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Summary Anatomy Item Literature (444) Expression Attributions Wiki
XB-ANAT-3716

Papers associated with cilium (and pcbd1)

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PCD Genes-From Patients to Model Organisms and Back to Humans., Niziolek M., Int J Mol Sci. February 3, 2022; 23 (3):       

[Analysis of PIH1D3 variant in a Chinese pedigree affected with primary ciliary dyskinesia]., Wang S., Zhonghua Yi Xue Yi Chuan Xue Za Zhi. September 10, 2020; 37 (9): 1021-1024.

Rare Human Diseases: Model Organisms in Deciphering the Molecular Basis of Primary Ciliary Dyskinesia., Poprzeczko M., Cells. December 11, 2019; 8 (12):     

Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance., Bustamante-Marin XM., Am J Hum Genet. February 7, 2019; 104 (2): 229-245.                                  

TRRAP is a central regulator of human multiciliated cell formation., Wang Z., J Cell Biol. June 4, 2018; 217 (6): 1941-1955.                        

TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization., Wallmeier J., Am J Hum Genet. August 4, 2016; 99 (2): 460-9.

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6., Zariwala MA., Am J Hum Genet. August 8, 2013; 93 (2): 336-45.  

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