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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

115 related items for PubMed ID: 2512447

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  • 13. 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; 5(5):413-7. PubMed ID: 7441795
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  • 16. Evidence for direct binding of intracellularly distributed ganglioside GM2 to isolated vimentin intermediate filaments in normal and Tay-Sachs disease human fibroblasts.
    Kotani M, Hosoya H, Kubo H, Itoh K, Sakuraba H, Kusubata M, Inagaki M, Yazaki S, Suzuki Y, Tai T.
    Cell Struct Funct; 1994 Apr; 19(2):81-7. PubMed ID: 7923401
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  • 17. Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism.
    Sango K, Yamanaka S, Hoffmann A, Okuda Y, Grinberg A, Westphal H, McDonald MP, Crawley JN, Sandhoff K, Suzuki K, Proia RL.
    Nat Genet; 1995 Oct; 11(2):170-6. PubMed ID: 7550345
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  • 18. Adult-onset GM2 gangliosidosis. Seizures, dementia, and normal pressure hydrocephalus associated with glycolipid storage in the brain and arachnoid granulation.
    O'Neill B, Butler AB, Young E, Falk PM, Bass NH.
    Neurology; 1978 Nov; 28(11):1117-23. PubMed ID: 568730
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  • 19. Specific expression of unusual GM2 ganglioside with Hanganutziu-Deicher antigen activity on human colon cancers.
    Hirabayashi Y, Kasakura H, Matsumoto M, Higashi H, Kato S, Kasai N, Naiki M.
    Jpn J Cancer Res; 1987 Mar; 78(3):251-60. PubMed ID: 3106281
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  • 20. [Biosynthesis and biodegradation of GM2 ganglioside].
    Hirabayashi Y, Kasakura H, Matsumoto M.
    Tanpakushitsu Kakusan Koso; 1984 Sep; 29(9):708-22. PubMed ID: 6240072
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