The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation-Reference-Cited by-同舟云学术

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

Published:2010-12-05 Issue:1 Volume:43 Page:79-84
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Becker-Heck Anita,Zohn Irene E,Okabe Noriko,Pollock Andrew,Lenhart Kari Baker,Sullivan-Brown Jessica,McSheene Jason,Loges Niki T,Olbrich Heike,Haeffner Karsten,Fliegauf Manfred,Horvath Judith,Reinhardt Richard,Nielsen Kim G,Marthin June K,Baktai Gyorgy,Anderson Kathryn V,Geisler Robert,Niswander Lee,Omran Heymut,Burdine Rebecca D

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.727.pdf

Reference27 articles.

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2. Barbato, A. et al. Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children. Eur. Respir. J. 34, 1264–1276 (2009).

3. Duquesnoy, P. et al. Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia. Am. J. Hum. Genet. 85, 890–896 (2009).

4. Loges, N.T. et al. Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects. Am. J. Hum. Genet. 85, 883–889 (2009).

5. Omran, H. et al. Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins. Nature 456, 611–616 (2008).

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