about
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseaseCoenzyme Q and Its Role in the Dietary Therapy against AgingUncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletionsTreatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effectsBacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseasesCoenzyme Q10 and Neurological Diseases.In vivo screening reveals interactions between Drosophila Manf and genes involved in the mitochondria and the ubiquinone synthesis pathway.CoQ10 Deficiency May Indicate Mitochondrial Dysfunction in Cr(VI) Toxicity.Methods for Structural and Functional Analyses of Intramembrane Prenyltransferases in the UbiA Superfamily.Mitochondrial disorders and the eye.Coenzyme Q10 as a Peripheral Biomarker for Multiple System AtrophyPathomechanisms in coenzyme q10-deficient human fibroblasts.Biochemical rationale and experimental data on the antiaging properties of CoQ(10) at skin level.A Drosophila model for primary coenzyme Q deficiency and dietary rescue in the developing nervous systemReactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency.Dependence of brown adipose tissue function on CD36-mediated coenzyme Q uptake.Coenzyme 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.A randomized, double-blind, placebo-controlled study of oral coenzyme Q10 to relieve self-reported treatment-related fatigue in newly diagnosed patients with breast cancerPostprandial antioxidant gene expression is modified by Mediterranean diet supplemented with coenzyme Q(10) in elderly men and womenDrug development for rare mitochondrial disordersReview of clinical trials for mitochondrial disorders: 1997-2012.Supplementation of Coenzyme Q10 among Patients with Type 2 Diabetes Mellitus.Coenzyme Q10 effects in neurodegenerative disease.Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.Neurodevelopmental manifestations of mitochondrial disease.Coenzyme Q and mitochondrial diseaseDrugs and mitochondrial diseases: 40 queries and answers.Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency.The regulation of coenzyme q biosynthesis in eukaryotic cells: all that yeast can tell us.Recovery of MERRF fibroblasts and cybrids pathophysiology by coenzyme Q10.Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases.The role of DMQ(9) in the long-lived mutant clk-1.Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency.The Combination of Physical Exercise with Muscle-Directed Antioxidants to Counteract Sarcopenia: A Biomedical Rationale for Pleiotropic Treatment with Creatine and Coenzyme Q10.Coenzyme Q plays opposing roles on bacteria/fungi and viruses in Drosophila innate immunity.Potential clinical utility of multiple system atrophy biomarkers.ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic?Pediatric reference intervals for muscle coenzyme Q(10).Influence of liver-X-receptor on tissue cholesterol, coenzyme Q and dolichol content
P2860
Q24645475-B5647FF6-4633-4926-9C30-A7F1613EE81DQ26753050-D0E0E713-CC0D-4AA7-8E30-D0E22386377AQ27324674-7C0B2B6B-6A45-4D57-B138-03FCD329D4A2Q28474996-B8994720-DD20-441F-BC07-92D77E55AFEAQ28708978-D47B0777-DABF-4F61-9F5F-2E4F0DC2FDA8Q30440307-3A5316C8-3F53-466B-9DEF-83A4D2F31456Q30854473-8587FE3C-40FB-4BF5-B9FA-2EA823DEABC5Q33624716-52DE192F-5575-4356-ADF6-782751E2875DQ33688223-E081F626-DC86-4E86-B328-46BD4123F4DCQ33702120-A50D422B-5D3E-4461-BDC3-B37CD4FE71B2Q33851721-44091EE2-0268-40F1-B513-30A870CFEB66Q33956929-742B63EC-54C5-47B5-8D2A-6C0D806918E5Q34046916-0332F587-28CF-4D3A-A738-1542F145D055Q34247683-A724D8FA-93DD-43FA-8E12-255E884B0D29Q34378808-899DDA47-52CE-40A8-9695-66CD5EF6EF10Q35054576-AE60E69C-C10E-478E-BB5F-3743FCAD89E7Q35123883-4C957864-0A91-44DA-B565-955E3F17D594Q35926240-3EB59A25-5F9C-4F9D-8171-7704BC952B29Q36409534-40223A62-9B8F-4E2F-97EB-2D719802CB4EQ36528283-BE345148-4161-478D-A05F-8A5AED03C196Q36762826-886D7454-102E-408D-BD6C-8AA4122D8A06Q36762846-AC156F2C-9D4E-405F-B30A-BF4F42BF6ABDQ37081597-3DF37C2C-E3F8-4FBA-970E-3EA69E6D2627Q37448888-613C6A3E-3AB6-4E2D-B94D-924F607FA2F8Q37619548-F04D0AAE-D259-439F-8325-1999E68392D8Q37784963-65AECA03-6150-4129-9DDB-F20A0C928F9FQ37785517-1617BAE6-DCDA-418F-9D2C-1FF564C5D683Q37980195-B71D5560-B7FB-462A-B714-BD5D1CD04DF2Q38236847-03807420-D3E0-471B-96D8-7316BD4C6E79Q39144563-753397DF-9E70-4F7D-BD6B-BB5663CEAC32Q39392555-639C9A45-0239-4724-85D7-577D6E56A3DCQ40767246-472392DA-7EC7-4357-8BFA-B1F65F1774ABQ42867713-4FA99F32-36E2-45F8-897F-B2975BEDC529Q43988547-D813A5A2-CC93-4DD8-B4DF-B471AC44C2C2Q45833603-81F169E0-2F4D-4DA8-87EE-D615E8B18448Q47071332-20D2D4EA-81B8-460F-8641-FBBFDF041B44Q47663712-29CD127A-7474-49E1-9697-98680A635A0CQ48799556-847BF8EB-E12A-4568-9EDD-56A9527D842FQ50794617-51B07AC4-C3D0-4EBA-A297-228115E3C8F1Q58329651-E6596FD1-F4F1-4C31-B53C-9B17506BF1EF
P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Human CoQ10 deficiencies
@en
Human CoQ10 deficiencies.
@nl
type
label
Human CoQ10 deficiencies
@en
Human CoQ10 deficiencies.
@nl
prefLabel
Human CoQ10 deficiencies
@en
Human CoQ10 deficiencies.
@nl
P2093
P2860
P356
P1433
P1476
Human CoQ10 deficiencies
@en
P2093
P2860
P304
P356
10.1002/BIOF.5520320113
P577
2008-01-01T00:00:00Z