ライフサイエンスコーパス: mesonephros

1 coitum (dpc) on the ventromedial side of the mesonephros.

2 1(+) mesenchymal cells that migrate from the mesonephros.

3 by mature structures such as the somites or mesonephros.

4 ds arise on the ventromedial surface of each mesonephros.

5 rs that are repressed by the presence of the mesonephros.

6 y coelomic epithelium invagination along the mesonephros.

7 lockade on the WD cultured in the absence of mesonephros.

8 to become the nephric duct, pronephros, and mesonephros.

9 ation in the absence of a developing pro- or mesonephros.

10 of homeotic transformation of metanephros to mesonephros.

11 ue and Lmx-1 mRNA expression as a marker for mesonephros.

12 umber of endothelial cells from the adjacent mesonephros, a mechanism totally absent in XX gonads.

13 the PGE2-cAMP-PKA pathway in the aorta-gonad-mesonephros (AGM) abolished enhancement in hematopoietic

14 c stem cells (HSCs) arise in the aorta-gonad-mesonephros (AGM) and mature as they transit through the

15 c stem cell emergence, viz., the aorta-gonad-mesonephros (AGM) and the fetal liver at 10.5-11.5 dpc,

16 Moreover, we show that aorta-gonad-mesonephros (AGM) cells from Mll-deficient embryos lacke

17 tive direct Notch targets in the aorta-gonad-mesonephros (AGM) embryonic tissue by chromatin precipit

18 slightly later in the zebrafish aorta/gonad/mesonephros (AGM) equivalent.

19 identical manner to vertebrate aorta-gonadal-mesonephros (AGM) HSCs.

20 poietic stem cells (HSCs) in the aorta-gonad-mesonephros (AGM) of the developing mouse embryo.

21 radiated adult mice arise in the aorta-gonad-mesonephros (AGM) on embryonic day 11.5 (E11.5).

22 Of them, the aorta-gonad-mesonephros (AGM) region drew particular attention owing

23 e novo expression of Hes5 in the aorta/gonad/mesonephros (AGM) region of Hes1 mutants.

24 (CD34(+)c-kit(+)) cells from the aorta-gonad-mesonephros (AGM) region of the developing mouse are mul

25 stem cells (HSCs) emerge in the aorta-gonads-mesonephros (AGM) region of the embryo.

26 mogenic endothelium within the aorta, gonad, mesonephros (AGM) region of the mammalian embryo is cruc

27 fates concurrently occur in the aorta-gonad-mesonephros (AGM) region prior to haematopoietic stem ce

28 inactivated SCL in yolk sac, the aortagonad-mesonephros (AGM) region, and fetal liver hematopoietic

29 HSCs were not released from the aorta-gonad-mesonephros (AGM) region, as evidenced by the accumulati

30 tem cells (HSCs) emerge from the aorta-gonad-mesonephros (AGM) region, but the molecular regulation o

31 an intraembryonic location, the aorta-gonad-mesonephros (AGM) region, is a site of residence and, po

32 t human HSCs emerge first in the aorta-gonad-mesonephros (AGM) region, specifically in the dorsal aor

33 such as the dorsal aorta of the aorta-gonad-mesonephros (AGM) region, suggesting that signals from t

34 lly dissect HSC emergence in the aorta-gonad-mesonephros (AGM) region, we screened a collection of in

35 l population that resides in the aorta-gonad-mesonephros (AGM) region.

36 stem cells (HSCs) arise in the aorta-gonads-mesonephros (AGM) region.

37 ntral domain of the aorta in the aorta-gonad-mesonephros (AGM) region.

38 etic stem cells in amniotes, the aorta-gonad-mesonephros (AGM) region.

39 the zebrafish equivalent to the aorta-gonad-mesonephros (AGM) region.

40 pendent expansion of HSCs in the aorta-gonad-mesonephros (AGM) region.

41 the dorsal aorta in the aorta/genital ridge/mesonephros (AGM) region.

42 vested from embryonic day 9 (E9) aorta-gonad-mesonephros (AGM) regions of GATA2 null embryos showed r

43 topoietic stem cells (HSCs) from aorta/gonad/mesonephros (AGM) regions of midgestation mouse embryos

44 Rare endothelial cells in the aorta-gonad-mesonephros (AGM) transition into hematopoietic stem cel

45 similar to hematopoiesis in the aorta-gonad-mesonephros (AGM).

46 tic splanchnopleura known as the aorta-gonad-mesonephros (AGM).

47 mice lacking RA synthesis and signalling in mesonephros and adjacent gonad and reveal that Stra8 exp

48 embryonic day 10.5 by the thickening of the mesonephros and consist of somatic cells and migratory p

49 ls are required for proper patterning of the mesonephros and metanephros.

50 ullerian duct, and developing tubules in the mesonephros and metanephros.

51 12.0, transgene expression was absent in the mesonephros and metanephros.

52 We also show that the region between the mesonephros and the gonad harbors steroidogenic cell pre

53 successive formation of the pronephros, the mesonephros and the metanephros.

54 embryos, embryonic day (E) 12.5 female gonad/mesonephros, and newborn ovary.

