about
Functional reconstitution of human FcRn in Madin-Darby canine kidney cells requires co-expressed human beta 2-microglobulinPhosphatidylethanolamine biosynthesis in mitochondria: phosphatidylserine (PS) trafficking is independent of a PS decarboxylase and intermembrane space proteins UPS1P and UPS2P.Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzinsPhosphatidylserine decarboxylase 1 autocatalysis and function does not require a mitochondrial-specific factor.Defining functional classes of Barth syndrome mutation in humansDisorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genesThe topology and regulation of cardiolipin biosynthesis and remodeling in yeastCardiolipin, a critical determinant of mitochondrial carrier protein assembly and function.Acyl-CoA thioesterase-2 facilitates mitochondrial fatty acid oxidation in the liverNeonatal Fc receptor for IgG regulates mucosal immune responses to luminal bacteriaMetalloprotease OMA1 Fine-tunes Mitochondrial Bioenergetic Function and Respiratory Supercomplex Stability.Ca2+-dependent calmodulin binding to FcRn affects immunoglobulin G transport in the transcytotic pathwaySpecific degradation of phosphatidylglycerol is necessary for proper mitochondrial morphology and functionTafazzins from Drosophila and mammalian cells assemble in large protein complexes with a short half-life.Phosphatidylethanolamine Metabolism in Health and Disease.Seven functional classes of Barth syndrome mutationCardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membraneBidirectional transepithelial IgG transport by a strongly polarized basolateral membrane Fcgamma-receptor.The power of yeast to model diseases of the powerhouse of the cell.The Taz1p transacylase is imported and sorted into the outer mitochondrial membrane via a membrane anchor domain.Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondriaImpaired Cardiolipin Biosynthesis Prevents Hepatic Steatosis and Diet-Induced Obesity.The Mammalian Malonyl-CoA Synthetase ACSF3 Is Required for Mitochondrial Protein Malonylation and Metabolic Efficiency.Human adenine nucleotide translocases physically and functionally interact with respirasomes.Natural and Induced Mitochondrial Phosphate Carrier Loss: DIFFERENTIAL DEPENDENCE OF MITOCHONDRIAL METABOLISM AND DYNAMICS AND CELL SURVIVAL ON THE EXTENT OF DEPLETION.Role for two conserved intermembrane space proteins, Ups1p and Ups2p, in intra-mitochondrial phospholipid trafficking.Multitiered and Cooperative Surveillance of Mitochondrial Phosphatidylserine Decarboxylase 1.Human neonatal Fc receptor mediates transport of IgG into luminal secretions for delivery of antigens to mucosal dendritic cells.Krüppel-like factor 4 (KLF4) induces mitochondrial fusion and increases spare respiratory capacity of human glioblastoma cells.Developmental regulation of TCR delta locus accessibility and expression by the TCR delta enhancer.Cardiomyopathy-associated mutation in the ADP/ATP carrier reveals translation-dependent regulation of cytochrome c oxidase activity.IgG transport across mucosal barriers by neonatal Fc receptor for IgG and mucosal immunityAntigen presentation by intestinal epithelial cellsPhosphatidylethanolamine made in the inner mitochondrial membrane is essential for yeast cytochrome bc complex functionis a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changesProteolytic Control of Lipid MetabolismSystems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Steven M Claypool
@ast
Steven M Claypool
@en
Steven M Claypool
@es
Steven M Claypool
@nl
type
label
Steven M Claypool
@ast
Steven M Claypool
@en
Steven M Claypool
@es
Steven M Claypool
@nl
prefLabel
Steven M Claypool
@ast
Steven M Claypool
@en
Steven M Claypool
@es
Steven M Claypool
@nl
P106
P1153
6603089451
P31
P496
0000-0001-5316-1623