---
_id: '2709'
article_processing_charge: No
author:
- first_name: László
full_name: Erdös, László
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
citation:
ama: 'Erdös L. Long time dynamics of an electron in a weakly coupled phonon field.
In: 13th International Congress of Mathematical Physics. International
Press of Boston; 2001:273-281.'
apa: Erdös, L. (2001). Long time dynamics of an electron in a weakly coupled phonon
field. In 13th International Congress of Mathematical Physics (pp. 273–281). International
Press of Boston.
chicago: Erdös, László. “Long Time Dynamics of an Electron in a Weakly Coupled Phonon
Field.” In 13th International Congress of Mathematical Physics, 273–81. International
Press of Boston, 2001.
ieee: L. Erdös, “Long time dynamics of an electron in a weakly coupled phonon field,”
in 13th International Congress of Mathematical Physics, International
Press of Boston, 2001, pp. 273–281.
ista: 'Erdös L. 2001.Long time dynamics of an electron in a weakly coupled phonon
field. In: 13th International Congress of Mathematical Physics. , 273–281.'
mla: Erdös, László. “Long Time Dynamics of an Electron in a Weakly Coupled Phonon
Field.” 13th International Congress of Mathematical Physics, International
Press of Boston, 2001, pp. 273–81.
short: L. Erdös, in:, 13th International Congress of Mathematical Physics, International
Press of Boston, 2001, pp. 273–281.
date_created: 2018-12-11T11:59:11Z
date_published: 2001-01-01T00:00:00Z
date_updated: 2023-05-22T12:11:29Z
day: '01'
extern: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 273 - 281
publication: 13th International Congress of Mathematical Physics
publication_identifier:
isbn:
- '9781571460851'
publication_status: published
publisher: ' International Press of Boston'
publist_id: '4187'
quality_controlled: '1'
status: public
title: Long time dynamics of an electron in a weakly coupled phonon field
type: book_chapter
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
year: '2001'
...
---
_id: '2734'
abstract:
- lang: eng
text: In this paper we describe an intrinsically geometric way of producing magnetic
fields on S3 and R3 for which the corresponding Dirac operators have a non-trivial
kernel. In many cases we are able to compute the dimension of the kernel. In particular
we can give examples where the kernel has any given dimension. This generalizes
the examples of Loss and Yau [1].
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: László
full_name: Erdös, László
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
- first_name: Jan
full_name: Solovej, Jan
last_name: Solovej
citation:
ama: Erdös L, Solovej J. The kernel of Dirac operators on S3 and R3. Reviews
in Mathematical Physics. 2001;13(10):1247-1280. doi:10.1142/S0129055X01000983
apa: Erdös, L., & Solovej, J. (2001). The kernel of Dirac operators on S3 and
R3. Reviews in Mathematical Physics. World Scientific Publishing. https://doi.org/10.1142/S0129055X01000983
chicago: Erdös, László, and Jan Solovej. “The Kernel of Dirac Operators on S3 and
R3.” Reviews in Mathematical Physics. World Scientific Publishing, 2001.
https://doi.org/10.1142/S0129055X01000983.
ieee: L. Erdös and J. Solovej, “The kernel of Dirac operators on S3 and R3,” Reviews
in Mathematical Physics, vol. 13, no. 10. World Scientific Publishing, pp.
1247–1280, 2001.
ista: Erdös L, Solovej J. 2001. The kernel of Dirac operators on S3 and R3. Reviews
in Mathematical Physics. 13(10), 1247–1280.
mla: Erdös, László, and Jan Solovej. “The Kernel of Dirac Operators on S3 and R3.”
Reviews in Mathematical Physics, vol. 13, no. 10, World Scientific Publishing,
2001, pp. 1247–80, doi:10.1142/S0129055X01000983.
short: L. Erdös, J. Solovej, Reviews in Mathematical Physics 13 (2001) 1247–1280.
date_created: 2018-12-11T11:59:19Z
date_published: 2001-10-01T00:00:00Z
date_updated: 2023-05-16T12:24:25Z
day: '01'
doi: 10.1142/S0129055X01000983
extern: '1'
external_id:
arxiv:
- math-ph/0001036
intvolume: ' 13'
issue: '10'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/math-ph/0001036
month: '10'
oa: 1
oa_version: Published Version
page: 1247 - 1280
publication: Reviews in Mathematical Physics
publication_identifier:
issn:
- 0129-055X
publication_status: published
publisher: World Scientific Publishing
publist_id: '4158'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The kernel of Dirac operators on S3 and R3
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 13
year: '2001'
...
---
_id: '2735'
abstract:
- lang: eng
text: We establish the exact low-energy asymptotics of the integrated density of
states (Lifschitz tail) in a homogeneous magnetic field and Poissonian impurities
with a repulsive single-site potential of Gaussian decay. It has been known that
the Gaussian potential tail discriminates between the so-called “classical” and
“quantum” regimes, and precise asymptotics are known in these cases. For the borderline
case, the coexistence of the classical and quantum regimes was conjectured. Here
we settle this last remaining open case to complete the full picture of the magnetic
Lifschitz tails.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: László
full_name: Erdös, László
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
citation:
ama: 'Erdös L. Lifschitz tail in a magnetic field: Coexistence of classical and
quantum behavior in the borderline case. Probability Theory and Related Fields.
2001;121(2):219-236. doi:10.1007/PL00008803'
apa: 'Erdös, L. (2001). Lifschitz tail in a magnetic field: Coexistence of classical
and quantum behavior in the borderline case. Probability Theory and Related
Fields. Springer. https://doi.org/10.1007/PL00008803'
chicago: 'Erdös, László. “Lifschitz Tail in a Magnetic Field: Coexistence of Classical
and Quantum Behavior in the Borderline Case.” Probability Theory and Related
Fields. Springer, 2001. https://doi.org/10.1007/PL00008803.'
ieee: 'L. Erdös, “Lifschitz tail in a magnetic field: Coexistence of classical and
quantum behavior in the borderline case,” Probability Theory and Related Fields,
vol. 121, no. 2. Springer, pp. 219–236, 2001.'
ista: 'Erdös L. 2001. Lifschitz tail in a magnetic field: Coexistence of classical
and quantum behavior in the borderline case. Probability Theory and Related Fields.
121(2), 219–236.'
mla: 'Erdös, László. “Lifschitz Tail in a Magnetic Field: Coexistence of Classical
and Quantum Behavior in the Borderline Case.” Probability Theory and Related
Fields, vol. 121, no. 2, Springer, 2001, pp. 219–36, doi:10.1007/PL00008803.'
short: L. Erdös, Probability Theory and Related Fields 121 (2001) 219–236.
date_created: 2018-12-11T11:59:19Z
date_published: 2001-10-01T00:00:00Z
date_updated: 2023-05-16T12:20:42Z
day: '01'
doi: 10.1007/PL00008803
extern: '1'
external_id:
arxiv:
- math-ph/0003023
intvolume: ' 121'
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/math-ph/0003023
month: '10'
oa: 1
oa_version: Published Version
page: 219 - 236
publication: Probability Theory and Related Fields
publication_identifier:
issn:
- 0044-3719
publication_status: published
publisher: Springer
publist_id: '4157'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Lifschitz tail in a magnetic field: Coexistence of classical and quantum behavior
in the borderline case'
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 121
year: '2001'
...
---
_id: '2736'
abstract:
- lang: eng
text: We consider the time evolution of N bosonic particles interacting via a mean
field Coulomb potential. Suppose the initial state is a product wavefunction.
We show that at any finite time the correlation functions factorize in the limit
N → ∞. Furthermore, the limiting one particle density matrix satisfies the nonlinear
Hartree equation. The key ingredients are the uniqueness of the BBGKY hierarchy
for the correlation functions and a new apriori estimate for the many-body Schrödinger
equations.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: László
full_name: Erdös, László
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
- first_name: Horng
full_name: Yau, Horng
last_name: Yau
citation:
ama: Erdös L, Yau H. Derivation of the nonlinear Schrödinger equation from a many
body Coulomb system. Advances in Theoretical and Mathematical Physics.
2001;5(6):1169-1205. doi:10.48550/arXiv.math-ph/0111042
apa: Erdös, L., & Yau, H. (2001). Derivation of the nonlinear Schrödinger equation
from a many body Coulomb system. Advances in Theoretical and Mathematical Physics.
International Press. https://doi.org/10.48550/arXiv.math-ph/0111042
chicago: Erdös, László, and Horng Yau. “Derivation of the Nonlinear Schrödinger
Equation from a Many Body Coulomb System.” Advances in Theoretical and Mathematical
Physics. International Press, 2001. https://doi.org/10.48550/arXiv.math-ph/0111042.
ieee: L. Erdös and H. Yau, “Derivation of the nonlinear Schrödinger equation from
a many body Coulomb system,” Advances in Theoretical and Mathematical Physics,
vol. 5, no. 6. International Press, pp. 1169–1205, 2001.
ista: Erdös L, Yau H. 2001. Derivation of the nonlinear Schrödinger equation from
a many body Coulomb system. Advances in Theoretical and Mathematical Physics.
