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1 revents both the smad2-mediated induction of dorsal mesodermal and endodermal markers and the inducti
2 n, Noggin and Follistatin, are implicated in dorsal mesodermal and neural development.
3  and function of the homeobox gene tinman in dorsal mesodermal cells during early embryogenesis.
4                        In addition, although dorsal mesodermal cells from lithium- or Wnt-exposed emb
5 calization of Xdsh at the membrane of normal dorsal mesodermal cells is consistent with Xdsh controll
6 gion--has a central role in the induction of dorsal mesodermal cells to form the Spemann organizer.
7 prospective neural ectodermal cells, or upon dorsal mesodermal cells, to cause a loss of anterior pat
8 ion in the Xenopus gastrula is essential for dorsal mesodermal development and for Nodal expression i
9 e trunk mesoderm, then refinement to a broad dorsal mesodermal domain, and finally restricted express
10 lar machine separate from MIB that can drive dorsal mesodermal extension exists in the zebrafish gast
11 maternally encoded zebrafish wnt8 protein in dorsal mesodermal fate determination.
12 rises mutations that lead to deficiencies in dorsal mesodermal fates and affect central nervous syste
13 ne, tinman, is a key patterning mediator for dorsal mesodermal fates like the heart.
14 tions and global changes in the shape of the dorsal mesodermal field.
15 AST-En(R) in intact embryos prevents general/dorsal mesodermal gene expression and axial development.
16   Foxd3 gain-of-function results in expanded dorsal mesodermal gene expression, including the Nodal-r
17  directly induce the same set of general and dorsal mesodermal genes, as well as some endodermal gene
18                                Expression of dorsal mesodermal genes, including chordin, goosecoid an
19  the organizer formation and leads to severe dorsal mesodermal patterning defects.
20                                  Hh controls dorsal mesodermal Ras signaling by transcriptional regul
21 hese transcription factors strongly enlarges dorsal mesodermal territories.
22 nscription factor Tinman (Tin) to induce all dorsal mesodermal tissue derivatives, which include dors
23 e complex (Tin-C) controls the patterning of dorsal mesodermal tissues, including the dorsal vessel o

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