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Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies.
Science. 1985 Jan 4;227(4682):67-70
PMID: 3964959
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Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?
Clin Genet. 1984 Dec;26(6):579-86
PMID: 6209040
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Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly.
Science. 1988 Mar 25;239(4847):1536-8
PMID: 3281254
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Peroxisomal integral membrane proteins in control and Zellweger fibroblasts.
J Biol Chem. 1988 Jul 25;263(21):10502-9
PMID: 3292528
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A conserved tripeptide sorts proteins to peroxisomes.
J Cell Biol. 1989 May;108(5):1657-64
PMID: 2654139
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Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.
Pediatr Res. 1989 Jul;26(1):67-72
PMID: 2475849
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The 70-kDa peroxisomal membrane protein is a member of the Mdr (P-glycoprotein)-related ATP-binding protein superfamily.
J Biol Chem. 1990 Mar 15;265(8):4534-40
PMID: 1968461
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Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.
Eur J Cell Biol. 1989 Dec;50(2):407-17
PMID: 2697558
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Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.
Pediatr Res. 1990 Mar;27(3):304-10
PMID: 2181395
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The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor protein.
Pediatr Res. 1991 Feb;29(2):141-6
PMID: 1673025
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Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.
J Inherit Metab Dis. 1991;14(2):152-64
PMID: 1679469
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A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase.
EMBO J. 1991 Nov;10(11):3255-62
PMID: 1680677
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Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group.
Biochim Biophys Acta. 1991 Oct 21;1097(3):232-7
PMID: 1718439
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Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.
Biochem Biophys Res Commun. 1991 Dec 31;181(3):947-54
PMID: 1764107
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Transport of microinjected proteins into peroxisomes of mammalian cells: inability of Zellweger cell lines to import proteins with the SKL tripeptide peroxisomal targeting signal.
Mol Cell Biol. 1992 Feb;12(2):531-41
PMID: 1732729
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A human gene responsible for Zellweger syndrome that affects peroxisome assembly.
Science. 1992 Feb 28;255(5048):1132-4
PMID: 1546315
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Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.
Hum Genet. 1992 Mar;88(5):491-9
PMID: 1372585
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Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndrome.
J Cell Physiol. 1992 Apr;151(1):103-12
PMID: 1560037
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Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly.
Cell Struct Funct. 1992 Feb;17(1):1-8
PMID: 1586963
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Targeting efficiencies of various permutations of the consensus C-terminal tripeptide peroxisomal targeting signal.
FEBS Lett. 1992 Jun 29;305(2):133-6
PMID: 1618341
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Biochemistry of peroxisomes.
Annu Rev Biochem. 1992;61:157-97
PMID: 1353950
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Import of proteins into peroxisomes and other microbodies.
Biochem J. 1992 Sep 15;286 ( Pt 3):657-69
PMID: 1417723
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Peroxisomal disorders in man.
Cell Biochem Funct. 1992 Sep;10(3):201-7
PMID: 1423901
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Cytosol-dependent peroxisomal protein import in a permeabilized cell system.
J Cell Biol. 1993 Feb;120(3):675-85
PMID: 8425896
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Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome.
Nat Genet. 1992 Apr;1(1):16-23
PMID: 1301993
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Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome.
Science. 1973 Oct 5;182(4107):62-4
PMID: 4730055
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Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism.
J Pediatr. 1975 Mar;86(3):382-7
PMID: 1113225
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Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).
Nature. 1983 Nov 3-9;306(5938):69-70
PMID: 6633659
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The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.
N Engl J Med. 1984 May 3;310(18):1141-6
PMID: 6709009
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Ultrastructural and cytochemical demonstration of peroxisomes in cultured fibroblasts from patients with peroxisomal deficiency disorders.
J Cell Biol. 1985 May;100(5):1789-92
PMID: 3988808