ライフサイエンスコーパス: embryonic axis

1 of residual TAG were mostly confined to the embryonic axis.

2 pment including the formation of the primary embryonic axis.

3 generates head-to-tail polarity of the main embryonic axis.

4 ertebrate segmentation and elongation of the embryonic axis.

5 of cells with respect to the anteroposterior embryonic axis.

6 Nodal signaling during establishment of the embryonic axis.

7 oriented along the anterior-posterior (a-p) embryonic axis.

8 xpression along the anterior-posterior (A-P) embryonic axis.

9 predictable rostrocaudal positions along the embryonic axis.

10 embryo tissues and seedling leaves from the embryonic axis.

11 derlie Hox regulation along the rostrocaudal embryonic axis.

12 equently can induce ectopic formation of the embryonic axis.

13 ay patterns all ventral cell fates along the embryonic axis.

14 ontaneously initiate formation of a complete embryonic axis.

15 ical role in establishment of the Drosophila embryonic axis.

16 ical role in the establishment of the dorsal embryonic axis.

17 tterns of reporter gene expression along the embryonic axis.

18 o complete cytokinesis and pattern the first embryonic axis.

19 the timing of specification of the secondary embryonic axis.

20 ants have defective somites along the entire embryonic axis.

21 vements both narrow and lengthen the forming embryonic axis.

22 hen rotate to align with the anteroposterior embryonic axis.

23 F) is required for patterning of the Xenopus embryonic axis.

24 ll behaviors that drive the extension of the embryonic axis.

25 d FGF signaling to promote elongation of the embryonic axis.

26 gene expression and in the formation of the embryonic axis.

27 riented perpendicular to the anteroposterior embryonic axis.

28 ries of ATAC-seq and RNA-seq along the chick embryonic axis.

29 to recruit uncommitted host cells into a new embryonic axis and induce host neural tissue with poster

30 bits a graded distribution along the primary embryonic axis and is partitioned unequally between the

31 d2 plays an essential role in patterning the embryonic axis and specification of definitive endoderm.

32 known to play a crucial role in defining the embryonic axis and subsequent development of the body pl

33 hortening and medio-lateral expansion of the embryonic axis, as well as abnormal notochord cell polar

34 ll stage, providing the earliest evidence of embryonic axis asymmetry in the zebrafish embryo.

35 on of the archenteron and also of the entire embryonic axis (both during and after gastrulation), as

36 colysis controls posterior elongation of the embryonic axis by regulating cell motility in the presom

37 Somites form along the embryonic axis by sequential segmentation from the preso

38 ial patterning along the Dorsal-ventral (DV) embryonic axis depends on a morphogen gradient of Bone M

39 and differentiation, and in establishing the embryonic axis during development.

40 ts with affected convergent extension of the embryonic axis during gastrulation.

41 eggshell axis than in the patterning of the embryonic axis during oogenesis.

42 rd, a conserved axial structure required for embryonic axis elongation and spine development, consist

43 Embryonic axis elongation is a complex multi-tissue morp

44 culogenesis, chorioallantoic attachment, and embryonic axis elongation.

45 ing horizontal ACD along the anteroposterior embryonic axis, endosomes containing the Notch ligand De

46 highly efficient transformation system using embryonic axis explants isolated from imbibed mature see

47 lel with PCP during gastrulation to regulate embryonic axis extension cooperatively.

48 During Drosophila embryonic axis extension, actomyosin has a specific plan

49 Establishment of the embryonic axis foreshadows the main body axis of adults

50 nt5a are both required for the initiation of embryonic axis formation and that the two proteins physi

51 effects of inhibiting MocuFH1 expression on embryonic axis formation in ascidians are similar to tho

52 Wnt signaling and regulates an early step in embryonic axis formation in mammals and amphibians.

53 Nodal morphogens play critical roles in embryonic axis formation in many organisms.

54 Embryonic axis formation in vertebrates is initiated by

55 Axin is a negative regulator of embryonic axis formation in vertebrates, which acts thro

56 Embryonic axis formation is essential for patterning and

57 In this paper, we report that the site of embryonic axis formation is marked earlier at the late-b

58 During embryonic axis formation, deep cells migrate and converg

59 f anterior-posterior polarity and subsequent embryonic axis formation, the Drosophila par-1 gene is r

60 st Dkk-1, are required for the initiation of embryonic axis formation.

