ライフサイエンスコーパス: visceral mesoderm

1 hila develop from the hindgut primordium and visceral mesoderm.

2 ction of beta3 in embryos is in cells of the visceral mesoderm.

3 Ubx) in parasegment 7 (PS7) of the embryonic visceral mesoderm.

4 ation between the midgut and the surrounding visceral mesoderm.

5 represses Robo2 expression in the abdominal visceral mesoderm.

6 inman, but does not require a differentiated visceral mesoderm.

7 delayed in the outflow tract myocardium and visceral mesoderm.

8 while the remaining macromere generates the visceral mesoderm.

9 can differentiate into cells of limb bud and visceral mesoderm.

10 to facilitate correct dpp expression in the visceral mesoderm.

11 d reporter gene expression anteriorly in the visceral mesoderm.

12 r, in parasegments 3 and 7 of the Drosophila visceral mesoderm.

13 is case between the inner ectoderm and outer visceral mesoderm.

14 m depends on interactions with the overlying visceral mesoderm.

15 ila tinman gene, which specifies cardiac and visceral mesoderm.

16 nce of the homeotic gene Antennapedia in the visceral mesoderm.

17 t and visceral mesoderm, Nkx2-5 rescued only visceral mesoderm.

18 of the abdominal-A (abdA) Hox domain in the visceral mesoderm.

19 capentaplegic and Wingless secreted from the visceral mesoderm.

20 luding somatic myoblasts, cardial cells, and visceral mesoderm.

21 he NK-4 gene, mediate NK-4 expression in the visceral mesoderm.

22 ion by bagpipe, a gene that specifies nearby visceral mesoderm.

23 mesoderm or endoderm to DPP signals from the visceral mesoderm.

24 Removing PS integrin function from the visceral mesoderm alone results in visceral mesoderm dis

25 NETRIN expression is also required in the visceral mesoderm, along which the glands move during th

26 required for NK-4 activation in cells of the visceral mesoderm and also for NK-4 repression in cells

27 cell level, also differentiate into cells of visceral mesoderm and can be expanded extensively by mea

28 lso been isolated, and its expression in the visceral mesoderm and embryonic skeleton in the mouse ha

29 ithelium concomitantly becomes surrounded by visceral mesoderm and is characterized by distinct gene

30 n of the homeotic genes Ultrabithorax in the visceral mesoderm and labial in the subjacent endoderm.

31 he dpp enhancer is repression throughout the visceral mesoderm and that activation by Wingless signal

32 es, has a key role in the development of the visceral mesoderm and the derived gut musculature.

33 distinct mesodermal populations: the caudal visceral mesoderm and the gonadal mesoderm.

34 the function of FoxF1 in the development of visceral mesoderm and the organogenesis of the gut.

35 ed in the septum transversum and splanchnic (visceral) mesoderm and is required for proper developmen

36 The precursors of the visceral mesoderm are also absent and concomitantly the

37 Abnormalities in visceral mesoderm are also observed.

38 it sandwich") in which Robo2 on the thoracic visceral mesoderm binds to Slit and presents it to Robo

39 that are expressed ubiquitously in the trunk visceral mesoderm but also for the expression of dpp in

40 , bagpipe, which is normally only needed for visceral mesoderm but not heart development, cannot subs

41 s close to Dpp-and Wg-secreting cells of the visceral mesoderm, but is in the cytoplasm in more dista

42 Visceral mesoderm can nevertheless be induced by Dpp in

43 Caudal visceral mesoderm (CVM) cells migrate from posterior to

44 Caudal visceral mesoderm (CVM) cells migrate synchronously towa

45 t portion of the mesoderm, termed the caudal visceral mesoderm (CVM), and migrate onto the trunk visc

46 tory cell types, including hemocytes, caudal visceral mesoderm (CVM), the visceral branch of the trac

47 agpipe, Nkx3-1, is expressed in vascular and visceral mesoderm-derived muscle tissues and may influen

48 of NK2-type genes (in activating markers of visceral mesoderm development in Drosophila) is specific

49 ox gene that serves as an early regulator of visceral mesoderm development.

50 ne, jelly belly (jeb), which is required for visceral mesoderm development.

51 uential but interdependent phases of hindgut visceral mesoderm development.

