---
_id: '11863'
abstract:
- lang: eng
text: "Suppose you buy a new laptop and, simply because you like it so much, you
recommend it to friends, encouraging them to purchase it as well. What would be
an adequate price for the vendor of the laptop to pay for your recommendation?\r\n\r\nPersonal
recommendations like this are of considerable commercial interest, but unlike
in sponsored search auctions there can be no truthful prices. Despite this \"lack
of truthfulness\" the vendor of the product might still decide to pay you for
recommendation e.g. because she wants to (i) provide you with an additional incentive
to actually recommend her or to (ii) increase your satisfaction and/or brand loyalty.
This leads us to investigate a pricing scheme based on the Shapley value [5] that
satisfies certain \"axioms of fairness\". We find that it is vulnerable to manipulations
and show how to overcome these difficulties using the anonymity-proof Shapley
value of [4]."
article_processing_charge: No
author:
- first_name: Paul
full_name: Dütting, Paul
last_name: Dütting
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Ingmar
full_name: Weber, Ingmar
last_name: Weber
citation:
ama: 'Dütting P, Henzinger MH, Weber I. How much is your personal recommendation
worth? In: Proceedings of the 19th International Conference on World Wide Web
. Association for Computing Machinery; 2010:1085-1086. doi:10.1145/1772690.1772816'
apa: 'Dütting, P., Henzinger, M. H., & Weber, I. (2010). How much is your personal
recommendation worth? In Proceedings of the 19th international conference on
World wide web (pp. 1085–1086). Raleigh, NC, United States: Association for
Computing Machinery. https://doi.org/10.1145/1772690.1772816'
chicago: Dütting, Paul, Monika H Henzinger, and Ingmar Weber. “How Much Is Your
Personal Recommendation Worth?” In Proceedings of the 19th International Conference
on World Wide Web , 1085–86. Association for Computing Machinery, 2010. https://doi.org/10.1145/1772690.1772816.
ieee: P. Dütting, M. H. Henzinger, and I. Weber, “How much is your personal recommendation
worth?,” in Proceedings of the 19th international conference on World wide
web , Raleigh, NC, United States, 2010, pp. 1085–1086.
ista: 'Dütting P, Henzinger MH, Weber I. 2010. How much is your personal recommendation
worth? Proceedings of the 19th international conference on World wide web . WWW:
International Conference on World Wide Web, 1085–1086.'
mla: Dütting, Paul, et al. “How Much Is Your Personal Recommendation Worth?” Proceedings
of the 19th International Conference on World Wide Web , Association for Computing
Machinery, 2010, pp. 1085–86, doi:10.1145/1772690.1772816.
short: P. Dütting, M.H. Henzinger, I. Weber, in:, Proceedings of the 19th International
Conference on World Wide Web , Association for Computing Machinery, 2010, pp.
1085–1086.
conference:
end_date: 2010-04-30
location: Raleigh, NC, United States
name: 'WWW: International Conference on World Wide Web'
start_date: 2010-04-26
date_created: 2022-08-16T09:00:41Z
date_published: 2010-04-01T00:00:00Z
date_updated: 2023-02-17T10:14:10Z
day: '01'
doi: 10.1145/1772690.1772816
extern: '1'
language:
- iso: eng
month: '04'
oa_version: None
page: 1085-1086
publication: 'Proceedings of the 19th international conference on World wide web '
publication_identifier:
isbn:
- '9781605587998'
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
scopus_import: '1'
status: public
title: How much is your personal recommendation worth?
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2010'
...
---
_id: '11885'
abstract:
- lang: eng
text: Over the last years the h-index has gained popularity as a measure for comparing
the impact of scientists. We investigate if ranking according to the h-index is
stable with respect to (i) different choices of citation databases, (ii) normalizing
citation counts by the number of authors or by removing self-citations, (iii)
small amounts of noise created by randomly removing citations or publications
and (iv) small changes in the definition of the index. In experiments for 5,283
computer scientists and 1,354 physicists we show that although the ranking of
the h-index is stable under most of these changes, it is unstable when different
databases are used. Therefore, comparisons based on the h-index should only be
trusted when the rankings of multiple citation databases agree.
article_processing_charge: No
article_type: original
author:
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Jacob
full_name: Suñol, Jacob
last_name: Suñol
- first_name: Ingmar
full_name: Weber, Ingmar
last_name: Weber
citation:
ama: Henzinger MH, Suñol J, Weber I. The stability of the h-index. Scientometrics.
2010;84(2):465-479. doi:10.1007/s11192-009-0098-7
apa: Henzinger, M. H., Suñol, J., & Weber, I. (2010). The stability of the h-index.
Scientometrics. Springer Nature. https://doi.org/10.1007/s11192-009-0098-7
chicago: Henzinger, Monika H, Jacob Suñol, and Ingmar Weber. “The Stability of the
H-Index.” Scientometrics. Springer Nature, 2010. https://doi.org/10.1007/s11192-009-0098-7.
ieee: M. H. Henzinger, J. Suñol, and I. Weber, “The stability of the h-index,” Scientometrics,
vol. 84, no. 2. Springer Nature, pp. 465–479, 2010.
ista: Henzinger MH, Suñol J, Weber I. 2010. The stability of the h-index. Scientometrics.
84(2), 465–479.
mla: Henzinger, Monika H., et al. “The Stability of the H-Index.” Scientometrics,
vol. 84, no. 2, Springer Nature, 2010, pp. 465–79, doi:10.1007/s11192-009-0098-7.
short: M.H. Henzinger, J. Suñol, I. Weber, Scientometrics 84 (2010) 465–479.
date_created: 2022-08-17T07:51:23Z
date_published: 2010-08-01T00:00:00Z
date_updated: 2023-02-17T14:09:51Z
day: '01'
doi: 10.1007/s11192-009-0098-7
extern: '1'
intvolume: ' 84'
issue: '2'
language:
- iso: eng
month: '08'
oa_version: None
page: 465-479
publication: Scientometrics
publication_identifier:
eissn:
- 1588-2861
issn:
- 0138-9130
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: The stability of the h-index
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 84
year: '2010'
...
---
_id: '11975'
abstract:
- lang: eng
text: A new method was developed for the quantitative analysis of steryl glycosides
in biodiesel (fatty acid methyl esters). This method is much more sensitive than
existing methods and has minimum limits of quantification of 50 μg/kg, compared
to previously published minimum limits of quantification of about 15 mg/kg. The
analysis is based on gas chromatography–mass spectroscopy determination of simple
pre-treated and silylated samples via single ion monitoring at 147, 204, 217 m/z,
which are specific ions for the silylated sugar moiety. Quantification was carried
out using cholesteryl β-d-glucopyranoside as internal standard. The modified synthesis
and purification of the internal standard is also presented as well as the characterization
by NMR and mass spectroscopy. The advantage of the method compared with other
approaches is the simplified sample preparation avoiding extra pre-treatment steps
coupled with complete derivatization of the sugar hydroxyl groups by using N,O-bis(trimethylsilyl)acetamide
with 5% trimethylchlorosilane as derivatization reagent. On the given conditions
high recovery rates ≥89% can be obtained. Evaluation of lab specific variance
and intermediate precision underline the robustness of the method which will be
further assessed by Round robin tests.
article_processing_charge: No
article_type: original
author:
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Sigurd
full_name: Schober, Sigurd
last_name: Schober
- first_name: Christoph
full_name: Goebl, Christoph
last_name: Goebl
- first_name: Martin
full_name: Mittelbach, Martin
last_name: Mittelbach
citation:
ama: Pieber B, Schober S, Goebl C, Mittelbach M. Novel sensitive determination of
steryl glycosides in biodiesel by gas chromatography-mass spectroscopy. Journal
of Chromatography A. 2010;1217(42):6555-6561. doi:10.1016/j.chroma.2010.08.006
apa: Pieber, B., Schober, S., Goebl, C., & Mittelbach, M. (2010). Novel sensitive
determination of steryl glycosides in biodiesel by gas chromatography-mass spectroscopy.
Journal of Chromatography A. Elsevier. https://doi.org/10.1016/j.chroma.2010.08.006
chicago: Pieber, Bartholomäus, Sigurd Schober, Christoph Goebl, and Martin Mittelbach.
“Novel Sensitive Determination of Steryl Glycosides in Biodiesel by Gas Chromatography-Mass
Spectroscopy.” Journal of Chromatography A. Elsevier, 2010. https://doi.org/10.1016/j.chroma.2010.08.006.
ieee: B. Pieber, S. Schober, C. Goebl, and M. Mittelbach, “Novel sensitive determination
of steryl glycosides in biodiesel by gas chromatography-mass spectroscopy,” Journal
of Chromatography A, vol. 1217, no. 42. Elsevier, pp. 6555–6561, 2010.
ista: Pieber B, Schober S, Goebl C, Mittelbach M. 2010. Novel sensitive determination
of steryl glycosides in biodiesel by gas chromatography-mass spectroscopy. Journal
of Chromatography A. 1217(42), 6555–6561.
mla: Pieber, Bartholomäus, et al. “Novel Sensitive Determination of Steryl Glycosides
in Biodiesel by Gas Chromatography-Mass Spectroscopy.” Journal of Chromatography
A, vol. 1217, no. 42, Elsevier, 2010, pp. 6555–61, doi:10.1016/j.chroma.2010.08.006.
short: B. Pieber, S. Schober, C. Goebl, M. Mittelbach, Journal of Chromatography
A 1217 (2010) 6555–6561.
date_created: 2022-08-25T10:43:43Z
date_published: 2010-10-15T00:00:00Z
date_updated: 2023-02-21T10:09:59Z
day: '15'
doi: 10.1016/j.chroma.2010.08.006
extern: '1'
external_id:
pmid:
- '20846658'
intvolume: ' 1217'
issue: '42'
language:
- iso: eng
month: '10'
oa_version: None
page: 6555-6561
pmid: 1
publication: Journal of Chromatography A
publication_identifier:
issn:
- 0021-9673
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Novel sensitive determination of steryl glycosides in biodiesel by gas chromatography-mass
spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 1217
year: '2010'
...
