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1 ppearing sperm are not able to penetrate the zona pellucida.
2 l binding, penetration, and signaling by the zona pellucida.
3 ciated, sperm-binding ligand on the ovulated zona pellucida.
4 red for secretion and incorporation into the zona pellucida.
5  required for mouse sperm binding to the egg zona pellucida.
6 nd an inner, thick extracellular matrix, the zona pellucida.
7 and secreted prior to incorporation into the zona pellucida.
8 binding sulfated carbohydrates of the oocyte zona pellucida.
9  exocytosis, enabling sperm to penetrate the zona pellucida.
10 nding sites were distributed over the entire zona pellucida.
11  zonadhesin with differing avidities for the zona pellucida.
12 edominant form capable of binding to the pig zona pellucida.
13 induced acrosome reaction, and penetrate the zona pellucida.
14 cles in ovaries isolated from mice lacking a zona pellucida.
15 e involved in the sperm's passage across the zona pellucida.
16 e distinct native B cell determinants of the zona pellucida.
17 rior to secretion and incorporation into the zona pellucida.
18 fic and human sperm do not bind to the mouse zona pellucida.
19 rus into the oviduct, and binding to the egg zona pellucida.
20 mete recognition and penetration through the zona pellucida.
21 ible existence of a P-selectin ligand in the zona pellucida.
22 -selectin ligand is expressed in the porcine zona pellucida.
23 ion along the oviduct and penetration of the zona pellucida.
24 triggered by adhesion to the mammalian egg's zona pellucida.
25 l contact between the sperm and the oocyte's zona pellucida.
26 rovulated, adult mZP3-/- females also lack a zona pellucida.
27 grown oocytes, the oocytes completely lack a zona pellucida.
28 blocked hatching of the blastocysts from the zona pellucida.
29  are incapable of fusing with eggs that lack zona pellucida.
30 protein in the egg's extracellular coat, the zona pellucida.
31 ole in mediating the binding of sperm to the zona pellucida.
32 sperm binding and/or penetration through the zona pellucida.
33 ted the interaction of this protein with the zona pellucida.
34 ADAM2 with ADAM3 in sperm binding to the egg zona pellucida.
35 pigs and named for its binding to the oocyte zona pellucida.
36 rom these mutant mice cannot bind to the egg zona pellucida.
37 phic sperm with reduced ability to penetrate zona pellucida.
38 ire more thrust to penetrate the cumulus and zona pellucida.
39 acellular matrix of mouse eggs, known as the zona pellucida.
40 hrough the oocyte prior to assembly into the zona pellucida.
41 osis event that occurs upon contact with the zona pellucida.
42 drastically deficient in adhesion to the egg zona pellucida (0.3% of wild type) and to the egg plasma
43 -parathyroid hormone (Pth)-calcitonin (Calc)-zona pellucida 2 (2p2) was established.
44                            Autoantibody to a zona pellucida 3 (ZP3) epitope was found to induce autoi
45 olled by regulatory sequences from the mouse zona pellucida 3 (Zp3) gene, which is normally expressed
46 unction of CPEB after pachytene, we used the zona pellucida 3 (Zp3) promoter to generate transgenic m
47 t an analysis of the pattern of evolution of Zona Pellucida 3 (ZP3), a protein present on the avian e
48 ld-type mice, we have generated human ORMDL3 zona pellucida 3 Cre (hORMDL3(zp3-Cre)) mice that overex
49 n with the ZP3330-342 peptide of the ovarian zona pellucida 3 glycoprotein, ZP3.
50 h an epitope-specific autoantibody to murine zona pellucida 3 induces severe ovarian disease in neona
51 lgus macaques immunized with monkey or human zona pellucida 3 peptide (pZP3) in adjuvant, developed T
52 o found in an interaction domain of the ZP3 (zona pellucida 3) protein.
53 forms immune complex with endogenous ovarian zona pellucida 3, and a pathogenic CD4(+) T cell respons
54 ility and, given the conserved nature of the zona pellucida, a similar phenotype is expected in other
55                   To prevent polyspermy, the zona pellucida, a structure that surrounds mammalian egg
56 as a template the structure of CUB domain in zona pellucida adhesion protein PSP-I/PSP-II from porcin
57  of sperm to produce a secretory response to zona pellucida agonists.
