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1 e produce embryos that are both bicaudal and ventralized.
2 rogenitors in Pax6 mutants are progressively ventralized, acquiring expression of regulatory genes no
3 gion and antagonized its transcriptional and ventralizing activities by interfering with its lysine m
4                  Comparative analysis of the ventralizing activities of different N- and C-terminal l
5  because it ensures that the dorsalizing and ventralizing activities of Dpp and Wg are restricted to
6                                          The ventralizing activities of Tsg require an endogenous Xol
7 a a suppression of swirl-dependent, BMP-like ventralizing activities.
8 genes vox (vega1) and vent (vega2) both have ventralizing activity in overexpression assays, loss-of-
9 this transformation results from the loss of ventralizing activity in the developing eye field, and t
10 embrane association and multimerization, and ventralizing activity in the zebrafish forebrain.
11 A and catalytic C subunits of PP2A each have ventralizing activity in Xenopus embryos.
12  Mix.1, a PAX class homeodomain protein with ventralizing activity in Xenopus.
13  specifies dorsal fate by counteracting this ventralizing activity.
14 laborate with Hh signaling and reinforce its ventralizing activity.
15  we used nickel chloride (NiCl(2)), a potent ventralizing agent on echinoderm embryos, on the indirec
16  Thus, whereas both Wnt8 and zygotic BMP are ventralizing agents that regulate common target genes, t
17 e mesoderm is established by dorsalizing and ventralizing agents, which are presumably mediated by th
18 istent with the properties of experimentally ventralized amphibian embryos, cerebum mutants exhibit r
19 with SCL and LMO-2 leads to embryos that are ventralized and have blood throughout the dorsal-ventral
20 easome subunits were found to differ between ventralized and lateralized embryos.
21 genesis of the pronephros was examined in UV-ventralized and lithium-dorsalized embryos.
22 g, as eggs from aubergine mutant mothers are ventralized and seldom fertilized.
23  members such as BMPs 2, 4, and 7, which are ventralizing and anti-neuralizing signals.
24 ermomyotome involves antagonistic actions of ventralizing and dorsalizing signals originating from ti
25 rates axis formation largely by limiting the ventralizing and posteriorizing activity of bone morphog
26 s of both Medea and Mad (a class I Smad) are ventralized, as are embryos null for the TGF-beta-like l
27  biological effects of BMP-3 oppose those of ventralizing BMPs, but the mechanism for this antagonism
28 ssed antagonists Chordin and Noggin with the ventralizing BMPs.
29 is regulated by the antagonizing function of ventralizing bone morphogenetic proteins (BMPs) and dors
30 ogenous Sonic Hedgehog signalling activation ventralizes both the somites and the neural tube in a do
31                                  AFE is then ventralized by applying Wnt, BMP, fibroblast growth fact
32 f Mix.1 can restore a dorsal axis in embryos ventralized by ectopic BMP-4 expression.
33 oxus embryos, like those of vertebrates, are ventralized by exogenous BMP protein.
34   Unexpectedly, Msx-deficient embryos become ventralized by late gastrulation whereas misexpression o
35 also become L or Ser dependent when they are ventralized by removal of pnr or Iro-C gene function.
36 unable to rescue dorsal cell fate in embryos ventralized by UV irradiation.
37  Xwnt8 in animal caps, (2) rescue of embryos ventralized by Xwnt8 DNA and (3) inhibition of XmyoD exp
38 n allele is still functional but has reduced ventralizing capability compared to the wild type.
39 ants revealed that the expression of NckK229 ventralized dorsal mesoderm.
40 hat bind the third SH3 domain antagonize the ventralizing effect of the first two SH3 domains.
41 st beta-catenin-1 (MO1), by contrast, had no ventralizing effect on wild-type embryos.
42  Bmp4 knockdown was sufficient to rescue the ventralizing effects caused by loss of Chordin activity.
43                      Taken together with the ventralizing effects of a mutant from of the XTcf-3 tran
44         1) which is a likely mediator of the ventralizing effects of BMP4 in the mesoderm.
45 nopus embryo animal caps mimics the mesoderm-ventralizing effects of BMP4.
46 en provided that Sonic Hedgehog mediates the ventralizing effects of notochord and floor plate, but t
47                                          The ventralizing effects of the xTsg mutants were stronger t
48  axis duplication and completely rescued the ventralizing effects of UV irradiation through the activ
49 xpression of Tsg mRNA in Xenopus embryos has ventralizing effects similar to Xolloid, a metalloprotea
50                In contrast, pAbp mutants lay ventralized eggs and enhance grk haploinsufficiency.
51 fect germline cyst development and result in ventralized eggs as a result of reduced Grk protein expr
52                         Each mutant produces ventralized eggs, a phenotype typically associated with
53 hin the oocyte, leading to the production of ventralized eggs.
