Papers associated with mesoderm (and smad4.1)

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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.
	Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis., Saumweber E., Front Cell Dev Biol. January 1, 2024; 12 1316048.
	Head organizer: Cerberus and IGF cooperate in brain induction in Xenopus embryos., Azbazdar Y., Cells Dev. December 16, 2023; 203897.
	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.
	Smad2 and Smad3 differentially modulate chordin transcription via direct binding on the distal elements in gastrula Xenopus embryos., Kumar V., Biochem Biophys Res Commun. June 25, 2021; 559 168-175.
	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):
	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.
	A role for BMP-induced homeobox gene MIXL1 in acute myelogenous leukemia and identification of type I BMP receptor as a potential target for therapy., Raymond A., Oncotarget. December 30, 2014; 5 (24): 12675-93.
	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.
	The tumor suppressor Smad4/DPC4 is regulated by phosphorylations that integrate FGF, Wnt, and TGF-β signaling., Demagny H., Cell Rep. October 23, 2014; 9 (2): 688-700.
	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.
	Signaling crosstalk between TGFβ and Dishevelled/Par1b., Mamidi A., Cell Death Differ. October 1, 2012; 19 (10): 1689-97.
	Self-regulation of the head-inducing properties of the Spemann organizer., Inui M., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.
	Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.
	HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ., Genes Dev. August 1, 2011; 25 (15): 1654-61.
	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.
	Conservation and diversification of an ancestral chordate gene regulatory network for dorsoventral patterning., Kozmikova I., PLoS One. February 3, 2011; 6 (2): e14650.
	The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM., Development. June 1, 2010; 137 (11): 1919-29.
	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.
	Rab5-mediated endocytosis of activin is not required for gene activation or long-range signalling in Xenopus., Hagemann AI., Development. August 1, 2009; 136 (16): 2803-13.
	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.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	Negative regulation of Activin/Nodal signaling by SRF during Xenopus gastrulation., Yun CH., Development. February 1, 2007; 134 (4): 769-77.
	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.
	GDF3, a BMP inhibitor, regulates cell fate in stem cells and early embryos., Levine AJ., Development. January 1, 2006; 133 (2): 209-16.
	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.
	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.
	Evi3, a common retroviral integration site in murine B-cell lymphoma, encodes an EBFAZ-related Krüppel-like zinc finger protein., Warming S., Blood. March 1, 2003; 101 (5): 1934-40.
	Regulation of the Lim-1 gene is mediated through conserved FAST-1/FoxH1 sites in the first intron., Watanabe M., Dev Dyn. December 1, 2002; 225 (4): 448-56.
	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.
	TGF-beta signalling pathways in early Xenopus development., Hill CS., Curr Opin Genet Dev. October 1, 2001; 11 (5): 533-40.
	Swift is a novel BRCT domain coactivator of Smad2 in transforming growth factor beta signaling., Shimizu K., Mol Cell Biol. June 1, 2001; 21 (12): 3901-12.
	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.
	A novel smad nuclear interacting protein, SNIP1, suppresses p300-dependent TGF-beta signal transduction., Kim RH., Genes Dev. July 1, 2000; 14 (13): 1605-16.
	Cloning and characterization of zebrafish smad2, smad3 and smad4., Dick A., Gene. April 4, 2000; 246 (1-2): 69-80.
	Homeodomain and winged-helix transcription factors recruit activated Smads to distinct promoter elements via a common Smad interaction motif., Germain S., Genes Dev. February 15, 2000; 14 (4): 435-51.
	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.

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