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PUBMED FOR HANDHELDS

Journal Abstract Search


97 related items for PubMed ID: 2936060

  • 1. Tay-Sachs disease with conspicuous cranial computerized tomographic appearances.
    Watanabe K, Mukawa A, Muto K, Nishikawa J, Takahashi S.
    Acta Pathol Jpn; 1985 Nov; 35(6):1521-32. PubMed ID: 2936060
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  • 2. Naturally occurring GM2 gangliosidosis in two Muntjak deer with pathological and biochemical features of human classical Tay-Sachs disease (type B GM2 gangliosidosis).
    Fox J, Li YT, Dawson G, Alleman A, Johnsrude J, Schumacher J, Homer B.
    Acta Neuropathol; 1999 Jan; 97(1):57-62. PubMed ID: 9930895
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  • 4. Composition of gangliosides and neutral glycosphingolipids of brain in classical Tay-Sachs and Sandhoff disease: more lyso-GM2 in Sandhoff disease?
    Rosengren B, Månsson JE, Svennerholm L.
    J Neurochem; 1987 Sep; 49(3):834-40. PubMed ID: 3612128
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  • 6. Autophagic flux is impaired in the brain tissue of Tay-Sachs disease mouse model.
    Sengul T, Can M, Ateş N, Seyrantepe V.
    PLoS One; 2023 Sep; 18(3):e0280650. PubMed ID: 36928510
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  • 7. Apoptotic cell death in mouse models of GM2 gangliosidosis and observations on human Tay-Sachs and Sandhoff diseases.
    Huang JQ, Trasler JM, Igdoura S, Michaud J, Hanal N, Gravel RA.
    Hum Mol Genet; 1997 Oct; 6(11):1879-85. PubMed ID: 9302266
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  • 8. Tay-Sachs disease brain cells in culture: mobilization of stored GM2 after concanavalin A-mediated uptake of hexosaminidase A.
    Hoffman LM, Brooks SE, Amsterdam D, Oropello J, Schneck L.
    J Neurosci Res; 1980 Oct; 5(5):413-7. PubMed ID: 7441795
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  • 9. MR findings in Tay-Sachs disease.
    Mugikura S, Takahashi S, Higano S, Kurihara N, Kon K, Sakamoto K.
    J Comput Assist Tomogr; 1996 Oct; 20(4):551-5. PubMed ID: 8708054
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  • 10. Assay of the GM2-ganglioside cleaving hexosaminidase activity of skin fibroblasts for GM2-gangliosidoses.
    Harzer K.
    Clin Chim Acta; 1983 Nov 30; 135(1):89-93. PubMed ID: 6228344
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  • 11. Restoration of the GM2 ganglioside metabolism in bone marrow-derived stromal cells from Tay-Sachs disease animal model.
    Martino S, Cavalieri C, Emiliani C, Dolcetta D, Cusella De Angelis MG, Chigorno V, Severini GM, Sandhoff K, Bordignon C, Sonnino S, Orlacchio A.
    Neurochem Res; 2002 Aug 30; 27(7-8):793-800. PubMed ID: 12374215
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  • 12. Retinal amacrine cell involvement in Tay-Sachs disease.
    Nagashima K, Kikuchi F, Suzuki Y, Abe T.
    Acta Neuropathol; 1981 Aug 30; 53(4):333-6. PubMed ID: 7223376
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  • 13. Two siblings, including a fetus, with Tay-Sachs disease.
    Yamada E, Matsumoto M, Hazama F, Momoi T, Sudo M.
    Acta Pathol Jpn; 1981 Nov 30; 31(6):1053-61. PubMed ID: 7315310
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  • 14. Ganglioside GM2 N-acetyl-beta-D-galactosaminidase and asialo GM2 (GA2) N-acetyl-beta-D-galactosaminidase; studies in human skin fibroblasts.
    O'Brien JS, Norden GW, Miller AL, Frost RG, Kelly TE.
    Clin Genet; 1977 Mar 30; 11(3):171-83. PubMed ID: 13950
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  • 15. Differentiation of two variants of type-AB GM2-gangliosidosis using chromogenic substrates.
    Li YT, Hirabayashi Y, Li SC.
    Am J Hum Genet; 1983 May 30; 35(3):520-2. PubMed ID: 6222647
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  • 16. Therapeutic evaluation of GM2 gangliosidoses by ELISA using anti-GM2 ganglioside antibodies.
    Tsuji D, Higashine Y, Matsuoka K, Sakuraba H, Itoh K.
    Clin Chim Acta; 2007 Mar 30; 378(1-2):38-41. PubMed ID: 17196574
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  • 17. Gangliosides in SV-40-transformed cells derived from Tay-Sachs disease fetal brain.
    Hoffman LM, Brooks SE, Stein MR, Adachi M, Schneck L.
    Metab Brain Dis; 1989 Jun 30; 4(2):87-93. PubMed ID: 2547146
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  • 20. The mutation mechanism causing juvenile-onset Tay-Sachs disease among Lebanese.
    Hechtman P, Boulay B, Bayleran J, Andermann E.
    Clin Genet; 1989 May 30; 35(5):364-75. PubMed ID: 2527097
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