Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
about
Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damage.Coexpression within Integrated Mitochondrial Pathways Reveals Different Networks in Normal and Chemically Treated Transcriptomes.Granzyme B-induced mitochondrial ROS are required for apoptosisCaenorhabditis elegans expressing the Saccharomyces cerevisiae NADH alternative dehydrogenase Ndi1p, as a tool to identify new genes involved in complex I related diseases.Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome.Succination is Increased on Select Proteins in the Brainstem of the NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) Knockout Mouse, a Model of Leigh Syndrome.Mitochondrial complex I activity and NAD+/NADH balance regulate breast cancer progression.The opposite prognostic effect of NDUFS1 and NDUFS8 in lung cancer reflects the oncojanus role of mitochondrial complex IA recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype.Monoallelic loss of tumor suppressor GRIM-19 promotes tumorigenesis in mice.Mitochondrial encephalomyopathy due to a novel mutation in ACAD9.The genetics and pathology of mitochondrial disease.Mitochondrial disease associated with complex I (NADH-CoQ oxidoreductase) deficiency.Downregulation of kidney protective factors by inflammation: role of transcription factors and epigenetic mechanisms.Metabolic flexibility of mitochondrial respiratory chain disorders predicted by computer modelling.Novel insights into the role of Neurospora crassa NDUFAF2, an evolutionarily conserved mitochondrial complex I assembly factor.NDUFS8-related Complex I Deficiency Extends Phenotype from "PEO Plus" to Leigh SyndromeInsights into the pathogenic character of a common NUBPL branch-site mutation associated with mitochondrial disease and complex I deficiency using a yeast model.A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia.
P2860
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P2860
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
@en
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
@nl
type
label
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
@en
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
@nl
prefLabel
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
@en
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
@nl
P2093
P1476
Mitochondrial complex I deficiency of nuclear origin I. Structural genes.
@en
P2093
Abdelhamid Slama
Alain Legrand
Hélène Pagniez-Mammeri
Paule Bénit
Pierre Rustin
Sandrine Loublier
P304
P356
10.1016/J.YMGME.2011.11.188
P577
2011-11-18T00:00:00Z