コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ilamentous structures in prometaphase I upon oocyte maturation.
2 lasmic polyadenylation during Xenopus laevis oocyte maturation.
3 al transcripts that are normally lost during oocyte maturation.
4 se and mechanism of ER reorganisation during oocyte maturation.
5 yogenesis, cuticle turnover, egg laying, and oocyte maturation.
6 eal an important link between metabolism and oocyte maturation.
7 B)/Akt regulation of PDE3A and its impact on oocyte maturation.
8 ecially in expression of genes important for oocyte maturation.
9 rminal vesicle breakdown are major events in oocyte maturation.
10 ell interaction, an absolute requirement for oocyte maturation.
11 3/12 ligands SPC and S1P delayed spontaneous oocyte maturation.
12 reases early CPEB phosphorylation and delays oocyte maturation.
13 have an essential and redundant function in oocyte maturation.
14 fertilization-specific Ca(2+) signal during oocyte maturation.
15 d several aspects of PAR-3 expression during oocyte maturation.
16 n the early steps of progesterone-stimulated oocyte maturation.
17 gered by LH, including cumulus expansion and oocyte maturation.
18 tic spindle formation was observed following oocyte maturation.
19 ing mid-oogenesis and increases further upon oocyte maturation.
20 nt Ca(2+) release is greatly enhanced during oocyte maturation.
21 degraded within a several hour period during oocyte maturation.
22 rganelle positioning and distribution during oocyte maturation.
23 ns of maternal mRNAs observed during Xenopus oocyte maturation.
24 a(2+)(cyt)) plays a dual role during Xenopus oocyte maturation.
25 that prevents premature MAPK activation and oocyte maturation.
26 ytoplasmic polyadenylation, translation, and oocyte maturation.
27 n considered the primary mediator of Xenopus oocyte maturation.
28 changes in protein levels during Drosophila oocyte maturation.
29 d for the influence of overexpressed XGef on oocyte maturation.
30 , XKCM1, NuMA, and cytoplasmic dynein during oocyte maturation.
31 unction through the Mos pathway to influence oocyte maturation.
32 entity of the receptor as an intermediary in oocyte maturation.
33 MAP kinase kinase kinase, is a regulator of oocyte maturation.
34 PF is necessary for SOCE inactivation during oocyte maturation.
35 r (MPF) kinase cascade, which drives Xenopus oocyte maturation.
36 nal activation of mRNAs that are crucial for oocyte maturation.
37 the expression of CPEB during oogenesis and oocyte maturation.
38 that regulates translation during vertebrate oocyte maturation.
39 maturing oocytes and function redundantly in oocyte maturation.
40 st epithelial cells and induction of Xenopus oocyte maturation.
41 c prophase I arrest through a process termed oocyte maturation.
42 clusters at the microvillar subcortex during oocyte maturation.
43 ne, are the physiologic mediators of Xenopus oocyte maturation.
44 f SERCA is further indication of its role in oocyte maturation.
45 e, and is released into the egg cytoplasm at oocyte maturation.
46 imal synthesis of CPEB, <3.6%, occurs during oocyte maturation.
47 s sufficient to mediate these effects during oocyte maturation.
48 s Gbetagamma subunits constitutively inhibit oocyte maturation.
49 component of ring canals and is required for oocyte maturation.
50 quired for protein synthesis during starfish oocyte maturation.
51 ylation, which stimulates translation during oocyte maturation.
52 n B1 mRNA translational control during mouse oocyte maturation.
53 restore EGFR-dependent cumulus expansion and oocyte maturation.
54 s polyadenylation-induced translation during oocyte maturation.
55 otein accumulation has been shown to inhibit oocyte maturation.
56 activates MAP kinase, which in turn leads to oocyte maturation.
57 mRNA and its subsequent translation, and for oocyte maturation.
58 eiotic divisions during progesterone-induced oocyte maturation.
59 ctivation of a specific maternal mRNA during oocyte maturation.
60 (1) Both spermatids and spermatozoa induce oocyte maturation.
61 ch contributes to the all-or-none process of oocyte maturation.
62 phosphorylation state changes during Xenopus oocyte maturation.
63 be involved in progesterone-induced Xenopus oocyte maturation.
64 NAs and proteins deposited in the egg during oocyte maturation.
65 Interestingly, Zar2 levels decreased during oocyte maturation.
66 translation of reporter mRNAs during Xenopus oocyte maturation.
67 enter or exit the polysome pool during mouse oocyte maturation.
