Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases.
about
Identification and characterization of new long chain acyl-CoA dehydrogenasesPEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferationMolecular cloning, gene structure and expression profile of two mouse peroxisomal 3-ketoacyl-CoA thiolase genesOxidative Stress in the Healthy and Wounded Hepatocyte: A Cellular Organelles PerspectiveCYP4 enzymes as potential drug targets: focus on enzyme multiplicity, inducers and inhibitors, and therapeutic modulation of 20-hydroxyeicosatetraenoic acid (20-HETE) synthase and fatty acid ω-hydroxylase activitiesIdentification of a substrate-binding site in a peroxisomal beta-oxidation enzyme by photoaffinity labeling with a novel palmitoyl derivativePredicted mouse peroxisome-targeted proteins and their actual subcellular locationsConformational plasticity of the lipid transfer protein SCP2Defects in mitochondrial and peroxisomal β-oxidation influence virulence in the maize pathogen Ustilago maydis.Peroxisomal and mitochondrial β-oxidation pathways influence the virulence of the pathogenic fungus Cryptococcus neoformansPEX11β induces peroxisomal gene expression and alters peroxisome number during early Xenopus laevis development.Genetic and dietary regulation of lipid droplet expansion in Caenorhabditis elegans.AMACR is associated with advanced pathologic risk factors in sporadic colorectal adenomas.The human metabolic reconstruction Recon 1 directs hypotheses of novel human metabolic functionsLiver fatty acid-binding protein and obesity.PEX11 beta deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome functionTysnd1 deficiency in mice interferes with the peroxisomal localization of PTS2 enzymes, causing lipid metabolic abnormalities and male infertility.Capsinoids suppress fat accumulation via lipid metabolism.Peroxisomal multifunctional protein-2 deficiency causes motor deficits and glial lesions in the adult central nervous system.Elevated alpha-methylacyl-CoA racemase enzymatic activity in prostate cancer.MFE1, a member of the peroxisomal hydroxyacyl coenzyme A dehydrogenase family, affects fatty acid metabolism necessary for morphogenesis in Dictyostelium spp.Peroxisome proliferators and peroxisome proliferator-activated receptor alpha: biotic and xenobiotic sensingGene expression changes controlling distinct adaptations in the heart and skeletal muscle of a hibernating mammalAMACR polymorphisms, dietary intake of red meat and dairy and prostate cancer risk.Localization of MCT2 at peroxisomes is associated with malignant transformation in prostate cancerMetabolic plasticity in resting and thrombin activated plateletsMammalian peroxisomal ABC transporters: from endogenous substrates to pathology and clinical significance.Analysis of the bioactivity of magnetically immunoisolated peroxisomes.Metabolic dysfunctions in multiple sclerosis: implications as to causation, early detection, and treatment, a case control studyGenomewide transcriptional signatures of migratory flight activity in a globally invasive insect pest.Beneficial reward-to-risk action of glucosamine during pathogenesis of osteoarthritisPEX11 promotes peroxisome division independently of peroxisome metabolismMetabolite transport across the peroxisomal membrane.Functional characterization of electron-transferring flavoprotein and its dehydrogenase required for fungal development and plant infection by the rice blast fungus.ABCD2 is abundant in adipose tissue and opposes the accumulation of dietary erucic acid (C22:1) in fatPeroxisomes: a nexus for lipid metabolism and cellular signaling.Peroxisomes and disease - an overview.Exercise and Omega-3 Polyunsaturated Fatty Acid Supplementation for the Treatment of Hepatic Steatosis in Hyperphagic OLETF RatsReinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.Attenuated progression of diet-induced steatohepatitis in glutathione-deficient mice.
P2860
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P2860
Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@ast
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@en
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@nl
type
label
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@ast
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@en
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@nl
prefLabel
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@ast
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@en
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@nl
P2093
P1476
Peroxisomal fatty acid alpha- ...... ters and peroxisomal diseases.
@en
P2093
Ferdinandusse S
Van Grunsven EG
Wanders RJ
Waterham HR
van Roermund CW
P304
P356
10.1042/0300-5127:0290250
P577
2001-05-01T00:00:00Z