INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse-Reference-Cited by-同舟云学术

INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse

Published:2009-08-09 Issue:9 Volume:41 Page:1027-1031
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Jacoby Monique,Cox James J,Gayral Stéphanie,Hampshire Daniel J,Ayub Mohammed,Blockmans Marianne,Pernot Eileen,Kisseleva Marina V,Compère Philippe,Schiffmann Serge N,Gergely Fanni,Riley John H,Pérez-Morga David,Woods C Geoffrey,Schurmans Stéphane

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.427.pdf

Reference26 articles.

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3. Anderson, C.T. et al. Primary cilia: cellular sensors for the skeleton. Anat. Rec. 291, 1074–1078 (2008).

4. Blero, D., Payrastre, B., Schurmans, S. & Erneux, C.E. Phosphoinositide phosphatases in a network of signaling reactions. Pflugers Arch. 455, 31–44 (2007).

5. Astle, M.V., Horan, K.A., Ooms, L.M. & Mitchell, C.A. The inositol polyphosphate 5-phosphatases: traffic controllers, waistline watchers and tumour suppressors? Biochem. Soc. Symp. 74, 161–181 (2007).

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