---
_id: '3203'
abstract:
- lang: eng
text: In recent years the Markov Random Field (MRF) has become the de facto probabilistic
model for low-level vision applications. However, in a maximum a posteriori (MAP)
framework, MRFs inherently encourage delta function marginal statistics. By contrast,
many low-level vision problems have heavy tailed marginal statistics, making the
MRF model unsuitable. In this paper we introduce a more general Marginal Probability
Field (MPF), of which the MRF is a special, linear case, and show that convex
energy MPFs can be used to encourage arbitrary marginal statistics. We introduce
a flexible, extensible framework for effectively optimizing the resulting NP-hard
MAP problem, based around dual-decomposition and a modified mincost flow algorithm,
and which achieves global optimality in some instances. We use a range of applications,
including image denoising and texture synthesis, to demonstrate the benefits of
this class of MPF over MRFs.
author:
- first_name: Oliver
full_name: Woodford, Oliver J
last_name: Woodford
- first_name: Carsten
full_name: Rother, Carsten
last_name: Rother
- first_name: Vladimir
full_name: Vladimir Kolmogorov
id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
last_name: Kolmogorov
citation:
ama: 'Woodford O, Rother C, Kolmogorov V. A global perspective on MAP inference
for low level vision. In: IEEE; 2009:2319-2326. doi:10.1109/ICCV.2009.5459434'
apa: 'Woodford, O., Rother, C., & Kolmogorov, V. (2009). A global perspective
on MAP inference for low level vision (pp. 2319–2326). Presented at the ICCV:
International Conference on Computer Vision, IEEE. https://doi.org/10.1109/ICCV.2009.5459434'
chicago: Woodford, Oliver, Carsten Rother, and Vladimir Kolmogorov. “A Global Perspective
on MAP Inference for Low Level Vision,” 2319–26. IEEE, 2009. https://doi.org/10.1109/ICCV.2009.5459434.
ieee: 'O. Woodford, C. Rother, and V. Kolmogorov, “A global perspective on MAP inference
for low level vision,” presented at the ICCV: International Conference on Computer
Vision, 2009, pp. 2319–2326.'
ista: 'Woodford O, Rother C, Kolmogorov V. 2009. A global perspective on MAP inference
for low level vision. ICCV: International Conference on Computer Vision, 2319–2326.'
mla: Woodford, Oliver, et al. A Global Perspective on MAP Inference for Low Level
Vision. IEEE, 2009, pp. 2319–26, doi:10.1109/ICCV.2009.5459434.
short: O. Woodford, C. Rother, V. Kolmogorov, in:, IEEE, 2009, pp. 2319–2326.
conference:
name: 'ICCV: International Conference on Computer Vision'
date_created: 2018-12-11T12:01:59Z
date_published: 2009-05-01T00:00:00Z
date_updated: 2021-01-12T07:41:46Z
day: '01'
doi: 10.1109/ICCV.2009.5459434
extern: 1
month: '05'
page: 2319 - 2326
publication_status: published
publisher: IEEE
publist_id: '3481'
quality_controlled: 0
status: public
title: A global perspective on MAP inference for low level vision
type: conference
year: '2009'
...
---
_id: '3230'
abstract:
- lang: eng
text: 'We present a new approach to the design of IND-CCA2 secure hybrid encryption
schemes in the standard model. Our approach provides an efficient generic transformation
from 1-universal to 2-universal hash proof systems. The transformation involves
a randomness extractor based on a 4-wise independent hash function as the key
derivation function. Our methodology can be instantiated with efficient schemes
based on standard intractability assumptions such as Decisional Diffie-Hellman,
Quadratic Residuosity, and Paillier''s Decisional Composite Residuosity. Interestingly,
our framework also allows to prove IND-CCA2 security of a hybrid version of 1991''s
Damgård''s ElGamal public-key encryption scheme under the DDH assumption. '
alternative_title:
- LNCS
author:
- first_name: Eike
full_name: Kiltz, Eike
last_name: Kiltz
- first_name: Krzysztof Z
full_name: Krzysztof Pietrzak
id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
last_name: Pietrzak
orcid: 0000-0002-9139-1654
- first_name: Martijn
full_name: Stam, Martijn
last_name: Stam
- first_name: Moti
full_name: Yung, Moti
last_name: Yung
citation:
ama: 'Kiltz E, Pietrzak KZ, Stam M, Yung M. A new randomness extraction paradigm
for hybrid encryption. In: Vol 5479. Springer; 2009:590-609. doi:10.1007/978-3-642-01001-9_34'
apa: 'Kiltz, E., Pietrzak, K. Z., Stam, M., & Yung, M. (2009). A new randomness
extraction paradigm for hybrid encryption (Vol. 5479, pp. 590–609). Presented
at the EUROCRYPT: Theory and Applications of Cryptographic Techniques, Springer.
https://doi.org/10.1007/978-3-642-01001-9_34'
chicago: Kiltz, Eike, Krzysztof Z Pietrzak, Martijn Stam, and Moti Yung. “A New
Randomness Extraction Paradigm for Hybrid Encryption,” 5479:590–609. Springer,
2009. https://doi.org/10.1007/978-3-642-01001-9_34.
ieee: 'E. Kiltz, K. Z. Pietrzak, M. Stam, and M. Yung, “A new randomness extraction
paradigm for hybrid encryption,” presented at the EUROCRYPT: Theory and Applications
of Cryptographic Techniques, 2009, vol. 5479, pp. 590–609.'
ista: 'Kiltz E, Pietrzak KZ, Stam M, Yung M. 2009. A new randomness extraction paradigm
for hybrid encryption. EUROCRYPT: Theory and Applications of Cryptographic Techniques,
LNCS, vol. 5479, 590–609.'
mla: Kiltz, Eike, et al. A New Randomness Extraction Paradigm for Hybrid Encryption.
Vol. 5479, Springer, 2009, pp. 590–609, doi:10.1007/978-3-642-01001-9_34.
short: E. Kiltz, K.Z. Pietrzak, M. Stam, M. Yung, in:, Springer, 2009, pp. 590–609.
conference:
name: 'EUROCRYPT: Theory and Applications of Cryptographic Techniques'
date_created: 2018-12-11T12:02:09Z
date_published: 2009-05-28T00:00:00Z
date_updated: 2021-01-12T07:41:58Z
day: '28'
doi: 10.1007/978-3-642-01001-9_34
extern: 1
intvolume: ' 5479'
month: '05'
page: 590 - 609
publication_status: published
publisher: Springer
publist_id: '3449'
quality_controlled: 0
status: public
title: A new randomness extraction paradigm for hybrid encryption
type: conference
volume: 5479
year: '2009'
...
---
_id: '3231'
abstract:
- lang: eng
text: 'We investigate the security of "padding-based" encryption schemes
in the standard model. This class contains all public-key encryption schemes where
the encryption algorithm first applies some invertible public transformation to
the message (the "padding"), followed by a trapdoor permutation. In
particular, this class contains OAEP and its variants. Our main result is a black-box
impossibility result showing that one cannot prove any such padding-based scheme
chosen-ciphertext secure even assuming the existence of ideal trapdoor permutations.
The latter is a strong ideal abstraction of trapdoor permutations which inherits
all security properties of uniform random permutations. '
alternative_title:
- LNCS
author:
- first_name: Eike
full_name: Kiltz, Eike
last_name: Kiltz
- first_name: Krzysztof Z
full_name: Krzysztof Pietrzak
id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
last_name: Pietrzak
orcid: 0000-0002-9139-1654
citation:
ama: 'Kiltz E, Pietrzak KZ. On the security of padding based encryption schemes
Why We cannot prove OAEP secure in the standard model. In: Vol 5479. Springer;
2009:389-406. doi:10.1007/978-3-642-01001-9_23'
apa: 'Kiltz, E., & Pietrzak, K. Z. (2009). On the security of padding based
encryption schemes Why We cannot prove OAEP secure in the standard model (Vol.
5479, pp. 389–406). Presented at the EUROCRYPT: Theory and Applications of Cryptographic
Techniques, Springer. https://doi.org/10.1007/978-3-642-01001-9_23'
chicago: Kiltz, Eike, and Krzysztof Z Pietrzak. “On the Security of Padding Based
Encryption Schemes Why We Cannot Prove OAEP Secure in the Standard Model,” 5479:389–406.
Springer, 2009. https://doi.org/10.1007/978-3-642-01001-9_23.
ieee: 'E. Kiltz and K. Z. Pietrzak, “On the security of padding based encryption
schemes Why We cannot prove OAEP secure in the standard model,” presented at the
EUROCRYPT: Theory and Applications of Cryptographic Techniques, 2009, vol. 5479,
pp. 389–406.'
ista: 'Kiltz E, Pietrzak KZ. 2009. On the security of padding based encryption schemes
Why We cannot prove OAEP secure in the standard model. EUROCRYPT: Theory and Applications
of Cryptographic Techniques, LNCS, vol. 5479, 389–406.'
mla: Kiltz, Eike, and Krzysztof Z. Pietrzak. On the Security of Padding Based
Encryption Schemes Why We Cannot Prove OAEP Secure in the Standard Model.
