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COQ4
Location Analysis of Estrogen Receptor Target Promoters Reveals That
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Whole-Exome Sequencing Reveals a Novel Homozygous
Metabolic Targets of Coenzyme Q10 in Mitochondria
Whole Exome Sequencing Reveals NOTCH1 Mutations in Anaplastic Large Cell Lymphoma and Points to Notch Both As a Key Pathway and a Potential Therapeutic Target
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Disorders of Human Coenzyme Q10 Metabolism: an Overview
Mitochondrial Diseases: Expanding the Diagnosis in the Era of Genetic Testing
ARTICLE ADCK3, an Ancestral Kinase, Is Mutated in a Form Of
Exploring the Mitochondrial Function in Muscle and Molecular Dysregulation in Cerebellum in a Mouse Model for ARCA2, a Recessive
Clinical Whole-Exome Sequencing Reveals a Common Pathogenic Variant in Patients with Coq10 Deficiency an Underdiagnosed Cause O
Mutations in Ubiquinone Deficiency and Oxidative Phosphorylation Disorders
PARL Deficiency in Mouse Causes Complex III Defects, Coenzyme Q Depletion, and Leigh-Like Syndrome
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Rescue of Primary Ubiquinone Deficiency Due to a Novel COQ7 Defect Using 2,4–Dihydroxybensoic Acid
A Genome Wide Copper-Sensitized Screen Identifies Novel Regulators of Mitochondrial Cytochrome C Oxidase Activity
Suppl. Fig. Legends
A Personalized Model of COQ2 Nephropathy Rescued by the Wild-Type COQ2 Allele Or Dietary Coenzyme Q10 Supplementation
Top View
De Novo Mutations in the Gene Encoding STXBP1 (MUNC18-1) Cause Early Infantile Epileptic Encephalopathy
Vitamin K2 Cannot Substitute Coenzyme Q10 As Electron Carrier
Are Shown B Gene Numbera
Mitokondriesykdommer V03
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
Accepted Manuscript
Mitochondrial Metabolism in Major Neurological Diseases Zhengqiu Zhou University of Kentucky,
[email protected]
Hallmarks of a New Era in Mitochondrial Biochemistry
Fatal Neonatal Encephalopathy and Lactic Acidosis Caused by a Homozygous Loss-Of-Function Variant in COQ9
Prenyldiphosphate Synthase, Subunit 1 (PDSS1)
(Coq10) Deficiency
Leigh Syndrome Nuclear Gene Panel
Characterization of Coq10 Biosynthesis in Fibroblasts of Patients with Primary and Secondary Coq10 Deficiency
Inherited Metabolic Disorders Presenting with Ataxia
COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by Coq10 Administration
Impact of Chemical Analogs of 4-Hydroxybenzoic Acid on Coenzyme Q Biosynthesis: from Inhibition to Bypass of Coenzyme Q Deficiency Fabien Pierrel
Coenzyme Q10 in the Treatment of Mitochondrial Disease
Panel Nmg4 Mitocondriales