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.
181 related articles for article (PubMed ID: 15890513)
1. Detection of CFTR mutations using ARMS and low-density microarrays. Eaker S; Johnson M; Jenkins J; Bauer M; Little S Biosens Bioelectron; 2005 Dec; 21(6):933-9. PubMed ID: 15890513 [TBL] [Abstract][Full Text] [Related]
2. Rapid screening for 31 mutations and polymorphisms in the cystic fibrosis transmembrane conductance regulator gene by Lminex xMAP suspension array. Dunbar SA; Jacobson JW Methods Mol Med; 2005; 114():147-71. PubMed ID: 16156102 [TBL] [Abstract][Full Text] [Related]
3. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations. Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673 [TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of CFTR gene in 70 Iranian cystic fibrosis patients. Alibakhshi R; Zamani M Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):3-8. PubMed ID: 17242497 [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. First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations. Jalalirad M; Houshmand M; Mirfakhraie R; Goharbari MH; Mirzajani F J Trop Pediatr; 2004 Dec; 50(6):359-61. PubMed ID: 15537723 [TBL] [Abstract][Full Text] [Related]
7. Identification of the commonest cystic fibrosis transmembrane regulator gene DeltaF508 mutation: evaluation of PCR--single-strand conformational polymorphism and polyacrylamide gel electrophoresis. Kakavas KV; Noulas AV; Kanakis I; Bonanou S; Karamanos NK Biomed Chromatogr; 2006 Oct; 20(10):1120-5. PubMed ID: 16708396 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Allele-specific competitive blocker PCR: a one-step method with applicability to pool screening. Orou A; Fechner B; Utermann G; Menzel HJ Hum Mutat; 1995; 6(2):163-9. PubMed ID: 7581400 [TBL] [Abstract][Full Text] [Related]
10. An alternative method to amplify RNA without loss of signal conservation for expression analysis with a proteinase DNA microarray in the ArrayTube format. Schüler S; Wenz I; Wiederanders B; Slickers P; Ehricht R BMC Genomics; 2006 Jun; 7():144. PubMed ID: 16768788 [TBL] [Abstract][Full Text] [Related]
11. Genotyping of mutation in the beta-globin gene using DNA microarrays. Dufva M; Poulsen L Methods Mol Biol; 2009; 509():47-56. PubMed ID: 19212714 [TBL] [Abstract][Full Text] [Related]
12. Array-based mutation detection of BRCA1 using direct probe/target hybridization. Yim SC; Park HG; Chang HN; Cho DY Anal Biochem; 2005 Feb; 337(2):332-7. PubMed ID: 15691514 [TBL] [Abstract][Full Text] [Related]
13. On-chip oligonucleotide ligation assay using one-dimensional microfluidic beads array for the detection of low-abundant DNA point mutations. Zhang H; Yang X; Wang K; Tan W; Li H; Zuo X; Wen J Biosens Bioelectron; 2008 Feb; 23(7):945-51. PubMed ID: 17983740 [TBL] [Abstract][Full Text] [Related]
14. Microchamber array based DNA quantification and specific sequence detection from a single copy via PCR in nanoliter volumes. Matsubara Y; Kerman K; Kobayashi M; Yamamura S; Morita Y; Tamiya E Biosens Bioelectron; 2005 Feb; 20(8):1482-90. PubMed ID: 15626601 [TBL] [Abstract][Full Text] [Related]
15. A novel optical biosensor format for the detection of clinically relevant TP53 mutations. Wilson PK; Jiang T; Minunni ME; Turner AP; Mascini M Biosens Bioelectron; 2005 May; 20(11):2310-3. PubMed ID: 15797331 [TBL] [Abstract][Full Text] [Related]
17. Four-color multiplex 5' nuclease assay for the simultaneous detection of the factor V Leiden and the prothrombin G20210A mutations. Ugozzoli LA; Hamby K Mol Cell Probes; 2004 Jun; 18(3):161-6. PubMed ID: 15135449 [TBL] [Abstract][Full Text] [Related]
18. Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis. Takahashi Y; Seki N; Ishiura H; Mitsui J; Matsukawa T; Kishino A; Onodera O; Aoki M; Shimozawa N; Murayama S; Itoyama Y; Suzuki Y; Sobue G; Nishizawa M; Goto J; Tsuji S Arch Neurol; 2008 Oct; 65(10):1326-32. PubMed ID: 18852346 [TBL] [Abstract][Full Text] [Related]
19. DNA microarrays. Bier FF; von Nickisch-Rosenegk M; Ehrentreich-Förster E; Reiss E; Henkel J; Strehlow R; Andresen D Adv Biochem Eng Biotechnol; 2008; 109():433-53. PubMed ID: 17985099 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]