ライフサイエンスコーパス: intermediate mesoderm

1 erates progenitors for the lateral plate and intermediate mesoderm.

2 gonads, and reproductive ductal systems: the intermediate mesoderm.

3 erived from an embryonic germ layer known as intermediate mesoderm.

4 hesis that nephron epithelia derive from the intermediate mesoderm.

5 sis, three kidney structures form within the intermediate mesoderm.

6 anephric developmental program in responsive intermediate mesoderm.

7 alian metanephric kidney is derived from the intermediate mesoderm.

8 tion in the lateral mesoderm, but not in the intermediate mesoderm.

9 level tissue-specific expression within the intermediate mesoderm.

10 n kidney is derived from progenitor cells in intermediate mesoderm.

11 in the formation of organs derived from the intermediate mesoderm.

12 ertebrate kidney arises exclusively from the intermediate mesoderm.

13 on of lamprey FoxC genes in the paraxial and intermediate mesoderms.

14 tor in acquiring metanephric fate within the intermediate mesoderm and as a key regulator of Gdnf exp

15 ur results reveal transitions connecting the intermediate mesoderm and progenitors of organ primordia

16 pment, Fgf-8 transcripts are detected in the intermediate mesoderm and subsequently in the prelimb fi

17 ons: nephrogenic mesenchyme derived from the intermediate mesoderm and tailbud-derived mesoderm, whic

18 are responsible for the establishment of the intermediate mesoderm and the induction of the embryonic

19 The Wnt-2b gene is expressed in the intermediate mesoderm and the lateral plate mesoderm in

20 tions in the development of the paraxial and intermediate mesoderm and the neural crest in Xenopus.

21 such as Pax2/8, which are essential for the intermediate mesoderm and the renal epithelial lineage,

22 lopment are both believed to derive from the intermediate mesoderm and to be specified as the kidney

23 in with multiple functions in the developing intermediate mesoderm and urogenital tract.

24 nown Wnt11 gene is expressed in paraxial and intermediate mesoderm, and in differentiated myocardial

25 f Hensen's node to the somitic mesoderm, the intermediate mesoderm, and then to the prospective limb-

26 f Hensen's node to the somitic mesoderm, the intermediate mesoderm, and then to the prospective limb-

27 rast, their misexpression in the prospective intermediate mesoderm appears to drive cells to acquire

28 n the surface ectoderm, lateral mesoderm and intermediate mesoderm are essential for nephric duct for

29 We have defined regions of the intermediate mesoderm as candidates for the pronephric f

30 imb formation and that its expression in the intermediate mesoderm at the appropriate time and place

31 pecifies the metanephric blastema within the intermediate mesoderm at the caudal end of the nephrogen

32 is model, ablation of Fgf8 expression in the intermediate mesoderm before limb bud initiation had no

33 egulate the establishment of paraxial versus intermediate mesoderm cell fates in the vertebrate embry

34 ts in altered patterning of the mesoderm and intermediate mesoderm cell lineages, which give rise to

35 These human intermediate mesoderm cells can differentiate into multi

36 Following further differentiation of intermediate mesoderm cells, the mutant podocytes failed

37 an differentiate into multiple cell types of intermediate mesoderm-derived organs in vitro and in viv

38 the ureteropelvic junction were derived from intermediate mesoderm-derived renal progenitors and were

39 tutively active Hedgehog signaling in murine intermediate mesoderm-derived renal progenitors results

40 useful system to elucidate the mechanisms of intermediate mesoderm development and potentially provid

41 r analyses show that key regulators of early intermediate mesoderm development, including Lhx1, Pax2,

42 d show that Odd 1 is essential for heart and intermediate mesoderm development.

43 se embryonic day 8.5 (E8.5) in the region of intermediate mesoderm fated to become the nephric duct,

44 important role in regulating the balance of intermediate mesoderm fates by attenuating Fgf activity.

45 d into PAX2(+)GATA3(+) pronephric (anterior) intermediate mesoderm fates in monolayer cultures at hig

46 on along the medio-lateral axis, its role in intermediate mesoderm formation has not been well charac

47 embryo, Foxc1 and Foxc2 negatively regulate intermediate mesoderm formation.

48 induced to express markers specific for the intermediate mesoderm, from which the kidneys arise.

49 s high levels of Bmp repress both medial and intermediate mesoderm gene expression and activate later

50 tterning in which low levels of Bmp activate intermediate mesoderm gene expression by inhibition of r

51 Within the LPM, the so-called intermediate mesoderm (IM) forms kidney and urogenital t

52 riments in the chick, Fgf8 expression in the intermediate mesoderm (IM) has been proposed to play a c

53 erning of zebrafish renal progenitors in the intermediate mesoderm (IM) involves the formation of ros

54 ining as markers for the conversion of chick intermediate mesoderm (IM) to pronephric tissue and Lmx-

55 Amniote kidney tissue is derived from the intermediate mesoderm (IM), a strip of mesoderm that lie

56 onic red blood cells (RBCs) develop in trunk intermediate mesoderm (IM), and early macrophages develo

57 Kidney progenitors originate within the intermediate mesoderm (IM), but the pathways that establ

58 Kidney progenitors originate within the intermediate mesoderm (IM), but the pathways that set th

59 (UBs) in mutants emerge as doublets from the intermediate mesoderm (IM)-derived nephric duct (ND) wit

60 tly expressed in multiple derivatives of the intermediate mesoderm, implicating the cell of origin as

61 owed a strong beta-galactosidase activity in intermediate mesoderm in an embryonic day 10 embryo and

62 cific epithelial structures derived from the intermediate mesoderm in both males and females.

63 1), the earliest known gene expressed in the intermediate mesoderm, is blocked by cyclohexamide, indi

64 The intermediate mesoderm lies between the somites and the l

65 ced pluripotent stem cells through posterior intermediate mesoderm-like and adrenocortical progenitor

66 scence protein knocked into OSR1, a specific intermediate mesoderm marker.

67 cking both Foxc1 and Foxc2 show expansion of intermediate mesoderm markers into the paraxial domain,

68 class homeobox gene Lim1 is expressed in the intermediate mesoderm, nephric duct, mesonephric tubules

69 Moreover, expression in the intermediate mesoderm of Glial cell-derived neurotrophic

70 ndoderm and subsequently in the endoderm and intermediate mesoderm, prior to the expression of defini

71 In this study we identify the domain of intermediate mesoderm that gives rise to the nephric duc

72 irst epithelial tubule to differentiate from intermediate mesoderm that is essential for all further

73 there was a bounded contiguous region of the intermediate mesoderm that provides pronephric progenito

74 etanephric mesenchyme or blastema within the intermediate mesoderm, the earliest step of metanephric

75 Consistent with its expression in the intermediate mesoderm, the optic cup and stalk, and the

76 Odd1 is the earliest known marker of the intermediate mesoderm, the precursor to all kidney tissu

77 riction of the Eya1(+) population within the intermediate mesoderm to nephron-forming cell fates and

78 pronephric kidney which forms directly from intermediate mesoderm to test six2b function during pron

79 ox11 paralog expression is restricted in the intermediate mesoderm to the posterior, metanephric leve

80 established a robust induction protocol for intermediate mesoderm, which produces up to 90% OSR1(+)

81 hordamesoderm, embryoids display somitic and intermediate mesoderm, with beating cardiac tissue anter

82 kidney markers are expressed in a stripe of intermediate mesoderm, with distinct, overlapping antero