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COQ9
Metabolic Targets of Coenzyme Q10 in Mitochondria
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Disorders of Human Coenzyme Q10 Metabolism: an Overview
Familial Neonatal Isolated Cardiomyopathy Caused by a Mutation in the flavoprotein Subunit of Succinate Dehydrogenase
Mutations in Ubiquinone Deficiency and Oxidative Phosphorylation Disorders
Mevalonate Pathway Provides Ubiquinone to Maintain Pyrimidine
Molecular Diagnostic Testing Requisition
Enhancing Mitochondrial Activity in Neurons Protects Against
COQ9 (N-17): Sc-83392
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
Mitochondrial DNA (Mtdna) Test Requisition
A Personalized Model of COQ2 Nephropathy Rescued by the Wild-Type COQ2 Allele Or Dietary Coenzyme Q10 Supplementation
Genes and Variants Underlying Human Congenital Lactic Acidosis—From Genetics to Personalized Treatment
Metabolic Engineering of Coenzyme Q by Modification of Isoprenoid Side
Enzyme Polymorphism, Oxygen and Injury: a Lipidomic Analysis of Flight-Induced Oxidative Damage in a Succinate Dehydrogenase D (Sdhd)-Polymorphic Insect Julianne E
Hallmarks of a New Era in Mitochondrial Biochemistry
Fatal Neonatal Encephalopathy and Lactic Acidosis Caused by a Homozygous Loss-Of-Function Variant in COQ9
Top View
Prenyldiphosphate Synthase, Subunit 1 (PDSS1)
(Coq10) Deficiency
NIH Public Access Author Manuscript Circ J
Leigh Syndrome Nuclear Gene Panel
Comprehensive Diagnosis for Mitochondrial Disorders
Diagnostic Opportunities for Rare Disease with NGS
Characterization of Coq10 Biosynthesis in Fibroblasts of Patients with Primary and Secondary Coq10 Deficiency
Treatable Genetic Diseases Are Enriched in the General Psychiatric Population
A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency
Physician's Guide to the Diagnosis, Treatment, and Follow-Up Of
Impact of Chemical Analogs of 4-Hydroxybenzoic Acid on Coenzyme Q Biosynthesis: from Inhibition to Bypass of Coenzyme Q Deficiency Fabien Pierrel
Table S1. the Four TAZ Mutations Examined in This Study. Patients Were Diagnosed with Barth
Peroxisomal Targeting of a Protein Phosphatase Type 2C Via
Genome-Wide Crispri Screening Identifies OCIAD1 As a Prohibitin