Papers associated with lateral (and nkx2-5)

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	Normal Table of Xenopus development: a new graphical resource., Zahn N., Development. July 15, 2022; 149 (14):
	Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism., Vick P., Genes (Basel). November 24, 2021; 12 (12):
	Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
	Kindlin2 regulates neural crest specification via integrin-independent regulation of the FGF signaling pathway., Wang H., Development. May 15, 2021; 148 (10):
	Amphibian thalamic nuclear organization during larval development and in the adult frog Xenopus laevis: Genoarchitecture and hodological analysis., Morona R., J Comp Neurol. October 1, 2020; 528 (14): 2361-2403.
	Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation., Nasr T., Dev Cell. December 16, 2019; 51 (6): 665-674.e6.
	Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis., Schwenty-Lara J., Dev Dyn. June 1, 2019; 248 (6): 465-476.
	The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.
	RPSA, a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in Xenopus., Griffin JN., Development. October 18, 2018; 145 (20):
	Frizzled-7 is required for Xenopus heart development., Abu-Elmagd M., Biol Open. December 15, 2017; 6 (12): 1861-1868.
	Coordinating heart morphogenesis: A novel role for hyperpolarization-activated cyclic nucleotide-gated (HCN) channels during cardiogenesis in Xenopus laevis., Pitcairn E., Commun Integr Biol. May 10, 2017; 10 (3): e1309488.
	The CapZ interacting protein Rcsd1 is required for cardiogenesis downstream of Wnt11a in Xenopus laevis., Hempel A., Dev Biol. April 1, 2017; 424 (1): 28-39.
	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	The splicing factor SRSF1 modulates pattern formation by inhibiting transcription of tissue specific genes during embryogenesis., Lee SH., Biochem Biophys Res Commun. September 2, 2016; 477 (4): 1011-1016.
	A Retinoic Acid-Hedgehog Cascade Coordinates Mesoderm-Inducing Signals and Endoderm Competence during Lung Specification., Rankin SA, Rankin SA., Cell Rep. June 28, 2016; 16 (1): 66-78.
	pdzrn3 is required for pronephros morphogenesis in Xenopus laevis., Marracci S., Int J Dev Biol. January 1, 2016; 60 (1-3): 57-63.
	The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
	Tcf21 regulates the specification and maturation of proepicardial cells., Tandon P., Development. June 1, 2013; 140 (11): 2409-21.
	Islet1-expressing cardiac progenitor cells: a comparison across species., Pandur P., Dev Genes Evol. March 1, 2013; 223 (1-2): 117-29.
	Regulation of primitive hematopoiesis by class I histone deacetylases., Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.
	Prolonged FGF signaling is necessary for lung and liver induction in Xenopus., Shifley ET., BMC Dev Biol. September 18, 2012; 12 27.
	Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT., Genesis. August 1, 2010; 48 (8): 492-504.
	FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.
	Neural ectoderm-secreted FGF initiates the expression of Nkx2.5 in cardiac progenitors via a p38 MAPK/CREB pathway., Keren-Politansky A., Dev Biol. November 15, 2009; 335 (2): 374-84.
	Retinoic acid regulates anterior-posterior patterning within the lateral plate mesoderm of Xenopus., Deimling SJ., Mech Dev. October 1, 2009; 126 (10): 913-23.
	Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.
	Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1., Movassagh M., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.
	IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W., Nature. July 17, 2008; 454 (7202): 345-9.
	XHAPLN3 plays a key role in cardiogenesis by maintaining the hyaluronan matrix around heart anlage., Ito Y., Dev Biol. July 1, 2008; 319 (1): 34-45.
	A crucial role of a high mobility group protein HMGA2 in cardiogenesis., Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	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.
	Redundancy and evolution of GATA factor requirements in development of the myocardium., Peterkin T., Dev Biol. November 15, 2007; 311 (2): 623-35.
	Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination., Hilton EN., Hum Mol Genet. July 15, 2007; 16 (14): 1773-82.
	Myoskeletin, a factor related to Myocardin, is expressed in somites and required for hypaxial muscle formation in Xenopus., Zhao H., Int J Dev Biol. January 1, 2007; 51 (4): 315-20.
	Characterization of myeloid cells derived from the anterior ventral mesoderm in the Xenopus laevis embryo., Tashiro S., Dev Growth Differ. October 1, 2006; 48 (8): 499-512.
	Retinoic acid signaling is essential for formation of the heart tube in Xenopus., Collop AH., Dev Biol. March 1, 2006; 291 (1): 96-109.
	Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.
	Characterization of Xenopus Phox2a and Phox2b defines expression domains within the embryonic nervous system and early heart field., Talikka M., Gene Expr Patterns. September 1, 2004; 4 (5): 601-7.
	A role for the RNA-binding protein, hermes, in the regulation of heart development., Gerber WV., Dev Biol. July 1, 2002; 247 (1): 116-26.
	Endoderm specification and differentiation in Xenopus embryos., Horb ME., Dev Biol. August 15, 2001; 236 (2): 330-43.
	Inhibition of Wnt activity induces heart formation from posterior mesoderm., Marvin MJ., Genes Dev. February 1, 2001; 15 (3): 316-27.
	Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.
	Regulation of the tinman homologues in Xenopus embryos., Sparrow DB., Dev Biol. November 1, 2000; 227 (1): 65-79.
	Designation of the anterior/posterior axis in pregastrula Xenopus laevis., Lane MC., Dev Biol. September 1, 2000; 225 (1): 37-58.
	Serrate and Notch specify cell fates in the heart field by suppressing cardiomyogenesis., Rones MS., Development. September 1, 2000; 127 (17): 3865-76.
	BMP signaling is required for heart formation in vertebrates., Shi Y, Shi Y., Dev Biol. August 15, 2000; 224 (2): 226-37.
	Transient cardiac expression of the tinman-family homeobox gene, XNkx2-10., Newman CS., Mech Dev. March 1, 2000; 91 (1-2): 369-73.
	Subdivision of the cardiac Nkx2.5 expression domain into myogenic and nonmyogenic compartments., Raffin M., Dev Biol. February 15, 2000; 218 (2): 326-40.
	The morphology of heart development in Xenopus laevis., Mohun TJ., Dev Biol. February 1, 2000; 218 (1): 74-88.

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