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10.1016/j.gdata.2015.11.027

http://scihub22266oqcxt.onion/10.1016/j.gdata.2015.11.027
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C4778620!4778620!26981369
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suck abstract from ncbi


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pmid26981369      Genom+Data 2016 ; 7 (ä): 82-5
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  • Transcriptional profile of immediate response to ionizing radiation exposure #MMPMID26981369
  • Rouchka EC; Flight RM; Fasciotto BH; Estrada R; Eaton JW; Patibandla PK; Waigel SJ; Li D; Kirtley JK; Sethu P; Keynton RS
  • Genom Data 2016[Mar]; 7 (ä): 82-5 PMID26981369show ga
  • Astronauts participating in long duration space missions are likely to be exposed to ionizing radiation associated with highly energetic and charged heavy particles. Previously proposed gene biomarkers for radiation exposure include phosphorylated H2A Histone Family, Member X (?H2AX), Tumor Protein 53 (TP53), and Cyclin-Dependent Kinase Inhibitor 1A (CDKN1A). However, transcripts of these genes may not be the most suitable biomarkers for radiation exposure due to a lack of sensitivity or specificity. As part of a larger effort to develop lab-on-a-chip methods for detecting radiation exposure events using blood samples, we designed a dose?course microarray study in order to determine coding and non-coding RNA transcripts undergoing differential expression immediately following radiation exposure. The main goal was to elicit a small set of sensitive and specific radiation exposure biomarkers at low, medium, and high levels of ionizing radiation exposure. Four separate levels of radiation were considered: 0 Gray (Gy) control; 0.3 Gy; 1.5 Gy; and 3.0 Gy with four replicates at each radiation level. This report includes raw gene expression data files from the resulting microarray experiments from all three radiation levels ranging from a lower, typical exposure than an astronaut might see (0.3 Gy) to high, potentially lethal, levels of radiation (3.0 Gy). The data described here is available in NCBI's Gene Expression Omnibus (GEO), accession GSE64375.
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