نتایج جستجو برای: chek2

تعداد نتایج: 669  

Journal: :Nucleic acids research 2004
Edwin Haghnazari Wolf-Dietrich Heyer

A DNA gap repair assay was used to determine the effect of mutations in the DNA damage checkpoint system on the efficiency and outcome (crossover/non-crossover) of recombinational DNA repair. In Saccharomyces cerevisiae gap repair is largely achieved by homologous recombination. As a result the plasmid either integrates into the chromosome (indicative of a crossover outcome) or remains extrachr...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2015
Asfandyar Sheikh Syed Ather Hussain Quratulain Ghori Nida Naeem Abul Fazil Smith Giri Brijesh Sathian Prajeena Mainali Dalal M Al Tamimi

Breast cancer is the most common malignancy in women around the world. About one in 12 women in the West develop breast cancer at some point in life. It is estimated that 5%-10% of all breast cancer cases in women are linked to hereditary susceptibility due to mutations in autosomal dominant genes. The two key players associated with high breast cancer risk are mutations in BRCA 1 and BRCA 2. A...

2013
Nikola A. Bowden Katie A. Ashton Ricardo E. Vilain Kelly A. Avery-Kiejda Ryan J. Davey Heather C. Murray Timothy Budden Stephen G. Braye Xu Dong Zhang Peter Hersey Rodney J. Scott

Nucleotide excision repair (NER) orchestrates the repair of helix distorting DNA damage, induced by both ultraviolet radiation (UVR) and cisplatin. There is evidence that the global genome repair (GGR) arm of NER is dysfunctional in melanoma and it is known to have limited induction in melanoma cell lines after cisplatin treatment. The aims of this study were to examine mRNA transcript levels o...

Journal: :Cancer detection and prevention 2006
Ritva Karhu Eeva Laurila Anne Kallioniemi Kirsi Syrjäkoski

BACKGROUND Germ-line mutations of the BRCA2 gene are the highest known risk factors for male breast cancer (MBC). Mutations in BRCA2 are mainly point mutations in contrast to BRCA1 in which large genomic rearrangements are quite common. In recent literature, however, genomic alterations of BRCA2 have been linked especially to male breast cancer families. We wanted to screen large genomic deleti...

2010
Kim M. Hirshfield Timothy R. Rebbeck Arnold J. Levine

Several female malignancies including breast, ovarian, and endometrial cancers can be characterized based on known somatic and germline mutations. Initiation and propagation of tumors reflect underlying genomic alterations such as mutations, polymorphisms, and copy number variations found in genes of multiple cellular pathways. The contributions of any single genetic variation or mutation in a ...

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