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1 rucial function is to locate and fuse with a mature oocyte.
2 he follicle wall, causing the release of the mature oocyte.
3 through the female reproductive tract to the mature oocyte.
4    Percutaneous oocyte aspirations yielded a mature oocyte.
5 ries of contractions required to ovulate the mature oocyte.
6 ergoes monthly structural changes to release mature oocytes.
7 gh-quality mitochondria at extreme ploidy in mature oocytes.
8 y coordinated contractility for ovulation of mature oocytes.
9 s from polyubiquitination and degradation in mature oocytes.
10 ssenger RNA expression in frontal cortex and mature oocytes.
11 entifying over a thousand CGIs methylated in mature oocytes.
12 are unlimited number of sperm and paucity of mature oocytes.
13 ted that the proteins are not present in the mature oocytes.
14 esin complexes and chromosome segregation in mature oocytes.
15 cytes while the ratios increased markedly in mature oocytes.
16 es and is most abundant in spermatocytes and mature oocytes.
17 d was enriched in the animal pole cytosol of mature oocytes.
18 cillations observed during fertilizations of mature oocytes.
19 cted, and the cells were fused to enucleated mature oocytes.
20 size, egg production, and yolk deposition in mature oocytes.
21  oocytes yet were replicated in progesterone-matured oocytes.
22 gg extracts, but not in immature or in vitro matured oocytes.
23 epithelial follicle cells which surround the maturing oocyte.
24 rates are only observed in the presence of a maturing oocyte.
25 ransduce this signal to promote apoptosis in maturing oocytes.
26 ssociation with the condensed chromosomes of maturing oocytes.
27 e cells to provide cytoplasmic components to maturing oocytes.
28 1 and 7.8 +/- 0.9, respectively; P < .0001), mature oocytes (1.5 +/- 0.3 v 5.1 +/- 1.1 and 8.5 +/- 1.
29 stinct subset of mRNAs both in quiescent and maturing oocytes, a function recapitulated with YFP-3'UT
30 on the inner surface of the micropyle of the mature oocyte and propose that, as in the abalone system
31                                 We extracted mature oocytes and brain regions from a subset of rats a
32 re than 18,000 enhancers that were active in mature oocytes and developing embryos and documented a b
33 As are highly adenylated at their 3' ends in mature oocytes and early embryos.
34 ate mos maintains the metaphase II arrest of mature oocytes and prevents DNA replication between the
35 m manually dissected nuclei and cytoplasm of mature oocytes and subjected it to deep sequencing.
36  damage by preventing production of abnormal mature oocytes and subsequent embryos.
37 le phenotype characterized by the absence of mature oocytes and the presence of trapped, immature ooc
38 distinct functions of OMA-1 and OMA-2 in the maturing oocyte and 1-cell embryo, ensuring a normal ooc
39 TR decreases MEX-3 abundance specifically in maturing oocytes and early embryos during temperature st
40                                      Because maturing oocytes and early embryos lack appreciable tran
41                                       In the maturing oocytes and eggs of the frog Xenopus laevis, hi
42 ns, OMA-1 and OMA-2, express specifically in maturing oocytes and function redundantly in oocyte matu
43        In adult mice, Sebox RNA was found in maturing oocytes and in fertilized eggs; however, the ab
44 h accompanies cytoplasmic polyadenylation in maturing oocytes and in in vitro activated oocyte lysate
45 croH2A is associated with the chromosomes of mature oocytes, and abundant macroH2A is present in the
46 nation, during repair of radiation damage in mature oocytes, and in proliferating somatic cells, wher
47 on of cyclin B1 requires factors specific to mature oocytes, and that to overcome arrest at MII, Ca2+
48 et the high-energy demands of embryogenesis, mature oocytes are furnished with vast amounts of mitoch
49      Thus, it is important to understand how mature oocytes are generated.
50       Egg activation is the process in which mature oocytes are released from developmental arrest an
51                                              Mature oocytes are transcriptionally quiescent and posse
52                                     Isolated maturing oocytes autonomously synthesized betaine in vit
53 anslocation of cortical granules in in vitro-matured oocytes begins with the movement of the germinal
54 us p27kip1 in vitro to lysates of hormonally matured oocytes blocked the enzymatic activity of the ac
55 on of antibodies to either Mad1 or Mad2 into maturing oocytes blocks the establishment of CSF arrest
56                                (3 and 4) The maturing oocyte both induces spermathecal dilation and m
57 opus oocytes and translational activation in mature oocytes, but the protein that binds to the TCS an
58 onstrated the control of epigenetic marks in maturing oocytes by SGOC network.
59                With this method, hundreds of mature oocytes can be activated to resume and complete m
60                                              Mature oocytes can be fertilized, but embryos that canno
61 with gonadotropins allowed the generation of mature oocytes capable of undergoing early embryonic dev
62  in granulosa cells across species, although mature oocytes change more in humans.
