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 *

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.