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4. Competitive assay to improve the specificity of detection of single-point mutations in alpha 1-antitrypsin deficiency. Gunneberg A; Scobie G; Hayes K; Kalsheker N Clin Chem; 1993 Oct; 39(10):2157-62. PubMed ID: 8403402 [TBL] [Abstract][Full Text] [Related]
5. Ribonuclease A cleavage combined with the polymerase chain reaction for detection of the Z mutation of the alpha-1-antitrypsin gene. Abe T; Takahashi H; Holmes MD; Curiel DT; Crystal RG Am J Respir Cell Mol Biol; 1989 Oct; 1(4):329-34. PubMed ID: 2624766 [TBL] [Abstract][Full Text] [Related]
6. Detection of alpha-1-antitrypsin deficiency variants by synthetic oligonucleotide hybridization. Klasen EC; Hofker MH; van Paassen HM; Verlaan-de Vries M; Bos JL; Frants RR Clin Chim Acta; 1987 Dec; 170(2-3):201-7. PubMed ID: 3501742 [TBL] [Abstract][Full Text] [Related]
7. Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification. Okayama H; Curiel DT; Brantly ML; Holmes MD; Crystal RG J Lab Clin Med; 1989 Aug; 114(2):105-13. PubMed ID: 2787825 [TBL] [Abstract][Full Text] [Related]
8. [Analysis of alpha 1-antitrypsin deficiency using DNA methods]. Wick U; Kühnl P; Engel W Monatsschr Kinderheilkd; 1990 Aug; 138(8):438-42. PubMed ID: 2215506 [TBL] [Abstract][Full Text] [Related]
9. Sensitive and quantitative detection of PCR-amplified HIV-1 DNA products by an enzyme linked immunoassay following solution hybridization with two differently labelled oligonucleotide probes. Böni J; Schüpbach J Mol Cell Probes; 1993 Oct; 7(5):361-71. PubMed ID: 8264670 [TBL] [Abstract][Full Text] [Related]
10. Detection of human DNA mutations with nonradioactive, allele-specific oligonucleotide probes. Hajra A; Sorenson RC; La Du BN Pharmacogenetics; 1992 Apr; 2(2):78-88. PubMed ID: 1302045 [TBL] [Abstract][Full Text] [Related]
11. Rapid DNA analysis of alpha 1-antitrypsin deficiency: application of an improved method for amplifying mutated gene sequences. Dermer SJ; Johnson EM Lab Invest; 1988 Sep; 59(3):403-8. PubMed ID: 3261817 [TBL] [Abstract][Full Text] [Related]
12. Polymerase chain reaction for detection of the alpha-1-antitrypsin Z allele in chronic liver disease. Brind AM; McIntosh I; Brock DJ; James OF; Bassendine MF J Hepatol; 1990 Mar; 10(2):240-3. PubMed ID: 2332597 [TBL] [Abstract][Full Text] [Related]
13. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Newton CR; Graham A; Heptinstall LE; Powell SJ; Summers C; Kalsheker N; Smith JC; Markham AF Nucleic Acids Res; 1989 Apr; 17(7):2503-16. PubMed ID: 2785681 [TBL] [Abstract][Full Text] [Related]
14. Detection of alpha 1-antitrypsin Z and S mutations by polymerase chain reaction-mediated site-directed mutagenesis. Tazelaar JP; Friedman KJ; Kline RS; Guthrie ML; Farber RA Clin Chem; 1992 Aug; 38(8 Pt 1):1486-8. PubMed ID: 1643720 [TBL] [Abstract][Full Text] [Related]
15. Diagnosis of alpha 1-antitrypsin deficiency by enzymatic amplification of human genomic DNA and direct sequencing of polymerase chain reaction products. Newton CR; Kalsheker N; Graham A; Powell S; Gammack A; Riley J; Markham AF Nucleic Acids Res; 1988 Sep; 16(17):8233-43. PubMed ID: 3262215 [TBL] [Abstract][Full Text] [Related]
16. Polymerase chain reaction detection of S and Z alpha-1-antitrypsin variants by duplex PCR assay. Lucotte G; Sesboüé R Mol Cell Probes; 1999 Oct; 13(5):389-91. PubMed ID: 10508561 [TBL] [Abstract][Full Text] [Related]
17. Screening for hereditary fructose intolerance mutations by reverse dot-blot. Lau J; Tolan DR Mol Cell Probes; 1999 Feb; 13(1):35-40. PubMed ID: 10024431 [TBL] [Abstract][Full Text] [Related]
18. alpha 1-antitrypsin deficiency detection by direct analysis of the mutation in the gene. Kidd VJ; Wallace RB; Itakura K; Woo SL Nature; 1983 Jul 21-27; 304(5923):230-4. PubMed ID: 6306478 [TBL] [Abstract][Full Text] [Related]
19. Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis. Lodewyckx L; Vandevyver C; Vandervorst C; Van Steenbergen W; Raus J; Michiels L Hum Mutat; 2001 Sep; 18(3):243-50. PubMed ID: 11524735 [TBL] [Abstract][Full Text] [Related]
20. Molecular characterisation of two alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) Null(Newport) (Gly115----Ser) and (Pi) Z Wrexham (Ser-19----Leu). Graham A; Kalsheker NA; Bamforth FJ; Newton CR; Markham AF Hum Genet; 1990 Oct; 85(5):537-40. PubMed ID: 2227940 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]