5(6), 1169–1205.
mla: Erdös, László, and Horng Yau. “Derivation of the Nonlinear Schrödinger Equation
from a Many Body Coulomb System.” Advances in Theoretical and Mathematical
Physics, vol. 5, no. 6, International Press, 2001, pp. 1169–205, doi:10.48550/arXiv.math-ph/0111042.
short: L. Erdös, H. Yau, Advances in Theoretical and Mathematical Physics 5 (2001)
1169–1205.
date_created: 2018-12-11T11:59:20Z
date_published: 2001-11-01T00:00:00Z
date_updated: 2023-05-16T12:12:41Z
day: '01'
doi: 10.48550/arXiv.math-ph/0111042
extern: '1'
external_id:
arxiv:
- math-ph/0111042
intvolume: ' 5'
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://arxiv.org/abs/math-ph/0111042
month: '11'
oa: 1
oa_version: Published Version
page: 1169 - 1205
publication: Advances in Theoretical and Mathematical Physics
publication_identifier:
issn:
- 1095-0761
publication_status: published
publisher: International Press
publist_id: '4156'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Derivation of the nonlinear Schrödinger equation from a many body Coulomb system
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 5
year: '2001'
...
---
_id: '2981'
abstract:
- lang: eng
text: Plants contain a novel unique subfamily of Rho GTPases, vital components of
cellular signalling networks. Here we report a general role for some members of
this family in polarized plant growth processes. We show that Arabidopsis AtRop4
and AtRop6 encode functional GTPases with similar intrinsic GTP hydrolysis rates.
We localized AtRop proteins in root meristem cells to the cross-wall and cell
plate membranes. Polar localization of AtRops in trichoblasts specifies the growth
sites for emerging root hairs. These sites were visible before budding and elongation
of the Arabidopsis root hair when AtRops accumulated at their tips. Expression
of constitutively active AtRop4 and AtRop6 mutant proteins in root hairs of transgenic
Arabidopsis plants abolished polarized growth and delocalized the tip-focused
Ca2+ gradient. Polar localization of AtRops was inhibited by brefeldin A, but
not by other drugs such as latrunculin B, cytochalasin D or caffeine. Our results
demonstrate a general function of AtRop GTPases in tip growth and in polar diffuse
growth.
acknowledgement: We thank Drs Frantisek Baluška, Matthias Godde, Peter Huijser, Lars
Vahlkamp and Dieter Volkmann for help, criticism and constructive reading of the
manuscript. We are grateful to Dr N.-H.Chua for providing us with pTA7002. The work
was funded by the DFG, the European Communities Biotechnology Programme (Bio4-CT98
0239) and the INCO Copernicus Programme (IC15-CT96-0920). C.S.V.R. is the recipient
of an Alexander von Humboldt fellowship and J.F. of a DAAD fellowship.
article_processing_charge: No
article_type: original
author:
- first_name: Arthur
full_name: Molendijk, Arthur
last_name: Molendijk
- first_name: Friedrich
full_name: Bischoff, Friedrich
last_name: Bischoff
- first_name: Chadalavada
full_name: Rajendrakumar, Chadalavada
last_name: Rajendrakumar
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Markus
full_name: Braun, Markus
last_name: Braun
- first_name: Simon
full_name: Gilroy, Simon
last_name: Gilroy
- first_name: Klaus
full_name: Palme, Klaus
last_name: Palme
citation:
ama: Molendijk A, Bischoff F, Rajendrakumar C, et al. Arabidopsis thaliana Rop GTPases
are localized to tips of root hairs and control polar growth. EMBO Journal.
2001;20(11):2779-2788. doi:10.1093/emboj/20.11.2779
apa: Molendijk, A., Bischoff, F., Rajendrakumar, C., Friml, J., Braun, M., Gilroy,
S., & Palme, K. (2001). Arabidopsis thaliana Rop GTPases are localized to
tips of root hairs and control polar growth. EMBO Journal. Wiley-Blackwell.
https://doi.org/10.1093/emboj/20.11.2779
chicago: Molendijk, Arthur, Friedrich Bischoff, Chadalavada Rajendrakumar, Jiří
Friml, Markus Braun, Simon Gilroy, and Klaus Palme. “Arabidopsis Thaliana Rop
GTPases Are Localized to Tips of Root Hairs and Control Polar Growth.” EMBO
Journal. Wiley-Blackwell, 2001. https://doi.org/10.1093/emboj/20.11.2779.
ieee: A. Molendijk et al., “Arabidopsis thaliana Rop GTPases are localized
to tips of root hairs and control polar growth,” EMBO Journal, vol. 20,
no. 11. Wiley-Blackwell, pp. 2779–2788, 2001.
ista: Molendijk A, Bischoff F, Rajendrakumar C, Friml J, Braun M, Gilroy S, Palme
K. 2001. Arabidopsis thaliana Rop GTPases are localized to tips of root hairs
and control polar growth. EMBO Journal. 20(11), 2779–2788.
mla: Molendijk, Arthur, et al. “Arabidopsis Thaliana Rop GTPases Are Localized to
Tips of Root Hairs and Control Polar Growth.” EMBO Journal, vol. 20, no.
11, Wiley-Blackwell, 2001, pp. 2779–88, doi:10.1093/emboj/20.11.2779.
short: A. Molendijk, F. Bischoff, C. Rajendrakumar, J. Friml, M. Braun, S. Gilroy,
K. Palme, EMBO Journal 20 (2001) 2779–2788.
date_created: 2018-12-11T12:00:40Z
date_published: 2001-06-01T00:00:00Z
date_updated: 2023-05-16T12:07:45Z
day: '01'
doi: 10.1093/emboj/20.11.2779
extern: '1'
external_id:
pmid:
- '11387211'
intvolume: ' 20'
issue: '11'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC125484/
month: '06'
oa: 1
oa_version: Published Version
page: 2779 - 2788
pmid: 1
publication: EMBO Journal
publication_identifier:
issn:
- 0261-4189
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3721'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Arabidopsis thaliana Rop GTPases are localized to tips of root hairs and control
polar growth
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 20
year: '2001'
...
---
_id: '2982'
abstract:
- lang: eng
text: Polar auxin transport is crucial for the regulation of auxin action and required
for some light-regulated responses during plant development. We have found that
two mutants of Arabidopsis - doc1, which displays altered expression of light-regulated
genes, and tir3, known for its reduced auxin transport - have similar defects
and define mutations in a single gene that we have renamed BIG. BIG is very similar
to the Drosophila gene Calossin/Pushover, a member of a gene family also present
in Caenorhabditis elegans and human genomes. The protein encoded by BIG is extraordinary
in size, 560 kD, and contains several putative Zn-finger domains. Expression-profiling
experiments indicate that altered expression of multiple light-regulated genes
in doc1 mutants can be suppressed by elevated levels of auxin caused by overexpression
of an auxin biosynthetic gene, suggesting that normal auxin distribution is required
to maintain low-level expression of these genes in the dark. Double mutants of
tir3 with the auxin mutants pin1, pid, and axr1 display severe defects in auxin-dependent
growth of the inflorescence. Chemical inhibitors of auxin transport change the
intracellular localization of the auxin efflux carrier PIN1 in doc1/tir3 mutants,
supporting the idea that BIG is required for normal auxin efflux.
acknowledgement: "We thank Kim Hanson and Melissa McCarthy for technical support,
and Adan Colon-Carmona, Jianming Li, and Karin Schumacher for their help in generating
and identifying the doc1-3 T-DNA line. Seeds of ap3-1 and a cosmid library were
supplied by the ABRC stock center. Jennifer Nemhauser made useful comments concerning
this manuscript. This work was supported by grants from the Department of Energy
(DE-FG03-89ER13993) and the National Science Foundation (MCB96-31390) to J.C., by
grants from the Department of Energy (DE-FG02-98ER20313) and the National Institutes
of Health (GM43644) to M.E., by a grant from DAAD to J.F., by a grant from DFG to
K.P., and by a Marsden grant of New Zealand to J.P. and K.S. J.C. is an Associate
Investigator of the Howard Hughes Medical Institute (HHMI), and Y.Z. is a HHMI fellow
of the Life Sciences Research Foundation.\r\n\r\nThe publication costs of this article
were defrayed in part by payment of page charges. This article must therefore be
hereby marked “advertisement” in accordance with 18 USC section 1734 solely to indicate
this fact."
article_processing_charge: No
article_type: original
author:
- first_name: Pedro
full_name: Gil, Pedro
last_name: Gil
- first_name: Elizabeth
full_name: Dewey, Elizabeth
last_name: Dewey
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Yunde
full_name: Zhao, Yunde
last_name: Zhao
- first_name: Kimberley
full_name: Snowden, Kimberley
last_name: Snowden
- first_name: Jo
full_name: Putterill, Jo
last_name: Putterill
- first_name: Klaus
full_name: Palme, Klaus
last_name: Palme
- first_name: Mark
full_name: Estelle, Mark
last_name: Estelle
- first_name: Joanne
full_name: Chory, Joanne
last_name: Chory
citation:
ama: 'Gil P, Dewey E, Friml J, et al. BIG: A calossin-like protein required for
polar auxin transport in Arabidopsis. Genes and Development. 2001;15(15):1985-1997.
doi:10.1101/gad.905201'
apa: 'Gil, P., Dewey, E., Friml, J., Zhao, Y., Snowden, K., Putterill, J., … Chory,
J. (2001). BIG: A calossin-like protein required for polar auxin transport in
Arabidopsis. Genes and Development. Cold Spring Harbor Laboratory Press.
https://doi.org/10.1101/gad.905201'
chicago: 'Gil, Pedro, Elizabeth Dewey, Jiří Friml, Yunde Zhao, Kimberley Snowden,
Jo Putterill, Klaus Palme, Mark Estelle, and Joanne Chory. “BIG: A Calossin-like
Protein Required for Polar Auxin Transport in Arabidopsis.” Genes and Development.
