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The Journal of Biological Chemistry
|
July 16, 2020
Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondria
Catherine 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 pathway
Bonny 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 function
Corrine 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 humans
Ya-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 bacteria
Masaru 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 changes
Tian 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 relevant
Nanami 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 carrier
Nanami 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 membrane
Iryna 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 syndrome
Katharina B Kuentzel, Ana Vranešević, Samuel Aj Trammell, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 8
The Journal of Biological Chemistry
|
July 16, 2020
Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondria
Catherine 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 pathway
Bonny 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 function
Corrine 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 humans
Ya-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 bacteria
Masaru 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 changes
Tian 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 relevant
Nanami 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 carrier
Nanami 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 membrane
Iryna 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 syndrome
Katharina B Kuentzel, Ana Vranešević, Samuel Aj Trammell, et al.
Page
of 8