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1 orsal accumulates on the ventral side of the syncytial blastoderm.
2 ion of a small number of giant nuclei in the syncytial blastoderm.
3 ween the nuclei located at the cortex of the syncytial blastoderm.
4 g is required for the cellularization of the syncytial blastoderm.
5 e regulation of Cdk1 waves in the Drosophila syncytial blastoderm.
6 rent at nuclear cycle 7, two cycles prior to syncytial blastoderm.
8 alized in both pseudocleavage furrows at the syncytial blastoderm and in the cleavage furrows during
9 cluding a broad zen expression domain in the syncytial blastoderm and the complete absence of postgas
10 vage-stage embryos, patchy loss of nuclei in syncytial blastoderms, and cuticular pattern defects in
11 indicates that pseudocleavage furrows in the syncytial blastoderm are abnormal but not completely dis
14 t the development of a cell-free system from syncytial blastoderm Drosophila embryos that recapitulat
16 ated to form a gradient in the nuclei of the syncytial blastoderm embryo after fertilization [1-3].
17 hment of segmental pattern in the Drosophila syncytial blastoderm embryo depends on pair-rule transcr
19 orsal-ventral polarity within the Drosophila syncytial blastoderm embryo is determined by the materna
22 repress decapentaplegic and zerknullt in the syncytial blastoderm embryo, they are able to pattern th
24 s limited the sensitivity of analysis of pre-syncytial blastoderm embryos and precluded studies of oo
25 Drosophila that removes damaged nuclei from syncytial blastoderm embryos via DNA damage checkpoint k
26 methods to analyze stage 14 oocytes and pre-syncytial blastoderm embryos, and found that stage 14 oo
29 l division separates the 6,000 nuclei of the syncytial blastoderm into separate cells through the inv
30 , gap, pair-rule and HOX) that subdivide the syncytial blastoderm into sequentially finer-scale coord
31 e a straightforward alternative in which the syncytial blastoderm is approximated by a periodic arran
33 rtmentalized around individual nuclei in the syncytial blastoderm is likely to ensure that secretory
34 aneous diffusion coefficients throughout the syncytial blastoderm nuclear cycle phase of the early em
35 -associated units of ER and Golgi across the syncytial blastoderm produced secretory products that we
36 ere, we show that smaug mutants also disrupt syncytial blastoderm stage cell-cycle delays, DNA replic
38 ping regulatory elements, including ones for syncytial blastoderm stage stripes 1 and 5, while a sing
39 cript is maximally expressed during the late syncytial blastoderm stage, disappears rapidly during th
40 detected in anterior nuclei in the embryo at syncytial blastoderm stage, within 1.5-2.5 h after trans
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