68 on to stimulate MPK-1 activity essential for oocyte maturation.
69 a similar situation also occurs during mouse oocyte maturation.
70 terone-induced MAPK-signaling during Xenopus oocyte maturation.
71 ate translation of mRNA targets required for oocyte maturation.
72 synthesis and phosphorylation in vivo during oocyte maturation.
73 aternal mRNA translational activation during oocyte maturation.
74 ns co-localised with mitochondria throughout oocyte maturation.
75 tion of MAPK, and inhibited MebetaCD-induced oocyte maturation.
76 fertilization-specific Ca(2+) signal during oocyte maturation.
77 (2+), and whose amount increases during late oocyte maturation.
78 ne-signaling pathway that leads to amphibian oocyte maturation.
79 e that binds to the Eph receptor and induces oocyte maturation.
80 requirements for PMCA internalization during oocyte maturation.
81 nylation and translational activation during oocyte maturation.
85 of several integral membrane proteins during oocyte maturation, a requisite process for early embryog
86 act that carries out the signaling events of oocyte maturation after addition of the heat-stable inhi
87 were detectable during progesterone-induced oocyte maturation, after egg fertilization, or during th
88 ominant negative raf blocks JNK induction of oocyte maturation, again suggesting cross-talk between p
90 nd OMA-2 are redundant proteins required for oocyte maturation--an essential part of meiosis that pre
91 Overall, we find that ALADIN is critical for oocyte maturation and appears to be far more essential f
92 XGef and CPEB interact during oogenesis and oocyte maturation and are present in a c-mos messenger r
94 ogen-activated protein kinase during Xenopus oocyte maturation and during mitosis in Xenopus egg extr
96 period can induce remarkable effects on both oocyte maturation and early embryo development, which in
97 increases during oogenesis, persists during oocyte maturation and early embryogenesis, and then fall
99 is a recurring theme in the biochemistry of oocyte maturation and early embryogenesis; the Mos/MEK/p
100 the largest transcriptome data set of bovine oocyte maturation and early embryonic development and de
103 ise the hypothesis that MAPK activity during oocyte maturation and early fertilization is required fo
104 such as Drosophila, Xenopus, and the mouse, oocyte maturation and early pattern formation is mediate
106 egrating datasets on the proteome changes at oocyte maturation and egg activation uncovers dynamics i
107 a kinase that has multiple functions during oocyte maturation and egg activation, for example, spind
108 led diabetes mellitus (DM) adversely affects oocyte maturation and embryo development via mechanisms
111 ese vesicles undergo dynamic movement during oocyte maturation and exocytosis at the time of fertiliz
113 ts in the oocyte-to-embryo transition - upon oocyte maturation and fertilization - and is dependent o
114 imal end of the germline, signals coordinate oocyte maturation and fertilization in the presence of s
116 enorhabditis elegans, where no delay between oocyte maturation and fertilization is apparent, oocyte
117 te maturation and fertilization is apparent, oocyte maturation and fertilization must be tightly coor
120 m the classical progesterone receptor during oocyte maturation and from receptor tyrosine kinases dur
122 IP(3)-sensitivity that is observed following oocyte maturation and is necessary for the proper Ca(2+)
123 inase assays, and defective for induction of oocyte maturation and maintenance of the spindle assembl
124 nothing cell fate decisions for both Xenopus oocyte maturation and mammalian fibroblast proliferation
126 1 ligands called ephrins negatively regulate oocyte maturation and MPK-1 mitogen-activated protein ki
127 esponse factor family member EGRH-1 inhibits oocyte maturation and ovulation until sperm are availabl
129 miRNA function is globally suppressed during oocyte maturation and preimplantation development and th
130 Xenopus oocytes blocks progesterone-induced oocyte maturation and prevents the polyadenylation and t
131 to germinal vesicle breakdown during Xenopus oocyte maturation and remains active throughout meiosis
132 O-acetyl-ADP-ribose causes a delay/block in oocyte maturation and results in a delay/block in embryo
135 of the PP2A/B55-Greatwall interaction during oocyte maturation and suggest that the cognate Scant Gre
136 possible relationship between such a form of oocyte maturation and that observed in other animals is
137 diversity of protein products necessary for oocyte maturation and the initiation of development.