58 t resulted in human sperm penetration of the zona pellucida and accumulation in the perivitelline spa
59  mice lacking ZP3 (Zp3(tm/tm)) do not form a zona pellucida and are infertile.
60 in Zp3-null mice, which never form a visible zona pellucida and are sterile.
61 oviducts causes premature degradation of the zona pellucida and embryo lysis, and wild-type embryos t
62 epare for the prospective penetration of the zona pellucida and fusion with the egg.
63                Acrosome reaction, binding to zona pellucida and fusion with the oolemma were lower in
64 that they demonstrate maximal binding to the zona pellucida and greatly increased sensitivity to iono
65 tein specifically reacted with ZP3 of oocyte zona pellucida and its affinity-purified antibodies comp
66 MII) oocytes exhibited irregularities of the zona pellucida and meiotic spindle.
67 ly embryo transduction protocols (removal of zona pellucida and subzonal microinjection).
68 ole of ZP2 in mediating sperm binding to the zona pellucida and support a model in which human sperm-
69       Sperm also bind transiently to the egg zona pellucida and the egg plasma membrane and then fuse
70 ctions between the cumulus cells outside the zona pellucida and the oocyte within.
71  is incorporated throughout the width of the zona pellucida and the transgenic mice are fertile.
72 st undergo capacitation in order to bind the zona pellucida and undergo a Ca(2+) ionophore-induced ac
73 P3, human sperm did not bind to the chimeric zona pellucida, and notwithstanding the absence of mouse
74 he sperm is induced by sperm adhesion to the zona pellucida, and signaling in the egg by gamete fusio
75 nteracts with the female reproductive tract, zona pellucida, and the oolemma.
76 es is known to have binding activity for the zona pellucida, and this action may serve to anchor sper
77        The multimeric forms did not bind the zona pellucida as avidly as did the p105/45 monomer.
78 ting that the changes that take place in the zona pellucida at fertilization affected the interaction
79                              These include a zona pellucida binding domain, which is present in a num
80                                              Zona pellucida binding protein 1 (ZPBP1), a spermatid an
81 , regulatory inhibitor subunit 1B (PPP1R1B), zona pellucida binding protein 2 (ZPBP2), and gasdermin
82  family of zinc finger 3 (AIOLOS; IKZF3) and zona pellucida binding protein 2 (ZPBP2).
83 6p21 (HLA-DQA1), 9p24 (IL33), and 17q12-q21 (zona pellucida binding protein 2 [ZPBP2]-gasdermin A [GS
84 s that rabbit proacrosin contains a specific zona pellucida binding site and that the loop containing
85 ike the latter, does not inhibit human sperm-zona pellucida binding under hemizona assay conditions.
86 ed, there was no significant effect on sperm-zona pellucida binding; however, fertilization was reduc
87 uding motility, capacitation, binding to the zona pellucida, binding to the oocyte membrane, and pene
88        Many candidates have been proposed as zona pellucida-binding proteins.
89 les in mouse eggs is required to produce the zona pellucida block to polyspermy.
90 ontact with the egg extracellular matrix, or zona pellucida, by the matrix glycoprotein ZP3.
91                                   Although a zona pellucida composed of ZP2 and ZP3 was formed around
92                                    The mouse zona pellucida consists of three glycoproteins that are
93         The mouse egg extracellular coat, or zona pellucida, consists of three glycoproteins, called
94               Results show that the ovulated zona pellucida contains at least two distinct ligands fo
95                                    The mouse zona pellucida contains three glycoproteins, ZP1, ZP2, a
96      Rgs2(-/-) eggs also underwent premature zona pellucida conversion in vivo.
97 ases that were sufficient to cause premature zona pellucida conversion.
98  channels during gamete interaction inhibits zona pellucida-dependent Ca2+ elevations, as demonstrate
99         ZP3, the glycoprotein agonist of the zona pellucida, depolarizes sperm membranes by activatin
100 lass, DPY, and terminating in a crosslinking zona pellucida domain and membrane anchor sequence.
