Papers associated with ventral (and smad1)

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	Xenopus Mad proteins transduce distinct subsets of signals for the TGF beta superfamily., Graff JM., Cell. May 17, 1996; 85 (4): 479-87.
	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.
	The tumor suppressor Smad4/DPC 4 as a central mediator of Smad function., Zhang Y., Curr Biol. April 1, 1997; 7 (4): 270-6.
	Bmp-4 acts as a morphogen in dorsoventral mesoderm patterning in Xenopus., Dosch R., Development. June 1, 1997; 124 (12): 2325-34.
	Xenopus FK 506-binding protein homolog induces a secondary axis in frog embryos, which is inhibited by coexisting BMP 4 signaling., Nishinakamura R., Biochem Biophys Res Commun. October 20, 1997; 239 (2): 585-91.
	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.
	Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.
	Role of TAK1 and TAB1 in BMP signaling in early Xenopus development., Shibuya H., EMBO J. February 16, 1998; 17 (4): 1019-28.
	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.
	Smad6 functions as an intracellular antagonist of some TGF-beta family members during Xenopus embryogenesis., Nakayama T., Genes Cells. June 1, 1998; 3 (6): 387-94.
	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.
	Ventral and lateral regions of the zebrafish gastrula, including the neural crest progenitors, are established by a bmp2b/swirl pathway of genes., Nguyen VH., Dev Biol. July 1, 1998; 199 (1): 93-110.
	Smad7 inhibits mesoderm formation and promotes neural cell fate in Xenopus embryos., Bhushan A., Dev Biol. August 15, 1998; 200 (2): 260-8.
	Cloning of Mix-related homeodomain proteins using fast retrieval of gel shift activities, (FROGS), a technique for the isolation of DNA-binding proteins., Mead PE., Proc Natl Acad Sci U S A. September 15, 1998; 95 (19): 11251-6.
	Physical and functional interaction of murine and Xenopus Smad7 with bone morphogenetic protein receptors and transforming growth factor-beta receptors., Souchelnytskyi S., J Biol Chem. September 25, 1998; 273 (39): 25364-70.
	Identification of two Smad4 proteins in Xenopus. Their common and distinct properties., Masuyama N., J Biol Chem. April 23, 1999; 274 (17): 12163-70.
	Functional analysis of human Smad1: role of the amino-terminal domain., Xu RH., Biochem Biophys Res Commun. May 10, 1999; 258 (2): 366-73.
	A role for the homeobox gene Xvex-1 as part of the BMP-4 ventral signaling pathway., Shapira E., Mech Dev. August 1, 1999; 86 (1-2): 99-111.
	Characterization of zebrafish smad1, smad2 and smad5: the amino-terminus of smad1 and smad5 is required for specific function in the embryo., Müller F., Mech Dev. October 1, 1999; 88 (1): 73-88.
	Cardiac looping and the vertebrate left-right axis: antagonism of left-sided Vg1 activity by a right-sided ALK2-dependent BMP pathway., Ramsdell AF., Development. December 1, 1999; 126 (23): 5195-205.
	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.
	FOG acts as a repressor of red blood cell development in Xenopus., Deconinck AE., Development. May 1, 2000; 127 (10): 2031-40.
	Phenotypic effects in Xenopus and zebrafish suggest that one-eyed pinhead functions as antagonist of BMP signalling., Kiecker C., Mech Dev. June 1, 2000; 94 (1-2): 37-46.
	Endogenous patterns of TGFbeta superfamily signaling during early Xenopus development., Faure S., Development. July 1, 2000; 127 (13): 2917-31.
	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.
	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.
	Calmodulin differentially modulates Smad1 and Smad2 signaling., Scherer A., J Biol Chem. December 29, 2000; 275 (52): 41430-8.
	Suppression of head formation by Xmsx-1 through the inhibition of intracellular nodal signaling., Yamamoto TS., Development. July 1, 2001; 128 (14): 2769-79.
	Timing of endogenous activin-like signals and regional specification of the Xenopus embryo., Lee MA., Development. August 1, 2001; 128 (15): 2939-52.
	The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud., Beck CW., Dev Biol. October 15, 2001; 238 (2): 303-14.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	Autoregulation of Xvent-2B; direct interaction and functional cooperation of Xvent-2 and Smad1., Henningfeld KA., J Biol Chem. January 18, 2002; 277 (3): 2097-103.
	Action range of BMP is defined by its N-terminal basic amino acid core., Ohkawara B., Curr Biol. February 5, 2002; 12 (3): 205-9.
	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.
	Cooperative inhibition of bone morphogenetic protein signaling by Smurf1 and inhibitory Smads., Murakami G., Mol Biol Cell. July 1, 2003; 14 (7): 2809-17.
	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.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	Dorsal-ventral patterning and neural induction in Xenopus embryos., De Robertis EM., Annu Rev Cell Dev Biol. January 1, 2004; 20 285-308.
	Interaction with Smad4 is indispensable for suppression of BMP signaling by c-Ski., Takeda M., Mol Biol Cell. March 1, 2004; 15 (3): 963-72.
	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.
	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.
	Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation., Daniels M., Development. November 1, 2004; 131 (22): 5613-26.
	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.
	The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.
	BMP4-dependent expression of Xenopus Grainyhead-like 1 is essential for epidermal differentiation., Tao J., Development. March 1, 2005; 132 (5): 1021-34.
	Functional specificity of the Xenopus T-domain protein Brachyury is conferred by its ability to interact with Smad1., Messenger NJ., Dev Cell. April 1, 2005; 8 (4): 599-610.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.

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