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Paul C Marcogliese

Showing results (11-20 of 35) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 21, 2024
Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viabilityDebdeep Dutta, Oguz Kanca, Rishi V Shridharan, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
DJ-1 protects the nigrostriatal axis from the neurotoxin MPTP by modulation of the AKT pathwayHossein Aleyasin, Maxime W C Rousseaux, Paul C Marcogliese, et al.
Nature Communications|April 18, 2024
Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in DrosophilaJenny Zhe Liao, Hyung-Lok Chung, Claire Shih, et al.
Nature Metabolism|August 31, 2023
A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levelsDebdeep Dutta, Oguz Kanca, Seul Kee Byeon, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 2018
Regulation of myeloid cell phagocytosis by LRRK2 via WAVE2 complex stabilization is altered in Parkinson's diseaseKwang Soo Kim, Paul C Marcogliese, Jungwoo Yang, et al.
Cell Reports|December 8, 2022
Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategyShrestha Sinha Ray, Debdeep Dutta, Cassandra Dennys, et al.
The Journal of Biological Chemistry|November 6, 2015
BAG2 Gene-mediated Regulation of PINK1 Protein Is Critical for Mitochondrial Translocation of PARKIN and Neuronal SurvivalDianbo Qu, Ali Hage, Katie Don-Carolis, et al.
Human Molecular Genetics|March 2, 2022
De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in DrosophilaHyung-Lok Chung, Patrick Rump, Di Lu, et al.
Human Molecular Genetics|May 2, 2020
De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairmentDebdeep Dutta, Lauren C Briere, Oguz Kanca, et al.
American Journal of Human Genetics|April 25, 2020
De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic EncephalopathyHyung-Lok Chung, Xiao Mao, Hua Wang, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2024
Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viabilityDebdeep Dutta, Oguz Kanca, Rishi V Shridharan, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
DJ-1 protects the nigrostriatal axis from the neurotoxin MPTP by modulation of the AKT pathwayHossein Aleyasin, Maxime W C Rousseaux, Paul C Marcogliese, et al.
Nature Communications|April 18, 2024
Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in DrosophilaJenny Zhe Liao, Hyung-Lok Chung, Claire Shih, et al.
Nature Metabolism|August 31, 2023
A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levelsDebdeep Dutta, Oguz Kanca, Seul Kee Byeon, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 2018
Regulation of myeloid cell phagocytosis by LRRK2 via WAVE2 complex stabilization is altered in Parkinson's diseaseKwang Soo Kim, Paul C Marcogliese, Jungwoo Yang, et al.
Cell Reports|December 8, 2022
Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategyShrestha Sinha Ray, Debdeep Dutta, Cassandra Dennys, et al.
The Journal of Biological Chemistry|November 6, 2015
BAG2 Gene-mediated Regulation of PINK1 Protein Is Critical for Mitochondrial Translocation of PARKIN and Neuronal SurvivalDianbo Qu, Ali Hage, Katie Don-Carolis, et al.
Human Molecular Genetics|March 2, 2022
De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in DrosophilaHyung-Lok Chung, Patrick Rump, Di Lu, et al.
Human Molecular Genetics|May 2, 2020
De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairmentDebdeep Dutta, Lauren C Briere, Oguz Kanca, et al.
American Journal of Human Genetics|April 25, 2020
De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic EncephalopathyHyung-Lok Chung, Xiao Mao, Hua Wang, et al.
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