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Craig Blackstone

Showing results (71-80 of 125) with videos related to

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Molecular Biology of the Cell|August 20, 2010
SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesisBenoît Renvoisé, Rell L Parker, Dong Yang, et al.
Frontiers in Molecular Neuroscience|March 26, 2016
Protective LRRK2 R1398H Variant Enhances GTPase and Wnt Signaling ActivityJonathon Nixon-Abell, Daniel C Berwick, Simone Grannó, et al.
The Journal of Biological Chemistry|September 25, 2003
Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastinPeng-Peng Zhu, Andrew Patterson, Brigitte Lavoie, et al.
Experimental Cell Research|September 28, 2016
Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphologyGuohua Zhao, Peng-Peng Zhu, Benoît Renvoisé, et al.
Human Molecular Genetics|May 5, 2018
Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegiasKyle Denton, Yongchao Mou, Chong-Chong Xu, et al.
Brain Research|December 11, 2012
N-terminal cleavage of the mitochondrial fusion GTPase OPA1 occurs via a caspase-independent mechanism in cerebellar granule neurons exposed to oxidative or nitrosative stressJosie J Gray, Amelia E Zommer, Ron J Bouchard, et al.
Genes|June 24, 2022
Nonalcoholic Fatty Liver Disease in Patients with Inherited and Sporadic Motor Neuron DegenerationBrian Johnson, Angela Kokkinis, Neville Gai, et al.
Annals of Clinical and Translational Neurology|January 10, 2015
Laing distal myopathy pathologically resembling inclusion body myositisRicardo H Roda, Alice B Schindler, Craig Blackstone, et al.
Human Molecular Genetics|September 18, 2016
Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulationBenoît Renvoisé, Brianna Malone, Melanie Falgairolle, et al.
The Journal of Biological Chemistry|August 11, 2010
A lethal de novo mutation in the middle domain of the dynamin-related GTPase Drp1 impairs higher order assembly and mitochondrial divisionChuang-Rung Chang, Cara Marie Manlandro, Damien Arnoult, et al.
Pageof 13

Showing results (71-80 of 125) with videos related to

Sort By:
Pageof 13
Molecular Biology of the Cell|August 20, 2010
SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesisBenoît Renvoisé, Rell L Parker, Dong Yang, et al.
Frontiers in Molecular Neuroscience|March 26, 2016
Protective LRRK2 R1398H Variant Enhances GTPase and Wnt Signaling ActivityJonathon Nixon-Abell, Daniel C Berwick, Simone Grannó, et al.
The Journal of Biological Chemistry|September 25, 2003
Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastinPeng-Peng Zhu, Andrew Patterson, Brigitte Lavoie, et al.
Experimental Cell Research|September 28, 2016
Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphologyGuohua Zhao, Peng-Peng Zhu, Benoît Renvoisé, et al.
Human Molecular Genetics|May 5, 2018
Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegiasKyle Denton, Yongchao Mou, Chong-Chong Xu, et al.
Brain Research|December 11, 2012
N-terminal cleavage of the mitochondrial fusion GTPase OPA1 occurs via a caspase-independent mechanism in cerebellar granule neurons exposed to oxidative or nitrosative stressJosie J Gray, Amelia E Zommer, Ron J Bouchard, et al.
Genes|June 24, 2022
Nonalcoholic Fatty Liver Disease in Patients with Inherited and Sporadic Motor Neuron DegenerationBrian Johnson, Angela Kokkinis, Neville Gai, et al.
Annals of Clinical and Translational Neurology|January 10, 2015
Laing distal myopathy pathologically resembling inclusion body myositisRicardo H Roda, Alice B Schindler, Craig Blackstone, et al.
Human Molecular Genetics|September 18, 2016
Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulationBenoît Renvoisé, Brianna Malone, Melanie Falgairolle, et al.
The Journal of Biological Chemistry|August 11, 2010
A lethal de novo mutation in the middle domain of the dynamin-related GTPase Drp1 impairs higher order assembly and mitochondrial divisionChuang-Rung Chang, Cara Marie Manlandro, Damien Arnoult, et al.
Pageof 13