---
_id: '760'
abstract:
- lang: eng
text: A randomized implementation is given of a test-and-set register with O(log
log n) individual step complexity and O(n) total step complexity against an oblivious
adversary. The implementation is linearizable and multi-shot, and shows an exponential
complexity improvement over previous solutions designed to work against a strong
adversary.
acknowledgement: The work of Dan Alistarh was supported by the NCCR MICS Project.
The work of James Aspnes was supported in part by NSF grant CCF-0916389.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Dan-Adrian
full_name: Alistarh, Dan-Adrian
id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
last_name: Alistarh
orcid: 0000-0003-3650-940X
- first_name: James
full_name: Aspnes, James
last_name: Aspnes
citation:
ama: 'Alistarh D-A, Aspnes J. Sub-logarithmic test-and-set against a weak adversary.
In: Vol 6950 LNCS. Springer; 2011:97-109. doi:10.1007/978-3-642-24100-0_7'
apa: 'Alistarh, D.-A., & Aspnes, J. (2011). Sub-logarithmic test-and-set against
a weak adversary (Vol. 6950 LNCS, pp. 97–109). Presented at the DISC: Distributed
Computing, Springer. https://doi.org/10.1007/978-3-642-24100-0_7'
chicago: Alistarh, Dan-Adrian, and James Aspnes. “Sub-Logarithmic Test-and-Set against
a Weak Adversary,” 6950 LNCS:97–109. Springer, 2011. https://doi.org/10.1007/978-3-642-24100-0_7.
ieee: 'D.-A. Alistarh and J. Aspnes, “Sub-logarithmic test-and-set against a weak
adversary,” presented at the DISC: Distributed Computing, 2011, vol. 6950 LNCS,
pp. 97–109.'
ista: 'Alistarh D-A, Aspnes J. 2011. Sub-logarithmic test-and-set against a weak
adversary. DISC: Distributed Computing, LNCS, vol. 6950 LNCS, 97–109.'
mla: Alistarh, Dan-Adrian, and James Aspnes. Sub-Logarithmic Test-and-Set against
a Weak Adversary. Vol. 6950 LNCS, Springer, 2011, pp. 97–109, doi:10.1007/978-3-642-24100-0_7.
short: D.-A. Alistarh, J. Aspnes, in:, Springer, 2011, pp. 97–109.
conference:
name: 'DISC: Distributed Computing'
date_created: 2018-12-11T11:48:21Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2023-02-23T13:12:01Z
day: '01'
doi: 10.1007/978-3-642-24100-0_7
extern: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 97 - 109
publication_status: published
publisher: Springer
publist_id: '6896'
status: public
title: Sub-logarithmic test-and-set against a weak adversary
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6950 LNCS
year: '2011'
...
---
_id: '761'
abstract:
- lang: eng
text: We give two new randomized algorithms for strong renaming, both of which work
against an adaptive adversary in asynchronous shared memory. The first uses repeated
sampling over a sequence of arrays of decreasing size to assign unique names to
each of n processes with step complexity O(log3 n). The second transforms any
sorting network into a strong adaptive renaming protocol, with an expected cost
equal to the depth of the sorting network. Using an AKS sorting network, this
gives a strong adaptive renaming algorithm with step complexity O(log k), where
k is the contention in the current execution. We show this to be optimal based
on a classic lower bound of Jayanti. We also show that any such strong renaming
protocol can be used to build a monotone-consistent counter with logarithmic step
complexity (at the cost of adding a max register) or a linearizable fetch-and-increment
register (at the cost of increasing the step complexity by a logarithmic factor).
acknowledgement: "We would like to thank Hagit Attiya, Rachid Guerraoui\r\nand Prasad
Jayanti for useful discussions and support. We\r\nwould also like to thank the
anonymous reviewers for many\r\nuseful comments."
article_processing_charge: No
author:
- first_name: Dan-Adrian
full_name: Alistarh, Dan-Adrian
id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
last_name: Alistarh
orcid: 0000-0003-3650-940X
- first_name: James
full_name: Aspnes, James
last_name: Aspnes
- first_name: Keren
full_name: Censor Hillel, Keren
last_name: Censor Hillel
- first_name: Seth
full_name: Gilbert, Seth
last_name: Gilbert
- first_name: Morteza
full_name: Zadimoghaddam, Morteza
last_name: Zadimoghaddam
citation:
ama: 'Alistarh D-A, Aspnes J, Censor Hillel K, Gilbert S, Zadimoghaddam M. Optimal-time
adaptive strong renaming, with applications to counting. In: ACM; 2011:239-248.
doi:10.1145/1993806.1993850'
apa: 'Alistarh, D.-A., Aspnes, J., Censor Hillel, K., Gilbert, S., & Zadimoghaddam,
M. (2011). Optimal-time adaptive strong renaming, with applications to counting
(pp. 239–248). Presented at the PODC: Principles of Distributed Computing, ACM.
https://doi.org/10.1145/1993806.1993850'
chicago: Alistarh, Dan-Adrian, James Aspnes, Keren Censor Hillel, Seth Gilbert,
and Morteza Zadimoghaddam. “Optimal-Time Adaptive Strong Renaming, with Applications
to Counting,” 239–48. ACM, 2011. https://doi.org/10.1145/1993806.1993850.
ieee: 'D.-A. Alistarh, J. Aspnes, K. Censor Hillel, S. Gilbert, and M. Zadimoghaddam,
“Optimal-time adaptive strong renaming, with applications to counting,” presented
at the PODC: Principles of Distributed Computing, 2011, pp. 239–248.'
ista: 'Alistarh D-A, Aspnes J, Censor Hillel K, Gilbert S, Zadimoghaddam M. 2011.
Optimal-time adaptive strong renaming, with applications to counting. PODC: Principles
of Distributed Computing, 239–248.'
mla: Alistarh, Dan-Adrian, et al. Optimal-Time Adaptive Strong Renaming, with
Applications to Counting. ACM, 2011, pp. 239–48, doi:10.1145/1993806.1993850.
short: D.-A. Alistarh, J. Aspnes, K. Censor Hillel, S. Gilbert, M. Zadimoghaddam,
in:, ACM, 2011, pp. 239–248.
conference:
name: 'PODC: Principles of Distributed Computing'
date_created: 2018-12-11T11:48:22Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2023-02-23T13:12:17Z
day: '01'
doi: 10.1145/1993806.1993850
extern: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 239 - 248
publication_status: published
publisher: ACM
publist_id: '6897'
status: public
title: Optimal-time adaptive strong renaming, with applications to counting
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2011'
...
---
_id: '9943'
abstract:
- lang: eng
text: Segmentation is the process of partitioning digital images into meaningful
regions. The analysis of biological high content images often requires segmentation
as a first step. We propose ilastik as an easy-to-use tool which allows the user
without expertise in image processing to perform segmentation and classification
in a unified way. ilastik learns from labels provided by the user through a convenient
mouse interface. Based on these labels, ilastik infers a problem specific segmentation.
A random forest classifier is used in the learning step, in which each pixel's
neighborhood is characterized by a set of generic (nonlinear) features. ilastik
supports up to three spatial plus one spectral dimension and makes use of all
dimensions in the feature calculation. ilastik provides realtime feedback that
enables the user to interactively refine the segmentation result and hence further
fine-tune the classifier. An uncertainty measure guides the user to ambiguous
regions in the images. Real time performance is achieved by multi-threading which
fully exploits the capabilities of modern multi-core machines. Once a classifier
has been trained on a set of representative images, it can be exported and used
to automatically process a very large number of images (e.g. using the CellProfiler
pipeline). ilastik is an open source project and released under the BSD license
at www.ilastik.org.
article_processing_charge: No
author:
- first_name: Christoph M
full_name: Sommer, Christoph M
id: 4DF26D8C-F248-11E8-B48F-1D18A9856A87
last_name: Sommer
orcid: 0000-0003-1216-9105
- first_name: Christoph
full_name: Straehle, Christoph
last_name: Straehle
- first_name: Ullrich
full_name: Köthe, Ullrich
last_name: Köthe
- first_name: Fred A.
full_name: Hamprecht, Fred A.
last_name: Hamprecht
citation:
ama: 'Sommer CM, Straehle C, Köthe U, Hamprecht FA. Ilastik: Interactive learning
and segmentation toolkit. In: 2011 IEEE International Symposium on Biomedical
Imaging: From Nano to Micro. Institute of Electrical and Electronics Engineers;
2011. doi:10.1109/isbi.2011.5872394'
apa: 'Sommer, C. M., Straehle, C., Köthe, U., & Hamprecht, F. A. (2011). Ilastik:
Interactive learning and segmentation toolkit. In 2011 IEEE International Symposium
on Biomedical Imaging: from Nano to Micro. Chicago, Illinois, USA: Institute
of Electrical and Electronics Engineers. https://doi.org/10.1109/isbi.2011.5872394'
chicago: 'Sommer, Christoph M, Christoph Straehle, Ullrich Köthe, and Fred A. Hamprecht.
