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injection in mice, which provided 6d in a high protective index (TD50/ED50) of 37.4 comparable to the reference drugs.
Atherosclerosis research using mice began with the invention of traditional atherosclerotic mice including low-density lipoprotein receptor knockout (LDLR−/−) and apolipoprotein E knockout (apoE−/−) mice, which provided tremendous progress in atherosclerosis research.
The most active compound 8f has shown the MES-induced seizures with ED50 value of 28.05 mg/kg and TD50 value of 561 mg/kg after intraperitoneal injection to mice, which provided compound 8f with a protective index (TD50/ED50) of 20 in the MES test.
OA progression was significantly enhanced in the Tfap2e−/− mice, which provided evidence for in vivo relevance.
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It is suggested that the favorably altered stools as shown in the microbiome might promote the inflammation and proteinuria in ADR-sensitive mice, which provides a new insight on the pathogenicity of chronic kidney disease.
Similarly, B16 melanoma, previously reported to engage a vascular component in response to single dose radiotherapy[6], is radiosensitized by DC101 (Figure S11), but when implanted in bak−/− mice, which provides radioresistant vasculature [8], similarly exhibited resistance to DC101-induced radiosensitization.
Similar results were observed in HDM-exposed PARP-1−/− mice, which provide evidence for the specificity of such protective effects.
This notion is supported by the results obtained from gonadectomized mice, which provide an experimental model of high FSH levels observed in aging populations (Hsueh & Erickson, 1979).
Recently, Bostick and colleagues [ 22] reported that utrophin up-regulation alone (without dystrophin expression) leads to DCM in mice, which provides strong evidence in support of our hypothesis.
In apolipoprotein-E deficient mice, which provide a valid research model for atherosclerosis, inactivation of the gene encoding TNFα significantly reduces the size of atheroma plaques [ 8, 9].
The muscle content of PrxV was found to be increased in Sod1 −/− mice compared with WT mice which provides further support for a substantial increase in peroxynitrite generation in this model.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com