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Journal Abstract Search

267 related items for PubMed ID: 15879313

  • 1. 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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  • 2. 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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  • 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 Feb 01; 12(5-6):279-92. PubMed ID: 16531323
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  • 12. 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 01; 219(1-3):9-17. PubMed ID: 17687502
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  • 17. 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 01; 23(6):928-38. PubMed ID: 18269311
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  • 18. Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
    Amador C, Mathews AM, Del Carmen Montoya M, Laughridge ME, Everman DB, Holden KR.
    J Child Neurol; 2008 Aug 01; 23(8):901-5. PubMed ID: 18660473
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  • 20. Palmoplantar keratosis in oculodentodigital dysplasia with a GJA1 point mutation out of the C-terminal region of connexin 43.
    Kogame T, Dainichi T, Shimomura Y, Tanioka M, Kabashima K, Miyachi Y.
    J Dermatol; 2014 Dec 01; 41(12):1095-7. PubMed ID: 25388818
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