Papers associated with brain (and smad1)

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	Xenopus mothers against decapentaplegic is an embryonic ventralizing agent that acts downstream of the BMP-2/4 receptor., Thomsen GH., Development. August 1, 1996; 122 (8): 2359-66.
	Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning., Nakayama T., Development. March 1, 1998; 125 (5): 857-67.
	Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.
	Identification of two Smad4 proteins in Xenopus. Their common and distinct properties., Masuyama N., J Biol Chem. April 23, 1999; 274 (17): 12163-70.
	Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4., Nishinakamura R., Dev Biol. December 15, 1999; 216 (2): 481-90.
	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.
	FOG acts as a repressor of red blood cell development in Xenopus., Deconinck AE., Development. May 1, 2000; 127 (10): 2031-40.
	BMP signaling is required for heart formation in vertebrates., Shi Y, Shi Y., Dev Biol. August 15, 2000; 224 (2): 226-37.
	The role of Xenopus dickkopf1 in prechordal plate specification and neural patterning., Kazanskaya O., Development. November 1, 2000; 127 (22): 4981-92.
	Neurogenin promotes neurogenesis and inhibits glial differentiation by independent mechanisms., Sun Y., Cell. February 9, 2001; 104 (3): 365-76.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
	XMAN1, an inner nuclear membrane protein, antagonizes BMP signaling by interacting with Smad1 in Xenopus embryos., Osada S., Development. May 1, 2003; 130 (9): 1783-94.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	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.
	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.
	Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition., Delaune E., Development. January 1, 2005; 132 (2): 299-310.
	Conditional BMP inhibition in Xenopus reveals stage-specific roles for BMPs in neural and neural crest induction., Wawersik S., Dev Biol. January 15, 2005; 277 (2): 425-42.
	DRAGON, a bone morphogenetic protein co-receptor., Samad TA., J Biol Chem. April 8, 2005; 280 (14): 14122-9.
	Smad1 and Smad8 function similarly in mammalian central nervous system development., Hester M., Mol Cell Biol. June 1, 2005; 25 (11): 4683-92.
	Temporal analysis of the early BMP functions identifies distinct anti-organizer and mesoderm patterning phases., Marom K., Dev Biol. June 15, 2005; 282 (2): 442-54.
	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.
	Isolation and comparative expression analysis of the Myc-regulatory proteins Mad1, Mad3, and Mnt during Xenopus development., Juergens K., Dev Dyn. August 1, 2005; 233 (4): 1554-9.
	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.
	Eye and neural defects associated with loss of GDF6., Hanel ML., BMC Dev Biol. June 6, 2006; 6 43.
	Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/Smad1 pathway., Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.
	The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
	Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.
	The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.
	Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1., Herr P., Development. May 1, 2008; 135 (10): 1813-22.
	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.
	FGF-activated calcium channels control neural gene expression in Xenopus., Lee KW., Biochim Biophys Acta. June 1, 2009; 1793 (6): 1033-40.
	Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus., Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	The role and regulation of GDF11 in Smad2 activation during tailbud formation in the Xenopus embryo., Ho DM., Mech Dev. January 1, 2010; 127 (9-12): 485-95.
	The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM., Development. June 1, 2010; 137 (11): 1919-29.
	Neuronatin promotes neural lineage in ESCs via Ca(2+) signaling., Lin HH., Stem Cells. November 1, 2010; 28 (11): 1950-60.
	Origin of muscle satellite cells in the Xenopus embryo., Daughters RS., Development. March 1, 2011; 138 (5): 821-30.
	Role of BMP, FGF, calcium signaling, and Zic proteins in vertebrate neuroectodermal differentiation., Aruga J., Neurochem Res. July 1, 2011; 36 (7): 1286-92.
	Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
	Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.
	TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network., Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
	Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.
	Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA., Development. August 1, 2012; 139 (16): 3010-20.
	BMP signal attenuates FGF pathway in anteroposterior neural patterning., Cho GS., Biochem Biophys Res Commun. May 10, 2013; 434 (3): 509-15.
	Scaling of dorsal-ventral patterning by embryo size-dependent degradation of Spemann's organizer signals., Inomata H., Cell. June 6, 2013; 153 (6): 1296-311.
	Cubilin, a high affinity receptor for fibroblast growth factor 8, is required for cell survival in the developing vertebrate head., Cases O., J Biol Chem. June 7, 2013; 288 (23): 16655-16670.
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	Simultaneous rather than ordered cleavage of two sites within the BMP4 prodomain leads to loss of ligand in mice., Tilak A., Development. August 1, 2014; 141 (15): 3062-71.

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