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Debdeep Dutta

Showing results (11-20 of 21) with videos related to

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Elife|June 20, 2022
An expanded toolkit for <i>Drosophila</i> gene tagging using synthesized homology donor constructs for CRISPR-mediated homologous recombinationOguz Kanca, Jonathan Zirin, Yanhui Hu, et al.
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.
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.
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.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 7, 2024
Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalitiesMatthew J Moulton, Kristhen Atala, Yiming Zheng, et al.
Science Advances|January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signalingPaul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
<i>De novo</i> variants in <i>PLCG1</i> are associated with hearing impairment, ocular pathology, and cardiac defectsMengqi Ma, Yiming Zheng, Shenzhao Lu, et al.
Elife|August 27, 2025
Heterozygous variants in <i>PLCG1</i> affect hearing, vision, cardiac, and immune functionMengqi Ma, Yiming Zheng, Mingxi Deng, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Elife|June 20, 2022
An expanded toolkit for <i>Drosophila</i> gene tagging using synthesized homology donor constructs for CRISPR-mediated homologous recombinationOguz Kanca, Jonathan Zirin, Yanhui Hu, et al.
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.
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.
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.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 7, 2024
Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalitiesMatthew J Moulton, Kristhen Atala, Yiming Zheng, et al.
Science Advances|January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signalingPaul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
<i>De novo</i> variants in <i>PLCG1</i> are associated with hearing impairment, ocular pathology, and cardiac defectsMengqi Ma, Yiming Zheng, Shenzhao Lu, et al.
Elife|August 27, 2025
Heterozygous variants in <i>PLCG1</i> affect hearing, vision, cardiac, and immune functionMengqi Ma, Yiming Zheng, Mingxi Deng, et al.
Pageof 3