223 related articles for article (PubMed ID: 6566965)
1. Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes.
Datta NS; Wilson GN; Hajra AK
N Engl J Med; 1984 Oct; 311(17):1080-3. PubMed ID: 6566965
[TBL] [Abstract][Full Text] [Related]
2. Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.
Wilson GN; Holmes RG; Custer J; Lipkowitz JL; Stover J; Datta N; Hajra A
Am J Med Genet; 1986 May; 24(1):69-82. PubMed ID: 3706414
[TBL] [Abstract][Full Text] [Related]
3. The role of peroxisomes in glycerol ether lipid metabolism.
Hajra AK; Horie S; Webber KO
Prog Clin Biol Res; 1988; 282():99-116. PubMed ID: 3071810
[TBL] [Abstract][Full Text] [Related]
4. Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.
van den Bosch H; Schalkwijk CG; Schrakamp G; Wanders RJ; Schutgens RB; Schram AW; Tager JM
Prog Clin Biol Res; 1988; 282():139-50. PubMed ID: 3071794
[TBL] [Abstract][Full Text] [Related]
5. Properties of the enzymes catalyzing the biosynthesis of lysophosphatidate and its ether analog in cultured fibroblasts from Zellweger syndrome patients and normal controls.
Webber KO; Datta NS; Hajra AK
Arch Biochem Biophys; 1987 May; 254(2):611-20. PubMed ID: 3646870
[TBL] [Abstract][Full Text] [Related]
6. Deficiency of acyl-CoA:dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test.
Wanders RJ; van Weringh G; Schrakamp G; Tager JM; van den Bosch H; Schutgens RB
Clin Chim Acta; 1985 Oct; 151(3):217-21. PubMed ID: 4053381
[TBL] [Abstract][Full Text] [Related]
7. [Diagnosis of Zellweger's cerebrohepatorenal syndrome].
Schutgens RB; Heymans HS; Purvis R; Wanders RJ; Schrakamp G; van den Bosch H
Tijdschr Kindergeneeskd; 1984 Dec; 52(6):231-8. PubMed ID: 6528320
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.
Heymans HS; vd Bosch H; Schutgens RB; Tegelaers WH; Walther JU; Müller-Höcker J; Borst P
Eur J Pediatr; 1984 Apr; 142(1):10-5. PubMed ID: 6714253
[TBL] [Abstract][Full Text] [Related]
10. Immunological analyses of alkyl-dihydroxyacetone-phosphate synthase in human peroxisomal disorders.
Biermann J; Gootjes J; Humbel BM; Dansen TB; Wanders RJ; van den Bosch H
Eur J Cell Biol; 1999 May; 78(5):339-48. PubMed ID: 10384985
[TBL] [Abstract][Full Text] [Related]
11. The cerebro-hepato-renal (Zellweger) syndrome: prenatal detection based on impaired biosynthesis of plasmalogens.
Schutgens RB; Schrakamp G; Wanders RJ; Heymans HS; Moser HW; Moser AE; Tager JM; Bosch HV; Aubourg P
Prenat Diagn; 1985; 5(5):337-44. PubMed ID: 4070172
[TBL] [Abstract][Full Text] [Related]
12. Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.
Schutgens RB; Wanders RJ; Heymans HS; Schram AW; Tager JM; Schrakamp G; van den Bosch H
J Inherit Metab Dis; 1987; 10 Suppl 1():33-45. PubMed ID: 3119940
[TBL] [Abstract][Full Text] [Related]
13. Topography of ether phospholipid biosynthesis.
Hardeman D; van den Bosch H
Biochim Biophys Acta; 1989 Nov; 1006(1):1-8. PubMed ID: 2804060
[TBL] [Abstract][Full Text] [Related]
14. Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesis.
Infante JP; Huszagh VA
Mol Genet Metab; 2001 Jan; 72(1):1-7. PubMed ID: 11161822
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome.
Schrakamp G; Roosenboom CF; Schutgens RB; Wanders RJ; Heymans HS; Tager JM; van den Bosch H
J Lipid Res; 1985 Jul; 26(7):867-73. PubMed ID: 4031664
[TBL] [Abstract][Full Text] [Related]
18. Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome.
Wanders RJ; Kos M; Roest B; Meijer AJ; Schrakamp G; Heymans HS; Tegelaers WH; van den Bosch H; Schutgens RB; Tager JM
Biochem Biophys Res Commun; 1984 Sep; 123(3):1054-61. PubMed ID: 6148939
[TBL] [Abstract][Full Text] [Related]
19. Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome. Case study and review of peroxisomal disorders in relation to skin disease.
Emami S; Rizzo WB; Hanley KP; Taylor JM; Goldyne ME; Williams ML
Arch Dermatol; 1992 Sep; 128(9):1213-22. PubMed ID: 1519936
[TBL] [Abstract][Full Text] [Related]
20. Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger.
Kase BF; Björkhem I; Hågå P; Pedersen JI
J Clin Invest; 1985 Feb; 75(2):427-35. PubMed ID: 3973012
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
