on the original version of this paper.\r\n"
author:
- first_name: Caroline
full_name: Uhler, Caroline
id: 49ADD78E-F248-11E8-B48F-1D18A9856A87
last_name: Uhler
orcid: 0000-0002-7008-0216
citation:
ama: Uhler C. Geometry of maximum likelihood estimation in Gaussian graphical models.
Annals of Statistics. 2012;40(1):238-261. doi:10.1214/11-AOS957
apa: Uhler, C. (2012). Geometry of maximum likelihood estimation in Gaussian graphical
models. Annals of Statistics. Institute of Mathematical Statistics. https://doi.org/10.1214/11-AOS957
chicago: Uhler, Caroline. “Geometry of Maximum Likelihood Estimation in Gaussian
Graphical Models.” Annals of Statistics. Institute of Mathematical Statistics,
2012. https://doi.org/10.1214/11-AOS957.
ieee: C. Uhler, “Geometry of maximum likelihood estimation in Gaussian graphical
models,” Annals of Statistics, vol. 40, no. 1. Institute of Mathematical
Statistics, pp. 238–261, 2012.
ista: Uhler C. 2012. Geometry of maximum likelihood estimation in Gaussian graphical
models. Annals of Statistics. 40(1), 238–261.
mla: Uhler, Caroline. “Geometry of Maximum Likelihood Estimation in Gaussian Graphical
Models.” Annals of Statistics, vol. 40, no. 1, Institute of Mathematical
Statistics, 2012, pp. 238–61, doi:10.1214/11-AOS957.
short: C. Uhler, Annals of Statistics 40 (2012) 238–261.
date_created: 2018-12-11T12:00:33Z
date_published: 2012-02-01T00:00:00Z
date_updated: 2021-01-12T07:40:04Z
day: '01'
department:
- _id: CaUh
doi: 10.1214/11-AOS957
intvolume: ' 40'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://arxiv.org/abs/1012.2643
month: '02'
oa: 1
oa_version: Preprint
page: 238 - 261
publication: Annals of Statistics
publication_status: published
publisher: Institute of Mathematical Statistics
publist_id: '3767'
quality_controlled: '1'
scopus_import: 1
status: public
title: Geometry of maximum likelihood estimation in Gaussian graphical models
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 40
year: '2012'
...
---
_id: '2962'
abstract:
- lang: eng
text: The choice of summary statistics is a crucial step in approximate Bayesian
computation (ABC). Since statistics are often not sufficient, this choice involves
a trade-off between loss of information and reduction of dimensionality. The latter
may increase the efficiency of ABC. Here, we propose an approach for choosing
summary statistics based on boosting, a technique from the machine learning literature.
We consider different types of boosting and compare them to partial least squares
regression as an alternative. To mitigate the lack of sufficiency, we also propose
an approach for choosing summary statistics locally, in the putative neighborhood
of the true parameter value. We study a demographic model motivated by the re-introduction
of Alpine ibex (Capra ibex) into the Swiss Alps. The parameters of interest are
the mean and standard deviation across microsatellites of the scaled ancestral
mutation rate (θanc = 4 Ne u), and the proportion of males obtaining access to
matings per breeding season (ω). By simulation, we assess the properties of the
posterior distribution obtained with the various methods. According to our criteria,
ABC with summary statistics chosen locally via boosting with the L2-loss performs
best. Applying that method to the ibex data, we estimate θanc ≈ 1.288, and find
that most of the variation across loci of the ancestral mutation rate u is between
7.7×10−4 and 3.5×10−3 per locus per generation. The proportion of males with access
to matings is estimated to ω ≈ 0.21, which is in good agreement with recent independent
estimates.
acknowledged_ssus:
- _id: ScienComp
author:
- first_name: Simon
full_name: Aeschbacher, Simon
id: 2D35326E-F248-11E8-B48F-1D18A9856A87
last_name: Aeschbacher
- first_name: Mark
full_name: Beaumont, Mark
last_name: Beaumont
- first_name: Andreas
full_name: Futschik, Andreas
last_name: Futschik
citation:
ama: Aeschbacher S, Beaumont M, Futschik A. A novel approach for choosing summary
statistics in approximate Bayesian computation. Genetics. 2012;192(3):1027-1047.
doi:10.1534/genetics.112.143164
apa: Aeschbacher, S., Beaumont, M., & Futschik, A. (2012). A novel approach
for choosing summary statistics in approximate Bayesian computation. Genetics.
Genetics Society of America. https://doi.org/10.1534/genetics.112.143164
chicago: Aeschbacher, Simon, Mark Beaumont, and Andreas Futschik. “A Novel Approach
for Choosing Summary Statistics in Approximate Bayesian Computation.” Genetics.
Genetics Society of America, 2012. https://doi.org/10.1534/genetics.112.143164.
ieee: S. Aeschbacher, M. Beaumont, and A. Futschik, “A novel approach for choosing
summary statistics in approximate Bayesian computation,” Genetics, vol.
192, no. 3. Genetics Society of America, pp. 1027–1047, 2012.
ista: Aeschbacher S, Beaumont M, Futschik A. 2012. A novel approach for choosing
summary statistics in approximate Bayesian computation. Genetics. 192(3), 1027–1047.
mla: Aeschbacher, Simon, et al. “A Novel Approach for Choosing Summary Statistics
in Approximate Bayesian Computation.” Genetics, vol. 192, no. 3, Genetics
Society of America, 2012, pp. 1027–47, doi:10.1534/genetics.112.143164.
short: S. Aeschbacher, M. Beaumont, A. Futschik, Genetics 192 (2012) 1027–1047.
date_created: 2018-12-11T12:00:34Z
date_published: 2012-11-01T00:00:00Z
date_updated: 2021-01-12T07:40:05Z
day: '01'
department:
- _id: NiBa
doi: 10.1534/genetics.112.143164
external_id:
pmid:
- '22960215'
intvolume: ' 192'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522150/
month: '11'
oa: 1
oa_version: Submitted Version
page: 1027 - 1047
pmid: 1
publication: Genetics
publication_status: published
publisher: Genetics Society of America
publist_id: '3763'
quality_controlled: '1'
scopus_import: 1
status: public
title: A novel approach for choosing summary statistics in approximate Bayesian computation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 192
year: '2012'
...
---
_id: '2963'
abstract:
- lang: eng
text: 'Zebra finches are an ubiquitous model system for the study of vocal learning
in animal communication. Their song has been well described, but its possible
function(s) in social communication are only partly understood. The so-called
‘directed song’ is a high-intensity, high-performance song given during courtship
in close proximity to the female, which is known to mediate mate choice and mating.
However, this singing mode constitutes only a fraction of zebra finch males’ prolific
song output. Potential communicative functions of their second, ‘undirected’ singing
mode remain unresolved in the face of contradicting reports of both facilitating
and inhibiting effects of social company on singing. We addressed this issue by
experimentally manipulating social contexts in a within-subject design, comparing
a solo versus male or female only company condition, each lasting for 24 hours.
Males’ total song output was significantly higher when a conspecific was in audible
and visible distance than when they were alone. Male and female company had an
equally facilitating effect on song output. Our findings thus indicate that singing
motivation is facilitated rather than inhibited by social company, suggesting
that singing in zebra finches might function both in inter- and intrasexual communication. '
author:
- first_name: Fabienne
full_name: Jesse, Fabienne
id: 4C8C26A4-F248-11E8-B48F-1D18A9856A87
last_name: Jesse
- first_name: Katharina
full_name: Riebel, Katharina
last_name: Riebel
citation:
ama: Jesse F, Riebel K. Social facilitation of male song by male and female conspecifics
in the zebra finch, Taeniopygia guttata. Behavioural Processes. 2012;91(3):262-266.
doi:10.1016/j.beproc.2012.09.006
apa: Jesse, F., & Riebel, K. (2012). Social facilitation of male song by male
and female conspecifics in the zebra finch, Taeniopygia guttata. Behavioural
Processes. Elsevier. https://doi.org/10.1016/j.beproc.2012.09.006
chicago: Jesse, Fabienne, and Katharina Riebel. “Social Facilitation of Male Song
by Male and Female Conspecifics in the Zebra Finch, Taeniopygia Guttata.” Behavioural
Processes. Elsevier, 2012. https://doi.org/10.1016/j.beproc.2012.09.006.
ieee: F. Jesse and K. Riebel, “Social facilitation of male song by male and female
conspecifics in the zebra finch, Taeniopygia guttata,” Behavioural Processes,
vol. 91, no. 3. Elsevier, pp. 262–266, 2012.
ista: Jesse F, Riebel K. 2012. Social facilitation of male song by male and female
conspecifics in the zebra finch, Taeniopygia guttata. Behavioural Processes. 91(3),
262–266.
mla: Jesse, Fabienne, and Katharina Riebel. “Social Facilitation of Male Song by
Male and Female Conspecifics in the Zebra Finch, Taeniopygia Guttata.” Behavioural
Processes, vol. 91, no. 3, Elsevier, 2012, pp. 262–66, doi:10.1016/j.beproc.2012.09.006.
short: F. Jesse, K. Riebel, Behavioural Processes 91 (2012) 262–266.
date_created: 2018-12-11T12:00:35Z
date_published: 2012-11-01T00:00:00Z
date_updated: 2021-01-12T07:40:06Z
day: '01'
department:
- _id: JoBo
doi: 10.1016/j.beproc.2012.09.006
intvolume: ' 91'
issue: '3'
language:
- iso: eng
month: '11'
oa_version: None
page: 262 - 266
publication: Behavioural Processes
publication_status: published
publisher: Elsevier
publist_id: '3756'
quality_controlled: '1'
status: public
title: Social facilitation of male song by male and female conspecifics in the zebra
finch, Taeniopygia guttata
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 91
year: '2012'
...
