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XB--489237
Papers associated with gjb3
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Understanding the Role of ATP Release through Connexins Hemichannels during Neurulation., Tovar LM, Burgos CF, Yévenes GE, Moraga-Cid G, Fuentealba J, Coddou C, Bascunan-Godoy L, Catrupay C, Torres A, Castro PA., Int J Mol Sci. January 21, 2023; 24 (3):  |
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Connexins in epidermal homeostasis and skin disease., Scott CA, Tattersall D, O'Toole EA, Kelsell DP., Biochim Biophys Acta. August 1, 2012; 1818 (8): 1952-61.  |
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A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expression., Mencía A, González-Nieto D, Modamio-Høybjør S, Etxeberría A, Aránguez G, Salvador N, Del Castillo I, Villarroel A, Moreno F, Barrio L, Moreno-Pelayo MA., Hum Genet. February 1, 2008; 123 (1): 41-53. |
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Implication of gap junction coupling in amphibian vitellogenin uptake., Mónaco ME, Villecco EI, Sánchez SS., Zygote. May 1, 2007; 15 (2): 149-57. |
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Cloning, embryonic expression, and functional characterization of two novel connexins from Xenopus laevis., de Boer TP, Kok B, Roël G, van Veen TA, Destrée OH, Rook MB, Vos MA, de Bakker JM, van der Heyden MA., Biochem Biophys Res Commun. October 20, 2006; 349 (2): 855-62.  |
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Xenopus connexins: how frogs bridge the gap., de Boer TP, van der Heyden MA., Differentiation. September 1, 2005; 73 (7): 330-40. |
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Multiple connexins contribute to intercellular communication in the Xenopus embryo., Landesman Y, Postma FR, Goodenough DA, Paul DL., J Cell Sci. January 1, 2003; 116 (Pt 1): 29-38.  |
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Early embryonic expression of ion channels and pumps in chick and Xenopus development., Rutenberg J, Cheng SM, Levin M., Dev Dyn. December 1, 2002; 225 (4): 469-84.  |
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Molecular cloning, functional expression, and tissue distribution of a novel human gap junction-forming protein, connexin-31.9. Interaction with zona occludens protein-1., Nielsen PA, Beahm DL, Giepmans BN, Baruch A, Hall JE, Kumar NM., J Biol Chem. October 11, 2002; 277 (41): 38272-83. |
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Virtual cloning, functional expression, and gating analysis of human connexin31.9., White TW, Srinivas M, Ripps H, Trovato-Salinaro A, Condorelli DF, Bruzzone R., Am J Physiol Cell Physiol. September 1, 2002; 283 (3): C960-70. |
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Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT., Griffith AJ, Chowdhry AA, Kurima K, Hood LJ, Keats B, Berlin CI, Morell RJ, Friedman TB., Am J Hum Genet. September 1, 2000; 67 (3): 745-9.  |
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KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness., Kubisch C, Schroeder BC, Friedrich T, Lütjohann B, El-Amraoui A, Marlin S, Petit C, Jentsch TJ., Cell. February 5, 1999; 96 (3): 437-46. |
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Biological functions of connexin genes revealed by human genetic defects, dominant negative approaches and targeted deletions in the mouse., Willecke K, Kirchhoff S, Plum A, Temme A, Thönnissen E, Ott T., Novartis Found Symp. January 1, 1999; 219 76-88; discussion 88-96. |
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Two gap junction genes, connexin 31.1 and 30.3, are closely linked on mouse chromosome 4 and preferentially expressed in skin., Hennemann H, Dahl E, White JB, Schwarz HJ, Lalley PA, Chang S, Nicholson BJ, Willecke K., J Biol Chem. August 25, 1992; 267 (24): 17225-33. |
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Molecular cloning and characterization of a new member of the gap junction gene family, connexin-31., Hoh JH, John SA, Revel JP., J Biol Chem. April 5, 1991; 266 (10): 6524-31. |
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