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As control, mannitol which does not induce the Ca2+-mediated insulin response was injected at the same final concentration in order to maintain the same osmotic concentration (Figure 7I).
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Tested parameters for response were: injected activity, ILD (gray), HILD (gray), TD (gray), tumour to nontumour ratio, tumour activity (percent injected activity), alpha-fetoprotein level (kIU/l), and tumour size (cm).
To test the insulin response, insulin was injected into control and PRAS40 animals that were fasted for 6 h, and livers were collected after injection.
To evaluate effects on Myc's proliferative response BrdU was injected intraperitoneally into 4-week old Eμ- Myc; Nfkb2+/+ and Eμ- Myc; Nfkb2-/ littermates and after 12 hr B220+sIgM+ and B220+sIgM- cells were assessed for their S phase indices.
To investigate the contribution of conserved immune signaling pathways to antiviral innate immune responses, CrPV was injected into isogenic mutants of the Immune Deficiency (Imd) pathway, which resembles the mammalian Tumor Necrosis Factor Receptor (TNFR) pathway.
The objective of this study was to determined the role of voltage-sensitive calcium channels in angiotensin II-induced pressor response when it was injected into the third ventricle of conscious rats.
Therefore, lidocaine seemed to be effective immediately after the injection and maintained its effectiveness throughout the acquisition session, which lasted for about 25 min. There was no significant effect on the acquisition of the conditioned response when lidocaine was injected 1 h before commencement of the conditioning procedure.
To examine the modulation of CfDDC to the humoral immune response, DDC inhibitor methyldopa was injected to inhibit the CfDDC activity in vivo, and then the ROS level in haemocytes was detected in the present study.
However, when Pb-pulsed DC was injected, a Th2 response was observed in the draining lymph node (Figure 5).
However, no difference in response units was detected when FI-peptide was injected in either blank flow cells or flow cells coated with a non-specific P. falciparum recombinant protein (MSP-119).
In contrast, the magnitude of the response was strong when DivIVA-GFP was injected, and the signal remained when the flow of DivIVA-GFP ceased, indicating that the fusion protein strongly interacted with the phospholipid membranes (the initial sharp decrease was due to buffer effects).
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