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Patrick M Nolan

Showing results (41-50 of 71) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|April 9, 2009
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker miceEsther B E Becker, Peter L Oliver, Maike D Glitsch, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 12, 2021
Zfhx3 modulates retinal sensitivity and circadian responses to lightSteven Hughes, Jessica K Edwards, Ashleigh G Wilcox, et al.
Scientific Reports|December 21, 2017
The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasisSilvia Maggi, Edoardo Balzani, Glenda Lassi, et al.
Frontiers in Behavioral Neuroscience|July 5, 2016
Analysis of Individual Mouse Activity in Group Housed Animals of Different Inbred Strains using a Novel Automated Home Cage Analysis SystemRasneer S Bains, Heather L Cater, Rowland R Sillito, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2016
Early doors (Edo) mutant mouse reveals the importance of period 2 (PER2) PAS domain structure for circadian pacemakingStefania Militi, Elizabeth S Maywood, Colby R Sandate, et al.
Human Molecular Genetics|April 4, 2002
Novel ENU-induced eye mutations in the mouse: models for human eye diseaseCaroline Thaung, Katrine West, Brian J Clark, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
Disease Models & Mechanisms|January 30, 2019
Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalitiesMichelle Stewart, Petrina Lau, Gareth Banks, et al.
Plos Biology|June 9, 2016
Melanopsin Regulates Both Sleep-Promoting and Arousal-Promoting Responses to LightVioletta Pilorz, Shu K E Tam, Steven Hughes, et al.
Current Biology : CB|March 21, 2025
Deficient synaptic neurotransmission results in a persistent sleep-like cortical activity across vigilance states in miceMathilde C C Guillaumin, Christian D Harding, Lukas B Krone, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2009
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker miceEsther B E Becker, Peter L Oliver, Maike D Glitsch, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 12, 2021
Zfhx3 modulates retinal sensitivity and circadian responses to lightSteven Hughes, Jessica K Edwards, Ashleigh G Wilcox, et al.
Scientific Reports|December 21, 2017
The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasisSilvia Maggi, Edoardo Balzani, Glenda Lassi, et al.
Frontiers in Behavioral Neuroscience|July 5, 2016
Analysis of Individual Mouse Activity in Group Housed Animals of Different Inbred Strains using a Novel Automated Home Cage Analysis SystemRasneer S Bains, Heather L Cater, Rowland R Sillito, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2016
Early doors (Edo) mutant mouse reveals the importance of period 2 (PER2) PAS domain structure for circadian pacemakingStefania Militi, Elizabeth S Maywood, Colby R Sandate, et al.
Human Molecular Genetics|April 4, 2002
Novel ENU-induced eye mutations in the mouse: models for human eye diseaseCaroline Thaung, Katrine West, Brian J Clark, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
Disease Models & Mechanisms|January 30, 2019
Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalitiesMichelle Stewart, Petrina Lau, Gareth Banks, et al.
Plos Biology|June 9, 2016
Melanopsin Regulates Both Sleep-Promoting and Arousal-Promoting Responses to LightVioletta Pilorz, Shu K E Tam, Steven Hughes, et al.
Current Biology : CB|March 21, 2025
Deficient synaptic neurotransmission results in a persistent sleep-like cortical activity across vigilance states in miceMathilde C C Guillaumin, Christian D Harding, Lukas B Krone, et al.
Pageof 8