54 tion of eIF1A in spnB ovaries suppresses the ventralized eggshell phenotype by restoring Grk expressi
55 les are moderately fertile, laying eggs with ventralized eggshells that can hatch normal larvae.
56  that reducing tsg gene product results in a ventralized embryo, and that tsg morphants specifically
57 f both genes does not result in a completely ventralized embryo.
58  by antisense deoxyoligonucleotides leads to ventralized embryonic defects and a reduction of the exp
59  using antisense oligonucleotides results in ventralized embryos and reduced organizer gene expressio
60 nsible for both the loss of pronephroi in UV-ventralized embryos and the induction of pronephroi duri
61 ric mesoderm, as marginal zone explants from ventralized embryos are still competent to respond to pr
62         Dorsal development can be rescued in ventralized embryos if Tcf-dependent transcription is ac
63 oss of the capacity to form pronephroi in UV-ventralized embryos is caused by the loss of tissues cap
64                                      Because ventralized embryos still gastrulate, producing a mechan
65            This axis also arises in severely ventralized embryos, despite their deficient embryonic p
66 ut activation of Tcf after MBT cannot rescue ventralized embryos, suggesting that beta-catenin/Tcf-de
67                                        In UV-ventralized embryos, xBic-C is polyadenylated less than
68 ganizer formation, and ultimately results in ventralized embryos.
69 E and drives symmetric blastopore closure in ventralized embryos.
70 re of early embryos to UV irradiation, which ventralizes embryos and inhibits neural induction, reduc
71                  Ectopic expression of BMP-4 ventralizes embryos and positively regulates the express
72            Ectopic expression of XSox17 beta ventralizes embryos by inhibiting the Wnt pathway downst
73 overexpressed in isolated animal caps and it ventralizes embryos.
74 es, our understanding of the role of Wnts in ventralizing embryos is less complete.
75 ) superfamily of growth factors, is a potent ventralizing factor and has been implicated in the commi
76 m in animal cap explants is repressed by the ventralizing factor BMP-4.
77           Previously, we have shown that the ventralizing factor bone morphogenetic protein 4 (BMP-4)
78  assays, Frzb antagonized Xwnt-8, a proposed ventralizing factor with an expression pattern complemen
79 in early Xenopus development by acting as a "ventralizing factor' and as an epidermal determinant: lo
80 which we have named vox and vent, are potent ventralizing factors in both zebrafish and Xenopus embry
81 ow, at low penetrance, early lethality and a ventralized gastrulation phenotype.
82 1 is inducible in uncommited ectoderm by the ventralizing growth factor BMP4 and counteracts the dors
83                         In animal caps, PV.1 ventralizes induction by activin and inhibits expression
84  organizer, where it functions to oppose the ventralizing influence of bone morphogenetic proteins (B
85 vous system, and Sonic hedgehog (Shh), which ventralizes it.
86 y protein kinase A and is antagonized by the ventralizing morphogen Sonic hedgehog.
87  such as Vent 1, and, consequently, develops ventralized morphology.
88 o these elements, suggesting the presence of ventralized musculature at the fin tip analogous to a fl
89 lyzed in double mutant combinations with the ventralized mutants chordino/chordin and ogon, whose mol
90 in expression by midgastrulation, while some ventralized mutants had reduced expression; however, in
91                                         Some ventralized mutants recover and develop into fertile adu
92                         Using dorsalized and ventralized mutants, we demonstrate that these domains a
93 rve an expansion of LE fate in dorsalized or ventralized mutants.
94                     One hundred eighteen new ventralizing mutants on the second chromosome fell into
95 es in karyosome morphology, similar to other ventralizing mutants such as okra and spindle B.
96 tized system where subthreshold amounts of a ventralizing Nck mutant were expressed, co-expression of
97 llele (Gli3(Delta699)) can mostly rescue the ventralized neural tube phenotypes of Sufu mutant embryo
98 s to midgestation lethality and a completely ventralized neural tube, demonstrating that PKA is as st
99 7 in future dorsal blastomeres resulted in a ventralized or posteriorized phenotype in which the embr
100                                              Ventralized otic progenitors subsequently give rise to e
101 adhesion is observed, embryos display both a ventralized phenotype and reduced dye transfer.
