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Journal Abstract Search

384 related items for PubMed ID: 9645704

  • 1. Characterization of the testis and epididymis in mouse models of human Tay Sachs and Sandhoff diseases and partial determination of accumulated gangliosides.
    Trasler J, Saberi F, Somani IH, Adamali HI, Huang JQ, Fortunato SR, Ritter G, Gu M, Aebersold R, Gravel RA, Hermo L.
    Endocrinology; 1998 Jul; 139(7):3280-8. PubMed ID: 9645704
    [Abstract] [Full Text] [Related]

  • 2. I. Abnormalities in cells of the testis, efferent ducts, and epididymis in juvenile and adult mice with beta-hexosaminidase A and B deficiency.
    Adamali HI, Somani IH, Huang JQ, Mahuran D, Gravel RA, Trasler JM, Hermo L.
    J Androl; 1999 Jul; 20(6):779-802. PubMed ID: 10591618
    [Abstract] [Full Text] [Related]

  • 3. II. Characterization and development of the regional- and cellular-specific abnormalities in the epididymis of mice with beta-hexosaminidase A deficiency.
    Adamali HI, Somani IH, Huang JQ, Gravel RA, Trasler JM, Hermo L.
    J Androl; 1999 Jul; 20(6):803-24. PubMed ID: 10591619
    [Abstract] [Full Text] [Related]

  • 4. 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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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Inefficiency in GM2 ganglioside elimination by human lysosomal beta-hexosaminidase beta-subunit gene transfer to fibroblastic cell line derived from Sandhoff disease model mice.
    Itakura T, Kuroki A, Ishibashi Y, Tsuji D, Kawashita E, Higashine Y, Sakuraba H, Yamanaka S, Itoh K.
    Biol Pharm Bull; 2006 Aug; 29(8):1564-9. PubMed ID: 16880605
    [Abstract] [Full Text] [Related]

  • 7. Metabolic correction in microglia derived from Sandhoff disease model mice.
    Tsuji D, Kuroki A, Ishibashi Y, Itakura T, Itoh K.
    J Neurochem; 2005 Sep; 94(6):1631-8. PubMed ID: 16092933
    [Abstract] [Full Text] [Related]

  • 8. Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases.
    Phaneuf D, Wakamatsu N, Huang JQ, Borowski A, Peterson AC, Fortunato SR, Ritter G, Igdoura SA, Morales CR, Benoit G, Akerman BR, Leclerc D, Hanai N, Marth JD, Trasler JM, Gravel RA.
    Hum Mol Genet; 1996 Jan; 5(1):1-14. PubMed ID: 8789434
    [Abstract] [Full Text] [Related]

  • 9. Promoters for the human beta-hexosaminidase genes, HEXA and HEXB.
    Norflus F, Yamanaka S, Proia RL.
    DNA Cell Biol; 1996 Feb; 15(2):89-97. PubMed ID: 8634145
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  • 11. [Molecular pathogenesis and therapeutic approach of GM2 gangliosidosis].
    Tsuji D.
    Yakugaku Zasshi; 2013 Feb; 133(2):269-74. PubMed ID: 23370522
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  • 14. GM2 gangliosidoses in Spain: analysis of the HEXA and HEXB genes in 34 Tay-Sachs and 14 Sandhoff patients.
    Gort L, de Olano N, Macías-Vidal J, Coll MA, Spanish GM2 Working Group.
    Gene; 2012 Sep 10; 506(1):25-30. PubMed ID: 22789865
    [Abstract] [Full Text] [Related]

  • 15. A novel gene editing system to treat both Tay-Sachs and Sandhoff diseases.
    Ou L, Przybilla MJ, Tăbăran AF, Overn P, O'Sullivan MG, Jiang X, Sidhu R, Kell PJ, Ory DS, Whitley CB.
    Gene Ther; 2020 May 10; 27(5):226-236. PubMed ID: 31896760
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  • 17. Improvement of motor and behavioral activity in Sandhoff mice transplanted with human CD34+ cells transduced with a HexA/HexB expressing lentiviral vector.
    Beegle J, Hendrix K, Maciel H, Nolta JA, Anderson JS.
    J Gene Med; 2020 Sep 10; 22(9):e3205. PubMed ID: 32335981
    [Abstract] [Full Text] [Related]

  • 18. In cellulo examination of a beta-alpha hybrid construct of beta-hexosaminidase A subunits, reported to interact with the GM2 activator protein and hydrolyze GM2 ganglioside.
    Sinici I, Yonekawa S, Tkachyova I, Gray SJ, Samulski RJ, Wakarchuk W, Mark BL, Mahuran DJ.
    PLoS One; 2013 Sep 10; 8(3):e57908. PubMed ID: 23483939
    [Abstract] [Full Text] [Related]

  • 19. [Recent advances in molecular genetics of GM2 gangliosidosis].
    Wakamatsu N.
    Nihon Rinsho; 1995 Dec 10; 53(12):2988-93. PubMed ID: 8577047
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