---
_id: '12199'
abstract:
- lang: eng
text: The four microsporangia of the flowering plant anther develop from archesporial
cells in the L2 of the primordium. Within each microsporangium, developing microsporocytes
are surrounded by concentric monolayers of tapetal, middle layer and endothecial
cells. How this intricate array of tissues, each containing relatively few cells,
is established in an organ possessing no formal meristems is poorly understood.
We describe here the pivotal role of the LRR receptor kinase EXCESS MICROSPOROCYTES
1 (EMS1) in forming the monolayer of tapetal nurse cells in Arabidopsis. Unusually
for plants, tapetal cells are specified very early in development, and are subsequently
stimulated to proliferate by a receptor-like kinase (RLK) complex that includes
EMS1. Mutations in members of this EMS1 signalling complex and its putative ligand
result in male-sterile plants in which tapetal initials fail to proliferate. Surprisingly,
these cells continue to develop, isolated at the locular periphery. Mutant and
wild-type microsporangia expand at similar rates and the ‘tapetal’ space at the
periphery of mutant locules becomes occupied by microsporocytes. However, induction
of late expression of EMS1 in the few tapetal initials in ems1 plants results
in their proliferation to generate a functional tapetum, and this proliferation
suppresses microsporocyte number. Our experiments also show that integrity of
the tapetal monolayer is crucial for the maintenance of the polarity of divisions
within it. This unexpected autonomy of the tapetal ‘lineage’ is discussed in the
context of tissue development in complex plant organs, where constancy in size,
shape and cell number is crucial.
acknowledgement: 'We thank the following for providing mutant lines and reagents:
Hong Ma, De Ye, Sacco De Vries, and Rod Scott for providing the pA9::Barnase lines
and information on A9 expression patterns. Carla Galinha and Paolo Piazza gave valuable
help with in situ hybridisation and qRT-PCR, respectively, and we acknowledge Qing
Zhang, Helen Prescott and Matthew Dicks for providing excellent technical assistance.
We are indebted to Miltos Tsiantis and Angela Hay for helpful discussion, and the
research was funded by Oxford University through a Clarendon Scholarship to X.F.,
with additional financial support from Magdalen College (Oxford).'
article_processing_charge: No
article_type: original
author:
- first_name: Xiaoqi
full_name: Feng, Xiaoqi
id: e0164712-22ee-11ed-b12a-d80fcdf35958
last_name: Feng
orcid: 0000-0002-4008-1234
- first_name: Hugh G.
full_name: Dickinson, Hugh G.
last_name: Dickinson
citation:
ama: Feng X, Dickinson HG. Tapetal cell fate, lineage and proliferation in the Arabidopsis
anther. Development. 2010;137(14):2409-2416. doi:10.1242/dev.049320
apa: Feng, X., & Dickinson, H. G. (2010). Tapetal cell fate, lineage and proliferation
in the Arabidopsis anther. Development. The Company of Biologists. https://doi.org/10.1242/dev.049320
chicago: Feng, Xiaoqi, and Hugh G. Dickinson. “Tapetal Cell Fate, Lineage and Proliferation
in the Arabidopsis Anther.” Development. The Company of Biologists, 2010.
https://doi.org/10.1242/dev.049320.
ieee: X. Feng and H. G. Dickinson, “Tapetal cell fate, lineage and proliferation
in the Arabidopsis anther,” Development, vol. 137, no. 14. The Company
of Biologists, pp. 2409–2416, 2010.
ista: Feng X, Dickinson HG. 2010. Tapetal cell fate, lineage and proliferation in
the Arabidopsis anther. Development. 137(14), 2409–2416.
mla: Feng, Xiaoqi, and Hugh G. Dickinson. “Tapetal Cell Fate, Lineage and Proliferation
in the Arabidopsis Anther.” Development, vol. 137, no. 14, The Company
of Biologists, 2010, pp. 2409–16, doi:10.1242/dev.049320.
short: X. Feng, H.G. Dickinson, Development 137 (2010) 2409–2416.
date_created: 2023-01-16T09:21:54Z
date_published: 2010-07-15T00:00:00Z
date_updated: 2023-05-08T10:57:11Z
day: '15'
department:
- _id: XiFe
doi: 10.1242/dev.049320
extern: '1'
external_id:
pmid:
- '20570940'
intvolume: ' 137'
issue: '14'
keyword:
- Developmental Biology
- Molecular Biology
- Anther Tapetum
- Arabidopsis
- Cell Fate Establishment
- EMS1
- Reproductive Cell Lineage
language:
- iso: eng
month: '07'
oa_version: None
page: 2409-2416
pmid: 1
publication: Development
publication_identifier:
issn:
- 1477-9129
- 0950-1991
publication_status: published
publisher: The Company of Biologists
quality_controlled: '1'
scopus_import: '1'
status: public
title: Tapetal cell fate, lineage and proliferation in the Arabidopsis anther
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 137
year: '2010'
...
---
_id: '12200'
abstract:
- lang: eng
text: Key steps in the evolution of the angiosperm anther include the patterning
of the concentrically organized microsporangium and the incorporation of four
such microsporangia into a leaf-like structure. Mutant studies in the model plant
Arabidopsis thaliana are leading to an increasingly accurate picture of (i) the
cell lineages culminating in the different cell types present in the microsporangium
(the microsporocytes, the tapetum, and the middle and endothecial layers), and
(ii) some of the genes responsible for specifying their fates. However, the processes
that confer polarity on the developing anther and position the microsporangia
within it remain unclear. Certainly, data from a range of experimental strategies
suggest that hormones play a central role in establishing polarity and the patterning
of the anther initial, and may be responsible for locating the microsporangia.
But the fact that microsporangia were originally positioned externally suggests
that their development is likely to be autonomous, perhaps with the reproductive
cells generating signals controlling the growth and division of the investing
anther epidermis. These possibilities are discussed in the context of the expression
of genes which initiate and maintain male and female reproductive development,
and in the perspective of our current views of anther evolution.
article_processing_charge: No
article_type: original
author:
- first_name: Xiaoqi
full_name: Feng, Xiaoqi
id: e0164712-22ee-11ed-b12a-d80fcdf35958
last_name: Feng
orcid: 0000-0002-4008-1234
- first_name: Hugh G.
full_name: Dickinson, Hugh G.
last_name: Dickinson
citation:
ama: Feng X, Dickinson HG. Cell–cell interactions during patterning of the Arabidopsis
anther. Biochemical Society Transactions. 2010;38(2):571-576. doi:10.1042/bst0380571
apa: Feng, X., & Dickinson, H. G. (2010). Cell–cell interactions during patterning
of the Arabidopsis anther. Biochemical Society Transactions. Portland
Press Ltd. https://doi.org/10.1042/bst0380571
chicago: Feng, Xiaoqi, and Hugh G. Dickinson. “Cell–Cell Interactions during Patterning
of the Arabidopsis Anther.” Biochemical Society Transactions. Portland
Press Ltd., 2010. https://doi.org/10.1042/bst0380571.
ieee: X. Feng and H. G. Dickinson, “Cell–cell interactions during patterning of
the Arabidopsis anther,” Biochemical Society Transactions, vol.
38, no. 2. Portland Press Ltd., pp. 571–576, 2010.
ista: Feng X, Dickinson HG. 2010. Cell–cell interactions during patterning of the
Arabidopsis anther. Biochemical Society Transactions. 38(2), 571–576.
mla: Feng, Xiaoqi, and Hugh G. Dickinson. “Cell–Cell Interactions during Patterning
of the Arabidopsis Anther.” Biochemical Society Transactions, vol.
38, no. 2, Portland Press Ltd., 2010, pp. 571–76, doi:10.1042/bst0380571.
short: X. Feng, H.G. Dickinson, Biochemical Society Transactions 38 (2010) 571–576.
date_created: 2023-01-16T09:22:18Z
date_published: 2010-03-22T00:00:00Z
date_updated: 2023-05-08T10:57:59Z
day: '22'
department:
- _id: XiFe
doi: 10.1042/bst0380571
extern: '1'
external_id:
pmid:
- '20298223'
intvolume: ' 38'
issue: '2'
keyword:
- Biochemistry
- Anther Development
- Arabidopsis
- Cell Fate
- Microsporangium
- Polarity
- Receptor Kinase
language:
- iso: eng
month: '03'
oa_version: None
page: 571-576
pmid: 1
publication: Biochemical Society Transactions
publication_identifier:
issn:
- 0300-5127
- 1470-8752
publication_status: published
publisher: Portland Press Ltd.
