Literature DB >> 1718663

Amplification of nucleic acids by polymerase chain reaction (PCR) and other methods and their applications.

A K Bej1, M H Mahbubani, R M Atlas.   

Abstract

The in vitro replication of DNA, principally using the polymerase chain reaction (PCR), permits the amplification of defined sequences of DNA. By exponentially amplifying a target sequence, PCR significantly enhances the probability of detecting target gene sequences in complex mixtures of DNA. It also facilitates the cloning and sequencing of genes. Amplification of DNA by PCR and other newly developed methods has been applied in many areas of biological research, including molecular biology, biotechnology, and medicine, permitting studies that were not possible before. Nucleic acid amplification has added a new and revolutionary dimension to molecular biology. This review examines PCR and other in vitro nucleic acid amplification methodologies--examining the critical parameters and variations and their widespread applications--giving the strengths and limitations of these methodologies.

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Year:  1991        PMID: 1718663     DOI: 10.3109/10409239109114071

Source DB:  PubMed          Journal:  Crit Rev Biochem Mol Biol        ISSN: 1040-9238            Impact factor:   8.250


  24 in total

1.  Detection and quantification of protein phosphatase inhibitor-1 gene expression in total rat liver and isolated hepatocytes.

Authors:  E A Aleem; T Flohr; A Hunziker; D Mayer; P Bannasch; H W Thielmann
Journal:  Mol Cell Biochem       Date:  2001-01       Impact factor: 3.396

Review 2.  Multiplex PCR: optimization and application in diagnostic virology.

Authors:  E M Elnifro; A M Ashshi; R J Cooper; P E Klapper
Journal:  Clin Microbiol Rev       Date:  2000-10       Impact factor: 26.132

Review 3.  Advances in nucleic acid-based detection methods.

Authors:  M J Wolcott
Journal:  Clin Microbiol Rev       Date:  1992-10       Impact factor: 26.132

4.  Amplification of DNA from native populations of soil bacteria by using the polymerase chain reaction.

Authors:  K D Bruce; W D Hiorns; J L Hobman; A M Osborn; P Strike; D A Ritchie
Journal:  Appl Environ Microbiol       Date:  1992-10       Impact factor: 4.792

5.  Checklist for optimization and validation of real-time PCR assays.

Authors:  Marijke Raymaekers; Rita Smets; Brigitte Maes; Reinoud Cartuyvels
Journal:  J Clin Lab Anal       Date:  2009       Impact factor: 2.352

Review 6.  The use of reverse transcriptase-polymerase chain reaction (RT-PCR) to investigate specific gene expression in multidrug-resistant cells.

Authors:  L O'Driscoll; C Daly; M Saleh; M Clynes
Journal:  Cytotechnology       Date:  1993       Impact factor: 2.058

7.  18S rRNA suggests that Entoprocta are protostomes, unrelated to Ectoprocta.

Authors:  L Y Mackey; B Winnepenninckx; R De Wachter; T Backeljau; P Emschermann; J R Garey
Journal:  J Mol Evol       Date:  1996-05       Impact factor: 2.395

8.  Influence of design probe and sequence mismatches on the efficiency of fluorescent RPA.

Authors:  Xiaoqing Liu; Qiongying Yan; Jianfei Huang; Jing Chen; Zhengyang Guo; Zhongdong Liu; Lin Cai; Risheng Li; Yan Wang; Guowu Yang; Quanxue Lan
Journal:  World J Microbiol Biotechnol       Date:  2019-06-11       Impact factor: 3.312

9.  Diagnosis and differentiation of Mycoplasma hyopneumoniae and Mycoplasma hyorhinis infections in pigs by PCR amplification of the p36 and p46 genes.

Authors:  J Caron; M Ouardani; S Dea
Journal:  J Clin Microbiol       Date:  2000-04       Impact factor: 5.948

10.  Detection of viable Vibrio cholerae by reverse-transcriptase polymerase chain reaction (RT-PCR).

Authors:  A K Bej; W Y Ng; S Morgan; D D Jones; M H Mahbubani
Journal:  Mol Biotechnol       Date:  1996-02       Impact factor: 2.695

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