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Patrick M Nolan

Showing results (51-60 of 71) with videos related to

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Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Science (New York, N.Y.)|April 28, 2007
The after-hours mutant reveals a role for Fbxl3 in determining mammalian circadian periodSofia I H Godinho, Elizabeth S Maywood, Linda Shaw, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Plos Biology|October 9, 2019
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Biology|September 4, 2019
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 22, 2018
Differential roles for cryptochromes in the mammalian retinal clockJovi C Y Wong, Nicola J Smyllie, Gareth T Banks, et al.
Science Advances|August 28, 2020
Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficitsGareth T Banks, Mathilde C C Guillaumin, Ines Heise, et al.
Molecular Metabolism|November 7, 2017
Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxietyLee Moir, Elena G Bochukova, Rebecca Dumbell, et al.
Disease Models & Mechanisms|May 28, 2009
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathyFrancesca Achilli, Virginie Bros-Facer, Hazel P Williams, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2005
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screenDebora Bogani, Catherine Willoughby, Jennifer Davies, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Science (New York, N.Y.)|April 28, 2007
The after-hours mutant reveals a role for Fbxl3 in determining mammalian circadian periodSofia I H Godinho, Elizabeth S Maywood, Linda Shaw, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Plos Biology|October 9, 2019
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Biology|September 4, 2019
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 22, 2018
Differential roles for cryptochromes in the mammalian retinal clockJovi C Y Wong, Nicola J Smyllie, Gareth T Banks, et al.
Science Advances|August 28, 2020
Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficitsGareth T Banks, Mathilde C C Guillaumin, Ines Heise, et al.
Molecular Metabolism|November 7, 2017
Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxietyLee Moir, Elena G Bochukova, Rebecca Dumbell, et al.
Disease Models & Mechanisms|May 28, 2009
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathyFrancesca Achilli, Virginie Bros-Facer, Hazel P Williams, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2005
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screenDebora Bogani, Catherine Willoughby, Jennifer Davies, et al.
Pageof 8