Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter study-Reference-Cited by-同舟云学术

Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter study

Published:2013-07 Issue:7 Volume:45 Page:606-611
ISSN:1590-8658
Container-title:Digestive and Liver Disease
language:en
Short-container-title:Digestive and Liver Disease

Author:

Resta Nicoletta,Pierannunzio Daniela,Lenato Gennaro Mariano,Stella Alessandro,Capocaccia Riccardo,Bagnulo Rosanna,Lastella Patrizia,Susca Francesco Claudio,Bozzao Cristina,Loconte Daria Carmela,Sabbà Carlo,Urso Emanuele,Sala Paola,Fornasarig Mara,Grammatico Paola,Piepoli Ada,Host Cristina,Turchetti Daniela,Viel Alessandra,Memo Luigi,Giunti Laura,Stigliano Vittoria,Varesco Liliana,Bertario Lucio,Genuardi Maurizio,Lucci Cordisco Emanuela,Tibiletti Maria Grazia,Di Gregorio Carmela,Andriulli Angelo,Ponz de Leon Maurizio

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference26 articles.

1. High cancer risk in Peutz–Jeghers syndrome: a systematic review and surveillance recommendations;van Lier;American Journal of Gastroenterology,2010

2. A serine/threonine kinase gene defective in Peutz–Jeghers syndrome;Hemminki;Nature,1998

3. Peutz–Jeghers syndrome is caused by mutations in a novel serine threonine kinase;Jenne;Nature Genetics,1998

4. The LKB1 complex-AMPK pathway: the tree that hides the forest;Sebbagh;Familial Cancer,2011

5. Breakpoint determination of 15 large deletions in Peutz–Jeghers subjects;Resta;Human Genetics,2010

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