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Spectropolarimetric comparison of molecular-genetic study of BRCA1 gene mutation types in patients with breast cancer and their relatives

机译:BRCA1基因突变类型在乳腺癌及其亲属患者中BRCA1基因突变类型的分子遗传学研究

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This work is devoted to the substantiation and selection of patients with breast cancer (BC) for the purpose ofconducting expensive molecular genetic studies on genotyping. As diagnostic methods have been used ultravioletspectrometry samples of blood plasma in the liquid state, infrared spectroscopy middle range (2,5 - 25 microns)dry residue of plasma polarization and laser diagnostic technique of thin histological sections of biologicaltissues. Obtained results showed that the use of spectrophotometry in the range of 1000-3000 cm~(-1) allowed toestablish quantitative parameters of the plasma absorption rate of blood of patients in the third group in differentranges, which would allow in the future to conduct an express analysis of the patient's condition (procedurescreening) for further molecular-genetic typing on BRCA Ⅰ and Ⅱ.
机译:这项工作致力于证实和选择乳腺癌(BC)的患者的目的对基因分型进行昂贵的分子遗传研究。由于诊断方法已被使用紫外线液体状态下血浆的光谱法,红外光谱中间范围(2,5-25微米)生物学薄组织区等离子体偏振和激光诊断技术的干燥残余物组织。得到的结果表明,分光光度法在1000-3000cm〜(-1)的范围内允许建立不同的患者血液血浆吸收率的定量参数范围,这将允许在未来进行对患者状况的明确分析(程序用于在BRCAⅠ和Ⅱ的进一步分子遗传键入的筛选。

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