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The results from field outbreak tests and cell culture analysis along with measurements of specific antibodies against AIV demonstrate that the mortality associated with AI infection can be reduced by using a receptor blocker against AIV.
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The goal of this study is to establish a firm relationship between rat aortic EC [Ca2+]i elevation and vascular contractility by using a receptor-mediated agonist (acetylcholine, ACh) and a receptor-independent agonist (ionomycin).
Receptor selectivity was, in both these models, tested by using a GLP1 receptor antagonist (exendin 9-39 amide) and a VIP receptor antagonist (hybrid neurotensin 6-11 and VIP 7-28; hybVIP).
Our data set the basis for a novel strategy towards a prompt and more efficient therapeutic intervention with better outcome, i.e. identifying patients at risk of developing albuminuria and in whom enhancement of RAS blockade, probably by using a mineralocorticoid receptor antagonist, may be indicated.
Our study evaluated whether a greater PBM could be achieved either in the progesterone nuclear receptor knockout mice (PRKO) or by using a nuclear progesterone receptor (nPR) antagonist, RU486 in mice.
VaxInnate is testing a universal flu vaccine that would work against all strains of the disease by using a Toll-like receptor (TLR) technology platform.
In addition, animal studies demonstrated beneficial effects of ET-1 antagonism by using a selective ET receptor antagonist during septic shock [ 6- 9].
Activin neutralization by using a soluble ActRIIB receptor fused to the Fc portion of human IgG1 [ 12, 17] reduced bronchoalveolar lavage fluid (BALF) cellular responses to injury in two different mouse models but failed to show any significant antifibrotic effects.
In addition to IPC, we also evaluated the effects of BPC by using a β2 adrenergic receptor agonist, formoterol, which has been shown to be very effective in eliciting cardioprotection [[ 42]].
In support of this, Smith et al. [ 40] demonstrate that the effects of levodopa on glycogen storage could be reversed by using a beta 2 adrenergic receptor antagonist.
In support of this possibility, the H2d-H2a repeat, when taken out of its normal context, is able to promote formation of dimers, as shown by using a truncated nuclear hormone receptor lacking its own dimerization domain [ 17]).
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