ライフサイエンスコーパス: vitelline

1 ny of the same signaling factors used by the vitelline and cardiovascular systems, and they contained

2 nd in the aorta-gonad-mesonephros region and vitelline and umbilical arteries of the midgestation mou

3 However, not all HPCs in the aorta, vitelline and umbilical arteries, and fetal liver requir

4 ls expressing Cbfa2 are in the yolk sac, the vitelline and umbilical arteries, and in the ventral asp

5 ar regions of the mouse conceptus-the aorta, vitelline and umbilical arteries, yolk sac and placenta.

6 terns delineated flow through the umbilical, vitelline, and other major blood vessels.

7 s of the major embryonic vasculature (aorta, vitelline, and umbilical arteries) and are found in intr

8 Here we show that umbilical cord and vitelline arteries (VAs), but not veins, contain pre-HSC

9 the placental vessels, and the umbilical and vitelline arteries initiate expression of the transcript

10 ported locations, the proximal umbilical and vitelline arteries.

11 ns that experience the highest flow near the vitelline artery and vein.

12 rated all over the primordia surrounding the vitelline blood vessel at embryonic day 2 (E2), then bec

13 ding wide size variation among the precursor vitelline bodies and disorganization of follicle cell mi

14 ocess, proliferation, and differentiation of vitelline cells, expression of female-specific genes and

15 uld cause the resultant abnormalities in the vitelline circulation by affecting VEGF/VEGF receptor si

16 imilarities in the pathology of the abnormal vitelline circulation in many of these conditions, we hy

17 Establishment of the vitelline circulation is crucial for normal embryonic gr

18 formation and/or maintenance of a functional vitelline circulation.

19 us edulis found transcripts of male-specific vitelline coat lysin (VCL) and female-specific vitelline

20 activity of the FE, but did not inhibit the vitelline delaminase activity that has been implicated i

21 use 16 kDa lysin to create a hole in the egg vitelline envelope (VE) by a species-specific, nonenzyma

22 The rainbow trout egg vitelline envelope (VE) is constructed of three proteins

23 pecies selectively creates a hole in the egg vitelline envelope (VE) through which the sperm passes t

24 6-kDa protein that creates a hole in the egg vitelline envelope (VE) through which the sperm swims to

25 molecular basis of sperm binding to the egg vitelline envelope (VE), a competition assay was used an

26 The extracellular coat, or vitelline envelope (VE), of rainbow trout (Oncorhynchus

27 ze the constituent proteins of the egg coat [vitelline envelope (VE)] of abalone eggs and to provide

28 rix surrounding X. laevis eggs consists of a vitelline envelope and a jelly coat.

29 B46, and peptide A show clear inhibition of vitelline envelope liftoff by these three compounds.

30 de that the gp69/64 glycoproteins in the egg vitelline envelope mediate sperm-egg binding, an initial

31 Conversely, after fertilization, when the vitelline envelope of the egg is converted to the fertil

32 telline coat lysin (VCL) and female-specific vitelline envelope receptor for lysin (VERL) could ident

33 The egg vitelline envelope receptor for lysin had previously bee

34 versity of the amino-terminal end of the egg vitelline envelope receptor for lysin has been promoted

35 kDa abalone sperm protein that dissolves the vitelline envelope surrounding the egg.

36 -specificity in dissolving a hole in the egg vitelline envelope through which the sperm swims to reac

37 o the egg, its action required an intact egg vitelline envelope, and its action was independent of la

38 ring the conversion from the coelomic to the vitelline envelope, the gp69/64 sperm receptors become e

39 n is exposed that bonds the sperm to the egg vitelline envelope.

40 ently in the absence of the eggshell and the vitelline envelope.

41 in used by sperm to create a hole in the egg vitelline envelope.

42 receptor (gp69/64) in the Xenopus laevis egg vitelline envelope.

43 or sperm is localized on the plasma membrane-vitelline layer complex of the egg of the sea urchin Str

44 in which copurified with egg plasma membrane-vitelline layer complexes.

45 indicating that some of the receptor in the vitelline layer is cryptic and a possible function for t

46 d extends from a sperm cell, penetrating the vitelline layer surrounding the egg.

47 60 serves to link the plasma membrane to the vitelline layer until fertilization.

48 as part of the protein complex known as the vitelline layer which serves as a precursor of the FE.

49 is elegans eggshell was composed of an outer vitelline layer, a middle chitin layer, and an inner lay

50 apidly assemble into the egg's extracellular vitelline layer, forming the fertilization envelope, a p

51 ce required to extend the bundle through the vitelline layer.

52 rger than the force required to puncture the vitelline layer.

53 destined for either cortical granules or the vitelline layer.

