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The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus. , Beckers A., Sci Rep. June 25, 2021; 11 (1): 13333.
Protein turnover dynamics suggest a diffusion-to-capture mechanism for peri-basal body recruitment and retention of intraflagellar transport proteins. , Hibbard JVK., Mol Biol Cell. June 1, 2021; 32 (12): 1171-1180.
A liquid-like organelle at the root of motile ciliopathy. , Huizar RL., Elife. December 18, 2018; 7
Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development. , Konjikusic MJ., PLoS Genet. November 6, 2018; 14 (11): e1007817.
The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice. , Beckers A., Sci Rep. October 2, 2018; 8 (1): 14678.
Protein localization screening in vivo reveals novel regulators of multiciliated cell development and function. , Tu F., J Cell Sci. January 29, 2018; 131 (3):
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):
The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery. , Toriyama M., Nat Genet. June 1, 2016; 48 (6): 648-56.
Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling. , Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.
Basal bodies in Xenopus. , Zhang S ., Cilia. February 3, 2016; 5 2.
Huntingtin is required for ciliogenesis and neurogenesis during early Xenopus development. , Haremaki T ., Dev Biol. December 15, 2015; 408 (2): 305-15.
Centrin-2 (Cetn2) mediated regulation of FGF/FGFR gene expression in Xenopus. , Shi J., Sci Rep. May 27, 2015; 5 10283.
ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled. , Miyatake K., Nat Commun. March 31, 2015; 6 6666.
Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton. , Ioannou A ., Dev Biol. August 15, 2013; 380 (2): 243-58.
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. , Zariwala MA., Am J Hum Genet. August 8, 2013; 93 (2): 336-45.
Rab11 regulates planar polarity and migratory behavior of multiciliated cells in Xenopus embryonic epidermis. , Kim K., Dev Dyn. September 1, 2012; 241 (9): 1385-95.
Regulation of basal body and ciliary functions by Diversin. , Yasunaga T., Mech Dev. January 1, 2011; 128 (7-10): 376-86.
The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos. , Stubbs JL., Nat Genet. December 1, 2008; 40 (12): 1454-60.
Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells. , Park TJ., Nat Genet. July 1, 2008; 40 (7): 871-9.
Identification of novel ciliogenesis factors using a new in vivo model for mucociliary epithelial development. , Hayes JM., Dev Biol. December 1, 2007; 312 (1): 115-30.