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 *

130 related articles for article (PubMed ID: 9886734)

  • 1. 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]  

  • 2. Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type I.
    Endo S; Nguyen TH; Fujiki K; Hotta Y; Nakayasu K; Yamaguchi T; Ishida N; Kanai A
    Am J Ophthalmol; 1999 Jul; 128(1):104-6. PubMed ID: 10482106
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new mutation (A546T) of the betaig-h3 gene responsible for a French lattice corneal dystrophy type IIIA.
    Dighiero P; Drunat S; Ellies P; D'Hermies F; Savoldelli M; Legeais JM; Renard G; Delpech M; Grateau G; Valleix S
    Am J Ophthalmol; 2000 Feb; 129(2):248-51. PubMed ID: 10682981
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Corneal amyloidosis caused by Leu518Pro mutation of betaig-h3 gene.
    Hirano K; Hotta Y; Fujiki K; Kanai A
    Br J Ophthalmol; 2000 Jun; 84(6):583-5. PubMed ID: 10837380
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygotic patient with betaig-h3 gene mutation in granular dystrophy.
    Fujiki K; Hotta Y; Nakayasu K; Kanai A
    Cornea; 1998 May; 17(3):288-92. PubMed ID: 9603385
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gelatino-lattice corneal dystrophy: clinical features and mutational analysis.
    Nakamura T; Nishida K; Dota A; Adachi W; Yamamoto S; Maeda N; Okada M; Kinoshita S
    Am J Ophthalmol; 2000 May; 129(5):665-6. PubMed ID: 10844062
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?].
    Grünauer-Kloevekorn C; Bräutigam S; Wolter-Roessler M; Tost F; Weidle E; Froster U; Duncker GI
    Klin Monbl Augenheilkd; 2005 Dec; 222(12):1017-23. PubMed ID: 16380889
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Survey of patients with granular, lattice, avellino, and Reis-Bücklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes.
    Afshari NA; Mullally JE; Afshari MA; Steinert RF; Adamis AP; Azar DT; Talamo JH; Dohlman CH; Dryja TP
    Arch Ophthalmol; 2001 Jan; 119(1):16-22. PubMed ID: 11146721
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
    Stix B; Leber M; Bingemer P; Gross C; Rüschoff J; Fändrich M; Schorderet DF; Vorwerk CK; Zacharias M; Roessner A; Röcken C
    Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1133-9. PubMed ID: 15790870
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene.
    Okada M; Yamamoto S; Watanabe H; Inoue Y; Tsujikawa M; Maeda N; Shimomura Y; Nishida K; Kinoshita S; Tano Y
    Am J Ophthalmol; 1998 Aug; 126(2):169-76. PubMed ID: 9727509
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.
    Warren JF; Abbott RL; Yoon MK; Crawford JB; Spencer WH; Margolis TP
    Am J Ophthalmol; 2003 Nov; 136(5):872-8. PubMed ID: 14597039
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Severe corneal dystrophy phenotype caused by homozygous R124H keratoepithelin mutations.
    Okada M; Yamamoto S; Inoue Y; Watanabe H; Maeda N; Shimomura Y; Ishii Y; Tano Y
    Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1947-53. PubMed ID: 9727418
    [TBL] [Abstract][Full Text] [Related]  

  • 14. R124C mutation of the betaIGH3 gene leads to remarkable phenotypic variability in a Greek four-generation family with lattice corneal dystrophy type 1.
    Hellenbroich Y; Tzivras G; Neppert B; Schwinger E; Zühlke C
    Ophthalmologica; 2001; 215(6):444-7. PubMed ID: 11741113
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chronic clinical course of two patients with severe corneal dystrophy caused by homozygous R124H mutations in the betaig-h3 gene.
    Kaji Y; Amano S; Oshika T; Usui T; Kitagawa M; Mimura T; Matsubara M
    Am J Ophthalmol; 2000 May; 129(5):663-5. PubMed ID: 10844061
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.
    Hirano K; Hotta Y; Nakamura M; Fujiki K; Kanai A; Yamamoto N
    Cornea; 2001 Jul; 20(5):525-9. PubMed ID: 11413411
    [TBL] [Abstract][Full Text] [Related]  

  • 17. BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.
    Schmitt-Bernard CF; Guittard C; Arnaud B; Demaille J; Argiles A; Claustres M; Tuffery-Giraud S
    Invest Ophthalmol Vis Sci; 2000 May; 41(6):1302-8. PubMed ID: 10798644
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I.
    Tian X; Fujiki K; Wang W; Murakami A; Xie P; Kanai A; Liu Z
    Jpn J Ophthalmol; 2005; 49(2):84-8. PubMed ID: 15838722
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotype of lattice corneal dystrophy (R124C mutation in TGFBI) in a patient presenting with features of avellino corneal dystrophy.
    Edelstein SL; Huang AJ; Harocopos GJ; Waltman SR
    Cornea; 2010 Jun; 29(6):698-700. PubMed ID: 20458218
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
    Correa-Gomez V; Villalvazo-Cordero L; Zenteno JC
    Mol Vis; 2007 Sep; 13():1695-700. PubMed ID: 17893671
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.