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cell–cell interactions during patterning of the Arabidopsis anther
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 38
year: '2010'
...
---
_id: '12653'
abstract:
- lang: eng
text: 'Daily streamflow from stations close to five Swiss glaciers is analyzed for
trends with the Mann-Kendall test. We consider a common period of record (1974–2004)
and longer periods based on data availability. The trend statistical significance
is tested on annual and seasonal bases. We also examine changes in precipitation,
temperature, and snow cover characteristics. Highly glacierized basins show statistically
significant positive trends in annual streamflow caused by increasing streamflow
in spring and summer. Trends are more numerous and stronger at lower and mid than
at the upper quantiles. The basin characterized by lower glacier coverage, conversely,
does not exhibit consistently statistically significant trends. Changes in precipitation
are not sufficient to explain the observed streamflow trends. Air temperature
sees an increase in mean, minimum, and maximum values at all sites. Variations
in the seasonal snow accumulation and ablation process are evident. Solid precipitation
is decreasing at all sites and trends may be due to a shift from snowfall into
rainfall. Mean snow depth is also decreasing, and its duration is getting shorter
because of a decrease in solid precipitation and enhanced melting. Trend magnitude
attenuates with longer time series. Contrasting trends are detected for different
subperiods in the last 70 years: statistically significant negative trends are
observed in the periods 1944–1974 and 1954–1984 for Aletschgletscher, in contrast
with the results for the common period. These trends are explained by different
rates of ice volume changes, and the sign of trends is clearly related to phases
of positive or negative glacier mass balance.'
article_number: W10522
article_processing_charge: No
article_type: original
author:
- first_name: Francesca
full_name: Pellicciotti, Francesca
id: b28f055a-81ea-11ed-b70c-a9fe7f7b0e70
last_name: Pellicciotti
- first_name: A.
full_name: Bauder, A.
last_name: Bauder
- first_name: M.
full_name: Parola, M.
last_name: Parola
citation:
ama: Pellicciotti F, Bauder A, Parola M. Effect of glaciers on streamflow trends
in the Swiss Alps. Water Resources Research. 2010;46(10). doi:10.1029/2009wr009039
apa: Pellicciotti, F., Bauder, A., & Parola, M. (2010). Effect of glaciers on
streamflow trends in the Swiss Alps. Water Resources Research. American
Geophysical Union. https://doi.org/10.1029/2009wr009039
chicago: Pellicciotti, Francesca, A. Bauder, and M. Parola. “Effect of Glaciers
on Streamflow Trends in the Swiss Alps.” Water Resources Research. American
Geophysical Union, 2010. https://doi.org/10.1029/2009wr009039.
ieee: F. Pellicciotti, A. Bauder, and M. Parola, “Effect of glaciers on streamflow
trends in the Swiss Alps,” Water Resources Research, vol. 46, no. 10. American
Geophysical Union, 2010.
ista: Pellicciotti F, Bauder A, Parola M. 2010. Effect of glaciers on streamflow
trends in the Swiss Alps. Water Resources Research. 46(10), W10522.
mla: Pellicciotti, Francesca, et al. “Effect of Glaciers on Streamflow Trends in
the Swiss Alps.” Water Resources Research, vol. 46, no. 10, W10522, American
Geophysical Union, 2010, doi:10.1029/2009wr009039.
short: F. Pellicciotti, A. Bauder, M. Parola, Water Resources Research 46 (2010).
date_created: 2023-02-20T08:18:27Z
date_published: 2010-10-01T00:00:00Z
date_updated: 2023-02-20T09:39:29Z
day: '01'
doi: 10.1029/2009wr009039
extern: '1'
intvolume: ' 46'
issue: '10'
keyword:
- Water Science and Technology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1029/2009WR009039
month: '10'
oa: 1
oa_version: Published Version
publication: Water Resources Research
publication_identifier:
eissn:
- 1944-7973
issn:
- 0043-1397
publication_status: published
publisher: American Geophysical Union
quality_controlled: '1'
scopus_import: '1'
status: public
title: Effect of glaciers on streamflow trends in the Swiss Alps
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 46
year: '2010'
...
---
_id: '1300'
abstract:
- lang: eng
text: 'Motion vision is a major function of all visual systems, yet the underlying
neural mechanisms and circuits are still elusive. In the lamina, the first optic
neuropile of Drosophila melanogaster, photoreceptor signals split into five parallel
pathways, L1-L5. Here we examine how these pathways contribute to visual motion
detection by combining genetic block and reconstitution of neural activity in
different lamina cell types with whole-cell recordings from downstream motion-sensitive
neurons. We find reduced responses to moving gratings if L1 or L2 is blocked;
however, reconstitution of photoreceptor input to only L1 or L2 results in wild-type
responses. Thus, the first experiment indicates the necessity of both pathways,
whereas the second indicates sufficiency of each single pathway. This contradiction
can be explained by electrical coupling between L1 and L2, allowing for activation
of both pathways even when only one of them receives photoreceptor input. A fundamental
difference between the L1 pathway and the L2 pathway is uncovered when blocking
L1 or L2 output while presenting moving edges of positive (ON) or negative (OFF)
contrast polarity: blocking L1 eliminates the response to moving ON edges, whereas
blocking L2 eliminates the response to moving OFF edges. Thus, similar to the
segregation of photoreceptor signals in ON and OFF bipolar cell pathways in the
vertebrate retina, photoreceptor signals segregate into ON-L1 and OFF-L2 channels
in the lamina of Drosophila.'
author:
- first_name: Maximilian A
full_name: Maximilian Jösch
id: 2BD278E6-F248-11E8-B48F-1D18A9856A87
last_name: Jösch
orcid: 0000-0002-3937-1330
- first_name: Bettina
full_name: Schnell, Bettina
last_name: Schnell
- first_name: Shamprasad
full_name: Raghu, Shamprasad V
last_name: Raghu
- first_name: Dierk
full_name: Reiff, Dierk F
last_name: Reiff
- first_name: Alexander
full_name: Borst, Alexander
last_name: Borst
citation:
ama: Jösch MA, Schnell B, Raghu S, Reiff D, Borst A. ON and off pathways in Drosophila
motion vision. Nature. 2010;468(7321):300-304. doi:10.1038/nature09545
apa: Jösch, M. A., Schnell, B., Raghu, S., Reiff, D., & Borst, A. (2010). ON
and off pathways in Drosophila motion vision. Nature. Nature Publishing
Group. https://doi.org/10.1038/nature09545
chicago: Jösch, Maximilian A, Bettina Schnell, Shamprasad Raghu, Dierk Reiff, and
Alexander Borst. “ON and off Pathways in Drosophila Motion Vision.” Nature.
Nature Publishing Group, 2010. https://doi.org/10.1038/nature09545.
ieee: M. A. Jösch, B. Schnell, S. Raghu, D. Reiff, and A. Borst, “ON and off pathways
in Drosophila motion vision,” Nature, vol. 468, no. 7321. Nature Publishing
Group, pp. 300–304, 2010.
ista: Jösch MA, Schnell B, Raghu S, Reiff D, Borst A. 2010. ON and off pathways
in Drosophila motion vision. Nature. 468(7321), 300–304.
mla: Jösch, Maximilian A., et al. “ON and off Pathways in Drosophila Motion Vision.”
Nature, vol. 468, no. 7321, Nature Publishing Group, 2010, pp. 300–04,
doi:10.1038/nature09545.
short: M.A. Jösch, B. Schnell, S. Raghu, D. Reiff, A. Borst, Nature 468 (2010) 300–304.
date_created: 2018-12-11T11:51:14Z
date_published: 2010-11-11T00:00:00Z
date_updated: 2021-01-12T06:49:44Z
day: '11'
doi: 10.1038/nature09545
extern: 1
intvolume: ' 468'
issue: '7321'
month: '11'
page: 300 - 304
publication: Nature
publication_status: published
publisher: Nature Publishing Group
publist_id: '5970'
quality_controlled: 0
status: public
title: ON and off pathways in Drosophila motion vision
type: journal_article
volume: 468
year: '2010'
...
---
_id: '1301'
abstract:
- lang: eng
text: Motion vision is essential for navigating through the environment. Due to
its genetic amenability, the fruit fly Drosophila has been serving for a lengthy
period as a model organism for studying optomotor behavior as elicited by large-field
horizontal motion. However, the neurons underlying the control of this behavior
have not been studied in Drosophila so far. Here we report the first whole cell
recordings from three cells of the horizontal system (HSN, HSE, and HSS) in the
lobula plate of Drosophila. All three HS cells are tuned to large-field horizontal
motion in a direction-selective way; they become excited by front-to-back motion
and inhibited by back-to-front motion in the ipsilateral field of view. The response
properties of HS cells such as contrast and velocity dependence are in accordance
with the correlation-type model of motion detection. Neurobiotin injection suggests
extensive coupling among ipsilateral HS cells and additional coupling to tangential
cells that have their dendrites in the contralateral hemisphere of the brain.
