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Mark A Corbett

Showing results (1-10 of 68) with videos related to

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Aviation, Space, and Environmental Medicine|November 23, 2013
A potential aid to circadian adaptation: re-timerMark A Corbett
Aerospace Medicine and Human Performance|March 31, 2022
Student Drowsiness During Simulated Solo FlightMark A Corbett, David G Newman
European Journal of Human Genetics : EJHG|June 15, 2017
Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restrictionRenée Carroll, Raman Kumar, Marie Shaw, et al.
BMC Biology|September 28, 2024
CRISPR-mediated megabase-scale transgene de-duplication to generate a functional single-copy full-length humanized DMD mouse modelYu C J Chey, Mark A Corbett, Jayshen Arudkumar, et al.
Epilepsia|January 9, 2023
Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitabilityChristel Depienne, Arn M J M van den Maagdenberg, Theresa Kühnel, et al.
Scientific Reports|June 4, 2016
Paternal under-nutrition programs metabolic syndrome in offspring which can be reversed by antioxidant/vitamin food fortification in fathersNicole O McPherson, Tod Fullston, Wan Xian Kang, et al.
The Cochrane Database of Systematic Reviews|March 3, 2018
Workplace lighting for improving alertness and mood in daytime workersDaniela V Pachito, Alan L Eckeli, Ahmed S Desouky, et al.
American Journal of Medical Genetics. Part A|December 29, 2015
A mutation in COL4A2 causes autosomal dominant porencephaly with cataractsThuong T Ha, Lynette G Sadleir, Simone A Mandelstam, et al.
Epilepsia|April 6, 2023
Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansionsMark A Corbett, Christel Depienne, Liana Veneziano, et al.
Human Molecular Genetics|August 1, 2006
Skeletal muscle repair in a mouse model of nemaline myopathyDespina Sanoudou, Mark A Corbett, Mei Han, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Aviation, Space, and Environmental Medicine|November 23, 2013
A potential aid to circadian adaptation: re-timerMark A Corbett
Aerospace Medicine and Human Performance|March 31, 2022
Student Drowsiness During Simulated Solo FlightMark A Corbett, David G Newman
European Journal of Human Genetics : EJHG|June 15, 2017
Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restrictionRenée Carroll, Raman Kumar, Marie Shaw, et al.
BMC Biology|September 28, 2024
CRISPR-mediated megabase-scale transgene de-duplication to generate a functional single-copy full-length humanized DMD mouse modelYu C J Chey, Mark A Corbett, Jayshen Arudkumar, et al.
Epilepsia|January 9, 2023
Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitabilityChristel Depienne, Arn M J M van den Maagdenberg, Theresa Kühnel, et al.
Scientific Reports|June 4, 2016
Paternal under-nutrition programs metabolic syndrome in offspring which can be reversed by antioxidant/vitamin food fortification in fathersNicole O McPherson, Tod Fullston, Wan Xian Kang, et al.
The Cochrane Database of Systematic Reviews|March 3, 2018
Workplace lighting for improving alertness and mood in daytime workersDaniela V Pachito, Alan L Eckeli, Ahmed S Desouky, et al.
American Journal of Medical Genetics. Part A|December 29, 2015
A mutation in COL4A2 causes autosomal dominant porencephaly with cataractsThuong T Ha, Lynette G Sadleir, Simone A Mandelstam, et al.
Epilepsia|April 6, 2023
Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansionsMark A Corbett, Christel Depienne, Liana Veneziano, et al.
Human Molecular Genetics|August 1, 2006
Skeletal muscle repair in a mouse model of nemaline myopathyDespina Sanoudou, Mark A Corbett, Mei Han, et al.
Pageof 7