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Journal Abstract Search

308 related items for PubMed ID: 7959736

  • 1. 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]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Identification of an active acidic residue in the catalytic site of beta-hexosaminidase.
    Tse R, Vavougios G, Hou Y, Mahuran DJ.
    Biochemistry; 1996 Jun 11; 35(23):7599-607. PubMed ID: 8652542
    [Abstract] [Full Text] [Related]

  • 4. Structural organization, sequence, and expression of the mouse HEXA gene encoding the alpha subunit of hexosaminidase A.
    Wakamatsu N, Benoit G, Lamhonwah AM, Zhang ZX, Trasler JM, Triggs-Raine BL, Gravel RA.
    Genomics; 1994 Nov 01; 24(1):110-9. PubMed ID: 7896264
    [Abstract] [Full Text] [Related]

  • 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 01; 14(3):348-52. PubMed ID: 8896570
    [Abstract] [Full Text] [Related]

  • 6. Characterization of the human HEXB gene encoding lysosomal beta-hexosaminidase.
    Neote K, Bapat B, Dumbrille-Ross A, Troxel C, Schuster SM, Mahuran DJ, Gravel RA.
    Genomics; 1988 Nov 01; 3(4):279-86. PubMed ID: 2977375
    [Abstract] [Full Text] [Related]

  • 7. Sequencing, expression, and enzymatic characterization of beta-hexosaminidase in rabbit lacrimal gland and primary cultured acinar cells.
    Andersson SV, Sjögren EC, Magnusson C, Gierow JP.
    Glycobiology; 2005 Mar 01; 15(3):211-20. PubMed ID: 15483268
    [Abstract] [Full Text] [Related]

  • 8. Specific induction of macrophage inflammatory protein 1-alpha in glial cells of Sandhoff disease model mice associated with accumulation of N-acetylhexosaminyl glycoconjugates.
    Tsuji D, Kuroki A, Ishibashi Y, Itakura T, Kuwahara J, Yamanaka S, Itoh K.
    J Neurochem; 2005 Mar 01; 92(6):1497-507. PubMed ID: 15748167
    [Abstract] [Full Text] [Related]

  • 9. Metabolic correction in microglia derived from Sandhoff disease model mice.
    Tsuji D, Kuroki A, Ishibashi Y, Itakura T, Itoh K.
    J Neurochem; 2005 Sep 01; 94(6):1631-8. PubMed ID: 16092933
    [Abstract] [Full Text] [Related]

  • 10. Structure and distribution of an Alu-type deletion mutation in Sandhoff disease.
    Neote K, McInnes B, Mahuran DJ, Gravel RA.
    J Clin Invest; 1990 Nov 01; 86(5):1524-31. PubMed ID: 2147027
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 11(2):170-6. PubMed ID: 7550345
    [Abstract] [Full Text] [Related]

  • 12. Identification of functional domains within the alpha and beta subunits of beta-hexosaminidase A through the expression of alpha-beta fusion proteins.
    Tse R, Wu YJ, Vavougios G, Hou Y, Hinek A, Mahuran DJ.
    Biochemistry; 1996 Aug 20; 35(33):10894-903. PubMed ID: 8718882
    [Abstract] [Full Text] [Related]

  • 13. Common HEXB polymorphisms reduce serum HexA and HexB enzymatic activities, potentially masking Tay-Sachs disease carrier identification.
    Vallance H, Morris TJ, Coulter-Mackie M, Lim-Steele J, Kaback M.
    Mol Genet Metab; 2006 Feb 20; 87(2):122-7. PubMed ID: 16352452
    [Abstract] [Full Text] [Related]

  • 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]

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  • 18. Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis.
    Tanaka K, Fisher SE, Craig IW.
    Genomics; 1999 Jun 15; 58(3):281-92. PubMed ID: 10373326
    [Abstract] [Full Text] [Related]

  • 19. Cloning and functional characterization of the chicken c-ros promoter.
    Chen J, Tong J, Tanaka-Sukegawa I, Wang LH.
    Cell Growth Differ; 1995 Dec 15; 6(12):1523-30. PubMed ID: 9019157
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