Disorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genes

por Lu, Ya-Wen, Claypool, Steven M.
Publicado 2015

Emerging Roles in the Biogenesis of Cytochrome c Oxidase for Members of the Mitochondrial Carrier Family

por Ogunbona, Oluwaseun B., Claypool, Steven M.
Publicado 2019

Deacylation on the matrix side of the mitochondrial inner membrane regulates cardiolipin remodeling

por Baile, Matthew G., Whited, Kevin, Claypool, Steven M.
Publicado 2013

Phospholipid ebb and flow makes mitochondria go

por Acoba, Michelle Grace, Senoo, Nanami, Claypool, Steven M.
Publicado 2020

Cardiomyopathy-associated mutation in the ADP/ATP carrier reveals translation-dependent regulation of cytochrome c oxidase activity

por Ogunbona, Oluwaseun B., Baile, Matthew G., Claypool, Steven M.
Publicado 2018

Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins

por Claypool, Steven M., McCaffery, J. Michael, Koehler, Carla M.
Publicado 2006

Barth syndrome mutations that cause tafazzin complex lability

por Claypool, Steven M., Whited, Kevin, Srijumnong, Santi, Han, Xianlin, Koehler, Carla M.
Publicado 2011

Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane

por Claypool, Steven M., Oktay, Yavuz, Boontheung, Pinmanee, Loo, Joseph A., Koehler, Carla M.
Publicado 2008

Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane

por Claypool, Steven M., Oktay, Yavuz, Boontheung, Pinmanee, Loo, Joseph A., Koehler, Carla M.
Publicado 2012

Tim54p connects inner membrane assembly and proteolytic pathways in the mitochondrion

por Hwang, David K., Claypool, Steven M., Leuenberger, Danielle, Tienson, Heather L., Koehler, Carla M.
Publicado 2007

Cardiolipin, Mitochondria, and Neurological Disease

por Falabella, Micol, Vernon, Hilary J., Hanna, Michael G., Claypool, Steven M., Pitceathly, Robert D.S.
Publicado 2021

The Influence of Supplemental Dietary Linoleic Acid on Skeletal Muscle Contractile Function in a Rodent Model of Barth Syndrome

por Elkes, Mario, Andonovski, Martin, Vidal, Daislyn, Farago, Madison, Modafferi, Ryan, Claypool, Steven M., LeBlanc, Paul J.
Publicado 2021

Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria

por Steffen, Janos, Vashisht, Ajay A., Wan, Jijun, Jen, Joanna C., Claypool, Steven M., Wohlschlegel, James A., Koehler, Carla M.
Publicado 2017

Human adenine nucleotide translocases physically and functionally interact with respirasomes

por Lu, Ya-Wen, Acoba, Michelle Grace, Selvaraju, Kandasamy, Huang, Tai-Chung, Nirujogi, Raja S., Sathe, Gajanan, Pandey, Akhilesh, Claypool, Steven M.
Publicado 2017

Impaired Cardiolipin Biosynthesis Prevents Hepatic Steatosis and Diet-Induced Obesity

por Cole, Laura K., Mejia, Edgard M., Vandel, Marilyne, Sparagna, Genevieve C., Claypool, Steven M., Dyck-Chan, Laura, Klein, Julianne, Hatch, Grant M.
Publicado 2016

Erratum. Impaired Cardiolipin Biosynthesis Prevents Hepatic Steatosis and Diet-Induced Obesity. Diabetes 2016;65:3289–3300

por Cole, Laura K., Mejia, Edgard M., Vandel, Marilyne, Sparagna, Genevieve C., Claypool, Steven M., Dyck-Chan, Laura, Klein, Julianne, Hatch, Grant M.
Publicado 2017

Phosphatidylethanolamine made in the inner mitochondrial membrane is essential for yeast cytochrome bc(1) complex function

por Calzada, Elizabeth, Avery, Erica, Sam, Pingdewinde N., Modak, Arnab, Wang, Chunyan, McCaffery, J. Michael, Han, Xianlin, Alder, Nathan N., Claypool, Steven M.
Publicado 2019

Secretory pathway Ca(2+)-ATPase SPCA2 regulates mitochondrial respiration and DNA damage response through store-independent calcium entry

por Makena, Monish Ram, Ko, Myungjun, Mekile, Allatah X., Senoo, Nanami, Dang, Donna K., Warrington, John, Buckhaults, Phillip, Talbot, C. Conover, Claypool, Steven M., Rao, Rajini
Publicado 2022

Impaired phosphatidylethanolamine metabolism activates a reversible stress response that detects and resolves mutant mitochondrial precursors

por Sam, Pingdewinde N., Calzada, Elizabeth, Acoba, Michelle Grace, Zhao, Tian, Watanabe, Yasunori, Nejatfard, Anahita, Trinidad, Jonathan C., Shutt, Timothy E., Neal, Sonya E., Claypool, Steven M.
Publicado 2021

The mitochondrial carrier SFXN1 is critical for complex III integrity and cellular metabolism

por Acoba, Michelle Grace, Alpergin, Ebru S. Selen, Renuse, Santosh, Fernández-del-Río, Lucía, Lu, Ya-Wen, Khalimonchuk, Oleh, Clarke, Catherine F., Pandey, Akhilesh, Wolfgang, Michael J., Claypool, Steven M.
Publicado 2021