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 *

184 related articles for article (PubMed ID: 17303074)

  • 1. DNA damage reduces Taq DNA polymerase fidelity and PCR amplification efficiency.
    Sikorsky JA; Primerano DA; Fenger TW; Denvir J
    Biochem Biophys Res Commun; 2007 Apr; 355(2):431-7. PubMed ID: 17303074
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effect of DNA damage on PCR amplification efficiency with the relative threshold cycle method.
    Sikorsky JA; Primerano DA; Fenger TW; Denvir J
    Biochem Biophys Res Commun; 2004 Oct; 323(3):823-30. PubMed ID: 15381074
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel PCR-mediated mutagenesis employing DNA containing a natural abasic site as a template and translesional Taq DNA polymerase.
    Kobayashi A; Kitaoka M; Hayashi K
    J Biotechnol; 2005 Mar; 116(3):227-32. PubMed ID: 15707683
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG.
    Shibutani S; Takeshita M; Grollman AP
    Nature; 1991 Jan; 349(6308):431-4. PubMed ID: 1992344
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comparison of the mutagenic properties of 8-oxo-7,8-dihydro-2'-deoxyadenosine and 8-oxo-7,8-dihydro-2'-deoxyguanosine DNA lesions in mammalian cells.
    Tan X; Grollman AP; Shibutani S
    Carcinogenesis; 1999 Dec; 20(12):2287-92. PubMed ID: 10590221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of 2-chloro-2'-deoxyadenosine incorporation into cellular DNA by quantitative polymerase chain reaction.
    Yuh SH; Tibudan M; Hentosh P
    Anal Biochem; 1998 Aug; 262(1):1-8. PubMed ID: 9735141
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An approach to random mutagenesis of DNA using mixtures of triphosphate derivatives of nucleoside analogues.
    Zaccolo M; Williams DM; Brown DM; Gherardi E
    J Mol Biol; 1996 Feb; 255(4):589-603. PubMed ID: 8568899
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Oligoribonucleotide (ORN) interference-PCR (ORNi-PCR): a simple method for suppressing PCR amplification of specific DNA sequences using ORNs.
    Tanigawa N; Fujita T; Fujii H
    PLoS One; 2014; 9(11):e113345. PubMed ID: 25405983
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Optimal conditions to use Pfu exo(-) DNA polymerase for highly efficient ligation-mediated polymerase chain reaction protocols.
    Angers M; Cloutier JF; Castonguay A; Drouin R
    Nucleic Acids Res; 2001 Aug; 29(16):E83. PubMed ID: 11504891
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Miscoding properties of model estrogen-DNA adducts in reactions catalyzed by mammalian and Escherichia coli DNA polymerases.
    Shibutani S; Itoh S; Yoshizawa I
    Biochemistry; 1997 Feb; 36(7):1755-65. PubMed ID: 9048559
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Simultaneous determination of 8-oxo-2'-deoxyguanosine and 8-oxo-2'-deoxyadenosine in DNA using online column-switching liquid chromatography/tandem mass spectrometry.
    Singh R; Teichert F; Verschoyle RD; Kaur B; Vives M; Sharma RA; Steward WP; Gescher AJ; Farmer PB
    Rapid Commun Mass Spectrom; 2009 Jan; 23(1):151-60. PubMed ID: 19065576
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Discrimination between 8-oxo-2'-deoxyguanosine and 2'-deoxyguanosine in DNA by the single nucleotide primer extension reaction with adap triphosphate.
    Taniguchi Y; Kikukawa Y; Sasaki S
    Angew Chem Int Ed Engl; 2015 Apr; 54(17):5147-51. PubMed ID: 25727406
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analyses of PCR products using DNA templates containing a consecutive deoxyinosine sequence.
    Kobayashi A; Kitaoka M; Hayashi K
    Nucleic Acids Symp Ser (Oxf); 2004; (48):225-6. PubMed ID: 17150560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Miscoding during DNA synthesis on damaged DNA templates catalysed by mammalian cell extracts.
    Shibutani S; Grollman AP
    Cancer Lett; 1994 Aug; 83(1-2):315-22. PubMed ID: 8062231
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A simple and eficient method for high fidelity PCR cloning using antibody-neutralizing technology.
    Kitabayashi M; Nishiya Y; Esaka M
    Biosci Biotechnol Biochem; 2003 Sep; 67(9):2034-7. PubMed ID: 14519999
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A single highly mutable catalytic site amino acid is critical for DNA polymerase fidelity.
    Patel PH; Kawate H; Adman E; Ashbach M; Loeb LA
    J Biol Chem; 2001 Feb; 276(7):5044-51. PubMed ID: 11069916
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Discrimination of primer 3'-nucleotide mismatch by taq DNA polymerase during polymerase chain reaction.
    Ayyadevara S; Thaden JJ; Shmookler Reis RJ
    Anal Biochem; 2000 Aug; 284(1):11-8. PubMed ID: 10933850
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Taq polymerase (EC 2.7.7.7): with particular emphasis on its use in PCR protocols.
    Landgraf A; Wolfes H
    Methods Mol Biol; 1993; 16():31-58. PubMed ID: 19082968
    [No Abstract]   [Full Text] [Related]  

  • 19. Suicide polymerase endonuclease restriction, a novel technique for enhancing PCR amplification of minor DNA templates.
    Green SJ; Minz D
    Appl Environ Microbiol; 2005 Aug; 71(8):4721-7. PubMed ID: 16085868
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of mutations using PCR and denaturing gradient gel electrophoresis.
    Cariello NF; Swenberg JA; De Bellis A; Skopek TR
    Environ Mol Mutagen; 1991; 18(4):249-54. PubMed ID: 1748086
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.