These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
113 related articles for article (PubMed ID: 12543196)
1. Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese with Meesmann's corneal dystrophy. Takahashi K; Takahashi K; Murakami A; Okisaka S; Kimura T; Kanai A Jpn J Ophthalmol; 2002; 46(6):673-4. PubMed ID: 12543196 [TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 15148206 [TBL] [Abstract][Full Text] [Related]
3. A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy. Corden LD; Swensson O; Swensson B; Rochels R; Wannke B; Thiel HJ; McLean WH Br J Ophthalmol; 2000 May; 84(5):527-30. PubMed ID: 10781519 [TBL] [Abstract][Full Text] [Related]
4. 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 Nat Genet; 1997 Jun; 16(2):184-7. PubMed ID: 9171831 [TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 16227835 [TBL] [Abstract][Full Text] [Related]
6. 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 Br J Ophthalmol; 2002 Jul; 86(7):729-32. PubMed ID: 12084738 [TBL] [Abstract][Full Text] [Related]
7. [Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]. Swensson O; Swensson B; Nölle B; Rochels R; Wannke B; Thiel HJ Klin Monbl Augenheilkd; 2000 Jul; 217(1):43-51. PubMed ID: 10949816 [TBL] [Abstract][Full Text] [Related]
8. 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; 13():975-80. PubMed ID: 17653038 [TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 16352477 [TBL] [Abstract][Full Text] [Related]
10. [Analysis of mutation in KRT12 gene in a Chinese family with Meesmann's corneal dystrophy]. Wang LJ; Tian X; Zhang QS; Liu L Zhonghua Yan Ke Za Zhi; 2007 Oct; 43(10):885-9. PubMed ID: 18201524 [TBL] [Abstract][Full Text] [Related]
11. 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; 16():954-60. PubMed ID: 20577595 [TBL] [Abstract][Full Text] [Related]
12. A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy. Coleman CM; Hannush S; Covello SP; Smith FJ; Uitto J; McLean WH Am J Ophthalmol; 1999 Dec; 128(6):687-91. PubMed ID: 10612503 [TBL] [Abstract][Full Text] [Related]
13. 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 Exp Eye Res; 2000 Jan; 70(1):41-9. PubMed ID: 10644419 [TBL] [Abstract][Full Text] [Related]
14. Recurrent Meesmann's corneal epithelial dystrophy after penetrating keratoplasty. Chiou AG; Florakis GJ; Copeland RL; Williams VA; McCormick SA; Chiesa R Cornea; 1998 Sep; 17(5):566-70. PubMed ID: 9756454 [TBL] [Abstract][Full Text] [Related]
15. 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 Am J Hum Genet; 1997 Dec; 61(6):1268-75. PubMed ID: 9399908 [TBL] [Abstract][Full Text] [Related]
16. Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy. Ha NT; Chau HM; Cung le X; Thanh TK; Fujiki K; Murakami A; Hiratsuka Y; Kanai A Invest Ophthalmol Vis Sci; 2003 Aug; 44(8):3310-6. PubMed ID: 12882775 [TBL] [Abstract][Full Text] [Related]
17. Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to xp22.3. Lisch W; Büttner A; Oeffner F; Böddeker I; Engel H; Lisch C; Ziegler A; Grzeschik K Am J Ophthalmol; 2000 Oct; 130(4):461-8. PubMed ID: 11024418 [TBL] [Abstract][Full Text] [Related]
18. 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; 14():1713-8. PubMed ID: 18806880 [TBL] [Abstract][Full Text] [Related]
19. A novel mutation at codon 124 (R124L) in the BIGH3 gene is associated with a superficial variant of granular corneal dystrophy. Mashima Y; Nakamura Y; Noda K; Konishi M; Yamada M; Kudoh J; Shimizu N Arch Ophthalmol; 1999 Jan; 117(1):90-3. PubMed ID: 9930165 [TBL] [Abstract][Full Text] [Related]
20. Arg124Cys mutation of the betaig-h3 bene in a Japanese family with lattice corneal dystrophy type I. Hotta Y; Fujiki K; Ono K; Fujimaki T; Nakayasu K; Yamaguchi T; Kanai A Jpn J Ophthalmol; 1998; 42(6):450-5. PubMed ID: 9886734 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]