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
about
The diploid genome sequence of an individual humanGenetic variation in an individual human exomeC-terminal tripeptide Ser-Asn-Leu (SNL) of human D-aspartate oxidase is a functional peroxisome-targeting signalIdentification of PEX5p-related novel peroxisome-targeting signal 1 (PTS1)-binding proteins in mammalsEvidence for the existence of a pristanoyl-CoA oxidase gene in manPrenatal and postnatal development of peroxisomal lipid-metabolizing pathways in the mouseAbsence of spontaneous peroxisome proliferation in enoyl-CoA Hydratase/L-3-hydroxyacyl-CoA dehydrogenase-deficient mouse liver. Further support for the role of fatty acyl CoA oxidase in PPARalpha ligand metabolismMolecular cloning and expression of cDNA encoding 3alpha,7alpha,12alpha-trihydroxy-5beta-chole stanoyl-CoA oxidase from rabbit liver.Dose-dependent effects of morphine exposure on mRNA and microRNA (miR) expression in hippocampus of stressed neonatal mice.ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment.Predictive Structure and Topology of Peroxisomal ATP-Binding Cassette (ABC) Transporters.Cerebrospinal fluid steroidomics: are bioactive bile acids present in brain?Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency.Redox Regulation of Homeostasis and Proteostasis in Peroxisomes.Developmental changes of bile acid composition and conjugation in L- and D-bifunctional protein single and double knockout mice.cDNA cloning and analysis of tissue-specific expression of mouse peroxisomal straight-chain acyl-CoA oxidase.Peroxisomes contain a specific phytanoyl-CoA/pristanoyl-CoA thioesterase acting as a novel auxiliary enzyme in alpha- and beta-oxidation of methyl-branched fatty acids in mouse.Conserved expression of alternative splicing variants of peroxisomal acyl-CoA oxidase 1 in vertebrates and developmental and nutritional regulation in fish.ACOX2:FAD; ACOXL:FAD oxidise (2S)-pristanoyl-CoA to trans-2;3-dehydropristanoyl-CoA25(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-CoAC22-bronchial and T7-alveolar epithelial cell lines of the immortomouse are excellent murine cell culture model systems to study pulmonary peroxisome biology and metabolism.Preeclampsia and Related Cardiovascular Risk: Common Genetic Background
P2860
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P2860
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
description
1996 nî lūn-bûn
@nan
1996 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Molecular characterization of ...... protein in Zellweger syndrome
@ast
Molecular characterization of ...... protein in Zellweger syndrome
@en
Molecular characterization of ...... protein in Zellweger syndrome
@en-gb
Molecular characterization of ...... protein in Zellweger syndrome
@nl
type
label
Molecular characterization of ...... protein in Zellweger syndrome
@ast
Molecular characterization of ...... protein in Zellweger syndrome
@en
Molecular characterization of ...... protein in Zellweger syndrome
@en-gb
Molecular characterization of ...... protein in Zellweger syndrome
@nl
prefLabel
Molecular characterization of ...... protein in Zellweger syndrome
@ast
Molecular characterization of ...... protein in Zellweger syndrome
@en
Molecular characterization of ...... protein in Zellweger syndrome
@en-gb
Molecular characterization of ...... protein in Zellweger syndrome
@nl
P2093
P2860
P356
P1476
Molecular characterization of ...... protein in Zellweger syndrome
@en
P2093
E Baumgart
G P Mannaerts
H D Fahimi
J A Leunissen
J C Vanhooren
J Vandekerckhove
P P van Veldhoven
P2860
P304
13748-13753
P356
10.1073/PNAS.93.24.13748
P407
P50
P577
1996-11-01T00:00:00Z