BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 12661150)

  • 1. Single-tube method for determination of F508del genotype in the CFTR gene using bidirectional PCR amplification of specific alleles.
    Maciel P; Yan J; Feng J; Accurso F; Sommer S
    Biotechniques; 2003 Mar; 34(3):460-2. PubMed ID: 12661150
    [No Abstract]   [Full Text] [Related]  

  • 2. Introduction to PCR/OLA/SCS, a multiplex DNA test, and its application to cystic fibrosis.
    Brinson EC; Adriano T; Bloch W; Brown CL; Chang CC; Chen J; Eggerding FA; Grossman PD; Iovannisci DM; Madonik AM; Sherman DG; Tam RW; Winn-Deen ES; Woo SL; Fung S
    Genet Test; 1997; 1(1):61-8. PubMed ID: 10464627
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid detection of the delta F508 deletion in cystic fibrosis by allele specific PCR and electrochemiluminescent detection.
    Stern HJ; Carlos RD; Schutzbank TE
    Clin Biochem; 1995 Aug; 28(4):470-3. PubMed ID: 8521604
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Allelic dropout caused by allele-specific amplification failure in single-cell PCR of the cystic fibrosis delta F508 deletion.
    Dreesen JC; Bras M; Coonen E; Dumoulin JC; Evers JL; Geraedts JP
    J Assist Reprod Genet; 1996 Feb; 13(2):112-4. PubMed ID: 8688582
    [No Abstract]   [Full Text] [Related]  

  • 6. Rapid detection of CFTR gene rearrangements impacts on genetic counselling in cystic fibrosis.
    Niel F; Martin J; Dastot-Le Moal F; Costes B; Boissier B; Delattre V; Goossens M; Girodon E
    J Med Genet; 2004 Nov; 41(11):e118. PubMed ID: 15520400
    [No Abstract]   [Full Text] [Related]  

  • 7. Molecular basis of cystic fibrosis in Lithuania: incomplete CFTR mutation detection by PCR-based screening protocols.
    Giannattasio S; Bobba A; Jurgelevicius V; Vacca RA; Lattanzio P; Merafina RS; Utkus A; Kucinskas V; Marra E
    Genet Test; 2006; 10(3):169-73. PubMed ID: 17020467
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Impact on Genetic Testing of Mutational Patterns of CFTR Gene in Different Clinical Macrocategories of Cystic Fibrosis.
    Lucarelli M; Bruno SM; Pierandrei S; Ferraguti G; Testino G; Truglio G; Strom R; Quattrucci S
    J Mol Diagn; 2016 Jul; 18(4):554-65. PubMed ID: 27157324
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations.
    Messaoud T; Verlingue C; Denamur E; Pascaud O; Quéré I; Fattoum S; Elion J; Férec C
    Eur J Hum Genet; 1996; 4(1):20-4. PubMed ID: 8800923
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiplex allele-specific target amplification based on PCR suppression.
    Broude NE; Zhang L; Woodward K; Englert D; Cantor CR
    Proc Natl Acad Sci U S A; 2001 Jan; 98(1):206-11. PubMed ID: 11136256
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Solid phase fluorescent sequencing of the CFTR gene.
    Cuppens H; Cassiman JJ
    Methods Mol Biol; 2001; 167():63-88. PubMed ID: 11265322
    [No Abstract]   [Full Text] [Related]  

  • 12. Analysis of 31 CFTR mutations by polymerase chain reaction/oligonucleotide ligation assay in a pilot screening of 4476 newborns for cystic fibrosis.
    Gasparini P; Arbustini E; Restagno G; Zelante L; Stanziale P; Gatta L; Sbaiz L; Sedita AM; Banchieri N; Sapone L; Fiorucci GC; Brinson E; Shulse E; Rappaport E; Fortina P
    J Med Screen; 1999; 6(2):67-9. PubMed ID: 10444722
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cystic fibrosis transmembrane regulator haplotypes in households of patients with cystic fibrosis.
    Furgeri DT; Marson FAL; Correia CAA; Ribeiro JD; Bertuzzo CS
    Gene; 2018 Jan; 641():137-143. PubMed ID: 29054758
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular diagnosis of cystic fibrosis.
    Kant JA; Mifflin TE; McGlennen R; Rice E; Naylor E; Cooper DL
    Clin Lab Med; 1995 Dec; 15(4):877-98. PubMed ID: 8838228
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening.
    Hantash FM; Redman JB; Starn K; Anderson B; Buller A; McGinniss MJ; Quan F; Peng M; Sun W; Strom CM
    Hum Genet; 2006 Mar; 119(1-2):126-36. PubMed ID: 16362824
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Microarray analysis in cystic fibrosis.
    Galvin P; Clarke LA; Harvey S; Amaral MD
    J Cyst Fibros; 2004 Aug; 3 Suppl 2():29-33. PubMed ID: 15463921
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina.
    Roqué M; Godoy CP; Castellanos M; Pusiol E; Mayorga LS
    Hum Mutat; 2001 Aug; 18(2):167. PubMed ID: 11462248
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mismatch cleavage detects base deletion in cystic fibrosis gene.
    Hsu IC; Highsmith WE; Xu J; Kong D
    Biotechniques; 1998 Oct; 25(4):692-6. PubMed ID: 9793654
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Applying CFTR molecular genetics to facilitate the diagnosis of cystic fibrosis through screening.
    Bobadilla JL; Farrell MH; Farrell PM
    Adv Pediatr; 2002; 49():131-90. PubMed ID: 12214770
    [No Abstract]   [Full Text] [Related]  

  • 20. A simple, fast and inexpensive method for mutation scanning of CFTR gene.
    Figueredo Lago JE; Armas Cayarga A; González González YJ; Collazo Mesa T
    BMC Med Genet; 2017 May; 18(1):58. PubMed ID: 28545452
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.