A Comprehensive Focus on Global Spectrum of BRCA1 and BRCA2 Mutations in Breast Cancer

F Karami, P Mehdipour - BioMed research international, 2013 - Wiley Online Library
Breast cancer (BC) is the most common cancer of women all over the world. BRCA1 and
BRCA2 gene mutations comprise the most important genetic susceptibility of BC. Except for …

BRCA1 mutation spectrum, functions, and therapeutic strategies: The story so far

B Sharma, RP Kaur, S Raut, A Munshi - Current problems in cancer, 2018 - Elsevier
BRCA1 gene mutations account for about 25-28% of hereditary Breast Cancer as BRCA1 is
included in the category of high penetrance genes. Except for few commonmutations, there …

Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients

RI Dodova, AV Mitkova, DR Dacheva, LB Hadjo… - BMC cancer, 2015 - Springer
Background About 3885 women are diagnosed with breast cancer and 1285 die from the
disease each year in Bulgaria. However no genetic testing to identify the mutations in high …

[PDF][PDF] Absence of 185delAG and 6174delT mutations among breast cancer patients of eastern India

A Chakraborty, D Banerjee, J Basak… - Asian Pacific Journal …, 2015 - researchgate.net
Background: The incidence of breast cancer in India is on the rise and is rapidly becoming
the number one cancer in females, pushing the cervical cancer to the second position. Most …

Heterogeneity of germline variants in high risk breast and ovarian cancer susceptibility genes in India

A Sharma-Oates, AM Shaaban… - Precision Clinical …, 2018 - academic.oup.com
Breast and ovarian cancers now account for one in three cancers in Indian women and their
incidence is rising. Major differences in the clinical presentation of breast and ovarian …

Detection of a novel mutation in exon 20 of the BRCA1 gene

A Chakraborty, A Katarkar, K Chaudhuri… - Cellular & Molecular …, 2013 - Springer
Abstract Hereditary breast cancer constitutes 5–10% of all breast cancer cases. Inherited
mutations in the BRCA1 and BRCA2 tumor-suppressor genes account for the majority of …

A case–control study of BRCA1 founder mutations 185delAG and 5382insC in a cohort of Egyptian ovarian cancer patients using pyrosequencing technique

MM Rizk, NM El-etreby, LM El-Attar, EA Elzyat… - Egyptian Journal of …, 2022 - Springer
Background Ovarian cancer (OC) is considered a leading cause of death among women
with gynecological malignancies. OC, like breast cancer, shows a familial predisposition to …

Absence of germline BRCA1 c. 68_69delAG and c. 5266dupC mutations among hormone receptor-negative breast cancer patients: a first impression at a tertiary …

LP Rweyemamu, G Akan, CH Mbotwa… - Tanzania Journal of …, 2021 - ajol.info
Abstract The germline BRCA1 c. 68_69delAG (185delAG) and c. 5266dupC (5382insC)
mutations are associated with hormone receptor-negative breast cancer (BC). Limited …

ЭФФЕКТ ОСНОВАТЕЛЯ В СПЕКТРЕ МУТАЦИЙ В ГЕНАХ НАСЛЕДСТВЕННОЙ ПРЕДРАСПОЛОЖЕННОСТИ К РАКУ МОЛОЧНОЙ ЖЕЛЕЗЫ

ЗИ Бисултанова, ПМ Джамбетова - Ежегодная итоговая научно …, 2023 - elibrary.ru
Мутации в двух основных высокопенетрантных генах рака молочной железы BRCA1 и
BRCA2 ответственны за 20 и более процентов случаев наследственного рака …

[PDF][PDF] Molecular study of BRCA-1, 2 and P53 gene polymorphisms among post-operative breast cancer patients

H Al-Hilaly, A Rasool, R Magid - repository.qu.edu.iq
Address: 1 Professor, Department of Medical Microbiology, College of Medicine, University
of Al-Qadisiyah, Diwaniyah, Iraq, Email: hammadi. abttan@ qu. edu. iq, 2 Assist Professor …