[HTML][HTML] Germline variants profiling of BRCA1 and BRCA2 in Chinese Hakka breast and ovarian cancer patients

Y Zhang, H Wu, Z Yu, L Li, J Zhang, X Liang, Q Huang - BMC cancer, 2022 - Springer
Objective To investigate the prevalence and spectrum of BRCA1 and BRCA2 mutations in
Chinese Hakka patients with breast and ovarian cancer. Methods A total of 1,664 breast or …

[HTML][HTML] The clinical significance of genetic variation in ovarian cancer

D Ban, SN Housley, JF McDonald - International Journal of Molecular …, 2023 - mdpi.com
Genetic variation is a well-known contributor to the onset and progression of cancer. The
goal of this study is to provide a comprehensive examination of the nucleotide and …

[HTML][HTML] Clinical Evidence of Circulating Tumor DNA Application in Aggressive Breast Cancer

B El Hejjioui, L Bouguenouch, MA Melhouf, H El Mouhi… - Diagnostics, 2023 - mdpi.com
Breast cancer is clinically and biologically heterogeneous and is classified into different
subtypes according to the molecular landscape of the tumor. Triple-negative breast cancer is …

[HTML][HTML] Preliminary insights on the mutational spectrum of BRCA1 and BRCA2 genes in Pakhtun ethnicity breast cancer patients from Khyber Pakhtunkhwa (KP) …

H Ahmad, A Ali, R Ali, AT Khalil, I Khan, MM Khan… - Neoplasia, 2024 - Elsevier
Gene mutations are a source of genetic instability which fuels the progression of cancer.
Mutations in BRCA1 and BRCA2 are considered as major drivers in the progression of …

[HTML][HTML] CENPA and BRCA1 are potential biomarkers associated with immune infiltration in heart failure and pan-cancer

J Wang, L Cai, G Huang, C Wang, Z Zhang, J Xu - Heliyon, 2024 - cell.com
Heart failure (HF) and cancer are the two leading causes of death worldwide and affect one
another in a bidirectional way. We aimed to identify hub therapeutic genes as potential …

[HTML][HTML] Germline RECQL gene mutations in Chinese patients with breast cancer

J Hu, Y Shen, K Zhang, Y Chen - Frontiers in Medicine, 2024 - frontiersin.org
Introduction Breast cancer is the most common malignant tumor in women, seriously
threatening health and survival. TP-dependent DNA helicase Q1 (RECQL) is a breast …

三阴性乳腺癌遗传易感性研究进展

张丽佳, 刘佳芮, 张沅, 陈薪宇, 王信, 张怡 - 肿瘤防治研究, 2023 - zlfzyj.com
三阴性乳腺癌(TNBC) 是一类治疗困难, 预后较差, 术后早期易复发且易转移的乳腺癌.
发病呈低龄化趋势, 种族差异大, 具有明显的遗传易感性, 因此迫切需要阐明TNBC …

Three cases of colon cancer in four generations of the Saudi family, caused by endogamous germline mutations

DS Alshaya, TMI Al-Hazani, MA Alotaibi… - Cellular and Molecular …, 2023 - cellmolbiol.org
Various research pieces of evidence have been published in recent years, establishing the
increasing prevalence of early colon cancer among young people. In this background, the …

Prevalence of familial BRCA1/2 mutation in four cancer types in the United Arab Emirates and of Arab Nationals

AAAA Al-Ali, MMAA Al Ali, DMAH El-Shourbagy… - 2023 - researchsquare.com
Background/Objectives: The presence of BRCA1/2 gene mutation significantly impacts the
current and future management of patients. Germline BRCA1/2 mutations are associated …

[HTML][HTML] Turkish population-based screening for first identified changes of BRCA1 and BRCA2 genes in breast and/or ovarian cancer patients

T Semerci Sevimli, M Sevimli, AE Manguoğlu… - Egyptian Journal of …, 2024 - Springer
Introduction It is known that BRCA1 and BRCA2 genes' mutation carriers are predisposed to
breast and ovarian cancers and other organ cancers such as prostate, colon and cervix. In …