“Ilastik: Interactive Learning and Segmentation Toolkit.” In 2011 IEEE International
Symposium on Biomedical Imaging: From Nano to Micro. Institute of Electrical
and Electronics Engineers, 2011. https://doi.org/10.1109/isbi.2011.5872394.'
ieee: 'C. M. Sommer, C. Straehle, U. Köthe, and F. A. Hamprecht, “Ilastik: Interactive
learning and segmentation toolkit,” in 2011 IEEE International Symposium on
Biomedical Imaging: from Nano to Micro, Chicago, Illinois, USA, 2011.'
ista: 'Sommer CM, Straehle C, Köthe U, Hamprecht FA. 2011. Ilastik: Interactive
learning and segmentation toolkit. 2011 IEEE International Symposium on Biomedical
Imaging: from Nano to Micro. ISBI: International Symposium on Biomedical Imaging.'
mla: 'Sommer, Christoph M., et al. “Ilastik: Interactive Learning and Segmentation
Toolkit.” 2011 IEEE International Symposium on Biomedical Imaging: From Nano
to Micro, Institute of Electrical and Electronics Engineers, 2011, doi:10.1109/isbi.2011.5872394.'
short: 'C.M. Sommer, C. Straehle, U. Köthe, F.A. Hamprecht, in:, 2011 IEEE International
Symposium on Biomedical Imaging: From Nano to Micro, Institute of Electrical and
Electronics Engineers, 2011.'
conference:
end_date: 2011-04-02
location: Chicago, Illinois, USA
name: 'ISBI: International Symposium on Biomedical Imaging'
start_date: 2011-03-30
date_created: 2021-08-19T11:49:58Z
date_published: 2011-06-09T00:00:00Z
date_updated: 2023-02-23T14:13:38Z
day: '09'
department:
- _id: Bio
doi: 10.1109/isbi.2011.5872394
extern: '1'
keyword:
- image segmentation
- biomedical imaging
- three dimensional displays
- neurons
- retina
- observers
- image color analysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.researchgate.net/publication/224241106_Ilastik_Interactive_learning_and_segmentation_toolkit
month: '06'
oa: 1
oa_version: Preprint
publication: '2011 IEEE International Symposium on Biomedical Imaging: from Nano to
Micro'
publication_identifier:
eissn:
- 1945-8452
isbn:
- 978-1-4244-4127-3
issn:
- 1945-7928
publication_status: published
publisher: Institute of Electrical and Electronics Engineers
quality_controlled: '1'
status: public
title: 'Ilastik: Interactive learning and segmentation toolkit'
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2011'
...
---
_id: '3429'
abstract:
- lang: eng
text: Transcription factors are central to sustaining pluripotency, yet little is
known about transcription factor dynamics in defining pluripotency in the early
mammalian embryo. Here, we establish a fluorescence decay after photoactivation
(FDAP) assay to quantitatively study the kinetic behaviour of Oct4, a key transcription
factor controlling pre-implantation development in the mouse embryo. FDAP measurements
reveal that each cell in a developing embryo shows one of two distinct Oct4 kinetics,
before there are any morphologically distinguishable differences or outward signs
of lineage patterning. The differences revealed by FDAP are due to differences
in the accessibility of Oct4 to its DNA binding sites in the nucleus. Lineage
tracing of the cells in the two distinct sub-populations demonstrates that the
Oct4 kinetics predict lineages of the early embryo. Cells with slower Oct4 kinetics
are more likely to give rise to the pluripotent cell lineage that contributes
to the inner cell mass. Those with faster Oct4 kinetics contribute mostly to the
extra-embryonic lineage. Our findings identify Oct4 kinetics, rather than differences
in total transcription factor expression levels, as a predictive measure of developmental
cell lineage patterning in the early mouse embryo.
acknowledgement: This work was supported by the Beckman Institute and Biological Imaging
Center at the California Institute of Technology and by the NHGRI Center of Excellence
in Genomic Science grant P50HG004071.
article_processing_charge: No
author:
- first_name: Nicolas
full_name: Plachta, Nicolas
last_name: Plachta
- 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: Shirley
full_name: Pease, Shirley
last_name: Pease
- first_name: Scott
full_name: Fraser, Scott
last_name: Fraser
- first_name: Periklis
full_name: Pantazis, Periklis
last_name: Pantazis
citation:
ama: Plachta N, Bollenbach MT, Pease S, Fraser S, Pantazis P. Oct4 kinetics predict
cell lineage patterning in the early mammalian embryo. Nature Cell Biology.
2011;13(2):117-123. doi:10.1038/ncb2154
apa: Plachta, N., Bollenbach, M. T., Pease, S., Fraser, S., & Pantazis, P. (2011).
Oct4 kinetics predict cell lineage patterning in the early mammalian embryo. Nature
Cell Biology. Nature Publishing Group. https://doi.org/10.1038/ncb2154
chicago: Plachta, Nicolas, Mark Tobias Bollenbach, Shirley Pease, Scott Fraser,
and Periklis Pantazis. “Oct4 Kinetics Predict Cell Lineage Patterning in the Early
Mammalian Embryo.” Nature Cell Biology. Nature Publishing Group, 2011.
https://doi.org/10.1038/ncb2154.
ieee: N. Plachta, M. T. Bollenbach, S. Pease, S. Fraser, and P. Pantazis, “Oct4
kinetics predict cell lineage patterning in the early mammalian embryo,” Nature
Cell Biology, vol. 13, no. 2. Nature Publishing Group, pp. 117–123, 2011.
ista: Plachta N, Bollenbach MT, Pease S, Fraser S, Pantazis P. 2011. Oct4 kinetics
predict cell lineage patterning in the early mammalian embryo. Nature Cell Biology.
13(2), 117–123.
mla: Plachta, Nicolas, et al. “Oct4 Kinetics Predict Cell Lineage Patterning in
the Early Mammalian Embryo.” Nature Cell Biology, vol. 13, no. 2, Nature
Publishing Group, 2011, pp. 117–23, doi:10.1038/ncb2154.
short: N. Plachta, M.T. Bollenbach, S. Pease, S. Fraser, P. Pantazis, Nature Cell
Biology 13 (2011) 117–123.
date_created: 2018-12-11T12:03:17Z
date_published: 2011-01-23T00:00:00Z
date_updated: 2025-09-30T08:39:51Z
day: '23'
department:
- _id: ToBo
doi: 10.1038/ncb2154
external_id:
isi:
- '000286805900004'
intvolume: ' 13'
isi: 1
issue: '2'
language:
- iso: eng
month: '01'
oa_version: None
page: 117 - 123
publication: Nature Cell Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '2971'
scopus_import: '1'
status: public
title: Oct4 kinetics predict cell lineage patterning in the early mammalian embryo
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 13
year: '2011'
...
---
_id: '3505'
abstract:
- lang: eng
text: Cell migration on two-dimensional (2D) substrates follows entirely different
rules than cell migration in three-dimensional (3D) environments. This is especially
relevant for leukocytes that are able to migrate in the absence of adhesion receptors
within the confined geometry of artificial 3D extracellular matrix scaffolds and
within the interstitial space in vivo. Here, we describe in detail a simple and
economical protocol to visualize dendritic cell migration in 3D collagen scaffolds
along chemotactic gradients. This method can be adapted to other cell types and
may serve as a physiologically relevant paradigm for the directed locomotion of
most amoeboid cells.
alternative_title:
- Methods in Molecular Biology
article_processing_charge: No
article_type: original
author:
- first_name: Michael K
full_name: Sixt, Michael K
id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
last_name: Sixt
orcid: 0000-0002-6620-9179
- first_name: Tim
full_name: Lämmermann, Tim
last_name: Lämmermann
citation:
ama: Sixt MK, Lämmermann T. In vitro analysis of chemotactic leukocyte migration
in 3D environments. Cell Migration. 2011;769:149-165. doi:10.1007/978-1-61779-207-6_11
apa: Sixt, M. K., & Lämmermann, T. (2011). In vitro analysis of chemotactic
leukocyte migration in 3D environments. Cell Migration. Springer. https://doi.org/10.1007/978-1-61779-207-6_11
chicago: Sixt, Michael K, and Tim Lämmermann. “In Vitro Analysis of Chemotactic
Leukocyte Migration in 3D Environments.” Cell Migration. Springer, 2011.
https://doi.org/10.1007/978-1-61779-207-6_11.
ieee: M. K. Sixt and T. Lämmermann, “In vitro analysis of chemotactic leukocyte
migration in 3D environments,” Cell Migration, vol. 769. Springer, pp.
149–165, 2011.
ista: Sixt MK, Lämmermann T. 2011. In vitro analysis of chemotactic leukocyte migration
in 3D environments. Cell Migration. 769, 149–165.
mla: Sixt, Michael K., and Tim Lämmermann. “In Vitro Analysis of Chemotactic Leukocyte
Migration in 3D Environments.” Cell Migration, vol. 769, Springer, 2011,
pp. 149–65, doi:10.1007/978-1-61779-207-6_11.
short: M.K. Sixt, T. Lämmermann, Cell Migration 769 (2011) 149–165.
corr_author: '1'
date_created: 2018-12-11T12:03:41Z
date_published: 2011-05-17T00:00:00Z
date_updated: 2024-10-21T06:03:02Z
day: '17'
department:
- _id: MiSi
doi: 10.1007/978-1-61779-207-6_11
intvolume: ' 769'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://pure.mpg.de/pubman/item/item_3219628_1/component/file_3219630/Sixt%20et%20al..pdf
month: '05'
oa: 1
oa_version: Published Version
page: 149 - 165
publication: Cell Migration
publication_status: published
publisher: Springer
publist_id: '2882'
quality_controlled: '1'
scopus_import: '1'
status: public
title: In vitro analysis of chemotactic leukocyte migration in 3D environments
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 769
year: '2011'
...
---
_id: '3724'
abstract:
- lang: eng
text: 'Small photochromic molecules are widespread in nature and serve as switches
for a plethora of light-controlled processes. In a typical photoreceptor, the
different geometries and polarities of the photochrome isomers are tightly coupled
to functionally relevant conformational changes in the proteins. The past decade
has seen extensive efforts to mimic nature and create proteins controlled by synthetic
photochromes in the laboratory. Here, we discuss the role of molecular modeling
to gain a structural understanding of photochromes and to design light-controlled
peptides and proteins. We address several fundamental questions: What are the
molecular structures of photochromes, particularly for metastable isomers that
cannot be addressed experimentally? How are the structures of bistable photoisomers
coupled to the conformational states of peptides and proteins? Can we design light-controlled
proteins rapidly and reliably? After an introduction to the principles of molecular
modeling, we answer these questions by examining systems that range from the size
of isolated photochromes, to that of peptides and large cell surface receptors,
each from its unique computational perspective.'
author:
- first_name: Harald L
full_name: Harald Janovjak
id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
last_name: Janovjak
orcid: 0000-0002-8023-9315
- first_name: Ehud
full_name: Isacoff, Ehud Y
last_name: Isacoff
citation:
ama: 'Janovjak HL, Isacoff E. Structure-based design of light-controlled proteins.
