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Summary Expression Phenotypes Gene Literature (26) GO Terms (5) Nucleotides (90) Proteins (43) Interactants (101) Wiki
XB-GENEPAGE-977955

Papers associated with gja4



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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):                     

The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus., Melchert J, Henningfeld KA, Richts S, Lingner T, Jonigk D, Pieler T., Dev Biol. March 15, 2020; 459 (2): 138-148.                                

The Physiological Characterization of Connexin41.8 and Connexin39.4, Which Are Involved in the Striped Pattern Formation of Zebrafish., Watanabe M, Sawada R, Aramaki T, Skerrett IM, Kondo S., J Biol Chem. January 15, 2016; 291 (3): 1053-63.

Loss of functional endothelial connexin40 results in exercise-induced hypertension in mice., Morton SK, Chaston DJ, Howitt L, Heisler J, Nicholson BJ, Fairweather S, Bröer S, Ashton AW, Matthaei KI, Hill CE., Hypertension. March 1, 2015; 65 (3): 662-9.

MiR-142-3p controls the specification of definitive hemangioblasts during ontogeny., Nimmo R, Ciau-Uitz A, Ruiz-Herguido C, Soneji S, Bigas A, Patient R, Enver T., Dev Cell. August 12, 2013; 26 (3): 237-49.                    

Uncoupling VEGFA functions in arteriogenesis and hematopoietic stem cell specification., Leung A, Ciau-Uitz A, Pinheiro P, Monteiro R, Zuo J, Vyas P, Patient R, Porcher C., Dev Cell. January 28, 2013; 24 (2): 144-58.                                

An intact connexin N-terminus is required for function but not gap junction formation., Kyle JW, Minogue PJ, Thomas BC, Domowicz DA, Berthoud VM, Hanck DA, Beyer EC., J Cell Sci. August 15, 2008; 121 (Pt 16): 2744-50.

Conductance of connexin hemichannels segregates with the first transmembrane segment., Hu X, Ma M, Dahl G., Biophys J. January 1, 2006; 90 (1): 140-50.

The permeability of gap junction channels to probes of different size is dependent on connexin composition and permeant-pore affinities., Weber PA, Chang HC, Spaeth KE, Nitsche JM, Nicholson BJ., Biophys J. August 1, 2004; 87 (2): 958-73.

CO(2) sensitivity of voltage gating and gating polarity of gapjunction channels--connexin40 and its COOH-terminus-truncated mutant., Peracchia C, Chen JT, Peracchia LL., J Membr Biol. July 15, 2004; 200 (2): 105-13.

Gap junctions and the connexin protein family., Söhl G, Willecke K., Cardiovasc Res. May 1, 2004; 62 (2): 228-32.

Ribosomes stalling on uORF1 in the Xenopus Cx41 5' UTR inhibit downstream translation initiation., Meijer HA, Thomas AA., Nucleic Acids Res. June 15, 2003; 31 (12): 3174-84.

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.                            

trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation., Rouan F, White TW, Brown N, Taylor AM, Lucke TW, Paul DL, Munro CS, Uitto J, Hodgins MB, Richard G., J Cell Sci. June 1, 2001; 114 (Pt 11): 2105-13.

Size selectivity between gap junction channels composed of different connexins., Gong XQ, Nicholson BJ., Cell Commun Adhes. January 1, 2001; 8 (4-6): 187-92.

Translational control of the Xenopus laevis connexin-41 5'-untranslated region by three upstream open reading frames., Meijer HA, Dictus WJ, Keuning ED, Thomas AA., J Biol Chem. October 6, 2000; 275 (40): 30787-93.

Hetero-domain interactions as a mechanism for the regulation of connexin channels., Stergiopoulos K, Alvarado JL, Mastroianni M, Ek-Vitorin JF, Taffet SM, Delmar M., Circ Res. May 28, 1999; 84 (10): 1144-55.

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.

Identification of connexin43 as a functional target for Wnt signalling., van der Heyden MA, Rook MB, Hermans MM, Rijksen G, Boonstra J, Defize LH, Destrée OH., J Cell Sci. June 1, 1998; 111 ( Pt 12) 1741-9.

A role for an inhibitory connexin in testis?, Chang M, Werner R, Dahl G., Dev Biol. April 10, 1996; 175 (1): 50-6.

Molecular cloning, tissue distribution, and hormonal control in the ovary of Cx41 mRNA, a novel Xenopus connexin gene transcript., Yoshizaki G, Patiño R., Mol Reprod Dev. September 1, 1995; 42 (1): 7-18.

Functional analysis of selective interactions among rodent connexins., White TW, Paul DL, Goodenough DA, Bruzzone R., Mol Biol Cell. April 1, 1995; 6 (4): 459-70.

Expression of a dominant negative inhibitor of intercellular communication in the early Xenopus embryo causes delamination and extrusion of cells., Paul DL, Yu K, Bruzzone R, Gimlich RL, Goodenough DA., Development. February 1, 1995; 121 (2): 371-81.

Connexin40, a component of gap junctions in vascular endothelium, is restricted in its ability to interact with other connexins., Bruzzone R, Haefliger JA, Gimlich RL, Paul DL., Mol Biol Cell. January 1, 1993; 4 (1): 7-20.

Molecular cloning and functional expression of mouse connexin40, a second gap junction gene preferentially expressed in lung., Hennemann H, Suchyna T, Lichtenberg-Fraté H, Jungbluth S, Dahl E, Schwarz J, Nicholson BJ, Willecke K., J Cell Biol. June 1, 1992; 117 (6): 1299-310.

Mouse connexin37: cloning and functional expression of a gap junction gene highly expressed in lung., Willecke K, Heynkes R, Dahl E, Stutenkemper R, Hennemann H, Jungbluth S, Suchyna T, Nicholson BJ., J Cell Biol. September 1, 1991; 114 (5): 1049-57.

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