102 s partial axis duplication, which mimics the ventralized phenotype caused by reduced gurken-Egfr sign
103 ea activity in the early embryo results in a ventralized phenotype identical to that of null dpp muta
104                                          The ventralized phenotype is also dependent on the kinesin I
105 ing molecular markers indicates that the boz ventralized phenotype may be due, in part, to the derepr
106 Genetic epistasis experiments show that this ventralized phenotype occurs independently of Shh and th
107 Cactus-lacZ expressed in vivo normalizes the ventralized phenotype of embryos that lack Cactus and fa
108 i zygotic mutant embryos exhibit a partially ventralized phenotype similar to dpp embryonic lethal mu
109                                The resulting ventralized phenotype, the effective dose, and the NiCl(
110 wild-type Xom and results in a more strongly ventralized phenotype.
111 nergistically enhances the penetrance of the ventralized phenotype.
112 ific for this gene (MO2) results in the same ventralized phenotypes as seen in ichabod embryos, and a
113 eover, loss of tsg1 partially suppressed the ventralized phenotypes of mutants of the BMP antagonists
114 ession of eve1 in embryos results in similar ventralized phenotypes to that seen in embryos overexpre
115 m60), and short tail(b180) mutations produce ventralized phenotypes, including expanded bmp2b/4 expre
116 sulted in a range of concentration-dependent ventralized phenotypes, including those lacking a brain
117     The enhanced individuals die with weakly ventralized phenotypes.
118  naive neural plate cells are converted into ventralized progenitors and a late period that extends w
119 on during the late period determines whether ventralized progenitors differentiate into motor neurons
120 ring which SHH drives the differentiation of ventralized progenitors into motor neurons.
121 ain-containing gene that is activated by the ventralizing signal BMP-4.
122 rafish yolk syncytial layer (YSL) secretes a ventralizing signal during gastrulation.
123  neural tube can compete with the diffusible ventralizing signal from the notochord.
124 the floor plate of the neural tube provide a ventralizing signal(s) directing sclerotome development,
125 ion and is important for the function of the ventralizing signal, Shh.
126 lly, activated protease cascade produces the ventralizing signal, so a distinct downstream step in th
127 ls and participates in the activation of the ventralizing signal.
128 g of the Drosophila embryo is initiated by a ventralizing signal.
129 rmed the action of chordin (chd) in opposing ventralizing signals at gastrulation.
130 ovides genetic evidence for the existence of ventralizing signals in the zebrafish gastrula and for a
131 Noggin and SHH-N have been implicated as the ventralizing signals produced by the notochord.
132 The ventrally located notochord provides the ventralizing signals to specify the sclerotome, while th
133 ene may normally function as an inhibitor of ventralizing signals, a function previously ascribed to
134 e or reduced levels of the notochord-derived ventralizing signals, as well as to the presence of domi
135 eral tissue passively reads graded levels of ventralizing signals, or whether local self-organizing r
136 lished, the organizer releases inhibitors of ventralizing signals, such as BMPs, and promotes dorsoan
137 itional mechanisms must exist to block these ventralizing signals.
138                Overexpression of PV.1 yields ventralized tadpoles and rescues embryos partially dorsa
139 y vertebrate embryonic tissues by binding to ventralizing TGF-beta-like bone morphogenetic proteins a
140               Furthermore, nickel treatments ventralize the direct developing hemichordate, S. kowale
141 at both RA and FGF receptor (FGFR) signaling ventralize the eye, by expanding optic stalk and ventral
142 transcription factors are induced by Shh and ventralize the forebrain through a mechanism that is poo
143      We propose that Fgf signaling, known to ventralize the telencephalon in a Shh-independent manner
144  of Shh in the otic vesicle of ShhP1 embryos ventralized the adjacent hindbrain by inducing, rather t
145 terminal domain were unable to bind BMP, yet ventralized the embryo very effectively, indicating stro
146 , microinjection of RW(d) in Xenopus embryos ventralizes the dorsoventral embryonic patterning by upr
147 uctures that require organizer signaling and ventralizes the embryo.
148 of these is Vax2, a homeodomain protein that ventralizes the vertebrate eye field by repressing trans
149 ty of the eggs laid by asun(d93) females are ventralized to varying degrees, from mild to severe; thi
150                                              Ventralizing transcriptional repressors in the Vox/Vent
151 tered abundance levels or isoform changes in ventralized versus lateralized embryos.
152                      dino mutant embryos are ventralized, whereas swirl mutants are dorsalized.
153 oventral axis of the pituitary gland becomes ventralized, with dorsal extension of the transcriptiona
154             It also suggests that inhibiting ventralizing wnts parallels the opposition of BMPs by no
155 EH/eh-1 domain is necessary for rescue of UV-ventralized Xenopus embryos, it is dispensable for ectop
156 teins can rescue dorsoanterior structures in ventralized Xenopus embryos.

 
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