BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 9086825)

  • 1. [Gene diagnosis with an affinity sensor, BIACORE--principle and applications].
    Gotoh M; Hasebe M; Ohira T; Tosu M
    Rinsho Byori; 1997 Mar; 45(3):224-8. PubMed ID: 9086825
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detection of point mutation and insertion mutations in DNA using a quartz crystal microbalance and MutS, a mismatch binding protein.
    Su X; Robelek R; Wu Y; Wang G; Knoll W
    Anal Chem; 2004 Jan; 76(2):489-94. PubMed ID: 14719903
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fiberoptic DNA sensor array capable of detecting point mutations.
    Healey BG; Matson RS; Walt DR
    Anal Biochem; 1997 Sep; 251(2):270-9. PubMed ID: 9299026
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of basepair substitution mutation at a frequency of 1 x 10(-7) by combining two genotypic selection methods, MutEx enrichment and allele-specific competitive blocker PCR.
    Parsons BL; Heflich RH
    Environ Mol Mutagen; 1998; 32(3):200-11. PubMed ID: 9814434
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR.
    Feriotto G; Ferlini A; Ravani A; Calzolari E; Mischiati C; Bianchi N; Gambari R
    Hum Mutat; 2001; 18(1):70-81. PubMed ID: 11438995
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Non-radioactive detection of K-ras mutations by nested allele specific PCR and oligonucleotide hybridization.
    Paranavitana CM
    Mol Cell Probes; 1998 Oct; 12(5):309-15. PubMed ID: 9778456
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quantitative detection of mutant alleles of the K-ras gene with minor groove binder-conjugated fluorogenic DNA probes.
    Itabashi T; Maesawa C; Uchiyama M; Higuchi T; Masuda T
    Int J Oncol; 2004 Mar; 24(3):687-96. PubMed ID: 14767554
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of Ki-ras mutations by PCR and differential hybridization and of p53 mutations by SSCP analysis in endoscopically obtained lavage solution from patients with long-standing ulcerative colitis.
    Lang SM; Heinzlmann M; Stratakis DF; Teschauer W; Loeschke K
    Am J Gastroenterol; 1997 Dec; 92(12):2166-70. PubMed ID: 9399746
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of mutations in PCR products from clinical samples by surface plasmon resonance.
    Nilsson P; Persson B; Larsson A; Uhlén M; Nygren PA
    J Mol Recognit; 1997; 10(1):7-17. PubMed ID: 9179775
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Universal DNA microarray method for multiplex detection of low abundance point mutations.
    Gerry NP; Witowski NE; Day J; Hammer RP; Barany G; Barany F
    J Mol Biol; 1999 Sep; 292(2):251-62. PubMed ID: 10493873
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Electrochemical scanning of DNA point mutations via MutS protein-mediated mismatch recognition.
    Chen H; Liu XJ; Liu YL; Jiang JH; Shen GL; Yu RQ
    Biosens Bioelectron; 2009 Mar; 24(7):1955-61. PubMed ID: 19022650
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA hybridization in nanostructural molecular assemblies enables detection of gene mutations without a fluorescent probe.
    Maruyama T; Park LC; Shinohara T; Goto M
    Biomacromolecules; 2004; 5(1):49-53. PubMed ID: 14715007
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MutS as a tool for mutation detection.
    Stanisławska-Sachadyn A; Sachadyn P
    Acta Biochim Pol; 2005; 52(3):575-83. PubMed ID: 16082411
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low density DNA microarray for detection of most frequent TP53 missense point mutations.
    Rangel-López A; Maldonado-Rodríguez R; Salcedo-Vargas M; Espinosa-Lara JM; Méndez-Tenorio A; Beattie KL
    BMC Biotechnol; 2005 Feb; 5():8. PubMed ID: 15713227
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide detection of unknown subtle mutations in bacteria by combination of MutS and RDA.
    Gotoh K; Hata M; Miyajima M; Yokota H
    Biochem Biophys Res Commun; 2000 Feb; 268(2):535-40. PubMed ID: 10679239
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The use of immobilized mismatch binding protein in mutation/SNP detection.
    Wagner R; Dean A
    Methods Mol Biol; 2000; 152():159-68. PubMed ID: 10957976
    [No Abstract]   [Full Text] [Related]  

  • 17. Detection of clinically relevant point mutations by a novel piezoelectric biosensor.
    Dell'Atti D; Tombelli S; Minunni M; Mascini M
    Biosens Bioelectron; 2006 Apr; 21(10):1876-9. PubMed ID: 16388945
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polymerase chain reaction/ligase detection reaction/hybridization assays using flow-through microfluidic devices for the detection of low-abundant DNA point mutations.
    Hashimoto M; Barany F; Soper SA
    Biosens Bioelectron; 2006 Apr; 21(10):1915-23. PubMed ID: 16488597
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Approaching real-time molecular diagnostics: single-pair fluorescence resonance energy transfer (spFRET) detection for the analysis of low abundant point mutations in K-ras oncogenes.
    Wabuyele MB; Farquar H; Stryjewski W; Hammer RP; Soper SA; Cheng YW; Barany F
    J Am Chem Soc; 2003 Jun; 125(23):6937-45. PubMed ID: 12783546
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Design of electrochemical biosensor systems for the detection of specific DNA sequences in PCR-amplified nucleic acids related to the catechol-O-methyltransferase Val108/158Met polymorphism based on intrinsic guanine signal.
    Ozkan-Ariksoysal D; Tezcanli B; Kosova B; Ozsoz M
    Anal Chem; 2008 Feb; 80(3):588-96. PubMed ID: 18181582
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.