160 related articles for article (PubMed ID: 2842863)
1. Coding of two sphingolipid activator proteins (SAP-1 and SAP-2) by same genetic locus.
O'Brien JS; Kretz KA; Dewji N; Wenger DA; Esch F; Fluharty AL
Science; 1988 Aug; 241(4869):1098-101. PubMed ID: 2842863
[TBL] [Abstract][Full Text] [Related]
2. Nucleotide sequence of cloned cDNA for human sphingolipid activator protein 1 precursor.
Dewji NN; Wenger DA; O'Brien JS
Proc Natl Acad Sci U S A; 1987 Dec; 84(23):8652-6. PubMed ID: 2825202
[TBL] [Abstract][Full Text] [Related]
3. Molecular cloning of the sphingolipid activator protein-1 (SAP-1), the sulfatide sulfatase activator.
Dewji N; Wenger D; Fujibayashi S; Donoviel M; Esch F; Hill F; O'Brien JS
Biochem Biophys Res Commun; 1986 Jan; 134(2):989-94. PubMed ID: 2868718
[TBL] [Abstract][Full Text] [Related]
4. Human sphingolipid activator protein-1 and sphingolipid activator protein-2 are encoded by the same gene.
Reiner O; Dagan O; Horowitz M
J Mol Neurosci; 1989; 1(4):225-33. PubMed ID: 2484333
[TBL] [Abstract][Full Text] [Related]
5. Regional localization of the gene coding for sphingolipid activator protein SAP-1 on human chromosome 10.
Kao FT; Law ML; Hartz J; Jones C; Zhang XL; Dewji N; O'Brien JS; Wenger DA
Somat Cell Mol Genet; 1987 Nov; 13(6):685-8. PubMed ID: 3478817
[TBL] [Abstract][Full Text] [Related]
6. Biosynthesis and molecular cloning of sulfated glycoprotein 1 secreted by rat Sertoli cells: sequence similarity with the 70-kilodalton precursor to sulfatide/GM1 activator.
Collard MW; Sylvester SR; Tsuruta JK; Griswold MD
Biochemistry; 1988 Jun; 27(12):4557-64. PubMed ID: 3048385
[TBL] [Abstract][Full Text] [Related]
7. Molecular cloning of a human co-beta-glucosidase cDNA: evidence that four sphingolipid hydrolase activator proteins are encoded by single genes in humans and rats.
Rorman EG; Grabowski GA
Genomics; 1989 Oct; 5(3):486-92. PubMed ID: 2515150
[TBL] [Abstract][Full Text] [Related]
8. Expression of the three alternative forms of the sphingolipid activator protein precursor in baby hamster kidney cells and functional assays in a cell culture system.
Henseler M; Klein A; Glombitza GJ; Suziki K; Sandhoff K
J Biol Chem; 1996 Apr; 271(14):8416-23. PubMed ID: 8626540
[TBL] [Abstract][Full Text] [Related]
9. Detection of a point mutation in sphingolipid activator protein-1 mRNA in patients with a variant form of metachromatic leukodystrophy.
Rafi MA; Zhang XL; DeGala G; Wenger DA
Biochem Biophys Res Commun; 1990 Jan; 166(2):1017-23. PubMed ID: 2302219
[TBL] [Abstract][Full Text] [Related]
10. The primary structure of mouse saposin.
Tsuda M; Sakiyama T; Endo H; Kitagawa T
Biochem Biophys Res Commun; 1992 May; 184(3):1266-72. PubMed ID: 1590788
[TBL] [Abstract][Full Text] [Related]
11. Mouse testicular sulfated glycoprotein-1: sequence analysis of the common backbone structure of prosaposins.
Zhao Q; Bell AW; El-Alfy M; Morales CR
J Androl; 1998; 19(2):165-74. PubMed ID: 9570739
[TBL] [Abstract][Full Text] [Related]
12. Analysis of a splice-site mutation in the sap-precursor gene of a patient with metachromatic leukodystrophy.
Henseler M; Klein A; Reber M; Vanier MT; Landrieu P; Sandhoff K
Am J Hum Genet; 1996 Jan; 58(1):65-74. PubMed ID: 8554069
[TBL] [Abstract][Full Text] [Related]
13. Structure of the lysosomal sphingolipid activator protein 1 by homology with influenza virus neuraminidase.
Potier M
Biochem Biophys Res Commun; 1988 Aug; 155(1):32-7. PubMed ID: 3415686
[TBL] [Abstract][Full Text] [Related]
14. Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defect.
Kretz KA; Carson GS; Morimoto S; Kishimoto Y; Fluharty AL; O'Brien JS
Proc Natl Acad Sci U S A; 1990 Apr; 87(7):2541-4. PubMed ID: 2320574
[TBL] [Abstract][Full Text] [Related]
15. The precursor of sulfatide activator protein is processed to three different proteins.
Fürst W; Machleidt W; Sandhoff K
Biol Chem Hoppe Seyler; 1988 May; 369(5):317-28. PubMed ID: 3048308
[TBL] [Abstract][Full Text] [Related]
16. A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD).
Wrobe D; Henseler M; Huettler S; Pascual Pascual SI; Chabas A; Sandhoff K
J Inherit Metab Dis; 2000 Feb; 23(1):63-76. PubMed ID: 10682309
[TBL] [Abstract][Full Text] [Related]
17. Assignment of the gene for human sphingolipid activator protein-2 (SAP-2) to chromosome 10.
Fujibayashi S; Kao FT; Jones C; Morse H; Law M; Wenger DA
Am J Hum Genet; 1985 Jul; 37(4):741-8. PubMed ID: 9556662
[TBL] [Abstract][Full Text] [Related]
18. Structure of full-length cDNA coding for sulfatide activator, a Co-beta-glucosidase and two other homologous proteins: two alternate forms of the sulfatide activator.
Nakano T; Sandhoff K; Stümper J; Christomanou H; Suzuki K
J Biochem; 1989 Feb; 105(2):152-4. PubMed ID: 2498298
[TBL] [Abstract][Full Text] [Related]
19. Correction of sulfatide metabolism after transfer of prosaposin cDNA to cultured cells from a patient with SAP-1 deficiency.
Rafi MA; Amini S; Zhang XL; Wenger DA
Am J Hum Genet; 1992 Jun; 50(6):1252-8. PubMed ID: 1350885
[TBL] [Abstract][Full Text] [Related]
20. Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease.
Schnabel D; Schröder M; Sandhoff K
FEBS Lett; 1991 Jun; 284(1):57-9. PubMed ID: 2060627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]