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1 ion in which the somite pulls apart from the segmental plate.
3 rin and the catenins appear early within the segmental plate and are expressed as small patch-like fo
4 the first phase, dorsomedial quadrants from segmental plate and early stage somites (II and IV) form
6 , we first analyzed the effects of Wnt-3a on segmental plate and somite explants (from Hamburger and
7 Paraxis expression is evident in the rostral segmental plate and the newly formed somites, although t
8 adhesion molecules in cultures of epiblast, segmental plate, and somite cells and by determining the
9 ial and lateral, can be distinguished in the segmental plate by position, morphology and gene express
13 so discovered that 17% of stage 10-11 caudal segmental plate explants exhibited several MHC-positive
16 ves of newly formed somites, and presomitic (segmental plate) mesenchyme -- to participate in the dif
17 illin 2 particles initially deposited in the segmental plate mesoderm are translocated along an unexp
19 ing single somites or somite-sized pieces of segmental plate mesoderm from 2-day (stage 10-14) chicke
20 i3 regulation: these signals repress Gli3 in segmental plate mesoderm prior to somite formation and t
23 wing-level somites or pre-somitic mesoderm (segmental plate), myotome development was evident but wa
25 ssed in a highly dynamic manner in the chick segmental plate prior to somite formation and that lunat
26 se from distinct populations of cells in the segmental plate that develop in different cellular envir
28 usters are spaced wide apart in the anterior segmental plates that form the first 6 somite pairs, as
29 tic fringe modulates Notch signalling in the segmental plate to regulate somitogenesis and rostral-ca
30 e the functional significance of N-cadherin, segmental plates were exposed to antibodies that perturb
31 tted to their fates until much later, in the segmental plate when slow precursors become independent
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