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Astringency in vitro was defined as the mg of CT required to achieve half-maximal precipitation of 0.5 mg of protein (bovine serum albumin).
A cell that had the potential to expand unlimitedly in vitro was defined as clonogenic cell.
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Possible in vitro interaction was defined as known physical or chemical incompatibility (for example, different pH, oxidative potential).
The optimal biological GS of CSH as observed in the in vitro experiments was defined by comparing the optimal CSH theoretical prediction model with the most ideal parameters using a threshold of 18% for mouse probes [ 17] and 20% for human probes.
Susceptibility to cephalosporins was defined as in vitro susceptibility to cefotaxime or ceftazidime.
Resistance in new cases (primary) was defined as in vitro resistance in patients who did not have a history of anti-TB treatment, while retreatment resistance (secondary) was defined as in vitro resistance in patients previously treated with any anti-TB medication.
Appropriate empiric antibiotic therapy was defined as in vitro susceptibility to at least one antibiotic of the organism(s) recovered from the BAL or the protected telescoping catheter samples.
Recently, a new T suppressor population was defined, which could be generated in vitro from CD8+CD28- T cells [ 37].
Catheter bacterial colonization was defined as positive culture of explanted catheters in vitro.
An appropriate combination therapy was defined if two or more antibiotics showed in vitro susceptibility.
In our study, colistin monotherapy was defined as adequate if P. aeruginosa was susceptible to colistin in vitro.
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CEO of Professional Science Editing for Scientists @ prosciediting.com