ライフサイエンスコーパス: ventral mesoderm

1 muscle founder identity gene, slouch, in the ventral mesoderm.

2 buds caused by a defect in the formation of ventral mesoderm.

3 ed self-organizing properties of the extreme ventral mesoderm.

4 ion is required for proper patterning of the ventral mesoderm.

5 essor, which is selectively expressed in the ventral mesoderm.

6 hros and tail originate from both dorsal and ventral mesoderm.

7 , supporting a role for Xnr2 in induction of ventral mesoderm.

8 Wnt signaling, also induced cardiogenesis in ventral mesoderm.

9 restriction of the ventral blood islands to ventral mesoderm.

10 oietic and vascular progenitors develop from ventral mesoderm.

11 The hematopoietic system is derived from ventral mesoderm.

12 tem cells is specified from undifferentiated ventral mesoderm.

13 the embryo causes ventralization and induces ventral mesoderm.

14 on domains and an increase in derivatives of ventral mesoderm.

15 (embryonic, fetal, or adult) originate from ventral mesoderm.

16 gastrulation is expressed in the lateral and ventral mesoderm.

17 lude the progenitors of the endoderm and the ventral mesoderm.

18 1) that is capable of mediating induction of ventral mesoderm.

19 regulation of Xbra itself in dorsal, but not ventral, mesoderm.

20 ral-to-caudal progression of both dorsal and ventral mesoderm across the pre-gastrula axis historical

21 enitors arise along the entire extent of the ventral mesoderm and contribute solely to haematopoietic

22 t embryos concur that cell rearrangements in ventral mesoderm and ectoderm contribute to the autonomo

23 Xenopus embryos and directs the formation of ventral mesoderm and epidermis.

24 and trunk endothelium all originate from the ventral mesoderm and often share lineage with one anothe

25 is a critical component in the formation of ventral mesoderm and possibly mediates the effects of BM

26 morphogenetic protein (BMP) subclass pattern ventral mesoderm and regulate ectodermal cell fates.

27 stic effect, greatly inhibiting formation of ventral mesoderm and ventral fin tissue.

28 grg2 and Xgrg4, are expressed in lateral and ventral mesoderm, and inhibit expression of XmyoD.

29 tes in a BMP-4 signalling pathway to pattern ventral mesoderm, and suggest a model whereby dimerizati

30 ood and vascular precursors from the extreme ventral mesoderm, and we show that this domain is normal

31 Xmad1 produces ventral mesoderm, apparently transducing a signal for BM

32 pable of inducing either dorsal or posterior ventral mesoderm at different times in development.

33 and endodermal markers and the induction of ventral mesoderm by smad1.

34 rostralmost contributions to both dorsal and ventral mesoderm concomitantly from marginal zone progen

35 the ability of Derriere to induce dorsal or ventral mesoderm depends strictly on the location of exp

36 Bmp signaling changes over time to regulate ventral mesoderm development.

37 can act during gastrulation both to promote ventral mesoderm differentiation and to attenuate dorsal

38 y during development by comparing dorsal and ventral mesoderm dissected from early gastrula embryos.

39 The activation of tbx6 transcription in ventral mesoderm does not depend on no tail gene activit

40 eted embryos are deficient in dorsal but not ventral mesoderm due to the reduced expression of the wn

41 sim is not activated in the ventral mesoderm, due to inhibition by the localized zin

42 l organizer formation and for patterning the ventral mesoderm during early gastrulation.

43 Hematopoietic stem cells are derived from ventral mesoderm during vertebrate development.

44 We demonstrate that SCL is expressed in ventral mesoderm early in embryogenesis.

45 secondary body axis or dorsalization of the ventral mesoderm explant analyzed by histological and mo

46 growth factor signaling during endoderm and ventral mesoderm formation.

