ライフサイエンスコーパス: posterior mesoderm

1 tion and patterning of zebrafish ventral and posterior mesoderm.

2 been implicated as patterning factors of the posterior mesoderm.

3 that are required for the development of all posterior mesoderm.

4 mutant for fgf8 blocks the formation of most posterior mesoderm.

5 tion alone has no affect on the formation of posterior mesoderm.

6 tricting its expression and influence to the posterior mesoderm.

7 ricted gene that is expressed in the lateral posterior mesoderm.

8 and vein are spatially mixed in the lateral posterior mesoderm.

9 eural tube but fails to direct expression to posterior mesoderm.

10 continue to be expressed in the ventral and posterior mesoderm after gastrulation, it is likely that

11 e domains of ectopic Msx-2 expression in the posterior mesoderm also exhibit ectopic expression of BM

12 N), or an anti-APLNR mAb, were found in both posterior mesoderm and anterior mesendoderm populations

13 T protein is vital for the formation of posterior mesoderm and axial development in all vertebra

14 h is typically required for the formation of posterior mesoderm and axial development, suggesting tha

15 chyury (T) gene is required for formation of posterior mesoderm and for axial development in both mou

16 ortant for the development of streak-derived posterior mesoderm and lateral morphogenesis.

17 variety of developmental processes including posterior mesoderm and neural patterning.

18 Hoxd11/lacZ reporter in the embryo tailbud, posterior mesoderm and neurectoderm.

19 al gastrulation movements and ultimately for posterior mesoderm and notochord differentiation in the

20 er of the T-box gene family, is required for posterior mesoderm and notochord differentiation in vert

21 gene family and is required for formation of posterior mesoderm and notochord during vertebrate devel

22 ytes, including the normally non-cardiogenic posterior mesoderm and the extraembryonic mesoderm of th

23 chyury (T) is essential for formation of the posterior mesoderm and the notochord in vertebrate embry

24 zled protein results in expansion of ventral posterior mesoderm and the ventral blood islands, indica

25 e or anterior endoderm/lateral mesenchyme or posterior mesoderm are each alone sufficient to ensure t

26 ryos rescues embryonic erythropoiesis in the posterior mesoderm as well as the formation of HSCs in t

27 readily induce cardiac myocyte formation in posterior mesoderm, but shows no capacity to induce card

28 rm and mesoderm by late blastula, and to the posterior mesoderm by mid-gastrula.

29 the role of Bmp signaling in the ventral and posterior mesoderm changes as gastrulation proceeds.

30 ting that cdx4 and hox genes act to make the posterior mesoderm competent for blood development.

31 tation, COX-1 signaling is also required for posterior mesoderm development, including the formation

32 ng a dominant-negative Fgf receptor inhibits posterior mesoderm development.

33 ryos does not result from a general block in posterior mesoderm differentiation as endothelial cells

34 t COX-1 expression becomes restricted to the posterior mesoderm during somitogenesis and to posterior

35 the role of Bmp signaling in the ventral and posterior mesoderm during trunk and tail outgrowth, we g

36 nd found that they play an essential role in posterior mesoderm formation during gastrulation.

37 log no tail (ntl) are together essential for posterior mesoderm formation.

38 new pathway upstream of Nodal signaling and posterior mesoderm formation.

39 Within the posterior mesoderm, hand2 is expressed laterally adjacen

40 n the morphogenesis of large portions of the posterior mesoderm has been suppressed.

41 developing limbs, cFHF-1 is confined to the posterior mesoderm in an area that encompasses the zone

42 Despite the lack of posterior mesoderm in spt(-);ntl(-) embryos, dorsal-vent

43 lays an important role during development of posterior mesoderm in vertebrate embryos.

44 and (iii) in explants of dorsal ectoderm and posterior mesoderm in which FGF signaling is specificall

45 nd promoting apoptosis in the regions of the posterior mesoderm in which it is ectopically expressed.

46 displaced by a repulsion mechanism from the posterior mesoderm into the endoderm.

47 te that dorsoventral patterning of the mouse posterior mesoderm is regulated by Bmp signaling, as is

48 destined for the ISVs arise from the lateral posterior mesoderm (LPM), and migrate to the dorsal aort

49 nside the blastopore and subsequently in the posterior mesoderm, notochord, and somites.

50 t in egg cylinder embryos but present in the posterior mesoderm of late primitive streak embryos.

51 tgrowing mesodermal cells of explants of the posterior mesoderm of normal limb buds cultured in the a

52 -2 via a retroviral expression vector in the posterior mesoderm of the progress zone from the time of

53 reases gata1(+) erythroid progenitors in the posterior mesoderm of wild-type embryos and anemic cdx4(

54 sterior mesoderm during somitogenesis and to posterior mesoderm organs at pharyngula stage.

55 X-1 signaling is required for development of posterior mesoderm organs, specifically in the vascular

56 Recombinants of dorsal ectoderm and posterior mesoderm were made in which FGF was specifical