Rsph9 is critical for ciliary radial spoke assembly and central pair microtubule stability
Author:
Affiliation:
1. State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science; Shanghai Institute of Biochemistry and Cell Biology; Shanghai China
2. University of Chinese Academy of Sciences; Shanghai China
Funder
National Natural Science Foundation of China
National Key R&D Program of China
Chinese Academy of Sciences
Publisher
Wiley
Subject
Cell Biology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/boc.201800060/fullpdf
Reference36 articles.
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2. Multiciliated cells;Brooks;Curr. Biol.,2014
3. miR-129-3p controls cilia assembly by regulating CP110 and actin dynamics;Cao;Nat. Cell Biol.,2012
4. Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities;Castleman;Am. J. Hum Genet,2009
5. Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia;Daniels;Hum. Mutat.,2013
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