???pagination.result.count???
???pagination.result.page???
1
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes. , Marquez J ., J Med Genet. July 1, 2021; 58 (7): 453-464.
Xenopus epidermal and endodermal epithelia as models for mucociliary epithelial evolution, disease, and metaplasia. , Walentek P ., Genesis. February 1, 2021; 59 (1-2): e23406.
Functional partitioning of a liquid-like organelle during assembly of axonemal dyneins. , Lee C , Lee C ., Elife. December 2, 2020; 9
ΔN- Tp63 Mediates Wnt/ β-Catenin-Induced Inhibition of Differentiation in Basal Stem Cells of Mucociliary Epithelia. , Haas M., Cell Rep. September 24, 2019; 28 (13): 3338-3352.e6.
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.
What we can learn from a tadpole about ciliopathies and airway diseases: Using systems biology in Xenopus to study cilia and mucociliary epithelia. , Walentek P ., Genesis. January 1, 2017; 55 (1-2):
miR-34/449 miRNAs are required for motile ciliogenesis by repressing cp110. , Song R., Nature. June 5, 2014; 510 (7503): 115-20.
Myb promotes centriole amplification and later steps of the multiciliogenesis program. , Tan FE., Development. October 1, 2013; 140 (20): 4277-86.