This connectivity scheme accounts for the complex layout of their receptive fields
and explains their sensitivity both to ipsilateral and to contralateral motion.
Thus the main response properties of Drosophila HS cells are strikingly similar
to the responses of their counterparts in the blowfly Calliphora, although we
found substantial differences with respect to their dendritic structure and connectivity.
This long-awaited functional characterization of HS cells in Drosophila provides
the basis for the future dissection of optomotor behavior and the underlying neural
circuitry by combining genetics, physiology, and behavior.
acknowledgement: This work was supported by the Max-Planck-Society and by a Human
Frontier Science Program grant to K. Ito, A. Borst, and B. Nelson.
article_processing_charge: No
article_type: original
author:
- first_name: Bettina
full_name: Schnell, Bettina
last_name: Schnell
- first_name: Maximilian A
full_name: Jösch, Maximilian A
id: 2BD278E6-F248-11E8-B48F-1D18A9856A87
last_name: Jösch
orcid: 0000-0002-3937-1330
- first_name: Friedrich
full_name: Förstner, Friedrich
last_name: Förstner
- first_name: Shamprasad
full_name: Raghu, Shamprasad
last_name: Raghu
- first_name: Hideo
full_name: Otsuna, Hideo
last_name: Otsuna
- first_name: Kei
full_name: Ito, Kei
last_name: Ito
- first_name: Alexander
full_name: Borst, Alexander
last_name: Borst
- first_name: Dierk
full_name: Reiff, Dierk
last_name: Reiff
citation:
ama: Schnell B, Jösch MA, Förstner F, et al. Processing of horizontal optic flow
in three visual interneurons of the Drosophila brain. Journal of Neurophysiology.
2010;103(3):1646-1657. doi:10.1152/jn.00950.2009
apa: Schnell, B., Jösch, M. A., Förstner, F., Raghu, S., Otsuna, H., Ito, K., …
Reiff, D. (2010). Processing of horizontal optic flow in three visual interneurons
of the Drosophila brain. Journal of Neurophysiology. American Physiological
Society. https://doi.org/10.1152/jn.00950.2009
chicago: Schnell, Bettina, Maximilian A Jösch, Friedrich Förstner, Shamprasad Raghu,
Hideo Otsuna, Kei Ito, Alexander Borst, and Dierk Reiff. “Processing of Horizontal
Optic Flow in Three Visual Interneurons of the Drosophila Brain.” Journal of
Neurophysiology. American Physiological Society, 2010. https://doi.org/10.1152/jn.00950.2009.
ieee: B. Schnell et al., “Processing of horizontal optic flow in three visual
interneurons of the Drosophila brain,” Journal of Neurophysiology, vol.
103, no. 3. American Physiological Society, pp. 1646–1657, 2010.
ista: Schnell B, Jösch MA, Förstner F, Raghu S, Otsuna H, Ito K, Borst A, Reiff
D. 2010. Processing of horizontal optic flow in three visual interneurons of the
Drosophila brain. Journal of Neurophysiology. 103(3), 1646–1657.
mla: Schnell, Bettina, et al. “Processing of Horizontal Optic Flow in Three Visual
Interneurons of the Drosophila Brain.” Journal of Neurophysiology, vol.
103, no. 3, American Physiological Society, 2010, pp. 1646–57, doi:10.1152/jn.00950.2009.
short: B. Schnell, M.A. Jösch, F. Förstner, S. Raghu, H. Otsuna, K. Ito, A. Borst,
D. Reiff, Journal of Neurophysiology 103 (2010) 1646–1657.
date_created: 2018-12-11T11:51:14Z
date_published: 2010-03-01T00:00:00Z
date_updated: 2021-01-12T06:49:44Z
day: '01'
doi: 10.1152/jn.00950.2009
extern: '1'
external_id:
pmid:
- '20089816'
intvolume: ' 103'
issue: '3'
language:
- iso: eng
month: '03'
oa_version: None
page: 1646 - 1657
pmid: 1
publication: Journal of Neurophysiology
publication_identifier:
eissn:
- 1522-1598
issn:
- ' 0022-3077'
publication_status: published
publisher: American Physiological Society
publist_id: '5971'
quality_controlled: '1'
status: public
title: Processing of horizontal optic flow in three visual interneurons of the Drosophila
brain
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 103
year: '2010'
...
---
_id: '9764'
article_processing_charge: No
author:
- first_name: Ulises
full_name: Rosas, Ulises
last_name: Rosas
- first_name: Nicholas H
full_name: Barton, Nicholas H
id: 4880FE40-F248-11E8-B48F-1D18A9856A87
last_name: Barton
orcid: 0000-0002-8548-5240
- first_name: Lucy
full_name: Copsey, Lucy
last_name: Copsey
- first_name: Pierre
full_name: Barbier De Reuille, Pierre
last_name: Barbier De Reuille
- first_name: Enrico
full_name: Coen, Enrico
last_name: Coen
citation:
ama: Rosas U, Barton NH, Copsey L, Barbier De Reuille P, Coen E. Heterosis and the
drift load. 2010. doi:10.1371/journal.pbio.1000429.s003
apa: Rosas, U., Barton, N. H., Copsey, L., Barbier De Reuille, P., & Coen, E.
(2010). Heterosis and the drift load. Public Library of Science. https://doi.org/10.1371/journal.pbio.1000429.s003
chicago: Rosas, Ulises, Nicholas H Barton, Lucy Copsey, Pierre Barbier De Reuille,
and Enrico Coen. “Heterosis and the Drift Load.” Public Library of Science, 2010.
https://doi.org/10.1371/journal.pbio.1000429.s003.
ieee: U. Rosas, N. H. Barton, L. Copsey, P. Barbier De Reuille, and E. Coen, “Heterosis
and the drift load.” Public Library of Science, 2010.
ista: Rosas U, Barton NH, Copsey L, Barbier De Reuille P, Coen E. 2010. Heterosis
and the drift load, Public Library of Science, 10.1371/journal.pbio.1000429.s003.
mla: Rosas, Ulises, et al. Heterosis and the Drift Load. Public Library of
Science, 2010, doi:10.1371/journal.pbio.1000429.s003.
short: U. Rosas, N.H. Barton, L. Copsey, P. Barbier De Reuille, E. Coen, (2010).
date_created: 2021-08-02T09:45:39Z
date_published: 2010-07-20T00:00:00Z
date_updated: 2023-02-23T11:42:17Z
day: '20'
department:
- _id: NiBa
doi: 10.1371/journal.pbio.1000429.s003
month: '07'
oa_version: Published Version
publisher: Public Library of Science
related_material:
record:
- id: '3779'
relation: used_in_publication
status: public
status: public
title: Heterosis and the drift load
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2010'
...
---
_id: '3402'
abstract:
- lang: eng
text: Model checking transactional memories (TMs) is difficult because of the unbounded
number, length, and delay of concurrent transactions, as well as the unbounded
size of the memory. We show that, under certain conditions satisfied by most TMs
we know of, the model checking problem can be reduced to a finite-state problem,
and we illustrate the use of the method by proving the correctness of several
TMs, including two-phase locking, DSTM, and TL2. The safety properties we consider
include strict serializability and opacity; the liveness properties include obstruction
freedom, livelock freedom, and wait freedom. Our main contribution lies in the
structure of the proofs, which are largely automated and not restricted to the
TMs mentioned above. In a first step we show that every TM that enjoys certain
structural properties either violates a requirement on some program with two threads
and two shared variables, or satisfies the requirement on all programs. In the
second step, we use a model checker to prove the requirement for the TM applied
to a most general program with two threads and two variables. In the safety case,
the model checker checks language inclusion between two finite-state transition
systems, a nondeterministic transition system representing the given TM applied
to a most general program, and a deterministic transition system representing
a most liberal safe TM applied to the same program. The given TM transition system
is nondeterministic because a TM can be used with different contention managers,
which resolve conflicts differently. In the liveness case, the model checker analyzes
fairness conditions on the given TM transition system.
acknowledgement: This research was supported by the Swiss National Science Foundation.
This paper is an extended and revised version of our previous work on model checking
transactional memories.
author:
- first_name: Rachid
full_name: Guerraoui, Rachid
last_name: Guerraoui
- first_name: Thomas A
full_name: Thomas Henzinger
id: 40876CD8-F248-11E8-B48F-1D18A9856A87
last_name: Henzinger
orcid: 0000−0002−2985−7724
- first_name: Vasu
full_name: Vasu Singh
id: 4DAE2708-F248-11E8-B48F-1D18A9856A87
last_name: Singh
citation:
ama: Guerraoui R, Henzinger TA, Singh V. Model checking transactional memories.
Distributed Computing. 2010;22(3):129-145. doi:10.1007/s00446-009-0092-6
apa: Guerraoui, R., Henzinger, T. A., & Singh, V. (2010). Model checking transactional
memories. Distributed Computing. Springer. https://doi.org/10.1007/s00446-009-0092-6
chicago: Guerraoui, Rachid, Thomas A Henzinger, and Vasu Singh. “Model Checking
Transactional Memories.” Distributed Computing. Springer, 2010. https://doi.org/10.1007/s00446-009-0092-6.
ieee: R. Guerraoui, T. A. Henzinger, and V. Singh, “Model checking transactional
memories,” Distributed Computing, vol. 22, no. 3. Springer, pp. 129–145,
2010.
ista: Guerraoui R, Henzinger TA, Singh V. 2010. Model checking transactional memories.