47 The formation of ventral mesoderm has been traditionally viewed as a resu

48 er-S blocks the induction of both dorsal and ventral mesoderm in animal-vegetal Nieuwkoop-type recomb

49 Hematopoietic cells arise from ventral mesoderm in different vertebrates, but the mecha

50 and -4/7 heterodimers are potent inducers of ventral mesoderm in ectodermal explants, we show that th

51 ctor hes6, is also restricted to lateral and ventral mesoderm in gastrula stage Xenopus embryos, lead

52 lays an early role in specifying presumptive ventral mesoderm in the leading edge mesoderm, and that

53 netic protein signals, inducing formation of ventral mesoderm in Xenopus embryos, whereas Smad2 trans

54 e important for the early development of the ventral mesoderm, including blood, vasculature and kidne

55 gative form of XBMPRII (tBRII) can dorsalize ventral mesoderm, induce extensive secondary body axes,

56 of Xnr2 from a dorsal mesoderm inducer to a ventral mesoderm inducer, supporting a role for Xnr2 in

57 Dorsal mesoderm induction in arthropods and ventral mesoderm induction in vertebrates are closely re

58 od system in vertebrates is characterized by ventral mesoderm induction, hematopoietic stem cell spec

59 o respond to BMP signaling in the context of ventral mesoderm induction.

60 roles in embryogenesis, including dorsal and ventral mesoderm induction.

61 proteins (BMPs), which induce epidermis and ventral mesoderm instead.

62 enetic factor-4 (Bmp-4), a potent inducer of ventral mesoderm, is activated in the Organizer.

63 coding the BMP antagonist noggin in the tail ventral mesoderm, leading us to speculate that one of th

64 ne morphogenetic protein 4 (BMP4) can induce ventral mesoderm led to the suggestion that the inductio

65 In all three species, somitic, lateral, and ventral mesoderm move into the deep layer during gastrul

66 ctive epidermis to differentiate in vitro as ventral mesoderm, no loss-of-function studies have demon

67 la embryo and subsequently restricted to the ventral mesoderm of the gastrula embryo under the signal

68 nalling pathway in the posterior lateral and ventral mesoderm of the zebrafish embryo at the gastrula

69 mutants exhibit pronounced defects in dorso-ventral mesoderm patterning and in the antero-posterior

70 amine the temporal roles of Bmp signaling in ventral mesoderm patterning.

71 Lateral/ventral mesoderm progenitors represent a distinct commit

72 to the suggestion that the induction of the ventral mesoderm requires a different signaling pathway

73 that XOs4 can induce mesoderm and dorsalize ventral mesoderm resulting in ectopic dorsal axis format

74 Smad8 can block BMP-4-mediated induction of ventral mesoderm-specific gene expression in ectodermal

75 observations link the expression of tbx6 to ventral mesoderm specification.

76 superficial presumptive somitic and lateral-ventral mesoderm that initially separates the sub-blasto

77 l mesoderm and then extending to lateral and ventral mesoderm, that precedes and parallels blastopore

78 , low concentrations of XSmad7 dorsalize the ventral mesoderm, thus inducing a secondary axis.

79 etic development, either in specification of ventral mesoderm to a blood cell fate, or in formation o

80 g pathways might interact in the decision of ventral mesoderm to form blood.

81 eural tissue from ectoderm and can dorsalize ventral mesoderm to form muscle.

82 -stimulated erythroid differentiation in the ventral mesoderm was substantially inhibited by coinject

83 on screen for factors that pattern or induce ventral mesoderm, we isolated a complementary DNA encodi

84 XMad protein induces ventral mesoderm when overexpressed in isolated animal c

85 orphogenetic protein (BMP) signaling, induce ventral mesoderm whereas Smad2, activated by activin-lik

86 s (BMPs) are required for the development of ventral mesoderm, which contributes to the ventral blood

87 al during gastrulation for the generation of ventral mesoderm, which makes it a challenge to define f

88 on of low levels of Bix1 causes formation of ventral mesoderm, while high levels induce endodermal di