55 ube derived from an epithelial anlage at the mesonephros anterior end, which then segregates from the

56 d/or para-aorta-splanchno-pleura/aorta-gonad-mesonephros are hypothesized to colonize the fetal liver

57 anterior structures, the pronephros and the mesonephros, are transitory and largely non-functional,

58 ated embryos cultured for 3 days in ovo, the mesonephros as well as the pronephros failed to develop

59 TH-responsive cells are present at the gonad/mesonephros border and seem to migrate into the XY but n

60 helium and specialized cells along the gonad-mesonephros border.

61 opoietic stem cells (HSC) in the aorta-gonad-mesonephros by abrogating Smad1 expression and the conse

62 During mesonephros development, it was expressed in the Wolffia

63 WDs without mesonephros did not form ectopic buds even in the presen

64 n (area comprising dorsal aorta, gonads, and mesonephros) during day 10 of development.

65 assay and in embryonic day 10.5 aorta-gonad-mesonephros explants.

66 ve and excretory tissues, including livers > mesonephros > guts > gallbladder.

67 ack, unilateral anomalous development of the mesonephros in males causes atresia of the homolateral e

68 mination, mesenchymal cells migrate from the mesonephros into the adjacent developing testis.

69 elopment, endothelial cells migrate from the mesonephros into the gonad to form a coelomic blood vess

70 hat steroidogenic cells can migrate from the mesonephros into the XY gonad.

71 induction of somatic cell migration from the mesonephros into the XY gonad.

72 ortic splanchnopleura, yolk sac, aorta-gonad-mesonephros, liver, and bone marrow (BM).

73 e functioning in the mammalian aorta-gonadal-mesonephros mesoderm.

74 Thus, a failure of development of mesonephros/mesonephric duct gives rise to absent ureter

75 nted in the Wolffian (mesonephric) duct, the mesonephros, metanephros and fetal gonads.

76 Transgenic mice that express GFP in the mesonephros, metanephros, ureteric bud, and sex ducts ma

77 Flow sorting of thrombocytes from the mesonephros of adult CD41-GFP zebrafish showed a GFP(hig

78 the para-aortic splanchnopleura/aorta-gonads-mesonephros of mouse embryos and that abrogation of nitr

79 -aortic splanchnopleura/aorta-genital ridges-mesonephros (P-Sp/AGM) region are the main sites of haem

80 ting cells from murine yolk sac, aorta-gonad-mesonephros, placenta, fetal liver, and bone marrow with

81 ce in the normal position in the aorta-gonad-mesonephros region and also in the yolk sac.

82 undergoes dramatic growth in the aorta-gonad-mesonephros region and by E11.5 reaches the size that ma

83 ls (HSCs) are first found in the aorta-gonad-mesonephros region and vitelline and umbilical arteries

84 itors are first generated in the aorta-gonad-mesonephros region between days 27 and 40 of human embry

85 c stem cells (HSCs) in the mouse aorta-gonad-mesonephros region emerge between embryonic days 10.5 an

86 genitor cells derived from the aorto gonadal mesonephros region of day 11 mouse embryos on the Jagged

87 (HSCs) that first appear in the aorta-gonado-mesonephros region of the fetus on embryonic day (E) 10.

88 The aorta-gonad-mesonephros region plays an important role in hematopoie

89 ived during embryogenesis in the aorta-gonad-mesonephros region subsequently colonize fetal and adult

90 on and atria earlier than in the aorta-gonad-mesonephros region, and is transient and definitive in n

91 CX3CR1(+) cells localized to the aorta-gonad-mesonephros region, and visualized at embryonic day (E)9

92 they are first generated in the aorta-gonad-mesonephros region, but at later developmental stages, i

93 od vessel walls in the yolk sac, aorta-gonad-mesonephros region, embryonic liver, and fetal bone marr

94 os developed cd41(+) HSCs in the aorta-gonad-mesonephros region, which later migrated to the kidney,

95 cell induction in the zebrafish aorta-gonad-mesonephros region.

96 e hematopoietic stem cell in the aorta-gonad-mesonephros region.

97 poietic cluster formation in the aorta-gonad-mesonephros region; embryonic-to-adult transplantation s

98 centa parallels that of the AGM (aorta-gonad-mesonephros) region starting at E10.5-E11.0.

99 endent induction of Stra8, but only when the mesonephros remains attached, pointing to a non-RA signa

100 pression pattern of the transgene in the pro/mesonephros suggest an intraembryonic site of developmen

101 tached, pointing to a non-RA signal from the mesonephros that induces Stra8 in the adjacent gonad.

102 sult from failure of cell migration from the mesonephros, thought to be a possible source of Leydig c

103 OFFgration from the mesonephros to the gonad is male specific at this stage

104 ivity to identify cells contributed from the mesonephros to the male or female gonad.

105 When cultured with the surrounding mesonephros, WDs formed many ectopic buds in response to

106 d11 is ectopically activated in the anterior mesonephros, we observe a partial transformation to a me

107 Somatic cells contributed from the mesonephros were distinguished by their histological loc