TSP172-DrugMatrix - Toxicogenomic signatures after exposure to chlorambucil in the rat


TSA668-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (4.5 mg/kg, 5 days) in the rat


TSA669-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (4.5 mg/kg, 3 days) in the rat


TSA670-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (.6 mg/kg, 5 days) in the rat


TSA671-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (.6 mg/kg, .25 days) in the rat


TSA672-DrugMatrix - Toxicogenomic signatures of Heart after exposure to chlorambucil (4.5 mg/kg, 5 days) in the rat


TSA673-DrugMatrix - Toxicogenomic signatures of Heart after exposure to chlorambucil (4.5 mg/kg, 3 days) in the rat


TSF668-chlorambucil


1 subfactor(s)
TSF669-chlorambucil


1 subfactor(s)
TSF670-chlorambucil


1 subfactor(s)
TSF671-chlorambucil


1 subfactor(s)
TSF672-chlorambucil


1 subfactor(s)
TSF673-chlorambucil


1 subfactor(s)
TSS668-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (4.5 mg/kg, 5 days) in the rat


TSS669-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (4.5 mg/kg, 3 days) in the rat


TSS670-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (.6 mg/kg, 5 days) in the rat


TSS671-DrugMatrix - Toxicogenomic signatures of Liver after exposure to chlorambucil (.6 mg/kg, .25 days) in the rat


TSS672-DrugMatrix - Toxicogenomic signatures of Heart after exposure to chlorambucil (4.5 mg/kg, 5 days) in the rat


TSS673-DrugMatrix - Toxicogenomic signatures of Heart after exposure to chlorambucil (4.5 mg/kg, 3 days) in the rat



TSP172 - DrugMatrix - Toxicogenomic signatures after exposure to chlorambucil in the rat Public

DrugMatrix is the scientific communities' largest molecular toxicology reference database and informatics system. DrugMatrix is populated with the comprehensive results of thousands of highly controlled and standardized toxicological experiments in which rats or primary rat hepatocytes were systematically treated with therapeutic, industrial, and environmental chemicals at both non-toxic and toxic doses.

Interventional Experimental design

No experimental design provided

Results

No results provided