Literature DB >> 27035997

Enhanced gene targeting to evaluate Lynch syndrome alterations.

Richard Fishel1, Christopher D Heinen2.   

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Year:  2016        PMID： 27035997      PMCID： PMC4839465          DOI： 10.1073/pnas.1602650113

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  21 in total

Review 1.  The selection for mismatch repair defects in hereditary nonpolyposis colorectal cancer: revising the mutator hypothesis.

Authors:  R Fishel
Journal:  Cancer Res       Date:  2001-10-15       Impact factor: 12.701

Review 2.  Mismatch repair.

Authors:  Richard Fishel
Journal:  J Biol Chem       Date:  2015-09-09       Impact factor: 5.157

3.  Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage.

Authors:  P Branch; G Aquilina; M Bignami; P Karran
Journal:  Nature       Date:  1993-04-15       Impact factor: 49.962

4.  Mismatch correction at O6-methylguanine residues in E. coli DNA.

Authors:  P Karran; M G Marinus
Journal:  Nature       Date:  1982-04-29       Impact factor: 49.962

Review 5.  Genetic predisposition to colorectal cancer.

Authors:  Albert de la Chapelle
Journal:  Nat Rev Cancer       Date:  2004-10       Impact factor: 60.716

6.  Sequence context effect for hMSH2-hMSH6 mismatch-dependent activation.

Authors:  Anthony Mazurek; Christopher N Johnson; Markus W Germann; Richard Fishel
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-23       Impact factor: 11.205

7.  Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.

Authors:  Hellen Houlleberghs; Marleen Dekker; Hildo Lantermans; Roos Kleinendorst; Hendrikus Jan Dubbink; Robert M W Hofstra; Senno Verhoef; Hein Te Riele
Journal:  Proc Natl Acad Sci U S A       Date:  2016-03-07       Impact factor: 11.205

8.  Structure of the human MutSalpha DNA lesion recognition complex.

Authors:  Joshua J Warren; Timothy J Pohlhaus; Anita Changela; Ravi R Iyer; Paul L Modrich; Lorena S Beese
Journal:  Mol Cell       Date:  2007-05-25       Impact factor: 17.970

9.  Determining the functional significance of mismatch repair gene missense variants using biochemical and cellular assays.

Authors:  Christopher D Heinen; Lene Juel Rasmussen
Journal:  Hered Cancer Clin Pract       Date:  2012-07-23       Impact factor: 2.857

10.  Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

Authors:  Bryony A Thompson; Amanda B Spurdle; John-Paul Plazzer; Marc S Greenblatt; Kiwamu Akagi; Fahd Al-Mulla; Bharati Bapat; Inge Bernstein; Gabriel Capellá; Johan T den Dunnen; Desiree du Sart; Aurelie Fabre; Michael P Farrell; Susan M Farrington; Ian M Frayling; Thierry Frebourg; David E Goldgar; Christopher D Heinen; Elke Holinski-Feder; Maija Kohonen-Corish; Kristina Lagerstedt Robinson; Suet Yi Leung; Alexandra Martins; Pal Moller; Monika Morak; Minna Nystrom; Paivi Peltomaki; Marta Pineda; Ming Qi; Rajkumar Ramesar; Lene Juel Rasmussen; Brigitte Royer-Pokora; Rodney J Scott; Rolf Sijmons; Sean V Tavtigian; Carli M Tops; Thomas Weber; Juul Wijnen; Michael O Woods; Finlay Macrae; Maurizio Genuardi
Journal:  Nat Genet       Date:  2013-12-22       Impact factor: 38.330
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