Vol. 5479, Springer, 2009, pp. 389–406, doi:10.1007/978-3-642-01001-9_23.
short: E. Kiltz, K.Z. Pietrzak, in:, Springer, 2009, pp. 389–406.
conference:
name: 'EUROCRYPT: Theory and Applications of Cryptographic Techniques'
date_created: 2018-12-11T12:02:09Z
date_published: 2009-05-28T00:00:00Z
date_updated: 2021-01-12T07:41:58Z
day: '28'
doi: 10.1007/978-3-642-01001-9_23
extern: 1
intvolume: ' 5479'
month: '05'
page: 389 - 406
publication_status: published
publisher: Springer
publist_id: '3450'
quality_controlled: 0
status: public
title: On the security of padding based encryption schemes Why We cannot prove OAEP
secure in the standard model
type: conference
volume: 5479
year: '2009'
...
---
_id: '3232'
abstract:
- lang: eng
text: 'A weak pseudorandom function (wPRF) is a cryptographic primitive similar
to - but weaker than - a pseudorandom function: for wPRFs one only requires that
the output is pseudorandom when queried on random inputs.We show that unlike "normal"
PRFs, wPRFs are seedincompressible, in the sense that the output of a wPRF is
pseudorandom even if a bounded amount of information about the key is leaked.
As an application of this result we construct a simple mode of operation which
- when instantiated with any wPRF - gives a leakage-resilient stream-cipher. The
implementation of such a cipher is secure against every side-channel attack, as
long as the amount of information leaked per round is bounded, but overall can
be arbitrary large. The construction is simpler than the previous one (Dziembowski-Pietrzak
FOCS''08) as it only uses a single primitive (a wPRF) in a straight forward manner. '
alternative_title:
- LNCS
author:
- first_name: Krzysztof Z
full_name: Krzysztof Pietrzak
id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
last_name: Pietrzak
orcid: 0000-0002-9139-1654
citation:
ama: 'Pietrzak KZ. A leakage resilient mode of operation. In: Vol 5479. Springer;
2009:462-482. doi:10.1007/978-3-642-01001-9_27'
apa: 'Pietrzak, K. Z. (2009). A leakage resilient mode of operation (Vol. 5479,
pp. 462–482). Presented at the CRYPTO: International Cryptology Conference, Springer.
https://doi.org/10.1007/978-3-642-01001-9_27'
chicago: Pietrzak, Krzysztof Z. “A Leakage Resilient Mode of Operation,” 5479:462–82.
Springer, 2009. https://doi.org/10.1007/978-3-642-01001-9_27.
ieee: 'K. Z. Pietrzak, “A leakage resilient mode of operation,” presented at the
CRYPTO: International Cryptology Conference, 2009, vol. 5479, pp. 462–482.'
ista: 'Pietrzak KZ. 2009. A leakage resilient mode of operation. CRYPTO: International
Cryptology Conference, LNCS, vol. 5479, 462–482.'
mla: Pietrzak, Krzysztof Z. A Leakage Resilient Mode of Operation. Vol. 5479,
Springer, 2009, pp. 462–82, doi:10.1007/978-3-642-01001-9_27.
short: K.Z. Pietrzak, in:, Springer, 2009, pp. 462–482.
conference:
name: 'CRYPTO: International Cryptology Conference'
date_created: 2018-12-11T12:02:09Z
date_published: 2009-05-28T00:00:00Z
date_updated: 2021-01-12T07:41:59Z
day: '28'
doi: 10.1007/978-3-642-01001-9_27
extern: 1
intvolume: ' 5479'
month: '05'
page: 462 - 482
publication_status: published
publisher: Springer
publist_id: '3448'
quality_controlled: 0
status: public
title: A leakage resilient mode of operation
type: conference
volume: 5479
year: '2009'
...
---
_id: '3292'
abstract:
- lang: eng
text: Galactofuranose (Galf) containing molecules have been described at the cell
surface of several eukaryotes and shown to contribute to the virulence of the
parasite Leishmania major and the fungus Aspergillus fumigatus. It is anticipated
that a number of the surface glycoconjugates such as N-glycans or glycolipids
are galactofuranosylated in the Golgi apparatus. This raises the question of how
the substrate for galactofuranosylation reactions, UDP-Galf, which is synthesized
in the cytosol, translocates into the organelles of the secretory pathway. Here
we report the first identification of a Golgi-localized nucleotide sugar transporter,
named GlfB, with specificity for a UDP-Galf. In vitro transport assays established
binding of UDP-Galf to GlfB and excluded transport of several other nucleotide
sugars. Furthermore, the implication of glfB in the galactofuranosylation of A.
fumigatus glycoconjugates and galactomannan was demonstrated by a targeted gene
deletion approach. Our data reveal a direct connection between galactomannan and
the organelles of the secretory pathway that strongly suggests that the cell wall-bound
polysaccharide originates from its glycosylphosphatidylinositol-anchored form.
author:
- first_name: Jakob
full_name: Engel, Jakob
last_name: Engel
- first_name: Philipp S
full_name: Schmalhorst, Philipp S
id: 309D50DA-F248-11E8-B48F-1D18A9856A87
last_name: Schmalhorst
orcid: 0000-0002-5795-0133
- first_name: Thilo
full_name: Dörk Bousset, Thilo
last_name: Dörk Bousset
- first_name: Vincent
full_name: Ferrières, Vincent
last_name: Ferrières
- first_name: Françoise
full_name: Routier, Françoise
last_name: Routier
citation:
ama: Engel J, Schmalhorst PS, Dörk Bousset T, Ferrières V, Routier F. A single UDP
galactofuranose transporter is required for galactofuranosylation in Aspergillus
fumigatus. Journal of Biological Chemistry. 2009;284(49):33859-33868. doi:10.1074/jbc.M109.070219
apa: Engel, J., Schmalhorst, P. S., Dörk Bousset, T., Ferrières, V., & Routier,
F. (2009). A single UDP galactofuranose transporter is required for galactofuranosylation
in Aspergillus fumigatus. Journal of Biological Chemistry. American Society
for Biochemistry and Molecular Biology. https://doi.org/10.1074/jbc.M109.070219
chicago: Engel, Jakob, Philipp S Schmalhorst, Thilo Dörk Bousset, Vincent Ferrières,
and Françoise Routier. “A Single UDP Galactofuranose Transporter Is Required for
Galactofuranosylation in Aspergillus Fumigatus.” Journal of Biological Chemistry.
American Society for Biochemistry and Molecular Biology, 2009. https://doi.org/10.1074/jbc.M109.070219 .
ieee: J. Engel, P. S. Schmalhorst, T. Dörk Bousset, V. Ferrières, and F. Routier,
“A single UDP galactofuranose transporter is required for galactofuranosylation
in Aspergillus fumigatus,” Journal of Biological Chemistry, vol. 284, no.
49. American Society for Biochemistry and Molecular Biology, pp. 33859–33868,
2009.
ista: Engel J, Schmalhorst PS, Dörk Bousset T, Ferrières V, Routier F. 2009. A single
UDP galactofuranose transporter is required for galactofuranosylation in Aspergillus
fumigatus. Journal of Biological Chemistry. 284(49), 33859–33868.
mla: Engel, Jakob, et al. “A Single UDP Galactofuranose Transporter Is Required
for Galactofuranosylation in Aspergillus Fumigatus.” Journal of Biological
Chemistry, vol. 284, no. 49, American Society for Biochemistry and Molecular
Biology, 2009, pp. 33859–68, doi:10.1074/jbc.M109.070219 .
short: J. Engel, P.S. Schmalhorst, T. Dörk Bousset, V. Ferrières, F. Routier, Journal
of Biological Chemistry 284 (2009) 33859–33868.
date_created: 2018-12-11T12:02:30Z
date_published: 2009-12-04T00:00:00Z
date_updated: 2021-01-12T07:42:26Z
day: '04'
doi: '10.1074/jbc.M109.070219 '
extern: '1'
intvolume: ' 284'
issue: '49'
language:
- iso: eng
month: '12'
oa_version: None
page: 33859 - 33868
publication: Journal of Biological Chemistry
publication_status: published
publisher: American Society for Biochemistry and Molecular Biology
publist_id: '3353'
quality_controlled: '1'
status: public
title: A single UDP galactofuranose transporter is required for galactofuranosylation
in Aspergillus fumigatus
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 284
year: '2009'
...
---
_id: '3293'
abstract:
- lang: eng
text: Chemotactic responses of Drosophila to certain esters and alcohols are experience
dependent. When the flies are exposed after eclosion to these chemicals, the odorants
become strongly attractive. We show that behavioral conditioning is accompanied
by an increase in the electrophysiological responses of single neurons in sensilla
basiconica. Sensitization involves odorants that act on a common olfactory receptor.
The possible mechanism of imaginal conditioning and its ecological and evolutionary
significance are discussed.
author:
- first_name: Subhra
full_name: Chakraborty Tuhin, Subhra
last_name: Chakraborty Tuhin
- first_name: Sarit
full_name: Sarit Goswami
id: 3A578F32-F248-11E8-B48F-1D18A9856A87
last_name: Goswami
- first_name: Obaid
full_name: Siddiqi, Obaid
last_name: Siddiqi
citation:
ama: Chakraborty Tuhin S, Goswami S, Siddiqi O. Sensory correlates of imaginal conditioning
in Drosophila melanogaster. Journal of Neurogenetics. 2009;23(1-2):210-219.
doi:10.1080/01677060802491559
apa: Chakraborty Tuhin, S., Goswami, S., & Siddiqi, O. (2009). Sensory correlates
of imaginal conditioning in Drosophila melanogaster. Journal of Neurogenetics.
