The notion that some common variants of APC might confer an increased colorectal tumour risk is supported by studies of the I1307K polymorphism. Recently it has been proposed that the E1317Q variant is also associated with an increased risk. We have studied the prevalence of E1317Q in 364 colorectal cancer patients and in 290 controls. Two patients were shown to possess E1317Q. Neither had a family history of colorectal cancer or co-existent adenomatous polyps. Two controls also carried E1317Q. This finding suggests that E1317Q is unlikely to be associated with anything more than a moderate increase in risk of colorectal cancer
The probability of colorectal cancer is moderately increased among carriers of the APC I1307K polymo...
Familial adenomatous polyposis (FAP) is a dominantly inherited syndrome caused by germline mutations...
Background and Aims: Colorectal cancer is one of the most frequent cancers in humans. Recently, a ge...
The notion that some common variants of APC might confer an increased colorectal tumour risk is supp...
Genetic susceptibility may play a role in many colorectal cancers (CRCs). Known syndromes such as fa...
SummaryGerm-line and somatic truncating mutations of the APC gene are thought to initiate colorectal...
Classical familial adenomatous polyposis (FAP) is a high-penetrance autosomal dominant disease that ...
Classical familial adenomatous polyposis (FAP) is a high-penetrance autosomal dominant disease that ...
Mendelian tumour syndromes are caused by rare mutations, which usually lead to protein inactivation....
Adenomatous polyposis coli (APC) gene polymorphisms are believed to contribute to tumor susceptibili...
PURPOSE: The probability of colorectal cancer is moder-ately increased among carriers of the APC I13...
Germline and somatic truncating mutations of the adenomatous polyposis coli gene (APC) are thought t...
Mendelian tumour syndromes are caused by rare mutations, which usually lead to protein inactivation....
The APC I1307K allele is believed to predispose to multiple colorectal tumours because the change at...
The probability of colorectal cancer is moderately increased among carriers of the APC I1307K polymo...
Familial adenomatous polyposis (FAP) is a dominantly inherited syndrome caused by germline mutations...
Background and Aims: Colorectal cancer is one of the most frequent cancers in humans. Recently, a ge...
The notion that some common variants of APC might confer an increased colorectal tumour risk is supp...
Genetic susceptibility may play a role in many colorectal cancers (CRCs). Known syndromes such as fa...
SummaryGerm-line and somatic truncating mutations of the APC gene are thought to initiate colorectal...
Classical familial adenomatous polyposis (FAP) is a high-penetrance autosomal dominant disease that ...
Classical familial adenomatous polyposis (FAP) is a high-penetrance autosomal dominant disease that ...
Mendelian tumour syndromes are caused by rare mutations, which usually lead to protein inactivation....
Adenomatous polyposis coli (APC) gene polymorphisms are believed to contribute to tumor susceptibili...
PURPOSE: The probability of colorectal cancer is moder-ately increased among carriers of the APC I13...
Germline and somatic truncating mutations of the adenomatous polyposis coli gene (APC) are thought t...
Mendelian tumour syndromes are caused by rare mutations, which usually lead to protein inactivation....
The APC I1307K allele is believed to predispose to multiple colorectal tumours because the change at...
The probability of colorectal cancer is moderately increased among carriers of the APC I1307K polymo...
Familial adenomatous polyposis (FAP) is a dominantly inherited syndrome caused by germline mutations...
Background and Aims: Colorectal cancer is one of the most frequent cancers in humans. Recently, a ge...