SP-0101: A radiation systems biology view of radiation sensitivity of normal and tumour cells
نویسندگان
چکیده
منابع مشابه
Radiation - perturbed signalling and systems radiation biology
In deep space astronauts are usually exposed to doses of ~ 1 mSv/day of charged particles, including HZE. Due to the exposure to GCR (e.g. during a mission to Mars), each cell nucleus of an astronaut would be traversed by a proton or by a secondary electron every few days, but only by an HZE ion every few months [1]. For this reason, besides the clustered properties of the incoming radiation on...
متن کاملIntegrative radiation systems biology
Maximisation of the ratio of normal tissue preservation and tumour cell reduction is the main concept of radiotherapy alone or combined with chemo-, immuno- or biologically targeted therapy. The foremost parameter influencing this ratio is radiation sensitivity and its modulation towards a more efficient killing of tumour cells and a better preservation of normal tissue at the same time is the ...
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در این تحقیق دانش زبانشناسی و کاربردشناسی زبان آموزان ایرانی در سطح بالای متوسط مقایسه شد. 50 دانش آموز با سابقه آموزشی مشابه از شش آموزشگاه زبان مختلف در دو آزمون دانش زبانشناسی و آزمون دانش گفتار شناسی زبان انگلیسی شرکت کردند که سوالات هر دو تست توسط محقق تهیه شده بود. همچنین در این تحقیق کارایی کتابهای آموزشی زبان در فراهم آوردن درون داد کافی برای زبان آموزان ایرانی به عنوان هدف جانبی تحقیق ...
15 صفحه اولThe effects of radiation and alkylating agents on chromatin degradation in normal and tumour lymphoid cells.
The dynamic of chromatin degradation was studied in thymocytes and LS/BL tumour cells. In permeabilised LS/BL cells, the rate of DNA degradation induced by endogenous calcium and magnesium-dependent endonuclease was approx. 25 times slower than in thymocytes. In LS/BL cells irradiation does not induce chromatin degradation. The alkylating agent TS 160 induced chromatin degradation in both LS/BL...
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ژورنال
عنوان ژورنال: Radiotherapy and Oncology
سال: 2016
ISSN: 0167-8140
DOI: 10.1016/s0167-8140(16)31350-0