Papers associated with somite (and krt12.4)

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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.
	Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
	Maternal Wnt11b regulates cortical rotation during Xenopus axis formation: analysis of maternal-effect wnt11b mutants., Houston DW., Development. September 1, 2022; 149 (17):
	BMP signaling is enhanced intracellularly by FHL3 controlling WNT-dependent spatiotemporal emergence of the neural crest., Alkobtawi M., Cell Rep. June 22, 2021; 35 (12): 109289.
	Xenopus slc7a5 is essential for notochord function and eye development., Katada T., Mech Dev. February 1, 2019; 155 48-59.
	PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation., Figueiredo AL., Development. November 15, 2017; 144 (22): 4183-4194.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	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.
	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.
	Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
	Developmental expression and role of Kinesin Eg5 during Xenopus laevis embryogenesis., Fernández JP., Dev Dyn. April 1, 2014; 243 (4): 527-40.
	Two different vestigial like 4 genes are differentially expressed during Xenopus laevis development., Barrionuevo MG., Int J Dev Biol. January 1, 2014; 58 (5): 369-77.
	NumbL is essential for Xenopus primary neurogenesis., Nieber F., BMC Dev Biol. October 14, 2013; 13 36.
	Indian hedgehog signaling is required for proper formation, maintenance and migration of Xenopus neural crest., Agüero TH., Dev Biol. April 15, 2012; 364 (2): 99-113.
	The LIM adaptor protein LMO4 is an essential regulator of neural crest development., Ochoa SD., Dev Biol. January 15, 2012; 361 (2): 313-25.
	The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos., Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.
	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 role for the Endothelin-1/Endothelin-A receptor signaling during early neural crest specification., Bonano M., Dev Biol. November 1, 2008; 323 (1): 114-29.
	The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo., Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.
	The role of the Spemann organizer in anterior-posterior patterning of the trunk., Jansen HJ., Mech Dev. January 1, 2007; 124 (9-10): 668-81.
	Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field., Reversade B., Cell. December 16, 2005; 123 (6): 1147-60.
	Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK., Dev Cell. March 1, 2005; 8 (3): 401-11.
	BMP4-dependent expression of Xenopus Grainyhead-like 1 is essential for epidermal differentiation., Tao J., Development. March 1, 2005; 132 (5): 1021-34.
	Specification of the enveloping layer and lack of autoneuralization in zebrafish embryonic explants., Sagerström CG., Dev Dyn. January 1, 2005; 232 (1): 85-97.
	Tsukushi functions as an organizer inducer by inhibition of BMP activity in cooperation with chordin., Ohta K., Dev Cell. September 1, 2004; 7 (3): 347-358.
	Patterning and tissue movements in a novel explant preparation of the marginal zone of Xenopus laevis., Davidson LA., Gene Expr Patterns. July 1, 2004; 4 (4): 457-66.
	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.
	Regulation of Msx genes by a Bmp gradient is essential for neural crest specification., Tribulo C., Development. December 1, 2003; 130 (26): 6441-52.
	Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.
	Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
	Laser-mediated microdissection of paraffin sections from Xenopus embryos allows detection of tissue-specific expressed mRNAs., Imamichi Y., Dev Genes Evol. July 1, 2001; 211 (7): 361-6.
	Distinct effects of XBF-1 in regulating the cell cycle inhibitor p27(XIC1) and imparting a neural fate., Hardcastle Z., Development. March 1, 2000; 127 (6): 1303-14.
	Neural tube closure in Xenopus laevis involves medial migration, directed protrusive activity, cell intercalation and convergent extension., Davidson LA., Development. October 1, 1999; 126 (20): 4547-56.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	Xenopus Zic family and its role in neural and neural crest development., Nakata K., Mech Dev. July 1, 1998; 75 (1-2): 43-51.
	The homeobox gene PV.1 mediates specification of the prospective neural ectoderm in Xenopus embryos., Ault KT., Dev Biol. December 1, 1997; 192 (1): 162-71.
	Differential expression of Xenopus ribosomal protein gene XlrpS1c., Scholnick J., Biochim Biophys Acta. October 9, 1997; 1354 (1): 72-82.
	Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos., Coffman CR., Cell. May 21, 1993; 73 (4): 659-71.
	Distinct distribution of vimentin and cytokeratin in Xenopus oocytes and early embryos., Torpey NP., J Cell Sci. January 1, 1992; 101 ( Pt 1) 151-60.
	Expression of intermediate filament proteins during development of Xenopus laevis. I. cDNA clones encoding different forms of vimentin., Herrmann H., Development. February 1, 1989; 105 (2): 279-98.
	A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus., Dent JA., Development. January 1, 1989; 105 (1): 61-74.
	Immunocytochemical identification of non-neuronal intermediate filament proteins in the developing Xenopus laevis nervous system., Szaro BG., Dev Biol. October 1, 1988; 471 (2): 207-24.
	Expression of Xenopus N-CAM RNA in ectoderm is an early response to neural induction., Kintner CR., Development. March 1, 1987; 99 (3): 311-25.
	The appearance and distribution of intermediate filament proteins during differentiation of the central nervous system, skin and notochord of Xenopus laevis., Godsave SF., J Embryol Exp Morphol. September 1, 1986; 97 201-23.
	Cell type-specific expression of nuclear lamina proteins during development of Xenopus laevis., Benavente R., Cell. May 1, 1985; 41 (1): 177-90.

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