140 in oocytes accelerates progesterone-induced oocyte maturation and the polyadenylation and translatio
141 A reporter injection assays, maskin prevents oocyte maturation and the translation of the CPE-contain
142 Translational repression was relieved during oocyte maturation and this coincided with degradation of
143 ulate the poly(A) tail length of dmos during oocyte maturation and to maintain a high level of active
145 rom a dormant maternal mRNA recruited during oocyte maturation, and a similar situation also occurs d
146 embrane asymmetry that is established during oocyte maturation, and for the asymmetrical distribution
147 from the pituitary gland triggers ovulation, oocyte maturation, and luteinization for successful repr
149 lation despite tail-length shortening during oocyte maturation, and prevented essentially all transla
150 the time course of SOCE inactivation during oocyte maturation, and show that SOCE inactivates almost
151 he level of CPEB phosphorylated early during oocyte maturation, and this directly correlates with inc
152 of budding yeast, calcium signaling, Xenopus oocyte maturation, and various other processes use multi
153 transients have not been demonstrated during oocyte maturation, and yet, manipulating intracellular c
154 ed with defects in early follicle formation, oocyte maturation, and zygotic cleavage following ovulat
155 yrosine-phosphorylated Xp95 increased during oocyte maturation; and 3) microinjection of deregulated
156 ect and indirect repression by miRNAs during oocyte maturation appears to be small (4%), and the gene
157 how the dramatic cell biological changes of oocyte maturation are brought about, we have begun to id
159 dissociated, which underscores inhibition of oocyte maturation as a potential strategy for contracept
162 ors may be involved in progesterone-mediated oocyte maturation as well as in other nongenomic steroid
165 O-acetyl-ADP-ribose (OAADPr), shown to block oocyte maturation, bind to chromatin-related proteins, a
166 functions upstream of a Ras/MAPK pathway for oocyte maturation but is not required for EGL-15 functio
167 not prevent the formation of the CGFD during oocyte maturation, but did inhibit the maturation-associ
168 (2) (PGE(2)) is a known critical mediator of oocyte maturation, but the diverse function of this lipi
170 -2 (XFRS2) is essential for the induction of oocyte maturation by an XFGFR1 harboring an activating m
172 a suggest that SERCA participates in Xenopus oocyte maturation by controlling cytosolic Ca(2+) and/or
174 versed the inhibitory effect of adenosine on oocyte maturation by modulating intracellular AMP levels
175 2 may regulate translation initiation during oocyte maturation by phosphorylating the serine-209 resi
181 , cyclins and mos have the ability to induce oocyte maturation, causing the resumption of the cell cy
182 ggest that oma-1, in addition to its role in oocyte maturation, contributes to early embryonic develo
183 Emi2 antisense morpholino knockdown during oocyte maturation did not affect polar body (PB) extrusi
184 5 inhibited microtubule (MT) assembly during oocyte maturation, disrupting assembly of the MTOC-TMA a
185 regulatory control over PKC activity during oocyte maturation disrupts the critical MI-to-MII transi
189 a highly orchestrated fashion during Xenopus oocyte maturation endowing the egg with the capacity to
190 n of elementary Ca(2+) release events during oocyte maturation explain the continuous nature and slow
194 and oocytes by assessing cumulus expansion, oocyte maturation, fertilization, and preimplantation em
196 Following the completion of oogenesis and oocyte maturation, histone mRNAs are synthesized and sto
199 knowledge, of proteome changes accompanying oocyte maturation in any organism and provides a powerfu
201 gnals triggered by EGFR signaling to promote oocyte maturation in gonadotropin-stimulated follicles.
