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Thus, intermediate neural progenitors increase the overall output of cells derived from every division of a type II neuroblast.
By contrast, every asymmetric division of a type II neuroblast invariably leads to the generation of an immature INP that acquires an INP functional identity during maturation.
Pros segregates exclusively into GMCs where it suppresses a type I neuroblast functional identity during asymmetric division of a type I neuroblast, but is undetectable in mitotic type II neuroblasts (Knoblich et al., 1995; Spana and Doe, 1995; Choksi et al., 2006; Bayraktar et al., 2010).
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Liu (2002)'s proposal of internally vs. externally caused emotions may provide a principled account to integrate the distinction between inchoative vs. homogeneous state in Tsai et al. 蔡美智等 (1999) and the division of type A vs. type B verbs in Chang et al. (2000).
An asymmetrical division of type A undifferentiated spermatogonia was suggested previously in zebrafish based on morphological evidence [2].
This group showed that division of type A pericytes is required for scar formation following spinal cord injury.
This group also used a Glast-CreER/RASless mouse line to inhibit cell division of the type A pericytes in the spinal cord injury model [ 127].
Let us "watch" the colony grow by tracking each of N-1 cell divisions, see Figure 7. Whenever a cell division happens, it may be a division of a cycling wild-type cell, or a division of a cycling 1-hit mutant cell.
All differentiated cell types in the central complex arise from repeated rounds of self-renewing asymmetric divisions of type I and type II neuroblasts, which are molecularly and functionally distinct (Bello et al., 2008; Boone and Doe, 2008; Bowman et al., 2008).
The prolonged division of the type II lineage might allow more time for target expression to accumulate, compared with the more rapid progression of the type I lineage.
The type I cohesin modules are separated into two groups, which may suggest the division of the type I group into subtypes.
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