PubMed (OMIM) for id: 3859

Year	Number of Results
1954	2
1963	1
1964	1
1965	1
1966	1
1968	1
1977	1
1993	1
1994	1
1996	2
1997	2
1998	1
2000	1
2011	1
2015	1
2016	1
2024	0

1

Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy.

Chen JL, Lin BR, Gee KM, Gee JA, Chung DW, Frausto RF, Deng SX, Aldave AJ. Chen JL, et al. Mol Vis. 2015 Dec 31;21:1378-86. eCollection 2015. Mol Vis. 2015. PMID: 26788030 Free PMC article.

2

Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy.

Allen EH, Courtney DG, Atkinson SD, Moore JE, Mairs L, Poulsen ET, Schiroli D, Maurizi E, Cole C, Hickerson RP, James J, Murgatroyd H, Smith FJ, MacEwen C, Enghild JJ, Nesbit MA, Leslie Pedrioli DM, McLean WH, Moore CB. Allen EH, et al. Hum Mol Genet. 2016 Mar 15;25(6):1176-91. doi: 10.1093/hmg/ddw001. Epub 2016 Jan 11. Hum Mol Genet. 2016. PMID: 26758872 Free PMC article.

3

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. PLoS One. 2011;6(12):e28582. doi: 10.1371/journal.pone.0028582. Epub 2011 Dec 12. PLoS One. 2011. PMID: 22174841 Free PMC article.

4

Rare form of hereditary epithelial dystrophy of the cornea; genetic, clinical, and pathologic study.

STOCKER FW, HOLT LB. STOCKER FW, et al. AMA Arch Ophthalmol. 1954 Apr;53(4):536-41. AMA Arch Ophthalmol. 1954. PMID: 14360886 No abstract available.

5

MEESMANN'S CORNEAL DYSTROPHY. A PATHOLOGICAL STUDY.

KUWABARA T, CICCARELLI EC. KUWABARA T, et al. Arch Ophthalmol. 1964 May;71:672-82. doi: 10.1001/archopht.1964.00970010692015. Arch Ophthalmol. 1964. PMID: 14120659 No abstract available.

6

Hereditary epithelial corneal dystrophy.

SNYDER WB. SNYDER WB. Am J Ophthalmol. 1963 Jan;55:56-61. doi: 10.1016/0002-9394(63)91648-9. Am J Ophthalmol. 1963. PMID: 13993171 No abstract available.

7

A rare form of hereditary epithelial dystrophy of the cornea: a genetic, clinical, and pathologic study.

STOCKER FW, HOLT LB. STOCKER FW, et al. Trans Am Ophthalmol Soc. 1954-1955;52:133-44. Trans Am Ophthalmol Soc. 1954. PMID: 13274420 Free PMC article. No abstract available.

8

Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

Corden LD, Swensson O, Swensson B, Smith FJ, Rochels R, Uitto J, McLEAN WH. Corden LD, et al. Exp Eye Res. 2000 Jan;70(1):41-9. doi: 10.1006/exer.1999.0769. Exp Eye Res. 2000. PMID: 10644419

9

Meesmann corneal epithelial dystrophy in a Saudi Arabian family.

Badr IA, Basaffar S, Jabak M, Wagoner MD. Badr IA, et al. Am J Ophthalmol. 1998 Feb;125(2):182-6. doi: 10.1016/s0002-9394(99)80089-0. Am J Ophthalmol. 1998. PMID: 9467444

10

Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy.

Nishida K, Honma Y, Dota A, Kawasaki S, Adachi W, Nakamura T, Quantock AJ, Hosotani H, Yamamoto S, Okada M, Shimomura Y, Kinoshita S. Nishida K, et al. Am J Hum Genet. 1997 Dec;61(6):1268-75. doi: 10.1086/301650. Am J Hum Genet. 1997. PMID: 9399908 Free PMC article.

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