Heterogeneity in mucolipidosis II (l-cell disease)-Reference-Cited by-同舟云学术

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Heterogeneity in mucolipidosis II (l-cell disease)

Published:2008-04-23 Issue:2 Volume:23 Page:155-159
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Okada Shintaro,Kato Tomochika,Oshima Toshio,Yutaka Tohru,Yabuuchi Hyakuji

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1983.tb01865.x/fullpdf

Reference15 articles.

1. I-cell disease: deficiency of extracellular hydrolase phosphory-lation;Bach;Biochem. Biophys. Res. Commun.,1979

2. Chloroquine inhibits lysosomal enzyme pinocytosis and enhances lysosomal enzyme secretion by impairing receptor recycling;Gonzalez-Noriega;J. Cell Biol.,1980

3. Biosynthesis of lysosomal enzymes in fibroblasts: phosphorylation of mannose residues;Hasilik;J. Biol. Chem.,1980

4. Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in I-cell fibroblasts;Hasilik;Biochem. Biophys. Res. Commun.,1981

5. A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes;Hickman;Biochem. Biophys. Res. Commun.,1972

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 18 Metabolic and storage diseases;Weedon's Skin Pathology;2010

2. Metabolic and storage diseases;Weedon's Skin Pathology;2010

3. A variant of mucolipidosis;European Journal of Pediatrics;1988-04

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