A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern
about
Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapyThe human PICD gene encodes a cytoplasmic and peroxisomal NADP(+)-dependent isocitrate dehydrogenaseHomo- and heterodimerization of peroxisomal ATP-binding cassette half-transportersPEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesisCharacterization and functional analysis of the nucleotide binding fold in human peroxisomal ATP binding cassette transportersLive cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3)Peroxisomal ABC transporters: functions and mechanismA Saccharomyces cerevisiae homolog of the human adrenoleukodystrophy transporter is a heterodimer of two half ATP-binding cassette transporters.Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrations.Complete inventory of the yeast ABC proteins.ABC Transporter Subfamily D: Distinct Differences in Behavior between ABCD1-3 and ABCD4 in Subcellular Localization, Function, and Human DiseaseABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlationsATP binding/hydrolysis by and phosphorylation of peroxisomal ATP-binding cassette proteins PMP70 (ABCD3) and adrenoleukodystrophy protein (ABCD1)Molecular cloning of a mammalian ABC transporter homologous to Drosophila white geneThe Arabidopsis pxa1 mutant is defective in an ATP-binding cassette transporter-like protein required for peroxisomal fatty acid beta-oxidationIdentification of a substrate-binding site in a peroxisomal beta-oxidation enzyme by photoaffinity labeling with a novel palmitoyl derivativeX-linked adrenoleukodystrophy enigma: how does the ALD peroxisomal transporter mutation affect CNS glia?Structure-function analysis of peroxisomal ATP-binding cassette transporters using chimeric dimers.Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient miceABCD2 alters peroxisome proliferator-activated receptor α signaling in vitro, but does not impair responses to fenofibrate therapy in a mouse model of diet-induced obesityPathophysiology of X-linked adrenoleukodystrophy.Gene expression profiling of the long-term adaptive response to hypoxia in the gills of adult zebrafish.Genomic organization and chromosomal localization of the human peroxisomal membrane protein-1-like protein (PXMP1-L) gene encoding a peroxisomal ABC transporter.Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.Peroxisomal dysfunction in inflammatory childhood white matter disorders: an unexpected contributor to neuropathologyFraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromesInvolvement of the carboxyl-terminal region of the yeast peroxisomal half ABC transporter Pxa2p in its interaction with Pxa1p and in transporter function.ABCD1 deletion-induced mitochondrial dysfunction is corrected by SAHA: implication for adrenoleukodystrophy.Mammalian peroxisomal ABC transporters: from endogenous substrates to pathology and clinical significance.Comparative genomics and adaptive selection of the ATP-binding-cassette gene family in caenorhabditis species.Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophy.Discovery of regulatory elements in human ATP-binding cassette transporters through expression quantitative trait mapping.The absence of ABCD2 sensitizes mice to disruptions in lipid metabolism by dietary erucic acid.Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferatorPEX11 promotes peroxisome division independently of peroxisome metabolismBrain endothelial dysfunction in cerebral adrenoleukodystrophy.A mouse model for X-linked adrenoleukodystrophy.Caffeic acid phenethyl ester induces adrenoleukodystrophy (Abcd2) gene in human X-ALD fibroblasts and inhibits the proinflammatory response in Abcd1/2 silenced mouse primary astrocytes.Impaired very long-chain acyl-CoA β-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction.Role of ATP-binding cassette transporters in brain lipid transport and neurological disease.
P2860
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P2860
A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern
description
1996 nî lūn-bûn
@nan
1996 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի փետրվարին 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
A close relative of the adreno ...... a specific expression pattern
@ast
A close relative of the adreno ...... a specific expression pattern
@en
A close relative of the adreno ...... a specific expression pattern
@nl
type
label
A close relative of the adreno ...... a specific expression pattern
@ast
A close relative of the adreno ...... a specific expression pattern
@en
A close relative of the adreno ...... a specific expression pattern
@nl
prefLabel
A close relative of the adreno ...... a specific expression pattern
@ast
A close relative of the adreno ...... a specific expression pattern
@en
A close relative of the adreno ...... a specific expression pattern
@nl
P2093
P2860
P3181
P356
P1476
A close relative of the adreno ...... a specific expression pattern
@en
P2093
G Lombard-Platet
P2860
P304
P3181
P356
10.1073/PNAS.93.3.1265
P407
P577
1996-02-06T00:00:00Z