ライフサイエンスコーパス: mesodermal tissue

1 by coordinating the production of neural and mesodermal tissue.

2 t have been one of the earliest functions of mesodermal tissue.

3 ences the development of adjacent neural and mesodermal tissue.

4 signaling can occur without inducing ectopic mesodermal tissues.

5 trulation and is unlikely to operate through mesodermal tissues.

6 migration phase and aberrantly contribute to mesodermal tissues.

7 the axial midline, which patterns neural and mesodermal tissues.

8 the development and homeostasis of multiple mesodermal tissues.

9 it has a role in the development of specific mesodermal tissues.

10 genotypic and phenotypic characteristics of mesodermal tissues.

11 ession of an H19 reporter gene in a range of mesodermal tissues.

12 ene expression of H19 and Igf2 in a range of mesodermal tissues.

13 tion and differentiation in early Drosophila mesodermal tissues.

14 lier origin of NC, independent of neural and mesodermal tissues.

15 -catenin and the formation of endodermal and mesodermal tissues.

16 e segmented trunk in both the ectodermal and mesodermal tissues.

17 Mutant limbs possess a broad band of mesodermal tissue along the distal periphery that is abs

18 ic downregulation of Igf2 transcripts in all mesodermal tissues and the placenta.

19 prox1 expression in adjacent endodermal and mesodermal tissues appeared unaffected by these manipula

20 Mesodermal tissues arise from diverse cell lineages and

21 VegT is required for the formation of 90% of mesodermal tissue, as measured by the expression of meso

22 ere, we show that coordination of neural and mesodermal tissue at the zebrafish head-trunk transition

23 Changes in neural or mesodermal tissue configuration arising from defects in

24 ion factor Tinman (Tin) to induce all dorsal mesodermal tissue derivatives, which include dorsal soma

25 here appears to be expression of yps mRNA in mesodermal tissue during embryogenesis.

26 omologues are widely expressed in neural and mesodermal tissues during early embryogenesis.

27 differ in their abilities to activate dpp in mesodermal tissues during embryogenesis.

28 s of Xenopus Dishevelled (Xdsh) to neural or mesodermal tissues elicited different defects that were

29 is secreted extracellularly, and it induced mesodermal tissue formation in animal cap assays.

30 he axial skeleton with origins from distinct mesodermal tissues have repatterned over the course of e

31 idgestation with severe defects in posterior mesodermal tissues; heterozygous mice are viable but hav

32 perfamily member, activin, is able to induce mesodermal tissues in animal cap explants from Xenopus l

33 ole in the proper development of a subset of mesodermal tissues in C. elegans.

34 production is distributed between neural and mesodermal tissues in the dorsal isolate, and the notoch

35 d the developmental relationship between two mesodermal tissues in the Drosophila embryo, the gonadal

36 ired for the differentiation of a variety of mesodermal tissues in the Drosophila embryo, yet its lig

37 mportant role in growth control in embryonic mesodermal tissues in which it is selectively expressed.

38 A new fate map for mesodermal tissues in Xenopus laevis predicted that the

39 ly inhibited the formation of endodermal and mesodermal tissues including micromere-derived skeletoge

40 vents leading to the development of specific mesodermal tissues, including skeletal muscle; however,

41 TACC1 and TACC2, which are also expressed in mesodermal tissues, including somites.

42 ex (Tin-C) controls the patterning of dorsal mesodermal tissues, including the dorsal vessel or heart

43 During mesodermal tissue induction in Drosophila, various combi

44 Our understanding of how mesodermal tissue is formed has been limited by the abse

45 Prospective mesodermal tissue is, however, induced and we present ev

46 inducing and patterning adjacent neural and mesodermal tissues is well established.

47 ral mesendoderm, which give rise to nonaxial mesodermal tissues; its expression is extinguished as ti

48 DiI labelling, we show that the neural crest-mesodermal tissue juxtaposition that later forms the cor

49 BMP-11 induced axial mesodermal tissue (muscle and notochord) in a dose-depen

50 pathway - being robustly established within mesodermal tissue on the left side only.

51 The results suggest that mesodermal tissues originally evolved from endoderm tiss

52 During vertebrate embryogenesis, most of the mesodermal tissue posterior to the head forms from a pro

53 hancers identified by eFS as being active in mesodermal tissues revealed enriched DNA binding site mo

54 e mesoderm and allocate cells into different mesodermal tissues such as body muscle or heart is commo

55 t the functions of RA in aligning neural and mesodermal tissues temporally precede the specification

56 tion, patterning and alignment of neural and mesodermal tissues that are essential for the organizati

57 lyzed the effects of embryonic expression in mesodermal tissues that include the cardioblasts of the

58 e that, in addition to patterning neural and mesodermal tissues, the notochord plays an important rol

59 vivo for expression of both H19 and Igf2 in mesodermal tissues to sequences downstream of the H19 ge

60 ing cues specify germ layer contribution and mesodermal tissue type specification of multipotent stem

61 embryonic tissue from somitic and presomitic mesodermal tissue, we identified new genes enriched in t

62 ificant levels were consistently detected in mesodermal tissues which contribute nonmyogenic cells to

63 necessary to create many different types of mesodermal tissues while causing a dramatic expansion of

64 Mesodermal tissue with heart forming potential (cardioge