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1  only lay in the mid-region of the embryonic-abembryonic axis but, on discovering that early blastocy
2 ppears that the orientation of the embryonic-abembryonic axis is anticipated by earlier cell division
3 eless, we find that the blastocyst embryonic-abembryonic axis is not perfectly orthogonal to the firs
4 vegetal axis of the zygote and its embryonic-abembryonic axis is orthogonal to it.
5 wever, it is not known whether the embryonic-abembryonic axis is set up by the first cleavage itself,
6    This has revealed that both the embryonic-abembryonic axis of the blastocyst and its plane of bila
7 n mammalian development is how the embryonic-abembryonic axis of the blastocyst is first established.
8  influences the orientation of the embryonic-abembryonic axis.
9 TE-ICM bias arises separately from embryonic-abembryonic bias.
10 f the mouse egg and can define embryonic and abembryonic halves of the future blastocyst.
11  localization of clones in the embryonic and abembryonic hemispheres of the late blastocyst and their
12 e a greater proportion of its progeny to the abembryonic part of the blastocyst (region including the
13 tomere that contributes predominantly to the abembryonic part of the blastocyst.
14 ter dividing cell, contributes mainly to the abembryonic part.
15 t and the progeny of its sister populate the abembryonic part.
16 ls that comprise either the embryonic or the abembryonic parts of the blastocyst.
17 end to populate the respective embryonic and abembryonic parts of the blastocyst.
18 ed similar models in which the embryonic and abembryonic parts of the mouse blastocyst become separat
19 ends to divide the embryo into embryonic and abembryonic parts.
20 mbryonic ectoderm cells were detected at the abembryonic pole in postmitotic cells.
21 und that the blastocyst cavity, defining the abembryonic pole, forms where symmetric divisions predom

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