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To identify valid predictors of TNF-α antagonist response in RA, serum proteome profiles from responders (R) and non-responders (NR) to etanercept, a soluble recombinant TNF-α receptor/IgG Fc fusion protein receptor, were compared in a prospective cohort study.
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Having determined both the agonist and antagonist responses in the assay with wild type AR, we next wanted to examine the assay performance with an AR mutant relevant to prostate cancer.
However, in that study, the animals were not vasodilated at the time of antagonist administration and the antagonist responses were only considered at one time point (that is, 24 h) following the septic challenge.
Structural differences between ER-α and ER-β may explain agonist versus antagonist responses to the same ligand, although the full interaction between the AF-1 and AF-2 transactivation sites is not yet fully understood.
Data from the Tc1 mice, and their significant differences from those in the Ts65Dn mice that were used in pre-clinical evaluation of antioxidant, memantine and GABAA antagonist responses, indicate that a plausible cause of the failure of clinical trials is the quite different molecular basis of the phenotype in DS and consequent quite different drug responses.
It shows that PCB47 and PCB100 only act as GR antagonists, and this antagonistic response can only be envisaged when these compounds are co-exposed with 5 μM budesonide.
However, none of these studies could clearly identify valid predictors for TNF-alpha antagonist drug response.
Further characterization of this control structure, especially in terms of network properties, may elucidate a general mechanism underlying antagonist drug response and associated clinical outcome.
Data for tumor model Leiomyosarcoma (No. 2) (intraperitoneal) in CAF1 mice 856 (C) -0.04 -0.05 -0.04 Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA 232 -0.04 -0.05 -0.04 NCI In Vivo Anticancer Drug Screen.
The inhibitor of mast cell degranulation significantly reduced responses to compound 48/80 and histamine-1 receptor antagonist reduced responses to histamine in all 3 groups.
In psoriasis vulgaris trials, the emerging IL-17 antagonists yielded response rates that reflect virtual elimination of disease (45, 46).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com