Role of the deafness dystonia peptide 1 (DDP1) in import of human Tim23 into the inner membrane of mitochondria
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Organization and function of the small Tim complexes acting along the import pathway of metabolite carriers into mammalian mitochondriaMutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like conditionThe role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteinsThe C66W mutation in the deafness dystonia peptide 1 (DDP1) affects the formation of functional DDP1.TIM13 complexes in the mitochondrial intermembrane spaceThe Princeton Protein Orthology Database (P-POD): a comparative genomics analysis tool for biologistsA fluorescent two-hybrid assay for direct visualization of protein interactions in living cells.Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies.Mitochondrial assembly: protein import.Protein import into mitochondria: origins and functions today (review).Mitochondrial protein import and human health and disease.Folding and biogenesis of mitochondrial small Tim proteins.The power of yeast to model diseases of the powerhouse of the cell.Health risks of space exploration: targeted and nontargeted oxidative injury by high-charge and high-energy particles.Ionizing radiation-induced metabolic oxidative stress and prolonged cell injury.Mitochondrial disulfide relay and its substrates: mechanisms in health and disease.The TIM23 mitochondrial protein import complex: function and dysfunction.Novel variants of human SCaMC-3, an isoform of the ATP-Mg/P(i) mitochondrial carrier, generated by alternative splicing from 3'-flanking transposable elements.A trypanosomal orthologue of an intermembrane space chaperone has a non-canonical function in biogenesis of the single mitochondrial inner membrane protein translocase.Previously Unreported Biallelic Mutation in DNAJC19: Are Sensorineural Hearing Loss and Basal Ganglia Lesions Additional Features of Dilated Cardiomyopathy and Ataxia (DCMA) Syndrome?The role of Tim9p in the assembly of the TIM22 import complexes.Intra-mitochondrial degradation of Tim23 curtails the survival of cells rescued from apoptosis by caspase inhibitors.Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism.Defective mitochondrial protein import contributes to complex I-induced mitochondrial dysfunction and neurodegeneration in Parkinson's disease
P2860
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P2860
Role of the deafness dystonia peptide 1 (DDP1) in import of human Tim23 into the inner membrane of mitochondria
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Role of the deafness dystonia ...... inner membrane of mitochondria
@ast
Role of the deafness dystonia ...... inner membrane of mitochondria
@en
Role of the deafness dystonia ...... inner membrane of mitochondria
@nl
type
label
Role of the deafness dystonia ...... inner membrane of mitochondria
@ast
Role of the deafness dystonia ...... inner membrane of mitochondria
@en
Role of the deafness dystonia ...... inner membrane of mitochondria
@nl
prefLabel
Role of the deafness dystonia ...... inner membrane of mitochondria
@ast
Role of the deafness dystonia ...... inner membrane of mitochondria
@en
Role of the deafness dystonia ...... inner membrane of mitochondria
@nl
P2093
P2860
P356
P1476
Role of the deafness dystonia ...... inner membrane of mitochondria
@en
P2093
K D Gerbitz
N Mühlenbein
S A Paschen
P2860
P304
P356
10.1074/JBC.M105313200
P407
P577
2001-10-05T00:00:00Z