Thoracic aortic disease in tuberous sclerosis complex: molecular pathogenesis and potential therapies in Tsc2+/− mice-Reference-Cited by-同舟云学术

Thoracic aortic disease in tuberous sclerosis complex: molecular pathogenesis and potential therapies in Tsc2+/− mice

Published:2010-02-16 Issue:10 Volume:19 Page:1908-1920
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Cao Jiumei,Gong Limin,Guo Dong-chuan,Mietzsch Ulrike,Kuang Shao-Qing,Kwartler Callie S.,Safi Hazim,Estrera Anthony,Gambello Michael J.,Milewicz Dianna M.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/19/10/1908/17249209/ddq066.pdf

Reference50 articles.

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3. Identification and characterization of the tuberous sclerosis gene on chromosome 16;The European Chromosome 16 Tuberous Sclerosis Consortium;Cell,1993

4. Identification of tuberin, the tuberous sclerosis-2 product. Tuberin possesses specific Rap1GAP activity;Wienecke;J. Biol. Chem.,1995

5. The tuberous sclerosis 2 gene product, tuberin, functions as a Rab5 GTPase activating protein (GAP) in modulating endocytosis;Xiao;J. Biol. Chem.,1997

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