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With a focus on different combinations of these markers, we distinguished four distinct, non-overlapping classes: tumors positive for ER and/or PgR expression and negative for HER2 expression were designated as HR+/HER2- (57 cases, 49.1%).
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Since there is currently no microglia-specific marker available, we distinguished microglia from macrophages by their morphological phenotype.
With this combination of markers we can distinguish across the larval cuticle, Hml+Lz− from Hml+Lz+ sessile hemocytes.
Although we did not find any resemblances between expression patterns of Hoxd8, Hoxd9 and any of the fiber type-specific markers we could distinguish the gastrocnemius, quadriceps and soleus from each other.
With these markers, we can roughly distinguish mTECs and cTECs in immunofluorescence and flow cytometry assays.
Based on specific markers, we were able to distinguish the populations of progenitors of the four optic neuropils and map the neurons and their connections.
Using CD1 or MHC-II as DC markers, we were not able to distinguish CD172aneg from CD172pos DC (Figure 4A), however CadM1 expression (Figure 4H), a signature of CD172aneg DC, was observed in the dermis.
Without using specific markers, we were not able to distinguish objectively between venules and arterioles, but we did occasionally observe vessels with a thin smooth muscle layer (possibly veins or venules) that only expressed Kir6.1 faintly (if at all).
The sole marker we had to distinguish us was a sign that Isaac posted on the tree behind us every day: "What Crimes Against the Country have you committed today?" The first students who came to Isaac were cousins.
We used classification and regression tree methods ([Breiman et al. 1984]) to determine which markers best distinguished sub-population 5A from 5B.
T cell populations have been classified by several surface markers and distinguished by their functions and residency, along with their effector cytokine production.
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