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Summary Anatomy Item Literature (1422) Expression Attributions Wiki
XB-ANAT-206

Papers associated with blastopore (and tubb2b)

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TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9                                                                                           


Evolution of the Rho guanine nucleotide exchange factors Kalirin and Trio and their gene expression in Xenopus development., Kratzer MC., Gene Expr Patterns. June 1, 2019; 32 18-27.                              


Xenopus slc7a5 is essential for notochord function and eye development., Katada T., Mech Dev. February 1, 2019; 155 48-59.                


Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation., Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.                      


Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14., Takebayashi-Suzuki K., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.          


N1-Src Kinase Is Required for Primary Neurogenesis in Xenopus tropicalis., Lewis PA., J Neurosci. August 30, 2017; 37 (35): 8477-8485.          


Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.                                


sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis., Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.                                    


Tbx3 represses bmp4 expression and, with Pax6, is required and sufficient for retina formation., Motahari Z., Development. October 1, 2016; 143 (19): 3560-3572.                                      


A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT., Gao L., Development. February 1, 2016; 143 (3): 492-503.                            


Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  


The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.                                    


Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S., Development. December 1, 2014; 141 (24): 4794-805.                            


The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.                                          


FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.                              


Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein., Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.                              


NumbL is essential for Xenopus primary neurogenesis., Nieber F., BMC Dev Biol. October 14, 2013; 13 36.                          


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


Identification and characterization of ADAM41, a novel ADAM metalloproteinase in Xenopus., Xu G., Int J Dev Biol. January 1, 2012; 56 (5): 333-9.          


Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.                  


Delta-Notch signaling is involved in the segregation of the three germ layers in Xenopus laevis., Revinski DR., Dev Biol. March 15, 2010; 339 (2): 477-92.            


Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.                


Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos., Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.              


Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.                      


Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.              


A new triple staining method for double in situ hybridization in combination with cell lineage tracing in whole-mount Xenopus embryos., Koga M., Dev Growth Differ. October 1, 2007; 49 (8): 635-45.            


Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.                            


FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.            


Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.                


Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.                    


Xenopus Nbx, a novel NK-1 related gene essential for neural crest formation., Kurata T., Dev Biol. May 1, 2003; 257 (1): 30-40.                


XETOR regulates the size of the proneural domain during primary neurogenesis in Xenopus laevis., Cao Y., Mech Dev. November 1, 2002; 119 (1): 35-44.                      


foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.            


Gli2 functions in FGF signaling during antero-posterior patterning., Brewster R., Development. October 1, 2000; 127 (20): 4395-405.            


Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y., J Neurosci. November 1, 1999; 19 (21): 9364-73.          


A two-step mechanism generates the spacing pattern of the ciliated cells in the skin of Xenopus embryos., Deblandre GA., Development. November 1, 1999; 126 (21): 4715-28.                  


Geminin, a neuralizing molecule that demarcates the future neural plate at the onset of gastrulation., Kroll KL., Development. August 1, 1998; 125 (16): 3247-58.                


Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.              


Differential expression of nucleoside diphosphate kinases (NDPK/NM23) during Xenopus early development., Ouatas T., Int J Dev Biol. January 1, 1998; 42 (1): 43-52.              


The role of F-cadherin in localizing cells during neural tube formation in Xenopus embryos., Espeseth A., Development. January 1, 1998; 125 (2): 301-12.                    


Sizzled: a secreted Xwnt8 antagonist expressed in the ventral marginal zone of Xenopus embryos., Salic AN., Development. December 1, 1997; 124 (23): 4739-48.              


X-MyT1, a Xenopus C2HC-type zinc finger protein with a regulatory function in neuronal differentiation., Bellefroid EJ., Cell. December 27, 1996; 87 (7): 1191-202.              


The role of vertical and planar signals during the early steps of neural induction., Grunz H., Int J Dev Biol. June 1, 1995; 39 (3): 539-43.  


Overexpression of a cellular retinoic acid binding protein (xCRABP) causes anteroposterior defects in developing Xenopus embryos., Dekker EJ., Development. April 1, 1994; 120 (4): 973-85.                

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