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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
7 ion, nuclei of endodermal cells, primary and secondary mesenchyme cells (PMCs and SMCs), and small mi
9 study: genes expressed in the subset of the secondary mesenchyme cells (SMC) that will become pigmen
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
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
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
23 st prior to invagination, and signals to the secondary mesenchyme-derived tissues at least until the
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
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