Informa Healthcare. https://doi.org/10.1080/01677060802491559
chicago: Chakraborty Tuhin, Subhra, Sarit Goswami, and Obaid Siddiqi. “Sensory Correlates
of Imaginal Conditioning in Drosophila Melanogaster.” Journal of Neurogenetics.
Informa Healthcare, 2009. https://doi.org/10.1080/01677060802491559
.
ieee: S. Chakraborty Tuhin, S. Goswami, and O. Siddiqi, “Sensory correlates of imaginal
conditioning in Drosophila melanogaster,” Journal of Neurogenetics, vol.
23, no. 1–2. Informa Healthcare, pp. 210–9, 2009.
ista: Chakraborty Tuhin S, Goswami S, Siddiqi O. 2009. Sensory correlates of imaginal
conditioning in Drosophila melanogaster. Journal of Neurogenetics. 23(1–2), 210–9.
mla: Chakraborty Tuhin, Subhra, et al. “Sensory Correlates of Imaginal Conditioning
in Drosophila Melanogaster.” Journal of Neurogenetics, vol. 23, no. 1–2,
Informa Healthcare, 2009, pp. 210–19, doi:10.1080/01677060802491559 .
short: S. Chakraborty Tuhin, S. Goswami, O. Siddiqi, Journal of Neurogenetics 23
(2009) 210–9.
date_created: 2018-12-11T12:02:30Z
date_published: 2009-01-01T00:00:00Z
date_updated: 2021-01-12T07:42:27Z
day: '01'
doi: '10.1080/01677060802491559 '
extern: 1
intvolume: ' 23'
issue: 1-2
month: '01'
page: 210 - 9
publication: Journal of Neurogenetics
publication_status: published
publisher: Informa Healthcare
publist_id: '3348'
quality_controlled: 0
status: public
title: Sensory correlates of imaginal conditioning in Drosophila melanogaster
type: journal_article
volume: 23
year: '2009'
...
---
_id: '3304'
abstract:
- lang: eng
text: Complex traits often involve interactions between different genetic loci.
This can lead to sign epistasis, whereby mutations that are individually deleterious
or neutral combine to confer a fitness benefit. In order to acquire the beneficial
genotype, an asexual population must cross a fitness valley or plateau by first
acquiring the deleterious or neutral intermediates. Here, we present a complete,
intuitive theoretical description of the valley-crossing process across the full
spectrum of possible parameter regimes. We calculate the rate at which a population
crosses a fitness valley or plateau of arbitrary width, as a function of the mutation
rates, the population size, and the fitnesses of the intermediates. We find that
when intermediates are close to neutral, a large population can cross even wide
fitness valleys remarkably quickly, so that valley-crossing dynamics may be common
even when mutations that directly increase fitness are also possible. Thus the
evolutionary dynamics of large populations can be sensitive to the structure of
an extended region of the fitness landscape — the population may not take directly
uphill paths in favor of paths across valleys and plateaus that lead eventually
to fitter genotypes. In smaller populations, we find that below a threshold size,
which depends on the width of the fitness valley and the strength of selection
against intermediate genotypes, valley-crossing is much less likely and hence
the evolutionary dynamics are less influenced by distant regions of the fitness
landscape.
author:
- first_name: Daniel
full_name: Daniel Weissman
id: 2D0CE020-F248-11E8-B48F-1D18A9856A87
last_name: Weissman
- first_name: Michael
full_name: Desai, Michael M
last_name: Desai
- first_name: Daniel
full_name: Fisher, Daniel S
last_name: Fisher
- first_name: Marcus
full_name: Feldman, Marcus W
last_name: Feldman
citation:
ama: Weissman D, Desai M, Fisher D, Feldman M. The rate at which asexual populations
cross fitness valleys. Theoretical Population Biology. 2009;75(4):286-300.
doi:10.1016/j.tpb.2009.02.006
apa: Weissman, D., Desai, M., Fisher, D., & Feldman, M. (2009). The rate at
which asexual populations cross fitness valleys. Theoretical Population Biology.
Academic Press. https://doi.org/10.1016/j.tpb.2009.02.006
chicago: Weissman, Daniel, Michael Desai, Daniel Fisher, and Marcus Feldman. “The
Rate at Which Asexual Populations Cross Fitness Valleys.” Theoretical Population
Biology. Academic Press, 2009. https://doi.org/10.1016/j.tpb.2009.02.006.
ieee: D. Weissman, M. Desai, D. Fisher, and M. Feldman, “The rate at which asexual
populations cross fitness valleys,” Theoretical Population Biology, vol.
75, no. 4. Academic Press, pp. 286–300, 2009.
ista: Weissman D, Desai M, Fisher D, Feldman M. 2009. The rate at which asexual
populations cross fitness valleys. Theoretical Population Biology. 75(4), 286–300.
mla: Weissman, Daniel, et al. “The Rate at Which Asexual Populations Cross Fitness
Valleys.” Theoretical Population Biology, vol. 75, no. 4, Academic Press,
2009, pp. 286–300, doi:10.1016/j.tpb.2009.02.006.
short: D. Weissman, M. Desai, D. Fisher, M. Feldman, Theoretical Population Biology
75 (2009) 286–300.
date_created: 2018-12-11T12:02:34Z
date_published: 2009-06-01T00:00:00Z
date_updated: 2021-01-12T07:42:31Z
day: '01'
doi: 10.1016/j.tpb.2009.02.006
extern: 1
intvolume: ' 75'
issue: '4'
month: '06'
page: 286 - 300
publication: Theoretical Population Biology
publication_status: published
publisher: Academic Press
publist_id: '3336'
quality_controlled: 0
status: public
title: The rate at which asexual populations cross fitness valleys
type: journal_article
volume: 75
year: '2009'
...
---
_id: '3309'
abstract:
- lang: eng
text: |2-
Mastitis, a worldwide endemic disease of dairy cows, is an important cause of decreased efficiency in milk production. Early medical treatment can reduce the nonreversible losses in milk production caused by this infection. Various diagnostic tests for mastitis are available, including a test measuring the electrical conductivity of milk (MEC test), the industry standard of somatic cell counting (SCC test), a bacteriological test, and a recently developed test measuring mammary associated amyloid A (MAA test). None of these tests is considered a gold standard, however. The aim of the present study was to determine which of these tests provides the best results, and at what cost, to improve the efficiency of milk production. For this study, 25 cows were tested at all four quarters of the udder with each of the aforementioned mastitis diagnostic tests. Based on the data, the disease prevalence as well as the sensitivity and the specificity of the four tests were estimated with a Bayesian approach by extending the Hui and Walter model with two independent tests and two populations to a model with four partially dependent tests and one population. This model was further combined with a receiver operating characteristics analysis to estimate the overall test accuracy.
author:
- first_name: Caroline
full_name: Caroline Uhler
id: 49ADD78E-F248-11E8-B48F-1D18A9856A87
last_name: Uhler
orcid: 0000-0002-7008-0216
citation:
ama: 'Uhler C. Mastitis in dairy production: Estimation of sensitivity, specificity
and disease prevalence in the absence of a gold standard. Journal of Agricultural
Biological and Environmental Statistics. 2009;14(1):79-98. doi:10.1198/jabes.2009.0005'
apa: 'Uhler, C. (2009). Mastitis in dairy production: Estimation of sensitivity,
specificity and disease prevalence in the absence of a gold standard. Journal
of Agricultural Biological and Environmental Statistics. Springer. https://doi.org/10.1198/jabes.2009.0005'
chicago: 'Uhler, Caroline. “Mastitis in Dairy Production: Estimation of Sensitivity,
Specificity and Disease Prevalence in the Absence of a Gold Standard.” Journal
of Agricultural Biological and Environmental Statistics. Springer, 2009. https://doi.org/10.1198/jabes.2009.0005.'
ieee: 'C. Uhler, “Mastitis in dairy production: Estimation of sensitivity, specificity
and disease prevalence in the absence of a gold standard,” Journal of Agricultural
Biological and Environmental Statistics, vol. 14, no. 1. Springer, pp. 79–98,
2009.'
ista: 'Uhler C. 2009. Mastitis in dairy production: Estimation of sensitivity, specificity
and disease prevalence in the absence of a gold standard. Journal of Agricultural
Biological and Environmental Statistics. 14(1), 79–98.'
mla: 'Uhler, Caroline. “Mastitis in Dairy Production: Estimation of Sensitivity,
Specificity and Disease Prevalence in the Absence of a Gold Standard.” Journal
of Agricultural Biological and Environmental Statistics, vol. 14, no. 1, Springer,
2009, pp. 79–98, doi:10.1198/jabes.2009.0005.'
short: C. Uhler, Journal of Agricultural Biological and Environmental Statistics
14 (2009) 79–98.
date_created: 2018-12-11T12:02:35Z
date_published: 2009-03-01T00:00:00Z
date_updated: 2021-01-12T07:42:33Z
day: '01'
doi: 10.1198/jabes.2009.0005
extern: 1
intvolume: ' 14'
issue: '1'
month: '03'
page: 79 - 98
publication: Journal of Agricultural Biological and Environmental Statistics
publication_status: published
publisher: Springer
publist_id: '3331'
quality_controlled: 0
status: public
title: 'Mastitis in dairy production: Estimation of sensitivity, specificity and disease
prevalence in the absence of a gold standard'
type: journal_article
volume: 14
year: '2009'
...
