Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2-Reference-Cited by-同舟云学术

Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2

Published:2018-09 Issue:3 Volume:155 Page:844-851
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

ten Broeke Sanne W.,van Bavel Tom C.,Jansen Anne M.L.,Gómez-García Encarnca,Hes Frederik J.,van Hest Liselot P.,Letteboer Tom G.W.,Olderode-Berends Maran J.W.,Ruano Dina,Spruijt Liesbeth,Suerink Manon,Tops Carli M.,van Eijk Ronald,Morreau Hans,van Wezel Tom,Nielsen Maartje

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference23 articles.

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3. PD-1 blockade in tumors with mismatch-repair deficiency;Le;N Engl J Med,2015

4. Exon 3 beta-catenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome;Johnson;Gut,2005

5. Comprehensive mutation analysis of PMS2 in a large cohort of probands suspected of Lynch syndrome or constitutional mismatch repair deficiency (CMMRD) syndrome;van der Klift;Hum Mutat,2016

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