Literature DB >> 10084114

Recent enhancements in SSCP.

K Hayashi1.   

Abstract

High sensitivity, robustness and scalability are the three criteria which influence whether techniques for rapid mutation detection will be used in the future. PCR-SSCP, one of the most popular methods for detecting mutation, especially in the field of medical genetics, is being improved (1) to efficiently detect mutations in long stretches of PCR products; (2) to simplify data interpretation by removing PCR artifacts and (3) to minimize human involvement in the process of mutation detection by a simple post-PCR fluorescence labeling followed by separation using automated DNA sequencers.

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Year:  1999        PMID: 10084114     DOI: 10.1016/s1050-3862(98)00017-5

Source DB:  PubMed          Journal:  Genet Anal


  4 in total

1.  Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection.

Authors:  P Kozlowski; W J Krzyzosiak
Journal:  Nucleic Acids Res       Date:  2001-07-15       Impact factor: 16.971

2.  Analysis of the fungal flora in environmental dust samples by PCR-SSCP method.

Authors:  Tobias Janke; Karin Schwaiger; Markus Ege; Carmen Fahn; Erika von Mutius; Johann Bauer; Melanie Mayer
Journal:  Curr Microbiol       Date:  2013-03-10       Impact factor: 2.188

3.  Detection of point mutation in K-ras oncogene at codon 12 in pancreatic diseases.

Authors:  Yue-Xin Ren; Guo-Ming Xu; Zhao-Shen Li; Yu-Gang Song
Journal:  World J Gastroenterol       Date:  2004-03-15       Impact factor: 5.742

4.  SNP analysis of the inter-alpha-trypsin inhibitor family heavy chain-related protein (IHRP) gene by a fluorescence-adapted SSCP method.

Authors:  Teruaki Tozaki; Nam-Ho Choi-Miura; Matsuo Taniyama; Masahiko Kurosawa; Motowo Tomita
Journal:  BMC Med Genet       Date:  2002-07-29       Impact factor: 2.103

  4 in total

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