---
_id: '110'
abstract:
- lang: eng
text: In order to better understand magnetic reconnection and particle acceleration
in solar flares, we compare the RHESSI hard X-ray (HXR) footpoint motions of three
flares with a detailed study of the corresponding topology given by a Magnetic
Charge Topology model. We analyze the relationship between the footpoint motions
and topological spine lines and find that the examined footpoint sources move
along spine lines. We present a three-dimensional topological model in which this
movement can be understood. As reconnection proceeds, flux is transferred between
the reconnecting domains, causing the separator to move. The movement of the separator\'s
chromospheric ends, identified with the HXR footpoints, is along those spine lines
on which the separator ends.
acknowledgement: This work was supported by RHESSI funds from the University of California
at Berkeley through a contract, SA1868-26308PG, with Montana State University. Funding
for our Research Experience for Undergraduates (REU) students was provided by NSF
grant ATM-0243923.
author:
- first_name: Angela
full_name: Des Jardins, Angela
last_name: Des Jardins
- first_name: Richard
full_name: Canfield, Richard
last_name: Canfield
- first_name: Dana
full_name: Longcope, Dana
last_name: Longcope
- first_name: Crystal
full_name: Fordyce, Crystal
last_name: Fordyce
- first_name: Scott R
full_name: Waitukaitis, Scott R
id: 3A1FFC16-F248-11E8-B48F-1D18A9856A87
last_name: Waitukaitis
orcid: 0000-0002-2299-3176
citation:
ama: 'Des Jardins A, Canfield R, Longcope D, Fordyce C, Waitukaitis SR. Reconnection
in three dimensions: The role of spines in three eruptive flares. The Astrophysical
Journal. 2009;693(2):1628-1636. doi:10.1088/0004-637X/693/2/1628'
apa: 'Des Jardins, A., Canfield, R., Longcope, D., Fordyce, C., & Waitukaitis,
S. R. (2009). Reconnection in three dimensions: The role of spines in three eruptive
flares. The Astrophysical Journal. IOP Publishing Ltd. https://doi.org/10.1088/0004-637X/693/2/1628'
chicago: 'Des Jardins, Angela, Richard Canfield, Dana Longcope, Crystal Fordyce,
and Scott R Waitukaitis. “Reconnection in Three Dimensions: The Role of Spines
in Three Eruptive Flares.” The Astrophysical Journal. IOP Publishing Ltd.,
2009. https://doi.org/10.1088/0004-637X/693/2/1628.'
ieee: 'A. Des Jardins, R. Canfield, D. Longcope, C. Fordyce, and S. R. Waitukaitis,
“Reconnection in three dimensions: The role of spines in three eruptive flares,”
The Astrophysical Journal, vol. 693, no. 2. IOP Publishing Ltd., pp. 1628–1636,
2009.'
ista: 'Des Jardins A, Canfield R, Longcope D, Fordyce C, Waitukaitis SR. 2009. Reconnection
in three dimensions: The role of spines in three eruptive flares. The Astrophysical
Journal. 693(2), 1628–1636.'
mla: 'Des Jardins, Angela, et al. “Reconnection in Three Dimensions: The Role of
Spines in Three Eruptive Flares.” The Astrophysical Journal, vol. 693,
no. 2, IOP Publishing Ltd., 2009, pp. 1628–36, doi:10.1088/0004-637X/693/2/1628.'
short: A. Des Jardins, R. Canfield, D. Longcope, C. Fordyce, S.R. Waitukaitis, The
Astrophysical Journal 693 (2009) 1628–1636.
date_created: 2018-12-11T11:44:41Z
date_published: 2009-03-10T00:00:00Z
date_updated: 2021-01-12T06:48:16Z
day: '10'
doi: 10.1088/0004-637X/693/2/1628
extern: '1'
intvolume: ' 693'
issue: '2'
language:
- iso: eng
month: '03'
oa_version: None
page: 1628 - 1636
publication: The Astrophysical Journal
publication_status: published
publisher: IOP Publishing Ltd.
publist_id: '7944'
quality_controlled: '1'
status: public
title: 'Reconnection in three dimensions: The role of spines in three eruptive flares'
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 693
year: '2009'
...
---
_id: '111'
abstract:
- lang: eng
text: Thin streams of liquid commonly break up into characteristic droplet patterns
owing to the surface-tension-driven PlateauRayleigh instability 1-3. Very similar
patterns are observed when initially uniform streams of dry granular material
break up into clusters of grains4-6, even though flows of macroscopic particles
are considered to lack surface tension7,8. Recent studies on freely falling granular
streams tracked fluctuations in the stream profile9, but the clustering mechanism
remained unresolved because the full evolution of the instability could not be
observed. Here we demonstrate that the cluster formation is driven by minute,
nanoNewton cohesive forces that arise from a combination of van der Waals interactions
and capillary bridges between nanometre-scale surface asperities. Our experiments
involve high-speed video imaging of the granular stream in the co-moving frame,
control over the properties of the grain surfaces and the use of atomic force
microscopy to measure grain-grain interactions. The cohesive forces that we measure
correspond to an equivalent surface tension five orders of magnitude below that,
of ordinary liquids. We find that, the shapes of these weakly cohesive, non-thermal
clusters of macroscopic particles closely resemble droplets resulting from thermally
induced rupture of liquid nanojets 10-12.
acknowledgement: This work was supported by NSF through its MRSEC programme and the
Inter-American Materials Collaboration Chicago-Chile, and by the Keck Initiative
for Ultrafast Imaging at the University of Chicago.
author:
- first_name: John
full_name: Royer, John
last_name: Royer
- first_name: Daniel
full_name: Evans, Daniel
last_name: Evans
- first_name: Loreto
full_name: Oyarte, Loreto
last_name: Oyarte
- first_name: Qiti
full_name: Guo, Qiti
last_name: Guo
- first_name: Eliot
full_name: Kapit, Eliot
last_name: Kapit
- first_name: Matthias
full_name: Möbius, Matthias
last_name: Möbius
- first_name: Scott R
full_name: Waitukaitis, Scott R
id: 3A1FFC16-F248-11E8-B48F-1D18A9856A87
last_name: Waitukaitis
orcid: 0000-0002-2299-3176
- first_name: Heinrich
full_name: Jaeger, Heinrich
last_name: Jaeger
citation:
ama: Royer J, Evans D, Oyarte L, et al. High-speed tracking of rupture and clustering
in freely falling granular streams. Nature. 2009;459(7250):1110-1113. doi:10.1038/nature08115
apa: Royer, J., Evans, D., Oyarte, L., Guo, Q., Kapit, E., Möbius, M., … Jaeger,
H. (2009). High-speed tracking of rupture and clustering in freely falling granular
streams. Nature. Nature Publishing Group. https://doi.org/10.1038/nature08115
chicago: Royer, John, Daniel Evans, Loreto Oyarte, Qiti Guo, Eliot Kapit, Matthias
Möbius, Scott R Waitukaitis, and Heinrich Jaeger. “High-Speed Tracking of Rupture
and Clustering in Freely Falling Granular Streams.” Nature. Nature Publishing
Group, 2009. https://doi.org/10.1038/nature08115.
ieee: J. Royer et al., “High-speed tracking of rupture and clustering in
freely falling granular streams,” Nature, vol. 459, no. 7250. Nature Publishing
Group, pp. 1110–1113, 2009.
ista: Royer J, Evans D, Oyarte L, Guo Q, Kapit E, Möbius M, Waitukaitis SR, Jaeger
H. 2009. High-speed tracking of rupture and clustering in freely falling granular
streams. Nature. 459(7250), 1110–1113.
mla: Royer, John, et al. “High-Speed Tracking of Rupture and Clustering in Freely
Falling Granular Streams.” Nature, vol. 459, no. 7250, Nature Publishing
Group, 2009, pp. 1110–13, doi:10.1038/nature08115.
short: J. Royer, D. Evans, L. Oyarte, Q. Guo, E. Kapit, M. Möbius, S.R. Waitukaitis,
H. Jaeger, Nature 459 (2009) 1110–1113.
date_created: 2018-12-11T11:44:41Z
date_published: 2009-06-25T00:00:00Z
date_updated: 2021-01-12T06:48:21Z
day: '25'
doi: 10.1038/nature08115
extern: '1'
intvolume: ' 459'
issue: '7250'
language:
- iso: eng
month: '06'
oa_version: None
page: 1110 - 1113
publication: Nature
publication_status: published
publisher: Nature Publishing Group
publist_id: '7943'
quality_controlled: '1'
status: public
title: High-speed tracking of rupture and clustering in freely falling granular streams
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 459
year: '2009'
...