In: Photosensitive Molecules for the Control of Biological Function. Vol
55. Springer; 2011:233-266. doi:10.1007/978-1-61779-031-7_13'
apa: Janovjak, H. L., & Isacoff, E. (2011). Structure-based design of light-controlled
proteins. In Photosensitive Molecules for the Control of Biological Function
(Vol. 55, pp. 233–266). Springer. https://doi.org/10.1007/978-1-61779-031-7_13
chicago: Janovjak, Harald L, and Ehud Isacoff. “Structure-Based Design of Light-Controlled
Proteins.” In Photosensitive Molecules for the Control of Biological Function,
55:233–66. Springer, 2011. https://doi.org/10.1007/978-1-61779-031-7_13.
ieee: H. L. Janovjak and E. Isacoff, “Structure-based design of light-controlled
proteins,” in Photosensitive Molecules for the Control of Biological Function,
vol. 55, Springer, 2011, pp. 233–266.
ista: 'Janovjak HL, Isacoff E. 2011.Structure-based design of light-controlled proteins.
In: Photosensitive Molecules for the Control of Biological Function. vol. 55,
233–266.'
mla: Janovjak, Harald L., and Ehud Isacoff. “Structure-Based Design of Light-Controlled
Proteins.” Photosensitive Molecules for the Control of Biological Function,
vol. 55, Springer, 2011, pp. 233–66, doi:10.1007/978-1-61779-031-7_13.
short: H.L. Janovjak, E. Isacoff, in:, Photosensitive Molecules for the Control
of Biological Function, Springer, 2011, pp. 233–266.
date_created: 2018-12-11T12:04:49Z
date_published: 2011-03-16T00:00:00Z
date_updated: 2021-01-12T07:51:45Z
day: '16'
doi: 10.1007/978-1-61779-031-7_13
extern: 1
intvolume: ' 55'
month: '03'
page: 233 - 266
publication: Photosensitive Molecules for the Control of Biological Function
publication_status: published
publisher: Springer
publist_id: '2504'
quality_controlled: 0
status: public
title: Structure-based design of light-controlled proteins
type: book_chapter
volume: 55
year: '2011'
...
---
_id: '3770'
abstract:
- lang: eng
text: 'The pink dolphin (Inia geoffrensis) is widely distributed along the Amazon
and Orinoco basins, covering an area of approximately 7 million km2. Previous
morphological and genetic studies have proposed the existence of at least two
evolutionary significant units: one distributed across the Orinoco and Amazon
basins and another confined to the Bolivian Amazon. The presence of barriers in
the riverine environment has been suggested to play a significant role in shaping
present-day patterns of ecological and genetic structure for this species. In
the present study, we examined the phylogeographic structure, lineage divergence
time and historical demography using mitochondrial (mt)DNA sequences in different
pink dolphin populations distributed in large and small spatial scales, including
two neighbouring Brazilian Amazon populations. mtDNA control region (CR) analysis
revealed that the Brazilian haplotypes occupy an intermediate position compared
to three previously studied geographic locations: the Colombian Amazon, the Colombian
Orinoco, and the Bolivian Amazon. On a local scale, we have identified a pattern
of maternal isolation between two neighbouring populations from Brazil. Six mtDNA
CR haplotypes were identified in Brazil with no sharing between the two populations,
as well as specific cytochrome b (cyt b) haplotypes identified in each locality.
In addition, we analyzed autosomal microsatellites to investigate male-mediated
gene flow and demographic changes within the study area in Brazil. Data analysis
of 14 microsatellite loci failed to detect significant population subdivision,
suggesting that male-mediated gene flow may maintain homogeneity between these
two locations. Moreover, both mtDNA and microsatellite data indicate a major demographic
collapse within Brazil in the late Pleistocene. Bayesian skyline plots (BSP) of
mtDNA data revealed a stable population for Colombian and Brazilian Amazon lineages
through time, whereas a population decline was demonstrated in the Colombian Orinoco
lineage. Moreover, BSP and Tajima''s D and Fu''s Fs tests revealed a recent population
expansion exclusively in the Bolivian sample. Finally, we estimated that the diversification
of the Inia sp. lineage began in the Late Pliocene (approximately 3.1 Mya) and
continued throughout the Pleistocene.'
article_processing_charge: No
author:
- first_name: Claudia
full_name: Hollatz, Claudia
last_name: Hollatz
- first_name: Sibelle
full_name: Vilaça, Sibelle
last_name: Vilaça
- first_name: Rodrigo A
full_name: Fernandes Redondo, Rodrigo A
id: 409D5C96-F248-11E8-B48F-1D18A9856A87
last_name: Fernandes Redondo
orcid: 0000-0002-5837-2793
- first_name: Míriam
full_name: Marmontel, Míriam
last_name: Marmontel
- first_name: Cyndi
full_name: Baker, Cyndi
last_name: Baker
- first_name: Fabrício
full_name: Santos, Fabrício
last_name: Santos
citation:
ama: Hollatz C, Vilaça S, Fernandes Redondo RA, Marmontel M, Baker C, Santos F.
The Amazon River system as an ecological barrier driving genetic differentiation
of the pink dolphin (Inia geoffrensis). Biological Journal of the Linnean Society.
2011;102(4):812-827. doi:10.1111/j.1095-8312.2011.01616.x
apa: Hollatz, C., Vilaça, S., Fernandes Redondo, R. A., Marmontel, M., Baker, C.,
& Santos, F. (2011). The Amazon River system as an ecological barrier driving
genetic differentiation of the pink dolphin (Inia geoffrensis). Biological
Journal of the Linnean Society. Wiley. https://doi.org/10.1111/j.1095-8312.2011.01616.x
chicago: Hollatz, Claudia, Sibelle Vilaça, Rodrigo A Fernandes Redondo, Míriam Marmontel,
Cyndi Baker, and Fabrício Santos. “The Amazon River System as an Ecological Barrier
Driving Genetic Differentiation of the Pink Dolphin (Inia Geoffrensis).” Biological
Journal of the Linnean Society. Wiley, 2011. https://doi.org/10.1111/j.1095-8312.2011.01616.x.
ieee: C. Hollatz, S. Vilaça, R. A. Fernandes Redondo, M. Marmontel, C. Baker, and
F. Santos, “The Amazon River system as an ecological barrier driving genetic differentiation
of the pink dolphin (Inia geoffrensis),” Biological Journal of the Linnean
Society, vol. 102, no. 4. Wiley, pp. 812–827, 2011.
ista: Hollatz C, Vilaça S, Fernandes Redondo RA, Marmontel M, Baker C, Santos F.
2011. The Amazon River system as an ecological barrier driving genetic differentiation
of the pink dolphin (Inia geoffrensis). Biological Journal of the Linnean Society.
102(4), 812–827.
mla: Hollatz, Claudia, et al. “The Amazon River System as an Ecological Barrier
Driving Genetic Differentiation of the Pink Dolphin (Inia Geoffrensis).” Biological
Journal of the Linnean Society, vol. 102, no. 4, Wiley, 2011, pp. 812–27,
doi:10.1111/j.1095-8312.2011.01616.x.
short: C. Hollatz, S. Vilaça, R.A. Fernandes Redondo, M. Marmontel, C. Baker, F.
Santos, Biological Journal of the Linnean Society 102 (2011) 812–827.
date_created: 2018-12-11T12:05:04Z
date_published: 2011-04-01T00:00:00Z
date_updated: 2021-01-12T07:52:05Z
day: '01'
doi: 10.1111/j.1095-8312.2011.01616.x
extern: '1'
intvolume: ' 102'
issue: '4'
language:
- iso: eng
month: '04'
oa_version: None
page: 812 - 827
publication: Biological Journal of the Linnean Society
publication_status: published
publisher: Wiley
publist_id: '2457'
status: public
title: The Amazon River system as an ecological barrier driving genetic differentiation
of the pink dolphin (Inia geoffrensis)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 102
year: '2011'
...
---
_id: '3771'
abstract:
- lang: eng
text: The small-sized frugivorous bat Carollia perspicillata is an understory specialist
and occurs in a wide range of lowland habitats, tending to be more common in tropical
dry or moist forests of South and Central America. Its sister species, Carollia
brevicauda, occurs almost exclusively in the Amazon rainforest. A recent phylogeographic
study proposed a hypothesis of origin and subsequent diversification for C. perspicillata
along the Atlantic coastal forest of Brazil. Additionally, it also found two allopatric
clades for C. brevicauda separated by the Amazon Basin. We used cytochrome b gene
sequences and a more extensive sampling to test hypotheses related to the origin
and diversification of C. perspicillata plus C. brevicauda clade in South America.
The results obtained indicate that there are two sympatric evolutionary lineages
within each species. In C. perspicillata, one lineage is limited to the Southern
Atlantic Forest, whereas the other is widely distributed. Coalescent analysis
points to a simultaneous origin for C. perspicillata and C. brevicauda, although
no place for the diversification of each species can be firmly suggested. The
phylogeographic pattern shown by C. perspicillata is also congruent with the Pleistocene
refugia hypothesis as a likely vicariant phenomenon shaping the present distribution
of its intraspecific lineages.
article_processing_charge: No
author:
- first_name: Ana
full_name: Pavan, Ana
last_name: Pavan
- first_name: Felipe
full_name: Martins, Felipe
last_name: Martins
- first_name: Fabrício
full_name: Santos, Fabrício
last_name: Santos
- first_name: Albert
full_name: Ditchfield, Albert
last_name: Ditchfield
- first_name: Rodrigo A
full_name: Fernandes Redondo, Rodrigo A
id: 409D5C96-F248-11E8-B48F-1D18A9856A87
last_name: Fernandes Redondo
orcid: 0000-0002-5837-2793
citation:
ama: 'Pavan A, Martins F, Santos F, Ditchfield A, Fernandes Redondo RA. Patterns
of diversification in two species of short-tailed bats (Carollia Gray, 1838):
the effects of historical fragmentation of Brazilian rainforests. Biological
Journal of the Linnean Society. 2011;102(3):527-539. doi:10.1111/j.1095-8312.2010.01601.x'
apa: 'Pavan, A., Martins, F., Santos, F., Ditchfield, A., & Fernandes Redondo,
R. A. (2011). Patterns of diversification in two species of short-tailed bats
(Carollia Gray, 1838): the effects of historical fragmentation of Brazilian rainforests.
