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1 rease before gastrulation and induce ventral mesoderm formation.
2 embryo proper, Eomesodermin is essential for mesoderm formation.
3 ed to play an important part in endoderm and mesoderm formation.
4 endoderm morphology and severe disruption of mesoderm formation.
5 al VegT mRNA and have studied the effects on mesoderm formation.
6  GSK-3 is also required for zebrafish dorsal mesoderm formation.
7 blocking a direct route to embryonic cardiac mesoderm formation.
8 factor signaling during endoderm and ventral mesoderm formation.
9 pression of Xenopus Brachyury causes ectopic mesoderm formation.
10 , suggesting that ActRIB is not required for mesoderm formation.
11 nman gene, which is essential for the dorsal mesoderm formation.
12 of genes critical for the earliest events in mesoderm formation.
13 eveal a redundant function of oep and ntl in mesoderm formation.
14 ogenitors without affecting primitive streak mesoderm formation.
15 ing played an ancestral role in deuterostome mesoderm formation.
16 ay upstream of Nodal signaling and posterior mesoderm formation.
17 gene, which is required for posterior (tail) mesoderm formation.
18  the prominent role of XRCC1 in endoderm and mesoderm formation.
19 o tail (ntl), which is essential for correct mesoderm formation.
20 which act to mediate different mechanisms of mesoderm formation.
21 niche-establishing factor Brachyury to allow mesoderm formation.
22 eas ectopic expression of DeltaNp63 inhibits mesoderm formation.
23 re required in the YSL for endoderm and head mesoderm formation.
24 h factor-beta superfamily that induce dorsal mesoderm formation.
25  Wnt/beta-catenin signaling and required for mesoderm formation.
26 er and this function is essential for dorsal mesoderm formation.
27 1, Map4k4, and Bicc1 have essential roles in mesoderm formation.
28 1 and Foxc2 negatively regulate intermediate mesoderm formation.
29  hitherto been unclear, also plays a role in mesoderm formation.
30 f twist, a transcription factor required for mesoderm formation.
31 l (ntl) are together essential for posterior mesoderm formation.
32 posterior structure development and inhibits mesoderm formation.
33 activity of the Src and Laloo kinases during mesoderm formation.
34 s a gene crucial for proper gastrulation and mesoderm formation.
35 lls to investigate the role of cell cycle in mesoderm formation.
36 sses in the mouse embryo, beyond its role in mesoderm formation.
37  brain fates, without blocking ventrolateral mesoderm formation.
38 s by suppressing signals that promote dorsal mesoderm formation.
39 scriptional effector of Nodal signals during mesoderm formation [17], but no mutations in the Fast-1
40  the one in which BMP4 was reported to drive mesoderm formation, also differentiate at least partiall
41    Thus, Smad7 acts as a potent inhibitor of mesoderm formation and also activates the default neural
42 ssues at the time of gastrulation for normal mesoderm formation and also suggest that subsequent Alk2
43  gene, T or Brachyury, which is required for mesoderm formation and axial elongation during embryogen
44 that Brat plays a critical role in embryonic mesoderm formation and body patterning.
45 was used to evaluate TGF-beta involvement in mesoderm formation and cardiopoietic differentiation, wh
46 tch FGFR signal interpretation to coordinate mesoderm formation and cell movements during gastrulatio
47  amnion as a signaling center during primate mesoderm formation and demonstrates the potential of in
48 ed anterior neural markers in the absence of mesoderm formation and DN-IGFR inhibited neural inductio
49 on of FN-enriched ECM which is essential for mesoderm formation and efficient cardiac differentiation
50 igate whether their function is required for mesoderm formation and gastrulation as implicated in Xen
51          To assess the function of ActRIB in mesoderm formation and gastrulation, chimera analysis wa
52 rms that derriere plays an important role in mesoderm formation and it illustrates the complex regula
53 errant DS development during early stages of mesoderm formation and its possible connection to lower
54 that Snail2 and Twist1 are required for both mesoderm formation and neural crest induction.
55 teps in embryogenesis, such as gastrulation, mesoderm formation and neurulation.
56 ting at a gastrulation-like stage, mediating mesoderm formation and patterning (two prerequisites for
57 eta- and Bmp-regulated processes involved in mesoderm formation and patterning are surprisingly unaff
58 ming growth factor-beta signals required for mesoderm formation and patterning in zebrafish.
59 ling, Rspo2 acts as an FGF antagonist during mesoderm formation and patterning.
