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174 related items for PubMed ID: 2430454
1. Hepatic peroxisomes are deficient in infantile refsum disease: a cytochemical study of 4 cases. Roels F, Cornelis A, Poll-The BT, Aubourg P, Ogier H, Scotto J, Saudubray JM. Am J Med Genet; 1986 Oct; 25(2):257-71. PubMed ID: 2430454 [Abstract] [Full Text] [Related]
2. Biogenesis of peroxisomes in fetal liver. Espeel M, Depreter M, Nardacci R, D'Herde K, Kerckaert I, Stefanini S, Roels F. Microsc Res Tech; 1997 Dec 01; 39(5):453-66. PubMed ID: 9408912 [Abstract] [Full Text] [Related]
3. Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblasts. Beard ME, Moser AB, Sapirstein V, Holtzman E. J Inherit Metab Dis; 1986 Dec 01; 9(4):321-34. PubMed ID: 2435984 [Abstract] [Full Text] [Related]
4. Peroxisomes (microbodies) in human liver: cytochemical and quantitative studies of 85 biopsies. Roels F, Pauwels M, Cornelis A, Kerckaert I, Van der Spek P, Goovaerts G, Versieck J, Goldfischer S. J Histochem Cytochem; 1983 Jan 01; 31(1A Suppl):235-7. PubMed ID: 6186727 [Abstract] [Full Text] [Related]
5. [Cytochemical studies of catalase activity in the peroxisomes of human hepatocytes]. Gonciarz Z, Panz B, Petelenz M, Grzybek H, Kocek B. Z Mikrosk Anat Forsch; 1987 Jan 01; 101(5):795-805. PubMed ID: 3445662 [No Abstract] [Full Text] [Related]
6. Biogenesis of peroxisomes in regenerating rat liver. I. Sequential changes of catalase and urate oxidase detected by ultrastructural cytochemistry. Yamamoto K, Fahimi HD. Eur J Cell Biol; 1987 Jun 01; 43(3):293-300. PubMed ID: 3622522 [Abstract] [Full Text] [Related]
7. Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders. Hughes JL, Poulos A, Robertson E, Chow CW, Sheffield LJ, Christodoulou J, Carter RF. Virchows Arch A Pathol Anat Histopathol; 1990 Jun 01; 416(3):255-64. PubMed ID: 1689088 [Abstract] [Full Text] [Related]
8. [Peroxisomes and peroxisomal diseases]. Petelenz M, Gonciarz Z, Grzybek H, Panz B. Postepy Hig Med Dosw; 1991 Jun 01; 45(1-2):77-99. PubMed ID: 1717967 [Abstract] [Full Text] [Related]
9. Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data. Roels F, Pauwels M, Poll-Thé BT, Scotto J, Ogier H, Aubourg P, Saudubray JM. Virchows Arch A Pathol Anat Histopathol; 1988 Jun 01; 413(4):275-85. PubMed ID: 3140473 [Abstract] [Full Text] [Related]
10. Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders. Hughes JL, Crane DI, Robertson E, Poulos A. Virchows Arch A Pathol Anat Histopathol; 1993 Jun 01; 423(6):459-68. PubMed ID: 7507276 [Abstract] [Full Text] [Related]
11. Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins. Wanders RJ, Schutgens RB, Schrakamp G, van den Bosch H, Tager JM, Schram AW, Hashimoto T, Poll-Thé BT, Saudubrau JM. Eur J Pediatr; 1986 Aug 01; 145(3):172-5. PubMed ID: 2429839 [Abstract] [Full Text] [Related]
12. Polydispersity of rat liver peroxisomes induced by the hypolipidemic and carcinogenic agent clofibrate. Flatmark T, Christiansen EN, Kryvi H. Eur J Cell Biol; 1981 Apr 01; 24(1):62-9. PubMed ID: 7238535 [Abstract] [Full Text] [Related]
13. Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells. Yajima S, Suzuki Y, Shimozawa N, Yamaguchi S, Orii T, Fujiki Y, Osumi T, Hashimoto T, Moser HW. Hum Genet; 1992 Mar 01; 88(5):491-9. PubMed ID: 1372585 [Abstract] [Full Text] [Related]
14. Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders. Espeel M, Roels F, Giros M, Mandel H, Peltier A, Poggi F, Poll-The BT, Smeitink JA, Van Maldergem L, Santos MJ. Eur J Cell Biol; 1995 Aug 01; 67(4):319-27. PubMed ID: 8521871 [Abstract] [Full Text] [Related]
15. 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 01; 81(6):1710-5. PubMed ID: 2454948 [Abstract] [Full Text] [Related]
16. Cytochemistry of human catalase. The demonstration of hepatic and renal peroxisomes by a high temperature procedure. Roels F, Goldfischer S. J Histochem Cytochem; 1979 Nov 01; 27(11):1471-7. PubMed ID: 92501 [Abstract] [Full Text] [Related]
17. Zellweger syndrome: a histochemical diagnosis of two cases. Raafat F, Smith K, Halloran EA, Lacy D. Pediatr Pathol; 1991 Nov 01; 11(3):413-20. PubMed ID: 1714076 [Abstract] [Full Text] [Related]
18. [Structure and function of hepatocyte lysosomes and peroxisomes of rachitic rats]. Khomutovskiĭ OA, Mironova VN, Degtiareva II. Ukr Biokhim Zh; 1976 Nov 01; 48(4):437-40. PubMed ID: 982611 [Abstract] [Full Text] [Related]
19. Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata. Espeel M, Heikoop JC, Smeitink JA, Beemer FA, De Craemer D, Van den Berg M, Hashimoto T, Wanders RJ, Schutgens RB, Poll-The BT. Ultrastruct Pathol; 1993 Nov 01; 17(6):623-36. PubMed ID: 8122328 [Abstract] [Full Text] [Related]
20. Catalase in guinea pig hepatocytes is localized in cytoplasm, nuclear matrix and peroxisomes. Yamamoto K, Völkl A, Hashimoto T, Fahimi HD. Eur J Cell Biol; 1988 Apr 01; 46(1):129-35. PubMed ID: 3396586 [Abstract] [Full Text] [Related] Page: [Next] [New Search]