Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex
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Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficienciesMature DIABLO/Smac is produced by the IMP protease complex on the mitochondrial inner membraneMammalian polynucleotide phosphorylase is an intermembrane space RNase that maintains mitochondrial homeostasisOrganization and function of the small Tim complexes acting along the import pathway of metabolite carriers into mammalian mitochondriaThe role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteinsMitochondrial disease in childhood: nuclear encodedEssential role of Mia40 in import and assembly of mitochondrial intermembrane space proteins.Atp23 biogenesis reveals a chaperone-like folding activity of Mia40 in the IMS of mitochondria.Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stabilityInhibition of mitochondrial protein import by mutant huntingtinHistorical perspective on mitochondrial medicineImporting mitochondrial proteins: machineries and mechanismsNeuro-otological syndromes for the neurologist.Juxtaposition of the two distal CX3C motifs via intrachain disulfide bonding is essential for the folding of Tim10.The in-depth evaluation of suspected mitochondrial diseaseRedox regulation of protein folding in the mitochondrial intermembrane space.The 3-methylglutaconic acidurias: what's new?ALS-linked mutant superoxide dismutase 1 (SOD1) alters mitochondrial protein composition and decreases protein import.Is MAC the knife that cuts cytochrome c from mitochondria during apoptosis?Neuronal degeneration and mitochondrial dysfunction.Polyserase-I, a human polyprotease with the ability to generate independent serine protease domains from a single translation product.Mitochondriopathies.Proteomics to display tissue repair opposing injury response to LPS-induced liver injury.Convergent mechanisms in etiologically-diverse dystoniasMitochondrial transporters as novel targets for intracellular calcium signaling.Mitochondrial protein import and human health and disease.Catch me if you can! Oxidative protein trapping in the intermembrane space of mitochondriaOtopathology in Mohr-Tranebjaerg syndromeAmyloid precursor protein and mitochondrial dysfunction in Alzheimer's disease.Folding and biogenesis of mitochondrial small Tim proteins.The power of yeast to model diseases of the powerhouse of the cell.Neurodevelopmental manifestations of mitochondrial disease.The mitochondrial connection in auditory neuropathy.Mechanisms of mitochondrial diseases.Mitochondrial disulfide relay: redox-regulated protein import into the intermembrane space.Oxidative folding in the mitochondrial intermembrane space in human health and disease.Mechanisms of exercise-induced mitochondrial biogenesis in skeletal muscle: implications for health and disease.Mitochondrial protein translocases for survival and wellbeing.The TIM23 mitochondrial protein import complex: function and dysfunction.Mitochondrial import of the ADP/ATP carrier: the essential TIM complex of the intermembrane space is required for precursor release from the TOM complex.
P2860
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P2860
Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex
description
2002 nî lūn-bûn
@nan
2002 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մարտին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@ast
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@en
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@nl
type
label
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@ast
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@en
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@nl
prefLabel
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@ast
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@en
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@nl
P2093
P3181
P356
P1476
Human deafness dystonia syndro ...... the DDP1/TIMM8a-TIMM13 complex
@en
P2093
Carla M Koehler
Karin Roesch
Lisbeth Tranebjaerg
Sean P Curran
P304
P3181
P356
10.1093/HMG/11.5.477
P407
P577
2002-03-01T00:00:00Z