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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 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. [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]  

  • 3. 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]  

  • 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. 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]  

  • 6. 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]  

  • 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. 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]  

  • 9. 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]  

  • 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. 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]  

  • 15. 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]  

  • 16. 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]  

  • 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. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.