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

Papers associated with left (and foxj1)

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The histone H4K20 methyltransferase SUV4-20H1/KMT5B is required for multiciliated cell differentiation in Xenopus., Angerilli A., Life Sci Alliance. July 1, 2023; 6 (7):                         


Mink1 regulates spemann organizer cell fate in the xenopus gastrula via Hmga2., Colleluori V., Dev Biol. March 1, 2023; 495 42-53.                            


Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.                                            


Normal Table of Xenopus development: a new graphical resource., Zahn N., Development. July 15, 2022; 149 (14):                         


Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates., Szenker-Ravi E., Nat Genet. January 1, 2022; 54 (1): 62-72.


dmrt2 and myf5 Link Early Somitogenesis to Left-Right Axis Determination in Xenopus laevis., Tingler M., Front Cell Dev Biol. January 1, 2022; 10 858272.                  


FGF-mediated establishment of left-right asymmetry requires Rab7 function in the dorsal mesoderm in Xenopus., Kreis J., Front Cell Dev Biol. January 1, 2022; 10 981762.                  


Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):                                           


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.                    


Altering metabolite distribution at Xenopus cleavage stages affects left-right gene expression asymmetries., Onjiko RM., Genesis. June 1, 2021; 59 (5-6): e23418.          


Combinatorial transcription factor activities on open chromatin induce embryonic heterogeneity in vertebrates., Bright AR., EMBO J. May 3, 2021; 40 (9): e104913.                        


RNA demethylation by FTO stabilizes the FOXJ1 mRNA for proper motile ciliogenesis., Kim H., Dev Cell. April 19, 2021; 56 (8): 1118-1130.e6.                                  


Aquatic models of human ciliary diseases., Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410.          


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


The FOXJ1 target Cfap206 is required for sperm motility, mucociliary clearance of the airways and brain development., Beckers A., Development. June 15, 2020; 147 (21):                                       


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


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.                              


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.                                  


Mechanical strain, novel genes and evolutionary insights: news from the frog left-right organizer., Blum M., Curr Opin Genet Dev. June 1, 2019; 56 8-14.      


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


Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus., Date P., Sci Rep. April 17, 2019; 9 (1): 6196.                            


A liquid-like organelle at the root of motile ciliopathy., Huizar RL., Elife. December 18, 2018; 7                               


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


CDC20B is required for deuterosome-mediated centriole production in multiciliated cells., Revinski DR., Nat Commun. November 7, 2018; 9 (1): 4668.              


Evolutionarily conserved Tbx5-Wnt2/2b pathway orchestrates cardiopulmonary development., Steimle JD., Proc Natl Acad Sci U S A. November 6, 2018; 115 (45): E10615-E10624.                                  


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.            


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.                                        


A Conserved Role of the Unconventional Myosin 1d in Laterality Determination., Tingler M., Curr Biol. March 5, 2018; 28 (5): 810-816.e3.                


RAPGEF5 Regulates Nuclear Translocation of β-Catenin., Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.                                                


Candidate Heterotaxy Gene FGFR4 Is Essential for Patterning of the Left-Right Organizer in Xenopus., Sempou E., Front Physiol. January 1, 2018; 9 1705.              


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


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):       


Roles of the cilium-associated gene CCDC11 in left-right patterning and in laterality disorders in humans., Gur M., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 267-276.          


La-related protein 6 controls ciliated cell differentiation., Manojlovic Z., Cilia. January 1, 2017; 6 4.                


Foxn4 promotes gene expression required for the formation of multiple motile cilia., Campbell EP., Development. December 15, 2016; 143 (24): 4654-4664.                                  


CFAP157 is a murine downstream effector of FOXJ1 that is specifically required for flagellum morphogenesis and sperm motility., Weidemann M., Development. December 15, 2016; 143 (24): 4736-4748.    


Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia., Del Viso F., Dev Cell. September 12, 2016; 38 (5): 478-92.                        


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


ATP4a is required for development and function of the Xenopus mucociliary epidermis - a potential model to study proton pump inhibitor-associated pneumonia., Walentek P., Dev Biol. December 15, 2015; 408 (2): 292-304.                                


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.            


TGF-β Signaling Regulates the Differentiation of Motile Cilia., Tözser J., Cell Rep. May 19, 2015; 11 (7): 1000-7.                


ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles., Walentek P., Data Brief. April 20, 2015; 4 22-31.            


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


Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.                    


miR-34/449 miRNAs are required for motile ciliogenesis by repressing cp110., Song R., Nature. June 5, 2014; 510 (7503): 115-20.                                


Symmetry breakage in the frog Xenopus: role of Rab11 and the ventral-right blastomere., Tingler M., Genesis. June 1, 2014; 52 (6): 588-99.            


RFX7 is required for the formation of cilia in the neural tube., Manojlovic Z., Mech Dev. May 1, 2014; 132 28-37.                  


Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.                                                    


A novel serotonin-secreting cell type regulates ciliary motility in the mucociliary epidermis of Xenopus tadpoles., Walentek P., Development. April 1, 2014; 141 (7): 1526-33.                        

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