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285 related items for PubMed ID: 15233947
1. AAV-mediated intravitreal gene therapy reduces lysosomal storage in the retinal pigmented epithelium and improves retinal function in adult MPS VII mice. Hennig AK, Ogilvie JM, Ohlemiller KK, Timmers AM, Hauswirth WW, Sands MS. Mol Ther; 2004 Jul; 10(1):106-16. PubMed ID: 15233947 [Abstract] [Full Text] [Related]
2. Retinal function is improved in a murine model of a lysosomal storage disease following bone marrow transplantation. Ohlemiller KK, Vogler CA, Roberts M, Galvin N, Sands MS. Exp Eye Res; 2000 Nov; 71(5):469-81. PubMed ID: 11040082 [Abstract] [Full Text] [Related]
11. Phenotype correction in retinal pigment epithelium in murine mucopolysaccharidosis VII by adenovirus-mediated gene transfer. Li T, Davidson BL. Proc Natl Acad Sci U S A; 1995 Aug 15; 92(17):7700-4. PubMed ID: 7644479 [Abstract] [Full Text] [Related]
13. Genetic correction of the fetal brain increases the lifespan of mice with the severe multisystemic disease mucopolysaccharidosis type VII. Karolewski BA, Wolfe JH. Mol Ther; 2006 Jul 15; 14(1):14-24. PubMed ID: 16624622 [Abstract] [Full Text] [Related]
14. Intravitreal gene therapy reduces lysosomal storage in specific areas of the CNS in mucopolysaccharidosis VII mice. Hennig AK, Levy B, Ogilvie JM, Vogler CA, Galvin N, Bassnett S, Sands MS. J Neurosci; 2003 Apr 15; 23(8):3302-7. PubMed ID: 12716937 [Abstract] [Full Text] [Related]
16. Feline immunodeficiency virus vectors. Gene transfer to mouse retina following intravitreal injection. Derksen TA, Sauter SL, Davidson BL. J Gene Med; 2002 Apr 15; 4(5):463-9. PubMed ID: 12221638 [Abstract] [Full Text] [Related]
17. Evaluation of AAV-mediated Gene Therapy for Central Nervous System Disease in Canine Mucopolysaccharidosis VII. Gurda BL, De Guilhem De Lataillade A, Bell P, Zhu Y, Yu H, Wang P, Bagel J, Vite CH, Sikora T, Hinderer C, Calcedo R, Yox AD, Steet RA, Ruane T, O'Donnell P, Gao G, Wilson JM, Casal M, Ponder KP, Haskins ME. Mol Ther; 2016 Feb 15; 24(2):206-216. PubMed ID: 26447927 [Abstract] [Full Text] [Related]
19. 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 15; 25(9):798-810. PubMed ID: 25003807 [Abstract] [Full Text] [Related]
20. Long-term and significant correction of brain lesions in adult mucopolysaccharidosis type VII mice using recombinant AAV vectors. Bosch A, Perret E, Desmaris N, Heard JM. Mol Ther; 2000 Jan 15; 1(1):63-70. PubMed ID: 10933913 [Abstract] [Full Text] [Related] Page: [Next] [New Search]