Titlebook: Genotoxicity Assessment; Methods and Protocol Alok Dhawan,Mahima Bajpayee Book 2019Latest edition Springer Science+Business Media, LLC, par

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書目名稱Genotoxicity Assessment影響因子(影響力)




書目名稱Genotoxicity Assessment影響因子(影響力)學科排名




書目名稱Genotoxicity Assessment網(wǎng)絡公開度




書目名稱Genotoxicity Assessment網(wǎng)絡公開度學科排名




書目名稱Genotoxicity Assessment被引頻次




書目名稱Genotoxicity Assessment被引頻次學科排名




書目名稱Genotoxicity Assessment年度引用




書目名稱Genotoxicity Assessment年度引用學科排名




書目名稱Genotoxicity Assessment讀者反饋




書目名稱Genotoxicity Assessment讀者反饋學科排名

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Dicentric Chromosome Assay (DCA) and Cytokinesis-Block Micronucleus (CBMN) Assay in the Field of Biomes (Dic) and micronuclei (MN) in exposed individuals’ peripheral blood lymphocytes (PBL)..The present chapter does not claim to make an exhaustive and complete picture on the complex world of biodosimetry, to which a large number of specific guidelines for performing laboratory services by the Inte

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Micronucleus Cytome Assays in Human Lymphocytes and Buccal Cellsrs to the use of ex vivo whole blood method, involving 72?h of culture with the block of cytokinesis starting at 44?h. BMNCyt protocol reports the established method for sample collection, processing, slide preparation and scoring.

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Micronucleus Analysis by Flow Cytometry of the in vitro MN test Organization for Economic Cooperation and Development (OECD) guideline 487 (OECD, Guideline for testing of chemicals: in vitro mammalian cell micronucleus test 487: in vitro mammalian cell micronucleus test (MNVIT). Organization for Economic Cooperation and Development, Pari

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The Comet Assay in Human Biomonitoringder to remove all cellular contents except the DNA attached to a nuclear scaffold. Subsequent electrophoresis results in accumulation of undamaged DNA sequences at the proximity of the nuclear scaffold, while damaged sequences migrate toward the anode. When visualized with fluorochromes, these migra

FECK

Multicolor Laser Scanning Confocal Immunofluorescence Microscopy of DNA Damage Response Biomarkersing confocal immunofluorescence microscopy (LSCIM) of three-dimensionally preserved nuclei can be, quantitative and maintain the spatial information. Here we describe the experimental protocols to quantify individual key events of the DDR cascade in three-dimensionally preserved nuclei by LSCIM with

Processes

Detection of DNA Double-Strand Breaks Using Pulsed-Field Gel Electrophoresislly relevant cellular processes as well as to investigate the genotoxic or clastogenic effects of toxicants. Pulsed-field gel electrophoresis (PFGE) is a widely used method for direct quantification of DNA DSBs. In this method, the cells exposed to DSB-inducing agents are embedded in the agarose blo