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1 ion in which the somite pulls apart from the segmental plate.
2                   Heterotopic transplants of segmental plate along the axis from quail to chick were
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
5                                              Segmental plate and somite cells are similar to primitiv
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
10 omite cultures and only partially reduced in segmental plate cultures.
11 ons of MyoD positive cells were found in the segmental plate, epiblast, mesoderm, and hypoblast.
12 unlike stage 10-11 embryos, both somites and segmental plate exhibited a strong response.
13 so discovered that 17% of stage 10-11 caudal segmental plate explants exhibited several MHC-positive
14                    98% of stage 10-11 caudal segmental plate explants treated with bFGF plus TGF-beta
15 named the lateral population of cells in the segmental plate, lateral presomitic cells.
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
18                                        While segmental plate mesoderm cells did not migrate into the
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
21 s sufficient to induce paraxis expression in segmental plate mesoderm.
22 LH genes as epithelial somites condense from segmental plate mesoderm.
23  wing-level somites or pre-somitic mesoderm (segmental plate), myotome development was evident but wa
24                     In order to test whether segmental plate or somitic mesoderm has the ability to m
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
27 m the first 6 somite pairs, as contrasted to segmental plates that form somites 7 and beyond.
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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