Usher Syndrome Protein Network Functions in the Retina and their Relation to Other Retinal Ciliopathies-Reference-Cited by-同舟云学术

Usher Syndrome Protein Network Functions in the Retina and their Relation to Other Retinal Ciliopathies

Published:2014 Issue: Volume: Page:527-533
ISSN:0065-2598
Container-title:Retinal Degenerative Diseases
language:
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Author:

Sorusch Nasrin,Wunderlich Kirsten,Bauss Katharina,Nagel-Wolfrum Kerstin,Wolfrum Uwe

Publisher

Springer New York

Link

http://link.springer.com/content/pdf/10.1007/978-1-4614-3209-8_67

Reference24 articles.

1. Saihan Z et al (2009) Update on Usher syndrome. Curr Opin Neurol 22:19–27

2. Wolfrum U (2011) Protein networks related to the Usher syndrome gain insights in the molecular basis of the disease. In: Ahuja S (ed) Usher syndrome: pathogenesis, diagnosis and therapy. Nova Sci Pub Inc, USA, p. 51–73

3. Riazuddin S et al (2012) Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nat Genet 44:1265–1271

4. Ebermann I et al (2010) PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome. J Clin Invest 120:1812–1823

5. Reiners J et al (2006) Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease. Exp Eye Res 83:97–119

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