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This contrasts with another BMS drug development program in which 120 mg/kg/day of a 2-branched 40 kDa polyethylene glycol-maleimide conjugated to L-cysteine (2br-40kD PEG-cys) did not induce an increase in micronuclei in male or female rats following one-month of subcutaneous dosing. 发自小木虫Android客户端 |
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