نتایج جستجو برای: familial breast cancer

تعداد نتایج: 1032090  

Journal: :Carcinogenesis 2007
Michael Wirtenberger Julia Schmutzhard Kari Hemminki Alfons Meindl Christian Sutter Rita K Schmutzler Barbara Wappenschmidt Marion Kiechle Norbert Arnold Bernhard H F Weber Dieter Niederacher Claus R Bartram Barbara Burwinkel

Overexpression of cAMP-dependent protein kinase A (PKA) is a hallmark of the great majority of human cancers including breast cancer. A-kinase anchoring proteins (AKAPs) coordinate the specificity of PKA signalling by localizing the kinase to its subcellular sites. We tested the hypothesis whether the functional amino acid exchange Ile646Val, located in the kinase-binding domain of AKAP10, is a...

2004
Pål Møller

Inherited breast-ovarian cancer was described in 1866. The underlying genetic defects in BRCA1/2 were demonstrated 128 years later. We now have 10 years of experience with genetic testing in BRCA kindreds. The majority of breast cancer kindreds (familial breast cancer) do not demonstrate ovarian cancer and are not associated with BRCA mutations. The effect of early diagnosis and treatment is mo...

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 Background: Breast cancer is one of the most common cancer of women in the world.  Although different genetic alteration has been reported in this malignancy, but P 53 gene  mutations has more frequency. P 53 gene is one of the most important suppressor genes and it  play a central role in breast cancer and detecting of mutations in this gene would be very helpful in understanding of genetic m...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2016
Sören Möller Lorelei A Mucci Jennifer R Harris Thomas Scheike Klaus Holst Ulrich Halekoh Hans-Olov Adami Kamila Czene Kaare Christensen Niels V Holm Eero Pukkala Axel Skytthe Jaakko Kaprio Jacob B Hjelmborg

BACKGROUND Family history is an established risk factor for breast cancer. Although some important genetic factors have been identified, the extent to which familial risk can be attributed to genetic factors versus common environment remains unclear. METHODS We estimated the familial concordance and heritability of breast cancer among 21,054 monozygotic and 30,939 dizygotic female twin pairs ...

Journal: :Breast Cancer Research : BCR 2008
Felicity Lose Jeremy Arnold David B Young Carolyn J Brown Graham J Mann Gulietta M Pupo Kum Kum Khanna Georgia Chenevix-Trench Amanda B Spurdle

Reference 1. Lose F, Arnold J, Young DB, Brown CJ, Mann GJ, Pupo GM, The Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, Khanna KK, Chenevix-Trench G, Spurdle AB: BcoR-L1 variation and breast cancer. Breast Cancer Res 2007, 9:R54. Correction Correction: BCoR-L1 variation and breast cancer Felicity Lose1,2, Jeremy Arnold1, David B Young1, Carolyn J Brown3, Grah...

Journal: :PloS one 2016
Liisa M Pelttari Sofia Khan Mikko Vuorela Johanna I Kiiski Sara Vilske Viivi Nevanlinna Salla Ranta Johanna Schleutker Robert Winqvist Anne Kallioniemi Thilo Dörk Natalia V Bogdanova Jonine Figueroa Paul D P Pharoah Marjanka K Schmidt Alison M Dunning Montserrat García-Closas Manjeet K Bolla Joe Dennis Kyriaki Michailidou Qin Wang John L Hopper Melissa C Southey Efraim H Rosenberg Peter A Fasching Matthias W Beckmann Julian Peto Isabel Dos-Santos-Silva Elinor J Sawyer Ian Tomlinson Barbara Burwinkel Harald Surowy Pascal Guénel Thérèse Truong Stig E Bojesen Børge G Nordestgaard Javier Benitez Anna González-Neira Susan L Neuhausen Hoda Anton-Culver Hermann Brenner Volker Arndt Alfons Meindl Rita K Schmutzler Hiltrud Brauch Thomas Brüning Annika Lindblom Sara Margolin Arto Mannermaa Jaana M Hartikainen Georgia Chenevix-Trench Laurien Van Dyck Hilde Janssen Jenny Chang-Claude Anja Rudolph Paolo Radice Paolo Peterlongo Emily Hallberg Janet E Olson Graham G Giles Roger L Milne Christopher A Haiman Fredrick Schumacher Jacques Simard Martine Dumont Vessela Kristensen Anne-Lise Borresen-Dale Wei Zheng Alicia Beeghly-Fadiel Mervi Grip Irene L Andrulis Gord Glendon Peter Devilee Caroline Seynaeve Maartje J Hooning Margriet Collée Angela Cox Simon S Cross Mitul Shah Robert N Luben Ute Hamann Diana Torres Anna Jakubowska Jan Lubinski Fergus J Couch Drakoulis Yannoukakos Nick Orr Anthony Swerdlow Hatef Darabi Jingmei Li Kamila Czene Per Hall Douglas F Easton Johanna Mattson Carl Blomqvist Kristiina Aittomäki Heli Nevanlinna

Common variation on 14q24.1, close to RAD51B, has been associated with breast cancer: rs999737 and rs2588809 with the risk of female breast cancer and rs1314913 with the risk of male breast cancer. The aim of this study was to investigate the role of RAD51B variants in breast cancer predisposition, particularly in the context of familial breast cancer in Finland. We sequenced the coding region ...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2015
Amy L Gross Betty J May Jennifer E Axilbund Deborah K Armstrong Richard B S Roden Kala Visvanathan

BACKGROUND This study prospectively examines weight gain in breast cancer survivors compared with cancer-free women from a familial risk cohort. METHODS Absolute and percent weight change over 4 years was compared among 303 breast cancer survivors and 307 cancer-free women matched on age and menopausal status, from the same familial risk cohort. Linear and logistic regression was used to esti...

Journal: :International Journal of Medical Sciences 2008
Nancy Uhrhammer Amina Abdelouahab Laurence Lafarge Viviane Feillel Ahmed Ben Dib Yves-Jean Bignon

Breast cancer rates and median age of onset differ between Western Europe and North Africa. In Western populations, 5 to 10 % of breast cancer cases can be attributed to major genetic factors such as BRCA1 and BRCA2, while this attribution is not yet well defined among Africans. To help determine the contribution of BRCA1 mutations to breast cancer in a North African population, we analysed gen...

2013
Ella R. Thompson Simone M. Rowley Sarah Sawyer kConFab Diana M. Eccles Alison H. Trainer Gillian Mitchell Paul A. James Ian G. Campbell

Mutations in RAD51D have been associated with an increased risk of hereditary ovarian cancer and although they have been observed in the context of breast and ovarian cancer families, the association with breast cancer is unclear. The aim of this current study was to validate the reported association of RAD51D with ovarian cancer and assess for an association with breast cancer. We screened for...

Journal: :Journal of medical genetics 1999
H Tulinius H Sigvaldason G Olafsdóttir L Tryggvadóttir K Bjarnadóttir

Information in the Icelandic Cancer Registry on breast cancer and its collection of breast cancer families has been used to elucidate changes in breast cancer incidence by time period and by age, and the effect of degree of relationship and age on the familial risk of breast cancer. Since 1921 the incidence rates have increased, but the increase is significantly greater (2.06% per year) for age...

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