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1 e might modulate (but not, itself, activate) mesoderm induction.
2 are candidate morphogens involved in Xenopus mesoderm induction.
3 d to BMP signaling in the context of ventral mesoderm induction.
4 sis, with only Smad4beta being essential for mesoderm induction.
5 n while antagonizing Dpp/Tin during visceral mesoderm induction.
6 n of lineage-specific gene expression during mesoderm induction.
7 for specification of embryonic polarity and mesoderm induction.
8 unctions as a long-range Nodal signal during mesoderm induction.
9 astula and that this activity contributes to mesoderm induction.
10 Brg1 is required for enhancer activation in mesoderm induction.
11 nd, unlike other FGFs, FGF-8 interferes with mesoderm induction.
12 t distal enhancers that are activated during mesoderm induction.
13 ally to endoderm formation in the absence of mesoderm induction.
14 essential for primitive streak formation and mesoderm induction.
15 omodimers in a number of contexts, including mesoderm induction.
16 3, demonstrating multiple roles for BMPs in mesoderm induction.
17 signaling pathway, nor did p120(ctn) affect mesoderm induction.
18 that both AP-1 heterodimers are required for mesoderm induction.
19 because Smad7 can also block BMP-4-mediated mesoderm induction.
20 embryogenesis, including dorsal and ventral mesoderm induction.
21 r egg cylinder elongation, gastrulation, and mesoderm induction.
22 as on basic fibroblast growth factor-induced mesoderm induction.
23 t proliferation, egg cylinder formation, and mesoderm induction.
24 Src-related kinase is involved in vertebrate mesoderm induction.
26 yonic stem (ES) cells with Wnt-3A stimulates mesoderm induction, activates a feedback loop that subse
27 cate that the transcriptional repression and mesoderm induction activities of FoxD3 are dependent on
31 These complexes are long-range messages for mesoderm induction and establishment of the embryonic bo
32 s embryonic development, and is required for mesoderm induction and for the expression of several key
34 he classical three-signal model of amphibian mesoderm induction and more recent modifications togethe
38 n of Smad1 and Smad2 in pathways that signal mesoderm induction and patterning in Xenopus embryos, as
39 are unaffected by Xsprouty2, indicating that mesoderm induction and patterning occurs normally in the
42 r, XActRIIB (previously called XAR1), blocks mesoderm induction and promotes neuralization in Xenopus
43 GF pathway in early Xenopus embryos inhibits mesoderm induction and results in truncation of the ante
45 , but not activin, receptor signaling during mesoderm induction and the AP-1/Jun is a key signaling m
47 t extension movements associated with dorsal mesoderm induction and the expression of goosecoid, a do
48 its neural crest induction in the absence of mesoderm induction and without a requirement for BMP ant
49 stablishing the dorsal body axis; regulating mesoderm induction; and subsequent ventrolateral pattern
50 r to what extent the molecular mechanisms of mesoderm induction are conserved between gastrula and po
51 imal transcriptional activity in response to mesoderm induction are scattered across a 290-bp region.
52 ion and activation of these receptors during mesoderm induction are without obvious effect, whereas d
53 the Activin signal-transduction pathway for mesoderm induction as dominant-negative components of th
54 odimers in embryos null for twist can rescue mesoderm induction as well as somatic muscle development
55 lator of the XSmad2 pathway to ensure proper mesoderm induction at the appropriate time and in the ap
58 NA encoding various activated FGFRs inhibits mesoderm induction by a receptor activated by a transmem
59 ts noggin and gremlin both efficiently block mesoderm induction by BMP homo- and heterodimers in anim
61 induce extensive secondary body axes, block mesoderm induction by BMP4 and directly neuralize ectode
63 strate that FAST-1 is a central regulator of mesoderm induction by ectopic TGFbeta superfamily ligand
66 of a dominant-inhibitory Laloo mutant blocks mesoderm induction by FGF and causes severe posterior tr
68 he extracellular domain but does not inhibit mesoderm induction by receptors bearing a tyrosine kinas
69 ction analysis revealed that XPIASy inhibits mesoderm induction by specific and direct downregulation
71 growth factors may be endogenous factors in mesoderm induction, by studying their ability to rescue
72 ranscripts are significantly elevated during mesoderm induction caused by activin and FGF, but not du
74 om several vertebrate species indicates that mesoderm induction continues after gastrulation in neuro
76 )-beta family members play a central role in mesoderm induction during early embryogenesis in Xenopus
77 stigated the role of DeltaNp63 in regulating mesoderm induction during early Xenopus laevis developme
78 rowth factor (FGF) signaling is required for mesoderm induction during gastrulation through positive
82 ession has no effect on the initial steps of mesoderm induction, either dorsal or ventral, but instea
83 terized by initial uniform expression during mesoderm induction, followed by modulated expression at
84 d Tcf3 genes are non-redundantly required in mesoderm induction for mediating primarily transcription
86 neural induction in Xenopus embryos in which mesoderm induction has been blocked by Cerberus-short, a
87 cycle signal transduction pathway in Xenopus mesoderm induction has been revealed by observations of
88 show that activin, the function of which in mesoderm induction has hitherto been unclear, also plays
89 m in vertebrates is characterized by ventral mesoderm induction, hematopoietic stem cell specificatio
91 an rescue both the loss of cell adhesion and mesoderm induction in ectodermal explants expressing XLe
92 or) blocks this response and hyperdorsalizes mesoderm induction in intact embryos or augments growth
93 ed at the right time and location to mediate mesoderm induction in response to VegT during Xenopus em
94 Embryological experiments demonstrate that mesoderm induction in the archenteron requires contact w
95 mesoderm induction in arthropods and ventral mesoderm induction in vertebrates are closely related pr
96 more potent than each homodimers in bone and mesoderm induction in vitro, suggesting that BMP4 and BM
101 Here we report that the function of FoxD3 in mesoderm induction is dependent on the recruitment of tr
102 for mesoderm induction in Xenopus, in which mesoderm induction is mediated by a gradient of multiple
104 es whose homolog in Xenopus is implicated in mesoderm induction, is expressed in the PMZ of prestreak
105 NA encoding Vg1, a growth factor involved in mesoderm induction, is localized to the vegetal cortex o
106 orming growth factor-beta family involved in mesoderm induction, is translated subsequent to the loca
107 FGF function do not support a role in early mesoderm induction, making the ancestral roles of FGF si
108 om expressing a retinal fate, independent of mesoderm induction or anterior-posterior patterning.
109 promoter of the Mix.2 gene is responsive to mesoderm induction signals when linked to a CAT reporter
111 ited the well characterized model of Xenopus mesoderm induction to determine the intracellular intera
112 These results suggest that BMP-4 requires mesoderm induction to generate a program of gene express
113 Thus, different FGFs show specificity for mesoderm induction versus neurogenesis and this may be m
115 ngation of epiblast-like cells and delays in mesoderm induction were also observed in the Klf6-/- EBs
116 agonist cerberus, which completely abolishes mesoderm induction when misexpressed during early develo
117 (XFD) after the mid-blastula stage uncouples mesoderm induction, which is normal, from maintenance of
119 e-eyed pinhead mutant, which is defective in mesoderm induction, with the wild-type embryo shows that
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