Mitochondrial diseases and ATPase defects of nuclear origin.
about
Ecto-F₁-ATPase: a moonlighting protein complex and an unexpected apoA-I receptor.Understanding structure, function, and mutations in the mitochondrial ATP synthase.Genetics of stroke.Bioinformatics Study of m.9053G>A Mutation at the ATP6 Gene in Relation to Type 2 Diabetes Mellitus and Cataract Diseases.TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesis.Increasing mitochondrial substrate-level phosphorylation can rescue respiratory growth of an ATP synthase-deficient yeast.The short variant of the mitochondrial dynamin OPA1 maintains mitochondrial energetics and cristae structure.Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice.Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.Comparison of Pre- and Post-translational Expressions of and Genes in Colorectal Adenoma-Carcinoma Tissues
P2860
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P2860
Mitochondrial diseases and ATPase defects of nuclear origin.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Mitochondrial diseases and ATPase defects of nuclear origin.
@ast
Mitochondrial diseases and ATPase defects of nuclear origin.
@en
type
label
Mitochondrial diseases and ATPase defects of nuclear origin.
@ast
Mitochondrial diseases and ATPase defects of nuclear origin.
@en
prefLabel
Mitochondrial diseases and ATPase defects of nuclear origin.
@ast
Mitochondrial diseases and ATPase defects of nuclear origin.
@en
P1476
Mitochondrial diseases and ATPase defects of nuclear origin
@en
P2093
Alena Vojtísková
Josef Houstek
P304
P356
10.1016/J.BBABIO.2004.04.012
P407
P577
2004-07-01T00:00:00Z