Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Kevin Whited"'
Autor:
Nanami Senoo, Dinesh K. Chinthapalli, Matthew G. Baile, Vinaya K. Golla, Bodhisattwa Saha, Oluwaseun B. Ogunbona, James A. Saba, Teona Munteanu, Yllka Valdez, Kevin Whited, Dror Chorev, Nathan N. Alder, Eric R. May, Carol V. Robinson, Steven M. Claypool
Publikováno v:
bioRxiv
SummaryThe mitochondrial phospholipid cardiolipin (CL) promotes bioenergetics via oxidative phosphorylation (OXPHOS). Three tightly bound CLs are evolutionarily conserved in the ADP/ATP carrier (AAC in yeast; adenine nucleotide translocator, ANT in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62db7af3c461236f7d1ff1a4f2f4668b
https://europepmc.org/articles/PMC10187269/
https://europepmc.org/articles/PMC10187269/
Autor:
Nathan N. Alder, Xianlin Han, J. Michael McCaffery, Erin N. Pryce, Murugappan Sathappa, Ya-Wen Lu, Kevin Whited, Matthew G. Baile, Steven M. Claypool
Publikováno v:
Journal of Biological Chemistry. 289:1768-1778
After biosynthesis, an evolutionarily conserved acyl chain remodeling process generates a final highly homogeneous and yet tissue-specific molecular form of the mitochondrial lipid cardiolipin. Hence, cardiolipin molecules in different organisms, and
Publikováno v:
Molecular Biology of the Cell
Our understanding of the clinically relevant tafazzin-mediated cardiolipin (CL) remodeling pathway is incomplete. In this study, a new trafficking step required for CL remodeling has been identified. Further, it is demonstrated that flux through this
Publikováno v:
The Journal of cell biology, vol 192, iss 3
The Journal of Cell Biology
The Journal of Cell Biology
Complexes containing tafazzin, which remodels newly synthesized cardiolipin, are destabilized by mutations associated with Barth syndrome.
Deficits in mitochondrial function result in many human diseases. The X-linked disease Barth syndrome (BTH
Deficits in mitochondrial function result in many human diseases. The X-linked disease Barth syndrome (BTH
Publikováno v:
The FASEB Journal. 27
Publikováno v:
Human molecular genetics. 22(3)
Patients with Barth syndrome (BTHS), a rare X-linked disease, suffer from skeletal and cardiomyopathy and bouts of cyclic neutropenia. The causative gene encodes tafazzin, a transacylase, which is the major determinant of the final acyl chain composi
Publikováno v:
Genomics & Genetics Weekly; 6/24/2024, p247-247, 1p
Publikováno v:
MMWR: Morbidity & Mortality Weekly Report. 5/3/2002, Vol. 51 Issue 17, p365. 5p. 1 Black and White Photograph, 1 Map.
Autor:
DeWitt, David
Publikováno v:
Athens News; 5/26/2015, p9-10, 2p
Publikováno v:
Indianapolis Monthly; Jun/Jul2020, p59-85, 27p, 238 Color Photographs