Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment.

Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment.

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http://www.wikidata.org/entity/Q39318947
The WOMED model of benign thyroid disease: Acquired magnesium deficiency due to physical and psychological stressors relates to dysfunction of oxidative phosphorylationPathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substrates.Pathomechanisms in coenzyme q10-deficient human fibroblasts.Gene Therapy Corrects Mitochondrial Dysfunction in Hematopoietic Progenitor Cells and Fibroblasts from Coq9R239X Mice.Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes.The pleiotropic effects of decanoic acid treatment on mitochondrial function in fibroblasts from patients with complex I deficient Leigh syndrome.Redox Signaling Mediated by Thioredoxin and Glutathione Systems in the Central Nervous System.Impact of Chemical Analogs of 4-Hydroxybenzoic Acid on Coenzyme Q Biosynthesis: From Inhibition to Bypass of Coenzyme Q Deficiency.New susceptible variant of COQ2 gene in Japanese patients with sporadic multiple system atrophy.Coq6 is responsible for the C4-deamination reaction in coenzyme Q biosynthesis in Saccharomyces cerevisiae.Measurement of Respiratory Chain Enzyme Activity in Human Renal Biopsy Specimens'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich's ataxia'.Mitochondrial CoQ deficiency is a common driver of mitochondrial oxidants and insulin resistance.Neutrophil depletion improves diet-induced non-alcoholic fatty liver disease in mice.Drug-Induced Mitochondrial Toxicity.
P2860

Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment.

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http://www.wikidata.org/entity/Q39318947
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2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-my
2012年学术文章
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2012年學術文章
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2012年學術文章
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name
Human neuronal coenzyme Q10 de ...... or pathogenesis and treatment.
@en
Human neuronal coenzyme Q10 de ...... or pathogenesis and treatment.
@nl
type
label
Human neuronal coenzyme Q10 de ...... or pathogenesis and treatment.
@en
Human neuronal coenzyme Q10 de ...... or pathogenesis and treatment.
@nl
prefLabel
Human neuronal coenzyme Q10 de ...... or pathogenesis and treatment.
@en
Human neuronal coenzyme Q10 de ...... or pathogenesis and treatment.
@nl
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P433
P478
P50
P577
P698
P921
P356
P1433
P1476
Human neuronal coenzyme Q10 de ...... for pathogenesis and treatment
@en
P2093
P2860
P2888
P304
P31
P356
P433
P478
P50
P577
P698
P921