BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

270 related articles for article (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; 96(10):e83-91. PubMed ID: 15879313
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 119(Pt 3):532-41. PubMed ID: 16418219
    [TBL] [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; 12(5-6):279-92. PubMed ID: 16531323
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 132(19):4375-86. PubMed ID: 16155213
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 126(Pt 13):2857-66. PubMed ID: 23606748
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 80(3):385-95. PubMed ID: 18678643
    [TBL] [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; 282(26):19190-202. PubMed ID: 17420259
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 75():549-56. PubMed ID: 23727526
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).
    Debeer P; Van Esch H; Huysmans C; Pijkels E; De Smet L; Van de Ven W; Devriendt K; Fryns JP
    Eur J Med Genet; 2005; 48(4):377-87. PubMed ID: 16378922
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new GJA1 (connexin 43) mutation causing oculodentodigital dysplasia associated to uncommon features.
    de la Parra DR; Zenteno JC
    Ophthalmic Genet; 2007 Dec; 28(4):198-202. PubMed ID: 18161618
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 23(17):3312-21. PubMed ID: 22809623
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 219(1-3):9-17. PubMed ID: 17687502
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 27(14):2172-85. PubMed ID: 27226478
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis.
    Kelly SC; Ratajczak P; Keller M; Purcell SM; Griffin T; Richard G
    Eur J Dermatol; 2006; 16(3):241-5. PubMed ID: 16709485
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 280(12):11458-66. PubMed ID: 15644317
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 472(1):55-69. PubMed ID: 26349540
    [TBL] [Abstract][Full Text] [Related]  

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

  • 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; 23(8):901-5. PubMed ID: 18660473
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three novel GJA1 missense substitutions resulting in oculo-dento-digital dysplasia (ODDD) - further extension of the mutational spectrum.
    Jamsheer A; Sowińska-Seidler A; Socha M; Stembalska A; Kiraly-Borri C; Latos-Bieleńska A
    Gene; 2014 Apr; 539(1):157-61. PubMed ID: 24508941
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 41(12):1095-7. PubMed ID: 25388818
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.