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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 s begins after hatching, suggesting that the vitelline envelope acts as a microbial barrier.
29 rix surrounding X. laevis eggs consists of a vitelline envelope and a jelly coat.
30  B46, and peptide A show clear inhibition of vitelline envelope liftoff by these three compounds.
31 de that the gp69/64 glycoproteins in the egg vitelline envelope mediate sperm-egg binding, an initial
32    Conversely, after fertilization, when the vitelline envelope of the egg is converted to the fertil
33 iotemporal pattern of tissue adhesion to the vitelline envelope provides controllable, counteracting
34 telline coat lysin (VCL) and female-specific vitelline envelope receptor for lysin (VERL) could ident
35                                      The egg vitelline envelope receptor for lysin had previously bee
36 versity of the amino-terminal end of the egg vitelline envelope receptor for lysin has been promoted
37 kDa abalone sperm protein that dissolves the vitelline envelope surrounding the egg.
38 es in a temporally coordinated manner to the vitelline envelope that surrounds the embryo.
39 -specificity in dissolving a hole in the egg vitelline envelope through which the sperm swims to reac
40 o the egg, its action required an intact egg vitelline envelope, and its action was independent of la
41 ring the conversion from the coelomic to the vitelline envelope, the gp69/64 sperm receptors become e
42 s on adhesion between the blastoderm and the vitelline envelope.
43 n is exposed that bonds the sperm to the egg vitelline envelope.
44 ently in the absence of the eggshell and the vitelline envelope.
45 in used by sperm to create a hole in the egg vitelline envelope.
46 receptor (gp69/64) in the Xenopus laevis egg vitelline envelope.
47 or sperm is localized on the plasma membrane-vitelline layer complex of the egg of the sea urchin Str
48 in which copurified with egg plasma membrane-vitelline layer complexes.
49  indicating that some of the receptor in the vitelline layer is cryptic and a possible function for t
50                            Disruption of the vitelline layer of the embryo envelope, which activates
51 nhibiting the formation of the extracellular vitelline layer of the fertilized embryo inside the uter
52 d extends from a sperm cell, penetrating the vitelline layer surrounding the egg.
53 60 serves to link the plasma membrane to the vitelline layer until fertilization.
54  as part of the protein complex known as the vitelline layer which serves as a precursor of the FE.
55 is elegans eggshell was composed of an outer vitelline layer, a middle chitin layer, and an inner lay
56 apidly assemble into the egg's extracellular vitelline layer, forming the fertilization envelope, a p
57 r cells are essential for the opening of the vitelline layer, further facilitating the micropyle's ro
58 ence mediated by inhibition of the embryonic vitelline layer.
59 ce required to extend the bundle through the vitelline layer.
60 rger than the force required to puncture the vitelline layer.
61 destined for either cortical granules or the vitelline layer.
62          Thus, p160 is a key candidate for a vitelline-layer linker protein, the selective proteolysi
63  lies between the embryonic membrane and the vitelline membrane (VM), the inner layer of the eggshell
64                                          The vitelline membrane (VM), the oocyte proximal layer of th
65  blastoderm disk is under the tension of the vitelline membrane (VM).
66  derivatives are gradually released from the vitelline membrane and become localized within distinct
67  is involved in coordinating assembly of the vitelline membrane and is required for functional proper
68           During early chorion formation the vitelline membrane appears to act as a reservoir for cho
69                                 Although the vitelline membrane appears to be morphologically complet
70 n, is essential for the morphogenesis of the vitelline membrane as sV23 protein null mutants lay flac
71 ive targets of Pipe, this work points to the vitelline membrane as the source of signals that generat
72 ruptions during the initial synthesis of the vitelline membrane by somatic follicle cells surrounding
73  chorion is dependent upon the presence of a vitelline membrane component.
74 ase autoactivation temporally coincides with vitelline membrane cross-linking and can be triggered in
75 onal regulation (cup, orb, bru1, me31B), and vitelline membrane formation (fs(1)N, fs(1)M3, clos).
76                                          The vitelline membrane is a specialized extracellular matrix
77 n (stages 8-10), were distributed within the vitelline membrane layer at all stages.
