The mitochondrial contact site complex, a determinant of mitochondrial architecture.
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Sam50 functions in mitochondrial intermembrane space bridging and biogenesis of respiratory complexesDetailed analysis of the human mitochondrial contact site complex indicate a hierarchy of subunitsQIL1 is a novel mitochondrial protein required for MICOS complex stability and cristae morphologyMINOS1 is a conserved component of mitofilin complexes and required for mitochondrial function and cristae organizationThe connection between inner membrane topology and mitochondrial functionPhospholipid transport via mitochondriaMitochondrial form and functionEvolutionary origin of the mitochondrial cholesterol transport machinery reveals a universal mechanism of steroid hormone biosynthesis in animalsA splicing mutation in the novel mitochondrial protein DNAJC11 causes motor neuron pathology associated with cristae disorganization, and lymphoid abnormalities in micePhosphatidylethanolamine biosynthesis in mitochondria: phosphatidylserine (PS) trafficking is independent of a PS decarboxylase and intermembrane space proteins UPS1P and UPS2P.Intramitochondrial transport of phosphatidic acid in yeast by a lipid transfer protein.Role for two conserved intermembrane space proteins, Ups1p and Ups2p, [corrected] in intra-mitochondrial phospholipid trafficking.Aim24 and MICOS modulate respiratory function, tafazzin-related cardiolipin modification and mitochondrial architectureRole of the AAA protease Yme1 in folding of proteins in the intermembrane space of mitochondria.Oxidative folding in the mitochondrial intermembrane space: A regulated process important for cell physiology and diseaseMutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorderOPA1-dependent cristae modulation is essential for cellular adaptation to metabolic demandBioanalysis of eukaryotic organellesTransgenic overexpression of mitofilin attenuates diabetes mellitus-associated cardiac and mitochondria dysfunctionDisorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genesThe topology and regulation of cardiolipin biosynthesis and remodeling in yeastLearning from Heterogeneous Data Sources: An Application in Spatial ProteomicsMitochondria: in sickness and in healthBiogenesis of mitochondrial outer membrane proteins, problems and diseases.Analysis of mutations in Neurospora crassa ERMES components reveals specific functions related to β-barrel protein assembly and maintenance of mitochondrial morphology.Role of mitochondrial inner membrane organizing system in protein biogenesis of the mitochondrial outer membrane.The C-terminal domain of Fcj1 is required for formation of crista junctions and interacts with the TOB/SAM complex in mitochondria.Regulated membrane remodeling by Mic60 controls formation of mitochondrial crista junctionsQIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver diseaseAge-dependent dissociation of ATP synthase dimers and loss of inner-membrane cristae in mitochondriaTransient contraction of mitochondria induces depolarization through the inner membrane dynamin OPA1 protein.A foundation for reliable spatial proteomics data analysis.Translocation of glycogen synthase kinase-3β (GSK-3β), a trigger of permeability transition, is kinase activity-dependent and mediated by interaction with voltage-dependent anion channel 2 (VDAC2).In vivo functions of Drp1: lessons learned from yeast genetics and mouse knockoutsBridging the gap: membrane contact sites in signaling, metabolism, and organelle dynamics.Mitochondrial Nucleoid: Shield and Switch of the Mitochondrial Genome.The Emerging Network of Mitochondria-Organelle Contacts.Mitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusionMitochondrial protein synthesis, import, and assembly.Azole susceptibility and transcriptome profiling in Candida albicans mitochondrial electron transport chain complex I mutants.
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P2860
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
description
2011 nî lūn-bûn
@nan
2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@ast
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@en
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@nl
type
label
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@ast
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@en
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@nl
prefLabel
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@ast
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@en
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@nl
P2093
P2860
P50
P921
P3181
P356
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P1476
The mitochondrial contact site complex, a determinant of mitochondrial architecture.
@en
P2093
Christian Körner
Dirk Walther
Matthias Mann
Max Harner
Ulrich Welsch
P2860
P304
P3181
P356
10.1038/EMBOJ.2011.379
P407
P577
2011-10-18T00:00:00Z