(a) Peripheral blood mononuclear cells (PBMCs) from three MDS subjects were monitored for cytokine production over 10 months of treatment with lenalidomide.
Mature fish were placed in broodstock tanks at three different sex ratios (Group A, 4♀:1♂; Group B, 1♀:1♂; and Group C, 1♀:4♂) and regularly monitored for egg production.
The residual seaweed VS was determined weekly and headspace gases were monitored for methane production.
Measurements of cell biomass using optical-density readings or dcw were not possible, because of the particulate matter present from the pretreated biomass, therefore cultures were monitored for ethanol production every 24 hours.
To establish the threshold of ethylene needed to induce autocatalytic ethylene production, fruit at stage 88 were treated for different periods of 50 ul.l-1 ethylene (12, 24, 36 hours) and continuously monitored for ethylene production over the subsequent seven days.
To screen mutants for their ability to undergo sexual development and sporogony, groups of 3 4 outbred Theiler's Original mice were infected with 5 × 10 mutant or wild-type parasites intraperitoneally and monitored for gametocyte production on Giemsa-stained thin blood films.
Twenty-four patients with RA and 15 patients with AS, fulfilling the ACR criteria [ 22] and the modified New York criteria [ 23], respectively, were monitored for autoantibody production over a 2-year period during which they were good responders, as defined by the modified disease activity scores [ 24], to a combination of methotrexate and infliximab.
Further to investigate cellular responses in the presence of IDR-1002, human OA FLS were stimulated with pro-inflammatory cytokines, and the TC supernatant was monitored for MMP-3 production after 24 hours and IL-1RA production after 48 hours.
The culture was monitored for 6 days for production of extracellular laccase with the induction of the promoter being maintained by daily addition of 1% (v/v) methanol.
