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1 on and disruption of somite formation at the tailbud stage.
2 een the midblastula transition and the early tailbud stage.
3 defect in the mutant embryos until the early tailbud stage.
4 the developing retina beginning in the early tailbud stage.
5 n stabilised by binding to cdk2, persists to tailbud stages.
6 ning of ventral explants between neurula and tailbud stages.
7 arly stages into the long, thin shape of the tailbud stages.
8 n the left lateral plate mesoderm at neurula/tailbud stages.
9 ly at mid-gastrula but continuing as late as tailbud stages.
10 e elongation of segmented tissue during post-tailbud stages.
11 rivatives and other dorsal structures during tailbud stages.
12                    At gastrula, neurula, and tailbud stages, Axdazl RNA is widely distributed.
13                                       During tailbud stages, axial expression resolves to the neural
14 ylinositol-specific phospholipase C to early tailbud stage axolotl embryos reveals that a specific su
15 tead the archenteron cavity almost closes at tailbud stages before providing a nucleus for the defini
16 ebrate chordate Ciona forms a tapered rod at tailbud stages consisting of only 40 cylindrical cells i
17 of the germ line did not occur until the mid-tailbud stage, days after the somatic germ layers are es
18                           At the neurula and tailbud stages, dorsoanterior structures are affected: e
19         Whole-mount in situ hybridisation on tailbud stage embryo reveals strong expression of the ge
20 each ectoderm cell of the late neurula/early tailbud stage embryo, a time point just before onset of
21 ically blocks tail formation when induced in tailbud stage embryos, comfirming the importance of Xhox
22  progress faster through epiboly, leading to tailbud-stage embryos that have a narrow axis and an enl
23 late mesoderm restricted to the left side of tailbud-stage embryos.
24 en restarts in a second phase at neurula and tailbud stages, firstly in two symmetric patches near th
25                                           At tailbud stage, forerunner cells form the dorsal roof of
26 pecific expression pattern of xmdc11a at the tailbud stage in the cranial neural crest and in a subse
27 ay: inhibition with MEK or Fgfr inhibitor at tailbud stages in Ciona results in a larva which fails t
28                          When cultured until tailbud stages, Keller explants develop neural tissue wi
29 tion and axis formation, however, during the tailbud stage, MocuFH1 is also expressed in ventral cell
30                                    Until the tailbud stage of development, all ERK activation domains
31 d genetic inhibition of BMP signaling at the tailbud stage resulted in severe inhibition of endocardi
32 al crest cells from all axial levels, at the tailbud stage, Sox10 is downregulated in the cranial neu
33                                 By the early tailbud stages, these cells lie at the horizontal myosep
34 reshadowed by different somite counts at the tailbud stage, thought to be a highly conserved (phyloty
35 sufficiency of no tail expression as late as tailbud stage to drive medial precursor cells towards th
36 established as being between 60% epiboly and tailbud stages using the Fgf receptor inhibitor SU5402.