Cardiolipin, a critical determinant of mitochondrial carrier protein assembly and function

por Claypool, Steven M.
Publicado em 2009

The Complexity of Cardiolipin in Health and Disease

por Claypool, Steven M., Koehler, Carla M.
Publicado em 2011

The power of yeast to model diseases of the powerhouse of the cell

por Baile, Matthew G., Claypool, Steven M
Publicado em 2013

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

por Lu, Ya-Wen, Claypool, Steven M.
Publicado no Front Genet (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 no Front Cell Dev Biol (2019)

Phosphatidylethanolamine Metabolism in Health and Disease

por Calzada, Elizabeth, Onguka, Ouma, Claypool, Steven M.
Publicado no Int Rev Cell Mol Biol (2015)

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

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

Proteolytic Control of Lipid Metabolism

por Sam, Pingdewinde N., Avery, Erica, Claypool, Steven M.
Publicado no ACS Chem Biol (2019)

Phospholipid ebb and flow makes mitochondria go

por Acoba, Michelle Grace, Senoo, Nanami, Claypool, Steven M.
Publicado no J Cell Biol (2020)

The Taz1p Transacylase Is Imported and Sorted into the Outer Mitochondrial Membrane via a Membrane Anchor Domain

por Herndon, Jenny D., Claypool, Steven M., Koehler, Carla M.
Publicado em 2013

The topology and regulation of cardiolipin biosynthesis and remodeling in yeast

por Baile, Matthew G., Lu, Ya Wen, Claypool, Steven M.
Publicado em 2013

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 no Mol Biol Cell (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 em 2006

Seven functional classes of Barth syndrome mutation

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

Phosphatidylserine Decarboxylase 1 Autocatalysis and Function Does Not Require a Mitochondrial-specific Factor

por Onguka, Ouma, Calzada, Elizabeth, Ogunbona, Oluwaseun B., Claypool, Steven M.
Publicado no J Biol Chem (2015)

Multitiered and Cooperative Surveillance of Mitochondrial Phosphatidylserine Decarboxylase 1

por Ogunbona, Oluwaseun B., Onguka, Ouma, Calzada, Elizabeth, Claypool, Steven M.
Publicado no Mol Cell Biol (2017)

Tafazzinsfrom Drosophila and Mammalian Cells Assemble in Large Protein Complexes with a Short Half-Life

por Xu, Yang, Malhotra, Ashim, Claypool, Steven M., Ren, Mindong, Schlame, Michael
Publicado no Mitochondrion (2015)

Barth syndrome mutations that cause tafazzin complex lability

por Claypool, Steven M., Whited, Kevin, Srijumnong, Santi, Han, Xianlin, Koehler, Carla M.
Publicado em 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 em 2008

Functional Reconstitution of Human FcRn in Madin-Darby Canine Kidney Cells Requires Co-expressed Human β(2)-Microglobulin

por Claypool, Steven M., Dickinson, Bonny L., Yoshida, Masaru, Lencer, Wayne I., Blumberg, Richard S.
Publicado em 2002