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1 2 to ichabod embryos increases the extent of ventralization.
2 midneurogenesis, the entire dTel VZ exhibits ventralization.
3  injection into wild-type embryos does cause ventralization.
4 tial role in Nck-induced anterior truncation/ventralization.
5 s including anterior truncation and mesoderm ventralization.
6 lear accumulation of beta-catenin and caused ventralization.
7 rmorphamine (PMR) was added later to promote ventralization.
8 ceptor levels in Gpr161(mut1/mut1) prevented ventralization.
9 lbous cilia associated with mild neural tube ventralization.
10 06H mutant, resulting in increased embryonic ventralization.
11                                              Ventralization, a major patterning process in the develo
12  Misexpression of Smad5 in the embryo causes ventralization and induces ventral mesoderm.
13 msx1 in early Xenopus embryos leads to their ventralization as described for BMP4.
14 either dorsal or ventral, but instead causes ventralization during gastrulation.
15                                              Ventralization in Ankmy2 knockout is completely independ
16                                              Ventralization in Ankmy2 knockout requires both cilia an
17 ivity, as loss of dlx3b and dlx4b suppresses ventralization in Msx-depleted embryos.
18  inhibits axis duplication and leads to mild ventralization in Xenopus embryo development.
19                      Here, we show that this ventralization is dependent on the other members of the
20                                         This ventralization is followed by a marked decrease in termi
21 tivity in the developing eye field, and that ventralization is mediated, at least in part, via Vax re
22  transcription factor may be involved in the ventralization of all three germ layers.
23    Thus, PV.1 plays an important role in the ventralization of both mesoderm and ectoderm.
24 e-dependent effects of wg on dpp expression, ventralization of dorsal cells and transdetermination su
25                                              Ventralization of embryos by UV irradiation and dorsaliz
26        Defects include a specific failure in ventralization of the anterior neural plate, loss of hea
27  multiple developmental processes, including ventralization of the CNS, branching morphogenesis of th
28                                 This partial ventralization of the dorsal telencephalon does not appe
29                                         This ventralization of the dTel VZ is paralleled by the expre
30 k, ectopic expression of either Vax leads to ventralization of the early retina, as assayed by expres
31 issencephaly1 (DLis1) gene result in partial ventralization of the eggshell.
32 tion at both poles of the stage 8 oocyte and ventralization of the eggshell.
33 esults in apparently increased activity with ventralization of the embryo, an effect not observed wit
34 utations in the Schnurri homolog sma-9 cause ventralization of the M lineage and that wild-type SMA-9
35 point causes inefficient Grk translation and ventralization of the oocyte.
36 iformly in the follicle cell layer, a strong ventralization of the resulting embryos is observed.
37  reveal that Bmp2b and Bmp7 synergize in the ventralization of wild-type embryos through a cell-auton
38 o varying degrees, from mild to severe; this ventralization phenotype may be secondary to defective l
39 dha and organizer-specific genes, and causes ventralization resulting in a headless phenotype.
40                                     Instead, ventralization results from the reduced formation of Gli
41 results indicate that CDMP-1 antagonizes the ventralization signals from the notochord.
42 fish with morpholino oligonucleotides causes ventralization similar to that produced by chordin mutan