Papers associated with cardiovascular system (and smad2)

Limit to papers also referencing gene:
Show all cardiovascular system papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	Differential nuclear import sets the timing of protein access to the embryonic genome., Nguyen T., Nat Commun. October 6, 2022; 13 (1): 5887.
	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.
	Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
	Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing., Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.
	Dissecting BMP signaling input into the gene regulatory networks driving specification of the blood stem cell lineage., Kirmizitas A., Proc Natl Acad Sci U S A. June 6, 2017; 114 (23): 5814-5821.
	Nodal signalling in Xenopus: the role of Xnr5 in left/right asymmetry and heart development., Tadjuidje E., Open Biol. August 1, 2016; 6 (8):
	E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.
	Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression., Nelson AC., BMC Biol. October 3, 2014; 12 81.
	Stochastic specification of primordial germ cells from mesoderm precursors in axolotl embryos., Chatfield J., Development. June 1, 2014; 141 (12): 2429-40.
	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.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
	Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.
	Xenopus neurula left-right asymmetry is respeficied by microinjecting TGF-beta5 protein., Mogi K., Int J Dev Biol. February 1, 2003; 47 (1): 15-29.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	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.
	Calmodulin differentially modulates Smad1 and Smad2 signaling., Scherer A., J Biol Chem. December 29, 2000; 275 (52): 41430-8.
	Recombinant expression and purification of smad proteins., Funaba M., Protein Expr Purif. December 1, 2000; 20 (3): 507-13.
	Mesendoderm induction and reversal of left-right pattern by mouse Gdf1, a Vg1-related gene., Wall NA., Dev Biol. November 15, 2000; 227 (2): 495-509.
	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.
	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.

???pagination.result.page??? 1