Papers associated with embryonic structure (and gjb1)

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	Understanding the Role of ATP Release through Connexins Hemichannels during Neurulation., Tovar LM., Int J Mol Sci. January 21, 2023; 24 (3):
	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endoderm gene regulatory network., Mukherjee S., Elife. September 7, 2020; 9
	Cell communication across gap junctions: a historical perspective and current developments., Evans WH., Biochem Soc Trans. June 1, 2015; 43 (3): 450-9.
	Prolonged FGF signaling is necessary for lung and liver induction in Xenopus., Shifley ET., BMC Dev Biol. September 18, 2012; 12 27.
	Connexin26-mediated transfer of laterality cues in Xenopus., Beyer T., Biol Open. May 15, 2012; 1 (5): 473-81.
	The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps., Drews C., BMC Dev Biol. January 31, 2011; 11 5.
	Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin., Tao L., Dev Dyn. October 1, 2010; 239 (10): 2627-36.
	Cloning, embryonic expression, and functional characterization of two novel connexins from Xenopus laevis., de Boer TP., Biochem Biophys Res Commun. October 20, 2006; 349 (2): 855-62.
	Global analysis of the transcriptional network controlling Xenopus endoderm formation., Sinner D., Development. May 1, 2006; 133 (10): 1955-66.
	XEpac, a guanine nucleotide-exchange factor for Rap GTPase, is a novel hatching gland specific marker during the Xenopus embryogenesis., Lee SJ., Dev Dyn. April 1, 2005; 232 (4): 1091-7.
	Multiple connexins contribute to intercellular communication in the Xenopus embryo., Landesman Y., J Cell Sci. January 1, 2003; 116 (Pt 1): 29-38.
	K(ATP) channel activity is required for hatching in Xenopus embryos., Cheng SM., Dev Dyn. December 1, 2002; 225 (4): 588-91.
	Virtual cloning, functional expression, and gating analysis of human connexin31.9., White TW., Am J Physiol Cell Physiol. September 1, 2002; 283 (3): C960-70.
	Calmodulin colocalizes with connexins and plays a direct role in gap junction channel gating., Sotkis A., Cell Commun Adhes. January 1, 2001; 8 (4-6): 277-81.
	Expression of connexin 30 in Xenopus embryos and its involvement in hatching gland function., Levin M., Dev Dyn. September 1, 2000; 219 (1): 96-101.
	Expression of major gap junction connexin types in the working myocardium of eight chordates., Becker DL., Cell Biol Int. January 1, 1998; 22 (7-8): 527-43.
	A chimeric connexin forming gap junction hemichannels., Pfahnl A., Pflugers Arch. April 1, 1997; 433 (6): 773-9.
	Heteromeric connexons in lens gap junction channels., Jiang JX., Proc Natl Acad Sci U S A. February 6, 1996; 93 (3): 1287-91.
	A structural basis for the unequal sensitivity of the major cardiac and liver gap junctions to intracellular acidification: the carboxyl tail length., Liu S., Biophys J. May 1, 1993; 64 (5): 1422-33.
	Molecular cloning and functional expression of mouse connexin40, a second gap junction gene preferentially expressed in lung., Hennemann H., J Cell Biol. June 1, 1992; 117 (6): 1299-310.
	Connexin46, a novel lens gap junction protein, induces voltage-gated currents in nonjunctional plasma membrane of Xenopus oocytes., Paul DL., J Cell Biol. November 1, 1991; 115 (4): 1077-89.
	Gap junctions formed by connexins 26 and 32 alone and in combination are differently affected by applied voltage., Barrio LC., Proc Natl Acad Sci U S A. October 1, 1991; 88 (19): 8410-4.
	Molecular cloning and characterization of a new member of the gap junction gene family, connexin-31., Hoh JH., J Biol Chem. April 5, 1991; 266 (10): 6524-31.
	Formation of gap junctions by expression of connexins in Xenopus oocyte pairs., Swenson KI., Cell. April 7, 1989; 57 (1): 145-55.

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