BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

303 related articles for article (PubMed ID: 20092310)

  • 1. Detection of the most common corneal dystrophies caused by BIGH3 gene point mutations using a multispot gold-capped nanoparticle array chip.
    Yoo SY; Kim DK; Park TJ; Kim EK; Tamiya E; Lee SY
    Anal Chem; 2010 Feb; 82(4):1349-57. PubMed ID: 20092310
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development of a DNA chip for the diagnosis of the most common corneal dystrophies caused by mutations in the betaigh3 gene.
    Yoo SY; Kim TI; Lee SY; Kim EK; Keum KC; Yoo NC; Yoo WM
    Br J Ophthalmol; 2007 Jun; 91(6):722-7. PubMed ID: 17215264
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Identification of BIGH3 gene mutations in the patients with two types of corneal dystrophies].
    Jin T; Zou LH; Yang L; Dong WL; Yu J; Lu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):32-4. PubMed ID: 14767905
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Label-free detection of peptide nucleic acid-DNA hybridization using localized surface plasmon resonance based optical biosensor.
    Endo T; Kerman K; Nagatani N; Takamura Y; Tamiya E
    Anal Chem; 2005 Nov; 77(21):6976-84. PubMed ID: 16255598
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Analysis of mutation of BIGH3 gene in Chinese patients with corneal dystrophies].
    Yu J; Zou LH; He JC; Liu NP; Zhang W; Lu L; Sun XG; Dong DS; Wu YY; Yin XT
    Zhonghua Yan Ke Za Zhi; 2003 Oct; 39(10):582-6. PubMed ID: 14766070
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Disposable nucleic acid biosensors based on gold nanoparticle probes and lateral flow strip.
    Mao X; Ma Y; Zhang A; Zhang L; Zeng L; Liu G
    Anal Chem; 2009 Feb; 81(4):1660-8. PubMed ID: 19159221
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sensitive Surface Enhanced Raman Scattering-Based Detection of a BIGH3 Point Mutation Associated with Avellino Corneal Dystrophy.
    Kim S; Jeong SN; Bae S; Chung H; Yoo SY
    Anal Chem; 2016 Dec; 88(23):11288-11292. PubMed ID: 27934116
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.
    Zhao XC; Nakamura H; Subramanyam S; Stock LE; Gillette TE; Yoshikawa S; Ma X; Yee RW
    Ophthalmology; 2007 Nov; 114(11):e39-46. PubMed ID: 17980739
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Single gold nanoparticles counter: an ultrasensitive detection platform for one-step homogeneous immunoassays and DNA hybridization assays.
    Xie C; Xu F; Huang X; Dong C; Ren J
    J Am Chem Soc; 2009 Sep; 131(35):12763-70. PubMed ID: 19678640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A subset of patients with epithelial basement membrane corneal dystrophy have mutations in TGFBI/BIGH3.
    Boutboul S; Black GC; Moore JE; Sinton J; Menasche M; Munier FL; Laroche L; Abitbol M; Schorderet DF
    Hum Mutat; 2006 Jun; 27(6):553-7. PubMed ID: 16652336
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. TGFBI gene mutations in Brazilian patients with corneal dystrophy.
    Solari HP; Ventura MP; Perez AB; Sallum JM; Burnier MN; Belfort R
    Eye (Lond); 2007 May; 21(5):587-90. PubMed ID: 16440005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Detection of p53 gene mutation by using a novel biosensor based on localized surface plasmon resonance.
    Duan RQ; Yuan JL; Yang H; Luo XG; Xi MR
    Neoplasma; 2012; 59(3):348-53. PubMed ID: 22329850
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Genetics of anterior and stromal corneal dystrophies.
    Poulaki V; Colby K
    Semin Ophthalmol; 2008; 23(1):9-17. PubMed ID: 18214787
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 16.