These carbons were explored for their reactivity against sulphur mustard and data was compared with that of impregnated carbons consisted of above basic and oxidizing compounds.
Importantly, the phenotypes of aberrant floral organs in transgenic plants were shown to be identical with those of CMS stem mustard (supplementary data additional file 1 and [ 31]).
Mustard agents are mutagenic; data for cellular and laboratory animal assays are presented.
All of the up-regulated genes detected in transgenic stem mustard are listed in supplementary data (additional file 3).
Furthermore, scpt mutants were not sensitive to irinotecan, bleomycin, mechlorethamine (nitrogen mustard), methyl methanesulfonate, or hydroxyurea (data not shown).
B. rapa (mustard), BAC-based genome sequence data from GenBank BrGDB154 and the collected Brassica expressed sequence tag were as a source genome.
We also observed a mild sensitivity of cds1Δ cells to nitrogen mustard in our colony counting assay (data not shown).
Risk analysis derived from carcinogenesis data indicates that sulfur mustard possesses a carcinogenic potency similar to that of benzo[a]pyrene.
The level of ASAL expression observed in the transgenic mustard plants was fairly comparable to the data of Dutta et al. [ 11].
The degradation data revealed that the benzoic acid nitrogen mustard peptide (AAAK) conjugate vesicles are more stable than the parent drug in aqueous solution.
