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Steven M Claypool

Showing results (61-70 of 73) with videos related to

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The Journal of Biological Chemistry|July 16, 2020
Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondriaCatherine H Le, Lindsay G Benage, Kalyn S Specht, et al.
Molecular Biology of the Cell|November 16, 2007
Ca2+-dependent calmodulin binding to FcRn affects immunoglobulin G transport in the transcytotic pathwayBonny L Dickinson, Steven M Claypool, June A D'Angelo, et al.
Journal of Cell Science|February 2, 2021
Adenine nucleotide translocase regulates airway epithelial metabolism, surface hydration and ciliary functionCorrine R Kliment, Jennifer M K Nguyen, Mary Jane Kaltreider, et al.
Human Molecular Genetics|February 25, 2016
Defining functional classes of Barth syndrome mutation in humansYa-Wen Lu, Laura Galbraith, Jenny D Herndon, et al.
The Journal of Clinical Investigation|July 15, 2006
Neonatal Fc receptor for IgG regulates mucosal immune responses to luminal bacteriaMasaru Yoshida, Kanna Kobayashi, Timothy T Kuo, et al.
Life Science Alliance|March 13, 2019
<i>PISD</i> is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changesTian Zhao, Caitlin M Goedhart, Pingdewinde N Sam, et al.
Biorxiv : the Preprint Server for Biology|May 19, 2023
Conserved cardiolipin-mitochondrial ADP/ATP carrier interactions assume distinct structural and functional roles that are clinically relevantNanami Senoo, Dinesh K Chinthapalli, Matthew G Baile, et al.
The EMBO Journal|June 5, 2024
Functional diversity among cardiolipin binding sites on the mitochondrial ADP/ATP carrierNanami Senoo, Dinesh K Chinthapalli, Matthew G Baile, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
Mdm38/LETM1 couples ion homeostasis and proteostatic mechanisms in the inner mitochondrial membraneIryna Bohovych, Gabriella Menezes da Silva, Saieeda Fabia Ali, et al.
JCI Insight|June 9, 2026
Omega-3 fatty acid supplementation improves skeletal muscle mitochondrial function in a model of Barth syndromeKatharina B Kuentzel, Ana Vranešević, Samuel Aj Trammell, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
The Journal of Biological Chemistry|July 16, 2020
Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondriaCatherine H Le, Lindsay G Benage, Kalyn S Specht, et al.
Molecular Biology of the Cell|November 16, 2007
Ca2+-dependent calmodulin binding to FcRn affects immunoglobulin G transport in the transcytotic pathwayBonny L Dickinson, Steven M Claypool, June A D'Angelo, et al.
Journal of Cell Science|February 2, 2021
Adenine nucleotide translocase regulates airway epithelial metabolism, surface hydration and ciliary functionCorrine R Kliment, Jennifer M K Nguyen, Mary Jane Kaltreider, et al.
Human Molecular Genetics|February 25, 2016
Defining functional classes of Barth syndrome mutation in humansYa-Wen Lu, Laura Galbraith, Jenny D Herndon, et al.
The Journal of Clinical Investigation|July 15, 2006
Neonatal Fc receptor for IgG regulates mucosal immune responses to luminal bacteriaMasaru Yoshida, Kanna Kobayashi, Timothy T Kuo, et al.
Life Science Alliance|March 13, 2019
<i>PISD</i> is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changesTian Zhao, Caitlin M Goedhart, Pingdewinde N Sam, et al.
Biorxiv : the Preprint Server for Biology|May 19, 2023
Conserved cardiolipin-mitochondrial ADP/ATP carrier interactions assume distinct structural and functional roles that are clinically relevantNanami Senoo, Dinesh K Chinthapalli, Matthew G Baile, et al.
The EMBO Journal|June 5, 2024
Functional diversity among cardiolipin binding sites on the mitochondrial ADP/ATP carrierNanami Senoo, Dinesh K Chinthapalli, Matthew G Baile, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
Mdm38/LETM1 couples ion homeostasis and proteostatic mechanisms in the inner mitochondrial membraneIryna Bohovych, Gabriella Menezes da Silva, Saieeda Fabia Ali, et al.
JCI Insight|June 9, 2026
Omega-3 fatty acid supplementation improves skeletal muscle mitochondrial function in a model of Barth syndromeKatharina B Kuentzel, Ana Vranešević, Samuel Aj Trammell, et al.
Pageof 8