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1 ased on the expression of the engrailed (en) segmentation gene.
2 anscription factors encoded by the pair-rule segmentation genes.
3 anscription factors encoded by the pair-rule segmentation genes.
4 ctions among maternal coordinate and zygotic segmentation genes.
5 ridisation to the analysis of the Drosophila segmentation genes.
6 atterns of vertebrate homologs of Drosophila segmentation genes.
7 s a crucial member of the pair-rule class of segmentation genes.
8 yogenesis by the transient expression of the segmentation genes.
9 -8, and several chick homologs of Drosophila segmentation genes.
10 pression of mammalian homologs of Drosophila segmentation genes.
11 leads to differential expression of zygotic segmentation genes.
13 expression of orthologues of the Drosophila segmentation genes among various insects have served to
14 ryo, a system of coordinates is laid down by segmentation genes and dorsoventral patterning genes.
15 initially established by the activity of the segmentation genes and is subsequently maintained during
16 homologues of the Drosophila and vertebrate segmentation genes and show that members of the Notch si
17 ork has revealed that orthologues of several segmentation genes are expressed in the grasshopper embr
19 l expression is initially established by the segmentation gene cascade in the early Drosophila embryo
20 sion of key developmental genes, such as the segmentation genes controlling anteroposterior patternin
21 espite our increased knowledge of individual segmentation genes, details of their interactions in non
22 ks activation of the Drosophila melanogaster segmentation gene engrailed (en) in odd-numbered paraseg
23 otprint assays were used to confirm that the segmentation gene engrailed contains paused Pol II as se
25 Previous studies on the regulation of the segmentation gene even-skipped (eve) have centered on th
26 t be required for consistent localization of segmentation gene expression because embryo size, a gene
28 robust to variations in embryonic geometry; segmentation gene expression remains reproducible even w
31 , a small number of HOM-C genes, such as the segmentation gene fushi tarazu (ftz), have nonhomeotic f
32 vidence that beetles have a homologue of the segmentation gene fushi tarazu of similar genomic locati
34 determination gene Sex-lethal (Sxl) and the segmentation genes fushi tarazu and even-skipped are ect
35 he cell cycle regulatory gene string and the segmentation gene giant coincides with transcriptional a
36 f runt provides evidence that this pair-rule segmentation gene has a direct role in repressing transc
38 ax genes, which are homologues of Drosophila segmentation genes, have provided a critical genetic ent
40 We report the first characterization of a segmentation gene homologue in the basal polychaete Capi
44 the expression profiles of a complete set of segmentation genes in the early embryos of the mosquito,
46 tino is the zebrafish homologue of the mouse segmentation gene kreisler, which encodes a bZip transcr
48 fly Drosophila have revealed a hierarchy of segmentation genes (maternal, gap, pair-rule and HOX) th
49 initial 'salt and pepper' expression of the segmentation gene MESP2 in the newly formed segment is t
59 epistatic to hedgehog (hh), another secreted segmentation gene product, in its requirement for heart
60 y target such activation domains to specific segmentation gene promoters, leading to rapid induction
64 hierarchical levels, regulating first, other segmentation genes; second, other regulatory genes that
70 m makes use of the small intron from the ftz segmentation gene to provide efficient processing of syn
72 posterior compartment, are generated by the segmentation genes while the Hox genes provide each segm
73 tions as a gap gene to control expression of segmentation genes within the abdominal region of the em