Literature DB >> 2864474

Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver.

R J Wanders, R B Schutgens, J M Tager.   

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Year:  1985        PMID： 2864474     DOI： 10.1007/bf01811504

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  3 in total

Review 1.  Review: the cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects.

Authors:  R I Kelley
Journal:  Am J Med Genet       Date:  1983-12

2.  Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome.

Authors:  R B Schutgens; G J Romeyn; R J Wanders; H van den Bosch; G Schrakamp; H S Heymans
Journal:  Biochem Biophys Res Commun       Date:  1984-04-16       Impact factor: 3.575

3.  Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome.

Authors:  R J Wanders; M Kos; B Roest; A J Meijer; G Schrakamp; H S Heymans; W H Tegelaers; H van den Bosch; R B Schutgens; J M Tager
Journal:  Biochem Biophys Res Commun       Date:  1984-09-28       Impact factor: 3.575
  3 in total
  6 in total

1.  Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.

Authors:  A W Schram; A Strijland; T Hashimoto; R J Wanders; R B Schutgens; H van den Bosch; J M Tager
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

2.  Isolation of peroxisome-deficient mutants of Saccharomyces cerevisiae.

Authors:  R Erdmann; M Veenhuis; D Mertens; W H Kunau
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

Review 3.  Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.

Authors:  R B Schutgens; R J Wanders; H S Heymans; A W Schram; J M Tager; G Schrakamp; H van den Bosch
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

4.  Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism.

Authors:  C J Danpure; P Fryer; S Griffiths; K M Guttridge; P R Jennings; J Allsop; A B Moser; S Naidu; H W Moser; M MacCollin
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

5.  Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy.

Authors:  J Vamecq; J P Draye; F Van Hoof; J P Misson; P Evrard; G Verellen; H J Eyssen; J Van Eldere; R B Schutgens; R J Wanders
Journal:  Am J Pathol       Date:  1986-12       Impact factor: 4.307

6.  Histochemistry of peroxisomal enzyme activities: a tool in the diagnosis of Zellweger syndrome.

Authors:  W M Frederiks; K S Bosch; M Ankum; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982
  6 in total

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