Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis-Reference-Cited by-同舟云学术

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

Published:2007-07-08 Issue:8 Volume:39 Page:1018-1024
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Attanasio Massimo,Uhlenhaut N Henriette,Sousa Vitor H,O'Toole John F,Otto Edgar,Anlag Katrin,Klugmann Claudia,Treier Anna-Corina,Helou Juliana,Sayer John A,Seelow Dominik,Nürnberg Gudrun,Becker Christian,Chudley Albert E,Nürnberg Peter,Hildebrandt Friedhelm,Treier Mathias

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng2072.pdf

Reference30 articles.

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2. Otto, E.A. et al. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination. Nat. Genet. 34, 413–420 (2003).

3. Hildebrandt, F. & Otto, E. Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease? Nat. Rev. Genet. 6, 928–940 (2005).

4. Sayer, J.A. et al. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nat. Genet. 38, 674–681 (2006).

5. Watnick, T. & Germino, G. From cilia to cyst. Nat. Genet. 34, 355–356 (2003).

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