---
_id: '11103'
abstract:
- lang: eng
text: Over the last decade, the nuclear envelope (NE) has emerged as a key component
in the organization and function of the nuclear genome. As many as 100 different
proteins are thought to specifically localize to this double membrane that separates
the cytoplasm and the nucleoplasm of eukaryotic cells. Selective portals through
the NE are formed at sites where the inner and outer nuclear membranes are fused,
and the coincident assembly of ∼30 proteins into nuclear pore complexes occurs.
These nuclear pore complexes are essential for the control of nucleocytoplasmic
exchange. Many of the NE and nuclear pore proteins are thought to play crucial
roles in gene regulation and thus are increasingly linked to human diseases.
article_processing_charge: No
article_type: review
author:
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Susan R.
full_name: Wente, Susan R.
last_name: Wente
citation:
ama: 'Hetzer M, Wente SR. Border control at the nucleus: Biogenesis and organization
of the nuclear membrane and pore complexes. Developmental Cell. 2009;17(5):606-616.
doi:10.1016/j.devcel.2009.10.007'
apa: 'Hetzer, M., & Wente, S. R. (2009). Border control at the nucleus: Biogenesis
and organization of the nuclear membrane and pore complexes. Developmental
Cell. Elsevier. https://doi.org/10.1016/j.devcel.2009.10.007'
chicago: 'Hetzer, Martin, and Susan R. Wente. “Border Control at the Nucleus: Biogenesis
and Organization of the Nuclear Membrane and Pore Complexes.” Developmental
Cell. Elsevier, 2009. https://doi.org/10.1016/j.devcel.2009.10.007.'
ieee: 'M. Hetzer and S. R. Wente, “Border control at the nucleus: Biogenesis and
organization of the nuclear membrane and pore complexes,” Developmental Cell,
vol. 17, no. 5. Elsevier, pp. 606–616, 2009.'
ista: 'Hetzer M, Wente SR. 2009. Border control at the nucleus: Biogenesis and organization
of the nuclear membrane and pore complexes. Developmental Cell. 17(5), 606–616.'
mla: 'Hetzer, Martin, and Susan R. Wente. “Border Control at the Nucleus: Biogenesis
and Organization of the Nuclear Membrane and Pore Complexes.” Developmental
Cell, vol. 17, no. 5, Elsevier, 2009, pp. 606–16, doi:10.1016/j.devcel.2009.10.007.'
short: M. Hetzer, S.R. Wente, Developmental Cell 17 (2009) 606–616.
date_created: 2022-04-07T07:53:45Z
date_published: 2009-11-17T00:00:00Z
date_updated: 2022-07-18T08:55:01Z
day: '17'
doi: 10.1016/j.devcel.2009.10.007
extern: '1'
external_id:
pmid:
- '19922866'
intvolume: ' 17'
issue: '5'
keyword:
- Developmental Biology
- Cell Biology
- General Biochemistry
- Genetics and Molecular Biology
- Molecular Biology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.devcel.2009.10.007
month: '11'
oa: 1
oa_version: Published Version
page: 606-616
pmid: 1
publication: Developmental Cell
publication_identifier:
issn:
- 1534-5807
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Border control at the nucleus: Biogenesis and organization of the nuclear
membrane and pore complexes'
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 17
year: '2009'
...
---
_id: '11105'
abstract:
- lang: eng
text: Nuclear-pore complexes (NPCs) are large protein channels that span the nuclear
envelope (NE), which is a double membrane that encloses the nuclear genome of
eukaryotes. Each of the typically 2,000–4,000 pores in the NE of vertebrate cells
is composed of multiple copies of 30 different proteins known as nucleoporins.
The evolutionarily conserved NPC proteins have the well-characterized function
of mediating the transport of molecules between the nucleoplasm and the cytoplasm.
Mutations in nucleoporins are often linked to specific developmental defects and
disease, and the resulting phenotypes are usually interpreted as the consequences
of perturbed nuclear transport activity. However, recent evidence suggests that
NPCs have additional functions in chromatin organization and gene regulation,
some of which might be independent of nuclear transport. Here, we review the transport-dependent
and transport-independent roles of NPCs in the regulation of nuclear function
and gene expression.
article_processing_charge: No
article_type: original
author:
- first_name: Maya
full_name: Capelson, Maya
last_name: Capelson
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Capelson M, Hetzer M. The role of nuclear pores in gene regulation, development
and disease. EMBO reports. 2009;10(7):697-705. doi:10.1038/embor.2009.147
apa: Capelson, M., & Hetzer, M. (2009). The role of nuclear pores in gene regulation,
development and disease. EMBO Reports. EMBO. https://doi.org/10.1038/embor.2009.147
chicago: Capelson, Maya, and Martin Hetzer. “The Role of Nuclear Pores in Gene Regulation,
Development and Disease.” EMBO Reports. EMBO, 2009. https://doi.org/10.1038/embor.2009.147.
ieee: M. Capelson and M. Hetzer, “The role of nuclear pores in gene regulation,
development and disease,” EMBO reports, vol. 10, no. 7. EMBO, pp. 697–705,
2009.
ista: Capelson M, Hetzer M. 2009. The role of nuclear pores in gene regulation,
development and disease. EMBO reports. 10(7), 697–705.
mla: Capelson, Maya, and Martin Hetzer. “The Role of Nuclear Pores in Gene Regulation,
Development and Disease.” EMBO Reports, vol. 10, no. 7, EMBO, 2009, pp.
697–705, doi:10.1038/embor.2009.147.
short: M. Capelson, M. Hetzer, EMBO Reports 10 (2009) 697–705.
date_created: 2022-04-07T07:54:06Z
date_published: 2009-07-01T00:00:00Z
date_updated: 2022-07-18T08:42:44Z
day: '01'
doi: 10.1038/embor.2009.147
extern: '1'
external_id:
pmid:
- '19543230'
intvolume: ' 10'
issue: '7'
keyword:
- Genetics
- Molecular Biology
- Biochemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1038/embor.2009.147
month: '07'
oa: 1
oa_version: Published Version
page: 697-705
pmid: 1
publication: EMBO reports
publication_identifier:
eissn:
- 1469-3178
issn:
- 1469-221X
publication_status: published
publisher: EMBO
quality_controlled: '1'
related_material:
link:
- relation: erratum
url: https://doi.org/10.1038/embor.2009.176
scopus_import: '1'
status: public
title: The role of nuclear pores in gene regulation, development and disease
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 10
year: '2009'
...
---
_id: '11106'
abstract:
- lang: eng
text: Formation of the nuclear envelope (NE) around segregated chromosomes occurs
by the reshaping of the endoplasmic reticulum (ER), a reservoir for disassembled
nuclear membrane components during mitosis. In this study, we show that inner
nuclear membrane proteins such as lamin B receptor (LBR), MAN1, Lap2β, and the
trans-membrane nucleoporins Ndc1 and POM121 drive the spreading of ER membranes
into the emerging NE via their capacity to bind chromatin in a collaborative manner.
Despite their redundant functions, decreasing the levels of any of these trans-membrane
proteins by RNAi-mediated knockdown delayed NE formation, whereas increasing the
levels of any of them had the opposite effect. Furthermore, acceleration of NE
formation interferes with chromosome separation during mitosis, indicating that
the time frame over which chromatin becomes membrane enclosed is physiologically
relevant and regulated. These data suggest that functionally distinct classes
of chromatin-interacting membrane proteins, which are present at nonsaturating
levels, collaborate to rapidly reestablish the nuclear compartment at the end
of mitosis.
article_processing_charge: No
article_type: original
author:
- first_name: Daniel J.
full_name: Anderson, Daniel J.
last_name: Anderson
- first_name: Jesse D.
full_name: Vargas, Jesse D.
last_name: Vargas
- first_name: Joshua P.
full_name: Hsiao, Joshua P.
last_name: Hsiao
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Anderson DJ, Vargas JD, Hsiao JP, Hetzer M. Recruitment of functionally distinct
membrane proteins to chromatin mediates nuclear envelope formation in vivo. Journal
of Cell Biology. 2009;186(2):183-191. doi:10.1083/jcb.200901106
apa: Anderson, D. J., Vargas, J. D., Hsiao, J. P., & Hetzer, M. (2009). Recruitment
of functionally distinct membrane proteins to chromatin mediates nuclear envelope
formation in vivo. Journal of Cell Biology. Rockefeller University Press.
https://doi.org/10.1083/jcb.200901106
chicago: Anderson, Daniel J., Jesse D. Vargas, Joshua P. Hsiao, and Martin Hetzer.
“Recruitment of Functionally Distinct Membrane Proteins to Chromatin Mediates
Nuclear Envelope Formation in Vivo.” Journal of Cell Biology. Rockefeller
University Press, 2009. https://doi.org/10.1083/jcb.200901106.
ieee: D. J. Anderson, J. D. Vargas, J. P. Hsiao, and M. Hetzer, “Recruitment of
functionally distinct membrane proteins to chromatin mediates nuclear envelope
formation in vivo,” Journal of Cell Biology, vol. 186, no. 2. Rockefeller
University Press, pp. 183–191, 2009.
ista: Anderson DJ, Vargas JD, Hsiao JP, Hetzer M. 2009. Recruitment of functionally
distinct membrane proteins to chromatin mediates nuclear envelope formation in
vivo. Journal of Cell Biology. 186(2), 183–191.
mla: Anderson, Daniel J., et al. “Recruitment of Functionally Distinct Membrane
Proteins to Chromatin Mediates Nuclear Envelope Formation in Vivo.” Journal
of Cell Biology, vol. 186, no. 2, Rockefeller University Press, 2009, pp.