52 Region- and stage-specific markers of visceral mesoderm differentiation, such as Xbap and alph

53 from the visceral mesoderm alone results in visceral mesoderm disorganization, but only causes a mod

54 n, the lateral plate mesoderm, and later the visceral mesoderm, does not proliferate and differentiat

55 In Drosophila, induction of visceral mesoderm, dorsal muscles, and the heart by Dpp

56 The transformation of the visceral mesoderm during development is remarkable; it d

57 ma cells, and skeletal myoblasts) as well as visceral mesoderm (endothelial cells).

58 We demonstrate that the caudal visceral mesoderm facilitates the migration of germ cell

59 een the endodermal cells and the surrounding visceral mesoderm for integrin target gene expression.

60 ne, tinman, is required for heart as well as visceral mesoderm formation in Drosophila, and at least

61 the suppression of bagpipe (bap), and hence visceral mesoderm formation, and the promotion of somati

62 nds directly contact five other tissues: the visceral mesoderm, gastric caecae, somatic mesoderm, fat

63 is later refined to be most prevalent in the visceral mesoderm, gut, gonads and salivary glands.

64 m patterning and determines the formation of visceral mesoderm, heart progenitors, specific somatic m

65 directs expression of a reporter gene in the visceral mesoderm in a pattern indistinguishable from dp

66 ment of visceral/splanchnic mesoderm and non-visceral mesoderm in coelomate animals.

67 models, we reveal the important role of the visceral mesoderm in the ontogeny of the GI tract.

68 induction while antagonizing Dpp/Tin during visceral mesoderm induction.

69 Development of the visceral mesoderm is a critical process in the organogen

70 In the absence of the PS integrins, the visceral mesoderm is disorganised, the primordial midgut

71 tion of genes involved in the development of visceral mesoderm is therefore essential for an understa

72 e mesoderm, and later in its derivative, the visceral mesoderm, is the Fox gene FoxF1.

73 te the proper differentiation of the hindgut visceral mesoderm itself.

74 nly into mesenchymal cells but also cells of visceral mesoderm may be an ideal source of stem cells f

75 into mesenchymal cells, but also cells with visceral mesoderm, neuroectoderm and endoderm characteri

76 e tin itself strongly rescued both heart and visceral mesoderm, Nkx2-5 rescued only visceral mesoderm

77 that Mad is required for any response of the visceral mesoderm or endoderm to DPP signals from the vi

78 ecific cofactor of homeotic gene products in visceral mesoderm patterning.

79 antly suppresses the hbs myoblast fusion and visceral mesoderm phenotypes, and enhances Hbs overexpre

80 cing we observe bottle cells in anterior and visceral mesoderm precursors as gastrulation commences,

81 In jeb mutants, visceral mesoderm precursors form, but they fail to migr

82 es the activities of genes that position the visceral mesoderm precursors, such as heartless, thickve

83 biniou expression is activated in the trunk visceral mesoderm primordia downstream of dpp, tinman, a

84 h explains the periodic arrangement of trunk visceral mesoderm primordia in wild type embryos.

85 l mesoderm (CVM), and migrate onto the trunk visceral mesoderm prior to undergoing myoblast fusion an

86 In flies, the visceral mesoderm secretes signaling molecules that diff

87 We use dpp674, a visceral mesoderm-specific enhancer of decapentaplegic (

88 for Drosophila tinman function in promoting visceral mesoderm-specific marker gene expression, but m

89 lanchnic mesoderm, consistent with a role in visceral mesoderm specification, a function performed by

90 ation of the primordial midgut cells along a visceral mesoderm substratum.

91 es examined, including the patterning of the visceral mesoderm, the embryonic ectoderm and the imagin

92 salivary gland turns and migrates along the visceral mesoderm to become properly oriented with respe

93 sensory neurons) or in trans (on neighboring visceral mesoderm) transforms abdominal organs to a thor

94 xcept that they closely associate with trunk visceral mesoderm (TVM).

95 uired for proper development of the circular visceral mesoderm upon which the gland migrates.

96 nd invertebrates, the differential rescue of visceral mesoderm versus heart development suggests that

97 The Drosophila visceral mesoderm (VM) is a favorite system for studying

98 ), and to establish and maintain the hindgut visceral mesoderm (Wg and Hh).

99 short-range activation of Ubx by Dpp in the visceral mesoderm, whereas vg exhibits a long-range resp

100 ated mef2 expression in the caudal and trunk visceral mesoderm, which give rise to longitudinal and c

101 n of reporter gene expression throughout the visceral mesoderm, with no diminution of expression in t