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However, changes in the release of SP in response to intradermal injection of capsaicin still remain unknown.
The dose-dependence of the three characteristics of RP and SP in response to two-second square pheromone pulses are shown in Fig. 5.
Geometric means of IFNγ production levels were significantly (p<0.0001) higher in HHCs than in the SP in response to CFP (495.9 versus 154.7 pg/mL), CFP-10 (146.3 versus 44.4 pg/mL), HspX (31.9 versus 12.7 pg/mL), and Ag85A (31.5 versus 11.9 pg/mL) (Figure 2A).
Statistically significant decreases in SP in response to 3-day treatment with AG825 were also observed in GCC-BC4 cultures.
CD45+ and CD31+ cells did not rise in the SP in response to gemcitabine (p = 0.21 and p = 0.66, respectively) when compared to control mice.
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Despite research efforts, little is known about the physiological functions of exogenous Spd in response to salt-alkali mixed stress.
Spermidine (Spd) has an important role in plant defense mechanisms against abiotic stress; however, relatively few data are available regarding Spd in responses of tomato to saline-alkaline stress.
This indicated that SP-PrP accumulation in response to proteasome inhibition was due not to an indirect effect of ER stress, but to a pool of short-lived PrP molecules in the cytosol.
The fact that the amount of SP-PrP increased in response to CAM741, which interferes with the correct insertion of the signal peptide into the translocon [36], [37], suggests that a post-targeting interaction between the signal and the Sec61 channel is primarily involved in PrP translocation, a conclusion also emerging from other studies [18], [42].
The variation in time of the transmembrane (RP) and transepithelial (SP) potentials were simulated in response to two-second square pheromone pulses of various heights.
To address whether dendritic Na+ spikes affect the timing of AP output, we measured population spikes in the CA1 and CA2 stratum pyramidale (SP) cell body layers in response to a burst of PP stimuli (5 pulses at 50 Hz).
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