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1 gastrulation is expressed in the lateral and ventral mesoderm.
2 lude the progenitors of the endoderm and the ventral mesoderm.
3 muscle founder identity gene, slouch, in the ventral mesoderm.
4  buds caused by a defect in the formation of ventral mesoderm.
5 ed self-organizing properties of the extreme ventral mesoderm.
6 ion is required for proper patterning of the ventral mesoderm.
7 essor, which is selectively expressed in the ventral mesoderm.
8 , supporting a role for Xnr2 in induction of ventral mesoderm.
9 Wnt signaling, also induced cardiogenesis in ventral mesoderm.
10  restriction of the ventral blood islands to ventral mesoderm.
11 oietic and vascular progenitors develop from ventral mesoderm.
12     The hematopoietic system is derived from ventral mesoderm.
13 hros and tail originate from both dorsal and ventral mesoderm.
14 tem cells is specified from undifferentiated ventral mesoderm.
15 the embryo causes ventralization and induces ventral mesoderm.
16 on domains and an increase in derivatives of ventral mesoderm.
17  (embryonic, fetal, or adult) originate from ventral mesoderm.
18 1) that is capable of mediating induction of ventral mesoderm.
19 regulation of Xbra itself in dorsal, but not ventral, mesoderm.
20 ral-to-caudal progression of both dorsal and ventral mesoderm across the pre-gastrula axis historical
21 enitors arise along the entire extent of the ventral mesoderm and contribute solely to haematopoietic
22 t embryos concur that cell rearrangements in ventral mesoderm and ectoderm contribute to the autonomo
23 Xenopus embryos and directs the formation of ventral mesoderm and epidermis.
24    Loss of Ezh2 resulted in dorsalization of ventral mesoderm and formation of a secondary axis.
25 and trunk endothelium all originate from the ventral mesoderm and often share lineage with one anothe
26  is a critical component in the formation of ventral mesoderm and possibly mediates the effects of BM
27 morphogenetic protein (BMP) subclass pattern ventral mesoderm and regulate ectodermal cell fates.
28 stic effect, greatly inhibiting formation of ventral mesoderm and ventral fin tissue.
29 grg2 and Xgrg4, are expressed in lateral and ventral mesoderm, and inhibit expression of XmyoD.
30 tes in a BMP-4 signalling pathway to pattern ventral mesoderm, and suggest a model whereby dimerizati
31 ood and vascular precursors from the extreme ventral mesoderm, and we show that this domain is normal
32                               Xmad1 produces ventral mesoderm, apparently transducing a signal for BM
33 pable of inducing either dorsal or posterior ventral mesoderm at different times in development.
34  and endodermal markers and the induction of ventral mesoderm by smad1.
35 rostralmost contributions to both dorsal and ventral mesoderm concomitantly from marginal zone progen
36  the ability of Derriere to induce dorsal or ventral mesoderm depends strictly on the location of exp
37  Bmp signaling changes over time to regulate ventral mesoderm development.
38  can act during gastrulation both to promote ventral mesoderm differentiation and to attenuate dorsal
39 y during development by comparing dorsal and ventral mesoderm dissected from early gastrula embryos.
40      The activation of tbx6 transcription in ventral mesoderm does not depend on no tail gene activit
41 eted embryos are deficient in dorsal but not ventral mesoderm due to the reduced expression of the wn
42                  sim is not activated in the ventral mesoderm, due to inhibition by the localized zin
43 l organizer formation and for patterning the ventral mesoderm during early gastrulation.
44    Hematopoietic stem cells are derived from ventral mesoderm during vertebrate development.
45      We demonstrate that SCL is expressed in ventral mesoderm early in embryogenesis.
46  secondary body axis or dorsalization of the ventral mesoderm explant analyzed by histological and mo
47            Ezh2 promotes Stat3 activation in ventral mesoderm formation independently of epigenetic r
48 vity increase before gastrulation and induce ventral mesoderm formation.
49  growth factor signaling during endoderm and ventral mesoderm formation.
