ライフサイエンスコーパス: segmentation gene

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.

12 ct heart depends crucially upon the homeotic segmentation gene abdominal-A (abd-A).

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

18 The maternal transcript of the anterior segmentation gene bicoid (bcd) is localized at the anter

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

24 The pair-rule segmentation gene even skipped (eve) is required to acti

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

27 The regulation of segmentation gene expression is investigated by computat

28 fects as a result of improper maintenance of segmentation gene expression.

29 mesothorax (T2) due to abnormal patterns of segmentation gene expression.

30 , a small number of HOM-C genes, such as the segmentation gene fushi tarazu (ftz), have nonhomeotic f

31 vidence that beetles have a homologue of the segmentation gene fushi tarazu of similar genomic locati

32 e Runt-dependent activation of the pair-rule segmentation gene fushi-tarazu (ftz).

33 determination gene Sex-lethal (Sxl) and the segmentation genes fushi tarazu and even-skipped are ect

34 he cell cycle regulatory gene string and the segmentation gene giant coincides with transcriptional a

35 f runt provides evidence that this pair-rule segmentation gene has a direct role in repressing transc

36 Homologues of Drosophila segmentation genes have been cloned and their expression

37 ax genes, which are homologues of Drosophila segmentation genes, have provided a critical genetic ent

38 The segmentation gene hierarchy of Drosophila melanogaster r

39 We report the first characterization of a segmentation gene homologue in the basal polychaete Capi

40 In flies, the gap segmentation gene hunchback (hb) encodes a C(2)H(2) zinc

41 ropod evolution from Hox-like to a pair-rule segmentation gene in Drosophila.

42 a homeotic gene but functions as a pair-rule segmentation gene in Drosophila.

43 the expression profiles of a complete set of segmentation genes in the early embryos of the mosquito,

44 While Hairy is probably not the only segmentation gene interacting with dCtBP, we show dose-s

45 tino is the zebrafish homologue of the mouse segmentation gene kreisler, which encodes a bZip transcr

46 We find that the segmentation gene Kruppel is expressed in a subset of fo

47 fly Drosophila have revealed a hierarchy of segmentation genes (maternal, gap, pair-rule and HOX) th

48 The segmentation gene network in insects can produce equival

49 ons that the evolution of upper tiers in the segmentation gene network is more flexible.

50 Thus, the Drosophila segmentation gene network responds faithfully to Bcd con

51 ed as a zinc finger homolog of the pair-rule segmentation gene odd-skipped.

52 The Drosophila gap-like segmentation genes orthodenticle, empty spiracles and bu

53 Reminiscent of many segmentation gene paralogues, the closely linked odd and

54 In Drosophila, segmentation genes partition the early embryo into reite

55 A cascade of segmentation genes patterns the embryo along its anterio

56 A set of pair-rule (PR) segmentation genes (PRGs) promotes the formation of alte

57 epistatic to hedgehog (hh), another secreted segmentation gene product, in its requirement for heart

58 y target such activation domains to specific segmentation gene promoters, leading to rapid induction

59 cificity with another pdm repressor: the gap segmentation gene regulator Hunchback (Hb).

60 n of the transcription factor encoded by the segmentation gene runt in the blastoderm embryo.

61 The segmentation gene, runt, is expressed by a subset of the

62 hierarchical levels, regulating first, other segmentation genes; second, other regulatory genes that

63 scriptional activation and repression of the segmentation gene sloppy-paired-1 (slp1).

64 Recent experiments indicate that the segmentation genes specify neuroblast identity along the

65 The analysis of a number of segmentation genes suggests that the repressor function

66 hairy is a Drosophila pair-rule segmentation gene that functions genetically as a repres

67 ogenesis and results in misregulation of the segmentation genes that are Bcd targets.

68 m makes use of the small intron from the ftz segmentation gene to provide efficient processing of syn

69 fish with a loss-of-function mutation in the segmentation gene valentino.

70 posterior compartment, are generated by the segmentation genes while the Hox genes provide each segm

71 tions as a gap gene to control expression of segmentation genes within the abdominal region of the em