Literature DB >> 16622277

Is it time to abandon microsatellite instability as a pre-screen for selecting families for mutation testing for mismatch repair genes?

Gareth D Evans, Fiona Lalloo, Tony Mak, Doug Speake, James Hill.   

Abstract

Mesh:

Year:  2006        PMID: 16622277     DOI: 10.1200/JCO.2005.05.3207

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


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  4 in total

1.  Identification of cancer patients with Lynch syndrome: clinically significant discordances and problems in tissue-based mismatch repair testing.

Authors:  Angela N Bartley; Rajyalakshmi Luthra; Devki S Saraiya; Diana L Urbauer; Russell R Broaddus
Journal:  Cancer Prev Res (Phila)       Date:  2011-11-15

2.  Heterogeneous staining for mismatch repair proteins during population-based prescreening for hereditary nonpolyposis colorectal cancer.

Authors:  Natasha Watson; Fabienne Grieu; Melinda Morris; Jennet Harvey; Colin Stewart; Lyn Schofield; Jack Goldblatt; Barry Iacopetta
Journal:  J Mol Diagn       Date:  2007-07-25       Impact factor: 5.568

3.  Systematic study on genetic and epimutational profile of a cohort of Amsterdam criteria-defined Lynch Syndrome in Singapore.

Authors:  Yanqun Liu; Min Hoe Chew; Xue Wei Goh; Soo Yong Tan; Carol Tien Tau Loi; Yuen Ming Tan; Hai Yang Law; Poh Koon Koh; Choong Leong Tang
Journal:  PLoS One       Date:  2014-04-07       Impact factor: 3.240

4.  Tumour MLH1 promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC).

Authors:  K Newton; N M Jorgensen; A J Wallace; D D Buchanan; F Lalloo; R F T McMahon; J Hill; D G Evans
Journal:  J Med Genet       Date:  2014-10-03       Impact factor: 6.318

  4 in total

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