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Pristanic acid
Abstract DRAYTON, JOSEPHINE BENTLEY
Substrate Specificity of Rat Liver Mitochondrial Carnitine Palmitoyl Transferase I: Evidence Against S-Oxidation of Phytanic Acid in Rat Liver Mitochondria
Ataxia with Loss of Purkinje Cells in a Mouse Model for Refsum Disease
Oxidation of Pristanic Acid in Fibroblasts and Its Application to the Diagnosis of Peroxisomal -Oxidation Defects
LIPID METABOLISM-3 Regulation of Fatty Acid Oxidation
Thermal Alteration of Organic Matter in Recent Marine Sediments
Phytanic Acid, but Not Pristanic Acid, Mediates the Positive Effects of Phytol Derivatives on Brown Adipocyte Differentiation
Oxidation of Pristanic Acid in Fibroblasts and Its Application to the Diagnosis of Peroxisomal Beta-Oxidation Defects
In Vivo Study of Phytanic Acid &-Oxidation in Classic Refsum's
Determining the Reference Intervals of Long-Chain Fatty Acids, Phytanic Acid and Pristanic Acid for Diagnostics of Peroxisome Disorders in Children
A Review of Odd-Chain Fatty Acid Metabolism and the Role of Pentadecanoic Acid (C15:0) and Heptadecanoic Acid (C17:0) in Health and Disease
Details About Three Fatty Acid Oxidation Pathways Occurring in Man
Microbial Metabolism of the Isoprenoid Alkane Pristane (A-Methylglutarate/4,8,12-Trimethyltridecanoate/Fatty Acid Metabolism)
Peroxisomal Cofactor Transport
Genetic Disorders of Mitochondrial and Peroxisomal Fatty Acid Oxidation and Peroxisome Proliferator-Activated Receptors
Phytanic Acid, a Daily Consumed Chlorophyll-Yielded Phytol Bio-Metabolite: a Comprehensive Review
A New Defect of Peroxisomal Function Involving Pristanic Acid: a Case Report B N Mclean, J Allen, S Ferdinandusse,Rjawanders
Fibroblast-Specific Genome-Scale Modelling Predicts an Imbalance in Amino Acid Metabolism in Refsum Disease
Top View
Case Report Chinese Boy with Normal Initial Peroxisomal Blood Assays: a Diagnostic Pitfall in the Workup for Infantile Refsum Disease
Peroxisomal Acyl-Coa Synthetases☆
Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
Intraorganellar Localization of Coash-Independent Phytanic Acid Oxidation in Human Liver Peroxisomes
Kernel Methods for Virtual Screening
Chapter 1: Introduction
Localization of the Oxidative Defect in Phytanic Acid Degradation in Patients with Refsum's Disease
Zellweger Syndrome -Biopsychosocial Intervention
Peroxisomal Disorders: the Single Peroxisomal Enzyme Deficiencies ⁎ Ronald J.A
Utilization of Sterol Carrier Protein-2 by Phytanoyl-Coa 2-Hydroxylase in the Peroxisomal Oxidation of Phytanic Acid
Infantile Refsum Disease Commentary
Serum Phytanic and Pristanic Acid Levels and Prostate Cancer Risk in Finnish Smokers