EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients

Colon-specific phenotype in Lynch syndrome associated with EPCAM deletion

(2012) P Grandval et al.   CLINICAL GENETICS

Prevalence of mismatch repair-deficient crypt foci in Lynch syndrome: a pathological study

(2012) Matthias Kloor et al.   LANCET ONCOLOGY

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

(2012) Cathrin Huth et al.   MODERN PATHOLOGY

Lynch Syndrome-Associated Extracolonic Tumors Are Rare in Two Extended Families With the Same EPCAM Deletion

(2011) Henry T Lynch et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

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

(2011) Carlo Patriarca et al.   CANCER TREATMENT REVIEWS

Lessons from common markers of tumor-initiating cells in solid cancers

(2011) Olivier Gires   CELLULAR AND MOLECULAR LIFE SCIENCES

A founder effect at the EPCAM locus in Congenital Tufting Enteropathy in the Arabic Gulf

(2011) Julie Salomon et al.   European Journal of Medical Genetics

Recurrence and variability of germline EPCAM deletions in Lynch syndrome

(2011) Roland P. Kuiper et al.   HUMAN MUTATION

Frequency of Deletions of EPCAM (TACSTD1) in MSH2-Associated Lynch Syndrome Cases

(2011) Kandelaria Rumilla et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Somatic Hypermethylation of MSH2 Is a Frequent Event in Lynch Syndrome Colorectal Cancers

(2010) T. Nagasaka et al.   CANCER RESEARCH

Epimutations and cancer predisposition: importance and mechanisms

(2010) Luke B Hesson et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Germline Epigenetic Silencing of the Tumor Suppressor Gene PTPRJ in Early-Onset Familial Colorectal Cancer

(2010) Ramprasath Venkatachalam et al.   GASTROENTEROLOGY

Analysis of EPCAM Protein Expression in Diagnostics of Lynch Syndrome

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

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

(2010) Carla Guarinos et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

(2010) Marlies JE Kempers et al.   LANCET ONCOLOGY

Further evidence for EpCAM as the gene for congenital tufting enteropathy

(2009) Mamata Sivagnanam et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The Emerging Role of EpCAM in Cancer and Stem Cell Signaling

(2009) M. Munz et al.   CANCER RESEARCH

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

(2009) HT Lynch et al.   CLINICAL GENETICS

Germline hypermethylation ofMLH1andEPCAMdeletions are a frequent cause of Lynch syndrome

(2009) Renée C. Niessen et al.   GENES CHROMOSOMES & CANCER

Deletions removing the last exon ofTACSTD1constitute a distinct class of mutations predisposing to Lynch syndrome

(2009) Marietta E. Kovacs et al.   HUMAN MUTATION

Identification of EpCAM as the Gene for Congenital Tufting Enteropathy

(2008) Mamata Sivagnanam et al.   GASTROENTEROLOGY

Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA

(2008) Wenqiang Yu et al.   NATURE

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