Guest guest Posted April 4, 2012 Report Share Posted April 4, 2012 eg Micronuclei in neonates and children: effects of environmental, genetic, demographic and disease variables. <http://www.ncbi.nlm.nih.gov/pubmed/21164182> Holland N, Fucic A, Merlo DF, Sram R, Kirsch-Volders M. Mutagenesis. 2011 Jan;26(1):51-6. http://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21164182/?tool=pubmed Children may be more susceptible to the effects of the environmental exposure and medical treatments than adults; however, limited information is available about the differences in genotoxic effects in children by age, sex and health status. Micronucleus (MN) assay is a well established method of monitoring genotoxicity, and this approach is thoroughly validated for adult lymphocytes by the Human Micronucleus Biomonitoring project (HUMN.org). Similar international undertaking is in progress for exfoliated buccal cells. Most of the MN studies in children are focused on analyses of lymphocytes but in the recent years, more investigators are interested in using exfoliated cells from the oral cavity and other cell types that can be collected non-invasively, which is particularly important in paediatric cohorts. The baseline MN frequency is relatively low in newborns and its assessment requires large cohorts and cell sample counts. */Available results are mostly consistent in conclusion that environmental pollutants and radiation exposures lead to the increase in the MN frequency in children/*... - - - - Autism Mutations, Scattered Across Many Genes, Merge Into Common Network of Interactions http://www.sciencedaily.com/releases/2012/04/120404133700.htm ScienceDaily (Apr. 4, 2012) — UW researchers have announced their findings from a major study looking into the genetic basis of autism spectrum disorders (ASD) with an approach piloted at the UW. The researchers have been studying ASD in children who have no family history of this or related impairments -- so called " sporadic autism " -- and also why autism varies in its symptoms and severity. By focusing on " sporadic autism, " the researchers sought to evaluate a specific genetic model for ASD risk, namely the appearance of new mutations (termed de novo) in children with ASD that were not found in either parent. .. Their results are reported in the April 4 advanced online edition of the journal Nature.... - - - - J. O’Roak et al* Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations*. / Nature/, 2012; DOI: 10.1038/nature10989 <http://dx.doi.org/10.1038/nature10989> Quote Link to comment Share on other sites More sharing options...
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