---
_id: '2964'
abstract:
- lang: eng
text: 'CA3 pyramidal neurons are important for memory formation and pattern completion
in the hippocampal network. These neurons receive multiple excitatory inputs from
numerous sources. Therefore, the rules of spatiotemporal integration of multiple
synaptic inputs and propagation of action potentials are important to understand
how CA3 neurons contribute to higher brain functions at cellular level. By using
confocally targeted patch-clamp recording techniques, we investigated the biophysical
properties of rat CA3 pyramidal neuron dendrites. We found two distinct dendritic
domains critical for action potential initiation and propagation: In the proximal
domain, action potentials initiated in the axon backpropagate actively with large
amplitude and fast time course. In the distal domain, Na+-channel mediated dendritic
spikes are efficiently evoked by local dendritic depolarization or waveforms mimicking
synaptic events. These findings can be explained by a high Na+-to-K+ conductance
density ratio of CA3 pyramidal neuron dendrites. The results challenge the prevailing
view that proximal mossy fiber inputs activate CA3 pyramidal neurons more efficiently
than distal perforant inputs by showing that the distal synapses trigger a different
form of activity represented by dendritic spikes. The high probability of dendritic
spike initiation in the distal area may enhance the computational power of CA3
pyramidal neurons in the hippocampal network. '
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Sooyun
full_name: Kim, Sooyun
id: 394AB1C8-F248-11E8-B48F-1D18A9856A87
last_name: Kim
citation:
ama: Kim S. Active properties of hippocampal CA3 pyramidal neuron dendrites. 2012.
apa: Kim, S. (2012). Active properties of hippocampal CA3 pyramidal neuron dendrites.
Institute of Science and Technology Austria.
chicago: Kim, Sooyun. “Active Properties of Hippocampal CA3 Pyramidal Neuron Dendrites.”
Institute of Science and Technology Austria, 2012.
ieee: S. Kim, “Active properties of hippocampal CA3 pyramidal neuron dendrites,”
Institute of Science and Technology Austria, 2012.
ista: Kim S. 2012. Active properties of hippocampal CA3 pyramidal neuron dendrites.
Institute of Science and Technology Austria.
mla: Kim, Sooyun. Active Properties of Hippocampal CA3 Pyramidal Neuron Dendrites.
Institute of Science and Technology Austria, 2012.
short: S. Kim, Active Properties of Hippocampal CA3 Pyramidal Neuron Dendrites,
Institute of Science and Technology Austria, 2012.
date_created: 2018-12-11T12:00:35Z
date_published: 2012-06-01T00:00:00Z
date_updated: 2023-09-07T11:43:51Z
day: '01'
degree_awarded: PhD
department:
- _id: PeJo
- _id: GradSch
language:
- iso: eng
month: '06'
oa_version: None
page: '65'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '3755'
related_material:
record:
- id: '3258'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Peter M
full_name: Jonas, Peter M
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
title: Active properties of hippocampal CA3 pyramidal neuron dendrites
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2012'
...
---
_id: '2965'
abstract:
- lang: eng
text: Dieser Artikel soll die sechs verschiedenen Creative Commons Lizenzen erläutern
und ihre Bedeutung im Rahmen des wissenschaftlichen Publizierens und des Open
Access erklären (CC-BY, CC-BY-SA, CC-BY-NC, CC-BY-ND, CC-BYNC-SA, CC-BY-NC-ND).
author:
- first_name: Patrick
full_name: Danowski, Patrick
id: 2EBD1598-F248-11E8-B48F-1D18A9856A87
last_name: Danowski
orcid: 0000-0002-6026-4409
citation:
ama: 'Danowski P. Kontext Open Access: Creative Commons. Mitteilungen der Vereinigung
Österreichischer Bibliothekarinnen & Bibliothekare. 2012;65(2):200-212.'
apa: 'Danowski, P. (2012). Kontext Open Access: Creative Commons. Mitteilungen
der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare. VÖB.'
chicago: 'Danowski, Patrick. “Kontext Open Access: Creative Commons.” Mitteilungen
der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare. VÖB,
2012.'
ieee: 'P. Danowski, “Kontext Open Access: Creative Commons,” Mitteilungen der
Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare, vol. 65,
no. 2. VÖB, pp. 200–212, 2012.'
ista: 'Danowski P. 2012. Kontext Open Access: Creative Commons. Mitteilungen der
Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare. 65(2), 200–212.'
mla: 'Danowski, Patrick. “Kontext Open Access: Creative Commons.” Mitteilungen
der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare, vol.
65, no. 2, VÖB, 2012, pp. 200–12.'
short: P. Danowski, Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen
& Bibliothekare 65 (2012) 200–212.
date_created: 2018-12-11T12:00:35Z
date_published: 2012-09-01T00:00:00Z
date_updated: 2021-01-12T07:40:07Z
day: '01'
ddc:
- '020'
department:
- _id: E-Lib
file:
- access_level: open_access
checksum: 162eea47d9d840c26b496ba6ae4d1c09
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:08:42Z
date_updated: 2020-07-14T12:45:57Z
file_id: '4703'
file_name: IST-2012-95-v1+1_sp-beitrag_danowski_kontext_open_access_creative_commons.pdf
file_size: 503345
relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: ' 65'
issue: '2'
language:
- iso: ger
license: https://creativecommons.org/licenses/by/4.0/
main_file_link:
- open_access: '1'
url: ' http://hdl.handle.net/10760/17625'
month: '09'
oa: 1
oa_version: Published Version
page: 200 - 212
popular_science: '1'
publication: Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare
publication_status: published
publisher: VÖB
publist_id: '3754'
pubrep_id: '95'
scopus_import: 1
status: public
title: 'Kontext Open Access: Creative Commons'
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: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 65
year: '2012'
...
---
_id: '2966'
abstract:
- lang: eng
text: 'Background: The outcome of male-male competition can be predicted from the
relative fighting qualities of the opponents, which often depend on their age.
In insects, freshly emerged and still sexually inactive males are morphologically
indistinct from older, sexually active males. These young inactive males may thus
be easy targets for older males if they cannot conceal themselves from their attacks.
The ant Cardiocondyla obscurior is characterised by lethal fighting between wingless
(" ergatoid" ) males. Here, we analyse for how long young males are
defenceless after eclosion, and how early adult males can detect the presence
of rival males.Results: We found that old ergatoid males consistently won fights
against ergatoid males younger than two days. Old males did not differentiate
between different types of unpigmented pupae several days before emergence, but
had more frequent contact to ready-to-eclose pupae of female sexuals and winged
males than of workers and ergatoid males. In rare cases, old ergatoid males displayed
alleviated biting of pigmented ergatoid male pupae shortly before adult eclosion,
as well as copulation attempts to dark pupae of female sexuals and winged males.
Ergatoid male behaviour may be promoted by a closer similarity of the chemical
profile of ready-to-eclose pupae to the profile of adults than that of young pupae
several days prior to emergence.Conclusion: Young ergatoid males of C. obscurior
would benefit greatly by hiding their identity from older, resident males, as
they are highly vulnerable during the first two days of their adult lives. In
contrast to the winged males of the same species, which are able to prevent ergatoid
male attacks by chemical female mimicry, young ergatoids do not seem to be able
to produce a protective chemical profile. Conflicts in male-male competition between
ergatoid males of different age thus seem to be resolved in favour of the older
males. This might represent selection at the colony level rather than the individual
level. © 2012 Cremer et al.; licensee BioMed Central Ltd.'
article_number: '7'
author:
- first_name: Sylvia
full_name: Cremer, Sylvia
id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
last_name: Cremer
orcid: 0000-0002-2193-3868
- first_name: Masaki
full_name: Suefuji, Masaki
last_name: Suefuji
- first_name: Alexandra
full_name: Schrempf, Alexandra
last_name: Schrempf
- first_name: Jürgen
full_name: Heinze, Jürgen
last_name: Heinze
citation:
ama: Cremer S, Suefuji M, Schrempf A, Heinze J. The dynamics of male-male competition
in Cardiocondyla obscurior ants. BMC Ecology. 2012;12. doi:10.1186/1472-6785-12-7
apa: Cremer, S., Suefuji, M., Schrempf, A., & Heinze, J. (2012). The dynamics
of male-male competition in Cardiocondyla obscurior ants. BMC Ecology.
BioMed Central. https://doi.org/10.1186/1472-6785-12-7
chicago: Cremer, Sylvia, Masaki Suefuji, Alexandra Schrempf, and Jürgen Heinze.
“The Dynamics of Male-Male Competition in Cardiocondyla Obscurior Ants.” BMC
Ecology. BioMed Central, 2012. https://doi.org/10.1186/1472-6785-12-7.
ieee: S. Cremer, M. Suefuji, A. Schrempf, and J. Heinze, “The dynamics of male-male
competition in Cardiocondyla obscurior ants,” BMC Ecology, vol. 12. BioMed
Central, 2012.
ista: Cremer S, Suefuji M, Schrempf A, Heinze J. 2012. The dynamics of male-male
competition in Cardiocondyla obscurior ants. BMC Ecology. 12, 7.
mla: Cremer, Sylvia, et al. “The Dynamics of Male-Male Competition in Cardiocondyla
Obscurior Ants.” BMC Ecology, vol. 12, 7, BioMed Central, 2012, doi:10.1186/1472-6785-12-7.
short: S. Cremer, M. Suefuji, A. Schrempf, J. Heinze, BMC Ecology 12 (2012).
date_created: 2018-12-11T12:00:35Z
date_published: 2012-06-15T00:00:00Z
date_updated: 2021-01-12T07:40:07Z
day: '15'
ddc:
- '570'
department:
- _id: SyCr
doi: 10.1186/1472-6785-12-7
file:
- access_level: open_access
checksum: 03d004bdff3724fb1627e3f5004bad80
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:08:44Z
date_updated: 2020-07-14T12:45:57Z
file_id: '4706'
file_name: IST-2012-94-v1+1_1472-6785-12-7.pdf
file_size: 489994
relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: ' 12'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: BMC Ecology
publication_status: published
publisher: BioMed Central
publist_id: '3753'
pubrep_id: '94'
quality_controlled: '1'
scopus_import: 1
status: public
title: The dynamics of male-male competition in Cardiocondyla obscurior ants
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 12
year: '2012'
...
