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

Papers associated with cilium∨derBy=4 (and dnah9)

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GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base., Jang DG., Elife. August 25, 2022; 11                                       


DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes., Marquez J., J Med Genet. July 1, 2021; 58 (7): 453-464.                        


Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.                        


Functional partitioning of a liquid-like organelle during assembly of axonemal dyneins., Lee C, Lee C., Elife. December 2, 2020; 9                             


CFAP43 modulates ciliary beating in mouse and Xenopus., Rachev E., Dev Biol. March 15, 2020; 459 (2): 109-125.                                                                    


Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility., Robson A., Proc Natl Acad Sci U S A. July 9, 2019; 116 (28): 14049-14054.                                  


A dual function of FGF signaling in Xenopus left-right axis formation., Schneider I., Development. May 10, 2019; 146 (9):                               


WDR5 regulates left-right patterning via chromatin-dependent and -independent functions., Kulkarni SS., Development. November 28, 2018; 145 (23):                 


WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation., Kulkarni SS., Dev Cell. September 10, 2018; 46 (5): 595-610.e3.                              


An Early Function of Polycystin-2 for Left-Right Organizer Induction in Xenopus., Vick P., iScience. April 27, 2018; 2 76-85.                                        


Leftward Flow Determines Laterality in Conjoined Twins., Tisler M., Curr Biol. February 20, 2017; 27 (4): 543-548.                


CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus., Bhattacharya D., Dev Biol. December 15, 2015; 408 (2): 196-204.            


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


The nodal inhibitor Coco is a critical target of leftward flow in Xenopus., Schweickert A., Curr Biol. April 27, 2010; 20 (8): 738-43.      


Flow on the right side of the gastrocoel roof plate is dispensable for symmetry breakage in the frog Xenopus laevis., Vick P., Dev Biol. July 15, 2009; 331 (2): 281-91.                                        


FGF signalling during embryo development regulates cilia length in diverse epithelia., Neugebauer JM., Nature. April 2, 2009; 458 (7238): 651-4.      


The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos., Stubbs JL., Nat Genet. December 1, 2008; 40 (12): 1454-60.                


Cilia multifunctional organelles at the center of vertebrate left-right asymmetry., Basu B., Curr Top Dev Biol. January 1, 2008; 85 151-74.


Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros., Tran U., Dev Biol. July 1, 2007; 307 (1): 152-64.                  


Cilia-driven leftward flow determines laterality in Xenopus., Schweickert A., Curr Biol. January 9, 2007; 17 (1): 60-6.        


Localization and loss-of-function implicates ciliary proteins in early, cytoplasmic roles in left-right asymmetry., Qiu D., Dev Dyn. September 1, 2005; 234 (1): 176-89.      

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