Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (23) GO Terms (5) Nucleotides (110) Proteins (36) Interactants (671) Wiki
XB-GENEPAGE-920655

Papers associated with cetn4



Limit to papers also referencing gene:
8 paper(s) referencing morpholinos

Results 1 - 23 of 23 results

Page(s): 1

Sort Newest To Oldest Sort Oldest To Newest

The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus., Beckers A, Fuhl F, Ott T, Boldt K, Brislinger MM, Walentek P, Schuster-Gossler K, Hegermann J, Alten L, Kremmer E, Przykopanski A, Serth K, Ueffing M, Blum M, Gossler 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, Vazquez N, Satija R, Wallingford JB., Mol Biol Cell. June 1, 2021; 32 (12): 1171-1180.              


A liquid-like organelle at the root of motile ciliopathy., Huizar RL, Lee C, Boulgakov AA, Horani A, Tu F, Marcotte EM, Brody SL, Wallingford JB., Elife. December 18, 2018; 7                               


Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development., Konjikusic MJ, Yeetong P, Boswell CW, Lee C, Lee C, Roberson EC, Ittiwut R, Suphapeetiporn K, Ciruna B, Gurnett CA, Wallingford JB, Shotelersuk V, Gray RS., 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, Ott T, Schuster-Gossler K, Boldt K, Alten L, Ueffing M, Blum M, Gossler 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, Sedzinski J, Ma Y, Marcotte EM, Wallingford JB., 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, Lee C, Wentzensen IM, Parisi MA, Crenshaw MM, Sapp JC, Gross JM, Wallingford JB, Biesecker LG., 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, Quigley IK., Genesis. January 1, 2017; 55 (1-2):       


The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery., Toriyama M, Lee C, Taylor SP, Duran I, Cohn DH, Bruel AL, Tabler JM, Drew K, Kelly MR, Kim S, Park TJ, Braun DA, Pierquin G, Biver A, Wagner K, Malfroot A, Panigrahi I, Franco B, Al-Lami HA, Yeung Y, Choi YJ, University of Washington Center for Mendelian Genomics, Duffourd Y, Faivre L, Rivière JB, Chen J, Liu KJ, Liu KJ, Marcotte EM, Hildebrandt F, Thauvin-Robinet C, Krakow D, Jackson PK, Wallingford JB., 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, Shi J, Winey M, Klymkowsky MW., Dev Biol. March 15, 2016; 411 (2): 257-265.                      


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


Huntingtin is required for ciliogenesis and neurogenesis during early Xenopus development., Haremaki T, Deglincerti A, Brivanlou AH., Dev Biol. December 15, 2015; 408 (2): 305-15.            


Centrin-2 (Cetn2) mediated regulation of FGF/FGFR gene expression in Xenopus., Shi J, Zhao Y, Vonderfecht T, Winey M, Klymkowsky MW., Sci Rep. May 27, 2015; 5 10283.                    


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


Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN, Blackiston DJ, Rea AC, Dore TM, Levin M., 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, Santama N, Skourides PA., Dev Biol. August 15, 2013; 380 (2): 243-58.                                  


ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6., Zariwala MA, Gee HY, Kurkowiak M, Al-Mutairi DA, Leigh MW, Hurd TW, Hjeij R, Dell SD, Chaki M, Dougherty GW, Adan M, Spear PC, Esteve-Rudd J, Loges NT, Rosenfeld M, Diaz KA, Olbrich H, Wolf WE, Sheridan E, Batten TF, Halbritter J, Porath JD, Kohl S, Lovric S, Hwang DY, Pittman JE, Burns KA, Ferkol TW, Sagel SD, Olivier KN, Morgan LC, Werner C, Raidt J, Pennekamp P, Sun Z, Zhou W, Airik R, Natarajan S, Allen SJ, Amirav I, Wieczorek D, Landwehr K, Nielsen K, Schwerk N, Sertic J, Köhler G, Washburn J, Levy S, Fan S, Koerner-Rettberg C, Amselem S, Williams DS, Mitchell BJ, Drummond IA, Otto EA, Omran H, Knowles MR, Hildebrandt F., 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, Lake BB, Haremaki T, Weinstein DC, Sokol SY., Dev Dyn. September 1, 2012; 241 (9): 1385-95.            


Kendrin is a novel substrate for separase involved in the licensing of centriole duplication., Matsuo K, Ohsumi K, Iwabuchi M, Kawamata T, Ono Y, Takahashi M., Curr Biol. May 22, 2012; 22 (10): 915-21.        


Regulation of basal body and ciliary functions by Diversin., Yasunaga T, Itoh K, Sokol SY., 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, Oishi I, Izpisúa Belmonte JC, Kintner C., 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, Mitchell BJ, Abitua PB, Kintner C, Wallingford JB., 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, Kim SK, Abitua PB, Park TJ, Herrington ER, Kitayama A, Grow MW, Ueno N, Wallingford JB., Dev Biol. December 1, 2007; 312 (1): 115-30.                                          

Page(s): 1