178 related articles for article (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
[TBL] [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; 39(5):453-66. PubMed ID: 9408912
[TBL] [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; 9(4):321-34. PubMed ID: 2435984
[TBL] [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; 31(1A Suppl):235-7. PubMed ID: 6186727
[TBL] [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; 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; 43(3):293-300. PubMed ID: 3622522
[TBL] [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; 416(3):255-64. PubMed ID: 1689088
[TBL] [Abstract][Full Text] [Related]
8. [Peroxisomes and peroxisomal diseases].
Petelenz M; Gonciarz Z; Grzybek H; Panz B
Postepy Hig Med Dosw; 1991; 45(1-2):77-99. PubMed ID: 1717967
[TBL] [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; 413(4):275-85. PubMed ID: 3140473
[TBL] [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; 423(6):459-68. PubMed ID: 7507276
[TBL] [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; 145(3):172-5. PubMed ID: 2429839
[TBL] [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; 24(1):62-9. PubMed ID: 7238535
[TBL] [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; 88(5):491-9. PubMed ID: 1372585
[TBL] [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; 67(4):319-27. PubMed ID: 8521871
[TBL] [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; 81(6):1710-5. PubMed ID: 2454948
[TBL] [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; 27(11):1471-7. PubMed ID: 92501
[TBL] [Abstract][Full Text] [Related]
17. Zellweger syndrome: a histochemical diagnosis of two cases.
Raafat F; Smith K; Halloran EA; Lacy D
Pediatr Pathol; 1991; 11(3):413-20. PubMed ID: 1714076
[TBL] [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; 48(4):437-40. PubMed ID: 982611
[TBL] [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; 17(6):623-36. PubMed ID: 8122328
[TBL] [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; 46(1):129-35. PubMed ID: 3396586
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]