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Journal Abstract Search

577 related items for PubMed ID: 7550345

  • 1.
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  • 2. 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
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  • 3. 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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  • 5. Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis.
    Sango K, McDonald MP, Crawley JN, Mack ML, Tifft CJ, Skop E, Starr CM, Hoffmann A, Sandhoff K, Suzuki K, Proia RL.
    Nat Genet; 1996 Nov; 14(3):348-52. PubMed ID: 8896570
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  • 6. Characterization of inducible models of Tay-Sachs and related disease.
    Sargeant TJ, Drage DJ, Wang S, Apostolakis AA, Cox TM, Cachón-González MB.
    PLoS Genet; 2012 Sep; 8(9):e1002943. PubMed ID: 23028353
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  • 8. [Recent advances in molecular genetics of GM2 gangliosidosis].
    Wakamatsu N.
    Nihon Rinsho; 1995 Dec; 53(12):2988-93. PubMed ID: 8577047
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  • 11. Structure and expression of the mouse beta-hexosaminidase genes, Hexa and Hexb.
    Yamanaka S, Johnson ON, Norflus F, Boles DJ, Proia RL.
    Genomics; 1994 Jun; 21(3):588-96. PubMed ID: 7959736
    [Abstract] [Full Text] [Related]

  • 12. 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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  • 15. 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]

  • 16. [Molecular pathogenesis and therapeutic approach of GM2 gangliosidosis].
    Tsuji D.
    Yakugaku Zasshi; 2013 Sep 10; 133(2):269-74. PubMed ID: 23370522
    [Abstract] [Full Text] [Related]

  • 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. Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease.
    Yamanaka S, Johnson MD, Grinberg A, Westphal H, Crawley JN, Taniike M, Suzuki K, Proia RL.
    Proc Natl Acad Sci U S A; 1994 Oct 11; 91(21):9975-9. PubMed ID: 7937929
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  • 19. Mouse model of GM2 activator deficiency manifests cerebellar pathology and motor impairment.
    Liu Y, Hoffmann A, Grinberg A, Westphal H, McDonald MP, Miller KM, Crawley JN, Sandhoff K, Suzuki K, Proia RL.
    Proc Natl Acad Sci U S A; 1997 Jul 22; 94(15):8138-43. PubMed ID: 9223328
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  • 20. The biochemistry of HEXA and HEXB gene mutations causing GM2 gangliosidosis.
    Mahuran DJ.
    Biochim Biophys Acta; 1991 Feb 22; 1096(2):87-94. PubMed ID: 1825792
    [No Abstract] [Full Text] [Related]

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