Treatment of a Lysosomal Storage Disease, Mucopolysaccharidosis VII, with Microencapsulated Recombinant Cells-Reference-Cited by-同舟云学术

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Treatment of a Lysosomal Storage Disease, Mucopolysaccharidosis VII, with Microencapsulated Recombinant Cells

Published:2000-10 Issue:15 Volume:11 Page:2117-2127
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Ross C. J. D.¹,Bastedo L.¹,Maier S. A.²,Sands M. S.³,Chang P. L.⁴

Affiliation:

1. Department of Biology, McMaster University, Hamilton, Ontario, L8N 3Z5 Canada

2. Department of Pediatrics, McMaster University, Hamilton, Ontario, L8N 3Z5 Canada; Department of Genetics, University of Alberta, Alberta, Canada

3. Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110

4. Department of Biology; Department of Pediatrics, McMaster University, Hamilton, Ontario, L8N 3Z5 Canada

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/104303400750001426

Reference53 articles.

1. A triploblast origin for Myxozoa?

2. Behavioral consequences of bone marrow transplantation in the treatment of murine mucopolysaccharidosis type VII.

3. Gaucher disease as a paradigm of current issues regarding single gene mutations of humans.

4. Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency.

5. Increased life span and correction of metabolic defects in murine mucopolysaccharidosis type VII after syngeneic bone marrow transplantation

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