183–91, doi:10.1083/jcb.200901106.
short: D.J. Anderson, J.D. Vargas, J.P. Hsiao, M. Hetzer, Journal of Cell Biology
186 (2009) 183–191.
date_created: 2022-04-07T07:54:18Z
date_published: 2009-07-20T00:00:00Z
date_updated: 2022-07-18T08:58:35Z
day: '20'
doi: 10.1083/jcb.200901106
extern: '1'
external_id:
pmid:
- '19620630'
intvolume: ' 186'
issue: '2'
keyword:
- Cell Biology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1083/jcb.200901106
month: '07'
oa: 1
oa_version: Published Version
page: 183-191
pmid: 1
publication: Journal of Cell Biology
publication_identifier:
eissn:
- 1540-8140
issn:
- 0021-9525
publication_status: published
publisher: Rockefeller University Press
quality_controlled: '1'
related_material:
link:
- relation: erratum
url: https://doi.org/10.1083/jcb.20090110620090903c
scopus_import: '1'
status: public
title: Recruitment of functionally distinct membrane proteins to chromatin mediates
nuclear envelope formation in vivo
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 186
year: '2009'
...
---
_id: '11107'
abstract:
- lang: eng
text: Nucleocytoplasmic transport occurs exclusively through nuclear pore complexes
(NPCs) embedded in pores formed by inner and outer nuclear membrane fusion. The
mechanism for de novo pore and NPC biogenesis remains unclear. Reticulons (RTNs)
and Yop1/DP1 are conserved membrane protein families required to form and maintain
the tubular endoplasmic reticulum (ER) and the postmitotic nuclear envelope. In
this study, we report that members of the RTN and Yop1/DP1 families are required
for nuclear pore formation. Analysis of Saccharomyces cerevisiae prp20-G282S and
nup133Δ NPC assembly mutants revealed perturbations in Rtn1–green fluorescent
protein (GFP) and Yop1-GFP ER distribution and colocalization to NPC clusters.
Combined deletion of RTN1 and YOP1 resulted in NPC clustering, nuclear import
defects, and synthetic lethality with the additional absence of Pom34, Pom152,
and Nup84 subcomplex members. We tested for a direct role in NPC biogenesis using
Xenopus laevis in vitro assays and found that anti-Rtn4a antibodies specifically
inhibited de novo nuclear pore formation. We hypothesize that these ER membrane–bending
proteins mediate early NPC assembly steps.
article_processing_charge: No
article_type: original
author:
- first_name: T. Renee
full_name: Dawson, T. Renee
last_name: Dawson
- first_name: Michelle D.
full_name: Lazarus, Michelle D.
last_name: Lazarus
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Susan R.
full_name: Wente, Susan R.
last_name: Wente
citation:
ama: Dawson TR, Lazarus MD, Hetzer M, Wente SR. ER membrane–bending proteins are
necessary for de novo nuclear pore formation. Journal of Cell Biology.
2009;184(5):659-675. doi:10.1083/jcb.200806174
apa: Dawson, T. R., Lazarus, M. D., Hetzer, M., & Wente, S. R. (2009). ER membrane–bending
proteins are necessary for de novo nuclear pore formation. Journal of Cell
Biology. Rockefeller University Press. https://doi.org/10.1083/jcb.200806174
chicago: Dawson, T. Renee, Michelle D. Lazarus, Martin Hetzer, and Susan R. Wente.
“ER Membrane–Bending Proteins Are Necessary for de Novo Nuclear Pore Formation.”
Journal of Cell Biology. Rockefeller University Press, 2009. https://doi.org/10.1083/jcb.200806174.
ieee: T. R. Dawson, M. D. Lazarus, M. Hetzer, and S. R. Wente, “ER membrane–bending
proteins are necessary for de novo nuclear pore formation,” Journal of Cell
Biology, vol. 184, no. 5. Rockefeller University Press, pp. 659–675, 2009.
ista: Dawson TR, Lazarus MD, Hetzer M, Wente SR. 2009. ER membrane–bending proteins
are necessary for de novo nuclear pore formation. Journal of Cell Biology. 184(5),
659–675.
mla: Dawson, T. Renee, et al. “ER Membrane–Bending Proteins Are Necessary for de
Novo Nuclear Pore Formation.” Journal of Cell Biology, vol. 184, no. 5,
Rockefeller University Press, 2009, pp. 659–75, doi:10.1083/jcb.200806174.
short: T.R. Dawson, M.D. Lazarus, M. Hetzer, S.R. Wente, Journal of Cell Biology
184 (2009) 659–675.
date_created: 2022-04-07T07:54:44Z
date_published: 2009-03-09T00:00:00Z
date_updated: 2022-07-18T08:55:05Z
day: '09'
doi: 10.1083/jcb.200806174
extern: '1'
external_id:
pmid:
- '19273614'
intvolume: ' 184'
issue: '5'
keyword:
- Cell Biology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1083/jcb.200806174
month: '03'
oa: 1
oa_version: Published Version
page: 659-675
pmid: 1
publication: Journal of Cell Biology
publication_identifier:
eissn:
- 1540-8140
issn:
- 0021-9525
publication_status: published
publisher: Rockefeller University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: ER membrane–bending proteins are necessary for de novo nuclear pore formation
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 184
year: '2009'
...
---
_id: '11108'
abstract:
- lang: eng
text: In dividing cells, nuclear pore complexes (NPCs) disassemble during mitosis
and reassemble into the newly forming nuclei. However, the fate of nuclear pores
in postmitotic cells is unknown. Here, we show that NPCs, unlike other nuclear
structures, do not turn over in differentiated cells. While a subset of NPC components,
like Nup153 and Nup50, are continuously exchanged, scaffold nucleoporins, like
the Nup107/160 complex, are extremely long-lived and remain incorporated in the
nuclear membrane during the entire cellular life span. Besides the lack of nucleoporin
expression and NPC turnover, we discovered an age-related deterioration of NPCs,
leading to an increase in nuclear permeability and the leaking of cytoplasmic
proteins into the nucleus. Our finding that nuclear “leakiness” is dramatically
accelerated during aging and that a subset of nucleoporins is oxidatively damaged
in old cells suggests that the accumulation of damage at the NPC might be a crucial
aging event.
article_processing_charge: No
article_type: original
author:
- first_name: Maximiliano A.
full_name: D'Angelo, Maximiliano A.
last_name: D'Angelo
- first_name: Marcela
full_name: Raices, Marcela
last_name: Raices
- first_name: Siler H.
full_name: Panowski, Siler H.
last_name: Panowski
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: D’Angelo MA, Raices M, Panowski SH, Hetzer M. Age-dependent deterioration of
nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells.
Cell. 2009;136(2):284-295. doi:10.1016/j.cell.2008.11.037
apa: D’Angelo, M. A., Raices, M., Panowski, S. H., & Hetzer, M. (2009). Age-dependent
deterioration of nuclear pore complexes causes a loss of nuclear integrity in
postmitotic cells. Cell. Elsevier. https://doi.org/10.1016/j.cell.2008.11.037
chicago: D’Angelo, Maximiliano A., Marcela Raices, Siler H. Panowski, and Martin
Hetzer. “Age-Dependent Deterioration of Nuclear Pore Complexes Causes a Loss of
Nuclear Integrity in Postmitotic Cells.” Cell. Elsevier, 2009. https://doi.org/10.1016/j.cell.2008.11.037.
ieee: M. A. D’Angelo, M. Raices, S. H. Panowski, and M. Hetzer, “Age-dependent deterioration
of nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells,”
Cell, vol. 136, no. 2. Elsevier, pp. 284–295, 2009.
ista: D’Angelo MA, Raices M, Panowski SH, Hetzer M. 2009. Age-dependent deterioration
of nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells.
Cell. 136(2), 284–295.
mla: D’Angelo, Maximiliano A., et al. “Age-Dependent Deterioration of Nuclear Pore
Complexes Causes a Loss of Nuclear Integrity in Postmitotic Cells.” Cell,
vol. 136, no. 2, Elsevier, 2009, pp. 284–95, doi:10.1016/j.cell.2008.11.037.
short: M.A. D’Angelo, M. Raices, S.H. Panowski, M. Hetzer, Cell 136 (2009) 284–295.
date_created: 2022-04-07T07:54:52Z
date_published: 2009-01-23T00:00:00Z
date_updated: 2022-07-18T08:55:29Z
day: '23'
doi: 10.1016/j.cell.2008.11.037
extern: '1'
external_id:
pmid:
- '19167330'
intvolume: ' 136'
issue: '2'
keyword:
- General Biochemistry
- Genetics and Molecular Biology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.cell.2008.11.037
month: '01'
oa: 1
oa_version: Published Version
page: 284-295
pmid: 1
publication: Cell
publication_identifier:
issn:
- 0092-8674
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Age-dependent deterioration of nuclear pore complexes causes a loss of nuclear
integrity in postmitotic cells
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 136
year: '2009'
...