Biological Journal of the Linnean Society. Wiley-Blackwell. https://doi.org/10.1111/j.1095-8312.2010.01601.x'
chicago: 'Pavan, Ana, Felipe Martins, Fabrício Santos, Albert Ditchfield, and Rodrigo
A Fernandes Redondo. “Patterns of Diversification in Two Species of Short-Tailed
Bats (Carollia Gray, 1838): The Effects of Historical Fragmentation of Brazilian
Rainforests.” Biological Journal of the Linnean Society. Wiley-Blackwell,
2011. https://doi.org/10.1111/j.1095-8312.2010.01601.x.'
ieee: 'A. Pavan, F. Martins, F. Santos, A. Ditchfield, and R. A. Fernandes Redondo,
“Patterns of diversification in two species of short-tailed bats (Carollia Gray,
1838): the effects of historical fragmentation of Brazilian rainforests.,” Biological
Journal of the Linnean Society, vol. 102, no. 3. Wiley-Blackwell, pp. 527–539,
2011.'
ista: 'Pavan A, Martins F, Santos F, Ditchfield A, Fernandes Redondo RA. 2011. Patterns
of diversification in two species of short-tailed bats (Carollia Gray, 1838):
the effects of historical fragmentation of Brazilian rainforests. Biological Journal
of the Linnean Society. 102(3), 527–539.'
mla: 'Pavan, Ana, et al. “Patterns of Diversification in Two Species of Short-Tailed
Bats (Carollia Gray, 1838): The Effects of Historical Fragmentation of Brazilian
Rainforests.” Biological Journal of the Linnean Society, vol. 102, no.
3, Wiley-Blackwell, 2011, pp. 527–39, doi:10.1111/j.1095-8312.2010.01601.x.'
short: A. Pavan, F. Martins, F. Santos, A. Ditchfield, R.A. Fernandes Redondo, Biological
Journal of the Linnean Society 102 (2011) 527–539.
corr_author: '1'
date_created: 2018-12-11T12:05:05Z
date_published: 2011-02-10T00:00:00Z
date_updated: 2025-09-30T08:39:13Z
day: '10'
department:
- _id: FyKo
doi: 10.1111/j.1095-8312.2010.01601.x
external_id:
isi:
- '000287193800005'
intvolume: ' 102'
isi: 1
issue: '3'
language:
- iso: eng
month: '02'
oa_version: None
page: 527 - 539
publication: Biological Journal of the Linnean Society
publication_status: published
publisher: Wiley-Blackwell
publist_id: '2456'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Patterns of diversification in two species of short-tailed bats (Carollia
Gray, 1838): the effects of historical fragmentation of Brazilian rainforests.'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 102
year: '2011'
...
---
_id: '3778'
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. Estimating linkage disequilibria. Heredity. 2011;106(2):205-206.
doi:10.1038/hdy.2010.67
apa: Barton, N. H. (2011). Estimating linkage disequilibria. Heredity. Nature
Publishing Group. https://doi.org/10.1038/hdy.2010.67
chicago: Barton, Nicholas H. “Estimating Linkage Disequilibria.” Heredity.
Nature Publishing Group, 2011. https://doi.org/10.1038/hdy.2010.67.
ieee: N. H. Barton, “Estimating linkage disequilibria,” Heredity, vol. 106,
no. 2. Nature Publishing Group, pp. 205–206, 2011.
ista: Barton NH. 2011. Estimating linkage disequilibria. Heredity. 106(2), 205–206.
mla: Barton, Nicholas H. “Estimating Linkage Disequilibria.” Heredity, vol.
106, no. 2, Nature Publishing Group, 2011, pp. 205–06, doi:10.1038/hdy.2010.67.
short: N.H. Barton, Heredity 106 (2011) 205–206.
corr_author: '1'
date_created: 2018-12-11T12:05:07Z
date_published: 2011-02-01T00:00:00Z
date_updated: 2025-09-30T08:38:46Z
day: '01'
department:
- _id: NiBa
doi: 10.1038/hdy.2010.67
external_id:
isi:
- '000286375300002'
pmid:
- '20502479'
intvolume: ' 106'
isi: 1
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183869/
month: '02'
oa: 1
oa_version: Submitted Version
page: 205 - 206
pmid: 1
publication: Heredity
publication_status: published
publisher: Nature Publishing Group
publist_id: '2449'
scopus_import: '1'
status: public
title: Estimating linkage disequilibria
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 106
year: '2011'
...
---
_id: '3784'
abstract:
- lang: eng
text: Advanced stages of Scyllarus phyllosoma larvae were collected by demersal
trawling during fishery research surveys in the western Mediterranean Sea in 2003–2005.
Nucleotide sequence analysis of the mitochondrial 16S rDNA gene allowed the final-stage
phyllosoma of Scyllarus arctus to be identified among these larvae. Its morphology
is described and illustrated. This constitutes the second complete description
of a Scyllaridae phyllosoma with its specific identity being validated by molecular
techniques (the first was S. pygmaeus). These results also solved a long lasting
taxonomic anomaly of several species assigned to the ancient genus Phyllosoma
Leach, 1814. Detailed examination indicated that the final-stage phyllosoma of
S. arctus shows closer affinities with the American scyllarid Scyllarus depressus
or with the Australian Scyllarus sp. b (sensu Phillips et al., 1981) than to its
sympatric species S. pygmaeus.
article_processing_charge: No
article_type: original
author:
- first_name: Ferran
full_name: Palero, Ferran
id: 3F0E2A22-F248-11E8-B48F-1D18A9856A87
last_name: Palero
orcid: 0000-0002-0343-8329
- first_name: Guillermo
full_name: Guerao, Guillermo
last_name: Guerao
- first_name: Paul
full_name: Clark, Paul
last_name: Clark
- first_name: Pere
full_name: Abello, Pere
last_name: Abello
citation:
ama: 'Palero F, Guerao G, Clark P, Abello P. Scyllarus arctus (Crustacea: Decapoda:
Scyllaridae) final stage phyllosoma identified by DNA analysis, with morphological
description. Journal of the Marine Biological Association of the United Kingdom.
2011;91(2):485-492. doi:10.1017/S0025315410000287'
apa: 'Palero, F., Guerao, G., Clark, P., & Abello, P. (2011). Scyllarus arctus
(Crustacea: Decapoda: Scyllaridae) final stage phyllosoma identified by DNA analysis,
with morphological description. Journal of the Marine Biological Association
of the United Kingdom. Cambridge University Press. https://doi.org/10.1017/S0025315410000287'
chicago: 'Palero, Ferran, Guillermo Guerao, Paul Clark, and Pere Abello. “Scyllarus
Arctus (Crustacea: Decapoda: Scyllaridae) Final Stage Phyllosoma Identified by
DNA Analysis, with Morphological Description.” Journal of the Marine Biological
Association of the United Kingdom. Cambridge University Press, 2011. https://doi.org/10.1017/S0025315410000287.'
ieee: 'F. Palero, G. Guerao, P. Clark, and P. Abello, “Scyllarus arctus (Crustacea:
Decapoda: Scyllaridae) final stage phyllosoma identified by DNA analysis, with
morphological description,” Journal of the Marine Biological Association of
the United Kingdom, vol. 91, no. 2. Cambridge University Press, pp. 485–492,
2011.'
ista: 'Palero F, Guerao G, Clark P, Abello P. 2011. Scyllarus arctus (Crustacea:
Decapoda: Scyllaridae) final stage phyllosoma identified by DNA analysis, with
morphological description. Journal of the Marine Biological Association of the
United Kingdom. 91(2), 485–492.'
mla: 'Palero, Ferran, et al. “Scyllarus Arctus (Crustacea: Decapoda: Scyllaridae)
Final Stage Phyllosoma Identified by DNA Analysis, with Morphological Description.”
Journal of the Marine Biological Association of the United Kingdom, vol.
91, no. 2, Cambridge University Press, 2011, pp. 485–92, doi:10.1017/S0025315410000287.'
short: F. Palero, G. Guerao, P. Clark, P. Abello, Journal of the Marine Biological
Association of the United Kingdom 91 (2011) 485–492.
corr_author: '1'
date_created: 2018-12-11T12:05:09Z
date_published: 2011-03-01T00:00:00Z
date_updated: 2025-09-30T08:38:12Z
day: '01'
department:
- _id: NiBa
doi: 10.1017/S0025315410000287
external_id:
isi:
- '000287940400022'
intvolume: ' 91'
isi: 1
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://digital.csic.es/bitstream/10261/32783/3/Palero_et_al_2011.pdf
month: '03'
oa: 1
oa_version: Published Version
page: 485 - 492
publication: Journal of the Marine Biological Association of the United Kingdom
publication_status: published
publisher: Cambridge University Press
publist_id: '2443'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Scyllarus arctus (Crustacea: Decapoda: Scyllaridae) final stage phyllosoma
identified by DNA analysis, with morphological description'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 91
year: '2011'
...
