Literature DB >> 1482122

Genetic analysis using the polymerase chain reaction.

H A Erlich1, N Arnheim.   

Abstract

The ability of PCR to amplify a specific DNA segment from a complex template in an automated reaction has made molecular analysis more accessible both to basic research and diagnostic laboratories. Modifications of the basic PCR method using generic primers now allow DNA amplification even in the absence of specific nucleotide sequence information. Although PCR has proved extremely valuable for detecting the presence or absence of a given sequence (e.g. diagnosis of infectious disease pathogens like HIV), it is uniquely suited to analyze genetic variation in the amplified DNA. The capacity to analyze DNA variation from limited samples like hair or cheek scrapings has made genetic diagnosis and population genetics studies much simpler and the amplification of specific sequences from individual cells (e.g. sperm) has opened new approaches to genetic mapping.

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Year:  1992        PMID: 1482122     DOI: 10.1146/annurev.ge.26.120192.002403

Source DB:  PubMed          Journal:  Annu Rev Genet        ISSN: 0066-4197            Impact factor:   16.830


  13 in total

1.  Electrospray ionization Fourier transform ion cyclotron resonance analysis of large polymerase chain reaction products.

Authors:  D S Wunschel; L P Tolić; B Feng; R D Smith
Journal:  J Am Soc Mass Spectrom       Date:  2000-04       Impact factor: 3.109

2.  Inheritance of chloroplast and mitochondrial genomes in pedunculate oak investigated with an efficient PCR method.

Authors:  S Dumolin; B Demesure; R J Petit
Journal:  Theor Appl Genet       Date:  1995-12       Impact factor: 5.699

3.  Assessing dissimilarity of genes by comparing their RNAse A mismatch cleavage patterns.

Authors:  A Rzhetsky; J Dopazo; E Snyder; C A Dangler; F J Ayala
Journal:  Genetics       Date:  1996-12       Impact factor: 4.562

4.  Selection response in finite populations.

Authors:  M Wei; A Caballero; W G Hill
Journal:  Genetics       Date:  1996-12       Impact factor: 4.562

5.  Selection of specific gene probes by combined use of low-stringency PCR amplification and Southern-blot hybridization.

Authors:  U Magdolen; V Magdolen; M Schmitt; W Bandlow
Journal:  Curr Genet       Date:  1995-03       Impact factor: 3.886

6.  Effective amplification of long targets from cloned inserts and human genomic DNA.

Authors:  S Cheng; C Fockler; W M Barnes; R Higuchi
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-07       Impact factor: 11.205

7.  Allelic discrimination by nick-translation PCR with fluorogenic probes.

Authors:  L G Lee; C R Connell; W Bloch
Journal:  Nucleic Acids Res       Date:  1993-08-11       Impact factor: 16.971

8.  A simple procedure for optimising the polymerase chain reaction (PCR) using modified Taguchi methods.

Authors:  B D Cobb; J M Clarkson
Journal:  Nucleic Acids Res       Date:  1994-09-11       Impact factor: 16.971

Review 9.  DNA analysis in type III hyperlipoproteinemia.

Authors:  C C Walden; R A Hegele
Journal:  CMAJ       Date:  1993-08-15       Impact factor: 8.262

10.  The 2-aminoethylphosphonate-specific transaminase of the 2-aminoethylphosphonate degradation pathway.

Authors:  Alexander D Kim; Angela S Baker; Debra Dunaway-Mariano; W W Metcalf; B L Wanner; Brian M Martin
Journal:  J Bacteriol       Date:  2002-08       Impact factor: 3.490

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