Papers associated with tbx2 (and OMIM)

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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.
	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.
	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.
	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.
	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.
	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.
	Molecular characterization and regulation of the human endothelin receptors., Elshourbagy NA, Korman DR, Wu HL, Sylvester DR, Lee JA, Nuthalaganti P, Bergsma DJ, Kumar CS, Nambi P., J Biol Chem. February 25, 1993; 268 (6): 3873-9.

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