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Summary Anatomy Item Literature (994) Expression Attributions Wiki
XB-ANAT-95

Papers associated with pharyngeal arch (and nkx2-5)

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tinman, a Drosophila homeobox gene required for heart and visceral mesoderm specification, may be represented by a family of genes in vertebrates: XNkx-2.3, a second vertebrate homologue of tinman., Evans SM., Development. November 1, 1995; 121 (11): 3889-99.                


Chick NKx-2.3 represents a novel family member of vertebrate homologues to the Drosophila homeobox gene tinman: differential expression of cNKx-2.3 and cNKx-2.5 during heart and gut development., Buchberger A., Mech Dev. May 1, 1996; 56 (1-2): 151-63.


A new tinman-related gene, nkx2.7, anticipates the expression of nkx2.5 and nkx2.3 in zebrafish heart and pharyngeal endoderm., Lee KH., Dev Biol. December 15, 1996; 180 (2): 722-31.


Xbap, a vertebrate gene related to bagpipe, is expressed in developing craniofacial structures and in anterior gut muscle., Newman CS., Dev Biol. January 15, 1997; 181 (2): 223-33.            


Vertebrate homologs of tinman and bagpipe: roles of the homeobox genes in cardiovascular development., Tanaka M., Dev Genet. January 1, 1998; 22 (3): 239-49.


A GATA-dependent nkx-2.5 regulatory element activates early cardiac gene expression in transgenic mice., Searcy RD., Development. November 1, 1998; 125 (22): 4461-70.


Subdivision of the cardiac Nkx2.5 expression domain into myogenic and nonmyogenic compartments., Raffin M., Dev Biol. February 15, 2000; 218 (2): 326-40.                  


BMP signaling is required for heart formation in vertebrates., Shi Y, Shi Y., Dev Biol. August 15, 2000; 224 (2): 226-37.          


Designation of the anterior/posterior axis in pregastrula Xenopus laevis., Lane MC., Dev Biol. September 1, 2000; 225 (1): 37-58.                        


Regulation of the tinman homologues in Xenopus embryos., Sparrow DB., Dev Biol. November 1, 2000; 227 (1): 65-79.      


Embryonic expression of an Nkx2-5/Cre gene using ROSA26 reporter mice., Moses KA., Genesis. December 1, 2001; 31 (4): 176-80.


Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.            


The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.                                                    


HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.                        


A crucial role of a high mobility group protein HMGA2 in cardiogenesis., Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.                  


FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.                  


Prolonged FGF signaling is necessary for lung and liver induction in Xenopus., Shifley ET., BMC Dev Biol. September 18, 2012; 12 27.                      


pdzrn3 is required for pronephros morphogenesis in Xenopus laevis., Marracci S., Int J Dev Biol. January 1, 2016; 60 (1-3): 57-63.                  


The splicing factor SRSF1 modulates pattern formation by inhibiting transcription of tissue specific genes during embryogenesis., Lee SH., Biochem Biophys Res Commun. September 2, 2016; 477 (4): 1011-1016.                


Kindlin2 regulates neural crest specification via integrin-independent regulation of the FGF signaling pathway., Wang H., Development. May 15, 2021; 148 (10):                                           


Early life exposure to perfluorooctanesulfonate (PFOS) impacts vital biological processes in Xenopus laevis: Integrated morphometric and transcriptomic analyses., Ismail T., Ecotoxicol Environ Saf. January 1, 2024; 269 115820.                      

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