63 e, we investigated whether mating influences mature oocyte composition in Drosophila melanogaster usi
64                                          The mature oocyte contains the highest number of mitochondri
65  uniraptor, the position and number of AN in mature oocytes correspond to the position and number of
66                                              Mature oocyte cytoplasm can reprogram somatic cell nucle
67 n Drosophila oogenesis, the development of a mature oocyte depends on having properly developed ring
68 n vivo, intact bull sperm microinjected into mature oocytes do not undergo disassembly of the PT.
69 actor (MPF), prevented GVBD, indicating that maturing oocytes eventually need to elevate their MPF le
70                           No other kinase in mature oocyte extracts phosphorylated the xnf7 P2 site t
71 horylation of the P2 site were purified from mature oocyte extracts.
72 uperovulation is to obtain maximum number of mature oocytes/follicles within a particular size range.
73  belonging to the phylum Nemertea, the ER of maturing oocytes forms numerous distinct clusters that a
74 cle wall and follicle rupture to release the mature oocyte from a layer of somatic follicle cells.
75 dle domain (LISD), although fusing them into maturing oocytes generates LISD-like TACC3 condensates a
76 d the PLU and GNU activating subunits in the mature oocyte, GNU is phosphorylated at Cyclin B/CDK1sit
77                             In spontaneously maturing oocytes, GVB was preceded by AMPK activation an
78 localizes to cytoplasmic RNP granules in the mature oocyte, identifying GNU as a new component of a s
79                      Drosophila melanogaster mature oocytes in ovaries are arrested at metaphase I of
80                Ablation of these cells traps mature oocytes in the gonad arm where they endomitotical
81 rt all stages of follicle growth to generate mature oocytes in vitro and emerging prospects for makin
82 se data demonstrate the sensitivity of mouse maturing oocytes in vivo to maternal protein undernutrit
83 n mitochondrial quality at extreme ploidy in mature oocytes, in the absence of sex and recombination.
84 tiation of female germline stem cells into a mature oocyte includes the expression of RNAs and protei
85                                Activation of mature oocytes initiates development by releasing the pr
86 ecal valve, a critical step for the entry of mature oocytes into the spermatheca for fertilization.
87 n contraction that is required for expelling mature oocytes into the spermatheca where fertilization
88                                       As the mature oocyte is approximately 125 micro m in diameter (
89              During wild-type ovulation, the mature oocyte is expelled from the gonad arm by contract
90 rates and marine invertebrates begins when a mature oocyte is fertilized, resulting in a rise in intr
91 tion is a precisely timed process by which a mature oocyte is released from an ovarian follicle.
92                          Cryopreservation of mature oocytes is also becoming more commonplace as meth
93  production in the fat body and Vg uptake by maturing oocytes, is of great importance for the success
94 n immature oocytes (germinal vesicle stage), matured oocytes (metaphase II eggs) and 2-cell stage emb
95 ion at two key stages of bovine development, matured oocytes (MII) and 8-cell-stage embryos, constitu
96 o (DNMT1o), levels of which are decreased in mature oocytes of aging females.
97                                              Mature oocytes of Drosophila are arrested in metaphase o
98 t accurately predicts tail-length changes in maturing oocytes of frogs and mammals.
99 the effects of the hormonal triggers used to mature oocytes on the degree of luteal phase support req
100 oocyte representing the default fate and the mature oocyte representing the induced fate.
101 ecipitation analysis of soluble keratin from matured oocytes revealed the presence of type I and type
102 llicles were most important to the number of mature oocytes subsequently retrieved.
103 erved novel phenotypes in these precociously maturing oocytes, such as chromosome coalescence, aberra
104 ed chromosome scattering in Colcemid-treated mature oocytes, suggesting a role in mediating chromosom
105            CSF was defined as an activity in mature oocytes that caused mitotic arrest when injected
106  dictyate stage until recruited to grow into mature oocytes that divide at ovulation.
107   Genetically, Tgkd teratomas originate from mature oocytes that have completed meiosis I, suggesting
108 had little effect on clock gene abundance in mature oocytes that were dissected from female Ae. albop
109                                           In maturing oocytes, the nucleus underwent kinesin-dependen
110  they can neither be initiated nor erased in mature oocytes; these properties are unique to the devel
111                                           In maturing oocytes, this tail lengthening occurs against a
112 ortant role in early development by enabling mature oocytes to generate a normal calcium response.
113 During Drosophila oogenesis, RCs connect the maturing oocyte to nurse cells supporting its growth.
114                       The ER microdomains of mature oocytes typically reached widths of 1-8 micromete
115 g functions posttranscriptionally already in mature oocytes via Wnt/stabilization of proteins (STOP)
116                                   The mutant mature oocytes were almost entirely depleted of all miRN
117  [5], or retention of bcd at the anterior in mature oocytes, which can remain dormant for weeks befor
118 ' follicles generate 70-100% of the earliest mature oocytes, while fewer than 26 wave 1 follicles wit
119 a mutant frequency induced by irradiation of mature oocytes with 5 Gy increases approximately twofold
120                         After fertilization, mature oocytes with such aggregates generate a normal se
121  also describes the stage specific growth of maturing oocytes within the ovary and permits the presen

 
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