ライフサイエンスコーパス: pronephros

1 detected in a small region of the developing pronephros.

2 evelopment and differentiation in retina and pronephros.

3 in organs such as Kupffer's vesicle and the pronephros.

4 ed terminal differentiation of the amphibian pronephros.

5 s derived from other germ layers such as the pronephros.

6 the formation of motile sensory cilia in the pronephros.

7 as caused by impaired differentiation of the pronephros.

8 zed its function in the developing amphibian pronephros.

9 nt hematopoietic sites such as the thymus or pronephros.

10 entially new methods of gene delivery to the pronephros.

11 l derivatives such as vasculature, blood and pronephros.

12 ogenesis of the larval amphibian kidney, the pronephros.

13 d in the neural tube and disorganized in the pronephros.

14 he first kidney to form in the embryo is the pronephros.

15 duce the formation of somitic muscle and the pronephros.

16 te the role for pax2.1 in development of the pronephros.

17 ishment of the Xenopus embryonic kidney, the pronephros.

18 ive mutations that affect development of the pronephros.

19 ected in the developing nephric duct and the pronephros.

20 he neural crest, central nervous system, and pronephros, all defects that were rescued by a Cby-GFP c

21 vis embryos to manipulation make the Xenopus pronephros an attractive system in which to study organo

22 nal glomerulus but retention of a functional pronephros, an arrangement similar to the aglomerular ki

23 ations that perturb the entire length of the pronephros and body axis curvature.

24 also expressed in other organs, such as the pronephros and liver primordium.

25 s, podocytes are stationary in the zebrafish pronephros and neither migrate nor change their branchin

26 ongly affect cilia motility in the zebrafish pronephros and neural tube.

27 matically extends its effect to head, heart, pronephros and pronephric duct mesoderm inducing early b

28 ion of the late distal tubule of the Xenopus pronephros and regulates renal epithelial cell different

29 exclusive from the dorsal mesoderm whereas, pronephros and tail originate from both dorsal and ventr

30 The simple organisation of the pronephros and the amenability of Xenopus laevis embryos

31 The two most anterior structures, the pronephros and the mesonephros, are transitory and large

32 strate that vascularization of the zebrafish pronephros and the onset of glomerular filtration occurs

33 physiological degeneration of the amphibian pronephros and to the development of the cement gland an

34 CDC11 leads to defective ciliogenesis in the pronephros and within the Kupffer's vesicle and results

35 e mesoderm fated to become the nephric duct, pronephros, and mesonephros.

36 otch signalling patterns the early X. laevis pronephros anlagen, a function that might be conserved i

37 the medio-lateral axis of the dorso-anterior pronephros anlagen, permitting the glomus and tubules to

38 gnalling in the dorso-anterior region of the pronephros anlagen.

39 echanisms that regulate cell fate within the pronephros are poorly understood but are important for t

40 postfertilization and distension/dilation of pronephros at 5 d postfertilization (dpf).

41 es are primarily expressed in the spleen and pronephros (bone marrow equivalent), and ontogenically,

42 versus transporting epithelial cells in the pronephros by way of a genetic pathway involving repress

43 In this work, we test whether the zebrafish pronephros can be used as an assay system for the develo

44 The pronephros consists of two nephrons with fused glomeruli

45 ces lmx1b in a genetic hierarchy involved in pronephros development and suggests that it is the balan

46 essential and novel mechanisms that control pronephros development in the zebrafish.

47 Notch signaling is involved in pronephros development in Xenopus and in glomerulogenesi

48 MX1B and ABRA act in a common pathway during pronephros development.

49 es and is enriched in neural tissues and the pronephros during later embryogenesis.

50 days in ovo, the mesonephros as well as the pronephros failed to develop on the experimental side.

51 ecific gene expression in the portion of the pronephros fated to form its vascular structure, the glo

52 he kidney, such as tnnt2a, or elimination of pronephros fluid output through knockdown of the intrafl

53 h the normal pattern of Pax-2 expression and pronephros formation.

54 after focal destruction, such that a normal pronephros forms after laser-mediated removal of the wt1

55 ired and sufficient for the induction of the pronephros from the chick IM.

56 gene ift88, was not associated with ectopic pronephros gene expression, thus suggesting a unique rol

57 whether paraxial mesoderm is sufficient for pronephros induction, stage 7 or earlier chick lateral p

58 The fish larval pronephros is a relevant kidney in which to pursue many

59 The Xenopus pronephros is a simple paired organ; each nephron consis

60 The zebrafish pronephros is also associated with the corpuscles of Sta

61 The pronephros is the first to form and is the functional em

62 renal cyst formation because its kidney (the pronephros) is simple and genes that cause cystic kidney

63 The zebrafish embryonic kidney, or pronephros, is a simplified yet conserved genetic model

64 In the pronephros, kcnj1 transcript expression was restricted t

65 cyp2k22 and slco1f4 was demonstrated in the pronephros; lipca was detected in the liver, and sult2st

66 nd synergist cyst formation in the zebrafish pronephros model.

67 s, angiogenesis of intersomitic vessels, and pronephros morphogenesis.

68 In the zebrafish pronephros, multiciliated cells (MCCs) are specialized f

69 ent of other mesoderm derivatives, including pronephros, muscle and lateral plate is not disrupted.

70 malian metanephros and also in the primitive pronephros of fish and amphibian larvae.

71 To address this question, the pronephros of translucent zebrafish larvae (casper) expr

72 be so derived from the hematopoietic kidney (pronephros) of a red-blooded Antarctic rockcod, Notothen

73 l mesoderm and IM before stage 8 developed a pronephros on the control side only.

74 The zebrafish pronephros provides a conserved model to study kidney de

75 The zebrafish pronephros provides an excellent in vivo system to study

76 Progenitors of the zebrafish pronephros, red blood and trunk endothelium all originat

77 iption factors irx3b and sim1a that mitigate pronephros segment patterning.

78 in many physiological functions, influenced pronephros segmentation.

79 and functional analysis of newly identified pronephros-specific genes are also described.

80 ibuted in a ;salt-and-pepper' fashion in the pronephros, suggesting that a lateral inhibition mechani

81 ate-1, and Delta-1 in the developing Xenopus pronephros suggests a role for this pathway in cell fate

82 The pronephros, the major hematopoietic organ in the adult f

83 acterised by the successive formation of the pronephros, the mesonephros and the metanephros.

84 in the epithelial structures of the Xenopus pronephros, the tubules and the duct, but not the glomus

85 es recent progress in applying the zebrafish pronephros to issues of human health and development.

86 e partially redundant functions to establish pronephros tubule epithelium polarity.

87 rmined the precise timing of these events in pronephros tubulogenesis.

88 Morphogenesis of the pronephros was examined in UV-ventralized and lithium-do

89 To determine whether the pronephros was induced by adjacent tissues and, if so, t

90 In the current study, the chick pronephros was used as a model system to identify tissue

91 The Xenopus pronephros was used as a paradigm to address this questi

92 the experiments presented here, the Xenopus pronephros was used as a simple model system to examine

93 ession patterns of the embryonic kidney, the pronephros, will be described and compared to the more c