These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

574 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants.
    McLachlan E, Manias JL, Gong XQ, Lounsbury CS, Shao Q, Bernier SM, Bai D, Laird DW.
    Cell Commun Adhes; 2005 May 27; 12(5-6):279-92. PubMed ID: 16531323
    [Abstract] [Full Text] [Related]

  • 4. ODDD-linked Cx43 mutants reduce endogenous Cx43 expression and function in osteoblasts and inhibit late stage differentiation.
    McLachlan E, Plante I, Shao Q, Tong D, Kidder GM, Bernier SM, Laird DW.
    J Bone Miner Res; 2008 Jun 27; 23(6):928-38. PubMed ID: 18269311
    [Abstract] [Full Text] [Related]

  • 5. Cerebral ischemic injury is enhanced in a model of oculodentodigital dysplasia.
    Kozoriz MG, Lai S, Vega JL, Sáez JC, Sin WC, Bechberger JF, Naus CC.
    Neuropharmacology; 2013 Dec 27; 75():549-56. PubMed ID: 23727526
    [Abstract] [Full Text] [Related]

  • 6. Mutations in the second extracellular region of connexin 43 prevent localization to the plasma membrane, but do not affect its ability to suppress cell growth.
    Olbina G, Eckhart W.
    Mol Cancer Res; 2003 Jul 27; 1(9):690-700. PubMed ID: 12861055
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 10. Fate of connexin43 in cardiac tissue harbouring a disease-linked connexin43 mutant.
    Manias JL, Plante I, Gong XQ, Shao Q, Churko J, Bai D, Laird DW.
    Cardiovasc Res; 2008 Dec 01; 80(3):385-95. PubMed ID: 18678643
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 13. Dominant-negative connexin43-EGFP inhibits calcium-transient synchronization of primary neonatal rat cardiomyocytes.
    Oyamada Y, Zhou W, Oyamada H, Takamatsu T, Oyamada M.
    Exp Cell Res; 2002 Feb 01; 273(1):85-94. PubMed ID: 11795949
    [Abstract] [Full Text] [Related]

  • 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 01; 223(3):601-9. PubMed ID: 20127707
    [Abstract] [Full Text] [Related]

  • 15. Connexin 33 impairs gap junction functionality by accelerating connexin 43 gap junction plaque endocytosis.
    Carette D, Gilleron J, Decrouy X, Fiorini C, Diry M, Segretain D, Pointis G.
    Traffic; 2009 Sep 01; 10(9):1272-85. PubMed ID: 19548984
    [Abstract] [Full Text] [Related]

  • 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 01; 132(19):4375-86. PubMed ID: 16155213
    [Abstract] [Full Text] [Related]

  • 17. Connexin 43 hemichannels contribute to the propagation of apoptotic cell death in a rat C6 glioma cell model.
    Decrock E, De Vuyst E, Vinken M, Van Moorhem M, Vranckx K, Wang N, Van Laeken L, De Bock M, D'Herde K, Lai CP, Rogiers V, Evans WH, Naus CC, Leybaert L.
    Cell Death Differ; 2009 Jan 01; 16(1):151-63. PubMed ID: 18820645
    [Abstract] [Full Text] [Related]

  • 18. Connexin43 enhances glioma invasion by a mechanism involving the carboxy terminus.
    Bates DC, Sin WC, Aftab Q, Naus CC.
    Glia; 2007 Nov 15; 55(15):1554-64. PubMed ID: 17823969
    [Abstract] [Full Text] [Related]

  • 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 15; 9(2):149-55. PubMed ID: 11857032
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 29.