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1 d that the expression of NckK229 ventralized dorsal mesoderm.
2 ecifically affected neurogenesis but not the dorsal mesoderm.
3 ting that oep acts downstream of inducers of dorsal mesoderm.
4  signaling pathway than the induction of the dorsal mesoderm.
5  gland can be induced by neural plate and by dorsal mesoderm.
6 eta-catenin-deficient marginal zones to form dorsal mesoderm.
7 s directed extension in cultured explants of dorsal mesoderm.
8 quired for formation of the neural plate and dorsal mesoderm.
9 ocious mediolateral intercalation of caudal, dorsal mesoderm.
10 and can account for extension throughout the dorsal mesoderm.
11 mal cap explant assays and in the endogenous dorsal mesoderm.
12  definitive amnioserosa, dorsal ectoderm and dorsal mesoderm.
13  to prevent ectopic enhancer activity in the dorsal mesoderm.
14  even-skipped (eve) to a small region of the dorsal mesoderm.
15 ensive AP brain patterning in the absence of dorsal mesoderm.
16 ultiple anteroposterior locations within the dorsal mesoderm.
17 n, as well as cell autonomous suppression of dorsal mesoderm.
18 nsduces activin/TGF-beta signals, generating dorsal mesoderm.
19 ndicating an early role for FGF signaling in dorsal mesoderm.
20 xtension movements normally undergone by the dorsal mesoderm.
21 , activated by activin-like ligands, induces dorsal mesoderm.
22 cally in the YSL induces expanded or ectopic dorsal mesoderm.
23 ative differences in their ability to induce dorsal mesoderm.
24 in response to inductive signals from normal dorsal mesoderm.
25 like, like loss of wnt8, causes expansion of dorsal mesoderm, (4) sp5-like knockdown reduces the defe
26  that boz and sqt act in parallel to specify dorsal mesoderm and anterior neuroectoderm.
27 g sites and is responsible for repression in dorsal mesoderm and ectoderm at mid-gastrula stages.
28 tions of activin above those known to induce dorsal mesoderm and heart, in an FGF-independent manner.
29 events, inhibits convergent extension in the dorsal mesoderm and in the posterior neural ectoderm.
30 elevated C-cadherin adhesion activity in the dorsal mesoderm and interferes with the normal blastopor
31  that is required for the development of the dorsal mesoderm and its derivatives in the Drosophila em
32 yos, BMP-11 acts more like activin, inducing dorsal mesoderm and neural tissue, and less like other f
33 bm can regulate convergent extension in both dorsal mesoderm and neural tissue.
34 embryonic explants consisting of presumptive dorsal mesoderm and neurectoderm (Keller explants), and
35  Xenopus, convergent extension occurs in the dorsal mesoderm and posterior neural ectoderm, and is me
36 at the GATA gene pannier is expressed in the dorsal mesoderm and required for cardial cell formation
37 bers of the TGFbeta Nodal subfamily, pattern dorsal mesoderm and the embryonic axes.
38 ive in the early mesoderm, the second in the dorsal mesoderm and the third in cardioblasts.
39  is a wave of Xombi expression, beginning in dorsal mesoderm and then extending to lateral and ventra
40 t uniquely, as specification tests show that dorsal mesoderm arises in fragments of the embryo which
41                      Arg is expressed in the dorsal mesoderm at the onset of gastrulation, and both g
42                               Suppression of dorsal mesoderm by Hex is accompanied by the down-regula
43 of Goosecoid and Chordin, while induction of dorsal mesoderm by Hex-(lambda)VP2 results in activation
44 (DSCR6), a RIPPLY family member that induces dorsal mesoderm by releasing repressive polycomb group p
45 sing fluorescent fusion proteins that during dorsal mesoderm C&E, the noncanonical Wnt component Pric
46                 We also demonstrate that the dorsal mesoderm can be induced independently of signals
47 gnals regulate the polarity of intercalating dorsal mesoderm cells during convergent extension.
48 qt function to induce high levels of ectopic dorsal mesoderm, consistent with sqt acting either downs
49 on of cells during gastrulation and disrupts dorsal mesoderm convergent extension, responsible for he
50  regulator of the Nodal pathway in zebrafish dorsal mesoderm development and establish a broadly cons
51 A transcription factor pannier acts early in dorsal mesoderm development to promote the development o
52  indicated that boz and sqt are required for dorsal mesoderm development.
53  the broad phase 2 expression pattern in the dorsal mesoderm does not restrict to the constrained pha
54   Cell division is also absent in involuting dorsal mesoderm during gastrulation in Xenopus, and to a
55             During Xenopus gastrulation, the dorsal mesoderm exhibits two different cell behaviors in
56 n of eng2, normally restricted to first arch dorsal mesoderm, expands ventrally in hand2 and edn1 mut
57 rm identity requires continual repression of dorsal mesoderm factors, including repressors of ventral
58 scriptional regulator Foxd3 is essential for dorsal mesoderm formation in zebrafish, and that this fu
59               Second, a gene associated with dorsal mesoderm formation, brachyury, is expressed norma
60 es with Tbx transcription factors to promote dorsal mesoderm formation, but their role in myogenesis
61 g growth factor-beta superfamily that induce dorsal mesoderm formation.
62 organizer and this function is essential for dorsal mesoderm formation.
63 ructures by suppressing signals that promote dorsal mesoderm formation.
64 we show GSK-3 is also required for zebrafish dorsal mesoderm formation.
65 hila tinman gene, which is essential for the dorsal mesoderm formation.
