نتایج جستجو برای: brca genes

تعداد نتایج: 428134  

2015
Edward S. Y. Wong Sandhya Shekar Claire H. T. Chan Lewis Z. Hong Suk-Yean Poon Toomas Silla Clarabelle Lin Vikrant Kumar Sonia Davila Mathijs Voorhoeve Aye Aye Thike Gay Hui Ho Yoon Sim Yap Puay Hoon Tan Min-Han Tan Peter Ang Ann S. G. Lee Peiwen Fei

PURPOSE The National Comprehensive Cancer Network (NCCN) has proposed guidelines for the genetic testing of the BRCA1 and BRCA2 genes, based on studies in western populations. This current study assessed potential predictive factors for BRCA mutation probability, in an Asian population. METHODS A total of 359 breast cancer patients, who presented with either a family history (FH) of breast an...

Journal: :Health law journal 2002
Bryn Williams-Jones

The patenting and commercialization of human genetic material raises a host of complex social, ethical, and policy issues, such as the potential for discrimination or stigmatization in access to health care services or employment, the exploitation of minority or indigenous communities in DNA prospecting, and the implications for ongoing biomedical research and access to health care services. Bu...

2017
Davide Caruso Anselmo Papa Silverio Tomao Patrizia Vici Pierluigi Benedetti Panici Federica Tomao

Ovarian cancer is the first cause of death from gynaecological malignancy. Germline mutation in BRCA1 and 2, two genes involved in the mechanisms of reparation of DNA damage, are showed to be related with the incidence of breast and ovarian cancer, both sporadic and familiar. PARP is a family of enzymes involved in the base excision repair (BER) system. The introduction of inhibitors of PARP in...

Journal: :Journal of medical genetics 2005
S-W Kim C S Lee J V Fey P I Borgen J Boyd

E pidemiological data suggest that 7% of breast cancer cases and 10% of ovarian cancer cases in the general population are attributable to one or more autosomal dominant susceptibility alleles. The breast and ovarian cancer susceptibility genes BRCA1 and BRCA2 were isolated in 1994 and 1995, 4 respectively, and since then, a large volume of literature attests to the involvement of these genes i...

2015
Jae Myoung Noh Jihun Kim Dae Yeon Cho Doo Ho Choi Won Park Seung Jae Huh

PURPOSE We performed exome sequencing in a breast cancer family without BRCA mutations. MATERIALS AND METHODS A family that three sisters have a history of breast cancer was selected for analysis. There were no family members with breast cancer in the previous generation. Genetic testing for BRCA mutation was negative, even by the multiplex ligation-dependent probe amplification method. Two s...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2011
C Underhill M Toulmonde H Bonnefoi

BACKGROUND Poly(adenosine diphosphate [ADP]-ribose) polymerase (PARP) inhibitors, with novel and selective mechanisms of action, have moved from the laboratory to the clinic in just the last few years. DESIGN We conducted an extensive review of PARP inhibitors using a Medline search. We also searched abstracts in databases of major international oncology meetings from the last 4 years. RESU...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2011
D J Gallagher J A Konner K M Bell-McGuinn J Bhatia P Sabbatini C A Aghajanian K Offit R R Barakat D R Spriggs N D Kauff

BACKGROUND Patients with BRCA-associated ovarian cancer (OC) have a survival advantage over those with sporadic OC. To further explore this, we examined the impact of prognostic factors on disease-free survival (DFS) and overall survival (OS) in patients with known BRCA mutation status. PATIENTS AND METHODS We reviewed stage III-IV OC patients treated at our institution between 1 December 199...

2016
I Vergote V Bours B Blaumeiser J-F Baurain

Ovarian cancer (OC) is the seventh most common cancer in women. Although women diagnosed with OC are usually treated frontline with platinum-based chemotherapy, most of them relapse once treatment is halted. Therefore, maintenance therapies have been developed to secure the response and delay further chemotherapy. There are two established maintenance therapies for women affected by platinum-se...

Journal: :Journal of the National Cancer Institute 2006
Kenneth Offit

EDITORIALS 1675 More than a decade after the discovery of the BRCA1 and BRCA2 genes, a consensus has yet to emerge regarding the frequency and precise magnitude and spectrum of cancer risks for individuals carrying mutations of these genes. Although these questions constitute a topic of heated debate among cancer epidemiologists ( 1 – 9 ) , they are also of clinical concern to women and men con...

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