ライフサイエンスコーパス: embryonic mesoderm

1 FoxQ1, are involved in patterning the early embryonic mesoderm.

2 ems derived from two distinct populations of embryonic mesoderm.

3 , the decapentaplegic (dpp) gene, within the embryonic mesoderm.

4 riving Bmp4 expression in extraembryonic and embryonic mesoderm.

5 al system of vertebrates is derived from the embryonic mesoderm.

6 ft LPM, but is present in the head and extra-embryonic mesoderm.

7 erlapping subsets of trophectoderm and extra-embryonic mesoderm.

8 ls, in the maintenance and patterning of the embryonic mesoderm.

9 al decidua, the trophectoderm, and the extra-embryonic mesoderm.

10 sed in the primitive streak and newly formed embryonic mesoderm.

11 Somatic muscle is derived from a subset of embryonic mesoderm.

12 lls ("hemangioblasts") within the Drosophila embryonic mesoderm.

13 ouse placenta and for generating signals for embryonic mesoderm and axis formation.

14 vironment may alter differentiation of extra-embryonic mesoderm and result in an increased number of

15 lacZ expression in transgenic mice to extra-embryonic mesoderm and subsequently to both endothelial

16 roDpp is cleaved at the S1 site alone in the embryonic mesoderm and this generates sufficient ligand

17 development, Scl is first expressed in extra-embryonic mesoderm, and is required for the generation o

18 These cells derive from embryonic mesoderm, but how they are specified is unknow

19 ite happens: Xwnt-8 functions to pattern the embryonic mesoderm by promoting ventral and lateral meso

20 Overexpression of MBC and ELMO in the embryonic mesoderm causes defects in myoblast fusion rem

21 GF signal, medicated by PI3K, can facilitate embryonic mesoderm cell spreading on fibronectin.

22 t effect of PDGF AA on aggregates of Xenopus embryonic mesoderm cells.

23 gastrulating embryos, FOXF1 marks most extra-embryonic mesoderm derivatives including the chorion, th

24 1 marks all posterior primitive streak extra-embryonic mesoderm derivatives with the remarkable excep

25 co-expressed during Drosophila melanogaster embryonic mesoderm development or neural development sco

26 are not functionally interchangeable during embryonic mesoderm development.

27 Most of the post-embryonic mesoderm develops from a single lineage.

28 e Eomesodermin (Eomes) is required for early embryonic mesoderm differentiation in mouse, frog (Xenop

29 ablishing that Brat plays a critical role in embryonic mesoderm formation and body patterning.

30 Embryonic mesoderm in C. elegans derives from a number o

31 connection between initial formation of the embryonic mesoderm in Drosophila and subsequent cell-fat

32 cification of human hematopoietic cells from embryonic mesoderm in vivo.

33 Mutant embryos form abundant extra-embryonic mesoderm, including allantois, a rudimentary h

34 RLR immunoreactivity in tissues derived from embryonic mesoderm, including the periadrenal and perine

35 The 175-bp enhancer is also active in the embryonic mesoderm, indicating that this enhancer functi

36 function because misexpression of shd in the embryonic mesoderm instead of the epidermis, the normal

37 ast to absence of anterior structures, extra-embryonic mesoderm is abundant.

38 Establishment of the embryonic mesoderm is dependent on integration of multip

39 Very little embryonic mesoderm is produced; in contrast, extraembryo

40 In the embryonic mesoderm, Notch is involved in the process by

41 ior primitive streak, from which much of the embryonic mesoderm of the wild-type embryo is derived.

42 egion gives rise to germ cells and the extra-embryonic mesoderm of the yolk sac; the distal region ge

43 As a consequence, no embryonic mesoderm- or endoderm-derived tissues develop,

44 esponse elements from genes expressed during embryonic mesoderm patterning and midgut morphogenesis p

45 misshapen is also expressed in the embryonic mesoderm, pole plasm and other sites of cell s

46 These observations suggest that embryonic mesoderm regulatory protein may mimic physiolo

47 Patterning of the Drosophila embryonic mesoderm requires the regulation of cell type-

48 Inhibition of Smurf1 expression in embryonic mesoderm results in loss of ephrinB1-mediated

49 h during lateral inhibition processes in the embryonic mesoderm, sensory organ specification in imagi

50 In addition, the embryonic mesoderm that is produced does not become orga

51 rsoventral patterning of the C. elegans post-embryonic mesoderm, the M lineage.

52 usters of equivalent cells in the Drosophila embryonic mesoderm, the Ras/MAPK pathway--activated by b

53 tte (ABC) transporter Mdr49 functions in the embryonic mesoderm to facilitate the transmission of the

54 experiments, exclusively targeting the intra-embryonic mesoderm were combined with QH1 immunostaining

55 al for early migration and patterning of the embryonic mesoderm, while BREATHLESS is required for pro

56 rovide the first demonstration that in mouse embryonic mesoderm, while Dicer is dispensable for somit

57 tn2 expression was also present in posterior embryonic mesoderm, while GATA-1 and GATA-2 expression w