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To evaluate angiogenesis, the rat aorta ring assay was performed for both fresh and cryopreserved AM within 7 days.
The in vitro activities of these compounds were evaluated by a resting tension of isolated rat thoracic aorta ring assay.
The relaxant activity of 2- o, p-substituted phenyl)-1H-benzimidazole derivatives with various 5- and 6-position substituents (–H, –CH3, –NO2- oCF3), namely 1–7, was recorded using the in vitro rat aorta ring test.
In the present study, the effects of blocking PI3k activation on endothelioma cells derived from mice with vascular tumors were investigated using the crystal violet assay, real-time cell analysis, light microscopy, the aorta ring assay and antibody arrays.
The mean length of these ten branches was taken as the microvessel length of the aorta ring culture.
Sprouts originating from the aorta ring are referred to as microvessels, and branches refer to sprouts originating from a microvessel or another branch.
Similar(42)
Their vasodilatory activities were determined experimentally in rat aorta rings that were pretreated with phenylephrine (PE).
Their vasorelaxant activities were evaluated experimentally against rat aorta rings pretreated with phenylephrine (PE).
The norepinephrine-induced vasoconstriction in intact aorta rings was completely abolished by the α1-adrenoceptor antagonist prazosin.
All N,N-dimethyl amide derivatives showed a relaxant activity higher on guinea pig trachea rings than on rat aorta rings.
Interventions: Change in force of contraction was measured in isolated myocardial strips or in isolated descending thoracic aorta rings during exposure to propofol or intralipid.
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