Mitochondrial diseases and genetic defects of ATP synthase.
about
Regulation of mitochondrial ATP synthase in cardiac pathophysiologyMucosal effects of tenofovir 1% gelDevelopment of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.Consequences of the pathogenic T9176C mutation of human mitochondrial DNA on yeast mitochondrial ATP synthase.A yeast-based assay identifies drugs active against human mitochondrial disordersMitochondrial ATP synthase: architecture, function and pathology.ATPase may play a critical role in disturbance of energy metabolism in congestive heart failure rats.Stable nuclear expression of ATP8 and ATP6 genes rescues a mtDNA Complex V null mutantMitochondrial protein sorting as a therapeutic target for ATP synthase disorders.Mitochondrial genetic variants identified to be associated with posttraumatic stress disorderInhibition of the Warburg effect with a natural compound reveals a novel measurement for determining the metastatic potential of breast cancers.Mitochondrial GWA Analysis of Lipid Profile Identifies Genetic Variants to Be Associated with HDL Cholesterol and Triglyceride Levels.Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies.The antiapoptotic herpes simplex virus glycoprotein J localizes to multiple cellular organelles and induces reactive oxygen species formation.Response to immunotherapy in a patient with adult onset Leigh syndrome and T9176C mtDNA mutation.Mechanisms of YidC-mediated insertion and assembly of multimeric membrane protein complexes.Identification of G8969>A in mitochondrial ATP6 gene that severely compromises ATP synthase function in a patient with IgA nephropathy.Synthesis of cytochrome c oxidase subunit 1 is translationally downregulated in the absence of functional F1F0-ATP synthase.The power of yeast to model diseases of the powerhouse of the cell.Mechanisms of mitochondrial diseases.Perspectives and potential applications of mitochondria-targeted antioxidants in cardiometabolic diseases and type 2 diabetes.Loss of LRPPRC causes ATP synthase deficiencyAffinity-based target deconvolution of safranal.Bioinformatics Study of m.9053G>A Mutation at the ATP6 Gene in Relation to Type 2 Diabetes Mellitus and Cataract Diseases.Proteomic screening of molecular targets of crocin.Response to letter to the editor: Why does Leigh syndrome responds to immunotherapy?Structure of a Complete ATP Synthase Dimer Reveals the Molecular Basis of Inner Mitochondrial Membrane MorphologyPhylogenetic Profiling of Mitochondrial Proteins and Integration Analysis of Bacterial Transcription Units Suggest Evolution of F1Fo ATP Synthase from Multiple Modules.MiRNA-506 promotes primary biliary cholangitis-like features in cholangiocytes and immune activation.Genetic diversity of ATP8 and ATP6 genes is associated with high-altitude adaptation in yak.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.Episodic weakness and Charcot-marie-tooth disease due to a mitochondrial MT-ATP6 mutation.Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C.Mitochondrial targeting as a novel therapy for stroke
P2860
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P2860
Mitochondrial diseases and genetic defects of ATP synthase.
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-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
2006年學術文章
@zh-hant
name
Mitochondrial diseases and genetic defects of ATP synthase.
@ast
Mitochondrial diseases and genetic defects of ATP synthase.
@en
type
label
Mitochondrial diseases and genetic defects of ATP synthase.
@ast
Mitochondrial diseases and genetic defects of ATP synthase.
@en
prefLabel
Mitochondrial diseases and genetic defects of ATP synthase.
@ast
Mitochondrial diseases and genetic defects of ATP synthase.
@en
P2093
P50
P1476
Mitochondrial diseases and genetic defects of ATP synthase
@en
P2093
Alena Vojtísková
Andrea Pícková
Josef Houstek
P304
P356
10.1016/J.BBABIO.2006.04.006
P407
P577
2006-04-19T00:00:00Z