Papers associated with sensory system (and nkx2-5)

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	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.
	Impact of glyphosate-based herbicide on early embryonic development of the amphibian Xenopus laevis., Flach H., Aquat Toxicol. March 1, 2022; 244 106081.
	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):
	A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis., Pokrovsky D., PLoS Biol. September 1, 2021; 19 (9): e3001377.
	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.
	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 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.
	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.
	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.
	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.
	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.
	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.
	Reduction of XNkx2-10 expression leads to anterior defects and malformation of the embryonic heart., Allen BG., Mech Dev. October 1, 2006; 123 (10): 719-29.
	A gynogenetic screen to isolate naturally occurring recessive mutations in Xenopus tropicalis., Noramly S., Mech Dev. March 1, 2005; 122 (3): 273-87.
	Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.
	Transgenic analysis of the atrialnatriuretic factor (ANF) promoter: Nkx2-5 and GATA-4 binding sites are required for atrial specific expression of ANF., Small EM., Dev Biol. September 1, 2003; 261 (1): 116-31.
	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.
	Designation of the anterior/posterior axis in pregastrula Xenopus laevis., Lane MC., Dev Biol. September 1, 2000; 225 (1): 37-58.
	BMP signaling is required for heart formation in vertebrates., Shi Y, Shi Y., Dev Biol. August 15, 2000; 224 (2): 226-37.
	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.
	Amphibian embryos as a model system for organ engineering: in vitro induction and rescue of the heart anlage., Grunz H., Int J Dev Biol. July 1, 1999; 43 (4): 361-4.
	Tbx5 is essential for heart development., Horb ME., Development. April 1, 1999; 126 (8): 1739-51.
	Vertebrate tinman homologues XNkx2-3 and XNkx2-5 are required for heart formation in a functionally redundant manner., Fu Y., Development. November 1, 1998; 125 (22): 4439-49.
	Murine cerberus homologue mCer-1: a candidate anterior patterning molecule., Biben C., Dev Biol. February 15, 1998; 194 (2): 135-51.
	Homeobox genes in cardiovascular development., Patterson KD., Curr Top Dev Biol. January 1, 1998; 40 1-44.
	tinman, a Drosophila homeobox gene required for heart and visceral mesoderm specification, may be represented by a family of genes in vertebrates: XNkx-2.3, a second vertebrate homologue of tinman., Evans SM., Development. November 1, 1995; 121 (11): 3889-99.

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