Cold Spring Harbor Laboratory Press, 2001. https://doi.org/10.1101/gad.905201.'
ieee: 'P. Gil et al., “BIG: A calossin-like protein required for polar auxin
transport in Arabidopsis,” Genes and Development, vol. 15, no. 15. Cold
Spring Harbor Laboratory Press, pp. 1985–1997, 2001.'
ista: 'Gil P, Dewey E, Friml J, Zhao Y, Snowden K, Putterill J, Palme K, Estelle
M, Chory J. 2001. BIG: A calossin-like protein required for polar auxin transport
in Arabidopsis. Genes and Development. 15(15), 1985–1997.'
mla: 'Gil, Pedro, et al. “BIG: A Calossin-like Protein Required for Polar Auxin
Transport in Arabidopsis.” Genes and Development, vol. 15, no. 15, Cold
Spring Harbor Laboratory Press, 2001, pp. 1985–97, doi:10.1101/gad.905201.'
short: P. Gil, E. Dewey, J. Friml, Y. Zhao, K. Snowden, J. Putterill, K. Palme,
M. Estelle, J. Chory, Genes and Development 15 (2001) 1985–1997.
date_created: 2018-12-11T12:00:41Z
date_published: 2001-08-01T00:00:00Z
date_updated: 2023-05-16T11:59:47Z
day: '01'
doi: 10.1101/gad.905201
extern: '1'
external_id:
pmid:
- '11485992'
intvolume: ' 15'
issue: '15'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC312751/
month: '08'
oa: 1
oa_version: Published Version
page: 1985 - 1997
pmid: 1
publication: Genes and Development
publication_identifier:
issn:
- 0890-9369
publication_status: published
publisher: Cold Spring Harbor Laboratory Press
publist_id: '3720'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'BIG: A calossin-like protein required for polar auxin transport in Arabidopsis'
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 15
year: '2001'
...
---
_id: '2983'
abstract:
- lang: eng
text: Polar transport of the phytohormone auxin mediates various processes in plant
growth and development, such as apical dominance, tropisms, vascular patterning
and axis formation. This view is based largely on the effects of polar auxin transport
inhibitors. These compounds disrupt auxin efflux from the cell but their mode
of action is unknown. It is thought that polar auxin flux is caused by the asymmetric
distribution of efflux carriers acting at the plasma membrane. The polar localization
of efflux carrier candidate PIN1 supports this model. Here we show that the seemingly
static localization of PIN1 results from rapid actin-dependent cycling between
the plasma membrane and endosomal compartments. Auxin transport inhibitors block
PIN1 cycling and inhibit trafficking of membrane proteins that are unrelated to
auxin transport. Our data suggest that PIN1 cycling is of central importance for
auxin transport and that auxin transport inhibitors affect efflux by generally
interfering with membrane-trafficking processes. In support of our conclusion,
the vesicle-trafficking inhibitor brefeldin A mimics physiological effects of
auxin transport inhibitors.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Niko
full_name: Geldner, Niko
last_name: Geldner
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: York
full_name: Stierhof, York
last_name: Stierhof
- first_name: Gerd
full_name: Jürgens, Gerd
last_name: Jürgens
- first_name: Klaus
full_name: Palme, Klaus
last_name: Palme
citation:
ama: Geldner N, Friml J, Stierhof Y, Jürgens G, Palme K. Auxin transport inhibitors
block PIN1 cycling and vesicle trafficking. Nature. 2001;413(6854):425-428.
doi:10.1038/35096571
apa: Geldner, N., Friml, J., Stierhof, Y., Jürgens, G., & Palme, K. (2001).
Auxin transport inhibitors block PIN1 cycling and vesicle trafficking. Nature.
Nature Publishing Group. https://doi.org/10.1038/35096571
chicago: Geldner, Niko, Jiří Friml, York Stierhof, Gerd Jürgens, and Klaus Palme.
“Auxin Transport Inhibitors Block PIN1 Cycling and Vesicle Trafficking.” Nature.
Nature Publishing Group, 2001. https://doi.org/10.1038/35096571.
ieee: N. Geldner, J. Friml, Y. Stierhof, G. Jürgens, and K. Palme, “Auxin transport
inhibitors block PIN1 cycling and vesicle trafficking,” Nature, vol. 413,
no. 6854. Nature Publishing Group, pp. 425–428, 2001.
ista: Geldner N, Friml J, Stierhof Y, Jürgens G, Palme K. 2001. Auxin transport
inhibitors block PIN1 cycling and vesicle trafficking. Nature. 413(6854), 425–428.
mla: Geldner, Niko, et al. “Auxin Transport Inhibitors Block PIN1 Cycling and Vesicle
Trafficking.” Nature, vol. 413, no. 6854, Nature Publishing Group, 2001,
pp. 425–28, doi:10.1038/35096571.
short: N. Geldner, J. Friml, Y. Stierhof, G. Jürgens, K. Palme, Nature 413 (2001)
425–428.
date_created: 2018-12-11T12:00:41Z
date_published: 2001-09-27T00:00:00Z
date_updated: 2023-05-16T11:51:44Z
day: '27'
doi: 10.1038/35096571
extern: '1'
external_id:
pmid:
- '11574889'
intvolume: ' 413'
issue: '6854'
language:
- iso: eng
month: '09'
oa_version: None
page: 425 - 428
pmid: 1
publication: Nature
publication_identifier:
issn:
- 0028-0836
publication_status: published
publisher: Nature Publishing Group
publist_id: '3719'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Auxin transport inhibitors block PIN1 cycling and vesicle trafficking
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 413
year: '2001'
...
---
_id: '2984'
abstract:
- lang: eng
text: Auxins represent an important class of plant hormone that regulate plant development.
Plants use specialized carrier proteins to transport the auxin indole-3-acetic
acid (IAA) to target tissues. To date, efflux carrier-mediated polar auxin transport
has been assumed to represent the sole mode of long distance IAA movement. Localization
of the auxin permease AUX1 in the Arabidopsis root apex has revealed a novel phloem-based
IAA transport pathway. AUX1, asymmetrically localized to the plasma membrane of
root protophloem cells, is proposed to promote the acropetal, post-phloem movement
of auxin to the root apex. MS analysis shows that IAA accumulation in aux1 mutant
root apices is impaired, consistent with an AUX1 phloem unloading function. AUX1
localization to columella and lateral root cap tissues of the Arabidopsis root
apex reveals that the auxin permease regulates a second IAA transport pathway.
Expression studies using an auxin-regulated reporter suggest that AUX1 is necessary
for root gravitropism by facilitating basipetal auxin transport to distal elongation
zone tissues.
acknowledgement: "We thank Ben Scheres and Marcus Grebe for critically reading the
manuscript, Burkhard Schulz for providing advice about the HA epitope tag, and Denis
Baker for valuable discussion. This work was funded by the BBSRC and European Commission
grants to the LATIN and POPWOOD research consortia.\r\n\r\nThe publication costs
of this article were defrayed in part by payment of page charges. This article must
therefore be hereby marked “advertisement” in accordance with 18 USC section 1734
solely to indicate this fact."
article_processing_charge: No
article_type: original
author:
- first_name: Ranjan
full_name: Swarup, Ranjan
last_name: Swarup
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Alan
full_name: Marchant, Alan
last_name: Marchant
- first_name: Karin
full_name: Ljung, Karin
last_name: Ljung
- first_name: Göran
full_name: Sandberg, Göran
last_name: Sandberg
- first_name: Klaus
full_name: Palme, Klaus
last_name: Palme
- first_name: Malcolm
full_name: Bennett, Malcolm
last_name: Bennett
citation:
ama: Swarup R, Friml J, Marchant A, et al. Localization of the auxin permease AUX1
suggests two functionally distinct hormone transport pathways operate in the Arabidopsis
root apex. Genes and Development. 2001;15(20):2648-2653. doi:10.1101/gad.210501
apa: Swarup, R., Friml, J., Marchant, A., Ljung, K., Sandberg, G., Palme, K., &
Bennett, M. (2001). Localization of the auxin permease AUX1 suggests two functionally
distinct hormone transport pathways operate in the Arabidopsis root apex. Genes
and Development. Cold Spring Harbor Laboratory Press. https://doi.org/10.1101/gad.210501
chicago: Swarup, Ranjan, Jiří Friml, Alan Marchant, Karin Ljung, Göran Sandberg,
Klaus Palme, and Malcolm Bennett. “Localization of the Auxin Permease AUX1 Suggests
Two Functionally Distinct Hormone Transport Pathways Operate in the Arabidopsis
Root Apex.” Genes and Development. Cold Spring Harbor Laboratory Press,
2001. https://doi.org/10.1101/gad.210501.
ieee: R. Swarup et al., “Localization of the auxin permease AUX1 suggests
two functionally distinct hormone transport pathways operate in the Arabidopsis
root apex,” Genes and Development, vol. 15, no. 20. Cold Spring Harbor
Laboratory Press, pp. 2648–2653, 2001.
ista: Swarup R, Friml J, Marchant A, Ljung K, Sandberg G, Palme K, Bennett M. 2001.
