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1 ll death in both the pharyngeal endoderm and splanchnic mesoderm.
2 nd a loss of Id2 expression in the heart and splanchnic mesoderm.
3 es, cardiac outflow tract, inflow tract, and splanchnic mesoderm.
4 ermal epithelium and mesenchyme derived from splanchnic mesoderm.
5 buds of foregut endoderm into the underlying splanchnic mesoderm.
6 subpopulation of primordial cells within the splanchnic mesoderm.
7 ion and formation of the somatic and cardiac splanchnic mesoderm.
8 elium and mesenchymal cells derived from the splanchnic mesoderm.
9 ria and OFT and are found also in the dorsal splanchnic mesoderm accompanied by the expression of the
10 elopment, GATA-4 is expressed in cardiogenic splanchnic mesoderm and associated endoderm, suggesting
11 ed on its early expression in precardiogenic splanchnic mesoderm and its ability to activate the expr
12 ely, involved in the development of visceral/splanchnic mesoderm and non-visceral mesoderm in coeloma
13 ion of Bmp4 in the caudal branchial arch and splanchnic mesoderm and OFT myocardium by using a condit
14 es of origin of vagal neural crest cells and splanchnic mesoderm, are likely to be important.
15 t highly expressed within the precardiogenic splanchnic mesoderm at the posterior lip of the anterior
16 ated from a midline secondary heart field of splanchnic mesoderm beneath the floor of the foregut.
17 in anterior and posterior second heart field splanchnic mesoderm between E8 and E10.
18 , Bapx1 is an early developmental marker for splanchnic mesoderm, consistent with a role in visceral
19 ents, showing that both cranial paraxial and splanchnic mesoderm contribute to branchiomeric muscle a
20   SRF transcripts appeared in the precardiac splanchnic mesoderm in stage HH 9 embryos and was detect
21 atic mesoderm and for differentiation of the splanchnic mesoderm into midgut musculature.
22 sphorylated-Erk and Pea3, identifies the AHF splanchnic mesoderm itself as a target for Fgf8 signalin
23 on these and other data, we propose that the splanchnic mesoderm layers in Drosophila and vertebrate
24  in the pharyngeal endoderm and/or overlying splanchnic mesoderm of the AHF at a stage prior to heart
25 d with these great arteries are derived from splanchnic mesoderm of the second heart field (SHF), an
26 e early splenic primordium, derived from the splanchnic mesoderm, of homozygous mutant embryos.
27 heart field, derived from branchial arch and splanchnic mesoderm, patterns the forming outflow tract
28 ed together, these findings suggest that the splanchnic mesoderm responds to endodermal Hedgehog sign
29              Misexpression of DN-Tcf4 in the splanchnic mesoderm resulted in the failure of the gizza
30 urs while extensive morphogenesis, including splanchnic mesoderm sliding over the endoderm, results i
31 ield (SHF) progenitors in the pharyngeal and splanchnic mesoderm (SpM), but how these progenitors are
32 tion specifically in SHF cells in the caudal splanchnic mesoderm (SpM), where Wnt5a and Dvl2 are co-e
33 ry heart field within the branchial arch and splanchnic mesoderm that contributes to the aortic sac a
34  express Islet and Tbx1/10, evocative of the splanchnic mesoderm that produces the lower jaw muscles
35 ial mesoderm, to regulate eye muscle, and in splanchnic mesoderm to regulate OFT development.
36 ce demonstrated that these embryos developed splanchnic mesoderm, which differentiated into primitive
37 ription factor is expressed in the visceral (splanchnic) mesoderm, which is involved in mesenchymal-e
38 s have MF20-expressing cardiomyocytes in the splanchnic mesoderm within the second heart field (SHF).

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