Peroxisomal disorders: a newly recognised group of genetic diseases.
about
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiencyGenetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysisIsolation of peroxisome-deficient mutants of Saccharomyces cerevisiae.PAS3, a Saccharomyces cerevisiae gene encoding a peroxisomal integral membrane protein essential for peroxisome biogenesis.Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acidsLeber's congenital amaurosis--a new syndrome with a cardiomyopathy.Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy.The value of the study of natural history in genetic disorders and congenital anomaly syndromes.Biology of senescent liver peroxisomes: role in hepatocellular aging and diseaseTherapeutic developments in peroxisome biogenesis disorders.Peroxisomes in wild-type and rosy mutant Drosophila melanogasterDifferent types of peroxisomes in human duodenal epithelium.Purification, properties, and immunocytochemical localization of human liver peroxisomal enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase.A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy)Import of proteins into peroxisomes and other microbodies.Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndromeA novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase.A fibroblast cell line defective in alkyl-dihydroxyacetone phosphate synthase: a novel defect in plasmalogen biosynthesis.An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes.Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum diseasePresence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome)Organelle pathology in metabolic neuromuscular disease: an overview.Peroxisomal disorders. A review of a recently recognized group of clinical entities.Dysmorphic syndromes with demonstrable biochemical abnormalities.Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus.Synthesis and subcellular location of peroxisomal membrane proteins in a peroxisome-deficient mutant of the yeast Hansenula polymorpha.Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.Biogenesis of peroxisomes in fetal liver.Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophyAn efficient positive selection procedure for the isolation of peroxisomal import and peroxisome assembly mutants of Saccharomyces cerevisiae.Differential protein import deficiencies in human peroxisome assembly disorders.Immunocytochemical localization of peroxisomal enzymes in human liver biopsies.High incorporation of dietary 1-O-heptadecyl glycerol into tissue plasmalogens of young rats.D-aspartate oxidase in rat, bovine and sheep kidney cortex is localized in peroxisomesPeroxisomes protect lymphoma cells from HDAC inhibitor-mediated apoptosis.Adrenoleucodystrophy.The electroretinogram.The role of 15-lipoxygenase in disruption of the peroxisomal membrane and in programmed degradation of peroxisomes in normal rat liver.Beta-oxidation of polyunsaturated fatty acids in peroxisomes. Subcellular distribution of delta 3,delta 2-enoyl-CoA isomerase activity in rat liver.
P2860
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P2860
Peroxisomal disorders: a newly recognised group of genetic diseases.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Peroxisomal disorders: a newly recognised group of genetic diseases.
@en
Peroxisomal disorders: a newly recognised group of genetic diseases.
@nl
type
label
Peroxisomal disorders: a newly recognised group of genetic diseases.
@en
Peroxisomal disorders: a newly recognised group of genetic diseases.
@nl
prefLabel
Peroxisomal disorders: a newly recognised group of genetic diseases.
@en
Peroxisomal disorders: a newly recognised group of genetic diseases.
@nl
P2093
P2860
P356
P1476
Peroxisomal disorders: a newly recognised group of genetic diseases.
@en
P2093
H S Heymans
H van den Bosch
R B Schutgens
R J Wanders
P2860
P2888
P304
P356
10.1007/BF00441734
P577
1986-02-01T00:00:00Z