101 des a light-responsive and membrane-anchored Zona Pellucida domain protein that supports light-depend
102 eins possess an N-terminal signal peptide, a zona pellucida domain, a consensus furin-like cleavage s
103 ct structure and contained peptides from the zona pellucida domain, which is involved in cell differe
104  DYF-7 contain, respectively, zonadhesin and zona pellucida domains, and DYF-7 self-associates into m
105                        In the absence of the zona pellucida, embryos lacking CTNNB1 undergo fission a
106 ibit the in vitro binding of murine sperm to zona pellucida-enclosed eggs.
107 es of capacitation, the ability to undergo a zona pellucida-evoked acrosome reaction, develops more s
108 e shotgun cell adhesion protein gene and the zona pellucida family transmembrane protein gene, CG1319
109 w comparisons to be made with the process of zona pellucida formation in mammals.
110                            Oocyte growth and zona pellucida formation proceed normally, but other asp
111                                 Treatment of zona pellucida-free eggs with chymotrypsin reduces the a
112 e normal when null spermatozoa were added to zona pellucida-free eggs, but in the presence of the ext
113  the oocyte membrane, and penetration of the zona pellucida-free oocyte.
114 he ability of Tenr mutant sperm to fertilize zona pellucida-free oocytes and to bind to, but not fert
115 sults demonstrate that a genetic defect in a zona pellucida gene causes infertility and, given the co
116  in coordinating the expression of the three zona pellucida genes during oogenesis.
117 coproteins in this regard because only human zona pellucida glycoprotein 3 (ZP3) and bovine proopiome
118 eta1,3-galactosyltransferase 1 (C1galt1)(FF):zona pellucida glycoprotein 3 Cre (ZP3Cre)] and Control
119 erm to specific O-linked oligosaccharides on zona pellucida glycoprotein 3.
120                                         Each zona pellucida glycoprotein is synthesized in growing oo
121 rides located at the sperm combining site of zona pellucida glycoprotein mZP3.
122 to be a cell-surface receptor for the murine zona pellucida glycoprotein ZP3, standard immunoelectron
123                                  ZP3, an egg zona pellucida glycoprotein, produces a sustained increa
124 protein that functions as a receptor for the zona pellucida glycoprotein, ZP3, and as an inducer of t
125  specific oligosaccharide ligands within the zona pellucida glycoprotein, ZP3, via beta1,4-galactosyl
126                                              Zona pellucida glycoproteins are responsible for species
127 ctin glycoprotein ligand-1 (PSGL-1) and from zona pellucida glycoproteins of porcine oocytes indicate
128  of these female fertilization proteins, the zona pellucida glycoproteins ZP2 and ZP3, are part of th
129 mZP3 (approximately 83 000 Mr), one of three zona pellucida glycoproteins, and once bound undergo the
130 ess GalTase bound ZP3 but did not bind other zona pellucida glycoproteins.
131 ndings and reveal novel functions for murine zona pellucida glycoproteins.
132    This extracellular matrix is known as the zona pellucida in eutherian mammals and consists of thre
133                  This matrix is known as the zona pellucida in mammals and is critically important fo
134 tively induced Ab to ZP3335-342 bound to the zona pellucida in the functional and degenerative ovaria
135          These embryos do not hatch from the zona pellucida in vitro, fail to grow in culture, and ex
136 e and produced antibody that bound to native zona pellucida in vivo.
137 ere to the extracellular coat of the egg, or zona pellucida, in a species-specific manner.
138 tein tyrosine phosphorylation as well as the zona pellucida-induced acrosome reaction.
139 cous media and in their ability to fertilize zona pellucida-intact eggs.
140 e oocytes and to bind to, but not fertilize, zona pellucida-intact oocytes suggests that the normal-a
141 purified antibodies completely blocked sperm-zona pellucida interaction in mice.
