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Journal Abstract Search

113 related items for PubMed ID: 8574933

  • 1. Morphological alterations in dental and periodontal tissues in murine mucopolysaccharidosis type VII.
    Gritli-Linde A, Linde A, Goldberg M.
    Calcif Tissue Int; 1995 Sep; 57(3):178-84. PubMed ID: 8574933
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  • 2. Hepatic storage of glycosaminoglycans in feline and canine models of mucopolysaccharidoses I, VI, and VII.
    Haskins ME, Otis EJ, Hayden JE, Jezyk PF, Stramm L.
    Vet Pathol; 1992 Mar; 29(2):112-9. PubMed ID: 1632054
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  • 3. Abnormal osteoclast morphology and bone remodeling in a murine model of a lysosomal storage disease.
    Monroy MA, Ross FP, Teitelbaum SL, Sands MS.
    Bone; 2002 Feb; 30(2):352-9. PubMed ID: 11856642
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  • 4. EMMPRIN/CD147 deficiency disturbs ameloblast-odontoblast cross-talk and delays enamel mineralization.
    Khaddam M, Huet E, Vallée B, Bensidhoum M, Le Denmat D, Filatova A, Jimenez-Rojo L, Ribes S, Lorenz G, Morawietz M, Rochefort GY, Kiesow A, Mitsiadis TA, Poliard A, Petzold M, Gabison EE, Menashi S, Chaussain C.
    Bone; 2014 Sep; 66():256-66. PubMed ID: 24970041
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  • 5. A murine model of mucopolysaccharidosis VII. Gross and microscopic findings in beta-glucuronidase-deficient mice.
    Vogler C, Birkenmeier EH, Sly WS, Levy B, Pegors C, Kyle JW, Beamer WG.
    Am J Pathol; 1990 Jan; 136(1):207-17. PubMed ID: 2105058
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  • 6. Early onset of lysosomal storage disease in a murine model of mucopolysaccharidosis type VII: undegraded substrate accumulates in many tissues in the fetus and very young MPS VII mouse.
    Vogler C, Levy B, Galvin N, Lessard M, Soper B, Barker J.
    Pediatr Dev Pathol; 2005 Jan; 8(4):453-62. PubMed ID: 16222480
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  • 7. Production of MPS VII mouse (Gus(tm(hE540A x mE536A)Sly)) doubly tolerant to human and mouse beta-glucuronidase.
    Tomatsu S, Orii KO, Vogler C, Grubb JH, Snella EM, Gutierrez M, Dieter T, Holden CC, Sukegawa K, Orii T, Kondo N, Sly WS.
    Hum Mol Genet; 2003 May 01; 12(9):961-73. PubMed ID: 12700165
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  • 10. Glycosaminoglycan storage in cultured neonatal murine mucopolysaccharidosis type VII neuroglial cells and correction by beta-glucuronidase gene transfer.
    Taylor RM, Wolfe JH.
    J Neurochem; 1997 May 01; 68(5):2079-85. PubMed ID: 9109535
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  • 11. Missense models [Gustm(E536A)Sly, Gustm(E536Q)Sly, and Gustm(L175F)Sly] of murine mucopolysaccharidosis type VII produced by targeted mutagenesis.
    Tomatsu S, Orii KO, Vogler C, Grubb JH, Snella EM, Gutierrez MA, Dieter T, Sukegawa K, Orii T, Kondo N, Sly WS.
    Proc Natl Acad Sci U S A; 2002 Nov 12; 99(23):14982-7. PubMed ID: 12403825
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  • 12. Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin fibroblasts.
    Moullier P, Bohl D, Heard JM, Danos O.
    Nat Genet; 1993 Jun 12; 4(2):154-9. PubMed ID: 8348154
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  • 13. Active site mutant transgene confers tolerance to human beta-glucuronidase without affecting the phenotype of MPS VII mice.
    Sly WS, Vogler C, Grubb JH, Zhou M, Jiang J, Zhou XY, Tomatsu S, Bi Y, Snella EM.
    Proc Natl Acad Sci U S A; 2001 Feb 27; 98(5):2205-10. PubMed ID: 11226217
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  • 14. Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency.
    Birkenmeier EH, Davisson MT, Beamer WG, Ganschow RE, Vogler CA, Gwynn B, Lyford KA, Maltais LM, Wawrzyniak CJ.
    J Clin Invest; 1989 Apr 27; 83(4):1258-66. PubMed ID: 2495302
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  • 15. Lentiviral-mediated gene therapy results in sustained expression of β-glucuronidase for up to 12 months in the gus(mps/mps) and up to 18 months in the gus(tm(L175F)Sly) mouse models of mucopolysaccharidosis type VII.
    Derrick-Roberts AL, Pyragius CE, Kaidonis XM, Jackson MR, Anson DS, Byers S.
    Hum Gene Ther; 2014 Sep 27; 25(9):798-810. PubMed ID: 25003807
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  • 17. Suramin-induced mucopolysaccharidosis in rat incisor.
    Gritli A, Septier D, Goldberg M.
    Cell Tissue Res; 1993 Jul 27; 273(1):53-64. PubMed ID: 8364961
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  • 19. Enzyme replacement in murine mucopolysaccharidosis type VII: neuronal and glial response to beta-glucuronidase requires early initiation of enzyme replacement therapy.
    Vogler C, Levy B, Galvin NJ, Thorpe C, Sands MS, Barker JE, Baty J, Birkenmeier EH, Sly WS.
    Pediatr Res; 1999 Jun 27; 45(6):838-44. PubMed ID: 10367775
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