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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
Institution: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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