142 s that sp56 may function in acrosomal matrix-zona pellucida interactions during and immediately follo
143 l adhesion event between mouse sperm and the zona pellucida is a high affinity event which is suffici
144                                The mammalian zona pellucida is an egg extracellular matrix to which s
145                                          The zona pellucida is an extracellular matrix consisting of
146                                          The zona pellucida is an extracellular matrix that mediates
147                                    The mouse zona pellucida is composed of three glycoproteins (ZP1,
148                                    The mouse zona pellucida is composed of three glycoproteins (ZP1,
149                                    The mouse zona pellucida is composed of three glycoproteins (ZP1,
150                                 In mice, the zona pellucida is composed of three glycoproteins, but t
151                                    The mouse zona pellucida is composed of three glycoproteins, ZP1,
152                                The mouse egg zona pellucida is constructed of three glycoproteins, ca
153                     After fertilization, the zona pellucida is modified ad minimus by cleavage of ZP2
154 crosomes indicates that sperm binding to the zona pellucida is not sufficient to induce acrosome exoc
155  embryos, these data are consistent with the zona pellucida maintaining interactions between granulos
156 nal-vesicle-intact oocytes but that lacked a zona pellucida matrix and had a disorganized corona radi
157  present in MVA and is incorporated into the zona pellucida matrix of transgenic mice.
158 en mutated to prevent incorporation into the zona pellucida matrix, complementing earlier studies ind
159 rane domain and assembled into the insoluble zona pellucida matrix.
160                            Via its bipartite zona pellucida module (ZP-N/ZP-C), UMOD forms extracellu
161 erm initiate fertilization by binding to the zona pellucida (mZP), the specialized extracellular matr
162 uter covering of the egg known as the murine zona pellucida (mZP).
163 in which the supramolecular structure of the zona pellucida necessary for sperm binding is modulated
164       The antiserum also failed to label the zona pellucida of oocytes examined by laser scanning con
165  that mediate recognition and binding to the zona pellucida of the egg are still not understood.
166 ctivity interferes with sperm binding to the zona pellucida of the ovum.
167           Recombinant ZP3R/sp56 bound to the zona pellucida of unfertilized eggs but not to 2-cell em
168               SED1 binds specifically to the zona pellucida of unfertilized oocytes, but not to the z
169 specific manner to the extracellular matrix (zona pellucida) of the oocyte.
170                   The extracellular coat, or zona pellucida, of the mouse egg consists of three glyco
171 , that constitute the extracellular coat, or zona pellucida, of the oocyte.
172                        Adhesion to the egg's zona pellucida promotes Ca2+ influx through voltage-sens
173 ptor is closely related to that of the mouse zona pellucida protein ZP2.
174 hey do not acrosome-react in response to egg zona pellucida proteins and have reduced fertilizing abi
175 luorophore conjugated to solubilized porcine zona pellucida proteins to observe zona receptors on liv
176 ass spectrometric analysis of the native rat zona pellucida proteome (defined as the fraction of the
177 of the transient immunocontraceptive porcine zona pellucida (PZP), and found that repeated vaccinatio
178   However, the sperm proteins that recognise zona pellucida receptors remain contentious despite long
179                  Sperm at the surface of the zona pellucida remained acrosome-intact for more than 2
180 e folliculogenesis and those that encode the zona pellucida required for fertilization and early embr
181  present in a number of proteins such as the zona pellucida sperm binding proteins, and uromodulin, I
182 t occur until the morula stage, and that the zona pellucida suffices to maintain blastomere proximity
183                            The extracellular zona pellucida surrounding mammalian eggs is formed by i
184  required for formation of the extracellular zona pellucida surrounding mouse eggs.
185                                The mammalian zona pellucida surrounding ovulated eggs mediates sperm
186 tion in mammals is mediated primarily by the zona pellucida surrounding ovulated eggs.
187                                          The zona pellucida surrounding ovulated mouse eggs contains
188  fertilization occurs when sperm contact the zona pellucida surrounding the egg.
189 rcome barriers and penetrate the cumulus and zona pellucida surrounding the egg.
190                                          The zona pellucida surrounding the pig oocyte contains two M
191                            The extracellular zona pellucida surrounds mammalian eggs and mediates tax
192                            The extracellular zona pellucida surrounds ovulated eggs and mediates game
193 with high K(+) or by addition of solubilized zona pellucida (sZP).
