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R Cookson

Showing results (121-130 of 388) with videos related to

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Human Molecular Genetics|August 8, 2002
Differential gene expression in a cell culture model of SOD1-related familial motor neurone diseaseJanine Kirby, Fiona M Menzies, Mark R Cookson, et al.
Brain Research|August 21, 2001
Superoxide-induced nitric oxide release from cultured glial cellsP Manning, M R Cookson, C J McNeil, et al.
Stem Cell Research|August 22, 2021
Generation of iPSC line from a Parkinson patient with PARK7 mutation and CRISPR-edited Gibco human episomal iPSC line to mimic PARK7 mutationMelissa Conti Mazza, Alexandra Beilina, Dorien A Roosen, et al.
Neuroreport|June 14, 2000
Screening of AP endonuclease as a candidate gene for amyotrophic lateral sclerosis (ALS)J Tomkins, S Dempster, S J Banner, et al.
Human Molecular Genetics|August 22, 2013
Hexokinase activity is required for recruitment of parkin to depolarized mitochondriaMelissa K McCoy, Alice Kaganovich, Iakov N Rudenko, et al.
Plos One|April 12, 2014
Post-translational decrease in respiratory chain proteins in the Polg mutator mouse brainDavid N Hauser, Allissa A Dillman, Jinhui Ding, et al.
Neuroscience Letters|July 6, 2002
Normal localization of deltaF323-Y328 mutant torsinA in transfected human cellsCasey O'Farrell, Dena G Hernandez, Crystal Evey, et al.
Biochemical and Biophysical Research Communications|April 20, 2007
The R1441C mutation of LRRK2 disrupts GTP hydrolysisPatrick A Lewis, Elisa Greggio, Alexandra Beilina, et al.
Neuroscience Letters|January 25, 2005
Identification of the epitope of a monoclonal antibody to DJ-1David W Miller, Carmen R Wilson, Mona A Kaleem, et al.
Eneuro|October 15, 2015
The Polg Mutator Phenotype Does Not Cause Dopaminergic Neurodegeneration in DJ-1-Deficient MiceDavid N Hauser, Christopher T Primiani, Rebekah G Langston, et al.
Pageof 39

Showing results (121-130 of 388) with videos related to

Sort By:
Pageof 39
Human Molecular Genetics|August 8, 2002
Differential gene expression in a cell culture model of SOD1-related familial motor neurone diseaseJanine Kirby, Fiona M Menzies, Mark R Cookson, et al.
Brain Research|August 21, 2001
Superoxide-induced nitric oxide release from cultured glial cellsP Manning, M R Cookson, C J McNeil, et al.
Stem Cell Research|August 22, 2021
Generation of iPSC line from a Parkinson patient with PARK7 mutation and CRISPR-edited Gibco human episomal iPSC line to mimic PARK7 mutationMelissa Conti Mazza, Alexandra Beilina, Dorien A Roosen, et al.
Neuroreport|June 14, 2000
Screening of AP endonuclease as a candidate gene for amyotrophic lateral sclerosis (ALS)J Tomkins, S Dempster, S J Banner, et al.
Human Molecular Genetics|August 22, 2013
Hexokinase activity is required for recruitment of parkin to depolarized mitochondriaMelissa K McCoy, Alice Kaganovich, Iakov N Rudenko, et al.
Plos One|April 12, 2014
Post-translational decrease in respiratory chain proteins in the Polg mutator mouse brainDavid N Hauser, Allissa A Dillman, Jinhui Ding, et al.
Neuroscience Letters|July 6, 2002
Normal localization of deltaF323-Y328 mutant torsinA in transfected human cellsCasey O'Farrell, Dena G Hernandez, Crystal Evey, et al.
Biochemical and Biophysical Research Communications|April 20, 2007
The R1441C mutation of LRRK2 disrupts GTP hydrolysisPatrick A Lewis, Elisa Greggio, Alexandra Beilina, et al.
Neuroscience Letters|January 25, 2005
Identification of the epitope of a monoclonal antibody to DJ-1David W Miller, Carmen R Wilson, Mona A Kaleem, et al.
Eneuro|October 15, 2015
The Polg Mutator Phenotype Does Not Cause Dopaminergic Neurodegeneration in DJ-1-Deficient MiceDavid N Hauser, Christopher T Primiani, Rebekah G Langston, et al.
Pageof 39