60                     This treatment inhibited mesoderm formation and severely disrupted normal develop
61 oorly understood after the initial phases of mesoderm formation and spreading.
62                                              Mesoderm formation and subsequent anterior-posterior (A-
63 shRNA knockdown of FN prevented Brachyury(+) mesoderm formation and subsequent hPSC-CM generation.
64  body differentiation enhances both paraxial mesoderm formation and the myogenic potential of the cel
65 -mutant embryos to analyze the mechanisms of mesoderm formation and ventral specification in a teleos
66 , altered epiblast patterning, impairment of mesoderm formation, and embryonic lethality at embryonic
67            Simultaneously blocking, Chordin, mesoderm formation, and FGF signaling eliminates neural
68 al pathway in which pannier promotes cardiac mesoderm formation, and pointed acts subsequently in thi
69 ubstantially different during trunk and tail mesoderm formation, and propose a genetic model that acc
70 ression of bagpipe (bap), and hence visceral mesoderm formation, and the promotion of somatic muscle
71 al to the early vertebrate embryo, including mesoderm formation, anterior patterning, and left-right
72 that the mechanisms responsible for paraxial mesoderm formation are largely conserved across vertebra
73  Src is enzymatically capable of stimulating mesoderm formation, as an activated Src construct both p
74 eal an essential early role for scleraxis in mesoderm formation, as well as a later role in formation
75 nr1, Xnr2, Xnr4 and derriere mRNA all rescue mesoderm formation, as well as the formation of blastopo
76 XActRIIB, a truncated mutant (tXALK4) blocks mesoderm formation both in vitro and in vivo; moreover,
77        Second, a gene associated with dorsal mesoderm formation, brachyury, is expressed normally in
78          TGFbeta member Vg1 is implicated in mesoderm formation but the role of the zebrafish ortholo
79  to promote ventral cell invagination during mesoderm formation, but how the downstream genes regulat
80  the C2/C3 lineage of 32-cell embryos blocks mesoderm formation, but neural crest is lost only in the
81  Tbx transcription factors to promote dorsal mesoderm formation, but their role in myogenesis has bee
82 ngs reveal that cell cycle regulators direct mesoderm formation by controlling the activity of key de
83 nstrated the inhibition of Ras/AP-1-mediated mesoderm formation by dominant-negative mutants of the F
84 sted whether endogenous Brat is required for mesoderm formation by expressing a dominant-negative, tr
85 SNIP1 plays a role in regulating dorsomedial mesoderm formation by the TGF-beta family member nodal.
86 inant VegT is required for both endoderm and mesoderm formation by the Xenopus embryo.
87             This unique property of Snail in mesoderm formation can be attributed mostly to the CtBP
88                           In Xenopus, normal mesoderm formation depends on signaling through the fibr
89 mozygous mutant NSD1 embryos, which initiate mesoderm formation, display a high incidence of apoptosi
90 el, mutant ISL1 embryos display a failure in mesoderm formation due to reduced BMP4 signaling from th
91  and the importance of NF-kappa B pathway in mesoderm formation during early embryogenesis.
92 ty negatively affects growth factor-mediated mesoderm formation during early mouse development.
93       This is due to the paucity of paraxial mesoderm formation during embryoid body (EB) in vitro di
94 hat they play an essential role in posterior mesoderm formation during gastrulation.
95  on the dynamics of neural tube and paraxial mesoderm formation during mammalian development.
96 nsferases are required for cell survival and mesoderm formation during mammalian development.
97 rst transcriptome-wide in vivo view of early mesoderm formation during mammalian gastrulation.
98 t cell (M) is responsible for all nongonadal mesoderm formation during postembryonic development.
99 vents in vertebrate embryogenesis, including mesoderm formation, establishment of left-right asymmetr
100                            During vertebrate mesoderm formation, fates are established according to p
101 been demonstrated that snail is critical for mesoderm formation, for CNS development, and for wing ce
102 patterning of cardiovascular spheroids after mesoderm formation from hPSCs.
103 medio-lateral axis, its role in intermediate mesoderm formation has not been well characterized.
104  morpholino oligonucleotides interferes with mesoderm formation in a concentration-dependent manner a
105 astoma protein), are necessary for efficient mesoderm formation in a context-dependent manner.
106 ) produced posteriorized embryos and induced mesoderm formation in animal cap explants, indicating th
107 m induction and also play key roles in early mesoderm formation in ascidians and amphioxus.