Distributed Computing. 22(3), 129–145.
mla: Guerraoui, Rachid, et al. “Model Checking Transactional Memories.” Distributed
Computing, vol. 22, no. 3, Springer, 2010, pp. 129–45, doi:10.1007/s00446-009-0092-6.
short: R. Guerraoui, T.A. Henzinger, V. Singh, Distributed Computing 22 (2010) 129–145.
date_created: 2018-12-11T12:03:08Z
date_published: 2010-03-01T00:00:00Z
date_updated: 2021-01-12T07:43:14Z
day: '01'
doi: 10.1007/s00446-009-0092-6
extern: 1
intvolume: ' 22'
issue: '3'
main_file_link:
- open_access: '0'
url: http://infoscience.epfl.ch/record/117513/files/PLDI_paper.pdf
month: '03'
page: 129 - 145
publication: Distributed Computing
publication_status: published
publisher: Springer
publist_id: '3000'
pubrep_id: '74'
quality_controlled: 0
status: public
title: Model checking transactional memories
type: journal_article
volume: 22
year: '2010'
...
---
_id: '3403'
abstract:
- lang: eng
text: Rate remapping is a conjunctive code that potentially enables hippocampal
place cells to jointly represent spatial and nonspatial information. In this issue
of Neuron, Rennó-Costa et al. introduce a theoretical model wherein the convergence
of the medial and lateral entorhinal excitatory inputs, combined with local inhibition,
explains hippocampal rate remapping. © 2010 Elsevier Inc.
author:
- first_name: Barty
full_name: Pleydell-Bouverie, Barty
last_name: Pleydell Bouverie
- first_name: Jozsef L
full_name: Jozsef Csicsvari
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
citation:
ama: 'Pleydell Bouverie B, Csicsvari JL. Rate remapping: When the code goes beyond
space (preview). Neuron. 2010;68(6):1015-1016. doi:10.1016/j.neuron.2010.12.011'
apa: 'Pleydell Bouverie, B., & Csicsvari, J. L. (2010). Rate remapping: When
the code goes beyond space (preview). Neuron. Elsevier. https://doi.org/10.1016/j.neuron.2010.12.011'
chicago: 'Pleydell Bouverie, Barty, and Jozsef L Csicsvari. “Rate Remapping: When
the Code Goes beyond Space (Preview).” Neuron. Elsevier, 2010. https://doi.org/10.1016/j.neuron.2010.12.011.'
ieee: 'B. Pleydell Bouverie and J. L. Csicsvari, “Rate remapping: When the code
goes beyond space (preview),” Neuron, vol. 68, no. 6. Elsevier, pp. 1015–1016,
2010.'
ista: 'Pleydell Bouverie B, Csicsvari JL. 2010. Rate remapping: When the code goes
beyond space (preview). Neuron. 68(6), 1015–1016.'
mla: 'Pleydell Bouverie, Barty, and Jozsef L. Csicsvari. “Rate Remapping: When the
Code Goes beyond Space (Preview).” Neuron, vol. 68, no. 6, Elsevier, 2010,
pp. 1015–16, doi:10.1016/j.neuron.2010.12.011.'
short: B. Pleydell Bouverie, J.L. Csicsvari, Neuron 68 (2010) 1015–1016.
date_created: 2018-12-11T12:03:08Z
date_published: 2010-12-22T00:00:00Z
date_updated: 2019-05-10T12:19:51Z
day: '22'
doi: 10.1016/j.neuron.2010.12.011
extern: 1
intvolume: ' 68'
issue: '6'
month: '12'
page: 1015 - 1016
publication: Neuron
publication_status: published
publisher: Elsevier
publist_id: '2999'
quality_controlled: 0
status: public
title: 'Rate remapping: When the code goes beyond space (preview)'
type: review
volume: 68
year: '2010'
...
---
_id: '3406'
abstract:
- lang: eng
text: The impact of structural biology on the design of ligands (agonists, antagonists
and modulators) for ionotropic glutamate receptors is reviewed.
author:
- first_name: Philipp
full_name: Stawski, Philipp
last_name: Stawski
- first_name: Harald L
full_name: Harald Janovjak
id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
last_name: Janovjak
orcid: 0000-0002-8023-9315
- first_name: Dirk
full_name: Trauner, Dirk
last_name: Trauner
citation:
ama: 'Stawski P, Janovjak HL, Trauner D. Pharmacology of ionotropic glutamate receptors:
a structural perspective. Bioorganic and Medicinal Chemistry. 2010;18(22):7759-7772.
doi:10.1016/j.bmc.2010.09.012'
apa: 'Stawski, P., Janovjak, H. L., & Trauner, D. (2010). Pharmacology of ionotropic
glutamate receptors: a structural perspective. Bioorganic and Medicinal Chemistry.
Elsevier. https://doi.org/10.1016/j.bmc.2010.09.012'
chicago: 'Stawski, Philipp, Harald L Janovjak, and Dirk Trauner. “Pharmacology of
Ionotropic Glutamate Receptors: A Structural Perspective.” Bioorganic and Medicinal
Chemistry. Elsevier, 2010. https://doi.org/10.1016/j.bmc.2010.09.012.'
ieee: 'P. Stawski, H. L. Janovjak, and D. Trauner, “Pharmacology of ionotropic glutamate
receptors: a structural perspective,” Bioorganic and Medicinal Chemistry,
vol. 18, no. 22. Elsevier, pp. 7759–7772, 2010.'
ista: 'Stawski P, Janovjak HL, Trauner D. 2010. Pharmacology of ionotropic glutamate
receptors: a structural perspective. Bioorganic and Medicinal Chemistry. 18(22),
7759–7772.'
mla: 'Stawski, Philipp, et al. “Pharmacology of Ionotropic Glutamate Receptors:
A Structural Perspective.” Bioorganic and Medicinal Chemistry, vol. 18,
no. 22, Elsevier, 2010, pp. 7759–72, doi:10.1016/j.bmc.2010.09.012.'
short: P. Stawski, H.L. Janovjak, D. Trauner, Bioorganic and Medicinal Chemistry
18 (2010) 7759–7772.
date_created: 2018-12-11T12:03:10Z
date_published: 2010-11-15T00:00:00Z
date_updated: 2019-04-26T07:22:27Z
day: '15'
doi: 10.1016/j.bmc.2010.09.012
extern: 1
intvolume: ' 18'
issue: '22'
month: '11'
page: 7759 - 7772
publication: Bioorganic and Medicinal Chemistry
publication_status: published
publisher: Elsevier
publist_id: '2996'
quality_controlled: 0
status: public
title: 'Pharmacology of ionotropic glutamate receptors: a structural perspective'
type: review
volume: 18
year: '2010'
...
---
_id: '3407'
abstract:
- lang: eng
text: Genetically targeted light-activated ion channels and pumps make it possible
to determine the role of specific neurons in neuronal circuits, information processing
and behavior. We developed a K+-selective ionotropic glutamate receptor that reversibly
inhibits neuronal activity in response to light in dissociated neurons and brain
slice and also reversibly suppresses behavior in zebrafish. The receptor is a
chimera of the pore region of a K+-selective bacterial glutamate receptor and
the ligand-binding domain of a light-gated mammalian kainate receptor. This hyperpolarizing
light-gated channel, HyLighter, is turned on by a brief light pulse at one wavelength
and turned off by a pulse at a second wavelength. The control is obtained at moderate
intensity. After optical activation, the photocurrent and optical silencing of
activity persists in the dark for extended periods. The low light requirement
and bi-stability of HyLighter represent advantages for the dissection of neural
circuitry.
author:
- first_name: Harald L
full_name: Harald Janovjak
id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
last_name: Janovjak
orcid: 0000-0002-8023-9315
- first_name: Stephanie
full_name: Szobota, Stephanie
last_name: Szobota
- first_name: Claire
full_name: Wyart, Claire
last_name: Wyart
- first_name: Dirk
full_name: Trauner, Dirk
last_name: Trauner
- first_name: Ehud
full_name: Isacoff, Ehud Y
last_name: Isacoff
citation:
ama: Janovjak HL, Szobota S, Wyart C, Trauner D, Isacoff E. A light-gated, potassium-selective
glutamate receptor for the optical inhibition of neuronal firing. Nature Neuroscience.
2010;13:1027-1032. doi:10.1038/nn.2589
apa: Janovjak, H. L., Szobota, S., Wyart, C., Trauner, D., & Isacoff, E. (2010).