---
_id: '2967'
abstract:
- lang: eng
text: For programs whose data variables range over Boolean or finite domains, program
verification is decidable, and this forms the basis of recent tools for software
model checking. In this article, we consider algorithmic verification of programs
that use Boolean variables, and in addition, access a single read-only array whose
length is potentially unbounded, and whose elements range over an unbounded data
domain. We show that the reachability problem, while undecidable in general, is
(1) PSPACE-complete for programs in which the array-accessing for-loops are not
nested, (2) decidable for a restricted class of programs with doubly nested loops.
The second result establishes connections to automata and logics defining languages
over data words.
acknowledgement: This research was supported in part by the NSF Cybertrust award CNS
0524059, by the European Research Council (ERC) Advanced Investigator Grant QUAREM,
and by the Austrian Science Fund (FWF) project S11402-N23.
article_number: '27'
author:
- first_name: Rajeev
full_name: Alur, Rajeev
last_name: Alur
- first_name: Pavol
full_name: Cerny, Pavol
id: 4DCBEFFE-F248-11E8-B48F-1D18A9856A87
last_name: Cerny
- first_name: Scott
full_name: Weinstein, Scott
last_name: Weinstein
citation:
ama: Alur R, Cerny P, Weinstein S. Algorithmic analysis of array-accessing programs.
ACM Transactions on Computational Logic (TOCL). 2012;13(3). doi:10.1145/2287718.2287727
apa: Alur, R., Cerny, P., & Weinstein, S. (2012). Algorithmic analysis of array-accessing
programs. ACM Transactions on Computational Logic (TOCL). ACM. https://doi.org/10.1145/2287718.2287727
chicago: Alur, Rajeev, Pavol Cerny, and Scott Weinstein. “Algorithmic Analysis of
Array-Accessing Programs.” ACM Transactions on Computational Logic (TOCL).
ACM, 2012. https://doi.org/10.1145/2287718.2287727.
ieee: R. Alur, P. Cerny, and S. Weinstein, “Algorithmic analysis of array-accessing
programs,” ACM Transactions on Computational Logic (TOCL), vol. 13, no.
3. ACM, 2012.
ista: Alur R, Cerny P, Weinstein S. 2012. Algorithmic analysis of array-accessing
programs. ACM Transactions on Computational Logic (TOCL). 13(3), 27.
mla: Alur, Rajeev, et al. “Algorithmic Analysis of Array-Accessing Programs.” ACM
Transactions on Computational Logic (TOCL), vol. 13, no. 3, 27, ACM, 2012,
doi:10.1145/2287718.2287727.
short: R. Alur, P. Cerny, S. Weinstein, ACM Transactions on Computational Logic
(TOCL) 13 (2012).
date_created: 2018-12-11T12:00:36Z
date_published: 2012-08-01T00:00:00Z
date_updated: 2023-02-23T12:09:43Z
day: '01'
department:
- _id: ToHe
doi: 10.1145/2287718.2287727
ec_funded: 1
intvolume: ' 13'
issue: '3'
language:
- iso: eng
month: '08'
oa_version: None
project:
- _id: 25EE3708-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '267989'
name: Quantitative Reactive Modeling
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
publication: ACM Transactions on Computational Logic (TOCL)
publication_status: published
publisher: ACM
publist_id: '3748'
quality_controlled: '1'
related_material:
record:
- id: '4403'
relation: earlier_version
status: public
scopus_import: 1
status: public
title: Algorithmic analysis of array-accessing programs
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2012'
...
---
_id: '2968'
abstract:
- lang: eng
text: Little is known about the stability of trophic relationships in complex natural
communities over evolutionary timescales. Here, we use sequence data from 18 nuclear
loci to reconstruct and compare the intraspecific histories of major Pleistocene
refugial populations in the Middle East, the Balkans and Iberia in a guild of
four Chalcid parasitoids (Cecidostiba fungosa, Cecidostiba semifascia, Hobbya
stenonota and Mesopolobus amaenus) all attacking Cynipid oak galls. We develop
a likelihood method to numerically estimate models of divergence between three
populations from multilocus data. We investigate the power of this framework on
simulated data, and-using triplet alignments of intronic loci-quantify the support
for all possible divergence relationships between refugial populations in the
four parasitoids. Although an East to West order of population divergence has
highest support in all but one species, we cannot rule out alternative population
tree topologies. Comparing the estimated times of population splits between species,
we find that one species, M. amaenus, has a significantly older history than the
rest of the guild and must have arrived in central Europe at least one glacial
cycle prior to other guild members. This suggests that although all four species
may share a common origin in the East, they expanded westwards into Europe at
different times. © 2012 Blackwell Publishing Ltd.
acknowledgement: "This work was supported by funding from the UK Natural Environment
Research Council to KL (NE/I020288/1) and GS (NE/H000038/1, NE/E014453/1, NER/B/504406/1,
NER/B/S2003/00856) and a grant from the European Research Council (250152) to NB.\r\nWe
thank Majide Tavakoli, Juli Pujade-Villar and Pablo-Fuentes Utrilla for contributing
specimens. Mike Hickerson and three anonymous reviewers gave helpful comments on
earlier versions of the manuscript. "
author:
- first_name: Konrad
full_name: Lohse, Konrad
last_name: Lohse
- first_name: Nicholas H
full_name: Barton, Nicholas H
id: 4880FE40-F248-11E8-B48F-1D18A9856A87
last_name: Barton
orcid: 0000-0002-8548-5240
- first_name: George
full_name: Melika, George
last_name: Melika
- first_name: Graham
full_name: Stone, Graham
last_name: Stone
citation:
ama: Lohse K, Barton NH, Melika G, Stone G. A likelihood based comparison of population
histories in a parasitoid guild. Molecular Ecology. 2012;21(18):4605-4617.
doi:10.1111/j.1365-294X.2012.05700.x
apa: Lohse, K., Barton, N. H., Melika, G., & Stone, G. (2012). A likelihood
based comparison of population histories in a parasitoid guild. Molecular Ecology.
Wiley-Blackwell. https://doi.org/10.1111/j.1365-294X.2012.05700.x
chicago: Lohse, Konrad, Nicholas H Barton, George Melika, and Graham Stone. “A Likelihood
Based Comparison of Population Histories in a Parasitoid Guild.” Molecular
Ecology. Wiley-Blackwell, 2012. https://doi.org/10.1111/j.1365-294X.2012.05700.x.
ieee: K. Lohse, N. H. Barton, G. Melika, and G. Stone, “A likelihood based comparison
of population histories in a parasitoid guild,” Molecular Ecology, vol.
21, no. 18. Wiley-Blackwell, pp. 4605–4617, 2012.
ista: Lohse K, Barton NH, Melika G, Stone G. 2012. A likelihood based comparison
of population histories in a parasitoid guild. Molecular Ecology. 21(18), 4605–4617.
mla: Lohse, Konrad, et al. “A Likelihood Based Comparison of Population Histories
in a Parasitoid Guild.” Molecular Ecology, vol. 21, no. 18, Wiley-Blackwell,
2012, pp. 4605–17, doi:10.1111/j.1365-294X.2012.05700.x.
short: K. Lohse, N.H. Barton, G. Melika, G. Stone, Molecular Ecology 21 (2012) 4605–4617.
date_created: 2018-12-11T12:00:36Z
date_published: 2012-09-01T00:00:00Z
date_updated: 2023-05-30T13:07:47Z
day: '01'
ddc:
- '570'
- '579'
department:
- _id: NiBa
doi: 10.1111/j.1365-294X.2012.05700.x
ec_funded: 1
file:
- access_level: open_access
checksum: c14ee4cb2a8ba9575bfd8a9bb7a883bb
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:17:47Z
date_updated: 2020-07-14T12:45:57Z
file_id: '5304'
file_name: IST-2014-296-v1+1_4_wasps_revised3.pdf
file_size: 235820
relation: main_file
- access_level: open_access
checksum: f00afc5b887c8222014b57375b8caece
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:17:48Z
date_updated: 2020-07-14T12:45:57Z
file_id: '5305'
file_name: IST-2014-296-v1+2_4_wasps_Supporting2.pdf
file_size: 41975
relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: ' 21'
issue: '18'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Submitted Version
page: 4605 - 4617
project:
- _id: 25B07788-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '250152'
name: Limits to selection in biology and in evolutionary computation
publication: Molecular Ecology
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3746'
pubrep_id: '296'
quality_controlled: '1'
related_material:
record:
- id: '13075'
relation: research_data
status: public
scopus_import: 1
status: public
title: A likelihood based comparison of population histories in a parasitoid guild
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 21
year: '2012'
...
---
_id: '2969'
abstract:
- lang: eng
text: "The coupling between presynaptic Ca^(2+) channels and Ca^(2+) sensors of
exocytosis is a key determinant of synaptic transmission. Evoked release from
parvalbumin (PV)-expressing interneurons is triggered by nanodomain coupling of
P/Q-type Ca^(2+) channels, whereas release from cholecystokinin (CCK)-containing
interneurons is generated by microdomain coupling of N-type channels. Nanodomain
coupling has several functional advantages, including speed and efficacy of transmission.
