Disease models for the development of therapies for lysosomal storage diseases-Reference-Cited by-同舟云学术

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Disease models for the development of therapies for lysosomal storage diseases

Published:2016-05 Issue:1 Volume:1371 Page:15-29
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:Ann. N.Y. Acad. Sci.

Author:

Xu Miao¹²,Motabar Omid¹,Ferrer Marc¹,Marugan Juan J.¹,Zheng Wei¹,Ottinger Elizabeth A.¹

Affiliation:

1. National Center for Advancing Translational Sciences; National Institutes of Health; Rockville Maryland

2. Sir Run Run Shaw Hospital; Zhejiang University School of Medicine; Hangzhou China

Funder

National Center for Advancing Translational Sciences

National Institutes of Health

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/nyas.13052/fullpdf

Reference117 articles.

1. Epidemiology and diagnosis of lysosomal storage disorders; challenges of screening;Kingma;Best Pract. Res. Clin. Endocrinol. Metab,2015

2. Prevalence of lysosomal storage disorders;Meikle;JAMA,1999

3. The incidence of inherited metabolic disorders in the West Midlands, UK;Sanderson;Arch. Dis. Child,2006

4. The lysosome: from waste bag to potential therapeutic target;Appelqvist;J. Mol. Cell Biol,2013

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