194 ocytes and secreted to form an extracellular zona pellucida that mediates sperm binding and fertiliza
195       Specific binding of spermatozoa to the zona pellucida that surrounds mammalian eggs is a key st
196   Mammalian oocytes synthesize and secrete a zona pellucida that surrounds the growing oocytes, ovula
197  ZP3 is a protein in the mammalian egg coat (zona pellucida) that binds sperm and stimulates acrosoma
198 urrounded by a thick extracellular coat, the zona pellucida, that plays important roles during early
199 y a relatively thick extracellular coat, the zona pellucida, that plays vital roles during oogenesis,
200 ce of BSA, as measured by the ability of the zona pellucida to induce the acrosome reaction and by su
201 required for the structural integrity of the zona pellucida to minimize precocious hatching and reduc
202 n to the mammalian egg extracellular matrix (zona pellucida) to allow penetration of the egg coat.
203 at about 75-80% of the murine sperm bound to zona pellucida under well defined in vitro conditions is
204 rabbit sperm and shown to bind to homologous zona pellucida using an in vitro assay.
205     Although porcine sperm first contact the zona pellucida via their plasma membrane, the regions of
206 e sperm were able to fertilize eggs once the zona pellucida was removed but displayed persistent abno
207    At fertilization, mouse sperm bind to the zona pellucida (which consists of glycoproteins ZP1, ZP2
208 P-ZP3 associate with the inner aspect of the zona pellucida, which is distinct from the plasma membra
209 o establish a tenacious association with the zona pellucida, yet they are capable of fertilization.
210 odular extracellular segment that includes a zona pellucida (ZP) domain and several plasminogen N-ter
211                         Proteins harboring a zona pellucida (ZP) domain are prominent components of v
212                                          The zona pellucida (ZP) domain is a bipartite protein struct
213 ations; the Tecta(L1820F,G1824D/+) mouse for zona pellucida (ZP) domain mutations causing stable mid-
214 f protein, bone morphogenetic protein-1) and zona pellucida (ZP) domain-containing protein we find pr
215 h includes a domain of eight cysteines and a zona pellucida (ZP) domain.
216  proteins share a sequence designated as the zona pellucida (ZP) domain.
217 filaments and extracellular matrices through zona pellucida (ZP) domains.
218 f these proteins is related to mammalian egg zona pellucida (ZP) glycoproteins ZP1-3 and possesses an
219 ics (OMD), cortical granule (CG) status, and zona pellucida (ZP) hardening as well as the integrity o
220 ics (OMD), cortical granule (CG) exocytosis, zona pellucida (ZP) hardening, and spindle/chromatin int
221 e involved directly in binding to the female zona pellucida (ZP) in a species-specific manner.
222                                          The zona pellucida (ZP) is a highly organized extracellular
223 ) is essential to fertilization, and the egg zona pellucida (ZP) is generally believed to be an in vi
224 ge leading to conformational activation of a Zona Pellucida (ZP) polymerisation domain.
225            All mutant oocytes had an altered zona pellucida (ZP) that was thinner than the control ZP
226 tilization the spermatozoon binds to the egg zona pellucida (ZP) via sperm receptor(s) and undergoes
227 tion, mammalian sperm must first bind to the zona pellucida (ZP), a glycoprotein matrix surrounding t
228  expression of an antibody that binds to the zona pellucida (ZP), a glycoprotein matrix that surround
229                                          The zona pellucida (ZP), an ovarian extracellular structure,
230  spermatozoa bound tightly or penetrated the zona pellucida (ZP), and fewer underwent acrosome reacti
231 alpha-EC) binds to the microvillar region of zona pellucida (ZP)-free eggs, the region of the membran
232 r matrix coating of the oocyte, known as the zona pellucida (ZP).
233 pecies-specific binding activity for the egg zona pellucida (ZP).
234    At fertilization, spermatozoa bind to the zona pellucida (ZP1, ZP2, ZP3) surrounding ovulated mous

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