Motile ciliopathies-Reference-Cited by-同舟云学术

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Motile ciliopathies

Published:2020-09-17 Issue:1 Volume:6 Page:
ISSN:2056-676X
Container-title:Nature Reviews Disease Primers
language:en
Short-container-title:Nat Rev Dis Primers

Author:

Wallmeier Julia,Nielsen Kim G.,Kuehni Claudia E.,Lucas Jane S.,Leigh Margaret W.,Zariwala Maimoona A.,Omran Heymut

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

https://www.nature.com/articles/s41572-020-0209-6.pdf

Reference310 articles.

1. Fliegauf, M., Benzing, T. & Omran, H. When cilia go bad: cilia defects and ciliopathies. Nat. Rev. Mol. Cell Biol. 8, 880–893 (2007).

2. Reiter, J. F. & Leroux, M. R. Genes and molecular pathways underpinning ciliopathies. Nat. Rev. Mol. Cell Biol. 18, 533–547 (2017).

3. Kennedy, M. P. et al. Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia. Circulation 115, 2814–2821 (2007). This article reports, for the first time, the presence of situs ambiguus (heterotaxy) in a fraction of patients with well-characterized primary ciliary dyskinesia.

4. Essner, J. J. et al. Conserved function for embryonic nodal cilia. Nature 418, 37–38 (2002).

5. Shapiro, A. J. et al. Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy. Chest 146, 1176–1186 (2014).

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