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Mark Cooper

Showing results (111-120 of 201) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|June 7, 2006
Coordinating outcomes measurement in ataxia research: do some widely used generic rating scales tick the boxes?Afsane Riazi, Stefan J Cano, J Mark Cooper, et al.
Human Molecular Genetics|September 28, 2010
Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagyMatthew E Gegg, J Mark Cooper, Kai-Yin Chau, et al.
Trials|June 5, 2020
Evaluating the efficacy and safety of GKT137831 in adults with type 1 diabetes and persistently elevated urinary albumin excretion: a statistical analysis planAlysha M De Livera, Anne Reutens, Mark Cooper, et al.
Journal of Public Health Research|August 30, 2014
The effects of a novel high intensity exercise intervention on established markers of cardiovascular disease and health in Scottish adolescent youthDuncan S Buchan, John D Young, Alan D Simpson, et al.
Genetics|October 20, 2007
A mixed-model quantitative trait loci (QTL) analysis for multiple-environment trial data using environmental covariables for QTL-by-environment interactions, with an example in maizeMartin P Boer, Deanne Wright, Lizhi Feng, et al.
BMC Public Health|May 28, 2013
High intensity interval running enhances measures of physical fitness but not metabolic measures of cardiovascular disease risk in healthy adolescentsDuncan S Buchan, Stewart Ollis, John D Young, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2004
Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cellsAnjum Misbahuddin, Mark R Placzek, Jan-Willem Taanman, et al.
Experimental Neurology|May 6, 2008
MELAS mitochondrial DNA mutation A3243G reduces glutamate transport in cybrids cell linesJacopo C DiFrancesco, J Mark Cooper, Amanda Lam, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|February 15, 2021
Strategies and considerations for implementing genomic selection to improve traits with additive and non-additive genetic architectures in sugarcane breedingKai P Voss-Fels, Xianming Wei, Elizabeth M Ross, et al.
Journal of Neurochemistry|October 13, 2005
Human spastin has multiple microtubule-related functionsSara Salinas, Rafael E Carazo-Salas, Christos Proukakis, et al.
Pageof 21

Showing results (111-120 of 201) with videos related to

Sort By:
Pageof 21
Movement Disorders : Official Journal of the Movement Disorder Society|June 7, 2006
Coordinating outcomes measurement in ataxia research: do some widely used generic rating scales tick the boxes?Afsane Riazi, Stefan J Cano, J Mark Cooper, et al.
Human Molecular Genetics|September 28, 2010
Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagyMatthew E Gegg, J Mark Cooper, Kai-Yin Chau, et al.
Trials|June 5, 2020
Evaluating the efficacy and safety of GKT137831 in adults with type 1 diabetes and persistently elevated urinary albumin excretion: a statistical analysis planAlysha M De Livera, Anne Reutens, Mark Cooper, et al.
Journal of Public Health Research|August 30, 2014
The effects of a novel high intensity exercise intervention on established markers of cardiovascular disease and health in Scottish adolescent youthDuncan S Buchan, John D Young, Alan D Simpson, et al.
Genetics|October 20, 2007
A mixed-model quantitative trait loci (QTL) analysis for multiple-environment trial data using environmental covariables for QTL-by-environment interactions, with an example in maizeMartin P Boer, Deanne Wright, Lizhi Feng, et al.
BMC Public Health|May 28, 2013
High intensity interval running enhances measures of physical fitness but not metabolic measures of cardiovascular disease risk in healthy adolescentsDuncan S Buchan, Stewart Ollis, John D Young, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2004
Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cellsAnjum Misbahuddin, Mark R Placzek, Jan-Willem Taanman, et al.
Experimental Neurology|May 6, 2008
MELAS mitochondrial DNA mutation A3243G reduces glutamate transport in cybrids cell linesJacopo C DiFrancesco, J Mark Cooper, Amanda Lam, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|February 15, 2021
Strategies and considerations for implementing genomic selection to improve traits with additive and non-additive genetic architectures in sugarcane breedingKai P Voss-Fels, Xianming Wei, Elizabeth M Ross, et al.
Journal of Neurochemistry|October 13, 2005
Human spastin has multiple microtubule-related functionsSara Salinas, Rafael E Carazo-Salas, Christos Proukakis, et al.
Pageof 21