Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice-Reference-Cited by-同舟云学术

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice

Published:2023-06-13 Issue:5 Volume:17 Page:957-971
ISSN:2095-0217
Container-title:Frontiers of Medicine
language:en
Short-container-title:Front. Med.

Author:

Wang Rongchun,Yang Danhui,Tu Chaofeng,Lei Cheng,Ding Shuizi,Guo Ting,Wang Lin,Liu Ying,Lu Chenyang,Yang Binyi,Ouyang Shi,Gong Ke,Tan Zhiping,Deng Yun,Tan Yueqiu,Qing Jie,Luo Hong

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s11684-023-0988-8.pdf

Reference50 articles.

1. Lucas JS, Davis SD, Omran H, Shoemark A. Primary ciliary dyskinesia in the genomics age. Lancet Respir Med 2020; 8(2): 202–216

2. Wallmeier J, Nielsen KG, Kuehni CE, Lucas JS, Leigh MW, Zariwala MA, Omran H. Motile ciliopathies. Nat Rev Dis Primers 2020; 6(1): 77

3. Goutaki M, Meier AB, Halbeisen FS, Lucas JS, Dell SD, Maurer E, Casaulta C, Jurca M, Spycher BD, Kuehni CE. Clinical manifestations in primary ciliary dyskinesia: systematic review and meta-analysis. Eur Respir J 2016; 48(4): 1081–1095

4. Lucas JS, Barbato A, Collins SA, Goutaki M, Behan L, Caudri D, Dell S, Eber E, Escudier E, Hirst RA, Hogg C, Jorissen M, Latzin P, Legendre M, Leigh MW, Midulla F, Nielsen KG, Omran H, Papon JF, Pohunek P, Redfern B, Rigau D, Rindlisbacher B, Santamaria F, Shoemark A, Snijders D, Tonia T, Titieni A, Walker WT, Werner C, Bush A, Kuehni CE. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia. Eur Respir J 2017; 49(1): 1601090

5. Fliegauf M, Benzing T, Omran H. When cilia go bad: cilia defects and ciliopathies. Nat Rev Mol Cell Biol 2007; 8(11): 880–893

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