206 roposed for the dual control of the onset of oocyte maturation in teleosts by estrogens and progestin
208 at disrupts AKAP/PKA interactions stimulates oocyte maturation in the continued presence of high cAMP
210 lopments, including oocyte vitrification and oocyte maturation in vitro, has resulted in reasonable s
211 yn kinase deficiency was also evident during oocyte maturation in vivo since ovulated cumulus oocyte
214 translation of several dormant mRNAs during oocyte maturation in XENOPUS: Polyadenylation is regulat
216 ate MAPK phosphorylation, MPF activation, or oocyte maturation, indicating that XGef may function thr
217 the expression of mRNA for PTPN13 and blocks oocyte maturation induced by progesterone, a blockade th
218 , overcomes milrinone-mediated inhibition of oocyte maturation, induces MSY2 phosphorylation and the
219 an mRNA that normally is deadenylated during oocyte maturation instead receives poly(A) in the presen
221 riments reveal that ER reorganisation during oocyte maturation is a complex multi-step process involv
225 adation of maternal mRNAs that occurs during oocyte maturation is dramatically altered in eggs obtain
226 t of Ca(2+) signaling differentiation during oocyte maturation is internalization of the plasma membr
229 ctional data show that MPF activation during oocyte maturation is required for full PMCA internalizat
230 mplete meiotic block of the Pde3a null mice, oocyte maturation is restored in the double knockout, al
232 at Muskelin, found to be up-regulated during oocyte maturation, is required for timely nurse cell nuc
233 slational activation of mRNAs during Xenopus oocyte maturation, is the essential heat-labile componen
234 s no detectable effect on translation during oocyte maturation, it is critical for this protein to lo
235 perm-sensing control mechanism that inhibits oocyte maturation, MAPK activation, and ovulation when s
237 of sperm, egrh-1 mutants exhibit derepressed oocyte maturation marked by MAPK activation and ovulatio
238 or CEH-18 is required to negatively regulate oocyte maturation, mitogen-activated protein kinase (MAP
240 global range of miRNA-regulated genes during oocyte maturation of Drosophila, we compared the proteom
241 We examined the regulation during Xenopus oocyte maturation of store-operated Ca(2+) entry (SOCE),
246 to interact with CPEB, no longer accelerates oocyte maturation or Mos synthesis, suggesting that XGef
247 e diverse function of this lipid mediator in oocyte maturation, ovulation, and fertilization has not
251 Stimulation induced by mating and in vitro oocyte maturation produced the optimal oocyte recipient
252 ng the meiotic katanin subunit MEI-1 and the oocyte maturation protein OMA-1, must be degraded during
253 r, posttranscriptionally controlled, events: oocyte maturation (release of the prophase I primary arr
256 MA-1 and OMA-2, previously shown to regulate oocyte maturation, repress transcription in P0 and P1 by
258 tic cell cycle progression during vertebrate oocyte maturation requires the correct temporal translat
262 t interestingly, Ca(2+) puffs cluster during oocyte maturation resulting in a continuum of Ca(2+) rel
263 s2 mRNA was recruited for translation during oocyte maturation, resulting in approximately 20-fold mo
265 ergoes several phosphorylation events during oocyte maturation, some of which are important for its d
266 R1-mediated Ca2+ release is regulated during oocyte maturation such that it reaches maximal effective
267 rrest at the GV-stage and the progression of oocyte maturation, such as oxidative phosphorylation, en
268 counterpart, human Speedy is able to induce oocyte maturation, suggesting similar biological charact
270 enic (Val 12)-ras-p21 induces Xenopus laevis oocyte maturation that is selectively blocked by two ras
273 While CPEB and maskin remain together during oocyte maturation, the maskin-elF-4E interaction is subs
276 accumulation during progesterone-stimulated oocyte maturation, the timing of Wee1 mRNA translational
277 ity is essential for XFGFR1act/XFRS2-induced oocyte maturation, this activity is not required for mat
278 howed that Orai1 expression decreases during oocyte maturation; this is associated with the oocytes g
279 ome acidification also occurs during Xenopus oocyte maturation; thus, a lysosomal switch that enhance
280 RNA-binding protein Hermes functions during oocyte maturation to regulate the cleavage of specific v
282 ant maternal mRNAs that are recruited during oocyte maturation; translation of Mos mRNA results in th
284 level of maternal JNK activity spanning from oocyte maturation until the onset of gastrulation that h
286 ein and inhibition of progestin induction of oocyte maturation upon microinjection of antisense oligo
287 e present here a genetic characterization of oocyte maturation, using C. elegans as a model system.
289 nked to G(i) or G(z) was sufficient to cause oocyte maturation, we expressed mammalian G(i)- and G(z)
290 hesis that gap junctions negatively regulate oocyte maturation, we performed an RNAi screen of innexi
291 ze the function of the MAP kinase pathway in oocyte maturation, we used U0126, a potent inhibitor of
292 ated with granulosa cell differentiation and oocyte maturation were expressed in a normal pattern, an
293 ke kinase that prevents progesterone-induced oocyte maturation when expressed in Xenopus oocytes.
294 K-2 mRNAs were recruited to polysomes during oocyte maturation, whereas the BMP-7 and XSTK9 mRNAs wer
295 of days of hormonal stimulation required for oocyte maturation, whereas the daily dose of gonadotropi
296 rtilization-specific Ca(2+) transient during oocyte maturation, which encompasses dramatic potentiati
298 nd the eIF4E binding protein during starfish oocyte maturation, while PI3 kinase activates these prot
299 ranscript dosage of a cohort of genes during oocyte maturation, with enrichment observed for the YTHD
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。