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The mouse model considered in this study is the Apolipoprotein AI (ApoAI) knock-out, where ApoAI is a gene known to play a pivotal roles in HDL metabolism [ 11, 12].
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Based on these observations, we decided to investigate the expression of Yeats2 in this mouse model considering only the liver tissue, and we found that Yeats2 expression is strongly downregulated in HFD mouse liver (P-value of ) (Kapushesky et al., 2010; Kleemann et al., 2010).
The mouse model is considered to have close similarities to mechanisms of acetaminophen toxicity in human hepatocytes and to the mechanisms that occur in human overdose patients [ 36].
Since the Apc gene mutation plays a significant role in the pathogenesis of familial adenomatous polyposis and sporadic intestinal cancers in patients, Apcmin/+ mouse model is considered as an ideal genetic animal model mimicking human intestinal tumorigenesis.
Affinities were captured by the rate constants, all available in Table 2. Two main categories of ataxias in humans and mouse models are considered in this study: those with reduced IP3R1 and those with supersensitive IP3R1 (Table 1).
Therefore, investigation of nutritional effects on early anatomical brain development using the mouse model must consider the first three weeks postnatally.
With these results, this mouse model could be considered as an adequate tool for selecting and optimizing effective vaccines against OEA.
For this reason, we suggest that any psoriasis mouse model should be considered jointly with the genetic background with which it is associated (e.g., the "K5-Tie2/CD1 model", the "B6/IMQ model", etc).. Along these lines, an important avenue for future investigation is to evaluate background-dependence of manipulations that give rise to psoriasis-like phenotypes in mouse.
Similar protection was observed in the mouse model that is considered as the 'gold standard' for sepsis research, namely CLP (Dejager et al, 2011).
The wild type mouse model is not considered to be a viremia model for dengue virus and we also did not detect virus by plaque forming assay using serum from wild type mice after i.p. infection by the Eden2 strain.
Taken together, the increased infectivity of sheep BSE in the porcine PrP mouse model must be considered as increased pathogenicity of the agent attributable to its passage in sheep.
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