Common tumour p53 mutations in immortalized cells from Hupki mice heterozygous at codon 72

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“p53 Polymorphism at Codon 72 and Breast Cancer” - Letter

We read with interest the recently published systematic review and meta-analysis titled “The Evaluation of p53 Polymorphism at Codon 72 and Association With Breast Cancer in Iran: A Systematic Review and Meta-analysis”. We believe that there are few important issues in the systematic review and meta-analysis that require clarification. A key characteristic of a systematic review is a comprehens...

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Frequency of p53 Gene Codon 72 Polymorphisms in Women with Breast Cancer in Iran

Backgrounds and Aims: P53 gene is regarded important in pathogenesis of different cancers. Therefore, this study aimed to investigate the frequency of p53 gene codon 72 Arg/Pro polymorphism in women suffering from breast cancer. Materials and Methods: A total of 90 patients with breast cancer and 83 matched healthy control women participated in this case-control study. Genomic DNA was extrac...

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P-93: Analysis of P53 Codon 72 Gene Polymorphism in Isfahanian Patients With Endometriosis

Background: The p53 tumor suppressor gene plays important roles in genomic stability. Several reports have noted racial differences in the prevalence of p53 genotypes at the codon 72 in patients with endometriosis.To study the association of endometriosis with p53 codon 72 polymorphism in the population of Isfahan. Materials and Methods: We undertook a case–control study to examine the possible...

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P53 codon 72 polymorphism in Taiwanese breast cancer patients.

There are clear discrepancies between ethnicity and geographic area regarding the peak age incidence and mortality of breast cancer. Underlying variances include genetic, environmental, and socioeconomic factors. The wild-type p53 codon has two common polymorphic variants from a single-base-pair substitution at codon 72, where either C-C-C encodes proline (p53-p72) or C-G-C encodes arginine (p5...

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ژورنال

عنوان ژورنال: Oncogene

سال: 2007

ISSN: 0950-9232,1476-5594

DOI: 10.1038/sj.onc.1210932