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More specifically, we examined the effect of honeybush extract and fermented honeybush on UVB-induced photoaging in the skin of hairless mice by evaluating various parameters of photoaging.
We also determined whether other hormone genes that are primarily expressed in the pituitary gland were altered in pre-symptomatic scrapie-infected mice by evaluating expression levels of Lhb, Tshb, and Fshb in scrapie-and mock-infected mice.
Hence the present investigation was designed to assess the anti-initiating potential of Sulforaphane (SFN) against benzo(a pyrene [B(a P] induced lung carcinogenesis in female Swiss Albino Mice by evaluating the activities of xenobiotic markers, and the balance between phase I and phase II carcinogen/drug metabolizing enzymes.
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Here, we determine the mechanism for 3' overhang synthesis in mouse cells by evaluating changes in telomeric overhangs throughout the cell cycle and at leading- and lagging-end telomeres.
We initially characterized this novel mouse line by evaluating VAChT expression expecting that the new location chosen for the insertion of the TK-Neo cassette would not alter VAChT gene expression.
Therefore, these findings add significantly to advances from previous CPS immunization mouse models by evaluating the generation of immune memory after immunization with P. chabaudi by mosquito bite.
Using a human 11β-HSD1 selectinhibitoritor as a starting point, we designed and synthesized a new class of derivatives of 1-arylsulfonyl piperidine-3-carboxamides. It was found that the large lipophilic group on the amino moiety may lead to cross-species potency towards human and mouse, allowing drug development by evaluating compounds in rodent model.
In this study, we hypothesized that a non-invasive method to quantify bone loss in the CIA mouse model could be accomplished by evaluating reconstructed high quality micro-CT images.
Oxidative stress induced by PFOA on mice was evaluated by malondialdehyde (MDA) formation and hydrogen peroxide generation, which were considered as reliable biomarkers of anthropogenic stresses on mice.
The effects of GHS-R1A treatment on intake in mice were evaluated by a two-way ANOVA followed by Bonferroni post hoc test.
The cytokines produced by spleen cells from the four groups of mice were evaluated by ELISA.
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