66                 Skeletal muscle derives from dorsal mesoderm formed during vertebrate gastrulation.
67                                Madr2 induces dorsal mesoderm from Xenopus ectoderm and can mimic the
68       As a consequence of the suppression of dorsal mesoderm gene expression, bone morphogenetic fact
69 usly described function in the regulation of dorsal mesoderm gene expression.
70 n: lower levels of Smad7 block activation of dorsal mesoderm genes and higher levels block all mesode
71 ain occur normally in wnt8; swr mutants, but dorsal mesoderm genes eventually come to be expressed th
72  in specification and differentiation of the dorsal mesoderm have been studied, the role of these gen
73 ich patterns the ectoderm such that it forms dorsal mesoderm in response to ventral inductive signals
74                                          The dorsal mesoderm in the frog Hymenochirus forms by a mech
75  endodermal development and the induction of dorsal mesoderm in vivo.
76 al and lung cancer, has been shown to induce dorsal mesoderm in Xenopus laevis in response to transfo
77 tical roles in the formation of endoderm and dorsal mesoderm in zebrafish.
78 s required for development of the Drosophila dorsal mesoderm, including heart.
79  protein processing controls production of a dorsal mesoderm inducer in these two species.
80 aps results in the conversion of Xnr2 from a dorsal mesoderm inducer to a ventral mesoderm inducer, s
81   In Xenopus the activins and Vg1 are potent dorsal mesoderm inducers while members of the bone morph
82 beta family members, such as Vg1, are potent dorsal mesoderm inducers, the TGF-beta pathway only weak
83 the dorsal yolk syncytial layer, a source of dorsal mesoderm inducing signals, and mutational analysi
84 tralising signals from ALK-2* antagonise the dorsal mesoderm-inducing signal derived from ALK-4*, sug
85 f the early VegT- and beta-catenin-regulated dorsal-mesoderm-inducing gene Xnr5.
86 nvergent extension movements associated with dorsal mesoderm induction and the expression of goosecoi
87                                              Dorsal mesoderm induction in arthropods and ventral meso
88                                              Dorsal mesoderm is itself subdivided into posterior and
89 ochord domain is specified in the vertebrate dorsal mesoderm, it undergoes dramatic morphogenesis.
90 xplants of deep neural plate with underlying dorsal mesoderm, lateral neural plate cells show a monop
91 nal for BMP2 and BMP4, whereas Xmad2 induces dorsal mesoderm like Vg1, activin, and nodal.
92                                  Loss of the dorsal mesoderm lineages is due to a high incidence of a
93 retarded by 8.5 d.p.c. and they fail to form dorsal mesoderm lineages, including chordamesoderm and p
94                 In Xenopus, Smad2 can induce dorsal mesoderm, mimicking Vg-1, activin and nodal.
95  and somatic muscle progenitors in the early dorsal mesoderm of Drosophila.
96 ulate the gonad after transplantation to the dorsal mesoderm of host embryos following germ-band exte
97 play spatial regulation and are found in the dorsal mesoderm of the organizer.
98 al determinant, ladybird, is absent from the dorsal mesoderm of Tribolium embryos.
99 ession when the ectoderm was recombined with dorsal mesoderm or treated with fibroblast growth factor
100 le that can directly induce ectoderm to form dorsal mesoderm, or a member of the Wnt family, which pa
101 NS) is induced by signals emanating from the dorsal mesoderm, or organizer, that divert the ectoderm
102 lation of organizer signaling might regulate dorsal mesoderm patterning and axial morphogenesis.
103 ntagonist Chordin and other signals from the dorsal mesoderm play important roles in this process.
104 a embryo, cardioblasts emerge from bilateral dorsal mesoderm primordia, followed by alignment as rows
105 d2 mRNA also synergized to induce ventral or dorsal mesoderm, respectively.
106                               The subsequent dorsal mesoderm-restricted mef2 expression is mediated t
107 neural plate explants lacking the underlying dorsal mesoderm show a bipolar, mediolaterally directed
108 on, followed by restricted expression in the dorsal mesoderm, specific expression in muscle progenito
109 U 2 suppresses the expression of a number of dorsal mesoderm-specific genes, including gsc, Xlim-1, X
110      This frizzled -mediated wnt pathway for dorsal mesoderm specification provides the first evidenc
111 Drosophila tinman, which is required for the dorsal mesoderm specification.
112 t only pyr mutants exhibit severe defects in dorsal mesoderm specification.
113 led function is necessary and sufficient for dorsal mesoderm specification.
114 re induced within the segmental areas of the dorsal mesoderm that receive intersecting Dpp and Wg inp
115 ent of most cell types deriving from the non-dorsal mesoderm - the fat body, somatic cells of the gon
116 rom Xenopus embryos induced both ventral and dorsal mesoderm, thereby mimicking the effects of TGF-be
117 formation in the whole embryo and transforms dorsal mesoderm to a ventral fate.
118 erminant(s) functions as a direct inducer of dorsal mesoderm (Vg1-like) or whether it acts to pattern
119 en the development and cell behaviors of the dorsal mesoderm, we have examined these behaviors in dis
120 the homeobox gene tinman is expressed in the dorsal mesoderm where it functions in the specification
121 ate in spt mutants almost exclusive from the dorsal mesoderm whereas, pronephros and tail originate f
122 entifies one specific subset of cells in the dorsal mesoderm, which give rise to particular pericardi
123                     Signals from a region of dorsal mesoderm, which is termed the organizer, pattern

 
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