---
_id: '11752'
abstract:
- lang: eng
text: We propose a model which suggests that structural martensitic transitions
are related to significant changes in the electronic structure, and are effected
by high-magnetic fields. The magnetic field dependence is considered unusual as
many influential investigations of martensitic transitions have emphasized that
the structural transitions are primarily lattice dynamical and are driven by the
entropy due to the phonons. We provide a theoretical framework which can be used
to describe the effect of high magnetic field on the transition and lattice dynamics
in which the field dependence originates from the dielectric constant. The model
is compared with some recent experimental results.
alternative_title:
- JPCS
article_number: '032062'
article_processing_charge: No
author:
- first_name: Xiaodong
full_name: Yang, Xiaodong
last_name: Yang
- first_name: Peter S
full_name: Riseborough, Peter S
last_name: Riseborough
- first_name: Kimberly A
full_name: Modic, Kimberly A
id: 13C26AC0-EB69-11E9-87C6-5F3BE6697425
last_name: Modic
orcid: 0000-0001-9760-3147
- first_name: R A
full_name: Fisher, R A
last_name: Fisher
- first_name: C P
full_name: Oppeil, C P
last_name: Oppeil
- first_name: T R
full_name: Finlayson, T R
last_name: Finlayson
- first_name: J C
full_name: Cooley, J C
last_name: Cooley
- first_name: J L
full_name: Smith, J L
last_name: Smith
- first_name: P A
full_name: Goddard, P A
last_name: Goddard
- first_name: A V
full_name: Silhanek, A V
last_name: Silhanek
- first_name: J C
full_name: Lashley, J C
last_name: Lashley
citation:
ama: 'Yang X, Riseborough PS, Modic KA, et al. Influence of magnetic fields on structural
martensitic transitions. In: Journal of Physics: Conference Series. Vol
200. IOP Publishing; 2009. doi:10.1088/1742-6596/200/3/032062'
apa: 'Yang, X., Riseborough, P. S., Modic, K. A., Fisher, R. A., Oppeil, C. P.,
Finlayson, T. R., … Lashley, J. C. (2009). Influence of magnetic fields on structural
martensitic transitions. In Journal of Physics: Conference Series (Vol.
200). Karlsruhe, Germany: IOP Publishing. https://doi.org/10.1088/1742-6596/200/3/032062'
chicago: 'Yang, Xiaodong, Peter S Riseborough, Kimberly A Modic, R A Fisher, C P
Oppeil, T R Finlayson, J C Cooley, et al. “Influence of Magnetic Fields on Structural
Martensitic Transitions.” In Journal of Physics: Conference Series, Vol.
200. IOP Publishing, 2009. https://doi.org/10.1088/1742-6596/200/3/032062.'
ieee: 'X. Yang et al., “Influence of magnetic fields on structural martensitic
transitions,” in Journal of Physics: Conference Series, Karlsruhe, Germany,
2009, vol. 200, no. 3.'
ista: 'Yang X, Riseborough PS, Modic KA, Fisher RA, Oppeil CP, Finlayson TR, Cooley
JC, Smith JL, Goddard PA, Silhanek AV, Lashley JC. 2009. Influence of magnetic
fields on structural martensitic transitions. Journal of Physics: Conference Series.
ICM: International Conference on Magnetism, JPCS, vol. 200, 032062.'
mla: 'Yang, Xiaodong, et al. “Influence of Magnetic Fields on Structural Martensitic
Transitions.” Journal of Physics: Conference Series, vol. 200, no. 3, 032062,
IOP Publishing, 2009, doi:10.1088/1742-6596/200/3/032062.'
short: 'X. Yang, P.S. Riseborough, K.A. Modic, R.A. Fisher, C.P. Oppeil, T.R. Finlayson,
J.C. Cooley, J.L. Smith, P.A. Goddard, A.V. Silhanek, J.C. Lashley, in:, Journal
of Physics: Conference Series, IOP Publishing, 2009.'
conference:
end_date: 2009-07-31
location: Karlsruhe, Germany
name: 'ICM: International Conference on Magnetism'
start_date: 2009-07-26
date_created: 2022-08-08T08:43:04Z
date_published: 2009-07-01T00:00:00Z
date_updated: 2023-02-23T12:58:33Z
day: '01'
doi: 10.1088/1742-6596/200/3/032062
extern: '1'
intvolume: ' 200'
issue: '3'
language:
- iso: eng
month: '07'
oa_version: None
publication: 'Journal of Physics: Conference Series'
publication_identifier:
eissn:
- 1742-6596
issn:
- 1742-6588
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
related_material:
record:
- id: '7080'
relation: later_version
status: public
scopus_import: '1'
status: public
title: Influence of magnetic fields on structural martensitic transitions
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 200
year: '2009'
...
---
_id: '8026'
abstract:
- lang: eng
text: Recent theoretical work has provided a basic understanding of signal propagation
in networks of spiking neurons, but mechanisms for gating and controlling these
signals have not been investigated previously. Here we introduce an idea for the
gating of multiple signals in cortical networks that combines principles of signal
propagation with aspects of balanced networks. Specifically, we studied networks
in which incoming excitatory signals are normally cancelled by locally evoked
inhibition, leaving the targeted layer unresponsive. Transmission can be gated
'on' by modulating excitatory and inhibitory gains to upset this detailed balance.
We illustrate gating through detailed balance in large networks of integrate-and-fire
neurons. We show successful gating of multiple signals and study failure modes
that produce effects reminiscent of clinically observed pathologies. Provided
that the individual signals are detectable, detailed balance has a large capacity
for gating multiple signals.
article_processing_charge: No
article_type: original
author:
- first_name: Tim P
full_name: Vogels, Tim P
id: CB6FF8D2-008F-11EA-8E08-2637E6697425
last_name: Vogels
orcid: 0000-0003-3295-6181
- first_name: L F
full_name: Abbott, L F
last_name: Abbott
citation:
ama: Vogels TP, Abbott LF. Gating multiple signals through detailed balance of excitation
and inhibition in spiking networks. Nature Neuroscience. 2009;12(4):483-491.
doi:10.1038/nn.2276
apa: Vogels, T. P., & Abbott, L. F. (2009). Gating multiple signals through
detailed balance of excitation and inhibition in spiking networks. Nature Neuroscience.
Springer Nature. https://doi.org/10.1038/nn.2276
chicago: Vogels, Tim P, and L F Abbott. “Gating Multiple Signals through Detailed
Balance of Excitation and Inhibition in Spiking Networks.” Nature Neuroscience.
Springer Nature, 2009. https://doi.org/10.1038/nn.2276.
ieee: T. P. Vogels and L. F. Abbott, “Gating multiple signals through detailed balance
of excitation and inhibition in spiking networks,” Nature Neuroscience,
vol. 12, no. 4. Springer Nature, pp. 483–491, 2009.
ista: Vogels TP, Abbott LF. 2009. Gating multiple signals through detailed balance
of excitation and inhibition in spiking networks. Nature Neuroscience. 12(4),
483–491.
mla: Vogels, Tim P., and L. F. Abbott. “Gating Multiple Signals through Detailed
Balance of Excitation and Inhibition in Spiking Networks.” Nature Neuroscience,
vol. 12, no. 4, Springer Nature, 2009, pp. 483–91, doi:10.1038/nn.2276.
short: T.P. Vogels, L.F. Abbott, Nature Neuroscience 12 (2009) 483–491.
date_created: 2020-06-25T13:10:55Z
date_published: 2009-04-01T00:00:00Z
date_updated: 2021-01-12T08:16:36Z
day: '01'
doi: 10.1038/nn.2276
extern: '1'
external_id:
pmid:
- '19305402'
intvolume: ' 12'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693069/
month: '04'
oa: 1
oa_version: Submitted Version
page: 483-491
pmid: 1
publication: Nature Neuroscience
publication_identifier:
issn:
- 1097-6256
- 1546-1726
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Gating multiple signals through detailed balance of excitation and inhibition
in spiking networks
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 12
year: '2009'
...
---
_id: '8474'
abstract:
- lang: eng
text: Hydrogen bonds are ubiquitous interactions in proteins, and are important
for their folding and functionality. Scalar coupling constants across hydrogen
bonds in the protein backbone, some as small as 0.5 Hz, can be directly measured
in the solid state by NMR spectroscopy (see figure). The nuclei on both sides
of the hydrogen bond can be identified and the size of the coupling constant can
be measured accurately.
article_processing_charge: No
article_type: original
author:
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
- first_name: Matthias
full_name: Huber, Matthias
last_name: Huber
- first_name: René
full_name: Verel, René
last_name: Verel
- first_name: Matthias
full_name: Ernst, Matthias
last_name: Ernst
- first_name: "Beatâ\x80\NH."
full_name: "Meier, Beatâ\x80\NH."
last_name: Meier
citation:
ama: Schanda P, Huber M, Verel R, Ernst M, Meier B. Direct detection of 3hJN’ hydrogen-bond
scalar couplings in proteins by solid-state NMR spectroscopy. Angewandte Chemie
International Edition. 2009;48(49):9322-9325. doi:10.1002/anie.200904411
apa: Schanda, P., Huber, M., Verel, R., Ernst, M., & Meier, B. (2009). Direct
detection of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR
spectroscopy. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.200904411
chicago: "Schanda, Paul, Matthias Huber, René Verel, Matthias Ernst, and Beatâ\x80\NH.