Localization of the auxin permease AUX1 suggests two functionally distinct hormone
transport pathways operate in the Arabidopsis root apex. Genes and Development.
15(20), 2648–2653.
mla: Swarup, Ranjan, et al. “Localization of the Auxin Permease AUX1 Suggests Two
Functionally Distinct Hormone Transport Pathways Operate in the Arabidopsis Root
Apex.” Genes and Development, vol. 15, no. 20, Cold Spring Harbor Laboratory
Press, 2001, pp. 2648–53, doi:10.1101/gad.210501.
short: R. Swarup, J. Friml, A. Marchant, K. Ljung, G. Sandberg, K. Palme, M. Bennett,
Genes and Development 15 (2001) 2648–2653.
date_created: 2018-12-11T12:00:41Z
date_published: 2001-10-15T00:00:00Z
date_updated: 2023-05-16T11:37:53Z
day: '15'
doi: 10.1101/gad.210501
extern: '1'
external_id:
pmid:
- '11641271'
intvolume: ' 15'
issue: '20'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: ncbi.nlm.nih.gov/pmc/articles/PMC312818/
month: '10'
oa: 1
oa_version: Published Version
page: 2648 - 2653
pmid: 1
publication: Genes and Development
publication_identifier:
issn:
- Genes and Development
publication_status: published
publisher: Cold Spring Harbor Laboratory Press
publist_id: '3718'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Localization of the auxin permease AUX1 suggests two functionally distinct
hormone transport pathways operate in the Arabidopsis root apex
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 15
year: '2001'
...
---
_id: '2985'
abstract:
- lang: eng
text: The elimination voltammetry with linear scan (EVLS) was used to study adenine
and cytosine reduction signals at the mercury electrode. In comparison with the
linear scan voltammetry (which provides only one unresolved peak), two elimination
functions provide good resolution of individual peaks and significant increase
of sensitivity. The first elimination function eliminates the kinetic current
(Ik) and conserves the diffusion current (Id). The second elimination function
eliminates kinetic and charging currents (Ik and Ic) simultaneously and conserves
the diffusion current (Id). Both functions give two well-resolved peaks of adenine
and cytosine in a wide concentration range, while the linear sweep voltammetry
gives badly resolved peaks due to hydrogen evolution. The best resolution of peaks
is observed in acetate buffer at pH 3.8 and the detection limit for both substances
is 500 nM. The concentration dependence of EVLS peak heights for one substance
at the constant concentration of the other substance is linear. The peak potentials
differ in these elimination functions. The difference in EVLS peak potentials
gives the possibility to evaluate αna. Elimination voltammetry with linear scan
contributes to the resolution of cathodic signals of purine and pyrimidine bases
at very negative potentials near supporting electrolyte discharge. Copyright ©
2001 Elsevier Science B.V.
article_processing_charge: No
article_type: original
author:
- first_name: Libuše
full_name: Trnková, Libuše
last_name: Trnková
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Oldřich
full_name: Dračka, Oldřich
last_name: Dračka
citation:
ama: Trnková L, Friml J, Dračka O. Elimination voltammetry of adenine and cytosine
mixtures. Bioelectrochemistry. 2001;54(2):131-136. doi:10.1016/S1567-5394(01)00119-0
apa: Trnková, L., Friml, J., & Dračka, O. (2001). Elimination voltammetry of
adenine and cytosine mixtures. Bioelectrochemistry. Elsevier. https://doi.org/10.1016/S1567-5394(01)00119-0
chicago: Trnková, Libuše, Jiří Friml, and Oldřich Dračka. “Elimination Voltammetry
of Adenine and Cytosine Mixtures.” Bioelectrochemistry. Elsevier, 2001.
https://doi.org/10.1016/S1567-5394(01)00119-0.
ieee: L. Trnková, J. Friml, and O. Dračka, “Elimination voltammetry of adenine and
cytosine mixtures,” Bioelectrochemistry, vol. 54, no. 2. Elsevier, pp.
131–136, 2001.
ista: Trnková L, Friml J, Dračka O. 2001. Elimination voltammetry of adenine and
cytosine mixtures. Bioelectrochemistry. 54(2), 131–136.
mla: Trnková, Libuše, et al. “Elimination Voltammetry of Adenine and Cytosine Mixtures.”
Bioelectrochemistry, vol. 54, no. 2, Elsevier, 2001, pp. 131–36, doi:10.1016/S1567-5394(01)00119-0.
short: L. Trnková, J. Friml, O. Dračka, Bioelectrochemistry 54 (2001) 131–136.
date_created: 2018-12-11T12:00:42Z
date_published: 2001-11-01T00:00:00Z
date_updated: 2023-05-15T14:48:44Z
day: '01'
doi: 10.1016/S1567-5394(01)00119-0
extern: '1'
external_id:
pmid:
- '11694393'
intvolume: ' 54'
issue: '2'
language:
- iso: eng
month: '11'
oa_version: None
page: 131 - 136
pmid: 1
publication: Bioelectrochemistry
publication_identifier:
isbn:
- 1567-5394
publication_status: published
publisher: Elsevier
publist_id: '3717'
quality_controlled: '1'
status: public
title: Elimination voltammetry of adenine and cytosine mixtures
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 54
year: '2001'
...
---
_id: '3169'
abstract:
- lang: eng
text: Several new algorithms for visual correspondence based on graph cuts [7, 14,
17] have recently been developed. While these methods give very strong results
in practice, they do not handle occlusions properly. Specifically, they treat
the two input images asymmetrically, and they do not ensure that a pixel corresponds
to at most one pixel in the other image. In this paper, we present a new method
which properly addresses occlusions, while preserving the advantages of graph
cut algorithms. We give experimental results for stereo as well as motion, which
demonstrate that our method performs well both at detecting occlusions and computing
disparities.
article_processing_charge: No
author:
- first_name: Vladimir
full_name: Kolmogorov, Vladimir
id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
last_name: Kolmogorov
- first_name: Ramin
full_name: Zabih, Ramin
last_name: Zabih
citation:
ama: 'Kolmogorov V, Zabih R. Computing visual correspondence with occlusions using
graph cuts. In: Proceedings of the 8th IEEE International Conference on Computer
Vision. Vol 2. IEEE; 2001:508-515. doi:10.1109/ICCV.2001.937668'
apa: 'Kolmogorov, V., & Zabih, R. (2001). Computing visual correspondence with
occlusions using graph cuts. In Proceedings of the 8th IEEE International Conference
on Computer Vision (Vol. 2, pp. 508–515). Vancouver, Canada: IEEE. https://doi.org/10.1109/ICCV.2001.937668'
chicago: Kolmogorov, Vladimir, and Ramin Zabih. “Computing Visual Correspondence
with Occlusions Using Graph Cuts.” In Proceedings of the 8th IEEE International
Conference on Computer Vision, 2:508–15. IEEE, 2001. https://doi.org/10.1109/ICCV.2001.937668.
ieee: V. Kolmogorov and R. Zabih, “Computing visual correspondence with occlusions
using graph cuts,” in Proceedings of the 8th IEEE International Conference
on Computer Vision, Vancouver, Canada, 2001, vol. 2, pp. 508–515.
ista: 'Kolmogorov V, Zabih R. 2001. Computing visual correspondence with occlusions
using graph cuts. Proceedings of the 8th IEEE International Conference on Computer
Vision. ICCV: International Conference on Computer Vision vol. 2, 508–515.'
mla: Kolmogorov, Vladimir, and Ramin Zabih. “Computing Visual Correspondence with
Occlusions Using Graph Cuts.” Proceedings of the 8th IEEE International Conference
on Computer Vision, vol. 2, IEEE, 2001, pp. 508–15, doi:10.1109/ICCV.2001.937668.
short: V. Kolmogorov, R. Zabih, in:, Proceedings of the 8th IEEE International Conference
on Computer Vision, IEEE, 2001, pp. 508–515.
conference:
end_date: 2001-07-14
location: Vancouver, Canada
name: 'ICCV: International Conference on Computer Vision'
start_date: 2001-07-07
date_created: 2018-12-11T12:01:47Z
date_published: 2001-08-01T00:00:00Z
date_updated: 2023-05-15T14:45:50Z
day: '01'
doi: 10.1109/ICCV.2001.937668
extern: '1'
intvolume: ' 2'
language:
- iso: eng
month: '08'
oa_version: None
page: 508 - 515
publication: Proceedings of the 8th IEEE International Conference on Computer Vision
publication_identifier:
isbn:
- '0769511430'
publication_status: published
publisher: IEEE
publist_id: '3514'
quality_controlled: '1'
status: public
title: Computing visual correspondence with occlusions using graph cuts
type: conference
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 2
year: '2001'
...
