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1 istently required throughout the rest of the blastoderm stage.
2 efly with that of SxlPe during the syncytial blastoderm stage.
3 all of the body regions are specified by the blastoderm stage.
4 t anterior body regions are specified by the blastoderm stage.
5 ges to equivalent patterns at the end of the blastoderm stage.
6 nt but instead maintain repression after the blastoderm stage.
7 t at PS9, which shifts posteriorly after the blastoderm stage.
8 e traced these defects back to the syncytial blastoderm stage.
9 l germ cells are specified from at least the blastoderm stage.
10 s but becomes depleted at the termini by the blastoderm stage.
11 rule gene even skipped (eve) at the cellular blastoderm stage.
12 entrosomes in Drosophila embryos at cellular blastoderm stage.
13 tage, disappears rapidly during the cellular blastoderm stage and is not detected at any other point
14 this single mechanism functions in the early blastoderm stage and subsequently during germ-band elong
15  the anterior segments are formed during the blastoderm stage and the remaining posterior segments ar
16 as the embryo transits from preblastoderm to blastoderm stages and defines the onset of a checkpoint
17  axis, and all segments are patterned at the blastoderm stage, before gastrulation.
18 ow that smaug mutants also disrupt syncytial blastoderm stage cell-cycle delays, DNA replication chec
19 tes a sensitized non-lethal phenotype at the blastoderm stage (defined as six cycB phenotype).
20 aximally expressed during the late syncytial blastoderm stage, disappears rapidly during the cellular
21 o stripes of expression (stripes 3 and 7) in blastoderm stage Drosophila embryos.
22 egulating spatial expression patterns in the blastoderm-stage Drosophila embryo.
23 nes, one stripe for each parasegment, in the blastoderm stage embryo.
24 verlapping domains in the head region of the blastoderm stage embryo.
25 ural analysis of Drosophila chromosome 2L in blastoderm stage embryos.
26  the layer of peripheral nuclei in syncytial blastoderm stage embryos.
27 ng neuregulin-1 hammerhead-type ribozymes to blastoderm-stage embryos leads to an embryonic lethal ph
28 razu (ftz) of Drosophila is expressed at the blastoderm stage in seven stripes that serve to define t
29                                      At late blastoderm stages, none of the candidate genes we have t
30 mined their domains of expression during the blastoderm stage of development, in relation to one anot
31 ned a gene expressed specifically during the blastoderm stage of Drosophila embryogenesis.
32 form levels throughout the embryo during the blastoderm stage of embryogenesis.
33                                           In blastoderm stage Presenilin mutants, Arm is aberrantly d
34 ciate with the male X chromosome as early as blastoderm stage, slightly earlier than the histone H4 i
35 atory elements, including ones for syncytial blastoderm stage stripes 1 and 5, while a single element
36 ase, produced sharply defined stripes at the blastoderm stage that were coincident with eve stripe 2
37 ecified nearly simultaneously so that by the blastoderm stage, the entire body plan has been determin
38    Transcripts persist strongly during early blastoderm stages then fade dramatically by 3h of develo
39 el, we have ectopically expressed fog at the blastoderm stage using an inducible promoter.
40  sufficient for even skipped function at the blastoderm stage, while the homeodomain is sufficient to
41  only anterior segments are patterned at the blastoderm stage, with the remaining segments arising af
42 n anterior nuclei in the embryo at syncytial blastoderm stage, within 1.5-2.5 h after translation com

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