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 *

159 related articles for article (PubMed ID: 7511817)

  • 1. Mutation detection by mismatch binding protein, MutS, in amplified DNA: application to the cystic fibrosis gene.
    Lishanski A; Ostrander EA; Rine J
    Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2674-8. PubMed ID: 7511817
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MutS binding protects heteroduplex DNA from exonuclease digestion in vitro: a simple method for detecting mutations.
    Ellis LA; Taylor GR; Banks R; Baumberg S
    Nucleic Acids Res; 1994 Jul; 22(13):2710-1. PubMed ID: 7518920
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Mutation detection using immobilized mismatch binding protein (MutS).
    Wagner R; Debbie P; Radman M
    Nucleic Acids Res; 1995 Oct; 23(19):3944-8. PubMed ID: 7479040
    [TBL] [Abstract][Full Text] [Related]  

  • 5. One tube mutation detection using sensitive fluorescent dyeing of MutS protected DNA.
    Sachadyn P; Stanislawska A; Kur J
    Nucleic Acids Res; 2000 Apr; 28(8):E36. PubMed ID: 10734213
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A simplified method for detection of the mutations predominantly causing cystic fibrosis and phenylketonuria in Polish families.
    Witt M; Jaruzelska J; Kuczora I; Matuszak R; Cichy W; Borski K
    Clin Genet; 1993 Jul; 44(1):44-5. PubMed ID: 7691449
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the delta F508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Fortina P; Conant R; Parrella T; Rappaport E; Scanlin T; Schwartz E; Robertson JM; Surrey S
    Mol Cell Probes; 1992 Aug; 6(4):353-6. PubMed ID: 1382222
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cystic fibrosis patients with mutation 1949del84 in exon 13 of the CFTR gene have a similar clinical severity as delta F508 homozygotes.
    Nunes V; Casals T; Gaona A; Antiñolo G; Ferrer-Calvete J; Pérez-Frias J; Tardío E; Molano J; Estivill X
    Hum Mutat; 1992; 1(5):375-9. PubMed ID: 1284539
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation detection with MutH, MutL, and MutS mismatch repair proteins.
    Smith J; Modrich P
    Proc Natl Acad Sci U S A; 1996 Apr; 93(9):4374-9. PubMed ID: 8633074
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Simultaneous detection of the two prevalent mutations in the cystic fibrosis gene in Reunion Island.
    Bienvenu T; Bousquet S; Herbulot C; Cartault F; Kaplan JC; Beldjord C
    Hum Mutat; 1993; 2(4):306-8. PubMed ID: 7691353
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular and clinical findings in Austrian cystic fibrosis patients with mutations in exon 11 of the CFTR gene.
    Greil I; Wagner K; Eber E; Zach M; Rosenkranz W
    Wien Klin Wochenschr; 1995; 107(15):464-9. PubMed ID: 7545856
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hybridization of glass-tethered oligonucleotide probes to target strands preannealed with labeled auxiliary oligonucleotides.
    Maldonado-Rodriguez R; Espinosa-Lara M; Calixto-Suárez A; Beattie WG; Beattie KL
    Mol Biotechnol; 1999 Feb; 11(1):1-12. PubMed ID: 10367278
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (delta F508).
    Cui KH; Haan EA; Wang LJ; Matthews CD
    BMJ; 1995 Aug; 311(7004):536-40. PubMed ID: 7545043
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A 32-bp deletion (2991del32) in the cystic fibrosis gene associated with CFTR mRNA reduction.
    Dörk T; Will K; Grade K; Krawczak M; Tümmler B
    Hum Mutat; 1994; 4(1):65-70. PubMed ID: 7524915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Requirement for Phe36 for DNA binding and mismatch repair by Escherichia coli MutS protein.
    Yamamoto A; Schofield MJ; Biswas I; Hsieh P
    Nucleic Acids Res; 2000 Sep; 28(18):3564-9. PubMed ID: 10982877
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fluorescence-based oligonucleotide ligation assay for analysis of cystic fibrosis transmembrane conductance regulator gene mutations.
    Eggerding FA; Iovannisci DM; Brinson E; Grossman P; Winn-Deen ES
    Hum Mutat; 1995; 5(2):153-65. PubMed ID: 7538376
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the W1282X and delta F508 mutations.
    Avner R; Laufer N; Safran A; Kerem BS; Friedmann A; Mitrani-Rosenbaum S
    Hum Reprod; 1994 Sep; 9(9):1676-80. PubMed ID: 7530726
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Directionality of DNA replication fork movement strongly affects the generation of spontaneous mutations in Escherichia coli.
    Yoshiyama K; Higuchi K; Matsumura H; Maki H
    J Mol Biol; 2001 Apr; 307(5):1195-206. PubMed ID: 11292335
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel CFTR mutation, 4035delA, detected by non-radioactive SSCP analysis.
    Reiss J; Lenz U; Rininsland F; Ballhausen P; Drews D; Posselt HG
    Hum Genet; 1992 Nov; 90(3):303-4. PubMed ID: 1283151
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Strong TV; Smit LS; Nasr S; Wood DL; Cole JL; Iannuzzi MC; Stern RC; Collins FS
    Hum Mutat; 1992; 1(5):380-7. PubMed ID: 1284540
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.