---
_id: '3791'
abstract:
- lang: eng
text: During the development of multicellular organisms, cell fate specification
is followed by the sorting of different cell types into distinct domains from
where the different tissues and organs are formed. Cell sorting involves both
the segregation of a mixed population of cells with different fates and properties
into distinct domains, and the active maintenance of their segregated state. Because
of its biological importance and apparent resemblance to fluid segregation in
physics, cell sorting was extensively studied by both biologists and physicists
over the last decades. Different theories were developed that try to explain cell
sorting on the basis of the physical properties of the constituent cells. However,
only recently the molecular and cellular mechanisms that control the physical
properties driving cell sorting, have begun to be unraveled. In this review, we
will provide an overview of different cell-sorting processes in development and
discuss how these processes can be explained by the different sorting theories,
and how these theories in turn can be connected to the molecular and cellular
mechanisms driving these processes.
alternative_title:
- Current Topics in Developmental Biology
article_processing_charge: No
author:
- first_name: Gabriel
full_name: Krens, Gabriel
id: 2B819732-F248-11E8-B48F-1D18A9856A87
last_name: Krens
orcid: 0000-0003-4761-5996
- first_name: Carl-Philipp J
full_name: Heisenberg, Carl-Philipp J
id: 39427864-F248-11E8-B48F-1D18A9856A87
last_name: Heisenberg
orcid: 0000-0002-0912-4566
citation:
ama: 'Krens G, Heisenberg C-PJ. Cell sorting in development. In: Labouesse M, ed.
Forces and Tension in Development. Vol 95. Elsevier; 2011:189-213. doi:10.1016/B978-0-12-385065-2.00006-2'
apa: Krens, G., & Heisenberg, C.-P. J. (2011). Cell sorting in development.
In M. Labouesse (Ed.), Forces and Tension in Development (Vol. 95, pp.
189–213). Elsevier. https://doi.org/10.1016/B978-0-12-385065-2.00006-2
chicago: Krens, Gabriel, and Carl-Philipp J Heisenberg. “Cell Sorting in Development.”
In Forces and Tension in Development, edited by Michel Labouesse, 95:189–213.
Elsevier, 2011. https://doi.org/10.1016/B978-0-12-385065-2.00006-2.
ieee: G. Krens and C.-P. J. Heisenberg, “Cell sorting in development,” in Forces
and Tension in Development, vol. 95, M. Labouesse, Ed. Elsevier, 2011, pp.
189–213.
ista: 'Krens G, Heisenberg C-PJ. 2011.Cell sorting in development. In: Forces and
Tension in Development. Current Topics in Developmental Biology, vol. 95, 189–213.'
mla: Krens, Gabriel, and Carl-Philipp J. Heisenberg. “Cell Sorting in Development.”
Forces and Tension in Development, edited by Michel Labouesse, vol. 95,
Elsevier, 2011, pp. 189–213, doi:10.1016/B978-0-12-385065-2.00006-2.
short: G. Krens, C.-P.J. Heisenberg, in:, M. Labouesse (Ed.), Forces and Tension
in Development, Elsevier, 2011, pp. 189–213.
corr_author: '1'
date_created: 2018-12-11T12:05:11Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2025-09-30T08:37:44Z
day: '01'
department:
- _id: CaHe
doi: 10.1016/B978-0-12-385065-2.00006-2
editor:
- first_name: Michel
full_name: Labouesse, Michel
last_name: Labouesse
external_id:
isi:
- '000290454200007'
intvolume: ' 95'
isi: 1
language:
- iso: eng
month: '01'
oa_version: None
page: 189 - 213
publication: Forces and Tension in Development
publication_status: published
publisher: Elsevier
publist_id: '2436'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cell sorting in development
type: book_chapter
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 95
year: '2011'
...
---
_id: '3796'
abstract:
- lang: eng
text: We address the problem of covering ℝ n with congruent balls, while minimizing
the number of balls that contain an average point. Considering the 1-parameter
family of lattices defined by stretching or compressing the integer grid in diagonal
direction, we give a closed formula for the covering density that depends on the
distortion parameter. We observe that our family contains the thinnest lattice
coverings in dimensions 2 to 5. We also consider the problem of packing congruent
balls in ℝ n , for which we give a closed formula for the packing density as well.
Again we observe that our family contains optimal configurations, this time densest
packings in dimensions 2 and 3.
alternative_title:
- LNCS
author:
- first_name: Herbert
full_name: Edelsbrunner, Herbert
id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
last_name: Edelsbrunner
orcid: 0000-0002-9823-6833
- first_name: Michael
full_name: Kerber, Michael
id: 36E4574A-F248-11E8-B48F-1D18A9856A87
last_name: Kerber
orcid: 0000-0002-8030-9299
citation:
ama: 'Edelsbrunner H, Kerber M. Covering and packing with spheres by diagonal distortion
in R^n. In: Calude C, Rozenberg G, Salomaa A, eds. Rainbow of Computer Science.
Vol 6570. Dedicated to Hermann Maurer on the Occasion of His 70th Birthday. Springer;
2011:20-35. doi:10.1007/978-3-642-19391-0_2'
apa: Edelsbrunner, H., & Kerber, M. (2011). Covering and packing with spheres
by diagonal distortion in R^n. In C. Calude, G. Rozenberg, & A. Salomaa (Eds.),
Rainbow of Computer Science (Vol. 6570, pp. 20–35). Springer. https://doi.org/10.1007/978-3-642-19391-0_2
chicago: Edelsbrunner, Herbert, and Michael Kerber. “Covering and Packing with Spheres
by Diagonal Distortion in R^n.” In Rainbow of Computer Science, edited
by Cristian Calude, Grzegorz Rozenberg, and Arto Salomaa, 6570:20–35. Dedicated
to Hermann Maurer on the Occasion of His 70th Birthday. Springer, 2011. https://doi.org/10.1007/978-3-642-19391-0_2.
ieee: H. Edelsbrunner and M. Kerber, “Covering and packing with spheres by diagonal
distortion in R^n,” in Rainbow of Computer Science, vol. 6570, C. Calude,
G. Rozenberg, and A. Salomaa, Eds. Springer, 2011, pp. 20–35.
ista: 'Edelsbrunner H, Kerber M. 2011.Covering and packing with spheres by diagonal
distortion in R^n. In: Rainbow of Computer Science. LNCS, vol. 6570, 20–35.'
mla: Edelsbrunner, Herbert, and Michael Kerber. “Covering and Packing with Spheres
by Diagonal Distortion in R^n.” Rainbow of Computer Science, edited by
Cristian Calude et al., vol. 6570, Springer, 2011, pp. 20–35, doi:10.1007/978-3-642-19391-0_2.
short: H. Edelsbrunner, M. Kerber, in:, C. Calude, G. Rozenberg, A. Salomaa (Eds.),
Rainbow of Computer Science, Springer, 2011, pp. 20–35.
corr_author: '1'
date_created: 2018-12-11T12:05:13Z
date_published: 2011-05-03T00:00:00Z
date_updated: 2024-10-21T06:03:02Z
day: '03'
ddc:
- '000'
department:
- _id: HeEd
doi: 10.1007/978-3-642-19391-0_2
editor:
- first_name: Cristian
full_name: Calude, Cristian
last_name: Calude
- first_name: Grzegorz
full_name: Rozenberg, Grzegorz
last_name: Rozenberg
- first_name: Arto
full_name: Salomaa, Arto
last_name: Salomaa
file:
- access_level: open_access
checksum: aaf22b4d7bd4277ffe8db532119cf474
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:07:42Z
date_updated: 2020-07-14T12:46:16Z
file_id: '4640'
file_name: IST-2016-539-v1+1_2011-B-01-CoveringPacking.pdf
file_size: 436875
relation: main_file
file_date_updated: 2020-07-14T12:46:16Z
has_accepted_license: '1'
intvolume: ' 6570'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Submitted Version
page: 20 - 35
publication: Rainbow of Computer Science
publication_status: published
publisher: Springer
publist_id: '2427'
pubrep_id: '539'
quality_controlled: '1'
scopus_import: '1'
series_title: Dedicated to Hermann Maurer on the Occasion of His 70th Birthday
status: public
title: Covering and packing with spheres by diagonal distortion in R^n
type: book_chapter
user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87
volume: 6570
year: '2011'
...
---
_id: '386'
abstract:
- lang: eng
text: 'We present a detailed study of the local density of states (LDOS) associated
with the surface-state band near a step edge of the strong topological insulator
Bi2Te3 and reveal a one-dimensional bound state that runs parallel to the step
edge and is bound to it at some characteristic distance. This bound state is clearly
observed in the bulk gap region, while it becomes entangled with the oscillations
of the warped surface band at high energy, and with the valence-band states near
the Dirac point. We obtain excellent fits to theoretical predictions [Alpichshev,
2011] that properly incorporate the three-dimensional nature of the problem to
the surface state. Fitting the data at different energies, we can recalculate
the LDOS originating from the Dirac band without the contribution of the bulk
bands or incoherent tunneling effects. '
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Zhanybek
full_name: Alpichshev, Zhanybek
id: 45E67A2A-F248-11E8-B48F-1D18A9856A87
last_name: Alpichshev
orcid: 0000-0002-7183-5203
- first_name: J G
full_name: Analytis, J G
last_name: Analytis
- first_name: J H
full_name: Chu, J H
last_name: Chu
- first_name: I R
full_name: Fisher, I R
last_name: Fisher
- first_name: A
full_name: Kapitulnik, A
last_name: Kapitulnik
citation:
ama: Alpichshev Z, Analytis JG, Chu JH, Fisher IR, Kapitulnik A. STM imaging of
a bound state along a step on the surface of the topological insulator Bi2Te3.
Physical Review B - Condensed Matter and Materials Physics. 2011;84(4).
doi:10.1103/PhysRevB.84.041104
apa: Alpichshev, Z., Analytis, J. G., Chu, J. H., Fisher, I. R., & Kapitulnik,
A. (2011). STM imaging of a bound state along a step on the surface of the topological
insulator Bi2Te3. Physical Review B - Condensed Matter and Materials Physics.
American Physical Society. https://doi.org/10.1103/PhysRevB.84.041104
chicago: Alpichshev, Zhanybek, J G Analytis, J H Chu, I R Fisher, and A Kapitulnik.