A light-gated, potassium-selective glutamate receptor for the optical inhibition
of neuronal firing. Nature Neuroscience. Nature Publishing Group. https://doi.org/10.1038/nn.2589
chicago: Janovjak, Harald L, Stephanie Szobota, Claire Wyart, Dirk Trauner, and
Ehud Isacoff. “A Light-Gated, Potassium-Selective Glutamate Receptor for the Optical
Inhibition of Neuronal Firing.” Nature Neuroscience. Nature Publishing
Group, 2010. https://doi.org/10.1038/nn.2589.
ieee: H. L. Janovjak, S. Szobota, C. Wyart, D. Trauner, and E. Isacoff, “A light-gated,
potassium-selective glutamate receptor for the optical inhibition of neuronal
firing,” Nature Neuroscience, vol. 13. Nature Publishing Group, pp. 1027–1032,
2010.
ista: Janovjak HL, Szobota S, Wyart C, Trauner D, Isacoff E. 2010. A light-gated,
potassium-selective glutamate receptor for the optical inhibition of neuronal
firing. Nature Neuroscience. 13, 1027–1032.
mla: Janovjak, Harald L., et al. “A Light-Gated, Potassium-Selective Glutamate Receptor
for the Optical Inhibition of Neuronal Firing.” Nature Neuroscience, vol.
13, Nature Publishing Group, 2010, pp. 1027–32, doi:10.1038/nn.2589.
short: H.L. Janovjak, S. Szobota, C. Wyart, D. Trauner, E. Isacoff, Nature Neuroscience
13 (2010) 1027–1032.
date_created: 2018-12-11T12:03:10Z
date_published: 2010-06-27T00:00:00Z
date_updated: 2021-01-12T07:43:16Z
day: '27'
doi: 10.1038/nn.2589
extern: 1
intvolume: ' 13'
month: '06'
page: 1027 - 1032
publication: Nature Neuroscience
publication_status: published
publisher: Nature Publishing Group
publist_id: '2995'
quality_controlled: 0
status: public
title: A light-gated, potassium-selective glutamate receptor for the optical inhibition
of neuronal firing
type: journal_article
volume: 13
year: '2010'
...
---
_id: '3430'
abstract:
- lang: eng
text: These are notes for a set of 7 two-hour lectures given at the 2010 Summer
School on Quantitative Evolutionary and Comparative Genomics at OIST, Okinawa,
Japan. The emphasis is on understanding how biological systems process information.
We take a physicist's approach of looking for simple phenomenological descriptions
that can address the questions of biological function without necessarily modeling
all (mostly unknown) microscopic details; the example that is developed throughout
the notes is transcriptional regulation in genetic regulatory networks. We present
tools from information theory and statistical physics that can be used to analyze
noisy nonlinear biological networks, and build generative and predictive models
of regulatory processes.
author:
- first_name: Gasper
full_name: Gasper Tkacik
id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
citation:
ama: 'Tkačik G. Lecture notes for 2010 summer school on Quantitative Evolutionary
and Comparative Genomics. In: Elsevier; 2010.'
apa: Tkačik, G. (2010). Lecture notes for 2010 summer school on Quantitative Evolutionary
and Comparative Genomics. Presented at the Summer School on Quantitative Evolutionary
and Comparative Genomics, Elsevier.
chicago: Tkačik, Gašper. “Lecture Notes for 2010 Summer School on Quantitative Evolutionary
and Comparative Genomics.” Elsevier, 2010.
ieee: G. Tkačik, “Lecture notes for 2010 summer school on Quantitative Evolutionary
and Comparative Genomics,” presented at the Summer School on Quantitative Evolutionary
and Comparative Genomics, 2010.
ista: Tkačik G. 2010. Lecture notes for 2010 summer school on Quantitative Evolutionary
and Comparative Genomics. Summer School on Quantitative Evolutionary and Comparative
Genomics.
mla: Tkačik, Gašper. Lecture Notes for 2010 Summer School on Quantitative Evolutionary
and Comparative Genomics. Elsevier, 2010.
short: G. Tkačik, in:, Elsevier, 2010.
conference:
name: Summer School on Quantitative Evolutionary and Comparative Genomics
date_created: 2018-12-11T12:03:17Z
date_published: 2010-06-22T00:00:00Z
date_updated: 2021-01-12T07:43:25Z
day: '22'
extern: 1
main_file_link:
- open_access: '1'
url: http://arxiv.org/pdf/1006.4291
month: '06'
oa: 1
publication_status: published
publisher: Elsevier
publist_id: '2970'
quality_controlled: 0
status: public
title: Lecture notes for 2010 summer school on Quantitative Evolutionary and Comparative
Genomics
type: conference
year: '2010'
...
---
_id: '3441'
abstract:
- lang: eng
text: The hippocampus is an important brain circuit for spatial memory and the spatially
selective spiking of hippocampal neuronal assemblies is thought to provide a mnemonic
representation of space. We found that remembering newly learnt goal locations
required NMDA receptorĝ€"dependent stabilization and enhanced reactivation
of goal-related hippocampal assemblies. During spatial learning, place-related
firing patterns in the CA1, but not CA3, region of the rat hippocampus were reorganized
to represent new goal locations. Such reorganization did not occur when goals
were marked by visual cues. The stabilization and successful retrieval of these
newly acquired CA1 representations of behaviorally relevant places was NMDAR dependent
and necessary for subsequent memory retention performance. Goal-related assembly
patterns associated with sharp wave/ripple network oscillations, during both learning
and subsequent rest periods, predicted memory performance. Together, these results
suggest that the reorganization and reactivation of assembly firing patterns in
the hippocampus represent the formation and expression of new spatial memory traces.
© 2010 Nature America, Inc. All rights reserved.
acknowledgement: |
Discussed in the News and Views section of the journal by Jeffery and Cacucci
author:
- first_name: David
full_name: Dupret, David
last_name: Dupret
- first_name: Joseph
full_name: Joseph O'Neill
id: 426376DC-F248-11E8-B48F-1D18A9856A87
last_name: O'Neill
- first_name: Barty
full_name: Pleydell-Bouverie, Barty
last_name: Pleydell Bouverie
- first_name: Jozsef L
full_name: Jozsef Csicsvari
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
citation:
ama: Dupret D, O’Neill J, Pleydell Bouverie B, Csicsvari JL. The reorganization
and reactivation of hippocampal maps predict spatial memory performance. Nature
Neuroscience. 2010;13(8):995-1002. doi:10.1038/nn.2599
apa: Dupret, D., O’Neill, J., Pleydell Bouverie, B., & Csicsvari, J. L. (2010).
The reorganization and reactivation of hippocampal maps predict spatial memory
performance. Nature Neuroscience. Nature Publishing Group. https://doi.org/10.1038/nn.2599
chicago: Dupret, David, Joseph O’Neill, Barty Pleydell Bouverie, and Jozsef L Csicsvari.
“The Reorganization and Reactivation of Hippocampal Maps Predict Spatial Memory
Performance.” Nature Neuroscience. Nature Publishing Group, 2010. https://doi.org/10.1038/nn.2599.
ieee: D. Dupret, J. O’Neill, B. Pleydell Bouverie, and J. L. Csicsvari, “The reorganization
and reactivation of hippocampal maps predict spatial memory performance,” Nature
Neuroscience, vol. 13, no. 8. Nature Publishing Group, pp. 995–1002, 2010.
ista: Dupret D, O’Neill J, Pleydell Bouverie B, Csicsvari JL. 2010. The reorganization
and reactivation of hippocampal maps predict spatial memory performance. Nature
Neuroscience. 13(8), 995–1002.
mla: Dupret, David, et al. “The Reorganization and Reactivation of Hippocampal Maps
Predict Spatial Memory Performance.” Nature Neuroscience, vol. 13, no.
8, Nature Publishing Group, 2010, pp. 995–1002, doi:10.1038/nn.2599.
short: D. Dupret, J. O’Neill, B. Pleydell Bouverie, J.L. Csicsvari, Nature Neuroscience
13 (2010) 995–1002.
date_created: 2018-12-11T12:03:21Z
date_published: 2010-08-01T00:00:00Z
date_updated: 2021-01-12T07:43:29Z
day: '01'
doi: 10.1038/nn.2599
extern: 1
intvolume: ' 13'
issue: '8'
month: '08'
page: 995 - 1002
publication: Nature Neuroscience
publication_status: published
publisher: Nature Publishing Group
publist_id: '2946'
quality_controlled: 0
status: public
title: The reorganization and reactivation of hippocampal maps predict spatial memory
performance
type: journal_article
volume: 13
year: '2010'
...
---
_id: '3442'
abstract:
- lang: eng
text: Episodic and spatial memories each involve the encoding of complex associations
in hippocampal neuronal circuits. Such memory traces could be stabilised from
short- to long-term forms by consolidation processes involving the 'reactivation'
of the original network firing patterns during sleep and rest. Waking experience
can be replayed in many different brain areas, but an important role for the hippocampus
lies in the organisation of the 'reactivation' process. Emerging evidence suggests
that sharp wave/ripple (SWR) events in the hippocampus could coordinate the reactivation
of memory traces and direct their reinstatement in cortical circuits. Although
the mechanisms remain uncertain, there is a growing consensus that such SWR-directed
reactivation of brain-wide memory traces could underlie memory consolidation.