50                             The formation of ventral mesoderm has been traditionally viewed as a resu
51 er-S blocks the induction of both dorsal and ventral mesoderm in animal-vegetal Nieuwkoop-type recomb
52               Hematopoietic cells arise from ventral mesoderm in different vertebrates, but the mecha
53 and -4/7 heterodimers are potent inducers of ventral mesoderm in ectodermal explants, we show that th
54 ctor hes6, is also restricted to lateral and ventral mesoderm in gastrula stage Xenopus embryos, lead
55 lays an early role in specifying presumptive ventral mesoderm in the leading edge mesoderm, and that
56 netic protein signals, inducing formation of ventral mesoderm in Xenopus embryos, whereas Smad2 trans
57 e important for the early development of the ventral mesoderm, including blood, vasculature and kidne
58 n is 20% higher in the Organizer than in the ventral mesoderm, indicating an elevation in mitochondri
59 gative form of XBMPRII (tBRII) can dorsalize ventral mesoderm, induce extensive secondary body axes,
60  of Xnr2 from a dorsal mesoderm inducer to a ventral mesoderm inducer, supporting a role for Xnr2 in
61  Dorsal mesoderm induction in arthropods and ventral mesoderm induction in vertebrates are closely re
62 od system in vertebrates is characterized by ventral mesoderm induction, hematopoietic stem cell spec
63 o respond to BMP signaling in the context of ventral mesoderm induction.
64 roles in embryogenesis, including dorsal and ventral mesoderm induction.
65  proteins (BMPs), which induce epidermis and ventral mesoderm instead.
66 enetic factor-4 (Bmp-4), a potent inducer of ventral mesoderm, is activated in the Organizer.
67 coding the BMP antagonist noggin in the tail ventral mesoderm, leading us to speculate that one of th
68 ne morphogenetic protein 4 (BMP4) can induce ventral mesoderm led to the suggestion that the inductio
69  In all three species, somitic, lateral, and ventral mesoderm move into the deep layer during gastrul
70 ctive epidermis to differentiate in vitro as ventral mesoderm, no loss-of-function studies have demon
71 la embryo and subsequently restricted to the ventral mesoderm of the gastrula embryo under the signal
72 nalling pathway in the posterior lateral and ventral mesoderm of the zebrafish embryo at the gastrula
73  mutants exhibit pronounced defects in dorso-ventral mesoderm patterning and in the antero-posterior
74 amine the temporal roles of Bmp signaling in ventral mesoderm patterning.
75                                      Lateral/ventral mesoderm progenitors represent a distinct commit
76  to the suggestion that the induction of the ventral mesoderm requires a different signaling pathway
77  that XOs4 can induce mesoderm and dorsalize ventral mesoderm resulting in ectopic dorsal axis format
78  Smad8 can block BMP-4-mediated induction of ventral mesoderm-specific gene expression in ectodermal
79  observations link the expression of tbx6 to ventral mesoderm specification.
80  superficial presumptive somitic and lateral-ventral mesoderm that initially separates the sub-blasto
81 l mesoderm and then extending to lateral and ventral mesoderm, that precedes and parallels blastopore
82 , low concentrations of XSmad7 dorsalize the ventral mesoderm, thus inducing a secondary axis.
83 etic development, either in specification of ventral mesoderm to a blood cell fate, or in formation o
84 phogenetic protein (Bmp) signaling to enable ventral mesoderm to commit to a blood fate.
85 g pathways might interact in the decision of ventral mesoderm to form blood.
86 eural tissue from ectoderm and can dorsalize ventral mesoderm to form muscle.
87 -stimulated erythroid differentiation in the ventral mesoderm was substantially inhibited by coinject
88 on screen for factors that pattern or induce ventral mesoderm, we isolated a complementary DNA encodi
89                         XMad protein induces ventral mesoderm when overexpressed in isolated animal c
90 orphogenetic protein (BMP) signaling, induce ventral mesoderm whereas Smad2, activated by activin-lik
91 s (BMPs) are required for the development of ventral mesoderm, which contributes to the ventral blood
92 al during gastrulation for the generation of ventral mesoderm, which makes it a challenge to define f
93 on of low levels of Bix1 causes formation of ventral mesoderm, while high levels induce endodermal di