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In their sense, it seems difficult to identify each jump point at the branch cells.
Then, this delay makes the cumulative flow curves in the branch cells lift up (or down) by unit vehicle at time interval t.
Abnormal activation of the Bnl signaling pathway in hairy mutant tracheal cells is exemplified by increased number of dorsal branch cells expressing Bnl receptor, Breathless (Btl) and Pointed, a downstream target of the Bnl/Btl signaling pathway.
Here, we show that the tracheal defects in γCOP mutants can be genetically dissected into (i) defects due to a general requirement for γCOP in all tracheal cells (luminal protein secretion, tube expansion) and (ii) defects due to a specific requirement in distinct cell types (dorsal branch cells, fusion cells).
Increased biocompatibility is also associated with lower generation branch cells with anionic or neutral groups compared to similar branch cells of higher generations which have cationic surface groups.
Notch signaling is required by dorsal branch cells at the junction with the dorsal trunk.
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The vehicle occupancy heading for branch cell a from upstream adjacent diverge cell divided by all the vehicle occupancy in this upstream diverge cell at time interval t.
When an additional vehicle is added to cell i, we should compute Eq. (2) after each time interval to obtain the number of vehicles in the queue of cell i heading for each branch cell.
For instance, suppose a new vehicle is inserted at the congested upstream cell (a presentation of link segment) at time interval t, and the vehicle heading for another downstream branch cell (not the same as the direction of the additional vehicle) is delayed by unit time interval after the rounding calculation for transmission flow.
Our studies demonstrate a novel role for Hairy in restriction of the terminal cell fate by limiting the domain of bnl expression in surrounding muscle cells such that only a single dorsal branch cell becomes specified as a terminal cell.
During branch cell mitosis, Myo8A-GFP appears on the spindle and phragmoplast, and as the phragmoplast matures, Myo8A-GFP accumulates at the phragmoplast periphery.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com