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ACAD9
NDUFAF1 Antibody
Molecular Mechanism of ACAD9 in Mitochondrial Respiratory Complex 1 Assembly
Inborn Errors of Metabolism Test Requisition
Genes Investigated
An Essential Role for ECSIT in Mitochondrial Complex I Assembly and Mitophagy in Macrophages
Genetic and Genomic Analysis of Hyperlipidemia, Obesity and Diabetes Using (C57BL/6J × TALLYHO/Jngj) F2 Mice
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
New Perspective in Diagnostics of Mitochondrial Disorders
Understanding ACAD9 Function and the Physiologic Consequences of Its Deficiency
Clinical, Biochemical and Genetic Spectrum of 70 Patients with ACAD9
From Gene Expression to the Clinic
Statutory Approvals Committee – Minutes
Supplementary Table 1A. Genes Significantly Altered in A4573 ESFT
Clinical, Biochemical and Genetic Spectrum of 70 Patients with ACAD9 Deficiency: Is Riboflavin Supplementation Effective? Birgit M
Exploring Alternative Therapeutic Interventions for the Treatment of Leigh Syndrome
Arabidopsis Thaliana Alternative Dehydrogenases: a Potential
PLATFORM ABSTRACTS Abstract Abstract Numbers Numbers Tuesday 31 Advances and References in Genomic Technology Room 210 #196–#204 2
Elucidating the Mitochondrial Architecture of Branched-Chain Amino Acid Metabolism Enzymes: Implications for Treatment
Top View
An Atypical Presentation of ACAD9 Deficiency: Diagnosis by Whole
Phenotype – Genotype Correlations in Leigh Syndrome: New Insights from a Multicenter Study of 96 Patients
Complex I Assembly Function and Fatty Acid Oxidation Enzyme
Using Biobin to Explore Rare Variant Population Stratification*
A Bioinformatics Tool for Automating the Binning of Rare Variants
Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer
Assembly Factors for the Membrane Arm of Human Complex I
Severe Riboflavin Deficiency Induces Alterations in the Hepatic Proteome
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
Genomic Unity® Prenatal Analysis
Blueprint Genetics Fatty Acid Oxidation Syndrome Panel
Genetic'dissection'of'growth'and' Meat'quality'traits'in'pigs''
Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
Mitochondrial Fatty Acid Oxidation and Its Disorders : the Carnitine Cycle
Genetic Diagnosis of Mendelian Disorders Via RNA Sequencing
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Negative Female
Fig2s1 Matr3 Iclip in Kd and PTBP1 Replicates Reduced File Size
Mitochondrial Encephalomyopathy Due to a Novel Mutation in ACAD9
Comprehensive Diagnosis for Mitochondrial Disorders
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
ACAD9 Deficiency
Technische Universität München
Refinement of the Locus for Hereditary Congenital Facial Palsy on Chromosome 3Q21 in Two Unrelated Families and Screening of Positional Candidate Genes
ACAD9 Gene Acyl-Coa Dehydrogenase Family Member 9
Invitae Carrier Screening (Continued)
High Incidence and Variable Clinical Outcome of Cardiac Hypertrophy Due to ACAD9 Mutations in Childhood
Biallelic Mutations in TMEM126B Cause Severe Complex I
Evaluation of Mitochondrial Bioenergetics, Dynamics
Whole Exome Sequencing to Elucidate the Molecular Basis of Cardiac Disease
A SARS-Cov-2-Human Protein-Protein Interaction Map Reveals Drug Targets and Potential Drug- Repurposing
Genomic Unity® Neurology Analysis
Genetic Diagnostics Test(S)/Gene(S)/Panel(S)