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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.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.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.Frontiers in Neuroscience|January 24, 2020
Vesicular Dysfunction and the Pathogenesis of Parkinson's Disease: Clues From Genetic StudiesKirsten Ebanks, Patrick A Lewis, Rina BandopadhyayJournal of Cell Science|September 12, 2023
Leucine-rich repeat kinase 2 at a glanceChristiane Zhu, Susanne Herbst, Patrick A LewisNeuroscience 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.BMC Genomics|November 14, 2012
Cell population-specific expression analysis of human cerebellumAlexandre Kuhn, Azad Kumar, Alexandra Beilina, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 6, 2007
The roles of kinases in familial Parkinson's diseaseMark R Cookson, William Dauer, Ted Dawson, et al.Pageof 39