Papers associated with ectoderm∨derBy=4 (and smad4)

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	Highly conserved and extremely evolvable: BMP signalling in secondary axis patterning of Cnidaria and Bilateria., Mörsdorf D., Dev Genes Evol. March 13, 2024;
	ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.
	Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis., Saumweber E., Front Cell Dev Biol. January 1, 2024; 12 1316048.
	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.
	HMCES modulates the transcriptional regulation of nodal/activin and BMP signaling in mESCs., Liang T., Cell Rep. July 12, 2022; 40 (2): 111038.
	Signaling Control of Mucociliary Epithelia: Stem Cells, Cell Fates, and the Plasticity of Cell Identity in Development and Disease., Walentek P., Cells Tissues Organs. January 1, 2022; 211 (6): 736-753.
	Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage., Castro Colabianchi AM., Biol Open. February 25, 2021; 10 (2):
	Dusp1 modulates activin/smad2 mediated germ layer specification via FGF signal inhibition in Xenopus embryos., Umair Z., Anim Cells Syst (Seoul). November 27, 2020; 24 (6): 359-370.
	Tbx2 mediates dorsal patterning and germ layer suppression through inhibition of BMP/GDF and Activin/Nodal signaling., Reich S., BMC Mol Cell Biol. May 28, 2020; 21 (1): 39.
	Repression of Inappropriate Gene Expression in the Vertebrate Embryonic Ectoderm., Reich S., Genes (Basel). November 6, 2019; 10 (11):
	Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus., Watanabe T., Development. October 26, 2018; 145 (20):
	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.
	Identification of p62/SQSTM1 as a component of non-canonical Wnt VANGL2-JNK signalling in breast cancer., Puvirajesinghe TM., Nat Commun. January 12, 2016; 7 10318.
	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.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus., Young JJ., Development. April 1, 2014; 141 (8): 1683-93.
	A potential molecular pathogenesis of cardiac/laterality defects in Oculo-Facio-Cardio-Dental syndrome., Tanaka K., Dev Biol. March 1, 2014; 387 (1): 28-36.
	Dynamics of TGF-β signaling reveal adaptive and pulsatile behaviors reflected in the nuclear localization of transcription factor Smad4., Warmflash A., Proc Natl Acad Sci U S A. July 10, 2012; 109 (28): E1947-56.
	Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.
	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.
	ZFP423 coordinates Notch and bone morphogenetic protein signaling, selectively up-regulating Hes5 gene expression., Masserdotti G., J Biol Chem. October 1, 2010; 285 (40): 30814-24.
	TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y., Mol Cell. January 15, 2010; 37 (1): 123-34.
	A crucial role of a high mobility group protein HMGA2 in cardiogenesis., Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	Negative regulation of Activin/Nodal signaling by SRF during Xenopus gastrulation., Yun CH., Development. February 1, 2007; 134 (4): 769-77.
	The MH1 domain of Smad3 interacts with Pax6 and represses autoregulation of the Pax6 P1 promoter., Grocott T., Nucleic Acids Res. January 1, 2007; 35 (3): 890-901.
	Function of the two Xenopus smad4s in early frog development., Chang C., J Biol Chem. October 13, 2006; 281 (41): 30794-803.
	Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.
	XBP1 forms a regulatory loop with BMP-4 and suppresses mesodermal and neural differentiation in Xenopus embryos., Cao Y, Cao Y., Mech Dev. January 1, 2006; 123 (1): 84-96.
	The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo., Collart C., Development. October 1, 2005; 132 (20): 4575-86.
	Notch signaling modulates the nuclear localization of carboxy-terminal-phosphorylated smad2 and controls the competence of ectodermal cells for activin A., Abe T., Mech Dev. May 1, 2005; 122 (5): 671-80.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1., Baldessari D., BMC Cell Biol. December 21, 2004; 5 (1): 48.
	The POU factor Oct-25 regulates the Xvent-2B gene and counteracts terminal differentiation in Xenopus embryos., Cao Y, Cao Y., J Biol Chem. October 15, 2004; 279 (42): 43735-43.
	Evidence for antagonism of BMP-4 signals by MAP kinase during Xenopus axis determination and neural specification., Sater AK., Differentiation. September 1, 2003; 71 (7): 434-44.
	Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
	A novel Xenopus Smad-interacting forkhead transcription factor (XFast-3) cooperates with XFast-1 in regulating gastrulation movements., Howell M., Development. June 1, 2002; 129 (12): 2823-34.
	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.
	Ski represses bone morphogenic protein signaling in Xenopus and mammalian cells., Wang W., Proc Natl Acad Sci U S A. December 19, 2000; 97 (26): 14394-9.
	Cloning and characterization of zebrafish smad2, smad3 and smad4., Dick A., Gene. April 4, 2000; 246 (1-2): 69-80.
	OAZ uses distinct DNA- and protein-binding zinc fingers in separate BMP-Smad and Olf signaling pathways., Hata A., Cell. January 21, 2000; 100 (2): 229-40.
	FAST-1 is a key maternal effector of mesoderm inducers in the early Xenopus embryo., Watanabe M., Development. December 1, 1999; 126 (24): 5621-34.
	Identification of two Smad4 proteins in Xenopus. Their common and distinct properties., Masuyama N., J Biol Chem. April 23, 1999; 274 (17): 12163-70.
	A mouse homologue of FAST-1 transduces TGF beta superfamily signals and is expressed during early embryogenesis., Weisberg E., Mech Dev. December 1, 1998; 79 (1-2): 17-27.
	Failure of egg cylinder elongation and mesoderm induction in mouse embryos lacking the tumor suppressor smad2., Weinstein M., Proc Natl Acad Sci U S A. August 4, 1998; 95 (16): 9378-83.
	Identification of receptors and Smad proteins involved in activin signalling in a human epidermal keratinocyte cell line., Shimizu A., Genes Cells. February 1, 1998; 3 (2): 125-34.
	Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.
	Smad5 induces ventral fates in Xenopus embryo., Suzuki A., Dev Biol. April 15, 1997; 184 (2): 402-5.

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