Davies V - Search Results

1

Davies V, Votruba M. Davies V, et al. Exp Eye Res. 2006 Nov;83(5):1003-4. doi: 10.1016/j.exer.2005.11.021. Epub 2006 Mar 23. Exp Eye Res. 2006. PMID: 16563384 Review. No abstract available.

2

Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.

Davies VJ, Hollins AJ, Piechota MJ, Yip W, Davies JR, White KE, Nicols PP, Boulton ME, Votruba M. Davies VJ, et al. Hum Mol Genet. 2007 Jun 1;16(11):1307-18. doi: 10.1093/hmg/ddm079. Epub 2007 Apr 11. Hum Mol Genet. 2007. PMID: 17428816

3

A missense mutation in the murine Opa3 gene models human Costeff syndrome.

Davies VJ, Powell KA, White KE, Yip W, Hogan V, Hollins AJ, Davies JR, Piechota M, Brownstein DG, Moat SJ, Nichols PP, Wride MA, Boulton ME, Votruba M. Davies VJ, et al. Among authors: davies jr. Brain. 2008 Feb;131(Pt 2):368-80. doi: 10.1093/brain/awm333. Brain. 2008. PMID: 18222992

4

OPA1 deficiency associated with increased autophagy in retinal ganglion cells in a murine model of dominant optic atrophy.

White KE, Davies VJ, Hogan VE, Piechota MJ, Nichols PP, Turnbull DM, Votruba M. White KE, et al. Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2567-71. doi: 10.1167/iovs.08-2913. Epub 2009 Feb 21. Invest Ophthalmol Vis Sci. 2009. PMID: 19234344 Free article.

5

Specific deficits in visual electrophysiology in a mouse model of dominant optic atrophy.

Barnard AR, Charbel Issa P, Perganta G, Williams PA, Davies VJ, Sekaran S, Votruba M, MacLaren RE. Barnard AR, et al. Exp Eye Res. 2011 Nov;93(5):771-7. doi: 10.1016/j.exer.2011.07.004. Epub 2011 Jul 22. Exp Eye Res. 2011. PMID: 21803037

6

OPA1 mutation and late-onset cardiomyopathy: mitochondrial dysfunction and mtDNA instability.

Chen L, Liu T, Tran A, Lu X, Tomilov AA, Davies V, Cortopassi G, Chiamvimonvat N, Bers DM, Votruba M, Knowlton AA. Chen L, et al. Among authors: davies v. J Am Heart Assoc. 2012 Oct;1(5):e003012. doi: 10.1161/JAHA.112.003012. Epub 2012 Oct 25. J Am Heart Assoc. 2012. PMID: 23316298 Free PMC article.

7

Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy.

Yu-Wai-Man P, Davies VJ, Piechota MJ, Cree LM, Votruba M, Chinnery PF. Yu-Wai-Man P, et al. Invest Ophthalmol Vis Sci. 2009 Oct;50(10):4561-6. doi: 10.1167/iovs.09-3634. Epub 2009 May 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19443720 Free PMC article.

8

Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome.

Wells T, Davies JR, Guschina IA, Ball DJ, Davies JS, Davies VJ, Evans BA, Votruba M. Wells T, et al. Hum Mol Genet. 2012 Nov 15;21(22):4836-44. doi: 10.1093/hmg/dds315. Epub 2012 Aug 6. Hum Mol Genet. 2012. PMID: 22869679

9

Impaired processing of local geometric features during navigation in a water maze following hippocampal lesions in rats.

Jones PM, Pearce JM, Davies VJ, Good MA, McGregor A. Jones PM, et al. Behav Neurosci. 2007 Dec;121(6):1258-71. doi: 10.1037/0735-7044.121.6.1258. Behav Neurosci. 2007. PMID: 18085879

10

Re-amputation occurrence in the diabetic population in South Wales, UK.

Kanade R, van Deursen R, Burton J, Davies V, Harding K, Price P. Kanade R, et al. Among authors: davies v. Int Wound J. 2007 Dec;4(4):344-52. doi: 10.1111/j.1742-481X.2007.00313.x. Epub 2007 Oct 24. Int Wound J. 2007. PMID: 17961158 Free PMC article.

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