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Summary Anatomy Item Literature (4897) Expression Attributions Wiki
XB-ANAT-3713

Papers associated with left (and cetn4)

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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.                    


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):             


Compound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel Joubert and oral-facial-digital overlap syndrome., Johnston JJ., Cold Spring Harb Mol Case Stud. July 1, 2017; 3 (4):       


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.                              


Basal bodies in Xenopus., Zhang S., Cilia. February 3, 2016; 5 2.      


ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled., Miyatake K., Nat Commun. March 31, 2015; 6 6666.                


Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.                


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.                                  


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.                


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.                                          

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