Principles and applications of polymerase chain reaction: Basic science for the practicing physician

被引:25
作者
Ishmael, Faoud T. [1 ]
Stellato, Cristiana [1 ]
机构
[1] Johns Hopkins Asthma & Allergy Ctr, Div Clin Immunol & Allergy, Baltimore, MD 21224 USA
关键词
D O I
10.1016/S1081-1206(10)60323-7
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Objective: To review the technology of polymerase chain reaction (PCR) and its use in diagnostic medicine and biomedical research. Data Sources: A literature review was performed using the PubMed database for English-language articles published between January 1, 1985, and November 31, 2007, using the following keywords: polymerase chain. reaction, real-time polymerase chain reaction, and applications of real-time polymerase chain reaction. Study Selection: Select review articles and primary articles relevant to medical applications of PCR were chosen. Results: As a revolutionary technique, PCR provides a rapid and accurate means of amplifying DNA. It has enabled the cloning and manipulation of genes for biomedical research and has facilitated the diagnosis of genetic, infectious, and oncologic diseases. The use of reverse transcriptases to evaluate RNA levels and the extension of PCR technology to quantify DNA amplification in real time has brought major advances to the application of PCR. By allowing the determination and quantification of changes in gene expression, these techniques have provided a greater understanding of disease processes and now serve as a foundation for diagnostics and basic science research. Conclusions: Both PCR and real-time PCR have dramatically changed the field of basic science and diagnostic medicine. These technologies are now a well-established, indispensable part of research and clinical laboratories.
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收藏
页码:437 / 443
页数:7
相关论文
共 20 条
  • [11] A COMMON LANGUAGE FOR PHYSICAL MAPPING OF THE HUMAN GENOME
    OLSON, M
    HOOD, L
    CANTOR, C
    BOTSTEIN, D
    [J]. SCIENCE, 1989, 245 (4925) : 1434 - 1435
  • [12] New real-time reverse transcriptase-initiated PCR assay with single-copy sensitivity for human immunodeficiency virus type 1 RNA in plasma
    Palmer, S
    Wiegand, AP
    Maldarelli, F
    Bazmi, H
    Mican, JM
    Polis, M
    Dewar, RL
    Planta, A
    Liu, SY
    Metcalf, JA
    Mellors, JW
    Coffin, JM
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (10) : 4531 - 4536
  • [13] PANET A, 1974, J BIOL CHEM, V249, P5213
  • [14] ENZYMATIC AMPLIFICATION OF BETA-GLOBIN GENOMIC SEQUENCES AND RESTRICTION SITE ANALYSIS FOR DIAGNOSIS OF SICKLE-CELL ANEMIA
    SAIKI, RK
    SCHARF, S
    FALOONA, F
    MULLIS, KB
    HORN, GT
    ERLICH, HA
    ARNHEIM, N
    [J]. SCIENCE, 1985, 230 (4732) : 1350 - 1354
  • [15] Tamaki Keiji, 2005, Legal Medicine, V7, P244, DOI 10.1016/j.legalmed.2005.02.002
  • [16] Tang YW, 1997, CLIN CHEM, V43, P2021
  • [17] Standardized determination of real-time PCR efficiency from a single reaction set-up
    Tichopad, A
    Dilger, M
    Schwarz, G
    Pfaffl, MW
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (20) : e122
  • [18] The power of real-time PCR
    Valasek, MA
    Repa, JJ
    [J]. ADVANCES IN PHYSIOLOGY EDUCATION, 2005, 29 (03) : 151 - 159
  • [19] Continuous fluorescence monitoring of rapid cycle DNA amplification
    Wittwer, CT
    Herrmann, MG
    Moss, AA
    Rasmussen, RP
    [J]. BIOTECHNIQUES, 1997, 22 (01) : 130 - &
  • [20] Real-time PCR for mRNA quantitation
    Wong, ML
    Medrano, JF
    [J]. BIOTECHNIQUES, 2005, 39 (01) : 75 - 85