PubMed (GeneRIF) for id: 3859

Year	Number of Results
2002	1
2005	2
2007	1
2008	2
2010	1
2012	1
2013	4
2014	2
2016	1
2017	2
2018	2
2019	1
2024	0

1

In vivo histology and p.L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophy.

Nishino T, Kobayashi A, Mori N, Masaki T, Yokogawa H, Fujiki K, Yanagawa A, Murakami A, Sugiyama K. Nishino T, et al. Jpn J Ophthalmol. 2019 Jan;63(1):46-55. doi: 10.1007/s10384-018-00643-6. Epub 2018 Dec 7. Jpn J Ophthalmol. 2019. PMID: 30535821

2

Human aniridia limbal epithelial cells lack expression of keratins K3 and K12.

Latta L, Viestenz A, Stachon T, Colanesi S, Szentmáry N, Seitz B, Käsmann-Kellner B. Latta L, et al. Exp Eye Res. 2018 Feb;167:100-109. doi: 10.1016/j.exer.2017.11.005. Epub 2017 Nov 21. Exp Eye Res. 2018. PMID: 29162348

3

Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.

Du X, Chen P, Sun D. Du X, et al. Graefes Arch Clin Exp Ophthalmol. 2017 Sep;255(9):1779-1786. doi: 10.1007/s00417-017-3699-5. Epub 2017 May 31. Graefes Arch Clin Exp Ophthalmol. 2017. PMID: 28567551

4

PAX6 Isoforms, along with Reprogramming Factors, Differentially Regulate the Induction of Cornea-specific Genes.

Sasamoto Y, Hayashi R, Park SJ, Saito-Adachi M, Suzuki Y, Kawasaki S, Quantock AJ, Nakai K, Tsujikawa M, Nishida K. Sasamoto Y, et al. Sci Rep. 2016 Feb 22;6:20807. doi: 10.1038/srep20807. Sci Rep. 2016. PMID: 26899008 Free PMC article.

5

siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy.

Courtney DG, Atkinson SD, Allen EH, Moore JE, Walsh CP, Pedrioli DM, MacEwen CJ, Pellegrini G, Maurizi E, Serafini C, Fantacci M, Liao H, Irvine AD, McLean WH, Moore CB. Courtney DG, et al. Invest Ophthalmol Vis Sci. 2014 May 6;55(5):3352-60. doi: 10.1167/iovs.13-12957. Invest Ophthalmol Vis Sci. 2014. PMID: 24801514

6

KRT12 mutations and in vivo confocal microscopy in two Japanese families with Meesmann corneal dystrophy.

Ogasawara M, Matsumoto Y, Hayashi T, Ohno K, Yamada H, Kawakita T, Dogru M, Shimazaki J, Tsubota K, Tsuneoka H. Ogasawara M, et al. Am J Ophthalmol. 2014 Jan;157(1):93-102.e1. doi: 10.1016/j.ajo.2013.08.008. Epub 2013 Oct 5. Am J Ophthalmol. 2014. PMID: 24099278

7

Autosomal-dominant Meesmann epithelial corneal dystrophy without an exon mutation in the keratin-3 or keratin-12 gene in a Chinese family.

Cao W, Yan M, Hao Q, Wang S, Wu L, Liu Q, Li M, Biddle FG, Wu W. Cao W, et al. J Int Med Res. 2013 Apr;41(2):511-8. doi: 10.1177/0300060513477306. Epub 2013 Mar 12. J Int Med Res. 2013. PMID: 23569037 Free article.

8

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. 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.

9

Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.

Hassan H, Thaung C, Ebenezer ND, Larkin G, Hardcastle AJ, Tuft SJ. Hassan H, et al. Eye (Lond). 2013 Mar;27(3):367-73. doi: 10.1038/eye.2012.261. Epub 2012 Dec 7. Eye (Lond). 2013. PMID: 23222558 Free PMC article.

10

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. Clausen I, et al. Mol Vis. 2010 May 29;16:954-60. Mol Vis. 2010. PMID: 20577595 Free PMC article.

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