© 2010 Elsevier Ltd.
author:
- first_name: Joseph
full_name: Joseph O'Neill
id: 426376DC-F248-11E8-B48F-1D18A9856A87
last_name: O'Neill
- first_name: Barty
full_name: Pleydell-Bouverie, Barty
last_name: Pleydell Bouverie
- first_name: David
full_name: Dupret, David
last_name: Dupret
- first_name: Jozsef L
full_name: Jozsef Csicsvari
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
citation:
ama: 'O’Neill J, Pleydell Bouverie B, Dupret D, Csicsvari JL. Play it again: reactivation
of waking experience and memory. Trends in Neurosciences. 2010;33(5):220-229.
doi:10.1016/j.tins.2010.01.006'
apa: 'O’Neill, J., Pleydell Bouverie, B., Dupret, D., & Csicsvari, J. L. (2010).
Play it again: reactivation of waking experience and memory. Trends in Neurosciences.
Elsevier. https://doi.org/10.1016/j.tins.2010.01.006'
chicago: 'O’Neill, Joseph, Barty Pleydell Bouverie, David Dupret, and Jozsef L Csicsvari.
“Play It Again: Reactivation of Waking Experience and Memory.” Trends in Neurosciences.
Elsevier, 2010. https://doi.org/10.1016/j.tins.2010.01.006.'
ieee: 'J. O’Neill, B. Pleydell Bouverie, D. Dupret, and J. L. Csicsvari, “Play it
again: reactivation of waking experience and memory,” Trends in Neurosciences,
vol. 33, no. 5. Elsevier, pp. 220–229, 2010.'
ista: 'O’Neill J, Pleydell Bouverie B, Dupret D, Csicsvari JL. 2010. Play it again:
reactivation of waking experience and memory. Trends in Neurosciences. 33(5),
220–229.'
mla: 'O’Neill, Joseph, et al. “Play It Again: Reactivation of Waking Experience
and Memory.” Trends in Neurosciences, vol. 33, no. 5, Elsevier, 2010, pp.
220–29, doi:10.1016/j.tins.2010.01.006.'
short: J. O’Neill, B. Pleydell Bouverie, D. Dupret, J.L. Csicsvari, Trends in Neurosciences
33 (2010) 220–229.
date_created: 2018-12-11T12:03:21Z
date_published: 2010-05-01T00:00:00Z
date_updated: 2021-01-12T07:43:29Z
day: '01'
doi: 10.1016/j.tins.2010.01.006
extern: 1
intvolume: ' 33'
issue: '5'
month: '05'
page: 220 - 229
publication: Trends in Neurosciences
publication_status: published
publisher: Elsevier
publist_id: '2945'
quality_controlled: 0
status: public
title: 'Play it again: reactivation of waking experience and memory'
type: journal_article
volume: 33
year: '2010'
...
---
_id: '3459'
author:
- first_name: Bernd
full_name: Fakler, Bernd
last_name: Fakler
- first_name: Peter M
full_name: Peter Jonas
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
citation:
ama: 'Fakler B, Jonas PM. Grundlagen zellulärer Erregbarkeit. In: Schmidt R, Heckmann
M, Lang F, eds. Physiologie Des Menschen. Springer; 2010.'
apa: Fakler, B., & Jonas, P. M. (2010). Grundlagen zellulärer Erregbarkeit.
In R. Schmidt, M. Heckmann, & F. Lang (Eds.), Physiologie Des Menschen.
Springer.
chicago: Fakler, Bernd, and Peter M Jonas. “Grundlagen Zellulärer Erregbarkeit.”
In Physiologie Des Menschen, edited by R. Schmidt, M. Heckmann, and Florian
Lang. Springer, 2010.
ieee: B. Fakler and P. M. Jonas, “Grundlagen zellulärer Erregbarkeit,” in Physiologie
Des Menschen, R. Schmidt, M. Heckmann, and F. Lang, Eds. Springer, 2010.
ista: 'Fakler B, Jonas PM. 2010.Grundlagen zellulärer Erregbarkeit. In: Physiologie
Des Menschen. .'
mla: Fakler, Bernd, and Peter M. Jonas. “Grundlagen Zellulärer Erregbarkeit.” Physiologie
Des Menschen, edited by R. Schmidt et al., Springer, 2010.
short: B. Fakler, P.M. Jonas, in:, R. Schmidt, M. Heckmann, F. Lang (Eds.), Physiologie
Des Menschen, Springer, 2010.
date_created: 2018-12-11T12:03:26Z
date_published: 2010-01-01T00:00:00Z
date_updated: 2021-01-12T07:43:35Z
day: '01'
editor:
- first_name: R.
full_name: Schmidt, R. F.
last_name: Schmidt
- first_name: M.
full_name: Heckmann, M.
last_name: Heckmann
- first_name: Florian
full_name: Lang, Florian
last_name: Lang
extern: 1
month: '01'
publication: Physiologie Des Menschen
publication_status: published
publisher: Springer
publist_id: '2928'
quality_controlled: 0
status: public
title: Grundlagen zellulärer Erregbarkeit
type: book_chapter
year: '2010'
...
---
_id: '3498'
abstract:
- lang: eng
text: "Purpose\r\nCalcifying tendinitis is a common condition of the shoulder. In
many cases, arthroscopic reduction in the deposit is indicated. The localization
of the deposit is sometimes challenging and time-consuming. Pre-operative ultrasound
(US)-guided needle placement in the deposit and pre-operative US marking of the
deposit at the skin with a ballpoint are described and recommended methods to
alleviate the procedure without using ionizing radiation by fluoroscopy.\r\nMethods\r\nIntra-operative
sonography of the shoulder is introduced as a new method to localize the calcific
deposit with high accuracy. After standard arthroscopic buresectomy, the surgeon
performs an ultrasound examination under sterile conditions to localize the deposits.
A ventral longitudinal US section is recommended, and the upper arm is rotated
until the deposit is visible. Subsequently, perpendicular to the skin at the position
of the transducer, a needle is introduced under arthroscopic and ultrasound visualization
to puncture the deposit.\r\nResults\r\nThe presence of snow-white crystals at
the tip of the needle proves the exact localization. Consecutively, the curettage
can be accomplished. Another intra-operative sonography evaluates possible calcific
remnants and the tendon structure.\r\nConclusion\r\nThis new technique may alleviate
arthroscopic calcific deposit curettage by visualizing the deposit without using
ionizing radiation. Additionally, soft tissue damage due to decreased number of
punctures to detect the deposit may be achieved. Both factors may contribute to
reduced operation time."
author:
- first_name: M.
full_name: Sabeti Aschraf, M.
last_name: Sabeti Aschraf
- first_name: C.
full_name: Gonano, C.
last_name: Gonano
- first_name: E.
full_name: Nemecek, E.
last_name: Nemecek
- first_name: Lisa
full_name: Cichocki, Lisa
id: 3BC78B60-F248-11E8-B48F-1D18A9856A87
last_name: Cichocki
- first_name: C.
full_name: Schueller Weidekamm, C.
last_name: Schueller Weidekamm
citation:
ama: Sabeti Aschraf M, Gonano C, Nemecek E, Cichocki L, Schueller Weidekamm C. Intra-operative
ultrasound facilitates the localization of the calcific deposit during arthroscopic
treatment of calcifying tendinitis. Knee Surgery, Sports Traumatology, Arthroscopy.
2010;18(12):1792-1794. doi:10.1007/s00167-010-1227-9
apa: Sabeti Aschraf, M., Gonano, C., Nemecek, E., Cichocki, L., & Schueller
Weidekamm, C. (2010). Intra-operative ultrasound facilitates the localization
of the calcific deposit during arthroscopic treatment of calcifying tendinitis.
Knee Surgery, Sports Traumatology, Arthroscopy. Springer. https://doi.org/10.1007/s00167-010-1227-9
chicago: Sabeti Aschraf, M., C. Gonano, E. Nemecek, Lisa Cichocki, and C. Schueller
Weidekamm. “Intra-Operative Ultrasound Facilitates the Localization of the Calcific
Deposit during Arthroscopic Treatment of Calcifying Tendinitis.” Knee Surgery,
Sports Traumatology, Arthroscopy. Springer, 2010. https://doi.org/10.1007/s00167-010-1227-9.
ieee: M. Sabeti Aschraf, C. Gonano, E. Nemecek, L. Cichocki, and C. Schueller Weidekamm,
“Intra-operative ultrasound facilitates the localization of the calcific deposit
during arthroscopic treatment of calcifying tendinitis,” Knee Surgery, Sports
Traumatology, Arthroscopy, vol. 18, no. 12. Springer, pp. 1792–1794, 2010.
ista: Sabeti Aschraf M, Gonano C, Nemecek E, Cichocki L, Schueller Weidekamm C.
2010. Intra-operative ultrasound facilitates the localization of the calcific
deposit during arthroscopic treatment of calcifying tendinitis. Knee Surgery,
Sports Traumatology, Arthroscopy. 18(12), 1792–1794.
mla: Sabeti Aschraf, M., et al. “Intra-Operative Ultrasound Facilitates the Localization
of the Calcific Deposit during Arthroscopic Treatment of Calcifying Tendinitis.”
