122 related articles for article (PubMed ID: 1718439)
1. Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group.
Wiemer EA; Out M; Schelen A; Wanders RJ; Schutgens RB; Van den Bosch H; Tager JM
Biochim Biophys Acta; 1991 Oct; 1097(3):232-7. PubMed ID: 1718439
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.
Schram AW; Strijland A; Hashimoto T; Wanders RJ; Schutgens RB; van den Bosch H; Tager JM
Proc Natl Acad Sci U S A; 1986 Aug; 83(16):6156-8. PubMed ID: 2426710
[TBL] [Abstract][Full Text] [Related]
4. Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.
Roscher AA; Hoefler S; Hoefler G; Paschke E; Paltauf F; Moser A; Moser H
Pediatr Res; 1989 Jul; 26(1):67-72. PubMed ID: 2475849
[TBL] [Abstract][Full Text] [Related]
5. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.
Tager JM; Brul S; Wiemer EA; Strijland A; Van Driel R; Schutgens RB; Van den Bosch H; Wanders RJ; Westerveld A
Prog Clin Biol Res; 1990; 321():545-58. PubMed ID: 2183242
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia.
Wanders RJ; van Roermund CW; van Wijland MJ; Schutgens RB; Tager JM; van den Bosch H; Thomas GH
J Inherit Metab Dis; 1988; 11 Suppl 2():161-4. PubMed ID: 3141699
[No Abstract] [Full Text] [Related]
8. 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]
9. In situ genetic complementation analysis of cells with generalized peroxisomal dysfunction.
Singh AK; Kulvatunyou N; Singh I; Stanley WS
Hum Hered; 1989; 39(5):298-301. PubMed ID: 2482247
[TBL] [Abstract][Full Text] [Related]
10. Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts.
Heikoop JC; Van den Berg M; Strijland A; Weijers PJ; Schutgens RB; Just WW; Wanders RJ; Tager JM
Biochim Biophys Acta; 1991 Jul; 1097(1):62-70. PubMed ID: 1677591
[TBL] [Abstract][Full Text] [Related]
11. Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.
Wiemer EA; Brul S; Just WW; Van Driel R; Brouwer-Kelder E; Van Den Berg M; Weijers PJ; Schutgens RB; Van Den Bosch H; Schram A
Eur J Cell Biol; 1989 Dec; 50(2):407-17. PubMed ID: 2697558
[TBL] [Abstract][Full Text] [Related]
12. Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.
Tateishi K; Okumoto K; Shimozawa N; Tsukamoto T; Osumi T; Suzuki Y; Kondo N; Okano I; Fujiki Y
Eur J Cell Biol; 1997 Aug; 73(4):352-9. PubMed ID: 9270878
[TBL] [Abstract][Full Text] [Related]
13. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
Aubourg P; Kremser K; Roland MO; Rocchiccioli F; Singh I
Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868
[TBL] [Abstract][Full Text] [Related]
14. Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly.
Suzuki Y; Shimozawa N; Yajima S; Orii T; Yokota S; Tashiro Y; Osumi T; Hashimoto T
Cell Struct Funct; 1992 Feb; 17(1):1-8. PubMed ID: 1586963
[TBL] [Abstract][Full Text] [Related]
15. Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease.
Wanders RJ; Heymans HS; Schutgens RB; Poll-Thé BT; Saudubray JM; Tager JM; Schrakamp G; van den Bosch H
J Neurol Sci; 1988 Apr; 84(2-3):147-55. PubMed ID: 2454298
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.
Zoeller RA; Allen LA; Santos MJ; Lazarow PB; Hashimoto T; Tartakoff AM; Raetz CR
J Biol Chem; 1989 Dec; 264(36):21872-8. PubMed ID: 2689450
[TBL] [Abstract][Full Text] [Related]
18. Investigation of peroxisomal lipid beta-oxidation enzymes in guinea pig liver peroxisomes by immunoblotting and immunocytochemistry.
Yamamoto K; Völkl A; Fahimi HD
J Histochem Cytochem; 1992 Dec; 40(12):1909-18. PubMed ID: 1360481
[TBL] [Abstract][Full Text] [Related]
19. Resistance to erucic acid as a selectable marker for peroxisomal activity: isolation of revertants of an infantile Refsum disease cell line.
Bachir Bioukar E; Straehli F; Ng KH; Rolland MO; Hashimoto T; Carreau JP; Deschatrette J
J Inherit Metab Dis; 1994; 17(1):41-59. PubMed ID: 7519689
[TBL] [Abstract][Full Text] [Related]
20. [Clinical biochemical and genetic aspects of peroxisome-deficient disorders].
Suzuki Y
No To Hattatsu; 1992 Mar; 24(2):194-7. PubMed ID: 1373633
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
