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Clinical data demonstrates that gastrointestinal side effects follow a predictable pattern of being most prominent during treatment initiation and dose escalation periods, then declining substantially as the body adapts
Both cell lines were maintained under standard conditions in specific DMEM/F-12 media supplemented with serum
Exclusion criteria subjects with conditions that have so far been identified as modulators of RBC survival must be excluded from participation [89]
Shi ZZ, et al
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