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1               These are the skeletogenic and secondary mesenchyme and gut.
2 ransiently in the embryonic skeletogenic and secondary mesenchyme and, later in development, is perma
3 , expressed in archenteron, skeletogenic and secondary mesenchyme, and the Endo16 gene, expressed in
4 t of cells of the archenteron giving rise to secondary mesenchyme at the archenteron tip followed by
5           Later the gene is expressed in the secondary mesenchyme, but expression is no longer detect
6 to homogeneous clones consisting of a single secondary mesenchyme cell (SMC) type.
7 ion, nuclei of endodermal cells, primary and secondary mesenchyme cells (PMCs and SMCs), and small mi
8 consist of two cell populations, primary and secondary mesenchyme cells (PMCs and SMCs).
9  study: genes expressed in the subset of the secondary mesenchyme cells (SMC) that will become pigmen
10                                       Later, secondary mesenchyme cells (SMCs) also enter the blastoc
11 o regulate the differential specification of secondary mesenchyme cells (SMCs) and endoderm in the se
12 s play an important role in the induction of secondary mesenchyme cells (SMCs), possibly by activatin
13  the failure of macromere progeny to specify secondary mesenchyme cells (SMCs).
14 s known to be necessary for specification of secondary mesenchyme cells (SMCs).
15 h functions sequentially in the vegetal-most secondary mesenchyme cells and later in the endoderm.
16 ssively displaced towards the animal pole by secondary mesenchyme cells and the elongating archentero
17 acterizes the ingression of both primary and secondary mesenchyme cells coincides with a rapid and dr
18                                         When secondary mesenchyme cells convert to a skeletogenic fat
19 tulates CyIIa expression in both primary and secondary mesenchyme cells suggests the existence of a p
20 iciencies in the organization of primary and secondary mesenchyme cells within the blastocoelic cavit
21 ogram of expression in both skeletogenic and secondary mesenchyme cells, contains the consensus-bindi
22 n, but particularly strongly in delaminating secondary mesenchyme cells.
23 st prior to invagination, and signals to the secondary mesenchyme-derived tissues at least until the
24 ere lineages diverts adjacent mesendoderm to secondary mesenchyme fates.
25 yogenesis in the embryonic vegetal plate and secondary mesenchyme founder cells, and expression is th
26 y and exclusively in part of the prospective secondary mesenchyme (mesodermal) domain at late-cleavag
27  central veg(2) mesodermal domain (i.e., the secondary mesenchyme progenitor field) from the peripher
28                                          New secondary mesenchyme specific genes, expressed exclusive
29 -mesodermal territory and embryos blocked in secondary mesenchyme specification.

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