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Summary Expression Phenotypes Gene Literature (91) GO Terms (12) Nucleotides (174) Proteins (66) Interactants (795) Wiki
XB--484864

Papers associated with sox17b.1 (and morpholino)



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Mezzo, a paired-like homeobox protein is an immediate target of Nodal signalling and regulates endoderm specification in zebrafish., Poulain M, Lepage T., Development. November 1, 2002; 129 (21): 4901-14.


Xhex-expressing endodermal tissues are essential for anterior patterning in Xenopus., Smithers LE, Jones CM., Mech Dev. December 1, 2002; 119 (2): 191-200.            


The secreted Frizzled-related protein Sizzled functions as a negative feedback regulator of extreme ventral mesoderm., Collavin L, Kirschner MW., Development. February 1, 2003; 130 (4): 805-16.        


The secreted Frizzled-related protein Sizzled functions as a negative feedback regulator of extreme ventral mesoderm., Collavin L, Kirschner MW., Development. February 1, 2003; 130 (4): 805-16.        


Redundant early and overlapping larval roles of Xsox17 subgroup genes in Xenopus endoderm development., Clements D, Cameleyre I, Woodland HR., Mech Dev. March 1, 2003; 120 (3): 337-48.            


PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J, Wu J, Tan C, Klein PS., Development. December 1, 2003; 130 (23): 5569-78.            


Repression of nodal expression by maternal B1-type SOXs regulates germ layer formation in Xenopus and zebrafish., Zhang C, Basta T, Hernandez-Lagunas L, Simpson P, Stemple DL, Artinger KB, Klymkowsky MW., Dev Biol. September 1, 2004; 273 (1): 23-37.


A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y, Smith JC., Dev Biol. September 15, 2004; 273 (2): 210-25.                      


The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo., Collart C, Verschueren K, Rana A, Smith JC, Huylebroeck D., Development. October 1, 2005; 132 (20): 4575-86.        


SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C, Basta T, Klymkowsky MW., Dev Dyn. December 1, 2005; 234 (4): 878-91.                    


Negative regulation of Activin/Nodal signaling by SRF during Xenopus gastrulation., Yun CH, Choi SC, Park E, Kim SJ, Chung AS, Lee HK, Lee HK, Lee HJ, Lee HJ, Han JK., Development. February 1, 2007; 134 (4): 769-77.              


Bmp signaling is necessary and sufficient for ventrolateral endoderm specification in Xenopus., Wills A, Dickinson K, Khokha M, Baker JC., Dev Dyn. August 1, 2008; 237 (8): 2177-86.      


Bmp signaling is necessary and sufficient for ventrolateral endoderm specification in Xenopus., Wills A, Dickinson K, Khokha M, Baker JC., Dev Dyn. August 1, 2008; 237 (8): 2177-86.      


Identification of a novel negative regulator of activin/nodal signaling in mesendodermal formation of Xenopus embryos., Cheong SM, Kim H, Han JK., J Biol Chem. June 19, 2009; 284 (25): 17052-60.                        


A conserved mechanism for vertebrate mesoderm specification in urodele amphibians and mammals., Swiers G, Chen YH, Johnson AD, Loose M., Dev Biol. July 1, 2010; 343 (1-2): 138-52.                              


Geminin cooperates with Polycomb to restrain multi-lineage commitment in the early embryo., Lim JW, Hummert P, Mills JC, Kroll KL., Development. January 1, 2011; 138 (1): 33-44.                    


HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ, Wills AE, Chuong E, Gupta R, Baker JC., Genes Dev. August 1, 2011; 25 (15): 1654-61.            


HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ, Wills AE, Chuong E, Gupta R, Baker JC., Genes Dev. August 1, 2011; 25 (15): 1654-61.            


fus/TLS orchestrates splicing of developmental regulators during gastrulation., Dichmann DS, Harland RM., Genes Dev. June 15, 2012; 26 (12): 1351-63.                        


fus/TLS orchestrates splicing of developmental regulators during gastrulation., Dichmann DS, Harland RM., Genes Dev. June 15, 2012; 26 (12): 1351-63.                        


Klf4 is required for germ-layer differentiation and body axis patterning during Xenopus embryogenesis., Cao Q, Zhang X, Lu L, Yang L, Gao J, Gao Y, Ma H, Cao Y., Development. November 1, 2012; 139 (21): 3950-61.                  


Lin28 proteins are required for germ layer specification in Xenopus., Faas L, Warrander FC, Maguire R, Ramsbottom SA, Quinn D, Genever P, Isaacs HV., Development. March 1, 2013; 140 (5): 976-86.                      


Lin28 proteins are required for germ layer specification in Xenopus., Faas L, Warrander FC, Maguire R, Ramsbottom SA, Quinn D, Genever P, Isaacs HV., Development. March 1, 2013; 140 (5): 976-86.                      


Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling., Bates TJ, Vonica A, Heasman J, Brivanlou AH, Bell E., Development. October 1, 2013; 140 (20): 4177-81.              


Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling., Bates TJ, Vonica A, Heasman J, Brivanlou AH, Bell E., Development. October 1, 2013; 140 (20): 4177-81.              


Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I, Le Bouffant R, Futel M, Riou JF, Umbhauer M., Dev Biol. January 15, 2015; 397 (2): 175-90.                            

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