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Summary Expression Phenotypes Gene Literature (1784) GO Terms (7) Nucleotides (155) Proteins (54) Interactants (2620) Wiki
XB--1018114

Papers associated with tbx2 (and Disease Ontology)



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referenced by:


The Role of RNA-Binding Proteins in Vertebrate Neural Crest and Craniofacial Development., Forman TE, Dennison BJC, Fantauzzo KA., J Dev Biol. August 27, 2021; 9 (3):   


Molecular mechanisms of hearing loss in Nager syndrome., Maharana SK, Saint-Jeannet JP., Dev Biol. August 1, 2021; 476 200-208.            


Long-range gap junctional signaling controls oncogene-mediated tumorigenesis in Xenopus laevis embryos., Chernet BT, Fields C, Levin M., Front Physiol. January 19, 2015; 5 519.                


Effect of the CALHM1 G330D and R154H human variants on the control of cytosolic Ca2+ and Aβ levels., Vingtdeux V, Tanis JE, Chandakkar P, Zhao H, Dreses-Werringloer U, Campagne F, Foskett JK, Marambaud P., PLoS One. November 6, 2014; 9 (11): e112484.        


Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTR., Cui G, Rahman KS, Infield DT, Kuang C, Prince CZ, McCarty NA., J Gen Physiol. August 1, 2014; 144 (2): 159-79.                          


The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L, Sindelka R, Chen J, Rothman A, Dickinson A, Sive H., Cell Rep. July 24, 2014; 8 (2): 596-609.                            


A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle., Sartelet A, Stauber T, Coppieters W, Ludwig CF, Fasquelle C, Druet T, Zhang Z, Ahariz N, Cambisano N, Jentsch TJ, Charlier C., Dis Model Mech. January 1, 2014; 7 (1): 119-28.                


Simple and efficient CRISPR/Cas9-mediated targeted mutagenesis in Xenopus tropicalis., Nakayama T, Fish MB, Fisher M, Oomen-Hajagos J, Thomsen GH, Grainger RM., Genesis. December 1, 2013; 51 (12): 835-43.            


Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicity., Srivastava S, Li D, Edwards N, Hynes AM, Wood K, Al-Hamed M, Wroe AC, Reaich D, Moochhala SH, Welling PA, Sayer JA., Physiol Rep. November 1, 2013; 1 (6): e00160.          


Modeling human neurodevelopmental disorders in the Xenopus tadpole: from mechanisms to therapeutic targets., Pratt KG, Khakhalin AS., Dis Model Mech. September 1, 2013; 6 (5): 1057-65.  


Transmembrane voltage potential is an essential cellular parameter for the detection and control of tumor development in a Xenopus model., Chernet BT, Levin M., Dis Model Mech. May 1, 2013; 6 (3): 595-607.                  


Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA, Gallas AL, Neto A, Gómez-Skarmeta JL, Zorn AM., Development. August 1, 2012; 139 (16): 3010-20.                                                                                


Control of vertebrate intraflagellar transport by the planar cell polarity effector Fuz., Brooks ER, Wallingford JB., J Cell Biol. July 9, 2012; 198 (1): 37-45.          


Transient expression of Ngn3 in Xenopus endoderm promotes early and ectopic development of pancreatic beta and delta cells., Oropeza D, Horb M., Genesis. March 1, 2012; 50 (3): 271-85.                        


Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium., Rubinos C, Sánchez HA, Verselis VK, Srinivas M., J Gen Physiol. January 1, 2012; 139 (1): 69-82.                    


Embryonic frog epidermis: a model for the study of cell-cell interactions in the development of mucociliary disease., Dubaissi E, Papalopulu N., Dis Model Mech. March 1, 2011; 4 (2): 179-92.                        


Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S, Yabe S, Uchiyama H., Dev Biol. October 15, 2010; 346 (2): 170-80.                                


Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing., Naranjo S, Voesenek K, de la Calle-Mustienes E, Robert-Moreno A, Kokotas H, Grigoriadou M, Economides J, Van Camp G, Hilgert N, Moreno F, Alsina B, Petersen MB, Kremer H, Gómez-Skarmeta JL., Hum Genet. October 1, 2010; 128 (4): 411-9.          


The miR-30 miRNA family regulates Xenopus pronephros development and targets the transcription factor Xlim1/Lhx1., Agrawal R, Tran U, Wessely O., Development. December 1, 2009; 136 (23): 3927-36.              


Learning about cancer from frogs: analysis of mitotic spindles in Xenopus egg extracts., Cross MK, Powers MA., Dis Model Mech. January 1, 2009; 2 (11-12): 541-7.      


Identification, developmental expression and regulation of the Xenopus ortholog of human FANCG/XRCC9., Stone S, Sobeck A, van Kogelenberg M, de Graaf B, Joenje H, Christian J, Hoatlin ME., Genes Cells. July 1, 2007; 12 (7): 841-51.        


Characterization of atrazine-induced gonadal malformations in African clawed frogs (Xenopus laevis) and comparisons with effects of an androgen antagonist (cyproterone acetate) and exogenous estrogen (17beta-estradiol): Support for the demasculinization/feminization hypothesis., Hayes TB, Stuart AA, Mendoza M, Collins A, Noriega N, Vonk A, Johnston G, Liu R, Kpodzo D., Environ Health Perspect. April 1, 2006; 114 Suppl 1 (Suppl 1): 134-41.                          


Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T., Skerrett IM, Di WL, Kasperek EM, Kelsell DP, Nicholson BJ., FASEB J. May 1, 2004; 18 (7): 860-2.


Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels., Kronengold J, Trexler EB, Bukauskas FF, Bargiello TA, Verselis VK., J Gen Physiol. October 1, 2003; 122 (4): 389-405.                    


Two different mechanisms of disinhibition produced by GABAA receptor mutations linked to epilepsy in humans., Bianchi MT, Song L, Zhang H, Macdonald RL., J Neurosci. July 1, 2002; 22 (13): 5321-7.


Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome., He Ml, Wen L, Campbell CE, Wu JY, Rao Y., Proc Natl Acad Sci U S A. August 31, 1999; 96 (18): 10212-7.

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