These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 49545)

  • 21. Alpha-L-iduronidase in human semen.
    Herd JK; Hayhome B
    Lancet; 1976 Jul; 2(7978):206. PubMed ID: 73832
    [No Abstract]   [Full Text] [Related]  

  • 22. Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.
    Hall CW; Neufeld EF
    Arch Biochem Biophys; 1973 Oct; 158(2):817-21. PubMed ID: 4205743
    [No Abstract]   [Full Text] [Related]  

  • 23. A radioactive substrate and assay for alpha-L-iduronidase.
    Di Natale P; Leder IG; Neufeld EF
    Clin Chim Acta; 1977 Jun; 77(3):211-8. PubMed ID: 406106
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hurler's syndromes without alpha-L-iduronidase deficiency.
    Orii T; Sukegawa K; Minami R; Nakao T
    Pediatrics; 1977 Nov; 60(5):764-5. PubMed ID: 411107
    [No Abstract]   [Full Text] [Related]  

  • 25. alpha-L-iduronidase deficiency and possible Hurler-Scheie genetic compound. Clinical, pathologic, and biochemical findings.
    Winters PR; Harrod MJ; Molenich-Heetred SA; Kirkpatrick J; Rosenberg RN
    Neurology; 1976 Nov; 26(11):1003-7. PubMed ID: 824566
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Neurochemical characterization of canine alpha-L-iduronidase deficiency disease (model of human mucopolysaccharidosis I).
    Constantopoulos G; Shull RM; Hastings N; Neufeld EF
    J Neurochem; 1985 Oct; 45(4):1213-7. PubMed ID: 3928817
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie case.
    Tondeur M; Vamos-Hurwitz E; Cantz M; Cremer N; Libert J; Pardou A
    Acta Paediatr Belg; 1976; 29(2):109-15. PubMed ID: 826105
    [No Abstract]   [Full Text] [Related]  

  • 29. Hurler-Scheie phenotype associated with consanguinity.
    Davies DL; Dutton GN; Farquharson J; Logan RW; Tolmie JL
    J Inherit Metab Dis; 1989; 12 Suppl 2():365-8. PubMed ID: 2512446
    [No Abstract]   [Full Text] [Related]  

  • 30. [Psychotic symptoms during the evolution of dementia in muco- polysaccharidosis of Hurler-Scheie phenotype].
    Dugas M; Le Heuzey MF; Mayer M
    Arch Fr Pediatr; 1985 May; 42(5):373-5. PubMed ID: 3935090
    [TBL] [Abstract][Full Text] [Related]  

  • 31. L-iduronidase in cultured human fibroblasts and liver.
    Matalon R; Cifonelli JA; Dorfman A
    Biochem Biophys Res Commun; 1971 Jan; 42(2):340-5. PubMed ID: 4993544
    [No Abstract]   [Full Text] [Related]  

  • 32. A method for alpha-L-iduronidase assay.
    Singh J; Niebes P; Di Ferrante N
    FEBS Lett; 1974 Sep; 45(1):248-51. PubMed ID: 4212889
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. Biochemical and histopathological studies on patients with mucopolysaccharidoses, two of whom had been treated by fibroblast transplantation.
    Crow J; Gibbs DA; Cozens W; Spellacy E; Watts RW
    J Clin Pathol; 1983 Apr; 36(4):415-30. PubMed ID: 6403596
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Mucopolisaccharidoses, Enzyme deficiencies (author's transl)].
    Gniot-Szulzycka J
    Postepy Biochem; 1976; 22(1):17-26. PubMed ID: 814540
    [No Abstract]   [Full Text] [Related]  

  • 36. Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients.
    O'Brien JS
    Proc Natl Acad Sci U S A; 1972 Jul; 69(7):1720-2. PubMed ID: 4261742
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fucosidosis: deficiency of alpha-L-fucosidase in cultured skin fibroblasts.
    Zielke K; Veath ML; O'Brien JS
    J Exp Med; 1972 Jul; 136(1):197-9. PubMed ID: 4624449
    [No Abstract]   [Full Text] [Related]  

  • 38. Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes.
    Mueller OT; Shows TB; Opitz JM
    Am J Med Genet; 1984 Jul; 18(3):547-56. PubMed ID: 6433708
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Correction of mucopolysaccharidosis type I fibroblasts by retroviral-mediated transfer of the human alpha-L-iduronidase gene.
    Anson DS; Bielicki J; Hopwood JJ
    Hum Gene Ther; 1992 Aug; 3(4):371-9. PubMed ID: 1525210
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The William Allan Memorial Award address: cell mixing and its sequelae.
    Neufeld EF
    Am J Hum Genet; 1983 Nov; 35(6):1081-5. PubMed ID: 6417999
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.