“STM Imaging of a Bound State along a Step on the Surface of the Topological Insulator
Bi2Te3.” Physical Review B - Condensed Matter and Materials Physics. American
Physical Society, 2011. https://doi.org/10.1103/PhysRevB.84.041104.
ieee: Z. Alpichshev, J. G. Analytis, J. H. Chu, I. R. Fisher, and A. Kapitulnik,
“STM imaging of a bound state along a step on the surface of the topological insulator
Bi2Te3,” Physical Review B - Condensed Matter and Materials Physics, vol.
84, no. 4. American Physical Society, 2011.
ista: Alpichshev Z, Analytis JG, Chu JH, Fisher IR, Kapitulnik A. 2011. STM imaging
of a bound state along a step on the surface of the topological insulator Bi2Te3.
Physical Review B - Condensed Matter and Materials Physics. 84(4).
mla: Alpichshev, Zhanybek, et al. “STM Imaging of a Bound State along a Step on
the Surface of the Topological Insulator Bi2Te3.” Physical Review B - Condensed
Matter and Materials Physics, vol. 84, no. 4, American Physical Society, 2011,
doi:10.1103/PhysRevB.84.041104.
short: Z. Alpichshev, J.G. Analytis, J.H. Chu, I.R. Fisher, A. Kapitulnik, Physical
Review B - Condensed Matter and Materials Physics 84 (2011).
date_created: 2018-12-11T11:46:10Z
date_published: 2011-07-21T00:00:00Z
date_updated: 2021-01-12T07:52:44Z
day: '21'
doi: 10.1103/PhysRevB.84.041104
extern: '1'
external_id:
arxiv:
- '1003.2233'
intvolume: ' 84'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1003.2233
month: '07'
oa: 1
oa_version: Preprint
publication: Physical Review B - Condensed Matter and Materials Physics
publication_status: published
publisher: American Physical Society
publist_id: '7443'
quality_controlled: '1'
status: public
title: STM imaging of a bound state along a step on the surface of the topological
insulator Bi2Te3
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 84
year: '2011'
...
---
_id: '3965'
abstract:
- lang: eng
text: The elevation function on a smoothly embedded 2-manifold in R-3 reflects the
multiscale topography of cavities and protrusions as local maxima. The function
has been useful in identifying coarse docking configurations for protein pairs.
Transporting the concept from the smooth to the piecewise linear category, this
paper describes an algorithm for finding all local maxima. While its worst-case
running time is the same as of the algorithm used in prior work, its performance
in practice is orders of magnitudes superior. We cast light on this improvement
by relating the running time to the total absolute Gaussian curvature of the 2-manifold.
author:
- first_name: Bei
full_name: Wang, Bei
last_name: Wang
- first_name: Herbert
full_name: Edelsbrunner, Herbert
id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
last_name: Edelsbrunner
orcid: 0000-0002-9823-6833
- first_name: Dmitriy
full_name: Morozov, Dmitriy
last_name: Morozov
citation:
ama: Wang B, Edelsbrunner H, Morozov D. Computing elevation maxima by searching
the Gauss sphere. Journal of Experimental Algorithmics. 2011;16(2.2):1-13.
doi:10.1145/1963190.1970375
apa: Wang, B., Edelsbrunner, H., & Morozov, D. (2011). Computing elevation maxima
by searching the Gauss sphere. Journal of Experimental Algorithmics. ACM.
https://doi.org/10.1145/1963190.1970375
chicago: Wang, Bei, Herbert Edelsbrunner, and Dmitriy Morozov. “Computing Elevation
Maxima by Searching the Gauss Sphere.” Journal of Experimental Algorithmics.
ACM, 2011. https://doi.org/10.1145/1963190.1970375.
ieee: B. Wang, H. Edelsbrunner, and D. Morozov, “Computing elevation maxima by searching
the Gauss sphere,” Journal of Experimental Algorithmics, vol. 16, no. 2.2.
ACM, pp. 1–13, 2011.
ista: Wang B, Edelsbrunner H, Morozov D. 2011. Computing elevation maxima by searching
the Gauss sphere. Journal of Experimental Algorithmics. 16(2.2), 1–13.
mla: Wang, Bei, et al. “Computing Elevation Maxima by Searching the Gauss Sphere.”
Journal of Experimental Algorithmics, vol. 16, no. 2.2, ACM, 2011, pp.
1–13, doi:10.1145/1963190.1970375.
short: B. Wang, H. Edelsbrunner, D. Morozov, Journal of Experimental Algorithmics
16 (2011) 1–13.
date_created: 2018-12-11T12:06:09Z
date_published: 2011-05-01T00:00:00Z
date_updated: 2021-01-12T07:53:31Z
day: '01'
department:
- _id: HeEd
doi: 10.1145/1963190.1970375
intvolume: ' 16'
issue: '2.2'
language:
- iso: eng
month: '05'
oa_version: None
page: 1 - 13
publication: Journal of Experimental Algorithmics
publication_status: published
publisher: ACM
publist_id: '2161'
quality_controlled: '1'
scopus_import: 1
status: public
title: Computing elevation maxima by searching the Gauss sphere
type: journal_article
user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2011'
...
---
OA_place: publisher
_id: '3275'
abstract:
- lang: eng
text: 'Chemokines organize immune cell trafficking by inducing either directed (tactic)
or random (kinetic) migration and by activating integrins in order to support
surface adhesion (haptic). Beyond that the same chemokines can establish clearly
defined functional areas in secondary lymphoid organs. Until now it is unclear
how chemokines can fulfill such diverse functions. One decisive prerequisite to
explain these capacities is to know how chemokines are presented in tissue. In
theory chemokines could occur either soluble or immobilized, and could be distributed
either homogenously or as a concentration gradient. To dissect if and how the
presenting mode of chemokines influences immune cells, I tested the response of
dendritic cells (DCs) to differentially displayed chemokines. DCs are antigen
presenting cells that reside in the periphery and migrate into draining lymph
nodes (LNs) once exposed to inflammatory stimuli to activate naïve T cells. DCs
are guided to and within the LN by the chemokine receptor CCR7, which has two
ligands, the chemokines CCL19 and CCL21. Both CCR7 ligands are expressed by fibroblastic
reticular cells in the LN, but differ in their ability to bind to heparan sulfate
residues. CCL21 has a highly charged C-terminal extension, which mediates binding
to anionic surfaces, whereas CCL19 is lacking such residues and likely distributes
as a soluble molecule. This study shows that surface-bound CCL21 causes random,
haptokinetic DC motility, which is confined to the chemokine coated area by insideout
activation of β2 integrins that mediate cell binding to the surface. CCL19 on
the other hand forms concentration gradients which trigger directional, chemotactic
movement, but no surface adhesion. In addition DCs can actively manipulate this
system by recruiting and activating serine proteases on their surfaces, which
create - by proteolytically removing the adhesive C-terminus - a solubilized variant
of CCL21 that functionally resembles CCL19. By generating a CCL21 concentration
gradient DCs establish a positive feedback loop to recruit further DCs from the
periphery to the CCL21 coated region. In addition DCs can sense chemotactic gradients
as well as immobilized haptokinetic fields at the same time and integrate these
signals. The result is chemotactically biased haptokinesis - directional migration
confined to a chemokine coated track or area - which could explain the dynamic
but spatially tightly controlled swarming leukocyte locomotion patterns that have
been observed in lymphatic organs by intravital microscopists. The finding that
DCs can approach soluble cues in a non-adhesive manner while they attach to surfaces
coated with immobilized cues raises the question how these cells transmit intracellular
forces to the environment, especially in the non-adherent migration mode. In order
to migrate, cells have to generate and transmit force to the extracellular substrate.
Force transmission is the prerequisite to procure an expansion of the leading
edge and a forward motion of the whole cell body. In the current conceptions actin
polymerization at the leading edge is coupled to extracellular ligands via the
integrin family of transmembrane receptors, which allows the transmission of intracellular
force. Against the paradigm of force transmission during migration, leukocytes,
like DCs, are able to migrate in threedimensional environments without using integrin
transmembrane receptors (Lämmermann et al., 2008). This reflects the biological
function of leukocytes, as they can invade almost all tissues, whereby their migration
has to be independent from the extracellular environment. How the cells can achieve
this is unclear. For this study I examined DC migration in a defined threedimensional
environment and highlighted actin-dynamics with the probe Lifeact-GFP. The result
was that chemotactic DCs can switch between integrin-dependent and integrin- independent
locomotion and can thereby adapt to the adhesive properties of their environment.
If the cells are able to couple their actin cytoskeleton to the substrate, actin
polymerization is entirely converted into protrusion. Without coupling the actin
cortex undergoes slippage and retrograde actin flow can be observed. But retrograde
actin flow can be completely compensated by higher actin polymerization rate keeping
the migration velocity and the shape of the cells unaltered. Mesenchymal cells
like fibroblast cannot balance the loss of adhesive interaction, cannot protrude
into open space and, therefore, strictly depend on integrinmediated force coupling.
This leukocyte specific phenomenon of “adaptive force transmission” endows these
cells with the unique ability to transit and invade almost every type of tissue. '
acknowledgement: "I would like to express my sincere gratitude to the following people
who made with their continuous support and encouragement this thesis possible: First,
I want to thank Prof. Dr. Michael Sixt for his excellent supervision and mentoring,
especially for the nice, relaxed working atmosphere, a lot of brilliant ideas and
the freedom to work in my own way.\r\n\r\nProf. Dr. Reinhard Fässler for his constant
support of the Sixt lab and for providing excellent working conditions. \r\n\r\nProf.
