Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model-Reference-Cited by-同舟云学术

Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model

Published:2012-09 Issue:9 Volume:18 Page:1423-1428
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

McIntyre Jeremy C,Davis Erica E,Joiner Ariell,Williams Corey L,Tsai I-Chun,Jenkins Paul M,McEwen Dyke P,Zhang Lian,Escobado John,Thomas Sophie,Szymanska Katarzyna,Johnson Colin A,Beales Philip L,Green Eric D,Mullikin James C,Program NISC Comparative Sequencing,Sabo Aniko,Muzny Donna M,Gibbs Richard A,Attié-Bitach Tania,Yoder Bradley K,Reed Randall R,Katsanis Nicholas,Martens Jeffrey R

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.2860.pdf

Reference40 articles.

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3. Lancaster, M.A. & Gleeson, J.G. The primary cilium as a cellular signaling center: lessons from disease. Curr. Opin. Genet. Dev. 19, 220–229 (2009).

4. Badano, J.L., Mitsuma, N., Beales, P.L. & Katsanis, N. The ciliopathies: an emerging class of human genetic disorders. Annu. Rev. Genomics Hum. Genet. 7, 125–148 (2006).

5. Lehman, J.M. et al. The Oak Ridge Polycystic Kidney mouse: modeling ciliopathies of mice and men. Dev. Dyn. 237, 1960–1971 (2008).

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