Keighren MA - Search Results

1

Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical model.

Mort RL, Ross RJH, Hainey KJ, Harrison OJ, Keighren MA, Landini G, Baker RE, Painter KJ, Jackson IJ, Yates CA. Mort RL, et al. Among authors: keighren ma. Nat Commun. 2016 Jan 6;7:10288. doi: 10.1038/ncomms10288. Nat Commun. 2016. PMID: 26732977 Free PMC article.

2

Genomic localization of a Dct-LacZ transgene locus: a simple assay for transgene status.

Takemoto Y, Keighren M, Jackson IJ, Yamamoto H. Takemoto Y, et al. Pigment Cell Res. 2006 Dec;19(6):644-5. doi: 10.1111/j.1600-0749.2006.00343.x. Pigment Cell Res. 2006. PMID: 17083491 No abstract available.

3

Humanized MC1R transgenic mice reveal human specific receptor function.

Jackson IJ, Budd PS, Keighren M, McKie L. Jackson IJ, et al. Hum Mol Genet. 2007 Oct 1;16(19):2341-8. doi: 10.1093/hmg/ddm191. Epub 2007 Jul 25. Hum Mol Genet. 2007. PMID: 17652101

4

Palmitoylation regulates epidermal homeostasis and hair follicle differentiation.

Mill P, Lee AW, Fukata Y, Tsutsumi R, Fukata M, Keighren M, Porter RM, McKie L, Smyth I, Jackson IJ. Mill P, et al. PLoS Genet. 2009 Nov;5(11):e1000748. doi: 10.1371/journal.pgen.1000748. Epub 2009 Nov 26. PLoS Genet. 2009. PMID: 19956733 Free PMC article.

5

Involvement of the melanocortin-1 receptor in acute pain and pain of inflammatory but not neuropathic origin.

Delaney A, Keighren M, Fleetwood-Walker SM, Jackson IJ. Delaney A, et al. PLoS One. 2010 Sep 13;5(9):e12498. doi: 10.1371/journal.pone.0012498. PLoS One. 2010. PMID: 20856883 Free PMC article.

6

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Mill P, Lockhart PJ, Fitzpatrick E, Mountford HS, Hall EA, Reijns MA, Keighren M, Bahlo M, Bromhead CJ, Budd P, Aftimos S, Delatycki MB, Savarirayan R, Jackson IJ, Amor DJ. Mill P, et al. Among authors: keighren m. Am J Hum Genet. 2011 Apr 8;88(4):508-15. doi: 10.1016/j.ajhg.2011.03.015. Am J Hum Genet. 2011. PMID: 21473986 Free PMC article.

7

A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.

Jadeja S, Mort RL, Keighren M, Hart AW, Joynson R, Wells S, Potter PK, Jackson IJ. Jadeja S, et al. Invest Ophthalmol Vis Sci. 2013 May 1;54(5):3569-78. doi: 10.1167/iovs.12-11125. Invest Ophthalmol Vis Sci. 2013. PMID: 23633653 Free PMC article.

8

A trans-acting protein effect causes severe eye malformation in the Mp mouse.

Rainger J, Keighren M, Keene DR, Charbonneau NL, Rainger JK, Fisher M, Mella S, Huang JT, Rose L, van't Hof R, Sakai LY, Jackson IJ, Fitzpatrick DR. Rainger J, et al. PLoS Genet. 2013;9(12):e1003998. doi: 10.1371/journal.pgen.1003998. Epub 2013 Dec 12. PLoS Genet. 2013. PMID: 24348270 Free PMC article.

9

Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes.

Hall EA, Keighren M, Ford MJ, Davey T, Jarman AP, Smith LB, Jackson IJ, Mill P. Hall EA, et al. PLoS Genet. 2013;9(12):e1003928. doi: 10.1371/journal.pgen.1003928. Epub 2013 Dec 26. PLoS Genet. 2013. PMID: 24415959 Free PMC article.

10

A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected].

Cross SH, Macalinao DG, McKie L, Rose L, Kearney AL, Rainger J, Thaung C, Keighren M, Jadeja S, West K, Kneeland SC, Smith RS, Howell GR, Young F, Robertson M, van T' Hof R, John SW, Jackson IJ. Cross SH, et al. PLoS Genet. 2014 May 8;10(5):e1004359. doi: 10.1371/journal.pgen.1004359. eCollection 2014 May. PLoS Genet. 2014. PMID: 24809698 Free PMC article.

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