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Journal Abstract Search

169 related items for PubMed ID: 6767344

  • 41. Prenatal diagnosis of GM1-gangliosidosis: biochemical manifestations in fetal tissues.
    Kudoh T, Kikuchi K, Nakamura F, Yokoyama S, Karube K, Tsugawa S, Minami R, Nakao T.
    Hum Genet; 1978 Nov 16; 44(3):287-93. PubMed ID: 103801
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  • 42. A comparison of the properties and bile salt specificities of galactosylceramide and lactosyl ceramide beta-galactosidase activities in human leucocytes and fibroblasts.
    Poulos A, Beckman K.
    Clin Chim Acta; 1980 Feb 28; 101(2-3):277-85. PubMed ID: 6766828
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  • 43. GM1-Gangliosidosis: a molecular abnormality of acid beta-galactosidase in fibroblasts.
    Furuya T, Suzuki Y.
    J Inherit Metab Dis; 1984 Feb 28; 7(3):145-6. PubMed ID: 6438402
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  • 45. Generation and characterization of recombinant feline beta-galactosidase for preclinical enzyme replacement therapy studies in GM1 gangliosidosis.
    Samoylova TI, Martin DR, Morrison NE, Hwang M, Cochran AM, Samoylov AM, Baker HJ, Cox NR.
    Metab Brain Dis; 2008 Jun 28; 23(2):161-73. PubMed ID: 18421424
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  • 49. The role of lysosomal sialidase and beta-galactosidase in processing the complex carbohydrate chains on lysosomal enzymes and possibly other glycoproteins.
    Swallow DM, West LF, Van Elsen A.
    Ann Hum Genet; 1984 Jul 28; 48(3):215-21. PubMed ID: 6431895
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  • 52. GM1-gangliosidosis. Defective recognition site on beta-galactosidase precursor.
    Hoogeveen AT, Reuser AJ, Kroos M, Galjaard H.
    J Biol Chem; 1986 May 05; 261(13):5702-4. PubMed ID: 3084469
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  • 56. GM1-ganglioside accumulation and beta-galactosidase deficiency in a case of GM1-gangliosidosis (Landing disease).
    Dacremont G, Kint JA.
    Clin Chim Acta; 1968 Sep 05; 21(3):421-5. PubMed ID: 5725200
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