One potential disadvantage is that stochastic\r\nopening of presynaptic Ca^(2+)
channels may trigger spontaneous transmitter release. We addressed this possibility
in rat hippocampal\r\ngranule cells, which receive converging inputs from different
inhibitory sources. Both reduction of extracellular Ca^(2+) concentration and
the unselective Ca^(2+) channel blocker Cd^(2+) reduced the frequency of miniature
IPSCs (mIPSCs) in granule cells by ~50%, suggesting that the opening of presynaptic
Ca^(2+) channels contributes to spontaneous release. Application of the selective
P/Q-type Ca^(2+) channel blocker\r\nω-agatoxin IVa had no detectable effects,
whereas both the N-type blocker ω-conotoxin GVIa and the L-type blocker nimodipine
reduced\r\nmIPSC frequency. Furthermore, both the fast Ca^(2+) chelator BAPTA-AM
and the slow chelator EGTA-AM reduced the mIPSC frequency,\r\nsuggesting that
Ca^(2+)-dependent spontaneous release is triggered by microdomain rather than
nanodomain coupling. The CB_(1) receptor\r\nagonist WIN 55212-2 also decreased
spontaneous release; this effect was occluded by prior application of ω-conotoxin
GVIa, suggesting that a major fraction of Ca^(2+)-dependent spontaneous release
was generated at the terminals of CCK-expressing interneurons. Tonic inhibition
generated by spontaneous opening of presynaptic N- and L-type Ca^(2+) channels
may be important for hippocampal information processing.\r\n"
acknowledgement: This work was supported by grants from the Deutsche Forschungsgemeinschaft
(TR 3/B10, Leibniz program, GSC-4 Spemann Graduate School) and the European Union
(European Research Council Advanced Grant).
author:
- first_name: Sarit
full_name: Goswami, Sarit
id: 3A578F32-F248-11E8-B48F-1D18A9856A87
last_name: Goswami
- first_name: Iancu
full_name: Bucurenciu, Iancu
last_name: Bucurenciu
- first_name: Peter M
full_name: Jonas, Peter M
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
citation:
ama: Goswami S, Bucurenciu I, Jonas PM. Miniature IPSCs in hippocampal granule cells
are triggered by voltage-gated Ca^(2+) channels via microdomain coupling. Journal
of Neuroscience. 2012;32(41):14294-14304. doi:10.1523/JNEUROSCI.6104-11.2012
apa: Goswami, S., Bucurenciu, I., & Jonas, P. M. (2012). Miniature IPSCs in
hippocampal granule cells are triggered by voltage-gated Ca^(2+) channels via
microdomain coupling. Journal of Neuroscience. Society for Neuroscience.
https://doi.org/10.1523/JNEUROSCI.6104-11.2012
chicago: Goswami, Sarit, Iancu Bucurenciu, and Peter M Jonas. “Miniature IPSCs in
Hippocampal Granule Cells Are Triggered by Voltage-Gated Ca^(2+) Channels via
Microdomain Coupling.” Journal of Neuroscience. Society for Neuroscience,
2012. https://doi.org/10.1523/JNEUROSCI.6104-11.2012.
ieee: S. Goswami, I. Bucurenciu, and P. M. Jonas, “Miniature IPSCs in hippocampal
granule cells are triggered by voltage-gated Ca^(2+) channels via microdomain
coupling,” Journal of Neuroscience, vol. 32, no. 41. Society for Neuroscience,
pp. 14294–14304, 2012.
ista: Goswami S, Bucurenciu I, Jonas PM. 2012. Miniature IPSCs in hippocampal granule
cells are triggered by voltage-gated Ca^(2+) channels via microdomain coupling.
Journal of Neuroscience. 32(41), 14294–14304.
mla: Goswami, Sarit, et al. “Miniature IPSCs in Hippocampal Granule Cells Are Triggered
by Voltage-Gated Ca^(2+) Channels via Microdomain Coupling.” Journal of Neuroscience,
vol. 32, no. 41, Society for Neuroscience, 2012, pp. 14294–304, doi:10.1523/JNEUROSCI.6104-11.2012.
short: S. Goswami, I. Bucurenciu, P.M. Jonas, Journal of Neuroscience 32 (2012)
14294–14304.
date_created: 2018-12-11T12:00:36Z
date_published: 2012-10-10T00:00:00Z
date_updated: 2021-01-12T07:40:08Z
day: '10'
department:
- _id: PeJo
doi: 10.1523/JNEUROSCI.6104-11.2012
external_id:
pmid:
- '23055500'
intvolume: ' 32'
issue: '41'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3632771/
month: '10'
oa: 1
oa_version: Submitted Version
page: 14294 - 14304
pmid: 1
project:
- _id: 25BDE9A4-B435-11E9-9278-68D0E5697425
grant_number: SFB-TR3-TP10B
name: Glutamaterge synaptische Übertragung und Plastizität in hippocampalen Mikroschaltkreisen
publication: Journal of Neuroscience
publication_status: published
publisher: Society for Neuroscience
publist_id: '3744'
quality_controlled: '1'
scopus_import: 1
status: public
title: Miniature IPSCs in hippocampal granule cells are triggered by voltage-gated
Ca^(2+) channels via microdomain coupling
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2012'
...
---
_id: '2970'
abstract:
- lang: eng
text: Morphogen gradients regulate the patterning and growth of many tissues, hence
a key question is how they are established and maintained during development.
Theoretical descriptions have helped to explain how gradient shape is controlled
by the rates of morphogen production, spreading and degradation. These effective
rates have been measured using fluorescence recovery after photobleaching (FRAP)
and photoactivation. To unravel which molecular events determine the effective
rates, such tissue-level assays have been combined with genetic analysis, high-resolution
assays, and models that take into account interactions with receptors, extracellular
components and trafficking. Nevertheless, because of the natural and experimental
data variability, and the underlying assumptions of transport models, it remains
challenging to conclusively distinguish between cellular mechanisms.
acknowledgement: AK is currently supported by an MRC CDF. MGG and OW were supported
by the Swiss National Science Foundation, grants from the Swiss SystemsX.ch initiative,
LipidX-2008/011, an ERC advanced investigator grant and the Polish-Swiss research
program.
author:
- first_name: Anna
full_name: Kicheva, Anna
id: 3959A2A0-F248-11E8-B48F-1D18A9856A87
last_name: Kicheva
orcid: 0000-0003-4509-4998
- first_name: Mark Tobias
full_name: Bollenbach, Mark Tobias
id: 3E6DB97A-F248-11E8-B48F-1D18A9856A87
last_name: Bollenbach
orcid: 0000-0003-4398-476X
- first_name: Ortrud
full_name: Wartlick, Ortrud
last_name: Wartlick
- first_name: Frank
full_name: Julicher, Frank
last_name: Julicher
- first_name: Marcos
full_name: Gonzalez Gaitan, Marcos
last_name: Gonzalez Gaitan
citation:
ama: 'Kicheva A, Bollenbach MT, Wartlick O, Julicher F, Gonzalez Gaitan M. Investigating
the principles of morphogen gradient formation: from tissues to cells. Current
Opinion in Genetics & Development. 2012;22(6):527-532. doi:10.1016/j.gde.2012.08.004'
apa: 'Kicheva, A., Bollenbach, M. T., Wartlick, O., Julicher, F., & Gonzalez
Gaitan, M. (2012). Investigating the principles of morphogen gradient formation:
from tissues to cells. Current Opinion in Genetics & Development. Elsevier.
https://doi.org/10.1016/j.gde.2012.08.004'
chicago: 'Kicheva, Anna, Mark Tobias Bollenbach, Ortrud Wartlick, Frank Julicher,
and Marcos Gonzalez Gaitan. “Investigating the Principles of Morphogen Gradient
Formation: From Tissues to Cells.” Current Opinion in Genetics & Development.
Elsevier, 2012. https://doi.org/10.1016/j.gde.2012.08.004.'
ieee: 'A. Kicheva, M. T. Bollenbach, O. Wartlick, F. Julicher, and M. Gonzalez Gaitan,
“Investigating the principles of morphogen gradient formation: from tissues to
cells,” Current Opinion in Genetics & Development, vol. 22, no. 6.
Elsevier, pp. 527–532, 2012.'
ista: 'Kicheva A, Bollenbach MT, Wartlick O, Julicher F, Gonzalez Gaitan M. 2012.
Investigating the principles of morphogen gradient formation: from tissues to
cells. Current Opinion in Genetics & Development. 22(6), 527–532.'
mla: 'Kicheva, Anna, et al. “Investigating the Principles of Morphogen Gradient
Formation: From Tissues to Cells.” Current Opinion in Genetics & Development,
vol. 22, no. 6, Elsevier, 2012, pp. 527–32, doi:10.1016/j.gde.2012.08.004.'
short: A. Kicheva, M.T. Bollenbach, O. Wartlick, F. Julicher, M. Gonzalez Gaitan,
Current Opinion in Genetics & Development 22 (2012) 527–532.
date_created: 2018-12-11T12:00:37Z
date_published: 2012-12-01T00:00:00Z
date_updated: 2021-01-12T07:40:09Z
day: '01'
department:
- _id: ToBo
doi: 10.1016/j.gde.2012.08.004
intvolume: ' 22'
issue: '6'
language:
- iso: eng
month: '12'
oa_version: None
page: 527 - 532
publication: Current Opinion in Genetics & Development
publication_status: published
publisher: Elsevier
publist_id: '3739'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Investigating the principles of morphogen gradient formation: from tissues
to cells'
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 22
year: '2012'
...
---
_id: '2971'
abstract:
- lang: eng
text: 'We study the task of interactive semantic labeling of a segmentation hierarchy.
To this end we propose a framework interleaving two components: an automatic labeling
step, based on a Conditional Random Field whose dependencies are defined by the
inclusion tree of the segmentation hierarchy, and an interaction step that integrates
incremental input from a human user. Evaluated on two distinct datasets, the proposed
interactive approach efficiently integrates human interventions and illustrates
the advantages of structured prediction in an interactive framework. '
author:
- first_name: Georg
full_name: Zankl, Georg
last_name: Zankl
- first_name: Yll
full_name: Haxhimusa, Yll
last_name: Haxhimusa
- first_name: Adrian
full_name: Ion, Adrian
id: 29F89302-F248-11E8-B48F-1D18A9856A87
last_name: Ion
citation:
ama: 'Zankl G, Haxhimusa Y, Ion A. Interactive labeling of image segmentation hierarchies.