Dr. Sanjiv Luther and Prof. Dr. Tobias Bollenbach for agreeing to be member of my
thesis committee and to evaluate my work.\r\n\r\nDr. Walther Göhring, Carmen Schmitz,
the Recombinant Protein Production core facility and the animal care takers for
providing the “infrastructure” for this thesis. \r\n\r\nProf. Dr. Daniel Legler,
Markus Bruckner and Dr. Julien Polleux for very fruitful collaborations and discussions.\r\n\r\nMy
labmates for their help, a lot of discussions and to make the Sixt lab to a convenient
place to work : Karin Hirsch, Tim Lämmeramnn, Holger Pflicke, Jörg Renkawitz, Michele
Weber and Alexander Eichner All members of the Department of Molecular Medicine
for their help. Especially I want to thank Sarah Schmidt, Karin Hirsch and Raphael
Ruppert for their friendship, nice chats and their uncensored point of view. "
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Kathrin
full_name: Schumann, Kathrin
id: F44D762E-4F9D-11E9-B64C-9EB26CEFFB5F
last_name: Schumann
citation:
ama: Schumann K. The role of chemotactic gradients in dendritic cell migration.
2011.
apa: Schumann, K. (2011). The role of chemotactic gradients in dendritic cell
migration. Institute of Science and Technology Austria.
chicago: Schumann, Kathrin. “The Role of Chemotactic Gradients in Dendritic Cell
Migration.” Institute of Science and Technology Austria, 2011.
ieee: K. Schumann, “The role of chemotactic gradients in dendritic cell migration,”
Institute of Science and Technology Austria, 2011.
ista: Schumann K. 2011. The role of chemotactic gradients in dendritic cell migration.
Institute of Science and Technology Austria.
mla: Schumann, Kathrin. The Role of Chemotactic Gradients in Dendritic Cell Migration.
Institute of Science and Technology Austria, 2011.
short: K. Schumann, The Role of Chemotactic Gradients in Dendritic Cell Migration,
Institute of Science and Technology Austria, 2011.
corr_author: '1'
date_created: 2018-12-11T12:02:24Z
date_published: 2011-03-01T00:00:00Z
date_updated: 2026-04-09T14:36:24Z
day: '01'
ddc:
- '570'
- '579'
degree_awarded: PhD
department:
- _id: MiSi
file:
- access_level: closed
checksum: e69eee6252660f0b694a2ea8923ddc72
content_type: application/pdf
creator: dernst
date_created: 2019-03-26T08:12:21Z
date_updated: 2020-07-14T12:46:06Z
file_id: '6177'
file_name: 2011_Thesis_Kathrin_Schumann.pdf
file_size: 4487708
relation: main_file
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checksum: 71727d63f424b5b446f68f4b87ecadc0
content_type: application/pdf
creator: dernst
date_created: 2021-02-22T11:24:30Z
date_updated: 2021-02-22T11:24:30Z
file_id: '9175'
file_name: 2011_Thesis_Schumann_noS.pdf
file_size: 4313127
relation: main_file
success: 1
file_date_updated: 2021-02-22T11:24:30Z
has_accepted_license: '1'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: '141'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '3371'
pubrep_id: '11'
status: public
supervisor:
- first_name: Michael K
full_name: Sixt, Michael K
id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
last_name: Sixt
orcid: 0000-0002-6620-9179
title: The role of chemotactic gradients in dendritic cell migration
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2011'
...
---
OA_place: publisher
_id: '3273'
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Jean-Léon
full_name: Maître, Jean-Léon
id: 48F1E0D8-F248-11E8-B48F-1D18A9856A87
last_name: Maître
orcid: 0000-0002-3688-1474
citation:
ama: Maître J-L. Mechanics of adhesion and de‐adhesion in zebrafish germ layer progenitors.
2011.
apa: Maître, J.-L. (2011). Mechanics of adhesion and de‐adhesion in zebrafish
germ layer progenitors. Institute of Science and Technology Austria.
chicago: Maître, Jean-Léon. “Mechanics of Adhesion and De‐adhesion in Zebrafish
Germ Layer Progenitors.” Institute of Science and Technology Austria, 2011.
ieee: J.-L. Maître, “Mechanics of adhesion and de‐adhesion in zebrafish germ layer
progenitors,” Institute of Science and Technology Austria, 2011.
ista: Maître J-L. 2011. Mechanics of adhesion and de‐adhesion in zebrafish germ
layer progenitors. Institute of Science and Technology Austria.
mla: Maître, Jean-Léon. Mechanics of Adhesion and De‐adhesion in Zebrafish Germ
Layer Progenitors. Institute of Science and Technology Austria, 2011.
short: J.-L. Maître, Mechanics of Adhesion and De‐adhesion in Zebrafish Germ Layer
Progenitors, Institute of Science and Technology Austria, 2011.
corr_author: '1'
date_created: 2018-12-11T12:02:23Z
date_published: 2011-12-12T00:00:00Z
date_updated: 2026-04-09T14:36:45Z
day: '12'
degree_awarded: PhD
department:
- _id: CaHe
language:
- iso: eng
month: '12'
oa_version: None
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '3373'
status: public
supervisor:
- first_name: Carl-Philipp J
full_name: Heisenberg, Carl-Philipp J
id: 39427864-F248-11E8-B48F-1D18A9856A87
last_name: Heisenberg
orcid: 0000-0002-0912-4566
title: Mechanics of adhesion and de‐adhesion in zebrafish germ layer progenitors
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2011'
...
---
_id: '9648'
abstract:
- lang: eng
text: In this paper, we establish a correspondence between the incremental algorithm
for computing AT-models [8,9] and the one for computing persistent homology [6,14,15].
We also present a decremental algorithm for computing AT-models that allows to
extend the persistence computation to a wider setting. Finally, we show how to
combine incremental and decremental techniques for persistent homology computation.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Rocio
full_name: Gonzalez-Diaz, Rocio
last_name: Gonzalez-Diaz
- first_name: Adrian
full_name: Ion, Adrian
id: 29F89302-F248-11E8-B48F-1D18A9856A87
last_name: Ion
- first_name: Maria Jose
full_name: Jimenez, Maria Jose
last_name: Jimenez
- first_name: Regina
full_name: Poyatos, Regina
last_name: Poyatos
citation:
ama: 'Gonzalez-Diaz R, Ion A, Jimenez MJ, Poyatos R. Incremental-decremental algorithm
for computing AT-models and persistent homology. In: Computer Analysis of Images
and Patterns. Vol 6854. Springer Nature; 2011:286-293. doi:10.1007/978-3-642-23672-3_35'
apa: 'Gonzalez-Diaz, R., Ion, A., Jimenez, M. J., & Poyatos, R. (2011). Incremental-decremental
algorithm for computing AT-models and persistent homology. In Computer Analysis
of Images and Patterns (Vol. 6854, pp. 286–293). Seville, Spain: Springer
Nature. https://doi.org/10.1007/978-3-642-23672-3_35'
chicago: Gonzalez-Diaz, Rocio, Adrian Ion, Maria Jose Jimenez, and Regina Poyatos.
“Incremental-Decremental Algorithm for Computing AT-Models and Persistent Homology.”
In Computer Analysis of Images and Patterns, 6854:286–93. Springer Nature,
2011. https://doi.org/10.1007/978-3-642-23672-3_35.
ieee: R. Gonzalez-Diaz, A. Ion, M. J. Jimenez, and R. Poyatos, “Incremental-decremental
algorithm for computing AT-models and persistent homology,” in Computer Analysis
of Images and Patterns, Seville, Spain, 2011, vol. 6854, pp. 286–293.
ista: 'Gonzalez-Diaz R, Ion A, Jimenez MJ, Poyatos R. 2011. Incremental-decremental
algorithm for computing AT-models and persistent homology. Computer Analysis of
Images and Patterns. CAIP: International Conference on Computer Analysis of Images
and Patterns, LNCS, vol. 6854, 286–293.'
mla: Gonzalez-Diaz, Rocio, et al. “Incremental-Decremental Algorithm for Computing
AT-Models and Persistent Homology.” Computer Analysis of Images and Patterns,
vol. 6854, Springer Nature, 2011, pp. 286–93, doi:10.1007/978-3-642-23672-3_35.
short: R. Gonzalez-Diaz, A. Ion, M.J. Jimenez, R. Poyatos, in:, Computer Analysis
of Images and Patterns, Springer Nature, 2011, pp. 286–293.
conference:
end_date: 2011-08-31
location: Seville, Spain
name: 'CAIP: International Conference on Computer Analysis of Images and Patterns'
start_date: 2011-08-29
date_created: 2021-07-11T22:01:19Z
date_published: 2011-08-01T00:00:00Z
date_updated: 2026-04-16T10:09:19Z
day: '01'
department:
- _id: HeEd
doi: 10.1007/978-3-642-23672-3_35
intvolume: ' 6854'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://hdl.handle.net/11441/30766
month: '08'
oa: 1
oa_version: Published Version
page: 286-293
publication: Computer Analysis of Images and Patterns
publication_identifier:
eissn:
- 1611-3349
isbn:
- '9783642236716'
issn:
- 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Incremental-decremental algorithm for computing AT-models and persistent homology
type: conference
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 6854
year: '2011'
...
---
_id: '3315'
abstract:
- lang: eng
text: We consider two-player games played in real time on game structures with clocks
where the objectives of players are described using parity conditions. The games
are concurrent in that at each turn, both players independently propose a time
delay and an action, and the action with the shorter delay is chosen. To prevent
a player from winning by blocking time, we restrict each player to play strategies
that ensure that the player cannot be responsible for causing a zeno run. First,
we present an efficient reduction of these games to turn-based (i.e., not concurrent)
finite-state (i.e., untimed) parity games. Our reduction improves the best known
complexity for solving timed parity games. Moreover, the rich class of algorithms
for classical parity games can now be applied to timed parity games. The states
of the resulting game are based on clock regions of the original game, and the
state space of the finite game is linear in the size of the region graph. Second,
we consider two restricted classes of strategies for the player that represents
the controller in a real-time synthesis problem, namely, limit-robust and bounded-robust
winning strategies. Using a limit-robust winning strategy, the controller cannot
choose an exact real-valued time delay but must allow for some nonzero jitter
in each of its actions. If there is a given lower bound on the jitter, then the
strategy is bounded-robust winning. We show that exact strategies are more powerful
than limit-robust strategies, which are more powerful than bounded-robust winning
strategies for any bound. For both kinds of robust strategies, we present efficient
reductions to standard timed automaton games. These reductions provide algorithms
for the synthesis of robust real-time controllers.
