Peroxisomal disorders: clinical, biochemical, and molecular aspects.
about
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group GA PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsPeroxisomal membrane proteins insert into the endoplasmic reticulum.Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in miceAdrenoleukodystrophy and related disorders.Therapeutic developments in peroxisome biogenesis disorders.Refsum disease, peroxisomes and phytanic acid oxidation: a review.Normal peroxisome development from vesicles induced by truncated Hansenula polymorpha Pex3p.Multivoxel magnetic resonance spectroscopy in a rhizomelic chondrodysplasia punctata case.Domain mapping of human PEX5 reveals functional and structural similarities to Saccharomyces cerevisiae Pex18p and Pex21p.Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum Disorder.Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.Approaching complete peroxisome characterization by gas-phase fractionation.PTS1-independent targeting of isocitrate lyase to peroxisomes requires the PTS1 receptor Pex5p.An Arabidopsis pex10 null mutant is embryo lethal, implicating peroxisomes in an essential role during plant embryogenesis.The peroxisome deficient Arabidopsis mutant sse1 exhibits impaired fatty acid synthesis.New amperometric biosensors based on diamond paste for the assay of L- and D-pipecolic acids in serum samples.RNA interference of peroxisome-related genes in C. elegans: a new model for human peroxisomal disorders.Peripheral ethanolamine plasmalogen deficiency: a logical causative factor in Alzheimer's disease and dementia.Pichia pastoris Pex14p, a phosphorylated peroxisomal membrane protein, is part of a PTS-receptor docking complex and interacts with many peroxins.Regulation of Oligodendrocyte Differentiation and Myelination by Nuclear Receptors: Role in Neurodegenerative Disorders.Antibodies against pex14p block ATP-independent binding of matrix proteins to peroxisomes in vitro.Diamond Paste Based Amperometric Biosensors for the Determination ofl- andd-Pipecolic Acid
P2860
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P2860
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
@ast
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
@en
type
label
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
@ast
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
@en
prefLabel
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
@ast
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
@en
P356
P1476
Peroxisomal disorders: clinical, biochemical, and molecular aspects.
@en
P2093
Wanders RJ
P2888
P304
P356
10.1023/A:1022592014988
P577
1999-04-01T00:00:00Z
P6179
1046161904