Decreased lysosomal storage in the adult MPS VII mouse brain in the vicinity of grafts of retroviral vector-corrected fibroblasts secreting high levels of β-glucuronidase

Author:

Taylor Rosanne M,Wolfe John H

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference19 articles.

1. Sly, W.S., Quinton, B.A., McAlister, W.H. & Rimoin, D.L. Beta glucuronidase deficiency: Report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis. J. Pediatr. 82, 249–257 (1973).

2. Neufeld, E.F. & Muenzer, J. The mucopolysaccharidoses. in Metabolic Basis of Inherited Disease, 7th edn. (eds. Scriver, C.R., Beaudet, A.L, Sly, W.S. & Valle, D.) 2465–2494 (McCraw Hill, NY, 1995).

3. Haskins, M.E., Desnick, R.J., DiFerrante, N., Jezyk, P.F. & Patterson, D.F. Beta-glucuronidase deficiency in a dog: A model of mucopolysaccharidosis VII. Pediatr. Res. 18, 980–984 (1984).

4. Birkenmeier, E.H. et al. Murine mucopolysaccharidosis type VII: Characterization of a mouse with beta-glucuronidase deficiency. J. Clin. Invest. 83, 1258–1256 (1989).

5. Wolfe, J.H. & Sands, M.S. Murine mucopolysaccharidosis type VII: A model system for somatic gene therapy of the central nervous system, in Protocols for Gene Transfer in Neuroscience: Towards Gene Therapy of Neurologic Disorders . (eds. P.R. Lowenstein & L.W. Enquist) 263–274 (John Wiley and Sons, Essex, England, 1996).

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