---
_id: '3434'
abstract:
- lang: eng
text: "This chapter contains sections titled:\r\n\r\nIntroduction\r\n\r\n- History\r\n\r\n-
Developing an Intuition of Likelihood\r\n\r\n- Method of Maximum Likelihood\r\n\r\n-
Bayesian Inference\r\n\r\n- Markov Chain Monte Carlo\r\n\r\n- Assessing Uncertainty
of Phylogenies\r\n\r\n- Hypothesis Testing and Model Choice\r\n\r\n- Comparative
Analysis\r\n\r\n- Conclusions\r\n\r\n- References"
article_processing_charge: No
author:
- first_name: John
full_name: Huelsenbeck, John
last_name: Huelsenbeck
- first_name: Jonathan P
full_name: Bollback, Jonathan P
id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
last_name: Bollback
orcid: 0000-0002-4624-4612
citation:
ama: 'Huelsenbeck J, Bollback JP. Application of the likelihood function in phylogenetic
analysis. In: Balding D, Bishop M, Cannings C, eds. Handbook of Statistical
Genetics. Wiley-Blackwell; 2001:415-439. doi:10.1002/9780470061619.ch15'
apa: Huelsenbeck, J., & Bollback, J. P. (2001). Application of the likelihood
function in phylogenetic analysis. In D. Balding, M. Bishop, & C. Cannings
(Eds.), Handbook of Statistical Genetics (pp. 415–439). Wiley-Blackwell.
https://doi.org/10.1002/9780470061619.ch15
chicago: Huelsenbeck, John, and Jonathan P Bollback. “Application of the Likelihood
Function in Phylogenetic Analysis.” In Handbook of Statistical Genetics,
edited by David Balding, Martin Bishop, and Chriss Cannings, 415–39. Wiley-Blackwell,
2001. https://doi.org/10.1002/9780470061619.ch15.
ieee: J. Huelsenbeck and J. P. Bollback, “Application of the likelihood function
in phylogenetic analysis,” in Handbook of Statistical Genetics, D. Balding,
M. Bishop, and C. Cannings, Eds. Wiley-Blackwell, 2001, pp. 415–439.
ista: 'Huelsenbeck J, Bollback JP. 2001.Application of the likelihood function in
phylogenetic analysis. In: Handbook of Statistical Genetics. , 415–439.'
mla: Huelsenbeck, John, and Jonathan P. Bollback. “Application of the Likelihood
Function in Phylogenetic Analysis.” Handbook of Statistical Genetics, edited
by David Balding et al., Wiley-Blackwell, 2001, pp. 415–39, doi:10.1002/9780470061619.ch15.
short: J. Huelsenbeck, J.P. Bollback, in:, D. Balding, M. Bishop, C. Cannings (Eds.),
Handbook of Statistical Genetics, Wiley-Blackwell, 2001, pp. 415–439.
date_created: 2018-12-11T12:03:19Z
date_published: 2001-01-01T00:00:00Z
date_updated: 2023-05-15T14:43:39Z
day: '01'
doi: 10.1002/9780470061619.ch15
editor:
- first_name: David
full_name: Balding, David
last_name: Balding
- first_name: Martin
full_name: Bishop, Martin
last_name: Bishop
- first_name: Chriss
full_name: Cannings, Chriss
last_name: Cannings
extern: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 415 - 439
publication: Handbook of Statistical Genetics
publication_identifier:
isbn:
- '9781119429142 '
publication_status: published
publisher: Wiley-Blackwell
publist_id: '2966'
quality_controlled: '1'
status: public
title: Application of the likelihood function in phylogenetic analysis
type: book_chapter
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
year: '2001'
...
---
_id: '3438'
abstract:
- lang: eng
text: As a discipline, phylogenetics is becoming transformed by a flood of molecular
data. These data allow broad questions to be asked about the history of life,
but also present difficult statistical and computational problems. Bayesian inference
of phylogeny brings a new perspective to a number of outstanding issues in evolutionary
biology, including the analysis of large phylogenetic trees and complex evolutionary
models and the detection of the footprint of natural selection in DNA sequences.
article_processing_charge: No
author:
- first_name: John
full_name: Huelsenbeck, John
last_name: Huelsenbeck
- first_name: Fredrik
full_name: Ronquist, Fredrik
last_name: Ronquist
- first_name: Rasmus
full_name: Nielsen, Rasmus
last_name: Nielsen
- first_name: Jonathan P
full_name: Bollback, Jonathan P
id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
last_name: Bollback
orcid: 0000-0002-4624-4612
citation:
ama: Huelsenbeck J, Ronquist F, Nielsen R, Bollback JP. Bayesian inference of phylogeny
and its impact on evolutionary biology. Science. 2001;294(5550):2310-2314.
doi:10.1126/science.1065889
apa: Huelsenbeck, J., Ronquist, F., Nielsen, R., & Bollback, J. P. (2001). Bayesian
inference of phylogeny and its impact on evolutionary biology. Science.
American Association for the Advancement of Science. https://doi.org/10.1126/science.1065889
chicago: Huelsenbeck, John, Fredrik Ronquist, Rasmus Nielsen, and Jonathan P Bollback.
“Bayesian Inference of Phylogeny and Its Impact on Evolutionary Biology.” Science.
American Association for the Advancement of Science, 2001. https://doi.org/10.1126/science.1065889.
ieee: J. Huelsenbeck, F. Ronquist, R. Nielsen, and J. P. Bollback, “Bayesian inference
of phylogeny and its impact on evolutionary biology,” Science, vol. 294,
no. 5550. American Association for the Advancement of Science, pp. 2310–2314,
2001.
ista: Huelsenbeck J, Ronquist F, Nielsen R, Bollback JP. 2001. Bayesian inference
of phylogeny and its impact on evolutionary biology. Science. 294(5550), 2310–2314.
mla: Huelsenbeck, John, et al. “Bayesian Inference of Phylogeny and Its Impact on
Evolutionary Biology.” Science, vol. 294, no. 5550, American Association
for the Advancement of Science, 2001, pp. 2310–14, doi:10.1126/science.1065889.
short: J. Huelsenbeck, F. Ronquist, R. Nielsen, J.P. Bollback, Science 294 (2001)
2310–2314.
date_created: 2018-12-11T12:03:20Z
date_published: 2001-12-14T00:00:00Z
date_updated: 2023-05-15T14:10:13Z
day: '14'
doi: 10.1126/science.1065889
extern: '1'
external_id:
pmid:
- '11743192 '
intvolume: ' 294'
issue: '5550'
language:
- iso: eng
month: '12'
oa_version: None
page: 2310 - 2314
pmid: 1
publication: Science
publication_identifier:
issn:
- 0036-8075
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '2962'
quality_controlled: '1'
status: public
title: Bayesian inference of phylogeny and its impact on evolutionary biology
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 294
year: '2001'
...
---
_id: '3439'
abstract:
- lang: eng
text: High molecular weight DNA was extracted from the primary Neotropical malaria
vector, Anopheles darlingi from Capanema, Pará, Brazil, to create a small insert
genomic library, and then a phagemid library. Enriched sublibraries were constructed
from the phagemid library using a microsatellite oligo primed second strand synthesis
protocol. The resulting 242 760 individual clones were screened. The mean clone
size of the positive clones was 302 bp. Flanking primers were designed for each
suitable microsatellite sequence. Eight polymorphic loci were optimized and characterized.
The allele size ranges are based on 253 samples of A. darlingi from eastern Amazonian
and central Brazil.
acknowledgement: For support in Brazil we thank D. Galiza, R.N.L. Lacerda,E.P.
Santa Rosa, M.N.O. Segura, and R.T.L. de Souza. We also thankM.J. Braun for allowing work on the library construction at theLaboratory
of Molecular Systematics, Washington. Supported byNIH AI 40116 to JEC and Instituto
Evandro Chagas, Belém, Brazil.
article_processing_charge: No
article_type: original
author:
- first_name: Jan
full_name: Conn, Jan
last_name: Conn
- first_name: Jonathan P
full_name: Bollback, Jonathan P
id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
last_name: Bollback
orcid: 0000-0002-4624-4612
- first_name: David
full_name: Onyabe, David
last_name: Onyabe
- first_name: Tessa
full_name: Robinson, Tessa
last_name: Robinson
- first_name: Richard
full_name: Wilkerson, Richard
last_name: Wilkerson
- first_name: Marinete
full_name: Povoa, Marinete
last_name: Povoa
citation:
ama: Conn J, Bollback JP, Onyabe D, Robinson T, Wilkerson R, Povoa M. Isolation
of polymorphic microsatellite markers from the malaria vector Anopheles darlingi.
Molecular Ecology Notes. 2001;1(4):223-225. doi: 10.1046/j.1471-8278.2001.00078.x
apa: Conn, J., Bollback, J. P., Onyabe, D., Robinson, T., Wilkerson, R., & Povoa,
M. (2001). Isolation of polymorphic microsatellite markers from the malaria vector
Anopheles darlingi. Molecular Ecology Notes. Wiley-Blackwell. https://doi.org/ 10.1046/j.1471-8278.2001.00078.x
chicago: Conn, Jan, Jonathan P Bollback, David Onyabe, Tessa Robinson, Richard Wilkerson,
and Marinete Povoa. “Isolation of Polymorphic Microsatellite Markers from the
Malaria Vector Anopheles Darlingi.” Molecular Ecology Notes. Wiley-Blackwell,
2001. https://doi.org/
10.1046/j.1471-8278.2001.00078.x.
ieee: J. Conn, J. P. Bollback, D. Onyabe, T. Robinson, R. Wilkerson, and M. Povoa,
“Isolation of polymorphic microsatellite markers from the malaria vector Anopheles
darlingi,” Molecular Ecology Notes, vol. 1, no. 4. Wiley-Blackwell, pp.
