BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 9611257)

  • 1. Detection of known mutation by proof-reading PCR.
    Bi W; Stambrook PJ
    Nucleic Acids Res; 1998 Jun; 26(12):3073-5. PubMed ID: 9611257
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PCR amplification of specific alleles: rapid detection of known mutations and polymorphisms.
    Bottema CD; Sommer SS
    Mutat Res; 1993 Jul; 288(1):93-102. PubMed ID: 7686270
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fidelity of Thermococcus litoralis DNA polymerase (Vent) in PCR determined by denaturing gradient gel electrophoresis.
    Cariello NF; Swenberg JA; Skopek TR
    Nucleic Acids Res; 1991 Aug; 19(15):4193-8. PubMed ID: 1870973
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PCR bias toward the wild-type k-ras and p53 sequences: implications for PCR detection of mutations and cancer diagnosis.
    Barnard R; Futo V; Pecheniuk N; Slattery M; Walsh T
    Biotechniques; 1998 Oct; 25(4):684-91. PubMed ID: 9793653
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Modified Proofreading PCR for Detection of Point Mutations, Insertions and Deletions Using a ddNTP-Blocked Primer.
    Hao W; Fan L; Chen Q; Chen X; Zhang S; Lan K; Lu J; Zhang C
    PLoS One; 2015; 10(4):e0123468. PubMed ID: 25915410
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutational analysis using denaturing gradient gel electrophoresis and PCR.
    Cariello NF; Skopek TR
    Mutat Res; 1993 Jul; 288(1):103-12. PubMed ID: 7686254
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High-fidelity DNA polymerase enhances the sensitivity of a peptide nucleic acid clamp PCR assay for K-ras mutations.
    Gilje B; Heikkilä R; Oltedal S; Tjensvoll K; Nordgård O
    J Mol Diagn; 2008 Jul; 10(4):325-31. PubMed ID: 18556764
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of 15 polymerases and phosphorothioate primer modification for detection of UV-induced C:G to T:A mutations by allele-specific PCR.
    Gale JM; Tafoya GB
    Photochem Photobiol; 2004 May; 79(5):461-9. PubMed ID: 15191056
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Direct cycle sequencing with delta Taq DNA polymerase.
    Fan J; Ranu RS
    DNA Seq; 1997; 7(5):285-8. PubMed ID: 9255519
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel assay for allelic discrimination that combines the fluorogenic 5' nuclease polymerase chain reaction (TaqMan) and mismatch amplification mutation assay.
    Glaab WE; Skopek TR
    Mutat Res; 1999 Nov; 430(1):1-12. PubMed ID: 10592313
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluation of MutS as a tool for direct measurement of point mutations in genomic DNA.
    Parsons BL; Heflich RH
    Mutat Res; 1997 Mar; 374(2):277-85. PubMed ID: 9100851
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the allele-specific PCR method for the detection of neoplastic disease.
    Rhodes CH; Honsinger C; Porter DM; Sorenson GD
    Diagn Mol Pathol; 1997 Feb; 6(1):49-57. PubMed ID: 9028737
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Context-dependent Taq-polymerase-mediated nucleotide alterations, as revealed by direct sequencing of the ZNF189 gene: implications for mutation detection.
    Odeberg J; Ahmadian A; Williams C; Uhlén M; Pontén F; Lundeberg J
    Gene; 1999 Jul; 235(1-2):103-9. PubMed ID: 10415338
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of the amplification refractory mutation allele-specific polymerase chain reaction system for sensitive and specific detection of p53 mutations in DNA.
    Low EO; Jones AM; Gibbins JR; Walker DM
    J Pathol; 2000 Mar; 190(4):512-5. PubMed ID: 10700003
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation detection by TaqMan-allele specific amplification: application to molecular diagnosis of glycogen storage disease type Ia and medium-chain acyl-CoA dehydrogenase deficiency.
    Fujii K; Matsubara Y; Akanuma J; Takahashi K; Kure S; Suzuki Y; Imaizumi M; Iinuma K; Sakatsume O; Rinaldo P; Narisawa K
    Hum Mutat; 2000; 15(2):189-96. PubMed ID: 10649496
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An amplification and ligation-based method to scan for unknown mutations in DNA.
    Zhang Y; Kaur M; Price BD; Tetradis S; Makrigiorgos GM
    Hum Mutat; 2002 Aug; 20(2):139-47. PubMed ID: 12124995
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Polymerase specific error rates and profiles identified by single molecule sequencing.
    Hestand MS; Van Houdt J; Cristofoli F; Vermeesch JR
    Mutat Res; 2016; 784-785():39-45. PubMed ID: 26829216
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Highly selective isolation of unknown mutations in diverse DNA fragments: toward new multiplex screening in cancer.
    Chakrabarti S; Price BD; Tetradis S; Fox EA; Zhang Y; Maulik G; Makrigiorgos GM
    Cancer Res; 2000 Jul; 60(14):3732-7. PubMed ID: 10919642
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heterozygote and mutation detection by direct automated fluorescent DNA sequencing using a mutant Taq DNA polymerase.
    Chadwick RB; Conrad MP; McGinnis MD; Johnston-Dow L; Spurgeon SL; Kronick MN
    Biotechniques; 1996 Apr; 20(4):676-83. PubMed ID: 8800689
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High-throughput simultaneous detection of point mutations and large-scale rearrangements by CE.
    Weber J; Miserere S; Champ J; Looten R; Stoppa-Lyonnet D; Viovy JL; Houdayer C
    Electrophoresis; 2007 Dec; 28(23):4282-8. PubMed ID: 17990260
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.