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1 e might modulate (but not, itself, activate) mesoderm induction.
2 are candidate morphogens involved in Xenopus mesoderm induction.
3 P/UTP-specific P2Y2 receptor blocked EMT and mesoderm induction.
4 as overcome by increasing BMP4 levels during mesoderm induction.
5 d to BMP signaling in the context of ventral mesoderm induction.
6 sis, with only Smad4beta being essential for mesoderm induction.
7 n while antagonizing Dpp/Tin during visceral mesoderm induction.
8 n of lineage-specific gene expression during mesoderm induction.
9  for specification of embryonic polarity and mesoderm induction.
10 unctions as a long-range Nodal signal during mesoderm induction.
11 astula and that this activity contributes to mesoderm induction.
12  Brg1 is required for enhancer activation in mesoderm induction.
13 nd, unlike other FGFs, FGF-8 interferes with mesoderm induction.
14 t distal enhancers that are activated during mesoderm induction.
15 ally to endoderm formation in the absence of mesoderm induction.
16 essential for primitive streak formation and mesoderm induction.
17 omodimers in a number of contexts, including mesoderm induction.
18  3, demonstrating multiple roles for BMPs in mesoderm induction.
19  signaling pathway, nor did p120(ctn) affect mesoderm induction.
20 that both AP-1 heterodimers are required for mesoderm induction.
21  because Smad7 can also block BMP-4-mediated mesoderm induction.
22  embryogenesis, including dorsal and ventral mesoderm induction.
23 r egg cylinder elongation, gastrulation, and mesoderm induction.
24 as on basic fibroblast growth factor-induced mesoderm induction.
25 t proliferation, egg cylinder formation, and mesoderm induction.
26 Src-related kinase is involved in vertebrate mesoderm induction.
27                      These data suggest that mesoderm induction activates the position-specific recog
28 yonic stem (ES) cells with Wnt-3A stimulates mesoderm induction, activates a feedback loop that subse
29 cate that the transcriptional repression and mesoderm induction activities of FoxD3 are dependent on
30                       FGFs act in vertebrate mesoderm induction and also play key roles in early meso
31            In Xenopus, SHP-2 is required for mesoderm induction and completion of gastrulation.
32 l marginal zone explants, but did not affect mesoderm induction and differentiation.
33  These complexes are long-range messages for mesoderm induction and establishment of the embryonic bo
34 s embryonic development, and is required for mesoderm induction and for the expression of several key
35 tivin, GDF1, and Vg1 have been implicated in mesoderm induction and left-right patterning.
36 he classical three-signal model of amphibian mesoderm induction and more recent modifications togethe
37 ssociate the roles of FGF and WNT factors in mesoderm induction and neural patterning.
38                                              Mesoderm induction and patterning are primarily regulate
39           The existence of morphogens during mesoderm induction and patterning in vertebrates has bee
40 n of Smad1 and Smad2 in pathways that signal mesoderm induction and patterning in Xenopus embryos, as
41 are unaffected by Xsprouty2, indicating that mesoderm induction and patterning occurs normally in the
42 eam transcription step have crucial roles in mesoderm induction and patterning.
43 concentrations however, XSmad7 inhibits both mesoderm induction and primary axis specification.
44 r, XActRIIB (previously called XAR1), blocks mesoderm induction and promotes neuralization in Xenopus
45 GF pathway in early Xenopus embryos inhibits mesoderm induction and results in truncation of the ante
46                                              Mesoderm induction and specification of the axial domain
47 , but not activin, receptor signaling during mesoderm induction and the AP-1/Jun is a key signaling m
48                       For teleosts, however, mesoderm induction and the establishment of dorsoventral
49 t extension movements associated with dorsal mesoderm induction and the expression of goosecoid, a do
50 its neural crest induction in the absence of mesoderm induction and without a requirement for BMP ant
51 stablishing the dorsal body axis; regulating mesoderm induction; and subsequent ventrolateral pattern
52 r to what extent the molecular mechanisms of mesoderm induction are conserved between gastrula and po
53 imal transcriptional activity in response to mesoderm induction are scattered across a 290-bp region.
54 ion and activation of these receptors during mesoderm induction are without obvious effect, whereas d
55  the Activin signal-transduction pathway for mesoderm induction as dominant-negative components of th
56 odimers in embryos null for twist can rescue mesoderm induction as well as somatic muscle development
57 lator of the XSmad2 pathway to ensure proper mesoderm induction at the appropriate time and in the ap
58                                              Mesoderm induction begins during gastrulation.
59      Ectopic expression of Xema RNA inhibits mesoderm induction, both by growth factors and in the ma
60                    Both mutants have altered mesoderm induction, but only homozygous or heterozygous
61 NA encoding various activated FGFRs inhibits mesoderm induction by a receptor activated by a transmem
62 ts noggin and gremlin both efficiently block mesoderm induction by BMP homo- and heterodimers in anim
63                  Furthermore, Xnr3 can block mesoderm induction by BMP-4 and activin, but not by Xnr2
64  induce extensive secondary body axes, block mesoderm induction by BMP4 and directly neuralize ectode
65                       Additional analysis of mesoderm induction by Derriere and members of the Nodal
66 strate that FAST-1 is a central regulator of mesoderm induction by ectopic TGFbeta superfamily ligand
67                                              Mesoderm induction by eFGF is uninhibited in dril1 morph
68                                  In Xenopus, mesoderm induction by endoderm at the blastula stage is
69 of a dominant-inhibitory Laloo mutant blocks mesoderm induction by FGF and causes severe posterior tr
70 s, and inhibitors of Nodal signaling blocked mesoderm induction by FoxD3.
