Literature DB >> 8166397

The ligase chain reaction in DNA-based diagnosis.

T G Laffler1, J J Carrino, R L Marshall.   

Abstract

Clinical specimens containing a suspected pathogen often have too little of the pathogen's DNA to be detected directly. It is generally necessary to first amplify the DNA and then to detect the amplification products. An amplification technique called the ligase chain reaction (LCR) is described, which in conjunction with an automated, nonradioactive readout format allows less than 10 molecules of target DNA to be detected. A prototype HIV assay and two prototype Chlamydia assays have sensitivities and specificities equivalent to PCR.

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Year:  1993        PMID: 8166397

Source DB:  PubMed          Journal:  Ann Biol Clin (Paris)        ISSN: 0003-3898            Impact factor:   0.459


  9 in total

1.  A quantitative assay for assessing allelic proportions by iterative gap ligation.

Authors:  J Stewart; P Kozlowski; M Sowden; E Messing; H C Smith
Journal:  Nucleic Acids Res       Date:  1998-02-15       Impact factor: 16.971

2.  Combinatorial library diversity: probability assessment of library populations.

Authors:  B Ward; T Juehne
Journal:  Nucleic Acids Res       Date:  1998-02-15       Impact factor: 16.971

3.  Rapid diagnosis of extrapulmonary tuberculosis by ligase chain reaction amplification.

Authors:  F Gamboa; J Dominguez; E Padilla; J M Manterola; E Gazapo; J Lonca; L Matas; A Hernandez; P J Cardona; V Ausina
Journal:  J Clin Microbiol       Date:  1998-05       Impact factor: 5.948

4.  Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by ligase chain reaction-based assays with clinical specimens from various sites: implications for diagnostic testing and screening.

Authors:  M Buimer; G J van Doornum; S Ching; P G Peerbooms; P K Plier; D Ram; H H Lee
Journal:  J Clin Microbiol       Date:  1996-10       Impact factor: 5.948

5.  Evaluation of the semiautomated Abbott LCx Mycobacterium tuberculosis assay for direct detection of Mycobacterium tuberculosis in respiratory specimens.

Authors:  V Ausina; F Gamboa; E Gazapo; J M Manterola; J Lonca; L Matas; J R Manzano; C Rodrigo; P J Cardona; E Padilla
Journal:  J Clin Microbiol       Date:  1997-08       Impact factor: 5.948

6.  Highly sensitive multiplex assay for detection of human immunodeficiency virus type 1 and hepatitis C virus RNA.

Authors:  C Giachetti; J M Linnen; D P Kolk; J Dockter; K Gillotte-Taylor; M Park; M Ho-Sing-Loy; M K McCormick; L T Mimms; S H McDonough
Journal:  J Clin Microbiol       Date:  2002-07       Impact factor: 5.948

7.  Detection of point mutations with a modified ligase chain reaction (Gap-LCR).

Authors:  K Abravaya; J J Carrino; S Muldoon; H H Lee
Journal:  Nucleic Acids Res       Date:  1995-02-25       Impact factor: 16.971

8.  A single-molecule sequencing assay for the comprehensive profiling of T4 DNA ligase fidelity and bias during DNA end-joining.

Authors:  Vladimir Potapov; Jennifer L Ong; Bradley W Langhorst; Katharina Bilotti; Dan Cahoon; Barry Canton; Thomas F Knight; Thomas C Evans; Gregory J S Lohman
Journal:  Nucleic Acids Res       Date:  2018-07-27       Impact factor: 16.971

9.  Efficient DNA ligation in DNA-RNA hybrid helices by Chlorella virus DNA ligase.

Authors:  Gregory J S Lohman; Yinhua Zhang; Alexander M Zhelkovsky; Eric J Cantor; Thomas C Evans
Journal:  Nucleic Acids Res       Date:  2013-11-06       Impact factor: 16.971

  9 in total

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