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Mouse lymphoma thymidine kinase gene mutation assay: meeting of the International Workshop on Genotoxicity Testing, San Francisco, 2005, recommendations for 24-h treatment
Authors:Moore Martha M,Honma Masamitsu,Clements Julie,Bolcsfoldi George,Burlinson Brian,Cifone Maria,Clarke Jane,Clay Philip,Doppalapudi Rupa,Fellows Michael,Gollapudi Bhaskar,Hou Saimei,Jenkinson Peter,Muster Wolfgang,Pant Kamala,Kidd Darren A,Lorge Elisabeth,Lloyd Melvyn,Myhr Brian,O'Donovan Michael,Riach Colin,Stankowski Leon F,Thakur Ajit K,Van Goethem Freddy  Mouse Lymphoma Assay Workgroup, IWGT
Affiliation:National Center for Toxicological Research, Food and Drug Administration, Jefferson, AR 72079, USA. Martha.Moore@fda.hhs.gov
Abstract:The Mouse Lymphoma Assay (MLA) Workgroup of the International Workshop on Genotoxicity Testing (IWGT), comprised of experts from Japan, Europe and the United States, met on September 9, 2005, in San Francisco, CA, USA. This meeting of the MLA Workgroup was devoted to reaching a consensus on issues involved with 24-h treatment. Recommendations were made concerning the acceptable values for the negative/solvent control (mutant frequency, cloning efficiency and suspension growth) and the criteria to define an acceptable positive control response. Consensus was also reached concerning the use of the global evaluation factor (GEF) and appropriate statistical trend analysis to define positive and negative responses for the 24-h treatment. The Workgroup agreed to continue their support of the International Committee on Harmonization (ICH) recommendation that the MLA assay should include a 24-h treatment (without S-9) in those situations where the short treatment (3-4 h) gives negative results.
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