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 *

273 related articles for article (PubMed ID: 12700042)

  • 1. The molecular genetics of the corneal dystrophies--current status.
    Klintworth GK
    Front Biosci; 2003 May; 8():d687-713. PubMed ID: 12700042
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Advances in the molecular genetics of corneal dystrophies.
    Klintworth GK
    Am J Ophthalmol; 1999 Dec; 128(6):747-54. PubMed ID: 10612512
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy.
    Stewart H; Black GC; Donnai D; Bonshek RE; McCarthy J; Morgan S; Dixon MJ; Ridgway AA
    Ophthalmology; 1999 May; 106(5):964-70. PubMed ID: 10328397
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Corneal dystrophies in the light of modern molecular genetic research].
    Auw-Hädrich C; Witschel H
    Ophthalmologe; 2002 Jun; 99(6):418-26. PubMed ID: 12125408
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Corneal dystrophies in Japan.
    Fujiki K; Nakayasu K; Kanai A
    J Hum Genet; 2001; 46(8):431-5. PubMed ID: 11501939
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis.
    Stewart HS; Ridgway AE; Dixon MJ; Bonshek R; Parveen R; Black G
    Hum Mutat; 1999; 14(2):126-32. PubMed ID: 10425035
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetics of the corneal endothelial dystrophies: an evidence-based review.
    Aldave AJ; Han J; Frausto RF
    Clin Genet; 2013 Aug; 84(2):109-19. PubMed ID: 23662738
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Autosomal dominant inherited corneal dystrophies associated with TGFBI mutation].
    Mashima Y; Yamada M; Oguchi Y
    Nippon Ganka Gakkai Zasshi; 2001 Oct; 105(10):659-72. PubMed ID: 11692612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.
    Takács L; Losonczy G; Matesz K; Balogh I; Sohajda Z; Tóth K; Fazakas F; Vereb G; Berta A
    Mol Vis; 2007 Oct; 13():1976-83. PubMed ID: 17982422
    [TBL] [Abstract][Full Text] [Related]  

  • 10. IC3D classification of corneal dystrophies--edition 2.
    Weiss JS; Møller HU; Aldave AJ; Seitz B; Bredrup C; Kivelä T; Munier FL; Rapuano CJ; Nischal KK; Kim EK; Sutphin J; Busin M; Labbé A; Kenyon KR; Kinoshita S; Lisch W
    Cornea; 2015 Feb; 34(2):117-59. PubMed ID: 25564336
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [The revised newest IC³D classification of corneal dystrophies].
    Seitz B; Lisch W; Weiss J
    Klin Monbl Augenheilkd; 2015 Mar; 232(3):283-94. PubMed ID: 25803558
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Stage-related therapy of corneal dystrophies.
    Seitz B; Lisch W
    Dev Ophthalmol; 2011; 48():116-153. PubMed ID: 21540634
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Corneal dystrophies.
    Klintworth GK
    Orphanet J Rare Dis; 2009 Feb; 4():7. PubMed ID: 19236704
    [TBL] [Abstract][Full Text] [Related]  

  • 14. In vivo laser confocal microscopy findings for Bowman's layer dystrophies (Thiel-Behnke and Reis-Bücklers corneal dystrophies).
    Kobayashi A; Sugiyama K
    Ophthalmology; 2007 Jan; 114(1):69-75. PubMed ID: 17198850
    [TBL] [Abstract][Full Text] [Related]  

  • 15. IC3D Classification of Corneal Dystrophies-Edition 3.
    Weiss JS; Rapuano CJ; Seitz B; Busin M; Kivelä TT; Bouheraoua N; Bredrup C; Nischal KK; Chawla H; Borderie V; Kenyon KR; Kim EK; Møller HU; Munier FL; Berger T; Lisch W
    Cornea; 2024 Apr; 43(4):466-527. PubMed ID: 38359414
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and genetic aspects of the TGFBI-associated corneal dystrophies.
    Lakshminarayanan R; Chaurasia SS; Anandalakshmi V; Chai SM; Murugan E; Vithana EN; Beuerman RW; Mehta JS
    Ocul Surf; 2014 Oct; 12(4):234-51. PubMed ID: 25284770
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and genetic update of corneal dystrophies.
    Lisch W; Weiss JS
    Exp Eye Res; 2019 Sep; 186():107715. PubMed ID: 31301286
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.