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Journal Abstract Search

158 related items for PubMed ID: 4269276

  • 1. N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycans.
    Thompson JN, Stoolmiller AC, Matalon R, Dorfman A.
    Science; 1973 Aug 31; 181(4102):866-7. PubMed ID: 4269276
    [Abstract] [Full Text] [Related]

  • 2. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.
    Hickman S, Shapiro LJ, Neufeld EF.
    Biochem Biophys Res Commun; 1974 Mar 15; 57(1):55-61. PubMed ID: 4364008
    [No Abstract] [Full Text] [Related]

  • 3. -Galactosidase, N-acetyl- -glucosaminidase, and -glucuronidase activity in fibroblast cultures from patients with mucopolysaccharide storage disease.
    Lagunoff D, Pritzl P, Scott CR.
    Biochem Med; 1973 Jun 15; 7(3):343-9. PubMed ID: 4268484
    [No Abstract] [Full Text] [Related]

  • 4. Acid glycosidases in mucopolysaccharidoses fibroblasts.
    Fluharty AL, Porter MT, Lassila EL, Trammell J, Carrel RE, Kihara H.
    Biochem Med; 1970 Sep 15; 4(2):110-20. PubMed ID: 4257448
    [No Abstract] [Full Text] [Related]

  • 5. 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 15; 69(7):1720-2. PubMed ID: 4261742
    [Abstract] [Full Text] [Related]

  • 6. Enzyme defects of glycosaminoglycan degradation in the mucopolysaccharidoses.
    Benson PF.
    Dev Med Child Neurol; 1974 Aug 15; 16(4):534-9. PubMed ID: 4277471
    [No Abstract] [Full Text] [Related]

  • 7. [Recent data on mucopolysaccharidoses].
    Spranger J.
    Monatsschr Kinderheilkd (1902); 1973 May 15; 121(5):181-3. PubMed ID: 4268292
    [No Abstract] [Full Text] [Related]

  • 8. Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
    Kint JA, Dacremont G, Carton D, Orye E, Hooft C.
    Science; 1973 Jul 27; 181(4097):352-4. PubMed ID: 4268963
    [Abstract] [Full Text] [Related]

  • 9. Sandhoff disease: impaired catabolism of sulfated glycosaminoglycans in cultured fibroblasts.
    Cantz M, O'Brien JF, Kresse H.
    Birth Defects Orig Artic Ser; 1975 Jul 27; 11(6):261-7. PubMed ID: 127630
    [Abstract] [Full Text] [Related]

  • 10. Hexosaminidase C in Tay-Sachs and Sandhoff disease.
    Penton E, Poenaru L, Dreyfus JC.
    Biochim Biophys Acta; 1975 May 23; 391(1):162-9. PubMed ID: 237554
    [Abstract] [Full Text] [Related]

  • 11. Sanfilippo disease type B: enzyme replacement and metabolic correction in cultured fibroblasts.
    O'Brien JS, Miller AL, Loverde AW, Veath ML.
    Science; 1973 Aug 24; 181(4101):753-5. PubMed ID: 4269326
    [Abstract] [Full Text] [Related]

  • 12. Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
    Ockerman PA, Hultberg B, Eriksson O.
    Clin Chim Acta; 1969 Jul 24; 25(1):97-102. PubMed ID: 4240390
    [No Abstract] [Full Text] [Related]

  • 13. Lysosomal enzymes in cultured cells from mucopolysaccharidoses.
    Keyser AJ, Priest RE, Priest JH.
    Lab Invest; 1972 Dec 24; 27(6):600-5. PubMed ID: 4264608
    [No Abstract] [Full Text] [Related]

  • 14. Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome.
    Matalon R, Arbogast B, Dorfman A.
    Biochem Biophys Res Commun; 1974 Dec 23; 61(4):1450-7. PubMed ID: 4218107
    [No Abstract] [Full Text] [Related]

  • 15. Degradation of keratan sulfate by beta-N-acetylhexosaminidases in GM2-gangliosidosis.
    Yutaka T, Okada S, Kato T, Yabuuhi H.
    Clin Genet; 1982 Mar 23; 21(3):196-202. PubMed ID: 6212169
    [Abstract] [Full Text] [Related]

  • 16. Leroy's l-cell disease: markedly increased activity of plasma acid hydrolases.
    Den Tandt WR, Lassila E, Philippart M.
    J Lab Clin Med; 1974 Mar 23; 83(3):403-8. PubMed ID: 4359899
    [No Abstract] [Full Text] [Related]

  • 17. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts.
    Fluharty AL, Stevens RL, Sanders DL, Kihara H.
    Biochem Biophys Res Commun; 1974 Jul 24; 59(2):455-61. PubMed ID: 4277366
    [No Abstract] [Full Text] [Related]

  • 18. Deficiency of lysosomal enzymes in storage diseases.
    Den Tandt WR, Giesberts MA.
    Biochem Med; 1973 Jun 24; 7(3):441-51. PubMed ID: 4268487
    [No Abstract] [Full Text] [Related]

  • 19. Cleavage of the (1 goes to 3)-2-acetamido-2-deoxy-beta-D-glucopyranosyl linkage present in keratan sulfate. The A and B isoenzymes of human liver hexosaminidase (EC 3.2.1.30).
    Toma S, Coppa G, Donnelly PV, Ricci R, Di Ferrante N, Srivastava SK.
    Carbohydr Res; 1981 Oct 16; 96(2):271-90. PubMed ID: 6458358
    [Abstract] [Full Text] [Related]

  • 20. Abnormal arylsulphatase activities of fibroblasts cultured from patients with mucopolysaccharidosis and cystinosis.
    Furusho K, Vetrella M, Latta E.
    Z Kinderheilkd; 1971 Oct 16; 110(4):324-31. PubMed ID: 4254863
    [No Abstract] [Full Text] [Related]

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