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ACADM
Inborn Errors of Metabolism Test Requisition
Deciphering the Gene Expression Profile of Peroxisome Proliferator
Chain Acyl-Coa Dehydrogenase (Mcad) Deficiency
Thiazolidinediones Upregulate Fatty Acid Uptake and Oxidation in Adipose Tissue of Diabetic Patients Guenther Boden,1,2 Carol Homko,2 Maria Mozzoli,1,2 Louise C
Activation of Pparα by Fatty Acid Accumulation Enhances Fatty Acid Degradation and Sulfatide Synthesis
Ab118182 – Fatty Acid Oxidation Human In-Cell ELISA
Development of a Targeted Second-Tier Genetic Test For
Differential Expression of Pparγ, FASN, and ACADM Genes In
Endoplasmic Reticulum Stress Protein GRP78 Modulates Lipid Metabolism to Control Drug Sensitivity and Antitumor Immunity in Breast Cancer Katherine L
Medium-Chain Acyl Coa Dehydrogenase Protects Mitochondria from Lipid Peroxidation in Glioblastoma
Lipid Myopathies
Ab118183 Fatty Acid Oxidation Human Flow Cytometry Kit
The Role of Acetyl-Coa Carboxylase Activity in Normal Liver Metabolism And
Screening of Core Genes and Pathways in Breast Cancer Development Via Comprehensive Analysis of Multi Gene Expression Datasets
Medium-Chain Acyl-Coa Dehydrogenase (MCAD) Deficiency
Divergent Effects of Glucose and Fructose on Hepatic Lipogenesis and Insulin Signaling
Ab129734 – ACADM ELISA Kit
Abbreviations and Alternate Names for the Additional Newborn Screening Disorders
Top View
Thioesterase Induction by 2,3,7,8-Tetrachlorodibenzo-P-Dioxin
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Severe Riboflavin Deficiency Induces Alterations in the Hepatic Proteome
PAX2 Promotes Epithelial Ovarian Cancer Progression Involving Fatty Acid Metabolic Reprogramming
Genomic Unity® Prenatal Analysis
Blueprint Genetics Fatty Acid Oxidation Syndrome Panel
Variation in the Fatty Acid Synthase Gene (FASN) and Its Association with Milk Traits in Gannan Yaks
Spectrum Analysis of Inborn Errors of Metabolism for Expanded Newborn
Medium Chain Acyl-Coa Dehydrogenase Deficiency (ACADM) Sequencing ARUP Test Code 0051758 MCAD FGS Specimen Whole Blood
ETF-QO Mutants Uncoupled Fatty Acid Β-Oxidation and Mitochondrial Bioenergetics Leading to Lipid Pathology
Lipid Metabolism in Cancer Cells Under Metabolic Stress
Altered Skeletal Muscle Mitochondrial Proteome As the Basis of Disruption of Mitochondrial Function in Diabetic Mice Piotr Zabie
Supplementary Information
A Novel Mutation of the ACADM Gene
Local Versus Systemic Control of Bone and Skeletal Muscle Mass by Components of the Transforming Growth Factor-Β Signaling Pathway
LC-FAOD) Are a Group of 6 Rare Autosomal Recessive Disorders1, 2
Clinical and Genetic Characteristics of Patients with Fatty Acid Oxidation