In: Vol 7476. Springer; 2012:11-20. doi:10.1007/978-3-642-32717-9_2'
apa: 'Zankl, G., Haxhimusa, Y., & Ion, A. (2012). Interactive labeling of image
segmentation hierarchies (Vol. 7476, pp. 11–20). Presented at the Pattern Recognition,
Graz, Austria: Springer. https://doi.org/10.1007/978-3-642-32717-9_2'
chicago: Zankl, Georg, Yll Haxhimusa, and Adrian Ion. “Interactive Labeling of Image
Segmentation Hierarchies,” 7476:11–20. Springer, 2012. https://doi.org/10.1007/978-3-642-32717-9_2.
ieee: G. Zankl, Y. Haxhimusa, and A. Ion, “Interactive labeling of image segmentation
hierarchies,” presented at the Pattern Recognition, Graz, Austria, 2012, vol.
7476, pp. 11–20.
ista: Zankl G, Haxhimusa Y, Ion A. 2012. Interactive labeling of image segmentation
hierarchies. Pattern Recognition vol. 7476, 11–20.
mla: Zankl, Georg, et al. Interactive Labeling of Image Segmentation Hierarchies.
Vol. 7476, Springer, 2012, pp. 11–20, doi:10.1007/978-3-642-32717-9_2.
short: G. Zankl, Y. Haxhimusa, A. Ion, in:, Springer, 2012, pp. 11–20.
conference:
end_date: 2012-08-31
location: Graz, Austria
name: Pattern Recognition
start_date: 2012-08-28
date_created: 2018-12-11T12:00:37Z
date_published: 2012-01-01T00:00:00Z
date_updated: 2021-01-12T07:40:10Z
day: '01'
department:
- _id: HeEd
doi: 10.1007/978-3-642-32717-9_2
intvolume: ' 7476'
language:
- iso: eng
month: '01'
oa_version: None
page: 11 - 20
publication_status: published
publisher: Springer
publist_id: '3737'
quality_controlled: '1'
scopus_import: 1
status: public
title: Interactive labeling of image segmentation hierarchies
type: conference
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7476
year: '2012'
...
---
_id: '2972'
abstract:
- lang: eng
text: 'Energy parity games are infinite two-player turn-based games played on weighted
graphs. The objective of the game combines a (qualitative) parity condition with
the (quantitative) requirement that the sum of the weights (i.e., the level of
energy in the game) must remain positive. Beside their own interest in the design
and synthesis of resource-constrained omega-regular specifications, energy parity
games provide one of the simplest model of games with combined qualitative and
quantitative objectives. Our main results are as follows: (a) exponential memory
is sufficient and may be necessary for winning strategies in energy parity games;
(b) the problem of deciding the winner in energy parity games can be solved in
NP ∩ coNP; and (c) we give an algorithm to solve energy parity by reduction to
energy games. We also show that the problem of deciding the winner in energy parity
games is logspace-equivalent to the problem of deciding the winner in mean-payoff
parity games, which can thus be solved in NP ∩ coNP. As a consequence we also
obtain a conceptually simple algorithm to solve mean-payoff parity games.'
arxiv: 1
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Laurent
full_name: Doyen, Laurent
last_name: Doyen
citation:
ama: Chatterjee K, Doyen L. Energy parity games. Theoretical Computer Science.
2012;458:49-60. doi:10.1016/j.tcs.2012.07.038
apa: Chatterjee, K., & Doyen, L. (2012). Energy parity games. Theoretical
Computer Science. Elsevier. https://doi.org/10.1016/j.tcs.2012.07.038
chicago: Chatterjee, Krishnendu, and Laurent Doyen. “Energy Parity Games.” Theoretical
Computer Science. Elsevier, 2012. https://doi.org/10.1016/j.tcs.2012.07.038.
ieee: K. Chatterjee and L. Doyen, “Energy parity games,” Theoretical Computer
Science, vol. 458. Elsevier, pp. 49–60, 2012.
ista: Chatterjee K, Doyen L. 2012. Energy parity games. Theoretical Computer Science.
458, 49–60.
mla: Chatterjee, Krishnendu, and Laurent Doyen. “Energy Parity Games.” Theoretical
Computer Science, vol. 458, Elsevier, 2012, pp. 49–60, doi:10.1016/j.tcs.2012.07.038.
short: K. Chatterjee, L. Doyen, Theoretical Computer Science 458 (2012) 49–60.
date_created: 2018-12-11T12:00:37Z
date_published: 2012-11-02T00:00:00Z
date_updated: 2023-02-23T11:45:29Z
day: '02'
ddc:
- '004'
department:
- _id: KrCh
doi: 10.1016/j.tcs.2012.07.038
ec_funded: 1
external_id:
arxiv:
- '1001.5183'
file:
- access_level: open_access
checksum: 719e4a5af5a01ad3f2f7f7f05b3c2b09
content_type: application/pdf
creator: kschuh
date_created: 2019-02-06T11:56:22Z
date_updated: 2020-07-14T12:45:57Z
file_id: '5935'
file_name: 2012_Elsevier_Chatterjee.pdf
file_size: 351271
relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: ' 458'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '11'
oa: 1
oa_version: Published Version
page: 49 - 60
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P 23499-N23
name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
- _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: Theoretical Computer Science
publication_status: published
publisher: Elsevier
publist_id: '3736'
pubrep_id: '935'
quality_controlled: '1'
related_material:
record:
- id: '3851'
relation: earlier_version
status: public
scopus_import: 1
status: public
title: Energy parity games
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 458
year: '2012'
...
---
_id: '2974'
abstract:
- lang: eng
text: "We construct a perfectly binding string commitment scheme whose security
is based on the learning parity with noise (LPN) assumption, or equivalently,
the hardness of decoding random linear codes. Our scheme not only allows for a
simple and efficient zero-knowledge proof of knowledge for committed values (essentially
a Σ-protocol), but also for such proofs showing any kind of relation amongst committed
values, i.e. proving that messages m_0,...,m_u, are such that m_0=C(m_1,...,m_u)
for any circuit C.\r\n\r\nTo get soundness which is exponentially small in a security
parameter t, and when the zero-knowledge property relies on the LPN problem with
secrets of length l, our 3 round protocol has communication complexity O(t|C|l
log(l)) and computational complexity of O(t|C|l) bit operations. The hidden constants
are small, and the computation consists mostly of computing inner products of
bit-vectors."
acknowledgement: "We are grateful to Petros Mol for helpful discussions on the reduction
for the hardness of the xLPN problem.\r\n"
alternative_title:
- LNCS
author:
- first_name: Abhishek
full_name: Jain, Abhishek
last_name: Jain
- first_name: Stephan
full_name: Krenn, Stephan
id: 329FCCF0-F248-11E8-B48F-1D18A9856A87
last_name: Krenn
orcid: 0000-0003-2835-9093
- first_name: Krzysztof Z
full_name: Pietrzak, Krzysztof Z
id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
last_name: Pietrzak
orcid: 0000-0002-9139-1654
- first_name: Aris
full_name: Tentes, Aris
last_name: Tentes
citation:
ama: 'Jain A, Krenn S, Pietrzak KZ, Tentes A. Commitments and efficient zero knowledge
proofs from learning parity with noise. In: Wang X, Sako K, eds. Vol 7658. Springer;
2012:663-680. doi:10.1007/978-3-642-34961-4_40'
apa: 'Jain, A., Krenn, S., Pietrzak, K. Z., & Tentes, A. (2012). Commitments
and efficient zero knowledge proofs from learning parity with noise. In X. Wang
& K. Sako (Eds.) (Vol. 7658, pp. 663–680). Presented at the ASIACRYPT: Theory
and Application of Cryptology and Information Security, Beijing, China: Springer.
https://doi.org/10.1007/978-3-642-34961-4_40'
chicago: Jain, Abhishek, Stephan Krenn, Krzysztof Z Pietrzak, and Aris Tentes. “Commitments
and Efficient Zero Knowledge Proofs from Learning Parity with Noise.” edited by
Xiaoyun Wang and Kazue Sako, 7658:663–80. Springer, 2012. https://doi.org/10.1007/978-3-642-34961-4_40.
ieee: 'A. Jain, S. Krenn, K. Z. Pietrzak, and A. Tentes, “Commitments and efficient
zero knowledge proofs from learning parity with noise,” presented at the ASIACRYPT:
Theory and Application of Cryptology and Information Security, Beijing, China,
2012, vol. 7658, pp. 663–680.'
ista: 'Jain A, Krenn S, Pietrzak KZ, Tentes A. 2012. Commitments and efficient zero
knowledge proofs from learning parity with noise. ASIACRYPT: Theory and Application
of Cryptology and Information Security, LNCS, vol. 7658, 663–680.'
mla: Jain, Abhishek, et al. Commitments and Efficient Zero Knowledge Proofs from
Learning Parity with Noise. Edited by Xiaoyun Wang and Kazue Sako, vol. 7658,
Springer, 2012, pp. 663–80, doi:10.1007/978-3-642-34961-4_40.
short: A. Jain, S. Krenn, K.Z. Pietrzak, A. Tentes, in:, X. Wang, K. Sako (Eds.),
Springer, 2012, pp. 663–680.
conference:
end_date: 2012-12-06
location: Beijing, China
name: 'ASIACRYPT: Theory and Application of Cryptology and Information Security'
start_date: 2012-12-02
date_created: 2018-12-11T12:00:38Z
date_published: 2012-12-01T00:00:00Z
date_updated: 2021-01-12T07:40:11Z
day: '01'
ddc:
- '004'
- '005'
department:
- _id: KrPi
doi: 10.1007/978-3-642-34961-4_40
ec_funded: 1
editor:
- first_name: Xiaoyun
full_name: Wang, Xiaoyun
last_name: Wang
- first_name: Kazue
full_name: Sako, Kazue
last_name: Sako
file:
- access_level: open_access
checksum: ab879537385efc4cb4203e7ef0fea17b
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:14:00Z
date_updated: 2020-07-14T12:45:58Z
file_id: '5048'
file_name: IST-2016-721-v1+1_513.pdf
file_size: 482570
relation: main_file
file_date_updated: 2020-07-14T12:45:58Z
has_accepted_license: '1'
intvolume: ' 7658'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Submitted Version
page: 663 - 680
project:
- _id: 258C570E-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '259668'
name: Provable Security for Physical Cryptography
publication_status: published
publisher: Springer
publist_id: '3730'
pubrep_id: '721'
scopus_import: 1
status: public
title: Commitments and efficient zero knowledge proofs from learning parity with noise
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: conference
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7658
year: '2012'
...
