Papers associated with heart (and nkx2-5)

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	Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival., Griffin C., Dis Model Mech. March 1, 2025; 18 (3):
	Fbrsl1 is required for heart development in Xenopus laevis and de novo variants in FBRSL1 can cause human heart defects., Berger H., Dis Model Mech. June 1, 2024; 17 (6):
	Early life exposure to perfluorooctanesulfonate (PFOS) impacts vital biological processes in Xenopus laevis: Integrated morphometric and transcriptomic analyses., Ismail T., Ecotoxicol Environ Saf. January 1, 2024; 269 115820.
	Normal Table of Xenopus development: a new graphical resource., Zahn N., Development. July 15, 2022; 149 (14):
	Impact of glyphosate-based herbicide on early embryonic development of the amphibian Xenopus laevis., Flach H., Aquat Toxicol. March 1, 2022; 244 106081.
	Transcriptional regulatory elements of hif1α in a distal locus of islet1 in Xenopus laevis., Miyakawa M., Comp Biochem Physiol B Biochem Mol Biol. January 1, 2021; 255 110598.
	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.
	Evaluation of the toxic effects of celecoxib on Xenopus embryo development., Yoon YH., Biochem Biophys Res Commun. June 22, 2018; 501 (2): 329-335.
	Frizzled-7 is required for Xenopus heart development., Abu-Elmagd M., Biol Open. December 15, 2017; 6 (12): 1861-1868.
	Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
	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.
	CUG-BP, Elav-like family member 1 (CELF1) is required for normal myofibrillogenesis, morphogenesis, and contractile function in the embryonic heart., Blech-Hermoni Y., Dev Dyn. August 1, 2016; 245 (8): 854-73.
	Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos., Guo R., BMC Anesthesiol. April 18, 2016; 16 23.
	pdzrn3 is required for pronephros morphogenesis in Xenopus laevis., Marracci S., Int J Dev Biol. January 1, 2016; 60 (1-3): 57-63.
	Perfluoroheptanoic acid affects amphibian embryogenesis by inducing the phosphorylation of ERK and JNK., Kim M., Int J Mol Med. December 1, 2015; 36 (6): 1693-700.
	Characterization of ticlopidine-induced developmental and teratogenic defects in Xenopus embryos and human endothelial cells., Park MS., Chem Biol Interact. October 5, 2015; 240 172-8.
	Predicting Variabilities in Cardiac Gene Expression with a Boolean Network Incorporating Uncertainty., Grieb M., PLoS One. July 16, 2015; 10 (7): e0131832.
	Direct nkx2-5 transcriptional repression of isl1 controls cardiomyocyte subtype identity., Dorn T., Stem Cells. April 1, 2015; 33 (4): 1113-29.
	The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
	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.
	Nkx2.5 is involved in myeloid cell differentiation at anterior ventral blood islands in the Xenopus embryo., Sakata H., Dev Growth Differ. October 1, 2014; 56 (8): 544-54.
	Diverse functions of kindlin/fermitin proteins during embryonic development in Xenopus laevis., Rozario T., Mech Dev. August 1, 2014; 133 203-17.
	Hhex and Cer1 mediate the Sox17 pathway for cardiac mesoderm formation in embryonic stem cells., Liu Y., Stem Cells. June 1, 2014; 32 (6): 1515-26.
	Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis., Guo Y., PLoS One. January 17, 2014; 9 (1): e87294.
	Expression pattern of zcchc24 during early Xenopus development., Vitorino M., Int J Dev Biol. January 1, 2014; 58 (1): 45-50.
	In vivo evaluation and comparison of developmental toxicity and teratogenicity of perfluoroalkyl compounds using Xenopus embryos., Kim M., Chemosphere. October 1, 2013; 93 (6): 1153-60.
	Tcf21 regulates the specification and maturation of proepicardial cells., Tandon P., Development. June 1, 2013; 140 (11): 2409-21.
	sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling., Gibb N., Development. April 1, 2013; 140 (7): 1537-49.
	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.
	Dissociation of cardiogenic and postnatal myocardial activities of GATA4., Gallagher JM., Mol Cell Biol. June 1, 2012; 32 (12): 2214-23.
	SHP-2 acts via ROCK to regulate the cardiac actin cytoskeleton., Langdon Y., Development. March 1, 2012; 139 (5): 948-57.
	Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
	Tbx5 overexpression favors a first heart field lineage in murine embryonic stem cells and in Xenopus laevis embryos., Herrmann F., Dev Dyn. December 1, 2011; 240 (12): 2634-45.
	Canonical WNT signaling enhances stem cell expression in the developing heart without a corresponding inhibition of cardiogenic differentiation., Martin LK., Stem Cells Dev. November 1, 2011; 20 (11): 1973-83.
	Cardiac neural crest is dispensable for outflow tract septation in Xenopus., Lee YH., Development. May 1, 2011; 138 (10): 2025-34.
	Functional analysis of Rfx6 and mutant variants associated with neonatal diabetes., Pearl EJ., Dev Biol. March 1, 2011; 351 (1): 135-45.
	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.
	Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
	Claudin5 genes encoding tight junction proteins are required for Xenopus heart formation., Yamagishi M., Dev Growth Differ. September 1, 2010; 52 (7): 665-75.
	Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT., Genesis. August 1, 2010; 48 (8): 492-504.
	Examining the cardiac NK-2 genes in early heart development., Bartlett H., Pediatr Cardiol. April 1, 2010; 31 (3): 335-41.
	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.
	Characterization of molecular markers to assess cardiac cushions formation in Xenopus., Lee YH., Dev Dyn. December 1, 2009; 238 (12): 3257-65.
	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.

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