Meier. “Direct Detection of 3hJN’ Hydrogen-Bond Scalar Couplings in Proteins by
Solid-State NMR Spectroscopy.” Angewandte Chemie International Edition.
Wiley, 2009. https://doi.org/10.1002/anie.200904411."
ieee: P. Schanda, M. Huber, R. Verel, M. Ernst, and B. Meier, “Direct detection
of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy,”
Angewandte Chemie International Edition, vol. 48, no. 49. Wiley, pp. 9322–9325,
2009.
ista: Schanda P, Huber M, Verel R, Ernst M, Meier B. 2009. Direct detection of 3hJN’
hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy. Angewandte
Chemie International Edition. 48(49), 9322–9325.
mla: Schanda, Paul, et al. “Direct Detection of 3hJN’ Hydrogen-Bond Scalar Couplings
in Proteins by Solid-State NMR Spectroscopy.” Angewandte Chemie International
Edition, vol. 48, no. 49, Wiley, 2009, pp. 9322–25, doi:10.1002/anie.200904411.
short: P. Schanda, M. Huber, R. Verel, M. Ernst, B. Meier, Angewandte Chemie International
Edition 48 (2009) 9322–9325.
date_created: 2020-09-18T10:11:33Z
date_published: 2009-11-17T00:00:00Z
date_updated: 2021-01-12T08:19:31Z
day: '17'
doi: 10.1002/anie.200904411
extern: '1'
intvolume: ' 48'
issue: '49'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '11'
oa_version: None
page: 9322-9325
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
- 1521-3773
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Direct detection of 3hJN' hydrogen-bond scalar couplings in proteins by solid-state
NMR spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 48
year: '2009'
...
---
_id: '8475'
article_processing_charge: No
article_type: original
author:
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
citation:
ama: 'Schanda P. Fast-pulsing longitudinal relaxation optimized techniques: Enriching
the toolbox of fast biomolecular NMR spectroscopy. Progress in Nuclear Magnetic
Resonance Spectroscopy. 2009;55(3):238-265. doi:10.1016/j.pnmrs.2009.05.002'
apa: 'Schanda, P. (2009). Fast-pulsing longitudinal relaxation optimized techniques:
Enriching the toolbox of fast biomolecular NMR spectroscopy. Progress in Nuclear
Magnetic Resonance Spectroscopy. Elsevier. https://doi.org/10.1016/j.pnmrs.2009.05.002'
chicago: 'Schanda, Paul. “Fast-Pulsing Longitudinal Relaxation Optimized Techniques:
Enriching the Toolbox of Fast Biomolecular NMR Spectroscopy.” Progress in Nuclear
Magnetic Resonance Spectroscopy. Elsevier, 2009. https://doi.org/10.1016/j.pnmrs.2009.05.002.'
ieee: 'P. Schanda, “Fast-pulsing longitudinal relaxation optimized techniques: Enriching
the toolbox of fast biomolecular NMR spectroscopy,” Progress in Nuclear Magnetic
Resonance Spectroscopy, vol. 55, no. 3. Elsevier, pp. 238–265, 2009.'
ista: 'Schanda P. 2009. Fast-pulsing longitudinal relaxation optimized techniques:
Enriching the toolbox of fast biomolecular NMR spectroscopy. Progress in Nuclear
Magnetic Resonance Spectroscopy. 55(3), 238–265.'
mla: 'Schanda, Paul. “Fast-Pulsing Longitudinal Relaxation Optimized Techniques:
Enriching the Toolbox of Fast Biomolecular NMR Spectroscopy.” Progress in Nuclear
Magnetic Resonance Spectroscopy, vol. 55, no. 3, Elsevier, 2009, pp. 238–65,
doi:10.1016/j.pnmrs.2009.05.002.'
short: P. Schanda, Progress in Nuclear Magnetic Resonance Spectroscopy 55 (2009)
238–265.
date_created: 2020-09-18T10:11:42Z
date_published: 2009-10-01T00:00:00Z
date_updated: 2021-01-12T08:19:32Z
day: '01'
doi: 10.1016/j.pnmrs.2009.05.002
extern: '1'
intvolume: ' 55'
issue: '3'
language:
- iso: eng
month: '10'
oa_version: None
page: 238-265
publication: Progress in Nuclear Magnetic Resonance Spectroscopy
publication_identifier:
issn:
- 0079-6565
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: 'Fast-pulsing longitudinal relaxation optimized techniques: Enriching the toolbox
of fast biomolecular NMR spectroscopy'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 55
year: '2009'
...
---
_id: '8476'
abstract:
- lang: eng
text: Atomic-resolution information on the structure and dynamics of nucleic acids
is essential for a better understanding of the mechanistic basis of many cellular
processes. NMR spectroscopy is a powerful method for studying the structure and
dynamics of nucleic acids; however, solution NMR studies are currently limited
to relatively small nucleic acids at high concentrations. Thus, technological
and methodological improvements that increase the experimental sensitivity and
spectral resolution of NMR spectroscopy are required for studies of larger nucleic
acids or protein−nucleic acid complexes. Here we introduce a series of imino-proton-detected
NMR experiments that yield an over 2-fold increase in sensitivity compared to
conventional pulse schemes. These methods can be applied to the detection of base
pair interactions, RNA−ligand titration experiments, measurement of residual dipolar
15N−1H couplings, and direct measurements of conformational transitions. These
NMR experiments employ longitudinal spin relaxation enhancement techniques that
have proven useful in protein NMR spectroscopy. The performance of these new experiments
is demonstrated for a 10 kDa TAR-TAR*GA RNA kissing complex and a 26 kDa tRNA.
article_processing_charge: No
article_type: original
author:
- first_name: Jonathan
full_name: Farjon, Jonathan
last_name: Farjon
- first_name: Jérôme
full_name: Boisbouvier, Jérôme
last_name: Boisbouvier
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
- first_name: Arthur
full_name: Pardi, Arthur
last_name: Pardi
- first_name: Jean-Pierre
full_name: Simorre, Jean-Pierre
last_name: Simorre
- first_name: Bernhard
full_name: Brutscher, Bernhard
last_name: Brutscher
citation:
ama: Farjon J, Boisbouvier J, Schanda P, Pardi A, Simorre J-P, Brutscher B. Longitudinal-relaxation-enhanced
NMR experiments for the study of nucleic acids in solution. Journal of the
American Chemical Society. 2009;131(24):8571-8577. doi:10.1021/ja901633y
apa: Farjon, J., Boisbouvier, J., Schanda, P., Pardi, A., Simorre, J.-P., &
Brutscher, B. (2009). Longitudinal-relaxation-enhanced NMR experiments for the
study of nucleic acids in solution. Journal of the American Chemical Society.
American Chemical Society. https://doi.org/10.1021/ja901633y
chicago: Farjon, Jonathan, Jérôme Boisbouvier, Paul Schanda, Arthur Pardi, Jean-Pierre
Simorre, and Bernhard Brutscher. “Longitudinal-Relaxation-Enhanced NMR Experiments
for the Study of Nucleic Acids in Solution.” Journal of the American Chemical
Society. American Chemical Society, 2009. https://doi.org/10.1021/ja901633y.
ieee: J. Farjon, J. Boisbouvier, P. Schanda, A. Pardi, J.-P. Simorre, and B. Brutscher,
“Longitudinal-relaxation-enhanced NMR experiments for the study of nucleic acids
in solution,” Journal of the American Chemical Society, vol. 131, no. 24.
American Chemical Society, pp. 8571–8577, 2009.
ista: Farjon J, Boisbouvier J, Schanda P, Pardi A, Simorre J-P, Brutscher B. 2009.
Longitudinal-relaxation-enhanced NMR experiments for the study of nucleic acids
in solution. Journal of the American Chemical Society. 131(24), 8571–8577.
mla: Farjon, Jonathan, et al. “Longitudinal-Relaxation-Enhanced NMR Experiments
for the Study of Nucleic Acids in Solution.” Journal of the American Chemical
Society, vol. 131, no. 24, American Chemical Society, 2009, pp. 8571–77, doi:10.1021/ja901633y.
short: J. Farjon, J. Boisbouvier, P. Schanda, A. Pardi, J.-P. Simorre, B. Brutscher,
Journal of the American Chemical Society 131 (2009) 8571–8577.
date_created: 2020-09-18T10:11:49Z
date_published: 2009-06-01T00:00:00Z
date_updated: 2021-01-12T08:19:32Z
day: '01'
doi: 10.1021/ja901633y
extern: '1'
intvolume: ' 131'
issue: '24'
language:
- iso: eng
month: '06'
oa_version: None
page: 8571-8577
publication: Journal of the American Chemical Society
publication_identifier:
issn:
- 0002-7863
- 1520-5126
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
status: public
title: Longitudinal-relaxation-enhanced NMR experiments for the study of nucleic acids
in solution
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 131
year: '2009'
...