The molecular and cellular basis of exostosis formation in hereditary multiple exostoses-Reference-Cited by-同舟云学术

The molecular and cellular basis of exostosis formation in hereditary multiple exostoses

Published:2008-04-30 Issue:5 Volume:89 Page:321-331
ISSN:0959-9673
Container-title:International Journal of Experimental Pathology
language:en
Short-container-title:

Author:

Trebicz-Geffen Meirav,Robinson Dror,Evron Zoharia,Glaser Tova,Fridkin Mati,Kollander Yehuda,Vlodavsky Israel,Ilan Neta,Law Kit Fong,Cheah Kathryn S.E.,Chan Danny,Werner Haim,Nevo Zvi

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2613.2008.00589.x/fullpdf

Reference50 articles.

1. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1);Ahn;Nat. Genet.,1995

2. Functions of cell surface heparan sulfate proteoglycans;Bernfield;Annu. Rev. Biochem.,1999

3. Cervical cord compression due to exostosis in a patient with hereditary multiple exostoses. Case report;Carmel;J. Neurosurg.,1968

4. Role of heparan sulfate in the terminal differentiation of growth plate chondrocytes;Chintala;Arch. Biochem. Biophys.,1995

5. Genetic heterogeneity in families with hereditary multiple exostoses;Cook;Am. J. Hum. Genet.,1993

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