Exact(6)
Maybe the study will suggest that a little tinkering is needed, or maybe that the sheriff's office be abolished; either way, Mr. Rampe said, the time has come to take a good hard look.
It seems that hepatic upregulation of LDLr by thyromimetics occurs when SR-BI-mediated uptake of plasma cholesterol is reduced and/or abolished, either through plasma CETP activity or due to the lack of SR-BI.
As for controls, the metabolic flux differences between retro- and antegrade perfusion must be abolished either when excess substrate is added or when one of these competing pathways is inhibited.
The effect has now been shown positively to depend upon irradiation of the caecum, and can be abolished either by shielding the caecum from irradiation or by surgically removing it prior to irradiation.
The residual signal was then abolished either by blockade of α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate (AMPA)/kainate glutamatergic receptors (10 μM NBQX), or by blockade of voltage-gated Ca2+ channels (100 μM Ni2+/100 μM Cd2+).
Under these conditions, His10-AtoC binding to the biotin-labelled atoD probe was abolished either by the addition of excess amounts of unlabelled cognate (atoD) competitor or by unlabelled DNA competitors containing the novel, atypical binding sites, i.e. metR-metE, acrD, narG.
Similar(54)
We then tested whether AMPK activation targets the EBox, the GATA sequence, or both sequences to transcriptionally activate the PGC-1α promoter by generating mutations within the EBox/GATA oligonucleotides to abolish either Ebox or GATA binding separately (Fig. 4A).
They don't think much about God or Queen, would probably agree that both entail more than their fair share of absurdity, but they're quite pleased they are there and don't want to abolish either.
These effects were significantly abolished by either chemical sympathectomy or beta-adrenergic receptor antagonist propranolol.
The morphogenetic effect of chitosan was abolished by either ligand or receptor deprivation, or inhibition of downstream signaling transduction.
At intermediate concentration range, Bevacizumab showed only partial competition with EBV321 as compared to hEBV321 (Figure 3A), however EBV321 binding to VEGF was abolished by either competitor at the highest concentration tested (1000 fold excess).
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