78 ins since s36 was found predominantly in the vitelline membrane layer of stage 12 egg chambers.
79 s to several protein components of the inner vitelline membrane layer of the eggshell.
80 t between the embryo plasma membrane and the vitelline membrane layer of the eggshell.
81 hree proproteins that are cleaved within the vitelline membrane layer to multiple derivatives.
82          These results also suggest that the vitelline membrane layer, by acting as a transient stora
83 vatives are generated in the oocyte proximal vitelline membrane layer, they are differentially distri
84 t necessary for the assembly of a functional vitelline membrane layer.
85  in each row of cells drives adhesion to the vitelline membrane mediated by integrins, apical spreadi
86 ential role in aligning molecules within the vitelline membrane network, much like hydrophobic domain
87  eggs with a soluble, rather than insoluble, vitelline membrane network.
88 on process, removing the outer proteinaceous vitelline membrane of nematode eggs.
89 glycoprotein, and a major constituent of the vitelline membrane of the avian yolk.
90                       Ovomucin isolated from vitelline membrane prevented adhesion of fibroblasts but
91 e other cell differentiation events, such as vitelline membrane protein expression, that lead to the
92                             Cross-linking of vitelline membrane protein sV23 also increases progressi
93 rmal uptake into the oocyte of sV17, a major vitelline membrane protein, and defects in non-disulfide
94                                sV23, a major vitelline membrane protein, is essential for the morphog
95  These mutations also block cross-linking of vitelline membrane proteins that normally occurs upon eg
96 tical granule exocytosis, which modifies the vitelline membrane to prevent polyspermy.
97 t abundant proprotein, is cleaved within the vitelline membrane to three mature derivatives in a deve
98 that additional structural components of the vitelline membrane undergo Pipe-dependent sulfation.
99 r anti-adhesive quality as the ovomucin from vitelline membrane, and that this anti-adhesive property
100 ermost layer of the Drosophila eggshell, the vitelline membrane, provides structural support and posi
101 ence of mechanosensitivity is not due to the vitelline membrane, rapid MG channel adaptation or tensi
102 sts of three major proteinaceous layers: the vitelline membrane, the inner chorionic layer, and the o
103                        Here we show that the vitelline membrane-like (VML) protein undergoes Pipe-dep
104 ell to produce a ventral cue embedded in the vitelline membrane.
105 astic plates representing the blastoderm and vitelline membrane.
106 d growth of disulfide linked networks in the vitelline membrane.
107 os were transiently dissociated within their vitelline membranes at different time points prior to th
108           Embryos surrounded by the abnormal vitelline membranes synthesized when Palisade is reduced
109  Nudel protease function produce eggs having vitelline membranes that are abnormally permeable to the
110 he caudal arteries (dorsal aorta, umbilical, vitelline) of 9.5 days post coitus (dpc) to 11.5 dpc mou
111 a protein of the parasite Fasciola hepatica (vitelline protein B [VpB]) and containing live Brucella
112 r protein of the parasite Fasciola hepatica (vitelline protein B).
113 ignaling, ultimately resulting in embryonic (vitelline) vasculopathy.
114 abeled 40-kDa dextran microperfused into the vitelline vein of 3-day-old embryos.
115 linear heart tube and the dorsal half of the vitelline vein.
116 stages and gives rise to embryonic blood and vitelline veins in the anterior ventral blood island (aV
117  the dorsal pancreatic endoderm; whereas the vitelline veins, which are normally adjacent to the emer
118 chimeric embryos, the embryos failed to form vitelline vessels and died at E9.5.
119 he gene is also expressed in Rathke's pouch, vitelline vessels and the limb mesenchyme.
120                                              Vitelline vessels regress by E10.5 in the remaining TEL-
121 irds of TEL-deficient yolk sacs at E9.5 lack vitelline vessels, yet possess capillaries, indicative o
122 layed activity in fetal liver, dorsal aorta, vitelline vessels, yolk sac, and heart.
123  the yolk sac capillary network into complex vitelline vessels.

 
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