---
_id: '3104'
abstract:
- lang: eng
text: |2-
Gradients of the plant hormone auxin, which depend on its active intercellular transport, are crucial for the maintenance of root meristematic activity. This directional transport is largely orchestrated by a complex interaction of specific influx and efflux carriers that mediate the auxin flow into and out of cells, respectively. Besides these transport proteins, plant-specific polyphenolic compounds knownasflavonols have beenshownto act as endogenous regulators of auxin transport. However, only limited information is available on how flavonol synthesis is developmentally regulated. Using reduction-of-function and overexpression approaches in parallel, we demonstrate that the WRKY23 transcription factor is needed for proper root growth and development by stimulating the local biosynthesis of flavonols. The expression of WRKY23 itself is controlled by auxin through the AUXIN RESPONSE FACTOR 7 (ARF7) and ARF19 transcriptional response pathway. Our results suggest a model in which WRKY23 is part of a transcriptional feedback loop of auxin on its own transport through local regulation of flavonol biosynthesis.
author:
- first_name: Wim
full_name: Grunewald, Wim
last_name: Grunewald
- first_name: Ive
full_name: De Smet, Ive
last_name: De Smet
- first_name: Daniel
full_name: Lewis, Daniel R
last_name: Lewis
- first_name: Christian
full_name: Löfke, Christian
last_name: Löfke
- first_name: Leentje
full_name: Jansen, Leentje
last_name: Jansen
- first_name: Geert
full_name: Goeminne, Geert
last_name: Goeminne
- first_name: Robin
full_name: Vanden Bossche, Robin
last_name: Vanden Bossche
- first_name: Mansour
full_name: Karimi, Mansour
last_name: Karimi
- first_name: Bert
full_name: De Rybel, Bert
last_name: De Rybel
- first_name: Bartel
full_name: Vanholme, Bartel
last_name: Vanholme
- first_name: Thomas
full_name: Teichmann, Thomas
last_name: Teichmann
- first_name: Wout
full_name: Boerjan, Wout
last_name: Boerjan
- first_name: Marc
full_name: Van Montagu, Marc C
last_name: Van Montagu
- first_name: Godelieve
full_name: Gheysen, Godelieve
last_name: Gheysen
- first_name: Gloria
full_name: Muday, Gloria K
last_name: Muday
- first_name: Jirí
full_name: Jirí Friml
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Tom
full_name: Beeckman, Tom
last_name: Beeckman
citation:
ama: Grunewald W, De Smet I, Lewis D, et al. Transcription factor WRKY23 assists
auxin distribution patterns during Arabidopsis root development through local
control on flavonol biosynthesis. PNAS. 2012;109(5):1554-1559. doi:10.1073/pnas.1121134109
apa: Grunewald, W., De Smet, I., Lewis, D., Löfke, C., Jansen, L., Goeminne, G.,
… Beeckman, T. (2012). Transcription factor WRKY23 assists auxin distribution
patterns during Arabidopsis root development through local control on flavonol
biosynthesis. PNAS. National Academy of Sciences. https://doi.org/10.1073/pnas.1121134109
chicago: Grunewald, Wim, Ive De Smet, Daniel Lewis, Christian Löfke, Leentje Jansen,
Geert Goeminne, Robin Vanden Bossche, et al. “Transcription Factor WRKY23 Assists
Auxin Distribution Patterns during Arabidopsis Root Development through Local
Control on Flavonol Biosynthesis.” PNAS. National Academy of Sciences,
2012. https://doi.org/10.1073/pnas.1121134109.
ieee: W. Grunewald et al., “Transcription factor WRKY23 assists auxin distribution
patterns during Arabidopsis root development through local control on flavonol
biosynthesis,” PNAS, vol. 109, no. 5. National Academy of Sciences, pp.
1554–1559, 2012.
ista: Grunewald W, De Smet I, Lewis D, Löfke C, Jansen L, Goeminne G, Vanden Bossche
R, Karimi M, De Rybel B, Vanholme B, Teichmann T, Boerjan W, Van Montagu M, Gheysen
G, Muday G, Friml J, Beeckman T. 2012. Transcription factor WRKY23 assists auxin
distribution patterns during Arabidopsis root development through local control
on flavonol biosynthesis. PNAS. 109(5), 1554–1559.
mla: Grunewald, Wim, et al. “Transcription Factor WRKY23 Assists Auxin Distribution
Patterns during Arabidopsis Root Development through Local Control on Flavonol
Biosynthesis.” PNAS, vol. 109, no. 5, National Academy of Sciences, 2012,
pp. 1554–59, doi:10.1073/pnas.1121134109.
short: W. Grunewald, I. De Smet, D. Lewis, C. Löfke, L. Jansen, G. Goeminne, R.
Vanden Bossche, M. Karimi, B. De Rybel, B. Vanholme, T. Teichmann, W. Boerjan,
M. Van Montagu, G. Gheysen, G. Muday, J. Friml, T. Beeckman, PNAS 109 (2012) 1554–1559.
date_created: 2018-12-11T12:01:24Z
date_published: 2012-01-31T00:00:00Z
date_updated: 2021-01-12T07:41:05Z
day: '31'
doi: 10.1073/pnas.1121134109
extern: 1
intvolume: ' 109'
issue: '5'
month: '01'
page: 1554 - 1559
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3595'
quality_controlled: 0
status: public
title: Transcription factor WRKY23 assists auxin distribution patterns during Arabidopsis
root development through local control on flavonol biosynthesis
type: journal_article
volume: 109
year: '2012'
...
---
_id: '3105'
abstract:
- lang: eng
text: Growth and development are coordinated by an array of intercellular communications.
Known plant signaling molecules include phytohormones and hormone peptides. Although
both classes can be implicated in the same developmental processes, little is
known about the interplay between phytohormone action and peptide signaling within
the cellular microenvironment. We show that genes coding for small secretory peptides,
designated GOLVEN (GLV), modulate the distribution of the phytohormone auxin.
The deregulation of the GLV function impairs the formation of auxin gradients
and alters the reorientation of shoots and roots after a gravity stimulus. Specifically,
the GLV signal modulates the trafficking dynamics of the auxin efflux carrier
PIN-FORMED2 involved in root tropic responses and meristem organization. Our work
links the local action of secretory peptides with phytohormone transport. Root
growth factor (RGF) or GOLVEN (GLV) secreted peptides have previously been implicated
in meristem regulation. Whitford et al. now show that RGF/GLV peptides induce
rapid relocalization of the auxin efflux regulator PIN2, regulate auxin gradients,
and modulate auxin-dependent root responses to specific stimuli.
author:
- first_name: Ryan
full_name: Whitford, Ryan
last_name: Whitford
- first_name: Ana
full_name: Fernandez, Ana
last_name: Fernandez
- first_name: Ricardo
full_name: Tejos, Ricardo
last_name: Tejos
- first_name: Amparo
full_name: Pérez, Amparo Cuéllar
last_name: Pérez
- first_name: Jürgen
full_name: Kleine-Vehn, Jürgen
last_name: Kleine Vehn
- first_name: Steffen
full_name: Vanneste, Steffen
last_name: Vanneste
- first_name: Andrzej
full_name: Drozdzecki, Andrzej
last_name: Drozdzecki
- first_name: Johannes
full_name: Leitner, Johannes
last_name: Leitner
- first_name: Lindy
full_name: Abas, Lindy
last_name: Abas
- first_name: Maarten
full_name: Aerts, Maarten
last_name: Aerts
- first_name: Kurt
full_name: Hoogewijs, Kurt
last_name: Hoogewijs
- first_name: Pawel
full_name: Pawel Baster
id: 3028BD74-F248-11E8-B48F-1D18A9856A87
last_name: Baster
- first_name: Ruth
full_name: De Groodt, Ruth
last_name: De Groodt
- first_name: Yao
full_name: Lin, Yao-Cheng
last_name: Lin
- first_name: Véronique
full_name: Storme, Véronique
last_name: Storme
- first_name: Yves
full_name: Van de Peer, Yves
last_name: Van De Peer
- first_name: Tom
full_name: Beeckman, Tom
last_name: Beeckman
- first_name: Annemieke
full_name: Madder, Annemieke
last_name: Madder
- first_name: Bart
full_name: Devreese, Bart
last_name: Devreese
- first_name: Christian
full_name: Luschnig, Christian
last_name: Luschnig
- first_name: Jirí
full_name: Jirí Friml
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Pierre
full_name: Hilson, Pierre
last_name: Hilson
citation:
ama: Whitford R, Fernandez A, Tejos R, et al. GOLVEN secretory peptides regulate
auxin carrier turnover during plant gravitropic responses. Developmental Cell.
2012;22(3):678-685. doi:10.1016/j.devcel.2012.02.002
apa: Whitford, R., Fernandez, A., Tejos, R., Pérez, A., Kleine Vehn, J., Vanneste,
S., … Hilson, P. (2012). GOLVEN secretory peptides regulate auxin carrier turnover
during plant gravitropic responses. Developmental Cell. Cell Press. https://doi.org/10.1016/j.devcel.2012.02.002
chicago: Whitford, Ryan, Ana Fernandez, Ricardo Tejos, Amparo Pérez, Jürgen Kleine
Vehn, Steffen Vanneste, Andrzej Drozdzecki, et al. “GOLVEN Secretory Peptides
Regulate Auxin Carrier Turnover during Plant Gravitropic Responses.” Developmental
Cell. Cell Press, 2012. https://doi.org/10.1016/j.devcel.2012.02.002.
ieee: R. Whitford et al., “GOLVEN secretory peptides regulate auxin carrier
turnover during plant gravitropic responses,” Developmental Cell, vol.