223–225, 2001.
ista: Conn J, Bollback JP, Onyabe D, Robinson T, Wilkerson R, Povoa M. 2001. Isolation
of polymorphic microsatellite markers from the malaria vector Anopheles darlingi.
Molecular Ecology Notes. 1(4), 223–225.
mla: Conn, Jan, et al. “Isolation of Polymorphic Microsatellite Markers from the
Malaria Vector Anopheles Darlingi.” Molecular Ecology Notes, vol. 1, no.
4, Wiley-Blackwell, 2001, pp. 223–25, doi:
10.1046/j.1471-8278.2001.00078.x.
short: J. Conn, J.P. Bollback, D. Onyabe, T. Robinson, R. Wilkerson, M. Povoa, Molecular
Ecology Notes 1 (2001) 223–225.
date_created: 2018-12-11T12:03:20Z
date_published: 2001-12-01T00:00:00Z
date_updated: 2023-05-15T13:58:49Z
day: '01'
doi: ' 10.1046/j.1471-8278.2001.00078.x'
extern: '1'
intvolume: ' 1'
issue: '4'
language:
- iso: eng
month: '12'
oa_version: None
page: 223 - 225
publication: Molecular Ecology Notes
publication_identifier:
issn:
- 1471-8278
publication_status: published
publisher: Wiley-Blackwell
publist_id: '2961'
quality_controlled: '1'
status: public
title: Isolation of polymorphic microsatellite markers from the malaria vector Anopheles
darlingi
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 1
year: '2001'
...
---
_id: '3440'
abstract:
- lang: eng
text: "Several methods have been proposed to infer the states at the ancestral nodes
on a phylogeny. These methods assume a specific tree and set of branch lengths
when estimating the ancestral character state. Inferences of the ancestral states,
then, are conditioned on the tree and branch lengths being true. We develop a
hierarchical Bayes method for inferring the ancestral states on a tree. The method
integrates over uncertainty in the tree, branch lengths, and substitution model
parameters by using Markov chain Monte Carlo. We compare the hierarchical Bayes
inferences of ancestral states with inferences of ancestral states made under
the assumption that a specific tree is correct. We find that the methods are correlated,
but that accommodating uncertainty in parameters of the phylogenetic model can
make inferences of ancestral states even more uncertain than they would be in
an empirical Bayes analysis.\r\n"
article_processing_charge: No
article_type: original
author:
- first_name: John
full_name: Huelsenbeck, John
last_name: Huelsenbeck
- first_name: Jonathan P
full_name: Bollback, Jonathan P
id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
last_name: Bollback
orcid: 0000-0002-4624-4612
citation:
ama: Huelsenbeck J, Bollback JP. Empirical and hierarchical Bayesian estimation
of ancestral states. Systematic Biology. 2001;50(3):351-366. doi:10.1080/10635150119871
apa: Huelsenbeck, J., & Bollback, J. P. (2001). Empirical and hierarchical Bayesian
estimation of ancestral states. Systematic Biology. Oxford University Press.
https://doi.org/10.1080/10635150119871
chicago: Huelsenbeck, John, and Jonathan P Bollback. “Empirical and Hierarchical
Bayesian Estimation of Ancestral States.” Systematic Biology. Oxford University
Press, 2001. https://doi.org/10.1080/10635150119871.
ieee: J. Huelsenbeck and J. P. Bollback, “Empirical and hierarchical Bayesian estimation
of ancestral states,” Systematic Biology, vol. 50, no. 3. Oxford University
Press, pp. 351–366, 2001.
ista: Huelsenbeck J, Bollback JP. 2001. Empirical and hierarchical Bayesian estimation
of ancestral states. Systematic Biology. 50(3), 351–366.
mla: Huelsenbeck, John, and Jonathan P. Bollback. “Empirical and Hierarchical Bayesian
Estimation of Ancestral States.” Systematic Biology, vol. 50, no. 3, Oxford
University Press, 2001, pp. 351–66, doi:10.1080/10635150119871.
short: J. Huelsenbeck, J.P. Bollback, Systematic Biology 50 (2001) 351–366.
date_created: 2018-12-11T12:03:20Z
date_published: 2001-05-01T00:00:00Z
date_updated: 2023-05-15T13:54:01Z
day: '01'
doi: 10.1080/10635150119871
extern: '1'
external_id:
pmid:
- '12116580'
intvolume: ' 50'
issue: '3'
language:
- iso: eng
month: '05'
oa_version: None
page: 351 - 366
pmid: 1
publication: Systematic Biology
publication_identifier:
issn:
- 0039-7989
publication_status: published
publisher: Oxford University Press
publist_id: '2960'
quality_controlled: '1'
status: public
title: Empirical and hierarchical Bayesian estimation of ancestral states
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 50
year: '2001'
...
---
_id: '3447'
author:
- first_name: Krishnendu
full_name: Krishnendu Chatterjee
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Pallab
full_name: Dasgupta, Pallab
last_name: Dasgupta
- first_name: Partha
full_name: Chakrabarti, Partha P
last_name: Chakrabarti
citation:
ama: 'Chatterjee K, Dasgupta P, Chakrabarti P. Weighted quantified computation tree
logic. In: Elsevier; 2001.'
apa: 'Chatterjee, K., Dasgupta, P., & Chakrabarti, P. (2001). Weighted quantified
computation tree logic. Presented at the CIT: Conference on Information Technology,
Elsevier.'
chicago: Chatterjee, Krishnendu, Pallab Dasgupta, and Partha Chakrabarti. “Weighted
Quantified Computation Tree Logic.” Elsevier, 2001.
ieee: 'K. Chatterjee, P. Dasgupta, and P. Chakrabarti, “Weighted quantified computation
tree logic,” presented at the CIT: Conference on Information Technology, 2001.'
ista: 'Chatterjee K, Dasgupta P, Chakrabarti P. 2001. Weighted quantified computation
tree logic. CIT: Conference on Information Technology.'
mla: Chatterjee, Krishnendu, et al. Weighted Quantified Computation Tree Logic.
Elsevier, 2001.
short: K. Chatterjee, P. Dasgupta, P. Chakrabarti, in:, Elsevier, 2001.
conference:
name: 'CIT: Conference on Information Technology'
date_created: 2018-12-11T12:03:23Z
date_published: 2001-11-14T00:00:00Z
date_updated: 2021-01-12T07:43:31Z
day: '14'
extern: 1
month: '11'
publication_status: published
publisher: Elsevier
publist_id: '2940'
quality_controlled: 0
status: public
title: Weighted quantified computation tree logic
type: conference
year: '2001'
...
---
_id: '3493'
abstract:
- lang: eng
text: Although agonists and competitive antagonists presumably occupy overlapping
binding sites on ligand-gated channels, these interactions cannot be identical
because agonists cause channel opening whereas antagonists do not. One explanation
is that only agonist binding performs enough work on the receptor to cause the
conformational changes that lead to gating. This idea is supported by agonist
binding rates at GABAA and nicotinic acetylcholine receptors that are slower than
expected for a diffusion-limited process, suggesting that agonist binding involves
an energy-requiring event. This hypothesis predicts that competitive antagonist
binding should require less activation energy than agonist binding. To test this
idea, we developed a novel deconvolution-based method to compare binding and unbinding
kinetics of GABAA receptor agonists and antagonists in outside-out patches from
rat hippocampal neurons. Agonist and antagonist unbinding rates were steeply correlated
with affinity. Unlike the agonists, three of the four antagonists tested had binding
rates that were fast, independent of affinity, and could be accounted for by diffusion-
and dehydration-limited processes. In contrast, agonist binding involved additional
energy-requiring steps, consistent with the idea that channel gating is initiated
by agonist-triggered movements within the ligand binding site. Antagonist binding
does not appear to produce such movements, and may in fact prevent them.
article_processing_charge: No
article_type: original
author:
- first_name: M.V
full_name: Jones, M.V
last_name: Jones
- first_name: Peter M
full_name: Jonas, Peter M
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
- first_name: Y.
full_name: Sahara, Y.
last_name: Sahara
- first_name: G.
full_name: Westbrook, G.
last_name: Westbrook
citation:
ama: Jones M., Jonas PM, Sahara Y, Westbrook G. Microscopic kinetics and energetics
distinguish GABAA receptor agonists from antagonists. Biophysical Journal.
2001;81(5):2660-2670. doi:10.1016/S0006-3495(01)75909-7
apa: Jones, M. ., Jonas, P. M., Sahara, Y., & Westbrook, G. (2001). Microscopic
kinetics and energetics distinguish GABAA receptor agonists from antagonists.
Biophysical Journal. Biophysical Society. https://doi.org/10.1016/S0006-3495(01)75909-7
chicago: Jones, M.V, Peter M Jonas, Y. Sahara, and G. Westbrook. “Microscopic Kinetics
and Energetics Distinguish GABAA Receptor Agonists from Antagonists.” Biophysical
Journal. Biophysical Society, 2001. https://doi.org/10.1016/S0006-3495(01)75909-7 .
ieee: M. . Jones, P. M. Jonas, Y. Sahara, and G. Westbrook, “Microscopic kinetics
and energetics distinguish GABAA receptor agonists from antagonists,” Biophysical
Journal, vol. 81, no. 5. Biophysical Society, pp. 2660–2670, 2001.
ista: Jones M., Jonas PM, Sahara Y, Westbrook G. 2001. Microscopic kinetics and
energetics distinguish GABAA receptor agonists from antagonists. Biophysical Journal.
