Moore JE - Search Results

1

Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy.

Allen EHA, Atkinson SD, Liao H, Moore JE, Pedrioli DML, Smith FJD, McLean WHI, Moore CBT. Allen EHA, et al. Among authors: moore cbt, moore je. Invest Ophthalmol Vis Sci. 2013 Jan 17;54(1):494-502. doi: 10.1167/iovs.12-10528. Invest Ophthalmol Vis Sci. 2013. PMID: 23233254 Free PMC article.

2

Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy.

Liao H, Irvine AD, Macewen CJ, Weed KH, Porter L, Corden LD, Gibson AB, Moore JE, Smith FJ, McLean WH, Moore CB. Liao H, et al. Among authors: moore je, moore cb. PLoS One. 2011;6(12):e28582. doi: 10.1371/journal.pone.0028582. Epub 2011 Dec 12. PLoS One. 2011. PMID: 22174841 Free PMC article.

3

Effect of tear hyperosmolarity and signs of clinical ocular surface pathology upon conjunctival goblet cell function in the human ocular surface.

Moore JE, Vasey GT, Dartt DA, McGilligan VE, Atkinson SD, Grills C, Lamey PJ, Leccisotti A, Frazer DG, Moore TC. Moore JE, et al. Among authors: moore tc. Invest Ophthalmol Vis Sci. 2011 Aug 3;52(9):6174-80. doi: 10.1167/iovs.10-7022. Invest Ophthalmol Vis Sci. 2011. PMID: 21519030

4

Protection of corneal epithelial stem cells prevents ultraviolet A damage during corneal collagen cross-linking treatment for keratoconus.

Moore JE, Atkinson SD, Azar DT, Worthington J, Downes CS, Courtney DG, Moore CB. Moore JE, et al. Among authors: moore cb. Br J Ophthalmol. 2014 Feb;98(2):270-4. doi: 10.1136/bjophthalmol-2013-303816. Epub 2013 Nov 28. Br J Ophthalmol. 2014. PMID: 24288393

5

A novel role for CRIM1 in the corneal response to UV and pterygium development.

Maurizi E, Schiroli D, Atkinson SD, Mairs L, Courtney DG, O'Hagan B, McGilligan VE, Pagnamenta AT, Taylor JC, Vasquez JJD, Illanes-Velarde DE, Goldsmith D, Gouws P, Moore JE, Nesbit MA, Moore CBT. Maurizi E, et al. Among authors: moore cbt, moore je. Exp Eye Res. 2019 Feb;179:75-92. doi: 10.1016/j.exer.2018.10.012. Epub 2018 Oct 24. Exp Eye Res. 2019. PMID: 30365943

6

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy.

Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJ, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WH. Irvine AD, et al. Among authors: moore je. Nat Genet. 1997 Jun;16(2):184-7. doi: 10.1038/ng0697-184. Nat Genet. 1997. PMID: 9171831

7

CRISPR/Cas9 DNA cleavage at SNP-derived PAM enables both in vitro and in vivo KRT12 mutation-specific targeting.

Courtney DG, Moore JE, Atkinson SD, Maurizi E, Allen EH, Pedrioli DM, McLean WH, Nesbit MA, Moore CB. Courtney DG, et al. Among authors: moore je, moore cb. Gene Ther. 2016 Jan;23(1):108-12. doi: 10.1038/gt.2015.82. Epub 2015 Aug 20. Gene Ther. 2016. PMID: 26289666 Free PMC article.

8

A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy.

Irvine AD, Coleman CM, Moore JE, Swensson O, Morgan SJ, McCarthy JH, Smith FJ, Black GC, McLean WH. Irvine AD, et al. Among authors: moore je. Br J Ophthalmol. 2002 Jul;86(7):729-32. doi: 10.1136/bjo.86.7.729. Br J Ophthalmol. 2002. PMID: 12084738 Free PMC article.

9

P63 expression in conjunctival proliferative diseases: pterygium and laryngo-onycho-cutaneous (LOC) syndrome.

Atkinson SD, Moore JE, Shah S, Sharma A, Best RM, Leccisotti A, Alarbi M, Rimmer D, Gardiner T, Moore TC. Atkinson SD, et al. Among authors: moore je, moore tc. Curr Eye Res. 2008 Jul;33(7):551-8. doi: 10.1080/02713680802187453. Curr Eye Res. 2008. PMID: 18600487

10

An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.

McLean WH, Irvine AD, Hamill KJ, Whittock NV, Coleman-Campbell CM, Mellerio JE, Ashton GS, Dopping-Hepenstal PJ, Eady RA, Jamil T, Phillips R, Shabbir SG, Haroon TS, Khurshid K, Moore JE, Page B, Darling J, Atherton DJ, Van Steensel MA, Munro CS, Smith FJ, McGrath JA. McLean WH, et al. Among authors: moore je. Hum Mol Genet. 2003 Sep 15;12(18):2395-409. doi: 10.1093/hmg/ddg234. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915477

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