Papers associated with anterior (and smad3)

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	Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14., Takebayashi-Suzuki K., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.
	Conserved and novel functions of programmed cellular senescence during vertebrate development., Davaapil H., Development. January 1, 2017; 144 (1): 106-114.
	Small C-terminal Domain Phosphatase 3 Dephosphorylates the Linker Sites of Receptor-regulated Smads (R-Smads) to Ensure Transforming Growth Factor β (TGFβ)-mediated Germ Layer Induction in Xenopus Embryos., Sun G., J Biol Chem. July 10, 2015; 290 (28): 17239-49.
	Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT., Development. December 1, 2014; 141 (23): 4537-47.
	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.
	Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ., Genes Dev. August 1, 2011; 25 (15): 1654-61.
	Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus., Smith SJ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.
	The function of heterodimeric AP-1 comprised of c-Jun and c-Fos in activin mediated Spemann organizer gene expression., Lee SY., PLoS One. January 1, 2011; 6 (7): e21796.
	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.
	Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	deltaEF1 and SIP1 are differentially expressed and have overlapping activities during Xenopus embryogenesis., van Grunsven LA., Dev Dyn. June 1, 2006; 235 (6): 1491-500.
	The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo., Collart C., Development. October 1, 2005; 132 (20): 4575-86.
	Smad2 and Smad3 coordinately regulate craniofacial and endodermal development., Liu Y., Dev Biol. June 15, 2004; 270 (2): 411-26.
	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.
	Bone morphogenetic protein-4-induced activation of Xretpos is mediated by Smads and Olf-1/EBF associated zinc finger (OAZ)., Shim S., Nucleic Acids Res. July 15, 2002; 30 (14): 3107-17.
	The role of a Williams-Beuren syndrome-associated helix-loop-helix domain-containing transcription factor in activin/nodal signaling., Ring C., Genes Dev. April 1, 2002; 16 (7): 820-35.
	Xenopus Smad3 is specifically expressed in the chordoneural hinge, notochord and in the endocardium of the developing heart., Howell M., Mech Dev. June 1, 2001; 104 (1-2): 147-50.
	Nodal signaling uses activin and transforming growth factor-beta receptor-regulated Smads., Kumar A., J Biol Chem. January 5, 2001; 276 (1): 656-61.

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