Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy.
Allen EH, Atkinson SD, Liao H, Moore JE, Leslie Pedrioli DM, Smith FJ, McLean WH, Moore CB.
Invest Ophthalmol Vis Sci. 2013 Jan 17;54(1):494-502. doi: 10.1167/iovs.12-10528.
Related citations
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.
PLoS One. 2011;6(12):e28582. doi: 10.1371/journal.pone.0028582. Epub 2011 Dec 12.
Stage-related therapy of corneal dystrophies.
Seitz B, Lisch W.
Dev Ophthalmol. 2011;48:116-53. doi: 10.1159/000324081. Epub 2011 Apr 26. Review.
Morphological evaluation of normal human corneal epithelium.
Ehlers N, Heegaard S, Hjortdal J, Ivarsen A, Nielsen K, Prause JU.
Acta Ophthalmol. 2010 Dec;88(8):858-61. doi: 10.1111/j.1755-3768.2009.01610.x.
Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann's corneal dystrophy in a German family.
Clausen I, Duncker GI, Grünauer-Kloevekorn C.
Mol Vis. 2010 May 29;16:954-60.
Management of symptomatic Meesmann dystrophy.
Jalbert I, Stapleton F.
Optom Vis Sci. 2009 Oct;86(10):E1202-6. doi: 10.1097/OPX.0b013e3181baad27.
Recurrent Meesmann's corneal dystrophy: treatment with keratectomy and mitomycin C.
Yeung JY, Hodge WG.
Can J Ophthalmol. 2009 Feb;44(1):103-4. doi: 10.3129/i08-179. No abstract available.
Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.
Szaflik JP, Ołdak M, Maksym RB, Kamińska A, Pollak A, Udziela M, Płoski R, Szaflik J.
Mol Vis. 2008 Sep 15;14:1713-8.
A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy.
Seto T, Fujiki K, Kishishita H, Fujimaki T, Murakami A, Kanai A.
Jpn J Ophthalmol. 2008 May-Jun;52(3):224-6. doi: 10.1007/s10384-007-0518-2. Epub 2008 Jul 27.
Meesmann corneal dystrophy associated with epithelial basement membrane and posterior polymorphous corneal dystrophies.
Cremona FA, Ghosheh FR, Laibson PR, Rapuano CJ, Cohen EJ.
Cornea. 2008 Apr;27(3):374-7. doi: 10.1097/ICO.0b013e31815c18fa.
A novel mutation as the basis for asymptomatic meesmann dystrophy in a Danish family.
Nielsen K, Orntoft T, Hjortdal J, Rasmussen T, Ehlers N.
Cornea. 2008 Jan;27(1):100-2. doi: 10.1097/ICO.0b013e31815652fd.
Meesmann's corneal dystrophy managed with an epithelial delaminator.
Gooi P, Brownstein S, Jackson WB, Mintsioulis G.
Can J Ophthalmol. 2007 Dec;42(6):878-9. No abstract available.
Phenotypic variability in Meesmann's dystrophy: clinical review of the literature and presentation of a family genetically identical to the original family.
Ehlers N, Hjortdal J, Nielsen K, Thiel HJ, Ørntoft T.
Acta Ophthalmol. 2008 Feb;86(1):40-4. Epub 2007 Nov 6. Review.
A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.
Sullivan LS, Baylin EB, Font R, Daiger SP, Pepose JS, Clinch TE, Nakamura H, Zhao XC, Yee RW.
Mol Vis. 2007 Jun 21;13:975-80.
Imaging the microstructural abnormalities of Meesmann corneal dystrophy by in vivo confocal microscopy.
Tuft S, Bron AJ.
Cornea. 2006 Aug;25(7):868; author reply 868-70. No abstract available.
Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.
Nichini O, Manzi Vd, Munier FL, Schorderet DF.
Ophthalmic Genet. 2005 Dec;26(4):169-73.
Novel mutations in the helix termination motif of keratin 3 and keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy.
Chen YT, Tseng SH, Chao SC.
Cornea. 2005 Nov;24(8):928-32.
Imaging the microstructural abnormalities of meesmann corneal dystrophy by in vivo confocal microscopy.
Patel DV, Grupcheva CN, McGhee CN.
Cornea. 2005 Aug;24(6):669-73.
A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy.
Yoon MK, Warren JF, Holsclaw DS, Gritz DC, Margolis TP.
Br J Ophthalmol. 2004 Jun;88(6):752-6.
Comprehensive analysis of keratin gene clusters in humans and rodents.
Hesse M, Zimek A, Weber K, Magin TM.
Eur J Cell Biol. 2004 Feb;83(1):19-26.
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on