The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney

The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney

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http://www.wikidata.org/entity/Q28613019

Q28613019

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Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome Evidence for the existence of a pristanoyl-CoA oxidase gene in man Isolation of the human peroxisomal acyl-CoA oxidase gene: organization, promoter analysis, and chromosomal localization Metabolic Interplay between Peroxisomes and Other Subcellular Organelles Including Mitochondria and the Endoplasmic Reticulum Interplay between oxidant species and energy metabolism Identification of a substrate-binding site in a peroxisomal beta-oxidation enzyme by photoaffinity labeling with a novel palmitoyl derivative Molecular cloning and further characterization of rat peroxisomal trihydroxycoprostanoyl-CoA oxidase The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders High density genome wide genotyping-by-sequencing and association identifies common and low frequency SNPs, and novel candidate genes influencing cow milk traits ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment.Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects Bile acids: the role of peroxisomes.Peroxisomes: a nexus for lipid metabolism and cellular signaling.A new peroxisomal disorder with fetal and neonatal adrenal insufficiency.Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis.Higher-plant medium- and short-chain acyl-CoA oxidases: identification, purification and characterization of two novel enzymes of eukaryotic peroxisomal beta-oxidation.A single acyl-CoA dehydrogenase is required for catabolism of isoleucine, valine and short-chain fatty acids in Aspergillus nidulans.ACOX2:FAD; ACOXL:FAD oxidise (2S)-pristanoyl-CoA to trans-2;3-dehydropristanoyl-CoA 25(S) THCA-CoA is dehydrogenated to 3alpha;7alpha;12alpha-trihydroxy-5beta-cholest-24-enoyl-CoA (THCA-CoA)25(S) DHCA-CoA is dehydrogenated to 25(S) 3alpha;7alpha-dihydroxy-5beta-cholest-24-enoyl-CoA

P2860

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P2860

The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney

Item

http://www.wikidata.org/entity/Q28613019

description

1993 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

1993 թվականի մայիսին հրատարակված գիտական հոդված

@hy

article publié dans la revue scientifique Journal of Biological Chemistry

@fr

artículu científicu espublizáu en 1993

@ast

im Mai 1993 veröffentlichter wissenschaftlicher Artikel

@de

scientific journal article

@en

vedecký článok (publikovaný 1993/05/15)

@sk

vědecký článek publikovaný v roce 1993

@cs

wetenschappelijk artikel (gepubliceerd op 1993/05/15)

@nl

наукова стаття, опублікована в травні 1993

@uk