162 related articles for article (PubMed ID: 12084738)
1. 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]
2. 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]
3. [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]
4. 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]
5. 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
Eye (Lond); 2013 Mar; 27(3):367-73. PubMed ID: 23222558
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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
Mol Vis; 2015; 21():1378-86. PubMed ID: 26788030
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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
Invest Ophthalmol Vis Sci; 2014 May; 55(5):3352-60. PubMed ID: 24801514
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Identification of a Novel Missense
Dong PN; Cung LX; Sam TK; Hang DTT; Chung DD; Alkadi TA; Buckshey A; Zhang J; Kassels A; Aldave AJ
Case Rep Ophthalmol; 2020; 11(1):120-126. PubMed ID: 32308613
[TBL] [Abstract][Full Text] [Related]
18. 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
Hum Mol Genet; 2016 Mar; 25(6):1176-91. PubMed ID: 26758872
[TBL] [Abstract][Full Text] [Related]
19. Meesmann's corneal dystrophy: ultrastructural features.
Tremblay M; Dubé I
Can J Ophthalmol; 1982 Feb; 17(1):24-8. PubMed ID: 6979375
[TBL] [Abstract][Full Text] [Related]
20. Coexistence of Meesmann Corneal Dystrophy and a Pseudo-Unilateral Lattice Corneal Dystrophy in a Patient With a Novel Pathogenic Variant in the Keratin K3 Gene: A Case Report.
Abad-Morales V; Barbany M; Gris O; Güell JL; Pomares E
Cornea; 2021 Mar; 40(3):370-372. PubMed ID: 33346999
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
