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Summary Anatomy Item Literature (4079) Expression Attributions Wiki
XB-ANAT-3714

Papers associated with right (and arl13b)

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Mebendazole preferentially inhibits cilia formation and exerts anticancer activity by synergistically augmenting DNA damage., Hong J., Biomed Pharmacother. March 20, 2024; 174 116434.                              

TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):                                               

CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability., Deniz E., Dev Biol. July 1, 2023; 499 75-88.                              

Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease., Mishra-Gorur K., Proc Natl Acad Sci U S A. April 18, 2023; 120 (16): e2214997120.                                            

INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex., Mascibroda LG., Nat Commun. October 13, 2022; 13 (1): 6054.                    

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.                        

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.                                  

Characterization of potential TRPP2 regulating proteins in early Xenopus embryos., Futel M., J Cell Biochem. December 1, 2018; 119 (12): 10338-10350.  

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

High variability of expression profiles of homeologous genes for Wnt, Hh, Notch, and Hippo signaling pathways in Xenopus laevis., Michiue T., Dev Biol. June 15, 2017; 426 (2): 270-290.                  

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.                

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.                        

Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy., Duncan AR., Semin Cell Dev Biol. March 1, 2016; 51 73-9.    

The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality., Boskovski MT., Nature. December 19, 2013; 504 (7480): 456-9.    

Left-right asymmetry: lessons from Cancún., Burdine RD., Development. November 1, 2013; 140 (22): 4465-70.    

RFX2 is broadly required for ciliogenesis during vertebrate development., Chung MI., Dev Biol. March 1, 2012; 363 (1): 155-65.                                                          

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