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COQ2
Molecular Diagnostic Requisition
Yeast and Rat Coq3 and Escherichia Coli Ubig Polypeptides Catalyze Both O-Methyltransferase Steps in Coenzyme Q Biosynthesis*
Metabolic Targets of Coenzyme Q10 in Mitochondria
Clinical Laboratory Services
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
COQ2 Gene Coenzyme Q2, Polyprenyltransferase
Mitochondrial Diseases: Expanding the Diagnosis in the Era of Genetic Testing
SSIEM Classification of Inborn Errors of Metabolism 2011
Carrier Screening Panel
Mutations in Ubiquinone Deficiency and Oxidative Phosphorylation Disorders
Respiratory Chain Activity and Protein Expression in Skeletal Muscles from High and Low Feed Efficient Swine Within the Same Genetic Line
Combined Defects in Oxidative Phosphorylation and Fatty Acid Β-Oxidation in Mitochondrial Disease
Molecular Epidemiology of Mitochondrial Cardiomyopathy:A Search Among Mitochondrial and Nuclear Genes
Rescue of Primary Ubiquinone Deficiency Due to a Novel COQ7 Defect Using 2,4–Dihydroxybensoic Acid
Molecular Diagnosis of Mitochondrial Disorders
New Susceptible Variant of COQ2 Gene in Japanese Patients with Sporadic Multiple System Atrophy
Genetic Testing
Mitochondrial DNA (Mtdna) Test Requisition
Top View
Metabolic Alterations in Inherited Cardiomyopathies
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
Primary Coenzyme Q10 Deficiency Presenting As Fatal Neonatal
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
Cerebral Mitochondrial Electron Transport Chain Dysfunction In
Riboflavin Metabolism: Role in Mitochondrial Function
Fatal Neonatal Encephalopathy and Lactic Acidosis Caused by a Homozygous Loss-Of-Function Variant in COQ9
Neurometabolic Implications of Coenzyme Q10 Deficiency: Pathogenesis, Detection and Treatment 1
Prenyldiphosphate Synthase, Subunit 1 (PDSS1)
(Coq10) Deficiency
ATM Regulates ATP Levels Through NRF1)
Blueprint Genetics Comprehensive Metabolism Panel
PG0453 Germline Multi-Gene Panel Testing
Mitochondrial/Metabolic Oligonucleotide Array CGH Analysis
Comprehensive Diagnosis for Mitochondrial Disorders
Syndromic Inherited Retinal Diseases: Genetic, Clinical and Diagnostic Aspects
Physician's Guide to the Diagnosis, Treatment, and Follow-Up Of
COQ2 Nephropathy: a Newly Described Inherited Mitochondriopathy with Primary Renal Involvement Francesca Diomedi-Camassei,* Silvia Di Giandomenico,† Filippo M
Coenzyme Q10 in the Treatment of Mitochondrial Disease
Supplementary Table 1
Blue Cross Blue Shield of New Mexico
Supp Table 2.Pdf
Coenzyme Q Depletion Reshapes MCF-7 Cells Metabolism
List of Nephropathy Genes