AIMS: Germline mutation of the E-cadherin gene (CDH1) accounts for the Hereditary Diffuse Gastric Cancer (HDGC) syndrome. Fourteen pedigrees with Diffuse Gastric Cancer that fulfilled the International Gastric Cancer Linkage Consortium (IGCLC) criteria were selected and screened for CDH1 germline mutations. METHODS: The entire coding region of the CDH1 gene and all intron-exon boundaries were analyzed by direct sequencing in the 14 families fulfilling the IGCLC criteria. E-cadherin immunohistochemical expression was evaluated on tumour as well as normal formalin-fixed paraffin embedded tissues. RESULTS: A novel germline missense mutation was found. It was a single C-->T substitution in exon 8, resulting in a transition of ...
IMPORTANCE E-cadherin (CDH1) is a cancer predisposition gene mutated in families meeting clinically ...
E-cadherin germ-line mutations have recently been described as a molecular basis for early-onset fam...
IMPORTANCE E-cadherin (CDH1) is a cancer predisposition gene mutated in families meeting clinically...
AIMS: Germline mutation of the E-cadherin gene (CDH1) accounts for the Hereditary Diffuse Gastri...
Germline inactivation of the E-cadherin gene (CDH1) is associated with hereditary diffuse gastric ca...
Hereditary diffuse gastric cancer (HDGC) is a cancer predisposition syndrome caused by germline muta...
E-cadherin (CDH1 gene) germline mutations are associated with the development of diffuse gastric can...
Importance. Familial aggregation occurs in approximately 10% of gastric cancers, which are generally...
AIM: CDH1 germline alterations occur in about 40% of hereditary diffuse gastric cancer (HDGC) fami...
AIM: Hereditary diffuse gastric cancer (HDGC) is a cancer susceptibility syndrome caused by E-cadh...
To evaluate the frequency and nature of E-cadherin gene (CDH1) germline mutations in familial gastri...
11Germline mutations in CDH1, the gene coding for the E-cadherin adhesion protein, are known to caus...
Hereditary diffuse gastric cancer (HDGC) is a recently defined cancer syndrome caused by inactivatin...
Germline inactivation of the E‐cadherin gene (CDH1) is associated with hereditary diffuse gastric ca...
E-cadherin is involved in the formation of cell-junctions and the maintenance of epithelial integrit...
IMPORTANCE E-cadherin (CDH1) is a cancer predisposition gene mutated in families meeting clinically ...
E-cadherin germ-line mutations have recently been described as a molecular basis for early-onset fam...
IMPORTANCE E-cadherin (CDH1) is a cancer predisposition gene mutated in families meeting clinically...
AIMS: Germline mutation of the E-cadherin gene (CDH1) accounts for the Hereditary Diffuse Gastri...
Germline inactivation of the E-cadherin gene (CDH1) is associated with hereditary diffuse gastric ca...
Hereditary diffuse gastric cancer (HDGC) is a cancer predisposition syndrome caused by germline muta...
E-cadherin (CDH1 gene) germline mutations are associated with the development of diffuse gastric can...
Importance. Familial aggregation occurs in approximately 10% of gastric cancers, which are generally...
AIM: CDH1 germline alterations occur in about 40% of hereditary diffuse gastric cancer (HDGC) fami...
AIM: Hereditary diffuse gastric cancer (HDGC) is a cancer susceptibility syndrome caused by E-cadh...
To evaluate the frequency and nature of E-cadherin gene (CDH1) germline mutations in familial gastri...
11Germline mutations in CDH1, the gene coding for the E-cadherin adhesion protein, are known to caus...
Hereditary diffuse gastric cancer (HDGC) is a recently defined cancer syndrome caused by inactivatin...
Germline inactivation of the E‐cadherin gene (CDH1) is associated with hereditary diffuse gastric ca...
E-cadherin is involved in the formation of cell-junctions and the maintenance of epithelial integrit...
IMPORTANCE E-cadherin (CDH1) is a cancer predisposition gene mutated in families meeting clinically ...
E-cadherin germ-line mutations have recently been described as a molecular basis for early-onset fam...
IMPORTANCE E-cadherin (CDH1) is a cancer predisposition gene mutated in families meeting clinically...