312 related articles for article (PubMed ID: 16155213)
1. 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]
2. Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 gene.
van Es RJ; Wittebol-Post D; Beemer FA
Int J Oral Maxillofac Surg; 2007 Sep; 36(9):858-60. PubMed ID: 17509830
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43).
Musa FU; Ratajczak P; Sahu J; Pentlicky S; Fryer A; Richard G; Willoughby CE
Eye (Lond); 2009 Mar; 23(3):549-55. PubMed ID: 18425059
[TBL] [Abstract][Full Text] [Related]
9. 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; 223(3):601-9. PubMed ID: 20127707
[TBL] [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; 80(3):385-95. PubMed ID: 18678643
[TBL] [Abstract][Full Text] [Related]
11. Ocular pathology relevant to glaucoma in a Gja1(Jrt/+) mouse model of human oculodentodigital dysplasia.
Tsui E; Hill KA; Laliberte AM; Paluzzi D; Kisilevsky I; Shao Q; Heathcote JG; Laird DW; Kidder GM; Hutnik CM
Invest Ophthalmol Vis Sci; 2011 Jun; 52(6):3539-47. PubMed ID: 21273537
[TBL] [Abstract][Full Text] [Related]
12. 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; 18(15):2899-911. PubMed ID: 19439426
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.
Dobrowolski R; Sasse P; Schrickel JW; Watkins M; Kim JS; Rackauskas M; Troatz C; Ghanem A; Tiemann K; Degen J; Bukauskas FF; Civitelli R; Lewalter T; Fleischmann BK; Willecke K
Hum Mol Genet; 2008 Feb; 17(4):539-54. PubMed ID: 18003637
[TBL] [Abstract][Full Text] [Related]
15. The G60S Cx43 mutant enhances keratinocyte proliferation and differentiation.
Churko JM; Kelly JJ; Macdonald A; Lee J; Sampson J; Bai D; Laird DW
Exp Dermatol; 2012 Aug; 21(8):612-8. PubMed ID: 22775996
[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. 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]
18. The G60S connexin43 mutant regulates hair growth and hair fiber morphology in a mouse model of human oculodentodigital dysplasia.
Churko JM; Chan J; Shao Q; Laird DW
J Invest Dermatol; 2011 Nov; 131(11):2197-204. PubMed ID: 21716323
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
