Guest guest Posted June 9, 2011 Report Share Posted June 9, 2011 Perhaps aluminum adjuvants and thimerosal are contributing to the DNA aberrations described in autism Genotoxic effects of aluminum, iron and manganese in human cells and experimental systems: A review of the literature. <http://www.ncbi.nlm.nih.gov/pubmed/21247993> Lima P, Vaconcellos M, Montenegro R, Bahia M, Antunes L, Costa E, Burbano R. Hum Exp Toxicol. 2011 Jan 19. Aluminum-induced micronuclei and apoptosis in human peripheral-blood lymphocytes treated during different phases of the cell cycle. <http://www.ncbi.nlm.nih.gov/pubmed/16007643> Banasik A, Lankoff A, Piskulak A, Adamowska K, Lisowska H, Wojcik A. Environ Toxicol. 2005 Aug;20(4):402-6. Genotoxicity of thimerosal in cultured human lymphocytes with and without metabolic activation sister chromatid exchange analysis proliferation index and mitotic index. <http://www.ncbi.nlm.nih.gov/pubmed/18321677> Eke D, Celik A. Toxicol In Vitro. 2008 Jun;22(4):927-34. Thimerosal induces micronuclei in the cytochalasin B block micronucleus test with human lymphocytes. <http://www.ncbi.nlm.nih.gov/pubmed/12491041> Westphal GA, Asgari S, Schulz TG, Bünger J, Müller M, Hallier E. Arch Toxicol. 2003 Jan;77(1):50-5. - - - - Autism linked to hundreds of genetic mutations Three new studies conclude that autism disorders are genetically very complex, not caused by one or two gene defects. The potential changes in DNA may produce what are essentially different forms of autism. http://www.latimes.com/health/la-he-autism-20110609,0,2892508.story - - - - High Risk Genomic Loci in ASD Studies by Levy et al. <http://www.cell.com/neuron/abstract/S0896-6273%2811%2900396-5> and et al. <http://www.cell.com/neuron/abstract/S0896-6273%2811%2900374-6> examine the contribution of rare de novo genomic copy number variations (CNVs) in a large collection of families with one child with autism spectrum disorder (ASD) and revealed a number of loci associated with higher risk of ASD. In a related study, Gilman et al. <http://www.cell.com/neuron/abstract/S0896-6273%2811%2900439-9> used a novel network analysis approach to identify a network of genes affected by these rare de novo CNVs. Preview by Schaaf and Zoghbi <http://www.cell.com/neuron/abstract/S0896-6273%2811%2900443-0>. Quote Link to comment Share on other sites More sharing options...
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