Knee Surgery, Sports Traumatology, Arthroscopy, vol. 18, no. 12, Springer,
2010, pp. 1792–94, doi:10.1007/s00167-010-1227-9.
short: M. Sabeti Aschraf, C. Gonano, E. Nemecek, L. Cichocki, C. Schueller Weidekamm,
Knee Surgery, Sports Traumatology, Arthroscopy 18 (2010) 1792–1794.
date_created: 2018-12-11T12:03:39Z
date_published: 2010-08-20T00:00:00Z
date_updated: 2021-01-12T07:43:51Z
day: '20'
doi: 10.1007/s00167-010-1227-9
intvolume: ' 18'
issue: '12'
language:
- iso: eng
month: '08'
oa_version: None
page: 1792 - 1794
publication: Knee Surgery, Sports Traumatology, Arthroscopy
publication_status: published
publisher: Springer
publist_id: '2889'
quality_controlled: '1'
scopus_import: 1
status: public
title: Intra-operative ultrasound facilitates the localization of the calcific deposit
during arthroscopic treatment of calcifying tendinitis
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 18
year: '2010'
...
---
_id: '3538'
abstract:
- lang: eng
text: How seizures start is a major question in epilepsy research. Preictal EEG
changes occur in both human patients and animal models, but their underlying mechanisms
and relationship with seizure initiation remain unknown. Here we demonstrate the
existence, in the hippocampal CA1 region, of a preictal state characterized by
the progressive and global increase in neuronal activity associated with a widespread
buildup of low-amplitude high-frequency activity (HFA) (> 100 Hz) and reduction
in system complexity. HFA is generated by the firing of neurons, mainly pyramidal
cells, at much lower frequencies. Individual cycles of HFA are generated by the
near-synchronous (within similar to 5 ms) firing of small numbers of pyramidal
cells. The presence of HFA in the low-calcium model implicates nonsynaptic synchronization;
the presence of very similar HFA in the high-potassium model shows that it does
not depend on an absence of synaptic transmission. Immediately before seizure
onset, CA1 is in a state of high sensitivity in which weak depolarizing or synchronizing
perturbations can trigger seizures. Transition to seizure is characterized by
a rapid expansion and fusion of the neuronal populations responsible for HFA,
associated with a progressive slowing of HFA, leading to a single, massive, hypersynchronous
cluster generating the high-amplitude low-frequency activity of the seizure.
author:
- first_name: Premysl
full_name: Jiruska, Premysl
last_name: Jiruska
- first_name: Jozsef L
full_name: Csicsvari, Jozsef L
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
- first_name: Andrew
full_name: Powell, Andrew
last_name: Powell
- first_name: John
full_name: Fox, John
last_name: Fox
- first_name: Wei
full_name: Chang, Wei
last_name: Chang
- first_name: Martin
full_name: Vreugdenhil, Martin
last_name: Vreugdenhil
- first_name: Xiaoli
full_name: Li, Xiaoli
last_name: Li
- first_name: Milan
full_name: Palus, Milan
last_name: Palus
- first_name: Alejandro
full_name: Bujan, Alejandro
last_name: Bujan
- first_name: Richard
full_name: Dearden, Richard
last_name: Dearden
- first_name: John
full_name: Jefferys, John
last_name: Jefferys
citation:
ama: Jiruska P, Csicsvari JL, Powell A, et al. High-frequency network activity,
global increase in neuronal activity, and synchrony expansion precede epileptic
seizures in vitro. Journal of Neuroscience. 2010;30(16):5690-5701. doi:10.1523/JNEUROSCI.0535-10.2010
apa: Jiruska, P., Csicsvari, J. L., Powell, A., Fox, J., Chang, W., Vreugdenhil,
M., … Jefferys, J. (2010). High-frequency network activity, global increase in
neuronal activity, and synchrony expansion precede epileptic seizures in vitro.
Journal of Neuroscience. Society for Neuroscience. https://doi.org/10.1523/JNEUROSCI.0535-10.2010
chicago: Jiruska, Premysl, Jozsef L Csicsvari, Andrew Powell, John Fox, Wei Chang,
Martin Vreugdenhil, Xiaoli Li, et al. “High-Frequency Network Activity, Global
Increase in Neuronal Activity, and Synchrony Expansion Precede Epileptic Seizures
in Vitro.” Journal of Neuroscience. Society for Neuroscience, 2010. https://doi.org/10.1523/JNEUROSCI.0535-10.2010.
ieee: P. Jiruska et al., “High-frequency network activity, global increase
in neuronal activity, and synchrony expansion precede epileptic seizures in vitro,”
Journal of Neuroscience, vol. 30, no. 16. Society for Neuroscience, pp.
5690–5701, 2010.
ista: Jiruska P, Csicsvari JL, Powell A, Fox J, Chang W, Vreugdenhil M, Li X, Palus
M, Bujan A, Dearden R, Jefferys J. 2010. High-frequency network activity, global
increase in neuronal activity, and synchrony expansion precede epileptic seizures
in vitro. Journal of Neuroscience. 30(16), 5690–5701.
mla: Jiruska, Premysl, et al. “High-Frequency Network Activity, Global Increase
in Neuronal Activity, and Synchrony Expansion Precede Epileptic Seizures in Vitro.”
Journal of Neuroscience, vol. 30, no. 16, Society for Neuroscience, 2010,
pp. 5690–701, doi:10.1523/JNEUROSCI.0535-10.2010.
short: P. Jiruska, J.L. Csicsvari, A. Powell, J. Fox, W. Chang, M. Vreugdenhil,
X. Li, M. Palus, A. Bujan, R. Dearden, J. Jefferys, Journal of Neuroscience 30
(2010) 5690–5701.
date_created: 2018-12-11T12:03:51Z
date_published: 2010-04-21T00:00:00Z
date_updated: 2021-01-12T07:44:10Z
day: '21'
doi: 10.1523/JNEUROSCI.0535-10.2010
extern: '1'
intvolume: ' 30'
issue: '16'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://www.jneurosci.org/content/30/16/5690
month: '04'
oa: 1
oa_version: None
page: 5690 - 5701
publication: Journal of Neuroscience
publication_status: published
publisher: Society for Neuroscience
publist_id: '2848'
quality_controlled: '1'
status: public
title: High-frequency network activity, global increase in neuronal activity, and
synchrony expansion precede epileptic seizures in vitro
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 30
year: '2010'
...
---
_id: '3592'
abstract:
- lang: eng
text: The zebrafish is a favorite model organism to study tissue morphogenesis during
development at a subcellular level. This largely results from the fact that zebrafish
embryos are transparent and thus accessible to various imaging techniques, such
as confocal and two-photon excitation (2PE) microscopy. In particular, 2PE microscopy
has been shown to be useful for imaging deep cell layers within the embryo and
following tissue morphogenesis over long periods. This chapter describes how to
use 2PE microscopy to study morphogenetic movements during early zebrafish embryonic
development, providing a general blueprint for its use in zebrafish.
article_processing_charge: No
author:
- first_name: Lara
full_name: Carvalho, Lara
last_name: Carvalho
- first_name: Carl-Philipp J
full_name: Heisenberg, Carl-Philipp J
id: 39427864-F248-11E8-B48F-1D18A9856A87
last_name: Heisenberg
orcid: 0000-0002-0912-4566
citation:
ama: Carvalho L, Heisenberg C-PJ. Imaging zebrafish embryos by two-photon excitation
time-lapse microscopy. Methods in Molecular Biology. 2010;546(Part 5):273-287.
doi:10.1007/978-1-60327-977-2_17
apa: Carvalho, L., & Heisenberg, C.-P. J. (2010). Imaging zebrafish embryos
by two-photon excitation time-lapse microscopy. Methods in Molecular Biology.
Springer. https://doi.org/10.1007/978-1-60327-977-2_17
chicago: Carvalho, Lara, and Carl-Philipp J Heisenberg. “Imaging Zebrafish Embryos
by Two-Photon Excitation Time-Lapse Microscopy.” Methods in Molecular Biology.
Springer, 2010. https://doi.org/10.1007/978-1-60327-977-2_17.
ieee: L. Carvalho and C.-P. J. Heisenberg, “Imaging zebrafish embryos by two-photon
excitation time-lapse microscopy,” Methods in Molecular Biology, vol. 546,
no. Part 5. Springer, pp. 273–287, 2010.
ista: Carvalho L, Heisenberg C-PJ. 2010. Imaging zebrafish embryos by two-photon
excitation time-lapse microscopy. Methods in Molecular Biology. 546(Part 5), 273–287.
mla: Carvalho, Lara, and Carl-Philipp J. Heisenberg. “Imaging Zebrafish Embryos
by Two-Photon Excitation Time-Lapse Microscopy.” Methods in Molecular Biology,
vol. 546, no. Part 5, Springer, 2010, pp. 273–87, doi:10.1007/978-1-60327-977-2_17.
short: L. Carvalho, C.-P.J. Heisenberg, Methods in Molecular Biology 546 (2010)
273–287.
date_created: 2018-12-11T12:04:08Z
date_published: 2010-01-01T00:00:00Z
date_updated: 2021-01-12T07:44:31Z
day: '01'
doi: 10.1007/978-1-60327-977-2_17
extern: '1'
intvolume: ' 546'
issue: Part 5
language:
- iso: eng
month: '01'
oa_version: None
page: 273 - 287
publication: Methods in Molecular Biology
publication_status: published
publisher: Springer
publist_id: '2791'
status: public
title: Imaging zebrafish embryos by two-photon excitation time-lapse microscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 546
year: '2010'
...