183 related articles for article (PubMed ID: 19259389)
1. 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; 2(3-4):157-67. PubMed ID: 19259389
[TBL] [Abstract][Full Text] [Related]
2. 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; 281(42):31801-11. PubMed ID: 16891658
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. A dominant loss-of-function GJA1 (Cx43) mutant impairs parturition in the mouse.
Tong D; Lu X; Wang HX; Plante I; Lui E; Laird DW; Bai D; Kidder GM
Biol Reprod; 2009 Jun; 80(6):1099-106. PubMed ID: 19176884
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Mice harbouring an oculodentodigital dysplasia-linked Cx43 G60S mutation have severe hearing loss.
Abitbol JM; Kelly JJ; Barr KJ; Allman BL; Laird DW
J Cell Sci; 2018 May; 131(9):. PubMed ID: 29618634
[TBL] [Abstract][Full Text] [Related]
11. 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; 449(2):401-13. PubMed ID: 23075222
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Effects of reduced connexin43 function on skull development in the Cx43
Jarvis SE; Lee JE; Jewlal E; Barr K; Kelly GM; Laird DW; Willmore KE
Bone; 2020 Jul; 136():115365. PubMed ID: 32320893
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits.
Furuta N; Ikeda M; Hirayanagi K; Fujita Y; Amanuma M; Okamoto K
Intern Med; 2012; 51(1):93-8. PubMed ID: 22214631
[TBL] [Abstract][Full Text] [Related]
16. 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; 457(3):441-9. PubMed ID: 24228978
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