22, no. 3. Cell Press, pp. 678–685, 2012.
ista: Whitford R, Fernandez A, Tejos R, Pérez A, Kleine Vehn J, Vanneste S, Drozdzecki
A, Leitner J, Abas L, Aerts M, Hoogewijs K, Baster P, De Groodt R, Lin Y, Storme
V, Van De Peer Y, Beeckman T, Madder A, Devreese B, Luschnig C, Friml J, Hilson
P. 2012. GOLVEN secretory peptides regulate auxin carrier turnover during plant
gravitropic responses. Developmental Cell. 22(3), 678–685.
mla: Whitford, Ryan, et al. “GOLVEN Secretory Peptides Regulate Auxin Carrier Turnover
during Plant Gravitropic Responses.” Developmental Cell, vol. 22, no. 3,
Cell Press, 2012, pp. 678–85, doi:10.1016/j.devcel.2012.02.002.
short: R. Whitford, A. Fernandez, R. Tejos, A. Pérez, J. Kleine Vehn, S. Vanneste,
A. Drozdzecki, J. Leitner, L. Abas, M. Aerts, K. Hoogewijs, P. Baster, R. De Groodt,
Y. Lin, V. Storme, Y. Van De Peer, T. Beeckman, A. Madder, B. Devreese, C. Luschnig,
J. Friml, P. Hilson, Developmental Cell 22 (2012) 678–685.
date_created: 2018-12-11T12:01:25Z
date_published: 2012-03-13T00:00:00Z
date_updated: 2021-01-12T07:41:06Z
day: '13'
doi: 10.1016/j.devcel.2012.02.002
extern: 1
intvolume: ' 22'
issue: '3'
month: '03'
page: 678 - 685
publication: Developmental Cell
publication_status: published
publisher: Cell Press
publist_id: '3594'
quality_controlled: 0
status: public
title: GOLVEN secretory peptides regulate auxin carrier turnover during plant gravitropic
responses
type: journal_article
volume: 22
year: '2012'
...
---
_id: '3106'
abstract:
- lang: eng
text: Cell polarization via asymmetrical distribution of structures or molecules
is essential for diverse cellular functions and development of organisms, but
how polarity is developmentally controlled has been poorly understood. In plants,
the asymmetrical distribution of the PIN-FORMED (PIN) proteins involved in the
cellular efflux of the quintessential phytohormone auxin plays a central role
in developmental patterning, morphogenesis, and differential growth. Recently
we showed that auxin promotes cell interdigitation by activating the Rho family
ROP GTPases in leaf epidermal pavement cells. Here we found that auxin activation
of the ROP2 signaling pathway regulates the asymmetric distribution of PIN1 by
inhibiting its endocytosis. ROP2 inhibits PIN1 endocytosis via the accumulation
of cortical actin microfilaments induced by the ROP2 effector protein RIC4. Our
findings suggest a link between the developmental auxin signal and polar PIN1
distribution via Rho-dependent cytoskeletal reorganization and reveal the conservation
of a design principle for cell polarization that is based on Rho GTPase-mediated
inhibition of endocytosis.
author:
- first_name: Shingo
full_name: Nagawa, Shingo
last_name: Nagawa
- first_name: Tongda
full_name: Xu, Tongda
last_name: Xu
- first_name: Deshu
full_name: Lin, Deshu
last_name: Lin
- first_name: Pankaj
full_name: Dhonukshe, Pankaj
last_name: Dhonukshe
- first_name: Xingxing
full_name: Zhang, Xingxing
last_name: Zhang
- first_name: Jirí
full_name: Jirí Friml
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Ben
full_name: Scheres, Ben
last_name: Scheres
- first_name: Ying
full_name: Fu, Ying
last_name: Fu
- first_name: Zhenbiao
full_name: Yang, Zhenbiao
last_name: Yang
citation:
ama: Nagawa S, Xu T, Lin D, et al. ROP GTPase-dependent actin microfilaments promote
PIN1 polarization by localized inhibition of clathrin-dependent endocytosis. PLoS
Biology. 2012;10(4). doi:10.1371/journal.pbio.1001299
apa: Nagawa, S., Xu, T., Lin, D., Dhonukshe, P., Zhang, X., Friml, J., … Yang, Z.
(2012). ROP GTPase-dependent actin microfilaments promote PIN1 polarization by
localized inhibition of clathrin-dependent endocytosis. PLoS Biology. Public
Library of Science. https://doi.org/10.1371/journal.pbio.1001299
chicago: Nagawa, Shingo, Tongda Xu, Deshu Lin, Pankaj Dhonukshe, Xingxing Zhang,
Jiří Friml, Ben Scheres, Ying Fu, and Zhenbiao Yang. “ROP GTPase-Dependent Actin
Microfilaments Promote PIN1 Polarization by Localized Inhibition of Clathrin-Dependent
Endocytosis.” PLoS Biology. Public Library of Science, 2012. https://doi.org/10.1371/journal.pbio.1001299.
ieee: S. Nagawa et al., “ROP GTPase-dependent actin microfilaments promote
PIN1 polarization by localized inhibition of clathrin-dependent endocytosis,”
PLoS Biology, vol. 10, no. 4. Public Library of Science, 2012.
ista: Nagawa S, Xu T, Lin D, Dhonukshe P, Zhang X, Friml J, Scheres B, Fu Y, Yang
Z. 2012. ROP GTPase-dependent actin microfilaments promote PIN1 polarization by
localized inhibition of clathrin-dependent endocytosis. PLoS Biology. 10(4).
mla: Nagawa, Shingo, et al. “ROP GTPase-Dependent Actin Microfilaments Promote PIN1
Polarization by Localized Inhibition of Clathrin-Dependent Endocytosis.” PLoS
Biology, vol. 10, no. 4, Public Library of Science, 2012, doi:10.1371/journal.pbio.1001299.
short: S. Nagawa, T. Xu, D. Lin, P. Dhonukshe, X. Zhang, J. Friml, B. Scheres, Y.
Fu, Z. Yang, PLoS Biology 10 (2012).
date_created: 2018-12-11T12:01:25Z
date_published: 2012-04-01T00:00:00Z
date_updated: 2021-01-12T07:41:06Z
day: '01'
doi: 10.1371/journal.pbio.1001299
extern: 1
intvolume: ' 10'
issue: '4'
month: '04'
publication: PLoS Biology
publication_status: published
publisher: Public Library of Science
publist_id: '3593'
quality_controlled: 0
status: public
title: ROP GTPase-dependent actin microfilaments promote PIN1 polarization by localized
inhibition of clathrin-dependent endocytosis
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
volume: 10
year: '2012'
...
---
_id: '3107'
author:
- first_name: Steffen
full_name: Vanneste, Steffen
last_name: Vanneste
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: 'Vanneste S, Friml J. Plant Signaling: Deconstructing Auxin Sensing.
Vol 8. Nature Publishing Group; 2012:415-416. doi:10.1038/nchembio.943'
apa: 'Vanneste, S., & Friml, J. (2012). Plant signaling: Deconstructing auxin
sensing. Nature Chemical Biology (Vol. 8, pp. 415–416). Nature Publishing
Group. https://doi.org/10.1038/nchembio.943'
chicago: 'Vanneste, Steffen, and Jiří Friml. Plant Signaling: Deconstructing
Auxin Sensing. Nature Chemical Biology. Vol. 8. Nature Publishing Group,
2012. https://doi.org/10.1038/nchembio.943.'
ieee: 'S. Vanneste and J. Friml, Plant signaling: Deconstructing auxin sensing,
vol. 8, no. 5. Nature Publishing Group, 2012, pp. 415–416.'
ista: 'Vanneste S, Friml J. 2012. Plant signaling: Deconstructing auxin sensing,
Nature Publishing Group,p.'
mla: 'Vanneste, Steffen, and Jiří Friml. “Plant Signaling: Deconstructing Auxin
Sensing.” Nature Chemical Biology, vol. 8, no. 5, Nature Publishing Group,
2012, pp. 415–16, doi:10.1038/nchembio.943.'
short: 'S. Vanneste, J. Friml, Plant Signaling: Deconstructing Auxin Sensing, Nature
Publishing Group, 2012.'
date_created: 2018-12-11T12:01:26Z
date_published: 2012-05-01T00:00:00Z
date_updated: 2021-01-12T07:41:06Z
day: '01'
doi: 10.1038/nchembio.943
extern: '1'
intvolume: ' 8'
issue: '5'
language:
- iso: eng
month: '05'
oa_version: None
page: 415 - 416
publication: Nature Chemical Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '3592'
quality_controlled: '1'
status: public
title: 'Plant signaling: Deconstructing auxin sensing'
type: other_academic_publication
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2012'
...
