W. S. Sly

Photoreceptor degeneration and altered distribution of interphotoreceptor matrix proteoglycans in the mucopolysaccharidosis VII mouse.

W. Sly, G. Hageman, H. Lazarus, 1993, Experimental eye research.

Demonstration of the heterozygous state for I-cell disease and pseudo-Hurler polydystrophy by assay of N-acetylglucosaminylphosphotransferase in white blood cells and fibroblasts.

A. Varki, M. Reitman, J. Grubb, 1982, American journal of human genetics.

Murine mucopolysaccharidosis type VII: long term therapeutic effects of enzyme replacement and enzyme replacement followed by bone marrow transplantation.

W. Sly, M. Sands, B. Gwynn, 1997, The Journal of clinical investigation.

A murine model of mucopolysaccharidosis VII. Gross and microscopic findings in beta-glucuronidase-deficient mice.

W. Sly, W. Beamer, E. Birkenmeier, 1990, The American journal of pathology.

Molecular analysis of patients with beta-glucuronidase deficiency presenting as hydrops fetalis or as early mucopolysaccharidosis VII.

W. Sly, R. Vervoort, W. Lissens, 1996, American Journal of Human Genetics.

Four novel mutations in mucopolysaccharidosis type VII including a unique base substitution in exon 10 of the beta-glucuronidase gene that creates a novel 5'-splice site.

W. Sly, S. Fukuda, S. Tomatsu, 1995, Human molecular genetics.

Enzyme replacement therapy for murine mucopolysaccharidosis type VII leads to improvements in behavior and auditory function.

W. Sly, M. Sands, L. Erway, 1998, The Journal of clinical investigation.

Treatment of murine mucopolysaccharidosis type VII by syngeneic bone marrow transplantation in neonates.

W. Sly, M. Sands, B. Gwynn, 1993, Laboratory investigation; a journal of technical methods and pathology.

Cloning and characterization of the human beta-glucuronidase gene.

Robertv . Miller, W. S. Sly, J. Kyle, 1990, Genomics.