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1 l structures that originated out of existing intersomitic blood vessels (ISVs).
2 he fused somites (fss/tbx24) mutant, lack of intersomitic boundaries and epithelial somites is accomp
3 en at both the notochord-somite boundary and intersomitic boundaries, consistent with a role for Fak
4 d at the basal region of epithelial cells at intersomitic boundaries.
5 mptive epitheloid border cells along nascent intersomitic boundaries.
6 Dll3 and Dll1 coordinate in establishing the intersomitic boundaries.
7 ities in somitogenesis, including defects in intersomitic boundary formation and failure in maintenan
8 mitic mesoderm is disrupted, suggesting that intersomitic boundary formation and rostral-caudal patte
9                                        Thus, intersomitic boundary formation in zebrafish involves sh
10  from either the posterior sclerotome or the intersomitic boundary is sufficient to enforce the separ
11 ce pathways leads to ectopic invasion of the intersomitic furrows and posterior sclerotome halves, di
12 ood vessel maturation led to pericardial and intersomitic hemorrhage.
13 resomitic mesoderm (PSM), and is enriched at intersomitic junctions and at myotendinous junctions in
14 irst directs one population of NCCs from the intersomitic path into the sclerotome, and SEMA3F/NRP2 s
15 of cranial and spinal nerves, and in somitic/intersomitic regions along the presumptive spinal cord.
16 expression of zebrafish NgBR is localized in intersomitic vessel (ISV) and axial dorsal aorta during
17 fish to recapitulate the endogenous temporal intersomitic vessel expression pattern of robo4.
18  zebrafish, ecscr interacts with kdrl during intersomitic vessel sprouting.
19 e present not only in the CV but also in the intersomitic vessels (ISVs).
20 rdinated symmetric and directed sprouting of intersomitic vessels and provide mechanistic insights in
21 al aorta and hypobranched, stunted, and thin intersomitic vessels due to impaired migration and proli
22          By following the development of the intersomitic vessels in real-time, we show that, while r
23 ective vascular tube formation and shortened intersomitic vessels in the posterior body region.
24 hat, while rostrocaudal gradient of maturing intersomitic vessels occurs, it is not absolute.
25 that Rap1b is essential for the sprouting of intersomitic vessels, a process known to be dependent on
26 xpressed in the head folds, head mesenchyme, intersomitic vessels, and migratory cranial neural crest
27 of vascular tube structures, angiogenesis of intersomitic vessels, and pronephros morphogenesis.
28 acs, defective angiogenesis in the brain and intersomitic vessels, and smaller chambers and reduced m
29 r plexus, the cardinal vein, and presumptive intersomitic vessels, as well as in vessels of the limb
30 ssels, which form by vasculogenesis, and the intersomitic vessels, which form by angiogenesis.
31 ndbrain capillaries and, to a lesser extent, intersomitic vessels.
32 -D1-expressing endothelial cells of adjacent intersomitic vessels.
33 18 mRNA with robo4 transcripts in developing intersomitic vessels.

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