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1  from embryonic stem (ES) cells derived from primitive ectoderm.
2 4(+) cells predominantly differentiated into primitive ectoderm and contributed to chimera formation,
3 bserved in vivo, including the generation of primitive ectoderm and neurectoderm in embryoid body cul
4 steoblasts, the cells are then arrested in a primitive ectoderm and/or endoderm stage.
5 c studies have reported their induction from primitive ectoderm (animal cap).
6                      We show that in axolotl primitive ectoderm (animal caps; ACs) NANOG and NODAL ac
7 larity complex with PKCzeta/lambda regulates primitive ectoderm cell polarity and morphogenesis.
8 elieved to most closely resemble pluripotent primitive ectoderm cells derived directly from the ICM.
9    However, differences between ES cells and primitive ectoderm cells have caused developmental biolo
10 on from the totipotent zygote to pluripotent primitive ectoderm cells in the inner cell mass of mouse
11 ent state, which is first established in the primitive ectoderm cells of blastocysts, is lost progres
12                      Our study shows that in primitive ectoderm cells, the sphingolipid ceramide was
13 ss and subsequently becomes localized to the primitive ectoderm, developing central nervous system, a
14 biosynthesis enhanced apoptosis and impaired primitive ectoderm formation in embryoid bodies differen
15                                              Primitive ectoderm formation was restored by incubation
16 ent of post-implantation epiblast cells from primitive ectoderm involves significant transcriptional
17 ion of the neural plate from a region of the primitive ectoderm is accompanied by the onset of specif
18                              In mammals, the primitive ectoderm is an epithelium of polarized cells t
19 e mouse embryonic stem cells (ESCs) to early primitive ectoderm-like (EPL) cells - a transcriptionall
20 ntrols the transition from an Fgf5-positive, primitive ectoderm-like cell state to a neural progenito
21 tic barrier and prevent their reversion to a primitive-ectoderm-like state.
22 expression of pluripotency genes, upregulate primitive ectoderm markers, undergo a morphological chan
23             Pluripotency is conserved in the primitive ectoderm of embryos from mammals and urodele a
24 s in the later stages, i.e. the epiblast and primitive ectoderm (PrE).
25 sis suggested a differentiation block at the primitive ectoderm stage.
26 and contain cores apparently arrested at the primitive ectoderm stage.
27          Mix.3 and Mix.4 can directly induce primitive ectoderm to become endoderm whereas Mix.1 cann