EPCAM Germ Line Deletions as Causes of Lynch Syndrome in Spanish Patients-Reference-Cited by-同舟云学术

EPCAM Germ Line Deletions as Causes of Lynch Syndrome in Spanish Patients

Published:2010-11 Issue:6 Volume:12 Page:765-770
ISSN:1525-1578
Container-title:The Journal of Molecular Diagnostics
language:en
Short-container-title:The Journal of Molecular Diagnostics

Author:

Guarinos Carla,Castillejo Adela,Barberá Víctor-Manuel,Pérez-Carbonell Lucía,Sánchez-Heras Ana-Beatriz,Segura Ángel,Guillén-Ponce Carmen,Martínez-Cantó Ana,Castillejo María-Isabel,Egoavil Cecilia-Magdalena,Jover Rodrigo,Payá Artemio,Alenda Cristina,Soto José-Luís

Publisher

Elsevier BV

Subject

Molecular Medicine,Pathology and Forensic Medicine

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3. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1;Ligtenberg;Nat Genet,2009

4. Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome;Kovacs;Hum Mutat,2009

5. Frequent EpCam protein expression in human carcinomas;Went;Hum Pathol,2004

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1. High Probability of Lynch Syndrome Among Colorectal Cancer Patients Is Associated With Higher Occurrence of KRAS and PIK3CA Mutations;World Journal of Oncology;2024-08

2. Microsatellite Instability and Immune Response: From Microenvironment Features to Therapeutic Actionability—Lessons from Colorectal Cancer;Genes;2023-05-27

3. Whole-Genome Profiles of Malay Colorectal Cancer Patients with Intact MMR Proteins;Genes;2021-09-20

4. Microsatellite instability: a review of what the oncologist should know;Cancer Cell International;2020-01-13

5. EPCAMmutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome;Human Mutation;2018-11-29