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ACADVL
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Inborn Errors of Metabolism Test Requisition
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Ab118182 – Fatty Acid Oxidation Human In-Cell ELISA
Very Long-Chain Acyl-Coa Dehydrogenase (VLCAD) Deficiency
Development of a Targeted Second-Tier Genetic Test For
Proteomic and Biochemical Studies of Lysine Malonylation Suggests Its Malonic
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Fatty Acid Oxidation Gene Panel, Varies
Ab118183 Fatty Acid Oxidation Human Flow Cytometry Kit
(VLCAD) Deficiency
Long-Chain Fatty Acid Oxidation Disorders Biochemical, Pathophysiological and Clinical Aspects
Electrophysiological Abnormalities in VLCAD Deficient Hipsc
Benzene Exposure Alters Expression of Enzymes Involved in Fatty Acid Β-Oxidation in Male C3H/He Mice
ACADVL Gene Acyl-Coa Dehydrogenase Very Long Chain
Disorders of Mitochondrial Long-Chain Fatty Acid Oxidation and the Carnitine Shuttle
00735 Triheptanoin Oral Liquid (Dojolvi)
Palmitate Fatty Acid Oxidation
Top View
Fatty Acid Oxidation Defects Panel
Divergent Effects of Glucose and Fructose on Hepatic Lipogenesis and Insulin Signaling
Development of a New Enzymatic Diagnosis Method for Very-Long
Reduction of Serum Free Fatty Acids and Triglycerides by Liver-Targeted Expression of Long Chain Acyl-Coa Synthetase 3
Myopathic Form of Very-Long Chain Acyl-Coa Dehydrogenase Deficiency: Evidence for Temperature-Sensitive Mild Mutations in Both Mutant Alleles in a Japanese Girl
Proximal Muscle Weakness Pract Neurol: First Published As 10.1136/Practneurol-2019-002204 on 4 April 2019
Targeted Disruption of Mouse Long-Chain Acyl-Coa Dehydrogenase Gene Reveals Crucial Roles for Fatty Acid Oxidation
Mitochondrial PNAS PLUS Rate-Limiting Enzymes and Nutrient Utilization by PERIOD Proteins
Genomic Unity® Prenatal Analysis
Blueprint Genetics Fatty Acid Oxidation Syndrome Panel
Supplemental Tables 10-29-15Lt.Xlsx
Spectrum Analysis of Inborn Errors of Metabolism for Expanded Newborn
KRAS, a Prime Mediator in Pancreatic Lipid Synthesis Through Extra Mitochondrial Glutamine and Citrate Metabolism
Ontario Newborn Screening Laboratory
Zinc Supplementation Reverses Alcohol-Induced Steatosis in Mice Through Reactivating Hepatocyte Nuclear Factor-4Α and Peroxisome Proliferator-Activated Receptor-Α
Supplementary Data
Inborn Errors of Metabolism
Screening for Very Long-Chain Acyl- Coenzyme a Dehydrogenase Deficiency