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Mark R Cookson

Showing results (211-220 of 320) with videos related to

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Plos One|June 4, 2009
Mitochondrial alterations in PINK1 deficient cells are influenced by calcineurin-dependent dephosphorylation of dynamin-related protein 1Anna Sandebring, Kelly Jean Thomas, Alexandra Beilina, et al.
Neurochemical Research|October 7, 2018
Differences in Stability, Activity and Mutation Effects Between Human and Mouse Leucine-Rich Repeat Kinase 2Rebekah G Langston, Iakov N Rudenko, Ravindran Kumaran, et al.
Nature Neuroscience|September 1, 2014
Genetic variability in the regulation of gene expression in ten regions of the human brainAdaikalavan Ramasamy, Daniah Trabzuni, Sebastian Guelfi, et al.
Scientific Reports|June 13, 2018
AKT signalling selectively regulates PINK1 mitophagy in SHSY5Y cells and human iPSC-derived neuronsMarc P M Soutar, Liam Kempthorne, Shuichi Miyakawa, et al.
FEBS Open Bio|October 16, 2023
LRRK2 negatively regulates glucose tolerance via regulation of membrane translocation of GLUT4 in adipocytesFumitaka Kawakami, Motoki Imai, Yuki Isaka, et al.
Annals of Neurology|December 11, 2008
Mitochondrial function and morphology are impaired in parkin-mutant fibroblastsHeather Mortiboys, Kelly Jean Thomas, Werner J H Koopman, et al.
The Journal of Biological Chemistry|July 10, 2003
L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome systemDavid W Miller, Rili Ahmad, Stephen Hague, et al.
The International Journal of Neuropsychopharmacology|December 21, 2012
Age-modulated association between prefrontal NAA and the BDNF geneBasira Salehi, Nora Preuss, Jan Willem van der Veen, et al.
Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.
Human Molecular Genetics|June 20, 2018
Proteomic analysis reveals co-ordinated alterations in protein synthesis and degradation pathways in LRRK2 knockout miceLaura Pellegrini, David N Hauser, Yan Li, et al.
Pageof 32

Showing results (211-220 of 320) with videos related to

Sort By:
Pageof 32
Plos One|June 4, 2009
Mitochondrial alterations in PINK1 deficient cells are influenced by calcineurin-dependent dephosphorylation of dynamin-related protein 1Anna Sandebring, Kelly Jean Thomas, Alexandra Beilina, et al.
Neurochemical Research|October 7, 2018
Differences in Stability, Activity and Mutation Effects Between Human and Mouse Leucine-Rich Repeat Kinase 2Rebekah G Langston, Iakov N Rudenko, Ravindran Kumaran, et al.
Nature Neuroscience|September 1, 2014
Genetic variability in the regulation of gene expression in ten regions of the human brainAdaikalavan Ramasamy, Daniah Trabzuni, Sebastian Guelfi, et al.
Scientific Reports|June 13, 2018
AKT signalling selectively regulates PINK1 mitophagy in SHSY5Y cells and human iPSC-derived neuronsMarc P M Soutar, Liam Kempthorne, Shuichi Miyakawa, et al.
FEBS Open Bio|October 16, 2023
LRRK2 negatively regulates glucose tolerance via regulation of membrane translocation of GLUT4 in adipocytesFumitaka Kawakami, Motoki Imai, Yuki Isaka, et al.
Annals of Neurology|December 11, 2008
Mitochondrial function and morphology are impaired in parkin-mutant fibroblastsHeather Mortiboys, Kelly Jean Thomas, Werner J H Koopman, et al.
The Journal of Biological Chemistry|July 10, 2003
L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome systemDavid W Miller, Rili Ahmad, Stephen Hague, et al.
The International Journal of Neuropsychopharmacology|December 21, 2012
Age-modulated association between prefrontal NAA and the BDNF geneBasira Salehi, Nora Preuss, Jan Willem van der Veen, et al.
Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.
Human Molecular Genetics|June 20, 2018
Proteomic analysis reveals co-ordinated alterations in protein synthesis and degradation pathways in LRRK2 knockout miceLaura Pellegrini, David N Hauser, Yan Li, et al.
Pageof 32