BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

382 related articles for article (PubMed ID: 8661004)

  • 1. Cloning of the canine GALC cDNA and identification of the mutation causing globoid cell leukodystrophy in West Highland White and Cairn terriers.
    Victoria T; Rafi MA; Wenger DA
    Genomics; 1996 May; 33(3):457-62. PubMed ID: 8661004
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of the rhesus monkey galactocerebrosidase (GALC) cDNA and gene and identification of the mutation causing globoid cell leukodystrophy (Krabbe disease) in this primate.
    Luzi P; Rafi MA; Victoria T; Baskin GB; Wenger DA
    Genomics; 1997 Jun; 42(2):319-24. PubMed ID: 9192853
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Globoid cell leukodystrophy in cairn and West Highland white terriers.
    Wenger DA; Victoria T; Rafi MA; Luzi P; Vanier MT; Vite C; Patterson DF; Haskins MH
    J Hered; 1999; 90(1):138-42. PubMed ID: 9987921
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Generation of a mouse with low galactocerebrosidase activity by gene targeting: a new model of globoid cell leukodystrophy (Krabbe disease).
    Luzi P; Rafi MA; Zaka M; Curtis M; Vanier MT; Wenger DA
    Mol Genet Metab; 2001 Jul; 73(3):211-23. PubMed ID: 11461188
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications.
    Wenger DA; Rafi MA; Luzi P
    Hum Mutat; 1997; 10(4):268-79. PubMed ID: 9338580
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular basis of globoid cell leukodystrophy in Irish setters.
    McGraw RA; Carmichael KP
    Vet J; 2006 Mar; 171(2):370-2. PubMed ID: 16490723
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cloning and expression of cDNA encoding human galactocerebrosidase, the enzyme deficient in globoid cell leukodystrophy.
    Chen YQ; Rafi MA; de Gala G; Wenger DA
    Hum Mol Genet; 1993 Nov; 2(11):1841-5. PubMed ID: 8281145
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Suppression of galactosylceramidase (GALC) expression in the twitcher mouse model of globoid cell leukodystrophy (GLD) is caused by nonsense-mediated mRNA decay (NMD).
    Lee WC; Tsoi YK; Dickey CA; Delucia MW; Dickson DW; Eckman CB
    Neurobiol Dis; 2006 Aug; 23(2):273-80. PubMed ID: 16759875
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic galactocerebrosidase deficiency (globoid cell leukodystrophy, Krabbe disease) in rhesus monkeys (Macaca mulatta).
    Baskin GB; Ratterree M; Davison BB; Falkenstein KP; Clarke MR; England JD; Vanier MT; Luzi P; Rafi MA; Wenger DA
    Lab Anim Sci; 1998 Oct; 48(5):476-82. PubMed ID: 10090061
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular basis of late-life globoid cell leukodystrophy.
    De Gasperi R; Gama Sosa MA; Sartorato E; Battistini S; Raghavan S; Kolodny EH
    Hum Mutat; 1999; 14(3):256-62. PubMed ID: 10477434
    [TBL] [Abstract][Full Text] [Related]  

  • 11. AAV2/5 vector expressing galactocerebrosidase ameliorates CNS disease in the murine model of globoid-cell leukodystrophy more efficiently than AAV2.
    Lin D; Fantz CR; Levy B; Rafi MA; Vogler C; Wenger DA; Sands MS
    Mol Ther; 2005 Sep; 12(3):422-30. PubMed ID: 15996520
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Krabbe disease: isolation and characterization of a full-length cDNA for human galactocerebrosidase.
    Sakai N; Inui K; Fujii N; Fukushima H; Nishimoto J; Yanagihara I; Isegawa Y; Iwamatsu A; Okada S
    Biochem Biophys Res Commun; 1994 Jan; 198(2):485-91. PubMed ID: 8297359
    [TBL] [Abstract][Full Text] [Related]  

  • 13. AAV-mediated expression of galactocerebrosidase in brain results in attenuated symptoms and extended life span in murine models of globoid cell leukodystrophy.
    Rafi MA; Zhi Rao H; Passini MA; Curtis M; Vanier MT; Zaka M; Luzi P; Wolfe JH; Wenger DA
    Mol Ther; 2005 May; 11(5):734-44. PubMed ID: 15851012
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Krabbe disease (globoid cell leukodystrophy)].
    Sakai N; Inui K; Okada S
    Nihon Rinsho; 1995 Dec; 53(12):2947-51. PubMed ID: 8577041
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a 6 base pair insertion in West Highland White Terriers with erythrocyte pyruvate kinase deficiency.
    Skelly BJ; Wallace M; Rajpurohit YR; Wang P; Giger U
    Am J Vet Res; 1999 Sep; 60(9):1169-72. PubMed ID: 10490091
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Somatic cell genetic analysis of the galactocerebrosidase gene: lack of complementation in human Krabbe disease/twitcher mouse cell hybrids.
    Skiba MC; Lyerla TA; Konola JT; Raghavan S
    J Neurosci Res; 1990 Dec; 27(4):472-8. PubMed ID: 2079710
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Galactosylceramidase deficiency causes sperm abnormalities in the mouse model of globoid cell leukodystrophy.
    Luddi A; Strazza M; Carbone M; Moretti E; Costantino-Ceccarini E
    Exp Cell Res; 2005 Mar; 304(1):59-68. PubMed ID: 15707574
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cellular uptake and lysosomal delivery of galactocerebrosidase tagged with the HIV Tat protein transduction domain.
    Zhang XY; Dinh A; Cronin J; Li SC; Reiser J
    J Neurochem; 2008 Feb; 104(4):1055-64. PubMed ID: 17986221
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple mutations in the GALC gene in a patient with adult-onset Krabbe disease.
    Luzi P; Rafi MA; Wenger DA
    Ann Neurol; 1996 Jul; 40(1):116-9. PubMed ID: 8687180
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Retroviral vector-mediated transfer of the galactocerebrosidase (GALC) cDNA leads to overexpression and transfer of GALC activity to neighboring cells.
    Rafi MA; Fugaro J; Amini S; Luzi P; de Gala G; Victoria T; Dubell C; Shahinfar M; Wenger DA
    Biochem Mol Med; 1996 Aug; 58(2):142-50. PubMed ID: 8812733
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.