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

184 related items for PubMed ID: 17420259

  • 1. 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]

  • 2.
    ; . PubMed ID:
    [No 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 Jun 29; 12(5-6):279-92. PubMed ID: 16531323
    [Abstract] [Full Text] [Related]

  • 4. Functional characterization of a GJA1 frameshift mutation causing oculodentodigital dysplasia and palmoplantar keratoderma.
    Gong XQ, Shao Q, Lounsbury CS, Bai D, Laird DW.
    J Biol Chem; 2006 Oct 20; 281(42):31801-11. PubMed ID: 16891658
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels.
    Dobrowolski R, Sommershof A, Willecke K.
    J Membr Biol; 2007 Oct 27; 219(1-3):9-17. PubMed ID: 17687502
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia.
    Shao Q, Liu Q, Lorentz R, Gong XQ, Bai D, Shaw GS, Laird DW.
    Mol Biol Cell; 2012 Sep 01; 23(17):3312-21. PubMed ID: 22809623
    [Abstract] [Full Text] [Related]

  • 11. Manipulating Cx43 expression triggers gene reprogramming events in dermal fibroblasts from oculodentodigital dysplasia patients.
    Esseltine JL, Shao Q, Huang T, Kelly JJ, Sampson J, Laird DW.
    Biochem J; 2015 Nov 15; 472(1):55-69. PubMed ID: 26349540
    [Abstract] [Full Text] [Related]

  • 12. Specific functional pathologies of Cx43 mutations associated with oculodentodigital dysplasia.
    Kelly JJ, Esseltine JL, Shao Q, Jabs EW, Sampson J, Auranen M, Bai D, Laird DW.
    Mol Biol Cell; 2016 Jul 15; 27(14):2172-85. PubMed ID: 27226478
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 23(6):928-38. PubMed ID: 18269311
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 75():549-56. PubMed ID: 23727526
    [Abstract] [Full Text] [Related]

  • 15. Myogenic bladder defects in mouse models of human oculodentodigital dysplasia.
    Huang T, Shao Q, Barr K, Simek J, Fishman GI, Laird DW.
    Biochem J; 2014 Feb 01; 457(3):441-9. PubMed ID: 24228978
    [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. Oogenesis defects in a mutant mouse model of oculodentodigital dysplasia.
    Tong D, Colley D, Thoo R, Li TY, Plante I, Laird DW, Bai D, Kidder GM.
    Dis Model Mech; 2009 Oct 01; 2(3-4):157-67. PubMed ID: 19259389
    [Abstract] [Full Text] [Related]

  • 18. The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants.
    Churko JM, Langlois S, Pan X, Shao Q, Laird DW.
    Biochem J; 2010 Aug 01; 429(3):473-83. PubMed ID: 20515445
    [Abstract] [Full Text] [Related]

  • 19. Effects of reduced connexin43 function on skull development in the Cx43I130T/+ mutant mouse that models oculodentodigital dysplasia.
    Jarvis SE, Lee JE, Jewlal E, Barr K, Kelly GM, Laird DW, Willmore KE.
    Bone; 2020 Jul 01; 136():115365. PubMed ID: 32320893
    [Abstract] [Full Text] [Related]

  • 20. The severity of mammary gland developmental defects is linked to the overall functional status of Cx43 as revealed by genetically modified mice.
    Stewart MK, Gong XQ, Barr KJ, Bai D, Fishman GI, Laird DW.
    Biochem J; 2013 Jan 15; 449(2):401-13. PubMed ID: 23075222
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.