61 te annelid Tubifex tubifex are essential for embryonic axis formation.

62 s beta-catenin during cell proliferation and embryonic axis formation.

63 hat has been implicated in the regulation of embryonic axis formation.

64 the role of forces in tissue patterning and embryonic axis formation.

65 t the embryonic shield can organize a second embryonic axis; however, contrary to our expectations ba

66 ent may be involved in specifying the future embryonic axis; however, how and when this pattern becom

67 is on the left or right side of the primary embryonic axis, implicating a molecular pathway leading

68 otein (BMP) patterns the dorsal-ventral (DV) embryonic axis in all vertebrates, but it is unknown how

69 ptually novel insights into the formation of embryonic axis in Arabidopsis by identifying a crucial r

70 st time that although the anterior-posterior embryonic axis in C. elegans is specified by sperm, the

71 e fibers showed that they elongate along the embryonic axis in cranial and caudal directions, or in b

72 avage is critical in establishing the second embryonic axis in the leech Helobdella, as in other uneq

73 oposed to drive morphogenesis of the primary embryonic axis in Xenopus.

74 lly during gastrulation and extension of the embryonic axis, in contrast to the appearance of the lim

75 ion switch in Hwa/beta-catenin signaling for embryonic axis induction, regulated by multiple kinases.

76 f ectodermal specification and the secondary embryonic axis, instead restrict the expression of these

77 C and E) of the primary anteroposterior (AP) embryonic axis is driven by polarized mediolateral (ML)

78 In C. elegans, the first embryonic axis is established shortly after fertilizatio

79 In some animal groups, the secondary embryonic axis is patterned by a small group of cells, o

80 Elongation of the vertebrate embryonic axis necessitates rapid expansion of the epide

81 in (BMP) signaling patterns the dorsoventral embryonic axis of vertebrates and invertebrates.

82 n the same pathway during the genesis of the embryonic axis, or the T/t region itself is truly comple

83 calised within the enveloping tissues of the embryonic axis (particularly the coleorhiza) during the

84 d by cables and is polarized relative to the embryonic axis, preferentially cyclically shortening and

85 ll fates along the sea urchin animal-vegetal embryonic axis requires the opposing functions of nuclea

86 ne the self-organizing networks that control embryonic axis specification and digit patterning.

87 of the cytoskeletal polarity that initiates embryonic axis specification and for translational contr

88 ated in Wnt signaling and plays key roles in embryonic axis specification and stem cell differentiati

89 wo nematode species where the mechanisms for embryonic axis specification are different even though s

90 rtance in biological mechanisms ranging from embryonic axis specification to the formation of long-te

91 pathway genes armitage and aubergine disrupt embryonic axis specification, triggering defects in micr

92 NA localization during mid-oogenesis and for embryonic axis specification.

93 in a moderately strong dorsalization of the embryonic axis, suggesting that Tsg1 promotes ventral fa

94 ed to an ectopic site, it induces a complete embryonic axis that includes a fully patterned, host-der

95 expression of WDV replicons occurred in the embryonic axis tissue of wheat embryos but their express

96 nscription in AV canal cells, duplicates the embryonic axis upon ventral injections in Xenopus embryo

97 The embryonic axis was found to be particularly enriched in

98 ctopic sites along the anterior to posterior embryonic axis were performed to distinguish the contrib

99 nt-1 class) that promotes duplication of the embryonic axis, whereas Xwnt-5A, -4, and -11 define a di

100 plit top mutant females exhibit a dorsalized embryonic axis, which can be rescued by BMP misexpressio

101 this gene was activated specifically in the embryonic axis, which was still enclosed by the endosper

102 The reconstituted embryo formed a secondary embryonic axis with a duplicated head and/or tail.

103 of the marginal zone, it induces a complete embryonic axis, without making a cellular contribution t