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Journal Abstract Search

573 related items for PubMed ID: 16418219

  • 1. Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells.
    Lai A, Le DN, Paznekas WA, Gifford WD, Jabs EW, Charles AC.
    J Cell Sci; 2006 Feb 01; 119(Pt 3):532-41. PubMed ID: 16418219
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  • 2. Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia.
    Shibayama J, Paznekas W, Seki A, Taffet S, Jabs EW, Delmar M, Musa H.
    Circ Res; 2005 May 27; 96(10):e83-91. PubMed ID: 15879313
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  • 7. Differential potency of dominant negative connexin43 mutants in oculodentodigital dysplasia.
    Gong XQ, Shao Q, Langlois S, Bai D, Laird DW.
    J Biol Chem; 2007 Jun 29; 282(26):19190-202. PubMed ID: 17420259
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  • 8. Loss of connexin43-mediated gap junctional coupling in the mesenchyme of limb buds leads to altered expression of morphogens in mice.
    Dobrowolski R, Hertig G, Lechner H, Wörsdörfer P, Wulf V, Dicke N, Eckert D, Bauer R, Schorle H, Willecke K.
    Hum Mol Genet; 2009 Aug 01; 18(15):2899-911. PubMed ID: 19439426
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  • 9. In vivo analysis of undocked connexin43 gap junction hemichannels in ovarian granulosa cells.
    Tong D, Li TY, Naus KE, Bai D, Kidder GM.
    J Cell Sci; 2007 Nov 15; 120(Pt 22):4016-24. PubMed ID: 17971414
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  • 11. Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43.
    Roscoe W, Veitch GI, Gong XQ, Pellegrino E, Bai D, McLachlan E, Shao Q, Kidder GM, Laird DW.
    J Biol Chem; 2005 Mar 25; 280(12):11458-66. PubMed ID: 15644317
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  • 12. Tyrosine-dependent basolateral targeting of human connexin43-eYFP in Madin-Darby canine kidney cells can be disrupted by the oculodentodigital dysplasia mutation L90V.
    Chtchetinin J, Gifford WD, Li S, Paznekas WA, Jabs EW, Lai A.
    FEBS J; 2009 Dec 25; 276(23):6992-7005. PubMed ID: 19860828
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  • 14. Decreased levels of Cx43 gap junctions result in ameloblast dysregulation and enamel hypoplasia in Gja1Jrt/+ mice.
    Toth K, Shao Q, Lorentz R, Laird DW.
    J Cell Physiol; 2010 Jun 25; 223(3):601-9. PubMed ID: 20127707
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  • 16. A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
    Flenniken AM, Osborne LR, Anderson N, Ciliberti N, Fleming C, Gittens JE, Gong XQ, Kelsey LB, Lounsbury C, Moreno L, Nieman BJ, Peterson K, Qu D, Roscoe W, Shao Q, Tong D, Veitch GI, Voronina I, Vukobradovic I, Wood GA, Zhu Y, Zirngibl RA, Aubin JE, Bai D, Bruneau BG, Grynpas M, Henderson JE, Henkelman RM, McKerlie C, Sled JG, Stanford WL, Laird DW, Kidder GM, Adamson SL, Rossant J.
    Development; 2005 Oct 25; 132(19):4375-86. PubMed ID: 16155213
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  • 19. Connexin 43-mediated bystander effect in two rat glioma cell models.
    Sanson M, Marcaud V, Robin E, Valéry C, Sturtz F, Zalc B.
    Cancer Gene Ther; 2002 Feb 25; 9(2):149-55. PubMed ID: 11857032
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  • 20. Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms.
    Huang T, Shao Q, MacDonald A, Xin L, Lorentz R, Bai D, Laird DW.
    J Cell Sci; 2013 Jul 01; 126(Pt 13):2857-66. PubMed ID: 23606748
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