Papers associated with cardiac mesoderm (and pax3)

Limit to papers also referencing gene:
Show all cardiac mesoderm papers

???pagination.result.count???

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

Sort Newest To Oldest

Sort Oldest To Newest

	The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
	The RNA-binding protein Rbm24 is transiently expressed in myoblasts and is required for myogenic differentiation during vertebrate development., Grifone R., Mech Dev. November 1, 2014; 134 1-15.
	5-Mehtyltetrahydrofolate rescues alcohol-induced neural crest cell migration abnormalities., Shi Y, Shi Y., Mol Brain. September 16, 2014; 7 67.
	Evolutionarily conserved morphogenetic movements at the vertebrate head-trunk interface coordinate the transport and assembly of hypopharyngeal structures., Lours-Calet C., Dev Biol. June 15, 2014; 390 (2): 231-46.
	Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
	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.
	Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.
	Xenopus reduced folate carrier regulates neural crest development epigenetically., Li J., PLoS One. January 1, 2011; 6 (11): e27198.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Expression analysis of Runx3 and other Runx family members during Xenopus development., Park BY., Gene Expr Patterns. June 1, 2010; 10 (4-5): 159-66.
	The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.
	Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.
	Cardiovascular development and the colonizing cardiac neural crest lineage., Snider P., ScientificWorldJournal. July 3, 2007; 7 1090-113.
	XHas2 activity is required during somitogenesis and precursor cell migration in Xenopus development., Ori M., Development. February 1, 2006; 133 (4): 631-40.
	Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome., Pizzuti A., Am J Hum Genet. April 1, 1996; 58 (4): 722-9.

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