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First, we characterised the effects of cryopreservation on the recovery of cryopreserved CD14++CD16− monocytes.
We have further characterised the effects of these two mutations in combination with the Z mutation in a eukaryotic cell model of disease.
We have designed, synthesised and characterised the effects of a number of novel anthraquinone derivatives and assessed their effects on large conductance, Ca2+ activated K+ (BK) channels recorded from rabbit bladder smooth muscle cells using the excised, inside/out configuration of the patch clamp technique.
We also characterised the effects of temsirolimus on CD8 memory cell formation.
Nadia Rosenthal's group systematically characterised the effects of Cre activity on cardiac morphology, physiology and function (page 1470 ).
We have characterised the effects of genetic background and gender on a range of quantifiable behaviours and time to humane endpoint in the SOD1 G93Adl mouse.
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We have characterised the effect of PMCG concentration and time of exposure on microcapsule diameter and membrane thickness, selecting a PMCG concentration of 0.5% (v/v) and an exposure time of 1 min as optimal parameters for a correct coating.
We characterised the effect of inhibiting MIF expression on B16-F10 cell viability and proliferation.
Previous studies also characterised the effect of ethylene on gene expression during climacteric ripening [ 6- 9].
The majority of in vitro studies on p7 inhibitors have characterised the effect of compounds on virus assembly and the infectivity of secreted particles.
Given our previous data showing that DMXAA alone altered the tumour microenvironment, we characterised the effect of DMXAA alone and in combination with Ad.E7 on the tumour microenvironment.
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