71 he extracellular domain but does not inhibit mesoderm induction by receptors bearing a tyrosine kinas
72 ction analysis revealed that XPIASy inhibits mesoderm induction by specific and direct downregulation
73  essential role in controlling the amount of mesoderm induction by the vegetal cells.
74  growth factors may be endogenous factors in mesoderm induction, by studying their ability to rescue
75 ranscripts are significantly elevated during mesoderm induction caused by activin and FGF, but not du
76                               cmXnr2 blocked mesoderm induction caused by Xnr, but not activin, RNA.
77 om several vertebrate species indicates that mesoderm induction continues after gastrulation in neuro
78  tail in janus-mutant embryos indicates that mesoderm induction depends on a marginal position.
79 )-beta family members play a central role in mesoderm induction during early embryogenesis in Xenopus
80 stigated the role of DeltaNp63 in regulating mesoderm induction during early Xenopus laevis developme
81 rowth factor (FGF) signaling is required for mesoderm induction during gastrulation through positive
82 d derriere as modulators of ALK4 function in mesoderm induction during primary axis formation.
83 ype mesoderms that arise as a consequence of mesoderm induction during vertebrate development.
84                  Human/rat MAP3K1/Map3k1 and mesoderm induction early response (MIER; MIER3)/MIER3 ar
85 ession has no effect on the initial steps of mesoderm induction, either dorsal or ventral, but instea
86 terized by initial uniform expression during mesoderm induction, followed by modulated expression at
87 d Tcf3 genes are non-redundantly required in mesoderm induction for mediating primarily transcription
88                        It is unclear whether mesoderm induction generates a multipotent PS progenitor
89 neural induction in Xenopus embryos in which mesoderm induction has been blocked by Cerberus-short, a
90 cycle signal transduction pathway in Xenopus mesoderm induction has been revealed by observations of
91  show that activin, the function of which in mesoderm induction has hitherto been unclear, also plays
92 m in vertebrates is characterized by ventral mesoderm induction, hematopoietic stem cell specificatio
93                                       Dorsal mesoderm induction in arthropods and ventral mesoderm in
94 an rescue both the loss of cell adhesion and mesoderm induction in ectodermal explants expressing XLe
95 or) blocks this response and hyperdorsalizes mesoderm induction in intact embryos or augments growth
96 ed at the right time and location to mediate mesoderm induction in response to VegT during Xenopus em
97   Embryological experiments demonstrate that mesoderm induction in the archenteron requires contact w
98 mesoderm induction in arthropods and ventral mesoderm induction in vertebrates are closely related pr
99 more potent than each homodimers in bone and mesoderm induction in vitro, suggesting that BMP4 and BM
100 uired for the activity of the latter and for mesoderm induction in vivo.
101                             We conclude that mesoderm induction in Xenopus depends on a maternal tran
102        The data support a modified model for mesoderm induction in Xenopus, in which mesoderm inducti
103 the Src kinase-Csk regulatory circuit during mesoderm induction, in vivo.
104 yosin-driven contraction-which persists when mesoderm induction is blocked.
105 Here we report that the function of FoxD3 in mesoderm induction is dependent on the recruitment of tr
106  for mesoderm induction in Xenopus, in which mesoderm induction is mediated by a gradient of multiple
107 s formed mesoderm derivatives revealing that mesoderm induction is SMAD2 independent.
108 es whose homolog in Xenopus is implicated in mesoderm induction, is expressed in the PMZ of prestreak
109 NA encoding Vg1, a growth factor involved in mesoderm induction, is localized to the vegetal cortex o
110 orming growth factor-beta family involved in mesoderm induction, is translated subsequent to the loca
111  FGF function do not support a role in early mesoderm induction, making the ancestral roles of FGF si
112 om expressing a retinal fate, independent of mesoderm induction or anterior-posterior patterning.
113  promoter of the Mix.2 gene is responsive to mesoderm induction signals when linked to a CAT reporter
114   Therefore, EphB4 modulates the response to mesoderm induction signals.
115 ited the well characterized model of Xenopus mesoderm induction to determine the intracellular intera
116    These results suggest that BMP-4 requires mesoderm induction to generate a program of gene express
117    Thus, different FGFs show specificity for mesoderm induction versus neurogenesis and this may be m
118                           The FGF-stimulated mesoderm induction was markedly inhibited in animal cap
119 ngation of epiblast-like cells and delays in mesoderm induction were also observed in the Klf6-/- EBs
120 agonist cerberus, which completely abolishes mesoderm induction when misexpressed during early develo
121 (XFD) after the mid-blastula stage uncouples mesoderm induction, which is normal, from maintenance of
122           We suggest that Ndr1 has a role in mesoderm induction, while Ndr2 is involved in subsequent
123 e-eyed pinhead mutant, which is defective in mesoderm induction, with the wild-type embryo shows that
124                                       During mesoderm induction, XPIASy is expressed in the animal ha

 
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