54 Thus, p160 is a key candidate for a vitelline-layer linker protein, the selective proteolysi

55 lies between the embryonic membrane and the vitelline membrane (VM), the inner layer of the eggshell

56 The vitelline membrane (VM), the oocyte proximal layer of th

57 derivatives are gradually released from the vitelline membrane and become localized within distinct

58 is involved in coordinating assembly of the vitelline membrane and is required for functional proper

59 During early chorion formation the vitelline membrane appears to act as a reservoir for cho

60 Although the vitelline membrane appears to be morphologically complet

61 n, is essential for the morphogenesis of the vitelline membrane as sV23 protein null mutants lay flac

62 ive targets of Pipe, this work points to the vitelline membrane as the source of signals that generat

63 ruptions during the initial synthesis of the vitelline membrane by somatic follicle cells surrounding

64 chorion is dependent upon the presence of a vitelline membrane component.

65 ase autoactivation temporally coincides with vitelline membrane cross-linking and can be triggered in

66 The vitelline membrane is a specialized extracellular matrix

67 n (stages 8-10), were distributed within the vitelline membrane layer at all stages.

68 ins since s36 was found predominantly in the vitelline membrane layer of stage 12 egg chambers.

69 s to several protein components of the inner vitelline membrane layer of the eggshell.

70 t between the embryo plasma membrane and the vitelline membrane layer of the eggshell.

71 hree proproteins that are cleaved within the vitelline membrane layer to multiple derivatives.

72 These results also suggest that the vitelline membrane layer, by acting as a transient stora

73 vatives are generated in the oocyte proximal vitelline membrane layer, they are differentially distri

74 t necessary for the assembly of a functional vitelline membrane layer.

75 ential role in aligning molecules within the vitelline membrane network, much like hydrophobic domain

76 eggs with a soluble, rather than insoluble, vitelline membrane network.

77 on process, removing the outer proteinaceous vitelline membrane of nematode eggs.

78 glycoprotein, and a major constituent of the vitelline membrane of the avian yolk.

79 Ovomucin isolated from vitelline membrane prevented adhesion of fibroblasts but

80 e other cell differentiation events, such as vitelline membrane protein expression, that lead to the

81 Cross-linking of vitelline membrane protein sV23 also increases progressi

82 rmal uptake into the oocyte of sV17, a major vitelline membrane protein, and defects in non-disulfide

83 sV23, a major vitelline membrane protein, is essential for the morphog

84 These mutations also block cross-linking of vitelline membrane proteins that normally occurs upon eg

85 tical granule exocytosis, which modifies the vitelline membrane to prevent polyspermy.

86 t abundant proprotein, is cleaved within the vitelline membrane to three mature derivatives in a deve

87 that additional structural components of the vitelline membrane undergo Pipe-dependent sulfation.

88 r anti-adhesive quality as the ovomucin from vitelline membrane, and that this anti-adhesive property

89 ermost layer of the Drosophila eggshell, the vitelline membrane, provides structural support and posi

90 ence of mechanosensitivity is not due to the vitelline membrane, rapid MG channel adaptation or tensi

91 sts of three major proteinaceous layers: the vitelline membrane, the inner chorionic layer, and the o

92 Here we show that the vitelline membrane-like (VML) protein undergoes Pipe-dep

93 ell to produce a ventral cue embedded in the vitelline membrane.

94 astic plates representing the blastoderm and vitelline membrane.

95 d growth of disulfide linked networks in the vitelline membrane.

96 os were transiently dissociated within their vitelline membranes at different time points prior to th

97 Embryos surrounded by the abnormal vitelline membranes synthesized when Palisade is reduced

98 Nudel protease function produce eggs having vitelline membranes that are abnormally permeable to the

99 a protein of the parasite Fasciola hepatica (vitelline protein B [VpB]) and containing live Brucella

100 r protein of the parasite Fasciola hepatica (vitelline protein B).

101 ignaling, ultimately resulting in embryonic (vitelline) vasculopathy.

102 abeled 40-kDa dextran microperfused into the vitelline vein of 3-day-old embryos.

103 linear heart tube and the dorsal half of the vitelline vein.

104 stages and gives rise to embryonic blood and vitelline veins in the anterior ventral blood island (aV

105 the dorsal pancreatic endoderm; whereas the vitelline veins, which are normally adjacent to the emer

106 chimeric embryos, the embryos failed to form vitelline vessels and died at E9.5.

107 he gene is also expressed in Rathke's pouch, vitelline vessels and the limb mesenchyme.

108 Vitelline vessels regress by E10.5 in the remaining TEL-

109 irds of TEL-deficient yolk sacs at E9.5 lack vitelline vessels, yet possess capillaries, indicative o

110 layed activity in fetal liver, dorsal aorta, vitelline vessels, yolk sac, and heart.

111 the yolk sac capillary network into complex vitelline vessels.