81(5), 2660–2670.
mla: Jones, M. .., et al. “Microscopic Kinetics and Energetics Distinguish GABAA
Receptor Agonists from Antagonists.” Biophysical Journal, vol. 81, no.
5, Biophysical Society, 2001, pp. 2660–70, doi:10.1016/S0006-3495(01)75909-7 .
short: M.. Jones, P.M. Jonas, Y. Sahara, G. Westbrook, Biophysical Journal 81 (2001)
2660–2670.
date_created: 2018-12-11T12:03:37Z
date_published: 2001-11-01T00:00:00Z
date_updated: 2023-05-15T13:50:21Z
day: '01'
doi: '10.1016/S0006-3495(01)75909-7 '
extern: '1'
external_id:
pmid:
- '11606279'
intvolume: ' 81'
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1301733/
month: '11'
oa: 1
oa_version: Published Version
page: 2660 - 2670
pmid: 1
publication: Biophysical Journal
publication_identifier:
issn:
- 0006-3495
publication_status: published
publisher: Biophysical Society
publist_id: '2894'
quality_controlled: '1'
status: public
title: Microscopic kinetics and energetics distinguish GABAA receptor agonists from
antagonists
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 81
year: '2001'
...
---
_id: '3494'
abstract:
- lang: eng
text: 'Mutual synaptic interactions between GABAergic interneurons are thought to
be of critical importance for the generation of network oscillations and for temporal
encoding of information in the hippocampus. However, the functional properties
of synaptic transmission between hippocampal interneurons are largely unknown.
We have made paired recordings from basket cells (BCs) in the dentate gyrus of
rat hippocampal slices, followed by correlated light and electron microscopical
analysis. Unitary GABAAreceptor-mediated IPSCs at BC–BC synapses recorded at the
soma showed a fast rise and decay, with a mean decay time constant of 2.5 ± 0.2
msec (32°C). Synaptic transmission at BC–BC synapses showed paired-pulse depression
(PPD) (32 ± 5% for 10 msec interpulse intervals) and multiple-pulse depression
during repetitive stimulation. Detailed passive cable model simulations based
on somatodendritic morphology and localization of synaptic contacts further indicated
that the conductance change at the postsynaptic site was even faster, decaying
with a mean time constant of 1.8 ± 0.6 msec. Sequential triple recordings revealed
that the decay time course of IPSCs at BC–BC synapses was approximately twofold
faster than that at BC–granule cell synapses, whereas the extent of PPD was comparable.
To examine the consequences of the fast postsynaptic conductance change for the
generation of oscillatory activity, we developed a computational model of an interneuron
network. The model showed robust oscillations at frequencies >60 Hz if the
excitatory drive was sufficiently large. Thus the fast conductance change at interneuron–interneuron
synapses may promote the generation of high-frequency oscillations observed in
the dentate gyrusin vivo. '
acknowledgement: This work was supported by grants of the Deutsche Forschungsgemeinschaft
(SFB 505/C6) and the Human Frontiers Science Program Organization (RG0017/1998-B).
We thank Drs. M. V. Jones, J. Bischofberger, and U. Kraushaar for critically reading
this manuscript. We also thank B. Taskin and A. Roth for advice in the use of reconstruction
and modeling software, and S. Nestel, M. Winter, and A. Blomenkamp for technical
assistance.
article_processing_charge: No
article_type: original
author:
- first_name: Marlene
full_name: Bartos, Marlene
last_name: Bartos
- first_name: Imre
full_name: Vida, Imre
last_name: Vida
- first_name: Michael
full_name: Frotscher, Michael
last_name: Frotscher
- first_name: Jörg
full_name: Geiger, Jörg
last_name: Geiger
- first_name: Peter M
full_name: Jonas, Peter M
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
citation:
ama: Bartos M, Vida I, Frotscher M, Geiger J, Jonas PM. Rapid signaling at inhibitory
synapses in a dentate gyrus interneuron network. Journal of Neuroscience.
2001;21(8):2687-2698. doi:10.1523/JNEUROSCI.21-08-02687.2001
apa: Bartos, M., Vida, I., Frotscher, M., Geiger, J., & Jonas, P. M. (2001).
Rapid signaling at inhibitory synapses in a dentate gyrus interneuron network.
Journal of Neuroscience. Society for Neuroscience. https://doi.org/10.1523/JNEUROSCI.21-08-02687.2001
chicago: Bartos, Marlene, Imre Vida, Michael Frotscher, Jörg Geiger, and Peter M
Jonas. “Rapid Signaling at Inhibitory Synapses in a Dentate Gyrus Interneuron
Network.” Journal of Neuroscience. Society for Neuroscience, 2001. https://doi.org/10.1523/JNEUROSCI.21-08-02687.2001.
ieee: M. Bartos, I. Vida, M. Frotscher, J. Geiger, and P. M. Jonas, “Rapid signaling
at inhibitory synapses in a dentate gyrus interneuron network.,” Journal of
Neuroscience, vol. 21, no. 8. Society for Neuroscience, pp. 2687–2698, 2001.
ista: Bartos M, Vida I, Frotscher M, Geiger J, Jonas PM. 2001. Rapid signaling at
inhibitory synapses in a dentate gyrus interneuron network. Journal of Neuroscience.
21(8), 2687–2698.
mla: Bartos, Marlene, et al. “Rapid Signaling at Inhibitory Synapses in a Dentate
Gyrus Interneuron Network.” Journal of Neuroscience, vol. 21, no. 8, Society
for Neuroscience, 2001, pp. 2687–98, doi:10.1523/JNEUROSCI.21-08-02687.2001.
short: M. Bartos, I. Vida, M. Frotscher, J. Geiger, P.M. Jonas, Journal of Neuroscience
21 (2001) 2687–2698.
date_created: 2018-12-11T12:03:37Z
date_published: 2001-04-15T00:00:00Z
date_updated: 2023-05-15T13:47:04Z
day: '15'
doi: 10.1523/JNEUROSCI.21-08-02687.2001
extern: '1'
external_id:
pmid:
- '11306622'
intvolume: ' 21'
issue: '8'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: ncbi.nlm.nih.gov/pmc/articles/PMC6762544/
month: '04'
oa: 1
oa_version: Published Version
page: 2687 - 2698
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
issn:
- 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '2893'
quality_controlled: '1'
status: public
title: Rapid signaling at inhibitory synapses in a dentate gyrus interneuron network.
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 21
year: '2001'
...
---
_id: '3495'
abstract:
- lang: eng
text: High Ca2+ permeability and its control by voltage-dependent Mg2+ block are
defining features of NMDA receptors. These features are lost if the principal
NR1 subunit carries an asparagine (N) to arginine (R) substitution in a critical
channel site at NR1 position 598. NR1(R) expression from a single allele in gene-targeted
NR1+/R mice is lethal soon after birth, precluding analysis of altered synaptic
functions later in life. We therefore employed the forebrain specific αCaMKII
promoter to drive tTA-mediated tetracyclin sensitive transcription of transgenes
for NR1(R) and for lacZ as reporter. Transgene expression was observed in cortex,
striatum, hippocampus, amygdala and olfactory bulb and was mosaic in all these
forebrain regions. It was highest in olfactory bulb granule cells, in most of
which Ca2+ permeability and voltage-dependent Mg2+ block of NMDA receptors were
reduced to different extents. This indicates significant impairment of NMDA receptor
function by NR1(R) in presence of the wild-type NR1 complement. Indeed, even though
NR1(R) mRNA constituted only 18% of the entire NR1 mRNA population in forebrain,
the transgenic mice died during adolescence unless transgene expression was suppressed
by doxycycline. Thus, glutamate receptor function can be altered in the mouse
by regulated NR1(R) transgene expression.
acknowledgement: 'This work was supported in part by grants from the 358 (1992) 36–41.Deutsche
Forschungsgemeinschaft (Bi 642 / 1-2) and the Volkswagen foundation. '
article_processing_charge: No
article_type: original
author:
- first_name: Jasna
full_name: Jerecic, Jasna
last_name: Jerecic
- first_name: Christian
full_name: Schulze, Christian
last_name: Schulze
- first_name: Peter M
full_name: Jonas, Peter M
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
- first_name: Rolf
full_name: Sprengel, Rolf
last_name: Sprengel
- first_name: Peter
full_name: Seeburg, Peter
last_name: Seeburg
- first_name: Joseph
full_name: Bischofberger, Joseph
last_name: Bischofberger
citation:
ama: Jerecic J, Schulze C, Jonas PM, Sprengel R, Seeburg P, Bischofberger J. Impaired
NMDA receptor function in mouse olfactory bulb neurons by tetracycline-sensitive
NR1 (N598R) expression. Molecular Brain Research. 2001;94(1-2):96-104.
doi:10.1016/S0169-328X(01)00221-2
apa: Jerecic, J., Schulze, C., Jonas, P. M., Sprengel, R., Seeburg, P., & Bischofberger,
J. (2001). Impaired NMDA receptor function in mouse olfactory bulb neurons by
tetracycline-sensitive NR1 (N598R) expression. Molecular Brain Research.
