Papers associated with neural tube (and fgf8)

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	ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.
	Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans., Lansdon LA., Genetics. January 1, 2018; 208 (1): 283-296.
	Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.
	Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling., Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.
	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.
	Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.
	The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.
	Transcription factor AP2 epsilon (Tfap2e) regulates neural crest specification in Xenopus., Hong CS., Dev Neurobiol. September 1, 2014; 74 (9): 894-906.
	Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
	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.
	mRNA fluorescence in situ hybridization to determine overlapping gene expression in whole-mount mouse embryos., Neufeld SJ., Dev Dyn. September 1, 2013; 242 (9): 1094-100.
	Current perspectives of the signaling pathways directing neural crest induction., Stuhlmiller TJ., Cell Mol Life Sci. November 1, 2012; 69 (22): 3715-37.
	Characterization and expressional analysis of Dleu7 during Xenopus tropicalis embryogenesis., Zhu X., Gene. November 1, 2012; 509 (1): 77-84.
	Transcription factors involved in lens development from the preplacodal ectoderm., Ogino H., Dev Biol. March 15, 2012; 363 (2): 333-47.
	Xaml1/Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus., Park BY., Dev Biol. February 1, 2012; 362 (1): 65-75.
	Mef2d acts upstream of muscle identity genes and couples lateral myogenesis to dermomyotome formation in Xenopus laevis., Della Gaspera B., PLoS One. January 1, 2012; 7 (12): e52359.
	MicroRNA-9 reveals regional diversity of neural progenitors along the anterior-posterior axis., Bonev B., Dev Cell. January 18, 2011; 20 (1): 19-32.
	Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
	Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus., Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
	Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network., Yan B., Dev Dyn. December 1, 2010; 239 (12): 3467-80.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.
	Temporal and spatial expression of FGF ligands and receptors during Xenopus development., Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.
	Mix.1/2-dependent control of FGF availability during gastrulation is essential for pronephros development in Xenopus., Colas A., Dev Biol. August 15, 2008; 320 (2): 351-65.
	The homeodomain factor Xanf represses expression of genes in the presumptive rostral forebrain that specify more caudal brain regions., Ermakova GV., Dev Biol. July 15, 2007; 307 (2): 483-97.
	Temporal requirement for bone morphogenetic proteins in regeneration of the tail and limb of Xenopus tadpoles., Beck CW., Mech Dev. September 1, 2006; 123 (9): 674-88.
	FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.
	Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development., Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
	FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	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.
	Regulated expression pattern of gremlin during zebrafish development., Nicoli S., Gene Expr Patterns. April 1, 2005; 5 (4): 539-44.
	XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis., Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.
	Neural induction requires BMP inhibition only as a late step, and involves signals other than FGF and Wnt antagonists., Linker C., Development. November 1, 2004; 131 (22): 5671-81.
	R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis., Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
	Expression patterns of Xenopus FGF receptor-like 1/nou-darake in early Xenopus development resemble those of planarian nou-darake and Xenopus FGF8., Hayashi S., Dev Dyn. August 1, 2004; 230 (4): 700-7.
	PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud., Aoto K., Dev Biol. November 15, 2002; 251 (2): 320-32.
	The homeoprotein Xiro1 is required for midbrain-hindbrain boundary formation., Glavic A., Development. April 1, 2002; 129 (7): 1609-21.
	Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo., Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.
	The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.
	Foregut endoderm is required at head process stages for anteriormost neural patterning in chick., Withington S., Development. February 1, 2001; 128 (3): 309-20.
	A developmental pathway controlling outgrowth of the Xenopus tail bud., Beck CW., Development. April 1, 1999; 126 (8): 1611-20.
	FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus., Christen B., Dev Biol. December 15, 1997; 192 (2): 455-66.

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