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22. Isolation of rat liver peroxisomes. Baudhuin P Methods Enzymol; 1974; 31():356-68. PubMed ID: 4153621 [No Abstract] [Full Text] [Related]
23. Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome. Bleeker-Wagemakers EM; Oorthuys JW; Wanders RJ; Schutgens RB Clin Genet; 1986 Feb; 29(2):160-4. PubMed ID: 3955868 [TBL] [Abstract][Full Text] [Related]
24. Cytochemical and immunocytochemical study on the peroxisomes of rat liver after administration of a hypolipidemic drug, MLM-160. Yokota S Eur J Cell Biol; 1990 Oct; 53(1):112-21. PubMed ID: 1981745 [TBL] [Abstract][Full Text] [Related]
25. Microbodies in Leydig cell tumors of rat testis. Reddy J; Svoboda D J Histochem Cytochem; 1972 Oct; 20(10):793-803. PubMed ID: 4404751 [No Abstract] [Full Text] [Related]
27. Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome. van Roermund CW; Brul S; Tager JM; Schutgens RB; Wanders RJ J Inherit Metab Dis; 1991; 14(2):152-64. PubMed ID: 1679469 [TBL] [Abstract][Full Text] [Related]
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29. [Peroxisomes. 2. Intraparticulate localization of peroxisomal enzymes of the rat kidney]. Suzuki S; Hayashi H; Suga T Seikagaku; 1972; 44(2):69-74. PubMed ID: 4401930 [No Abstract] [Full Text] [Related]
30. [Effect of minimal hepatectomy on catalase and peroxisomal oxidase activity in rat liver]. Lamy J; Lamy JN; Schmitt M; Weill J Biochimie; 1973; 55(11):1491-4. PubMed ID: 4151476 [No Abstract] [Full Text] [Related]
31. Peroxisomal organization in normal and cerebrohepatorenal (Zellweger) syndrome fibroblasts. Santos MJ; Ojeda JM; Garrido J; Leighton F Proc Natl Acad Sci U S A; 1985 Oct; 82(19):6556-60. PubMed ID: 2995971 [TBL] [Abstract][Full Text] [Related]
32. Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata. Balfe A; Hoefler G; Chen WW; Watkins PA Pediatr Res; 1990 Mar; 27(3):304-10. PubMed ID: 2181395 [TBL] [Abstract][Full Text] [Related]
33. Cerebrohepatorenal syndrome of Zellweger: a peroxisomal deficiency disorder. Case report and review. Kaplan M; Eidelman AI; Shapira Y; Collins J; Goldfischer S Isr J Med Sci; 1988 Jun; 24(6):319-24. PubMed ID: 3042692 [TBL] [Abstract][Full Text] [Related]
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36. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis. Brul S; Westerveld A; Strijland A; Wanders RJ; Schram AW; Heymans HS; Schutgens RB; van den Bosch H; Tager JM J Clin Invest; 1988 Jun; 81(6):1710-5. PubMed ID: 2454948 [TBL] [Abstract][Full Text] [Related]
37. Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome. Schutgens RB; Romeyn GJ; Wanders RJ; van den Bosch H; Schrakamp G; Heymans HS Biochem Biophys Res Commun; 1984 Apr; 120(1):179-84. PubMed ID: 6712687 [TBL] [Abstract][Full Text] [Related]
38. Peroxisomal disorders. A review of a recently recognized group of clinical entities. Talwar D; Swaiman KF Clin Pediatr (Phila); 1987 Oct; 26(10):497-504. PubMed ID: 2443295 [TBL] [Abstract][Full Text] [Related]
39. Differentiation of liver peroxisomes in the foetal and newborn rat. Cytochemistry of catalase and D-aminoacid oxidase. Stefanini S; Farrace MG; Argento MP J Embryol Exp Morphol; 1985 Aug; 88():151-63. PubMed ID: 2867120 [TBL] [Abstract][Full Text] [Related]
40. Ultrastructural localization of catalase and D-amino acid oxidase in 'normal' fetal mouse liver. Dabholkar AS Experientia; 1986 Feb; 42(2):144-7. PubMed ID: 2868912 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]