Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/131130
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dc.titlePast exposure to densely ionizing radiation leaves a unique permanent signature in the genome
dc.contributor.authorHande, M.P.
dc.contributor.authorAzizova, T.V.
dc.contributor.authorGeard, C.R.
dc.contributor.authorBurak, L.E.
dc.contributor.authorMitchell, C.R.
dc.contributor.authorKhokhryakov, V.F.
dc.contributor.authorVasilenko, E.K.
dc.contributor.authorBrenner, D.J.
dc.date.accessioned2016-11-28T10:16:35Z
dc.date.available2016-11-28T10:16:35Z
dc.date.issued2003-05-01
dc.identifier.citationHande, M.P., Azizova, T.V., Geard, C.R., Burak, L.E., Mitchell, C.R., Khokhryakov, V.F., Vasilenko, E.K., Brenner, D.J. (2003-05-01). Past exposure to densely ionizing radiation leaves a unique permanent signature in the genome. American Journal of Human Genetics 72 (5) : 1162-1170. ScholarBank@NUS Repository.
dc.identifier.issn00029297
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/131130
dc.description.abstractSpeculation has long surrounded the question of whether past exposure to ionizing radiation leaves a unique permanent signature in the genome. Intrachromosomal rearrangements or deletions are produced much more efficiently by densely ionizing radiation than by chemical mutagens, x-rays, or endogenous aging processes. Until recently, such stable intrachromosomal aberrations have been very hard to detect, but a new chromosome band painting technique has made their detection practical. We report the detection and quantification of stable intrachromosomal aberrations in lymphocytes of healthy former nuclear-weapons workers who were exposed to plutonium many years ago. Even many years after occupational exposure, more than half the blood cells of the healthy plutonium workers contain large (>6 Mb) intrachromosomal rearrangements. The yield of these aberrations was highly correlated with plutonium dose to the bone marrow. The control groups contained very few such intrachromosomal aberrations. Quantification of this large-scale chromosomal damage in human populations exposed many years earlier will lead to new insights into the mechanisms and risks of cytogenetic damage.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1086/375041
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHYSIOLOGY
dc.description.sourcetitleAmerican Journal of Human Genetics
dc.description.volume72
dc.description.issue5
dc.description.page1162-1170
dc.description.codenAJHGA
dc.identifier.isiut000182474400009
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