The tuberous sclerosis proteins regulate formation of the primary cilium via a rapamycin-insensitive and polycystin 1-independent pathway-Reference-Cited by-同舟云学术

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The tuberous sclerosis proteins regulate formation of the primary cilium via a rapamycin-insensitive and polycystin 1-independent pathway

Published:2008-10-09 Issue:1 Volume:18 Page:151-163
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Hartman Tiffiney R.,Liu Dongyan,Zilfou Jack T.,Robb Victoria,Morrison Tasha,Watnick Terry,Henske Elizabeth P.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/18/1/151/14138553/ddn325.pdf

Reference96 articles.

1. Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene;Sampson;Am. J. Hum. Genet.,1997

2. A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney disease;Longa;Nephrol. Dial. Transplant.,1997

3. A germline insertion in the tuberous sclerosis (Tsc2) gene gives rise to the Eker rat model of dominantly inherited cancer;Kobayashi;Nat. Genet.,1995

4. Renal carcinogenesis, hepatic hemangiomatosis, and embryonic lethality caused by a germ-line Tsc2 mutation in mice;Kobayashi;Cancer Res.,1999

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