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Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 to enable coenzyme Q biosynthesisCOQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.Coenzyme Q and Its Role in the Dietary Therapy against AgingAutosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisationBacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseasesCoenzyme Q10 and Neurological Diseases.Coenzyme Q protects Caenorhabditis elegans GABA neurons from calcium-dependent degeneration.Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal diseaseCoenzyme q10 therapyAssociation between genetic variants in the Coenzyme Q10 metabolism and Coenzyme Q10 status in humansDecreased expression of prenyl diphosphate synthase subunit 2 correlates with reduced survival of patients with gastric cancerCoenzyme q10 administration in community-acquired pneumonia in the elderly.The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children.CLD1 Reverses the Ubiquinone Insufficiency of Mutant cat5/coq7 in a Saccharomyces cerevisiae Model System.The submitochondrial distribution of ubiquinone affects respiration in long-lived Mclk1+/- miceCoenzyme Q10: is there a clinical role and a case for measurement?Coenzyme Q10 supplementation rescues renal disease in Pdss2kd/kd mice with mutations in prenyl diphosphate synthase subunit 2Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency.How can we treat mitochondrial encephalomyopathies? Approaches to therapyCoenzyme Q10 effects in neurodegenerative disease.Therapeutic use of coenzyme Q10 and coenzyme Q10-related compounds and formulations.Drugs and mitochondrial diseases: 40 queries and answers.Coenzyme Q10 depletion in medical and neuropsychiatric disorders: potential repercussions and therapeutic implications.Human CoQ10 deficienciesGenome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases.Balanced CoQ6 biosynthesis is required for lifespan and mitophagy in yeast.Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency.A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency.Respiratory-induced coenzyme Q biosynthesis is regulated by a phosphorylation cycle of Cat5p/Coq7p.Coenzyme Q10-responsive ataxia: 2-year-treatment follow-upAtaxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Mutations in coenzyme Q10 biosynthetic genes.
@ast
Mutations in coenzyme Q10 biosynthetic genes.
@en
type
label
Mutations in coenzyme Q10 biosynthetic genes.
@ast
Mutations in coenzyme Q10 biosynthetic genes.
@en
prefLabel
Mutations in coenzyme Q10 biosynthetic genes.
@ast
Mutations in coenzyme Q10 biosynthetic genes.
@en
P2860
P356
P1476
Mutations in coenzyme Q10 biosynthetic genes.
@en
P2093
Catarina M Quinzii
Michio Hirano
P2860
P304
P356
10.1172/JCI31423
P407
P577
2007-03-01T00:00:00Z