111 related articles for article (PubMed ID: 2875937)
1. Attenuated activities and structural alterations of arylsulfatase A in tissues from subjects with pseudo arylsulfatase A deficiency.
Kihara H; Meek WE; Fluharty AL
Hum Genet; 1986 Sep; 74(1):59-62. PubMed ID: 2875937
[TBL] [Abstract][Full Text] [Related]
2. Pseudo arylsulfatase A deficiency: evidence for a structurally altered enzyme.
Fluharty AL; Meek WE; Kihara H
Biochem Biophys Res Commun; 1983 Apr; 112(1):191-7. PubMed ID: 6132605
[TBL] [Abstract][Full Text] [Related]
3. Pseudo arylsulfatase A deficiency. Biosynthesis of an abnormal arylsulfatase A.
Ameen M; Chang PL
FEBS Lett; 1987 Jul; 219(1):130-4. PubMed ID: 2885227
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase A activity.
Bach G; Neufeld EF
Biochem Biophys Res Commun; 1983 Apr; 112(1):198-205. PubMed ID: 6132606
[TBL] [Abstract][Full Text] [Related]
5. Deficient glycosylation of arylsulfatase A in pseudo arylsulfatase-A deficiency.
Ameen M; Lazzarino DA; Kelly BM; Gabel CA; Chang PL
Mol Cell Biochem; 1990 Feb; 92(2):117-27. PubMed ID: 1968615
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and stability of arylsulfatase A and B in fibroblasts from multiple sulfatase deficiency.
Steckel F; Hasilik A; von Figura K
Eur J Biochem; 1985 Aug; 151(1):141-5. PubMed ID: 2863138
[TBL] [Abstract][Full Text] [Related]
7. Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.
Chang PL; Davidson RG
Proc Natl Acad Sci U S A; 1980 Oct; 77(10):6166-70. PubMed ID: 6108562
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.
Kihara H; Ho CK; Fluharty AL; Tsay KK; Hartlage PL
Pediatr Res; 1980 Mar; 14(3):224-7. PubMed ID: 6104322
[TBL] [Abstract][Full Text] [Related]
9. [Arylsulfatase A--physico-chemical properties and the use of enzyme radioimmunoassay in medical diagnosis].
Laidler PM
Folia Med Cracov; 1991; 32(3-4):149-68. PubMed ID: 1688265
[TBL] [Abstract][Full Text] [Related]
10. Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts.
Kihara H; Tsay KK; Fluharty AL
Hum Genet; 1984; 66(4):300-1. PubMed ID: 6144627
[TBL] [Abstract][Full Text] [Related]
11. Synthesis and processing of arylsulfatase A in human skin fibroblasts.
Waheed A; Hasilik A; von Figura K
Hoppe Seylers Z Physiol Chem; 1982 Apr; 363(4):425-30. PubMed ID: 6122636
[TBL] [Abstract][Full Text] [Related]
12. Multiple sulfatase deficiency: degradation of arylsulfatase A and B after endocytosis in fibroblasts.
Steckel F; Hasilik A; von Figura K
Eur J Biochem; 1985 Aug; 151(1):147-52. PubMed ID: 2863139
[TBL] [Abstract][Full Text] [Related]
13. Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiency.
Waheed A; Hasilik A; von Figura K
Eur J Biochem; 1982 Apr; 123(2):317-21. PubMed ID: 6122572
[TBL] [Abstract][Full Text] [Related]
14. The activity of arylsulfatase A and B on tyrosine O-sulfates.
Fluharty AL; Stevens RL; Goldstein EB; Kihara H
Biochim Biophys Acta; 1979 Feb; 566(2):321-6. PubMed ID: 33715
[TBL] [Abstract][Full Text] [Related]
15. Diagnosis of arylsulfatase A deficiency.
Li ZG; Waye JS; Chang PL
Am J Med Genet; 1992 Aug; 43(6):976-82. PubMed ID: 1357970
[TBL] [Abstract][Full Text] [Related]
16. Microheterogeneity of arylsulfatase A from human tissues.
Stevens RL; Fluharty AL; Killgrove AR; Kihara H
Biochim Biophys Acta; 1976 Oct; 445(3):661-71. PubMed ID: 9992
[TBL] [Abstract][Full Text] [Related]
17. Targeting of phosphomannosyl-deficient arylsulfatase A to lysosomes of I-cell fibroblasts.
Waheed A; Van Etten RL; Koob R; Drenckhahn D
Eur J Cell Biol; 1988 Feb; 45(2):262-7. PubMed ID: 2896590
[TBL] [Abstract][Full Text] [Related]
18. Atypical metachromatic leukodystrophy? Problems with the biochemical diagnosis.
Tønnesen T; Vrang C; Wiesmann UN; Christomanou H; Lou HO
Hum Genet; 1984; 67(2):170-3. PubMed ID: 6146562
[TBL] [Abstract][Full Text] [Related]
19. A variant form of metachromatic leukodystrophy without arylsulfatase deficiency.
Hahn AF; Gordon BA; Hinton GG; Gilbert JJ
Ann Neurol; 1982 Jul; 12(1):33-6. PubMed ID: 6126151
[TBL] [Abstract][Full Text] [Related]
20. Phosphorylation and sulfation of arylsulfatase A accompanies biosynthesis of the enzyme in normal and carcinoma cell lines.
Waheed A; van Etten RL
Biochim Biophys Acta; 1985 Oct; 847(1):53-61. PubMed ID: 2864959
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
