Literature DB >> 2182014

Polymerase chain reaction (PCR) amplification with a single specific primer.

M Kalman1, E T Kalman, M Cashel.   

Abstract

A method is described for amplification of DNA fragments flanking a single known sequence that is sufficiently long to enable synthesis of a functional primer in polymerase chain reactions.

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Year:  1990        PMID： 2182014     DOI： 10.1016/0006-291x(90)92052-2

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


  6 in total

Review 1.  The polymerase chain reaction and other amplification techniques in immunological research and diagnosis.

Authors:  A M Lew; R B Brandon; M Panaccio; C J Morrow
Journal:  Immunology       Date:  1992-01       Impact factor: 7.397

2.  In situ amplification of single copy gene segments in individual cells by the polymerase chain reaction.

Authors:  W Spann; K Pachmann; H Zabnienska; A Pielmeier; B Emmerich
Journal:  Infection       Date:  1991 Jul-Aug       Impact factor: 3.553

3.  Isolation and detection of urease genes in Ureaplasma urealyticum.

Authors:  J J Willoughby; W C Russell; D Thirkell; M G Burdon
Journal:  Infect Immun       Date:  1991-07       Impact factor: 3.441

4.  Supported PCR: an efficient procedure to amplify sequences flanking a known DNA segment.

Authors:  G N Rudenko; C M Rommens; H J Nijkamp; J Hille
Journal:  Plant Mol Biol       Date:  1993-02       Impact factor: 4.076

5.  PCR walking from microdissection clone M54 identifies three exons from the human gene for the neural cell adhesion molecule L1 (CAM-L1).

Authors:  A Rosenthal; R N MacKinnon; D S Jones
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

6.  Genomic structure of the human caldesmon gene.

Authors:  K Hayashi; H Yano; T Hashida; R Takeuchi; O Takeda; K Asada; E Takahashi; I Kato; K Sobue
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-15       Impact factor: 11.205
  6 in total

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