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Since we cloned MS4a4B from the thymus of C57BL/6 mice, data from our studies and others have shown that MS4a4B is highly expressed in T cells and is closely related to the regulation of CD4+ T cell-mediated immune responses [1], [19], [20], suggesting its importance in adaptive immunity.
(B ) The mean ratio between grid periodicity (λ i ) and the diameter of grid fields (l i ) in mice (data from Giocomo et al., 2011a ).
For example, in order to compare the response to Qs and BALB/c mice, data from all Qs groups (infected with either N. caninum type and the two different time points) were considered as "Qs".
Although not fully investigated in Tc1 mice, data from human studies and from other mouse models would suggest that rest/activity and rhythm disturbances may arise as a consequence of either generalized synaptic deficits or disturbances in particular brain circuitries.
To gain insights on the effect of aging on circulating miRNAs, we compared the circulating miRNAs exhibiting significant GbA in N and df/df mice (data from the present study) with changes in circulating miRNAs reported for the hybrid long‐lived B6C3F1 mouse (Dhahbi et al., 2013d).
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Comparative analysis with B6C3F1 mouse data from a similarly designed study identified 2790 differentially expressed rat orthologs in the duodenum compared to 5013 mouse orthologs at day 8, and only 1504 rat and 3484 mouse orthologs at day 91.
First, we obtained the whole genome pairwise alignment (human vs rhesus and human vs mouse) data from the UCSC Genome Browser [41].
Every fifth trial was a probe trial (on which no puff was delivered) however as these amounted to only 10 probe trials per mouse, data from these trials have not been used for any specific analysis.
Assigning each identified structure in the eHistology Atlas to an appropriate EMAPA ID, allows the eHistology Atlas interface to be a portal to relevant mouse data from distributed resources.
Figure 1 shows our dose response data (in mice) for six different types of ultrafine carbonaceous particles (10 50 nm) and the data of Oberdörster et al. (2005) for fine (~ 250 nm) and ultrafine (~ 20 nm) TiO2 particles; we present the data for rats, which was reanalyzed by Wittmaack, and also the mouse data from Oberdörster et al. (2005).
All mice data was taken from a previously produced body of work.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com