Elsevier. https://doi.org/10.1016/S0169-328X(01)00221-2
chicago: Jerecic, Jasna, Christian Schulze, Peter M Jonas, Rolf Sprengel, Peter
Seeburg, and Joseph Bischofberger. “Impaired NMDA Receptor Function in Mouse Olfactory
Bulb Neurons by Tetracycline-Sensitive NR1 (N598R) Expression.” Molecular Brain
Research. Elsevier, 2001. https://doi.org/10.1016/S0169-328X(01)00221-2.
ieee: J. Jerecic, C. Schulze, P. M. Jonas, R. Sprengel, P. Seeburg, and J. Bischofberger,
“Impaired NMDA receptor function in mouse olfactory bulb neurons by tetracycline-sensitive
NR1 (N598R) expression,” Molecular Brain Research, vol. 94, no. 1–2. Elsevier,
pp. 96–104, 2001.
ista: Jerecic J, Schulze C, Jonas PM, Sprengel R, Seeburg P, Bischofberger J. 2001.
Impaired NMDA receptor function in mouse olfactory bulb neurons by tetracycline-sensitive
NR1 (N598R) expression. Molecular Brain Research. 94(1–2), 96–104.
mla: Jerecic, Jasna, et al. “Impaired NMDA Receptor Function in Mouse Olfactory
Bulb Neurons by Tetracycline-Sensitive NR1 (N598R) Expression.” Molecular Brain
Research, vol. 94, no. 1–2, Elsevier, 2001, pp. 96–104, doi:10.1016/S0169-328X(01)00221-2.
short: J. Jerecic, C. Schulze, P.M. Jonas, R. Sprengel, P. Seeburg, J. Bischofberger,
Molecular Brain Research 94 (2001) 96–104.
date_created: 2018-12-11T12:03:38Z
date_published: 2001-10-19T00:00:00Z
date_updated: 2023-05-15T13:42:32Z
day: '19'
doi: 10.1016/S0169-328X(01)00221-2
extern: '1'
external_id:
pmid:
- '11597769'
intvolume: ' 94'
issue: 1-2
language:
- iso: eng
month: '10'
oa_version: None
page: 96 - 104
pmid: 1
publication: Molecular Brain Research
publication_identifier:
issn:
- 0169-328X
publication_status: published
publisher: Elsevier
publist_id: '2892'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Impaired NMDA receptor function in mouse olfactory bulb neurons by tetracycline-sensitive
NR1 (N598R) expression
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 94
year: '2001'
...
---
_id: '3496'
abstract:
- lang: eng
text: 'The mossy fiber-CA3 pyramidal neuron synapse is a main component of the hippocampal
trisynaptic circuitry. Recent studies, however, suggested that inhibitory interneurons
are the major targets of the mossy fiber system. To study the regulation of mossy
fiber-interneuron excitation, we examined unitary and compound excitatory postsynaptic
currents in dentate gyrus basket cells, evoked by paired recording between granule
and basket cells or extracellular stimulation of mossy fiber collaterals. The
application of an associative high-frequency stimulation paradigm induced posttetanic
potentiation (PTP) followed by homosynaptic long-term potentiation (LTP). Analysis
of numbers of failures, coefficient of variation, and paired-pulse modulation
indicated that both PTP and LTP were expressed presynaptically. The Ca2+ chelator
1,2-bis(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid (BAPTA) did not affect
PTP or LTP at a concentration of 10 mM but attenuated LTP at a concentration of
30 mM. Both forskolin, an adenylyl cyclase activator, and phorbolester diacetate,
a protein kinase C stimulator, lead to a long-lasting increase in excitatory postsynaptic
current amplitude. H-89, a protein kinase A inhibitor, and bisindolylmaleimide,
a protein kinase C antagonist, reduced PTP, whereas only bisindolylmaleimide reduced
LTP. These results may suggest a differential contribution of protein kinase A
and C pathways to mossy fiber-interneuron plasticity. Interneuron PTP and LTP
may provide mechanisms to maintain the balance between synaptic excitation of
interneurons and that of principal neurons in the dentate gyrus-CA3 network. '
acknowledgement: We thank Drs. J. Bischofberger and M. Martina for critically reading
an earlier version of the manuscript and A. Blomenkamp for excellent technical assistance.
Supported by the Deutsche Forschungsgemeinschaft Sonderforschungsbereich 505/C5
and Human Frontiers Science Program Organization Grant RG0017/98.
article_processing_charge: No
article_type: original
author:
- first_name: Henrik
full_name: Alle, Henrik
last_name: Alle
- first_name: Peter M
full_name: Jonas, Peter M
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
- first_name: Jörg
full_name: Geiger, Jörg
last_name: Geiger
citation:
ama: Alle H, Jonas PM, Geiger J. PTP and LTP at a hippocampal mossy fiber-interneuron
synapse. PNAS. 2001;98(25):14708-14713. doi:10.1073/pnas.251610898
apa: Alle, H., Jonas, P. M., & Geiger, J. (2001). PTP and LTP at a hippocampal
mossy fiber-interneuron synapse. PNAS. National Academy of Sciences. https://doi.org/10.1073/pnas.251610898
chicago: Alle, Henrik, Peter M Jonas, and Jörg Geiger. “PTP and LTP at a Hippocampal
Mossy Fiber-Interneuron Synapse.” PNAS. National Academy of Sciences, 2001.
https://doi.org/10.1073/pnas.251610898
.
ieee: H. Alle, P. M. Jonas, and J. Geiger, “PTP and LTP at a hippocampal mossy fiber-interneuron
synapse,” PNAS, vol. 98, no. 25. National Academy of Sciences, pp. 14708–14713,
2001.
ista: Alle H, Jonas PM, Geiger J. 2001. PTP and LTP at a hippocampal mossy fiber-interneuron
synapse. PNAS. 98(25), 14708–14713.
mla: Alle, Henrik, et al. “PTP and LTP at a Hippocampal Mossy Fiber-Interneuron
Synapse.” PNAS, vol. 98, no. 25, National Academy of Sciences, 2001, pp.
14708–13, doi:10.1073/pnas.251610898
.
short: H. Alle, P.M. Jonas, J. Geiger, PNAS 98 (2001) 14708–14713.
date_created: 2018-12-11T12:03:38Z
date_published: 2001-12-04T00:00:00Z
date_updated: 2023-05-15T11:08:08Z
day: '04'
doi: '10.1073/pnas.251610898 '
extern: '1'
external_id:
pmid:
- '11734656'
intvolume: ' 98'
issue: '25'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC64746/
month: '12'
oa: 1
oa_version: None
page: 14708 - 14713
pmid: 1
publication: PNAS
publication_identifier:
issn:
- 0027-8424
publication_status: published
publisher: National Academy of Sciences
publist_id: '2891'
quality_controlled: '1'
scopus_import: '1'
status: public
title: PTP and LTP at a hippocampal mossy fiber-interneuron synapse
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 98
year: '2001'
...
---
_id: '3507'
abstract:
- lang: eng
text: A molecular classification method is based on a space filling description
of a molecule. The three dimensional body corresponding to the space filling molecular
structure is divided into Voronoi regions to provide a basis for efficiently processing
local structural information. A Delaunay triangulation provides a basis for systematically
processing information relating to the Voronoi regions into shape descriptors
in the form of topological elements. Preferably, additional shape and/or property
descriptors are included in the classification method. The classification methods
generally are used to identify similarities between molecules that can be used
as property predictors for a variety of applications. Generally, the property
predictions are the basis for selection of compounds for incorporation into efficacy
evaluations.
applicant:
- Jie Liang, Herbert Edelsbrunner
article_processing_charge: No
author:
- first_name: Jie
full_name: Liang, Jie
last_name: Liang
- first_name: Herbert
full_name: Edelsbrunner, Herbert
id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
last_name: Edelsbrunner
orcid: 0000-0002-9823-6833
citation:
ama: Liang J, Edelsbrunner H. Molecular classification for property prediction.
2001.
apa: Liang, J., & Edelsbrunner, H. (2001). Molecular classification for property
prediction.
chicago: Liang, Jie, and Herbert Edelsbrunner. “Molecular Classification for Property
Prediction,” 2001.
ieee: J. Liang and H. Edelsbrunner, “Molecular classification for property prediction.”
2001.
ista: Liang J, Edelsbrunner H. 2001. Molecular classification for property prediction.
mla: Liang, Jie, and Herbert Edelsbrunner. Molecular Classification for Property
Prediction. 2001.
short: J. Liang, H. Edelsbrunner, (2001).
date_created: 2018-12-11T12:03:41Z
date_published: 2001-01-30T00:00:00Z
date_updated: 2022-01-05T15:12:42Z
day: '30'
extern: '1'
ipc: G16C20/70 ; G16B15/00
ipn: US6182016B1
main_file_link:
- open_access: '1'
url: https://patents.google.com/patent/US6182016B1
month: '01'
oa: 1
oa_version: Published Version
publication_date: 2001-01-30
publist_id: '2880'
status: public
title: Molecular classification for property prediction
type: patent
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2001'
...