Treatment of the mouse model of mucopolysaccharidosis I with retrovirally transduced bone marrow-Reference-Cited by-同舟云学术

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Treatment of the mouse model of mucopolysaccharidosis I with retrovirally transduced bone marrow

Published:2003-08 Issue:4 Volume:79 Page:233-244
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Zheng Yi,Rozengurt Nora,Ryazantsev Sergey,Kohn Donald B,Satake Noriko,Neufeld Elizabeth F

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference43 articles.

1. The mucopolysaccharidoses;Neufeld,2001

2. The human gene mutation database;Krawczak;Trends Genet.,1997

3. Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications;Scott;Hum. Mutat.,1995

4. The defect in Hurler and Hunter syndromes. II. Deficiency of specific factors involved in mucopolysaccharide degradation;Fratantoni;Proc. Natl. Acad. Sci. USA,1969

5. The defect in the Hurler and Scheie syndromes: deficiency of α-l-iduronidase;Bach;Proc. Natl. Acad. Sci. USA,1972

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1. Identification of a novel fusion Iduronidase with improved activity in the cardiovascular system;Molecular Genetics and Metabolism Reports;2022-12

2. MPSI Manifestations and Treatment Outcome: Skeletal Focus;International Journal of Molecular Sciences;2022-09-22

3. Delivering gene therapy for mucopolysaccharide diseases;Frontiers in Molecular Biosciences;2022-09-12

4. Lysosomal storage diseases: mucopolysaccharidosis type I and II;Pediatrician (St. Petersburg);2021-10-13

5. Gene Therapy for Neuronopathic Mucopolysaccharidoses: State of the Art;International Journal of Molecular Sciences;2021-08-25

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