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Titlebook: Environmental Genomics; C. Cristofre Martin,C. Cristofre Martin Book 2008 Humana Press 2008 Bur.DNA.FISH.Fluoreszenz in situ-Hybridisierun

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https://doi.org/10.1007/978-3-658-43381-9ulation monitoring of genetic damage, screening of chemicals for genotoxic potential and for specific purposes such as the prediction of the radiosensitivity of tumors and the inter-individual variation in radiosensitivity. In its current basic form the CBMN assay can provide, using simple morpholog
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https://doi.org/10.1007/978-3-662-31518-7equence of specific chromosomes, if available, can be used to count the number of chromosomes in interphase nuclei to detect hyperploid cells possibly produced by chromosome nondisjunction. Finally, probes that hybridize to the telomeric sequence common to all chromosomes can be used to label telome
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https://doi.org/10.1007/978-3-322-87643-0e., species composition) and functional differences (i.e., gene composition) in the genomic content of two different rumen environmental communities (.). Through a series of hybridizations and polymerase chain reaction (PCR) amplifications, metagenomic differences between two environmental samples c
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High Throughput Whole Mount , Hybridization of Zebrafish Embryos for Analysis of Tissue-Specific Gengene expression domains between organisms that have been subjected to different environmental conditions, an understanding of the cellular and tissue-specific effects of these environmental exposures can be identified. This technique is complementary to gene expression profiling techniques such as D
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Constructing and Screening a cDNA Librarywith or survive different stresses. The construction of a cDNA library and subsequent screening for genes of interest allows researchers to select for genes that are likely to play key roles in the regulation or response to the condition or stress of interest, those that may not be expressed (or exi
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