نتایج جستجو برای: hereditary breast cancer

تعداد نتایج: 1055993  

Seyed Ali Reza Mortazavi Seyed Mohammad Javad Mortazavi,

Breast cancer is the most common malignancy among women, both in the developed and developing countries. Women with mutations in the BRCA1 and BRCA2 genes have an increased risk of breast and ovarian cancers. Recent studies show that short-wavelength visible light disturb the secretion of melatonin and causes circadian rhythm disruption. We have previously studied the health effects of exposure...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009
Sarah Louise Dombernowsky Maren Weischer Jacob Johannes Freiberg Stig Egil Bojesen Anne Tybjaerg-Hansen Børge Grønne Nordestgaard

PURPOSE BRCA1 and BRCA2 are key tumor suppressors with a role in cellular DNA repair, genomic stability, and checkpoint control. Mutations in BRCA1 and BRCA2 often cause hereditary breast and ovarian cancer; however, missense polymorphisms in these genes pose a problem in genetic counseling, as their impact on risk of breast and ovarian cancer is unclear. EXPERIMENTAL DESIGN We resequenced BR...

2014
Jung Min Park Min Kyu Kim

OBJECTIVES Borderline ovarian tumors (BOT) are premalignant lesions. Approximately 10% of all epithelial ovarian cancers are known to be hereditary with hereditary breast and ovarian cancer (HBOC) accounting for approximately 90% of cases; the remaining 10% are attributable to Lynch syndrome, also known as hereditary nonpolyposis colorectal cancer (HNPCC). The aim of our study is to estimate th...

2015
Yosuke Hirotsu Hiroshi Nakagomi Ikuko Sakamoto Kenji Amemiya Toshio Oyama Hitoshi Mochizuki Masao Omata

Approximately 5-10% of all breast and/or ovarian cancer cases are considered as inherited. BRCA1 and BRCA2 tumor suppressor genes account for a high penetrance of hereditary cases, but familial cases without mutations in these genes can also occur. Despite their low penetrance, other hereditary cancer-related genes are known to be associated with breast and ovarian cancer risk. However, the ext...

Journal: :نشریه پرستاری ایران 0
سکینه فقیه صفایی s faghyeh safaii اکرم نجف یارندی a nagaf yarandi افتخار السادات حاجی کاظمی es hajikazemi پرویز کمالی p kamali

the present research is a field study in order to investigate scale and ways of doing breast self examination (bse). 270 nurses employed by the medical sciences university’s hospitals related to the ministry of health, and medical education in city of tehran are selected and involved in research on the basis of simple random sampling. the data collection tool was a protrayed questionnaire which...

1999
Raquel Soares Ronald van Eijk Aureliano Dias Mónica Botelho Carla Costa Isabel Amendoeira Carlos Lopes Peter Devilee Fernando Schmitt

The aims of our study were: (1) to detect disease-associated BRCA1 mutations in a series of Portuguese patients with breast and/or ovarian cancer; (2) to evaluate the expression of molecular markers of biological behaviour, namely ER, proliferative index, c-erb-B2, p53, sialyl-Tn and angiogenic index in a series of hereditary breast cancer (HBC) in relation to sporadic cases. We selected 65 pat...

2007
Kristi D. Graves Lisa M. Moss Camille L. Jasper Tiffani A. DeMarco Beth N. Peshkin Claudine Isaacs Marc D. Schwartz

Background: Registries of individuals at risk for hereditary cancer syndromes are an invaluable resource for cancer research, yet little is known about the predictors of enrollment in hereditary cancer registries. We sought to identify the factors that characterize individuals who enroll versus those who decline participation in a Familial Cancer Registry (FCR). We also sought to identify the f...

2017
Michael Conroy Mitesh J Borad Alan H Bryce

Breast cancer 1 antigen (BRCA 1) and breast cancer 2 antigen (BRCA2) genes play a significant role in deoxyribonucleic acid (DNA) repair by means of interstrand crosslink repair, and deleterious germline mutations of these are responsible for most hereditary breast and ovarian cancers. Therapeutic strategies which specifically target interstrand crosslink repair can therefore be helpful in pati...

Journal: :Cancer research 2012
Göran Jönsson Johan Staaf Johan Vallon-Christersson Markus Ringnér Sofia K Gruvberger-Saal Lao H Saal Karolina Holm Cecilia Hegardt Adalgeir Arason Rainer Fagerholm Camilla Persson Dorthe Grabau Ellinor Johnsson Kristina Lövgren Linda Magnusson Päivi Heikkilä Bjarni A Agnarsson Oskar T Johannsson Per Malmström Mårten Fernö Håkan Olsson Niklas Loman Heli Nevanlinna Rosa B Barkardottir Åke Borg

Breast tumors from BRCA1 germ line mutation carriers typically exhibit features of the basal-like molecular subtype. However, the specific genes recurrently mutated as a consequence of BRCA1 dysfunction have not been fully elucidated. In this study, we used gene expression profiling to molecularly subtype 577 breast tumors, including 73 breast tumors from BRCA1/2 mutation carriers. Focusing on ...

Journal: :Vestnik Rossiiskoi akademii meditsinskikh nauk 2014
N V Cherdyntseva L F Pisareva A A Ivanova Ye V Panferova E A Malinovskaya I N Odintsova A V Doroshenko P A Gervas E M Slonimskaya A A Shivit-ool V V Dvornichenko Ye L Choinzonov

BACKGROUND Ethnic diversity of the population in the region of Siberia suggests the existence of different germline mutations in the BRCA1/2 genes associated with breast and ovarian cancer in different ethnic populations, but spectrum of these mutations has not been studied. OBJECTIVE Our aim was to evaluate the frequency of the most common mutations BRCA1/2 (BRCA1 5382insC, BRCA1 185delAG, B...

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