108  essential roles in regulating ventrolateral mesoderm formation in conjunction with wnt8, and in patt
109 n, is required for heart as well as visceral mesoderm formation in Drosophila, and at least one of se
110 odomain gene needed for visceral and cardiac mesoderm formation in Drosophila.
111 kappaB-Twist-Snail network controls axis and mesoderm formation in Drosophila.
112 h necessary and sufficient to direct cardiac mesoderm formation in frog embryos and human embryonic s
113 erm-mesoderm interaction promoted precardiac mesoderm formation in mouse embryonic stem cells and inv
114 anscription factor Foxh1 as regulating FLK1+ mesoderm formation in mouse embryonic stem cells, which
115      This model contrasts with the models of mesoderm formation in other vertebrates as it suggests t
116                                              Mesoderm formation in the amphibian embryo occurs throug
117              Here, we reinvestigate paraxial mesoderm formation in the chicken embryo and demonstrate
118 (SRF) is a transcription factor required for mesoderm formation in the developing mouse embryo that i
119                                              Mesoderm formation in the Drosophila embryo depends on t
120 es the genomic targets of a key regulator of mesoderm formation in the early mouse embryo, thereby pr
121 ve streak, resulting in severe disruption of mesoderm formation in the embryo proper.
122 tor tyrosine kinases play a critical role in mesoderm formation in the frog, Xenopus laevis, acting a
123                                              Mesoderm formation in the frog, Xenopus laevis, is depen
124 bryonic stem cells, is required for paraxial mesoderm formation in the mouse.
125  that QSulf1 inhibits FGF2- and FGF4-induced mesoderm formation in the Xenopus embryo and FGF-depende
126 target genes function to limit the extent of mesoderm formation in the Xenopus gastrula, and point to
127 t produce mesoderm-inducing signals and that mesoderm formation in these embryos occurred ectopically
128 ted transcription, has been shown to promote mesoderm formation in vitro.
129    Using this system, we were able to induce mesoderm formation in Xenopus animal-cap tissue and to d
130 ctivates a receptor tyrosine kinase, induces mesoderm formation in Xenopus embryos through activation
131 onal regulator Foxd3 is essential for dorsal mesoderm formation in zebrafish, and that this function
132 locus, display severe defects in midline and mesoderm formation including absence of most of the somi
133    Ezh2 promotes Stat3 activation in ventral mesoderm formation independently of epigenetic regulatio
134 gnalling pathways that regulate endoderm and mesoderm formation interact is crucial to understanding
135              Although the initiating step of mesoderm formation is well characterized, the subsequent
136 chyury is considered to have a major role in mesoderm formation, it is possible that Wnts might play
137 es have also been proposed to participate in mesoderm formation, neural crest cell migration, carcino
138 mpetition may be responsible for the lack of mesoderm formation observed in such injected embryos.
139 ve for Nodal signaling, Foxd3 did not rescue mesoderm formation or axial development, indicating that
140 nces revealed that Slugh is not required for mesoderm formation or for neural crest generation, migra
141 cleus to finally trigger gene expression for mesoderm formation remains unknown.
142 Tbx6, each of which is critical for paraxial mesoderm formation, since absence of any one of these fa
143 hese observations and with a role for ntl in mesoderm formation, some somites form within the tail re
144 l gene is required for non-notochordal trunk mesoderm formation; spadetail mutant embryos have major
145  by repressing two inhibitors of cardiogenic mesoderm formation-Tcf3 and Foxa2-and activating inducer
146 rsal argue against a proposed role for sc in mesoderm formation that had seemed potentially relevant
147 ed in the mesoderm maintenance machinery and mesoderm formation through the synergistic action of the
148 mutant combinations that disrupt Chordin and mesoderm formation to reveal additional signals that con
149 rder to better characterize the evolution of mesoderm formation, we have examined the role of FGF sig
150 rriere cleavage mutant completely blocks all mesoderm formation when ectopically expressed.
151 tion in the early Xenopus embryo potentiates mesoderm formation whereas ectopic expression of DeltaNp
152 ells skewed toward the Flk-1(+)PDGFRalpha(-) mesoderm formation, which generated hematopoietic and en
153 g activity specifically during lateral plate mesoderm formation while reducing fibroblast growth fact
154 myogenesis selectively, acting subsequent to mesoderm formation yet before induction of Mesp1 and Mes

 
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