---
_id: '3108'
abstract:
- lang: eng
text: The phytohormone auxin acts as a prominent signal, providing, by its local
accumulation or depletion in selected cells, a spatial and temporal reference
for changes in the developmental program. The distribution of auxin depends on
both auxin metabolism (biosynthesis, conjugation and degradation) and cellular
auxin transport. We identified in silico a novel putative auxin transport facilitator
family, called PIN-LIKES (PILS). Here we illustrate that PILS proteins are required
for auxin-dependent regulation of plant growth by determining the cellular sensitivity
to auxin. PILS proteins regulate intracellular auxin accumulation at the endoplasmic
reticulum and thus auxin availability for nuclear auxin signalling. PILS activity
affects the level of endogenous auxin indole-3-acetic acid (IAA), presumably via
intracellular accumulation and metabolism. Our findings reveal that the transport
machinery to compartmentalize auxin within the cell is of an unexpected molecular
complexity and demonstrate this compartmentalization to be functionally important
for a number of developmental processes.
author:
- first_name: Elke
full_name: Barbez, Elke
last_name: Barbez
- first_name: Martin
full_name: Kubeš, Martin
last_name: Kubeš
- first_name: Jakub
full_name: Rolčík, Jakub
last_name: Rolčík
- first_name: Chloe
full_name: Béziat, Chloe
last_name: Béziat
- first_name: Aleš
full_name: Pěnčík, Aleš
last_name: Pěnčík
- first_name: Bangjun
full_name: Wang, Bangjun
last_name: Wang
- first_name: Michel
full_name: Rosquete, Michel Ruiz
last_name: Rosquete
- first_name: Jinsheng
full_name: Zhu, Jinsheng
last_name: Zhu
- first_name: Petre
full_name: Dobrev, Petre I
last_name: Dobrev
- first_name: Yuree
full_name: Lee, Yuree
last_name: Lee
- first_name: Eva
full_name: Zašímalová, Eva
last_name: Zašímalová
- first_name: Jan
full_name: Petrášek, Jan
last_name: Petrášek
- first_name: Markus
full_name: Geisler, Markus
last_name: Geisler
- first_name: Jirí
full_name: Jirí Friml
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Jürgen
full_name: Kleine-Vehn, Jürgen
last_name: Kleine Vehn
citation:
ama: Barbez E, Kubeš M, Rolčík J, et al. A novel putative auxin carrier family regulates
intracellular auxin homeostasis in plants. Nature. 2012;485(7396):119-122.
doi:10.1038/nature11001
apa: Barbez, E., Kubeš, M., Rolčík, J., Béziat, C., Pěnčík, A., Wang, B., … Kleine
Vehn, J. (2012). A novel putative auxin carrier family regulates intracellular
auxin homeostasis in plants. Nature. Nature Publishing Group. https://doi.org/10.1038/nature11001
chicago: Barbez, Elke, Martin Kubeš, Jakub Rolčík, Chloe Béziat, Aleš Pěnčík, Bangjun
Wang, Michel Rosquete, et al. “A Novel Putative Auxin Carrier Family Regulates
Intracellular Auxin Homeostasis in Plants.” Nature. Nature Publishing Group,
2012. https://doi.org/10.1038/nature11001.
ieee: E. Barbez et al., “A novel putative auxin carrier family regulates
intracellular auxin homeostasis in plants,” Nature, vol. 485, no. 7396.
Nature Publishing Group, pp. 119–122, 2012.
ista: Barbez E, Kubeš M, Rolčík J, Béziat C, Pěnčík A, Wang B, Rosquete M, Zhu J,
Dobrev P, Lee Y, Zašímalová E, Petrášek J, Geisler M, Friml J, Kleine Vehn J.
2012. A novel putative auxin carrier family regulates intracellular auxin homeostasis
in plants. Nature. 485(7396), 119–122.
mla: Barbez, Elke, et al. “A Novel Putative Auxin Carrier Family Regulates Intracellular
Auxin Homeostasis in Plants.” Nature, vol. 485, no. 7396, Nature Publishing
Group, 2012, pp. 119–22, doi:10.1038/nature11001.
short: E. Barbez, M. Kubeš, J. Rolčík, C. Béziat, A. Pěnčík, B. Wang, M. Rosquete,
J. Zhu, P. Dobrev, Y. Lee, E. Zašímalová, J. Petrášek, M. Geisler, J. Friml, J.
Kleine Vehn, Nature 485 (2012) 119–122.
date_created: 2018-12-11T12:01:26Z
date_published: 2012-05-03T00:00:00Z
date_updated: 2021-01-12T07:41:07Z
day: '03'
doi: 10.1038/nature11001
extern: 1
intvolume: ' 485'
issue: '7396'
month: '05'
page: 119 - 122
publication: Nature
publication_status: published
publisher: Nature Publishing Group
publist_id: '3591'
quality_controlled: 0
status: public
title: A novel putative auxin carrier family regulates intracellular auxin homeostasis
in plants
type: journal_article
volume: 485
year: '2012'
...
---
_id: '3109'
abstract:
- lang: eng
text: Receptor-mediated endocytosis is an integral part of signal transduction as
it mediates signal attenuation and provides spatial and temporal dimensions to
signaling events. One of the best-studied leucine-rich repeat receptor-like kinases
in plants, BRASSINOSTEROID INSENSITIVE 1 (BRI1), perceives its ligand, the brassinosteroid
(BR) hormone, at the cell surface and is constitutively endocytosed. However,
the importance of endocytosis for BR signaling remains unclear. Here we developed
a bioactive, fluorescent BR analog, Alexa Fluor 647-castasterone (AFCS), and visualized
the endocytosis of BRI1-AFCS complexes in living Arabidopsis thaliana cells. Impairment
of endocytosis dependent on clathrin and the guanine nucleotide exchange factor
for ARF GTPases (ARF-GEF) GNOM enhanced BR signaling by retaining active BRI1-ligand
complexes at the plasma membrane. Increasing the trans-Golgi network/early endosome
pool of BRI1-BR complexes did not affect BR signaling. Our findings provide what
is to our knowledge the first visualization of receptor-ligand complexes in plants
and reveal clathrin-and ARF-GEF-dependent endocytic regulation of BR signaling
from the plasma membrane.
author:
- first_name: Niloufer
full_name: Irani, Niloufer G
last_name: Irani
- first_name: Simone
full_name: Di Rubbo, Simone
last_name: Di Rubbo
- first_name: Evelien
full_name: Mylle, Evelien
last_name: Mylle
- first_name: Jos
full_name: Van Den Begin, Jos
last_name: Van Den Begin
- first_name: Joanna
full_name: Schneider-Pizoń, Joanna
last_name: Schneider Pizoń
- first_name: Jaroslava
full_name: Hniliková, Jaroslava
last_name: Hniliková
- first_name: Miroslav
full_name: Šíša, Miroslav
last_name: Šíša
- first_name: Dieter
full_name: Buyst, Dieter
last_name: Buyst
- first_name: Josep
full_name: Vilarrasa-Blasi, Josep
last_name: Vilarrasa Blasi
- first_name: Anna
full_name: Szatmári, Anna-Maria
last_name: Szatmári
- first_name: Daniël
full_name: Van Damme, Daniël
last_name: Van Damme
- first_name: Kiril
full_name: Mishev, Kiril
last_name: Mishev
- first_name: Mirela
full_name: Codreanu, Mirela-Corina
last_name: Codreanu
- first_name: Ladislav
full_name: Kohout, Ladislav
last_name: Kohout
- first_name: Miroslav
full_name: Strnad, Miroslav
last_name: Strnad
- first_name: Ana
full_name: Caño-Delgado, Ana I
last_name: Caño Delgado
- first_name: Jirí
full_name: Jirí Friml
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Annemieke
full_name: Madder, Annemieke
last_name: Madder
- first_name: Eugenia
full_name: Russinova, Eugenia
last_name: Russinova
citation:
ama: Irani N, Di Rubbo S, Mylle E, et al. Fluorescent castasterone reveals BRI1
signaling from the plasma membrane. Nature Chemical Biology. 2012;8(6):583-589.
doi:10.1038/nchembio.958
apa: Irani, N., Di Rubbo, S., Mylle, E., Van Den Begin, J., Schneider Pizoń, J.,
Hniliková, J., … Russinova, E. (2012). Fluorescent castasterone reveals BRI1 signaling
from the plasma membrane. Nature Chemical Biology. Nature Publishing Group.
https://doi.org/10.1038/nchembio.958
chicago: Irani, Niloufer, Simone Di Rubbo, Evelien Mylle, Jos Van Den Begin, Joanna
Schneider Pizoń, Jaroslava Hniliková, Miroslav Šíša, et al. “Fluorescent Castasterone
Reveals BRI1 Signaling from the Plasma Membrane.” Nature Chemical Biology.
Nature Publishing Group, 2012. https://doi.org/10.1038/nchembio.958.
ieee: N. Irani et al., “Fluorescent castasterone reveals BRI1 signaling from
the plasma membrane,” Nature Chemical Biology, vol. 8, no. 6. Nature Publishing
Group, pp. 583–589, 2012.
ista: Irani N, Di Rubbo S, Mylle E, Van Den Begin J, Schneider Pizoń J, Hniliková
J, Šíša M, Buyst D, Vilarrasa Blasi J, Szatmári A, Van Damme D, Mishev K, Codreanu
M, Kohout L, Strnad M, Caño Delgado A, Friml J, Madder A, Russinova E. 2012. Fluorescent
castasterone reveals BRI1 signaling from the plasma membrane. Nature Chemical
Biology. 8(6), 583–589.
mla: Irani, Niloufer, et al. “Fluorescent Castasterone Reveals BRI1 Signaling from
the Plasma Membrane.” Nature Chemical Biology, vol. 8, no. 6, Nature Publishing
Group, 2012, pp. 583–89, doi:10.1038/nchembio.958.
short: N. Irani, S. Di Rubbo, E. Mylle, J. Van Den Begin, J. Schneider Pizoń, J.
Hniliková, M. Šíša, D. Buyst, J. Vilarrasa Blasi, A. Szatmári, D. Van Damme, K.
Mishev, M. Codreanu, L. Kohout, M. Strnad, A. Caño Delgado, J. Friml, A. Madder,
E. Russinova, Nature Chemical Biology 8 (2012) 583–589.
date_created: 2018-12-11T12:01:26Z
date_published: 2012-06-01T00:00:00Z
date_updated: 2021-01-12T07:41:07Z
day: '01'
doi: 10.1038/nchembio.958
extern: 1
intvolume: ' 8'
issue: '6'
month: '06'
page: 583 - 589
publication: Nature Chemical Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '3590'
quality_controlled: 0
status: public
title: Fluorescent castasterone reveals BRI1 signaling from the plasma membrane
type: journal_article
volume: 8
year: '2012'
...