نتایج جستجو برای: familial breast cancer

تعداد نتایج: 1032090  

2012
Irene Catucci Mara Colombo Paolo Verderio Loris Bernard Filomena Ficarazzi Frederique Mariette Monica Barile Bernard Peissel Elisa Cattaneo Siranoush Manoukian Paolo Radice Paolo Peterlongo

Breast cancer can be caused by germline mutations in several genes that are responsible for different hereditary cancer syndromes. Some of the genes causing the Fanconi anemia (FA) syndrome, such as BRCA2, BRIP1, PALB2, and RAD51C, are associated with high or moderate risk of developing breast cancer. Very recently, SLX4 has been established as a new FA gene raising the question of its implicat...

2009
Malinee Pongsavee Pimpicha Patmasiriwat Grady F. Saunders

Estrogen is believed to be pre-initiator in the risk of breast cancer. The BRCA1 is a tumor suppressor gene associated with breast and ovarian cancer risk. This report describes functional analysis of two BRCA1 missense mutations (Asp67Glu and Thr1051Ser) observed in the familial breast/ovarian cancer patients in Thailand. Levels of luciferase activity of the two mutations were relatively lower...

2015
Shuying Liu Funda Meric-Bernstam Napa Parinyanitikul Bailiang Wang Agda K. Eterovic Xiaofeng Zheng Mihai Gagea Mariana Chavez-MacGregor Naoto T. Ueno Xiudong Lei Wanding Zhou Lakshmy Nair Debu Tripathy Powel H. Brown Gabriel N. Hortobagyi Ken Chen John Mendelsohn Gordon B. Mills Ana M. Gonzalez-Angulo

Major breast cancer predisposition genes, only account for approximately 30% of high-risk breast cancer families and only explain 15% of breast cancer familial relative risk. The HGF growth factor receptor MET is potentially functionally altered due to an uncommon germline single nucleotide polymorphism (SNP), MET-T1010I, in many cancer lineages including breast cancer where the MET-T1010I SNP ...

Journal: :Cochrane Database of Systematic Reviews 2018

Journal: :Annals of the Academy of Medicine, Singapore 2004
L S J Sim J H C L Hendriks S M C Fook-Chong

INTRODUCTION The aim of this study was to assess the performance and value of breast ultrasound in women with familial risk of breast cancer. MATERIALS AND METHODS From an initial dataset of 245 women with positive family history who had breast cancer surveillance utilising mammography or magnetic resonance imaging (MRI) between November 1994 and February 2001, 179 subjects with follow-up dat...

Journal: :Cancer Epidemiology Biomarkers & Prevention 2005

Journal: :gastroenterology and hepatology from bed to bench 0
seyed mohammad hossein kashfi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran mina golmohammadi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran faeghe behboudi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran ehsan nazemalhosseini- mojarad gastroenterology and liver diseases research center, shahid beheshti university of medical science, tehran, iran mohammad reza zali gastroenterology and liver diseases research center, shahid beheshti university of medical science, tehran, iran

normal 0 false false false en-us x-none ar-sa microsoftinternetexplorer4 colorectal cancer is classified in to three forms: sporadic (70-75%), familial (20-25%) and hereditary (5-10%). hereditary colorectal cancer syndromes classified into two different subtypes: polyposis and non polyposis. familial adenomatous polyposis (fap; omim #175100) is the most common polyposis syndrome, account for <1...

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