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1 xpressed in the yolk syncytial layer and the hypochord.
2  to be specified as floorplate, notochord or hypochord.
3 ochord lies medially, flanked by presumptive hypochord and both overlie the deep region of the presum
4 cial cartilage, ear, notochord, floor plate, hypochord and fins in a pattern similar to the expressio
5 dorsal midline, prechordal plate, notochord, hypochord and floor plate share a common embryonic origi
6 dline structures, including notochord and/or hypochord and neural floorplate, regulate Xnr-1 expressi
7 inhibiting notochord formation and promoting hypochord and possibly floor plate development, but the
8 sion resolves to the neural tube floorplate, hypochord, and (transiently) the notochord anlage, and i
9 eginning of gastrulation caused expansion of hypochord at the expense of notochord, but floor plate w
10 ailbud to specify hypochord from a notochord/hypochord bipotential cell population.
11                                              Hypochord cells are also found at the midline of anamnio
12     We demonstrate here that floor plate and hypochord cells arise from distinct regions of the zebra
13 nk notochord cells and excess floorplate and hypochord cells.
14 mbryos had reduced numbers of floorplate and hypochord cells; these cells lie above and beneath the n
15 neurulation leads to the complete failure of hypochord development and to the elimination of expressi
16  in presumptive hypochord precursors and for hypochord development.
17 otochord signaling, a significantly enlarged hypochord develops.
18 ate during early neural stages, and that the hypochord does not depend on further notochord signals f
19 ells in the underlying endoderm to take on a hypochord fate during early neural stages, and that the
20     Notch signaling promotes floor plate and hypochord fates over notochord, but has variable effects
21 tants have significantly stronger defects in hypochord formation but not in somitogenesis or hindbrai
22 c effects on both hindbrain neurogenesis and hypochord formation.
23 ol of somite segmentation, neurogenesis, and hypochord formation.
24 eurulation, however, does not interfere with hypochord formation.
25 , continues to act in the tailbud to specify hypochord from a notochord/hypochord bipotential cell po
26  dorsal midline (floor plate, notochord, and hypochord) has been an area of classical research and de
27  both paraxial and axial mesoderm (including hypochord), in similar patterns and amounts in both spec
28                Notch signaling, required for hypochord induction during gastrulation, continues to ac
29                   It appears likely that the hypochord is required for the formation of the dorsal ao
30  and to the elimination of expression of the hypochord marker, VEGF.
31  required for her4 expression in presumptive hypochord precursors and for hypochord development.
32                         During gastrulation, hypochord precursors are closely associated with no tail
33                                 We show that hypochord precursors arise from the lateral edges of the
34 prechordal plate, notochord, floor plate and hypochord progenitors during gastrulation.
35 neighboring midline precursors to develop as hypochord, rather than as notochord.
36 aling during gastrulation entirely prevented hypochord specification but only reduced the number of f
37 hord are critical for the development of the hypochord, which is a transient, endodermally derived st
38  diffusible form of VEGF is expressed by the hypochord, which lies at the embryonic midline immediate
39                        One such cell type is hypochord, which lies ventral to notochord in anamniote

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