Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
about
A mitochondrial DNA hypomorph of cytochrome oxidase specifically impairs male fertility in Drosophila melanogasterA Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer.De novo mtDNA point mutations are common and have a low recurrence risk.Nongradient blue native gel analysis of serum proteins and in-gel detection of serum esterase activities.Mitochondrial complex 1 gene analysis in keratoconus.A mutation in the NADH-dehydrogenase subunit 2 suppresses fibroblast aging.Codon bias and gene expression of mitochondrial ND2 gene in chordates.Mitochondrial respiratory complex I: structure, function and implication in human diseases.Single gene deletions of mrpA to mrpG and mrpE point mutations affect activity of the Mrp Na+/H+ antiporter of alkaliphilic Bacillus and formation of hetero-oligomeric Mrp complexesA Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease.Resolving mitochondrial protein complexes using nongradient blue native polyacrylamide gel electrophoresis.The genetics and pathology of mitochondrial disease.COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation.Identification of key genes in Gram‑positive and Gram‑negative sepsis using stochastic perturbation.Dynamic comparisons of high-resolution expression profiles highlighting mitochondria-related genes between in vivo and in vitro fertilized early mouse embryos.Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene.Mitochondrial DNA Haplogroup A Decreases the Risk of Drug Addiction but Conversely Increases the Risk of HIV-1 Infection in Chinese Addicts.Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.Association of a missense nucleotide polymorphism in the MT-ND2 gene with mitochondrial reactive oxygen species production in the Tibet chicken embryo incubated in normoxia or simulated hypoxia.The expression characteristics of mt-ND2 gene in chicken.Mitochondrial Mutations in Cholestatic Liver Disease with Biliary Atresia.Study on heteroplasmic variation and the effect of chicken mitochondrial ND2.TMEM126B deficiency reduces mitochondrial SDH oxidation by LPS, attenuating HIF-1α stabilization and IL-1β expression
P2860
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P2860
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
@en
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
@nl
type
label
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
@en
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
@nl
prefLabel
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
@en
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
@nl
P2093
P50
P1476
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome
@en
P2093
Jan A M Smeitink
Johanna Uusimaa
Kari Majamaa
Lambert P van Heuvel
Leo G J Nijtmans
Roel Smeets
Sharita Timal
P356
10.1016/J.YMGME.2006.08.003
P577
2006-09-22T00:00:00Z