156 related articles for article (PubMed ID: 10553003)
1. Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities.
de Vet EC; Ijlst L; Oostheim W; Dekker C; Moser HW; van Den Bosch H; Wanders RJ
J Lipid Res; 1999 Nov; 40(11):1998-2003. PubMed ID: 10553003
[TBL] [Abstract][Full Text] [Related]
2. Alkyl-dihydroxyacetonephosphate synthase. Fate in peroxisome biogenesis disorders and identification of the point mutation underlying a single enzyme deficiency.
de Vet EC; Ijlst L; Oostheim W; Wanders RJ; van den Bosch H
J Biol Chem; 1998 Apr; 273(17):10296-301. PubMed ID: 9553082
[TBL] [Abstract][Full Text] [Related]
3. Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency).
Sztriha L; Al-Gazali LI; Wanders RJ; Ofman R; Nork M; Lestringant GG
Dev Med Child Neurol; 2000 Jul; 42(7):492-5. PubMed ID: 10972423
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Alkyl-dihydroxyacetonephosphate synthase.
de Vet EC; van den Bosch H
Cell Biochem Biophys; 2000; 32 Spring():117-21. PubMed ID: 11330037
[TBL] [Abstract][Full Text] [Related]
6. Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2.
Ofman R; Hettema EH; Hogenhout EM; Caruso U; Muijsers AO; Wanders RJ
Hum Mol Genet; 1998 May; 7(5):847-53. PubMed ID: 9536089
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiency.
Brookhyser KM; Lipson MH; Moser AB; Moser HW; Lachman RS; Rimoin DL
Prenat Diagn; 1999 Apr; 19(4):383-5. PubMed ID: 10327148
[TBL] [Abstract][Full Text] [Related]
8. Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata.
Kanzawa N; Shimozawa N; Wanders RJ; Ikeda K; Murakami Y; Waterham HR; Mukai S; Fujita M; Maeda Y; Taguchi R; Fujiki Y; Kinoshita T
J Lipid Res; 2012 Apr; 53(4):653-63. PubMed ID: 22253471
[TBL] [Abstract][Full Text] [Related]
9. Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findings.
Hebestreit H; Wanders RJ; Schutgens RB; Espeel M; Kerckaert I; Roels F; Schmausser B; Schrod L; Marx A
Eur J Pediatr; 1996 Dec; 155(12):1035-9. PubMed ID: 8956940
[TBL] [Abstract][Full Text] [Related]
10. [Dihydroxyacetonephosphate acyltransferase (DHAP-AT) deficiency and alkyl-DHAP synthase deficiency].
Shimozawa N
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):313-4. PubMed ID: 9645070
[No Abstract] [Full Text] [Related]
11. Mild reduction of plasmalogens causes rhizomelic chondrodysplasia punctata: functional characterization of a novel mutation.
Noguchi M; Honsho M; Abe Y; Toyama R; Niwa H; Sato Y; Ghaedi K; Rahmanifar A; Shafeghati Y; Fujiki Y
J Hum Genet; 2014 Jul; 59(7):387-92. PubMed ID: 24849933
[TBL] [Abstract][Full Text] [Related]
12. Peroxisomes and ether lipid biosynthesis in rat testis and epididymis.
Reisse S; Rothardt G; Völkl A; Beier K
Biol Reprod; 2001 Jun; 64(6):1689-94. PubMed ID: 11369596
[TBL] [Abstract][Full Text] [Related]
13. Stability of alkyl-dihydroxyacetonephosphate synthase in human control and peroxisomal disorder fibroblasts.
Biermann J; Gootjes J; Wanders RJ; van den Bosch H
IUBMB Life; 1999 Dec; 48(6):635-9. PubMed ID: 10683770
[TBL] [Abstract][Full Text] [Related]
14. Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.
Stevens VL; Raetz CR
J Biol Chem; 1990 Sep; 265(26):15653-8. PubMed ID: 1975590
[TBL] [Abstract][Full Text] [Related]
15. The native molecular size of alkyl-dihydroxyacetonephosphate synthase and dihydroxyacetonephosphate acyltransferase.
Biermann J; Schoonderwoerd K; Hom ML; Luthjens LH; Van den Bosch H
Biochim Biophys Acta; 1998 Jul; 1393(1):137-42. PubMed ID: 9714777
[TBL] [Abstract][Full Text] [Related]
16. The crucial step in ether phospholipid biosynthesis: structural basis of a noncanonical reaction associated with a peroxisomal disorder.
Razeto A; Mattiroli F; Carpanelli E; Aliverti A; Pandini V; Coda A; Mattevi A
Structure; 2007 Jun; 15(6):683-92. PubMed ID: 17562315
[TBL] [Abstract][Full Text] [Related]
17. Synthesis of plasmalogens in eye lens epithelial cells.
Thai TP; Rodemer C; Worsch J; Hunziker A; Gorgas K; Just WW
FEBS Lett; 1999 Aug; 456(2):263-8. PubMed ID: 10456321
[TBL] [Abstract][Full Text] [Related]
18. In vitro processing of the human alkyl-dihydroxyacetonephosphate synthase precursor.
Biermann J; van den Bosch H
Arch Biochem Biophys; 1999 Aug; 368(1):139-46. PubMed ID: 10415121
[TBL] [Abstract][Full Text] [Related]
19. Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation study.
Heikoop JC; Wanders RJ; Strijland A; Purvis R; Schutgens RB; Tager JM
Hum Genet; 1992 Jun; 89(4):439-44. PubMed ID: 1618493
[TBL] [Abstract][Full Text] [Related]
20. Alkyl-dihydroxyacetonephosphate synthase.
van den Bosch H; de Vet EC
Biochim Biophys Acta; 1997 Sep; 1348(1-2):35-44. PubMed ID: 9370314
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]