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3 nd gynoecium development, where we find that NUB acts redundantly with JAG to promote the growth of t
4 asciatus (milkweed bug), showed that nubbin (nub) affects antenna morphogenesis, labial patterning, t
6 lso show that despite shifting position, the Nub and Tsh domain boundaries, like compartment boundari
8 s of the wing and mammalian rhombomeres, the Nub and Tsh domains share some of the attributes of clas
10 due to regulation by Wingless signaling, the Nub and Tsh expression boundaries shift during developme
11 omains of two transcription factors, Nubbin (Nub) and Teashirt (Tsh), present in distal and proximal
13 e is nearly the same vesicle to vesicle, and nubs, at their sites of connection to the vesicle membra
14 ibia), and in this species we also show that nub expression in the legs is regulated by Notch signali
15 of-function experiments showing that ectopic NUB expression is sufficient to drive the proliferation
17 irst functional evidence defining a role for nub in leg segmentation and highlight the varying degree
22 In addition, we find that the distal factor Nub represses the ligand unpaired as well as Stat92E act
24 of these two segments and creates a chimeric nub-RNAi tibia-tarsus that retains a tibial identity in
27 2) "axial" filaments connect focal rings to nub tips, thereby organizing filament bundling and ensur
28 cromolecules attached by narrow projections, nubs, to the vesicle membrane at approximately 25 sites.
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