Papers associated with primordium (and sox3)

Limit to papers also referencing gene:
Show all primordium papers

???pagination.result.count???

???pagination.result.page??? 1 2 ???pagination.result.next???

Sort Newest To Oldest

Sort Oldest To Newest

	Phenotype-genotype relationships in Xenopus sox9 crispants provide insights into campomelic dysplasia and vertebrate jaw evolution., Hossain N., Dev Growth Differ. October 1, 2023; 65 (8): 481-497.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
	Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3., Juraver-Geslin HA., Genesis. February 1, 2015; 53 (2): 203-24.
	Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
	The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.
	The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube., Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.
	Early embryonic specification of vertebrate cranial placodes., Schlosser G., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
	NumbL is essential for Xenopus primary neurogenesis., Nieber F., BMC Dev Biol. October 14, 2013; 13 36.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	sox4 and sox11 function during Xenopus laevis eye development., Cizelsky W., PLoS One. July 1, 2013; 8 (7): e69372.
	Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene., Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
	Xmab21l3 mediates dorsoventral patterning in Xenopus laevis., Sridharan J., Mech Dev. July 1, 2012; 129 (5-8): 136-46.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.
	Short chain dehydrogenase/reductase rdhe2 is a novel retinol dehydrogenase essential for frog embryonic development., Belyaeva OV., J Biol Chem. March 16, 2012; 287 (12): 9061-71.
	The RNA-binding protein XSeb4R regulates maternal Sox3 at the posttranscriptional level during maternal-zygotic transition in Xenopus., Bentaya S., Dev Biol. March 15, 2012; 363 (2): 362-72.
	Expression of periostin during Xenopus laevis embryogenesis., Tao S., Dev Genes Evol. October 1, 2011; 221 (4): 247-54.
	Over-expression of atf4 in Xenopus embryos interferes with neurogenesis and eye formation., Liu JT., Dongwuxue Yanjiu. October 1, 2011; 32 (5): 485-91.
	Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53., Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.
	Xenopus laevis insulin receptor substrate IRS-1 is important for eye development., Bugner V., Dev Dyn. July 1, 2011; 240 (7): 1705-15.
	Peter Pan functions independently of its role in ribosome biogenesis during early eye and craniofacial cartilage development in Xenopus laevis., Bugner V., Development. June 1, 2011; 138 (11): 2369-78.
	Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus., Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
	Histone XH2AX is required for Xenopus anterior neural development: critical role of threonine 16 phosphorylation., Lee SY., J Biol Chem. September 17, 2010; 285 (38): 29525-34.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	FMR1/FXR1 and the miRNA pathway are required for eye and neural crest development., Gessert S., Dev Biol. May 1, 2010; 341 (1): 222-35.
	Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis., Illes JC., Dev Dyn. January 1, 2009; 238 (1): 194-203.
	Xenopus Sox3 activates sox2 and geminin and indirectly represses Xvent2 expression to induce neural progenitor formation at the expense of non-neural ectodermal derivatives., Rogers CD., Mech Dev. January 1, 2009; 126 (1-2): 42-55.
	Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.
	Evolution of non-coding regulatory sequences involved in the developmental process: reflection of differential employment of paralogous genes as highlighted by Sox2 and group B1 Sox genes., Kamachi Y., Proc Jpn Acad Ser B Phys Biol Sci. January 1, 2009; 85 (2): 55-68.
	Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
	Hairy2 functions through both DNA-binding and non DNA-binding mechanisms at the neural plate border in Xenopus., Nichane M., Dev Biol. October 15, 2008; 322 (2): 368-80.
	Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning., Ambrosio AL., Dev Cell. August 1, 2008; 15 (2): 248-60.
	The lens-regenerating competence in the outer cornea and epidermis of larval Xenopus laevis is related to pax6 expression., Gargioli C., J Anat. May 1, 2008; 212 (5): 612-20.
	PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
	FoxN3 is required for craniofacial and eye development of Xenopus laevis., Schuff M., Dev Dyn. January 1, 2007; 236 (1): 226-39.
	Expression of Sox1 during Xenopus early embryogenesis., Nitta KR., Biochem Biophys Res Commun. December 8, 2006; 351 (1): 287-93.
	Neural induction in Xenopus requires inhibition of Wnt-beta-catenin signaling., Heeg-Truesdell E., Dev Biol. October 1, 2006; 298 (1): 71-86.
	Isolation and characterization of a novel gene, xMADML, involved in Xenopus laevis eye development., Elkins MB., Dev Dyn. July 1, 2006; 235 (7): 1845-57.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	A dominant-negative form of the E3 ubiquitin ligase Cullin-1 disrupts the correct allocation of cell fate in the neural crest lineage., Voigt J., Development. February 1, 2006; 133 (3): 559-68.
	Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis., Ahrens K., Dev Biol. December 1, 2005; 288 (1): 40-59.
	Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.
	Inhibition of neurogenesis by SRp38, a neuroD-regulated RNA-binding protein., Liu KJ, Liu KJ., Development. April 1, 2005; 132 (7): 1511-23.
	Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
	Systematic screening for genes specifically expressed in the anterior neuroectoderm during early Xenopus development., Takahashi N., Int J Dev Biol. January 1, 2005; 49 (8): 939-51.
	A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y., Dev Biol. September 15, 2004; 273 (2): 210-25.
	Molecular anatomy of placode development in Xenopus laevis., Schlosser G., Dev Biol. July 15, 2004; 271 (2): 439-66.
	Connective-tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex., Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.
	Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation., Leise WF., Development. April 1, 2004; 131 (8): 1703-15.
	Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.

???pagination.result.page??? 1 2 ???pagination.result.next???