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Results: 1 to 20 of 117

Similar articles for PubMed (Select 21716323)

1.

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. doi: 10.1038/jid.2011.183. Epub 2011 Jun 30.

2.

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. doi: 10.1016/j.neuropharm.2013.05.003. Epub 2013 May 31.

PMID:
23727526
3.

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 Mar-Apr;2(3-4):157-67. doi: 10.1242/dmm.000935. Epub 2009 Feb 23.

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.

5.

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. doi: 10.1042/BJ20121070.

6.

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 15;17(4):539-54. Epub 2007 Nov 13.

7.

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. doi: 10.1111/j.1600-0625.2012.01532.x.

PMID:
22775996
8.

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. doi: 10.1091/mbc.E12-02-0128. Epub 2012 Jul 18.

9.

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 1;457(3):441-9. doi: 10.1042/BJ20130810.

10.

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 1;126(Pt 13):2857-66. doi: 10.1242/jcs.123315. Epub 2013 Apr 19.

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 1;52(6):3539-47. doi: 10.1167/iovs.10-6399.

PMID:
21273537
12.

Characterization of gap junction proteins in the bladder of Cx43 mutant mouse models of oculodentodigital dysplasia.

Lorentz R, Shao Q, Huang T, Fishman GI, Laird DW.

J Membr Biol. 2012 Jun;245(5-6):345-55. doi: 10.1007/s00232-012-9455-1. Epub 2012 Jul 3.

13.

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. Epub 2006 Aug 6.

14.

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 1;80(3):385-95. doi: 10.1093/cvr/cvn203. Epub 2008 Aug 4.

15.

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. Epub 2007 Apr 9.

16.

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. Epub 2005 May 5.

17.

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. Epub 2007 Aug 9.

PMID:
17687502
18.

Atrial tachycardia/fibrillation in the connexin 43 G60S mutant (Oculodentodigital dysplasia) mouse.

Tuomi JM, Tyml K, Jones DL.

Am J Physiol Heart Circ Physiol. 2011 Apr;300(4):H1402-11. doi: 10.1152/ajpheart.01094.2010. Epub 2011 Jan 14.

19.

Human dermal fibroblasts derived from oculodentodigital dysplasia patients suggest that patients may have wound-healing defects.

Churko JM, Shao Q, Gong XQ, Swoboda KJ, Bai D, Sampson J, Laird DW.

Hum Mutat. 2011 Apr;32(4):456-66. doi: 10.1002/humu.21472.

20.

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. doi: 10.1002/jcp.22046.

PMID:
20127707
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