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- 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: Vinayak
full_name: Prabhu, Vinayak
last_name: Prabhu
citation:
ama: 'Chatterjee K, Henzinger TA, Prabhu V. Timed parity games: Complexity and robustness.
Logical Methods in Computer Science. 2011;7(4). doi:10.2168/LMCS-7(4:8)2011'
apa: 'Chatterjee, K., Henzinger, T. A., & Prabhu, V. (2011). Timed parity games:
Complexity and robustness. Logical Methods in Computer Science. International
Federation of Computational Logic. https://doi.org/10.2168/LMCS-7(4:8)2011'
chicago: 'Chatterjee, Krishnendu, Thomas A Henzinger, and Vinayak Prabhu. “Timed
Parity Games: Complexity and Robustness.” Logical Methods in Computer Science.
International Federation of Computational Logic, 2011. https://doi.org/10.2168/LMCS-7(4:8)2011.'
ieee: 'K. Chatterjee, T. A. Henzinger, and V. Prabhu, “Timed parity games: Complexity
and robustness,” Logical Methods in Computer Science, vol. 7, no. 4. International
Federation of Computational Logic, 2011.'
ista: 'Chatterjee K, Henzinger TA, Prabhu V. 2011. Timed parity games: Complexity
and robustness. Logical Methods in Computer Science. 7(4).'
mla: 'Chatterjee, Krishnendu, et al. “Timed Parity Games: Complexity and Robustness.”
Logical Methods in Computer Science, vol. 7, no. 4, International Federation
of Computational Logic, 2011, doi:10.2168/LMCS-7(4:8)2011.'
short: K. Chatterjee, T.A. Henzinger, V. Prabhu, Logical Methods in Computer Science
7 (2011).
corr_author: '1'
date_created: 2018-12-11T12:02:37Z
date_published: 2011-12-14T00:00:00Z
date_updated: 2026-05-22T08:46:08Z
day: '14'
ddc:
- '000'
- '005'
department:
- _id: KrCh
- _id: ToHe
doi: 10.2168/LMCS-7(4:8)2011
ec_funded: 1
file:
- access_level: open_access
checksum: 3480e1594bbef25ff7462fa93a8a814e
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:16:42Z
date_updated: 2020-07-14T12:46:07Z
file_id: '5231'
file_name: IST-2016-86-v2+1_1011.0688_3_.pdf
file_size: 588863
relation: main_file
file_date_updated: 2020-07-14T12:46:07Z
has_accepted_license: '1'
intvolume: ' 7'
issue: '4'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nd/4.0/
month: '12'
oa: 1
oa_version: Published Version
project:
- _id: 25EFB36C-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '215543'
name: COMponent-Based Embedded Systems design Techniques
publication: Logical Methods in Computer Science
publication_status: published
publisher: International Federation of Computational Logic
publist_id: '3324'
pubrep_id: '506'
quality_controlled: '1'
related_material:
record:
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relation: earlier_version
status: public
scopus_import: 1
status: public
title: 'Timed parity games: Complexity and robustness'
tmp:
image: /image/cc_by_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nd/4.0/legalcode
name: Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0)
short: CC BY-ND (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2011'
...
---
_id: '2701'
abstract:
- lang: eng
text: We consider N × N Hermitian random matrices with independent identically distributed
entries (Wigner matrices). The matrices are normalized so that the average spacing
between consecutive eigenvalues is of order 1/ N. Under suitable assumptions on
the distribution of the single matrix element, we first prove that, away from
the spectral edges, the empirical density of eigenvalues concentrates around the
Wigner semicircle law on energy scales η ≫ N -1. This result establishes the semicircle
law on the optimal scale and it removes a logarithmic factor from our previous
result [6]. We then show a Wegner estimate, i.e., that the averaged density of
states is bounded. Finally, we prove that the eigenvalues of a Wigner matrix repel
each other, in agreement with the universality conjecture.
author:
- first_name: László
full_name: László Erdös
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
- first_name: Benjamin
full_name: Schlein, Benjamin
last_name: Schlein
- first_name: Horng
full_name: Yau, Horng-Tzer
last_name: Yau
citation:
ama: Erdös L, Schlein B, Yau H. Wegner estimate and level repulsion for Wigner random
matrices. International Mathematics Research Notices. 2010;(3):436-479.
doi:10.1093/imrn/rnp136
apa: Erdös, L., Schlein, B., & Yau, H. (2010). Wegner estimate and level repulsion
for Wigner random matrices. International Mathematics Research Notices.
Oxford University Press. https://doi.org/10.1093/imrn/rnp136
chicago: Erdös, László, Benjamin Schlein, and Horng Yau. “Wegner Estimate and Level
Repulsion for Wigner Random Matrices.” International Mathematics Research Notices.
Oxford University Press, 2010. https://doi.org/10.1093/imrn/rnp136.
ieee: L. Erdös, B. Schlein, and H. Yau, “Wegner estimate and level repulsion for
Wigner random matrices,” International Mathematics Research Notices, no.
3. Oxford University Press, pp. 436–479, 2010.
ista: Erdös L, Schlein B, Yau H. 2010. Wegner estimate and level repulsion for Wigner
random matrices. International Mathematics Research Notices. (3), 436–479.
mla: Erdös, László, et al. “Wegner Estimate and Level Repulsion for Wigner Random
Matrices.” International Mathematics Research Notices, no. 3, Oxford University
Press, 2010, pp. 436–79, doi:10.1093/imrn/rnp136.
short: L. Erdös, B. Schlein, H. Yau, International Mathematics Research Notices
(2010) 436–479.
date_created: 2018-12-11T11:59:09Z
date_published: 2010-01-01T00:00:00Z
date_updated: 2021-01-12T06:59:09Z
day: '01'
doi: 10.1093/imrn/rnp136
extern: 1
issue: '3'
main_file_link:
- open_access: '1'
url: http://arxiv.org/abs/0811.2591
month: '01'
oa: 1
page: 436 - 479
publication: International Mathematics Research Notices
publication_status: published
publisher: Oxford University Press
publist_id: '4195'
quality_controlled: 0
status: public
title: Wegner estimate and level repulsion for Wigner random matrices
type: journal_article
year: '2010'
...
---
_id: '2704'
abstract:
- lang: eng
text: Consider a system of N bosons in three dimensions interacting via a repulsive
short range pair potential N2V(N(xi-xj)), where x = (x1, ..., xN) denotes the
positions of the particles. Let HN, denote the Hamiltonian of the system and let
ψN,t be the solution to the Schrödinger equation. Suppose that the initial data
ψN,0 satisfies the energy condition 〈 ψ N,0,Hk N ψN,0〉 ≤ CkNk for k =1, 2, ....We
also assume that the k-particle density matrices of the initial state are asymptotically
factorized as N →∞1. We prove that the k-particle density matrices of ψN,t are
also asymptotically factorized and the one particle orbital wave function solves
the Gross-Pitaevskii equation, a cubic nonlinear Schrödinger equation with the
coupling constant given by the scattering length of the potential V. We also prove
the same conclusion if the energy condition holds only for k=1 but the factorization
of ψN,0 is assumed in a stronger sense.
author:
- first_name: László
full_name: László Erdös
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
- first_name: Benjamin
full_name: Schlein, Benjamin
last_name: Schlein
- first_name: Horng
full_name: Yau, Horng-Tzer
last_name: Yau
citation:
ama: Erdös L, Schlein B, Yau H. Derivation of the Gross-Pitaevskii equation for
the dynamics of Bose-Einstein condensate. Annals of Mathematics. 2010;172(1):291-370.
doi:10.4007/annals.2010.172.291
apa: Erdös, L., Schlein, B., & Yau, H. (2010). Derivation of the Gross-Pitaevskii
equation for the dynamics of Bose-Einstein condensate. Annals of Mathematics.
Princeton University Press. https://doi.org/10.4007/annals.2010.172.291
chicago: Erdös, László, Benjamin Schlein, and Horng Yau. “Derivation of the Gross-Pitaevskii
Equation for the Dynamics of Bose-Einstein Condensate.” Annals of Mathematics.
Princeton University Press, 2010. https://doi.org/10.4007/annals.2010.172.291.
ieee: L. Erdös, B. Schlein, and H. Yau, “Derivation of the Gross-Pitaevskii equation
for the dynamics of Bose-Einstein condensate,” Annals of Mathematics, vol.
172, no. 1. Princeton University Press, pp. 291–370, 2010.
ista: Erdös L, Schlein B, Yau H. 2010. Derivation of the Gross-Pitaevskii equation
for the dynamics of Bose-Einstein condensate. Annals of Mathematics. 172(1), 291–370.
mla: Erdös, László, et al. “Derivation of the Gross-Pitaevskii Equation for the
Dynamics of Bose-Einstein Condensate.” Annals of Mathematics, vol. 172,
no. 1, Princeton University Press, 2010, pp. 291–370, doi:10.4007/annals.2010.172.291.
short: L. Erdös, B. Schlein, H. Yau, Annals of Mathematics 172 (2010) 291–370.
date_created: 2018-12-11T11:59:10Z
date_published: 2010-07-01T00:00:00Z
date_updated: 2021-01-12T06:59:10Z
day: '01'
doi: 10.4007/annals.2010.172.291
extern: 1
intvolume: ' 172'
issue: '1'
main_file_link:
- open_access: '0'
url: http://xxx.lanl.gov/abs/math-ph/0606017
month: '07'
page: 291 - 370
publication: Annals of Mathematics
publication_status: published
publisher: Princeton University Press
publist_id: '4192'
quality_controlled: 0
status: public
title: Derivation of the Gross-Pitaevskii equation for the dynamics of Bose-Einstein
condensate
type: journal_article
volume: 172
year: '2010'
...