Differential Features of Microsatellite-Unstable Colorectal Carcinomas Depending on EPCAM Expression Status

Subsets of microsatellite-unstable colorectal cancers exhibit discordance between the CpG island methylator phenotype and MLH1 methylation status

(2013) Jung H Kim et al.   MODERN PATHOLOGY

Expression status of wild-type HSP110 correlates with HSP110 T17 deletion size and patient prognosis in microsatellite-unstable colorectal cancer

(2013) Jung Ho Kim et al.   MODERN PATHOLOGY

EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients

(2012) Marjolijn J. L. Ligtenberg et al.   Familial Cancer

Usefulness of epithelial cell adhesion molecule expression in the algorithmic approach to Lynch syndrome identification

(2012) Eva Musulen et al.   HUMAN PATHOLOGY

The molecular basis of EPCAM expression loss in Lynch syndrome-associated tumors

(2012) Cathrin Huth et al.   MODERN PATHOLOGY

EpCAM and its potential role in tumor-initiating cells

(2012) Sannia Imrich et al.   Cell Adhesion & Migration

Epithelial cell adhesion molecule expression (CD326) in cancer: A short review

(2011) Carlo Patriarca et al.   CANCER TREATMENT REVIEWS

Differential clinicopathological features in microsatellite instability-positive colorectal cancers depending on CIMP status

(2011) Jeong Mo Bae et al.   VIRCHOWS ARCHIV

Microsatellite instability in the management of colorectal cancer

(2011) Maria S Pino et al.   Expert Review of Gastroenterology & Hepatology

Microsatellite Instability in Colorectal Cancer

(2010) C. Richard Boland et al.   GASTROENTEROLOGY

Clinical Relevance of Microsatellite Instability in Colorectal Cancer

(2010) Albert de la Chapelle et al.   JOURNAL OF CLINICAL ONCOLOGY

Analysis of EPCAM Protein Expression in Diagnostics of Lynch Syndrome

(2010) Matthias Kloor et al.   JOURNAL OF CLINICAL ONCOLOGY

EpCAM-Positive Hepatocellular Carcinoma Cells Are Tumor-Initiating Cells With Stem/Progenitor Cell Features

(2008) Taro Yamashita et al.   GASTROENTEROLOGY

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

(2008) Marjolijn J L Ligtenberg et al.   NATURE GENETICS