127 related articles for article (PubMed ID: 6781103)
1. Fluorometric measurement of alpha-L-iduronidase activity using 4-methylumbelliferyl-alpha-L-iduronide.
Minami R; Watanabe Y; Kudoh T; Oyanagi K; Nakao T
Tohoku J Exp Med; 1980 Apr; 130(4):381-4. PubMed ID: 6781103
[TBL] [Abstract][Full Text] [Related]
2. A fluorometric assay using 4-methylumbelliferyl alpha-L-iduronide for the estimation of alpha-L-iduronidase activity and the detection of Hurler and Scheie syndromes.
Hopwood JJ; Muller V; Smithson A; Baggett N
Clin Chim Acta; 1979 Mar; 92(2):257-65. PubMed ID: 114339
[TBL] [Abstract][Full Text] [Related]
3. Comparison of the substrate 4-methylumbelliferyl-alpha-l-iduronide with phenyl-alpha-L-iduronide for the diagnosis of Hurler's disease in cultured cells.
Butterworth J; Broadhead DM
J Inherit Metab Dis; 1980; 2(3):71-4. PubMed ID: 6796763
[TBL] [Abstract][Full Text] [Related]
4. Fluorometric measurement of urinary alpha-L-iduronidase activity.
Isemura M; Kosaka H; Ikenaka T; Kido R; Yoshimura T
J Biochem; 1978 Sep; 84(3):627-32. PubMed ID: 102641
[TBL] [Abstract][Full Text] [Related]
5. Use of 4-trifluoromethylumbelliferyl-alpha-L-iduronide as a new substrate for detection of alpha-L-iduronidase deficiency in human tissues and for rapid prenatal diagnosis of Hurler disease.
Tsvetkova IV; Karpova EA; Voznyi YV; Zolotukhina TV; Biryukov VV; Semyachkina AN
J Inherit Metab Dis; 1991; 14(2):134-9. PubMed ID: 1909400
[TBL] [Abstract][Full Text] [Related]
6. Characteristics of leukocyte and plasma methylumbelliferyl-alpha-L-iduronide iduronidase.
Den Tandt WR; Scharpe S
Biochem Med Metab Biol; 1989 Feb; 41(1):18-24. PubMed ID: 2713148
[TBL] [Abstract][Full Text] [Related]
7. [Use of 4-methylumbelliferryl-alpha-L-iduronide and 4-trifluoromethylumbelliferryl-alpha-L-iduronide for detecting alpha-L-iduronidase deficiencies in human tissue and for rapid prenatal diagnosis of Hurler disease].
Tsvetkova IV; Karpova EA; Voznyĭ IaV; Zolotukhina TV; Biriukov VB; Semiachkina AN
Vopr Med Khim; 1991; 37(1):74-7. PubMed ID: 1907053
[TBL] [Abstract][Full Text] [Related]
8. [Fluorometric determination of alpha-L-iduronidase activity in leukocytes and blood plasma in Hurler's disease].
Gusina NB; Tsukerman GL
Lab Delo; 1988; (7):46-9. PubMed ID: 2460681
[No Abstract] [Full Text] [Related]
9. Diagnostic enzymology of alpha-L-iduronidase with special reference to a sulphated disaccharide derived from heparin.
Hopwood JJ; Muller V
Clin Sci (Lond); 1982 Feb; 62(2):193-201. PubMed ID: 6895615
[TBL] [Abstract][Full Text] [Related]
10. Fluorometric assay of alpha-L-iduronidase in serum for detection of affected and carrier animals in a canine model of mucopolysaccharidosis I.
Shull RM; Hastings NE
Clin Chem; 1985 Jun; 31(6):826-7. PubMed ID: 3922649
[TBL] [Abstract][Full Text] [Related]
11. Leucocyte values of alpha-L-iduronidase activity in mucopolysaccharidosis I.
Kelly TE; Taylor HA
J Med Genet; 1976 Apr; 13(2):149-51. PubMed ID: 819651
[TBL] [Abstract][Full Text] [Related]
12. The use of alpha-L-iduronidase activity determinations in leucocytes for the detection of Hurler and Scheie syndromes.
Liem KO; Hooghwinkel GJ
Clin Chim Acta; 1975 Apr; 60(2):259-62. PubMed ID: 805007
[No Abstract] [Full Text] [Related]
13. alpha-L-iduronidase activity in leukocytes: diagnosis of homozygotes and heterozygotes of the Hurler syndrome.
Omura K; Higami S; Tada K
Eur J Pediatr; 1976 May; 122(2):103-5. PubMed ID: 817912
[TBL] [Abstract][Full Text] [Related]
14. Detection of the carrier state of Hurler's syndrome by assay of alpha-L-iduronidase in leukocytes.
Dulaney JT; Milunsky A; Moser HW
Clin Chim Acta; 1976 Jun; 69(2):305-10. PubMed ID: 819189
[TBL] [Abstract][Full Text] [Related]
15. A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease).
Voznyi YV; Keulemans JL; van Diggelen OP
J Inherit Metab Dis; 2001 Nov; 24(6):675-80. PubMed ID: 11768586
[TBL] [Abstract][Full Text] [Related]
16. Standardization of α-L-iduronidase enzyme assay with Michaelis-Menten kinetics.
Ou L; Herzog TL; Wilmot CM; Whitley CB
Mol Genet Metab; 2014 Feb; 111(2):113-5. PubMed ID: 24332804
[TBL] [Abstract][Full Text] [Related]
17. Absence of alpha-L-iduronidase activity in various tissues from two sibs affected with presumably the Hurler-Scheie compound syndrome.
Thompson JN; Finley SC; Lorincz AE; Finley WH
Birth Defects Orig Artic Ser; 1975; 11(6):341-6. PubMed ID: 811284
[No Abstract] [Full Text] [Related]
18. alpha-L-Iduronidase activity in established lymphoblastoid cells from patients with Hurler and Scheie syndromes transformed by Epstein-Barr virus.
Minami R; Suzuki M; Kudoh T; Sato S; Oyanagi K
Tohoku J Exp Med; 1977 Aug; 122(4):393-6. PubMed ID: 199964
[TBL] [Abstract][Full Text] [Related]
19. Properties of alpha-L-iduronidase in cultured skin fibroblasts from alpha-L-iduronidase-deficient patients.
Fujibayashi S; Minami R; Ishikawa Y; Wagatsuma K; Nakao T; Tsugawa S
Hum Genet; 1984; 65(3):268-72. PubMed ID: 6421718
[TBL] [Abstract][Full Text] [Related]
20. Microtest for determination of alpha-L-iduronidase in plasma and leucocytes and its potential for diagnosing alpha-L-iduronidase deficiency.
Den Tandt WR; Scharpe S; Giesberts M; Poorthuis BJ
Lancet; 1984 Apr; 1(8380):794. PubMed ID: 6143109
[No Abstract] [Full Text] [Related]
[Next] [New Search]