Peroxisomal Matrix Enzymes in Zellweger Syndrome: Activity and Subcellular Localization in Liver

Overview

Journal J Inherit Metab Dis

Publisher Wiley

Date 1985 Jan 1

PMID 2864474

Citations 6

Authors

R J Wanders

R B Schutgens

J M Tager

Affiliations

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Citing Articles

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

Danpure C, Fryer P, Griffiths S, Guttridge K, Jennings P, Allsop J J Inherit Metab Dis. 1994; 17(1):27-40.

PMID: 8051936 DOI: 10.1007/BF00735393.

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

Frederiks W, Bosch K, Ankum M, Wanders R J Inherit Metab Dis. 1993; 16(6):921-8.

PMID: 7907383 DOI: 10.1007/BF00711506.

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

Schutgens R, Wanders R, Heymans H, Schram A, Tager J, Schrakamp G J Inherit Metab Dis. 1987; 10 Suppl 1:33-45.

PMID: 3119940 DOI: 10.1007/BF01812845.

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

Vamecq J, Draye J, Van Hoof F, Misson J, Evrard P, Verellen G Am J Pathol. 1986; 125(3):524-35.

PMID: 2879480 PMC: 1888479.

Isolation of peroxisome-deficient mutants of Saccharomyces cerevisiae.

Erdmann R, Veenhuis M, Mertens D, Kunau W Proc Natl Acad Sci U S A. 1989; 86(14):5419-23.

PMID: 2568633 PMC: 297634. DOI: 10.1073/pnas.86.14.5419.

References

Wanders R, Kos M, Roest B, Meijer A, Schrakamp G, Heymans H . Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome. Biochem Biophys Res Commun. 1984; 123(3):1054-61. DOI: 10.1016/s0006-291x(84)80240-5. View

Kelley R . Review: the cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects. Am J Med Genet. 1983; 16(4):503-17. DOI: 10.1002/ajmg.1320160409. View

Schutgens R, Romeyn G, Wanders R, van den Bosch H, Schrakamp G, Heymans H . Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome. Biochem Biophys Res Commun. 1984; 120(1):179-84. DOI: 10.1016/0006-291x(84)91430-x. View