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1 he follicle wall, causing the release of the mature oocyte.
2 through the female reproductive tract to the mature oocyte.
3 rucial function is to locate and fuse with a mature oocyte.
4 Percutaneous oocyte aspirations yielded a mature oocyte.
5 ries of contractions required to ovulate the mature oocyte.
6 size, egg production, and yolk deposition in mature oocytes.
7 s from polyubiquitination and degradation in mature oocytes.
8 ssenger RNA expression in frontal cortex and mature oocytes.
9 entifying over a thousand CGIs methylated in mature oocytes.
10 are unlimited number of sperm and paucity of mature oocytes.
11 ted that the proteins are not present in the mature oocytes.
12 cytes while the ratios increased markedly in mature oocytes.
13 es and is most abundant in spermatocytes and mature oocytes.
14 d was enriched in the animal pole cytosol of mature oocytes.
15 cillations observed during fertilizations of mature oocytes.
16 cted, and the cells were fused to enucleated mature oocytes.
17 y coordinated contractility for ovulation of mature oocytes.
18 gg extracts, but not in immature or in vitro matured oocytes.
19 oocytes yet were replicated in progesterone-matured oocytes.
20 rates are only observed in the presence of a maturing oocyte.
21 epithelial follicle cells which surround the maturing oocyte.
22 ssociation with the condensed chromosomes of maturing oocytes.
23 e cells to provide cytoplasmic components to maturing oocytes.
24 1 and 7.8 +/- 0.9, respectively; P < .0001), mature oocytes (1.5 +/- 0.3 v 5.1 +/- 1.1 and 8.5 +/- 1.
25 on the inner surface of the micropyle of the mature oocyte and propose that, as in the abalone system
28 ate mos maintains the metaphase II arrest of mature oocytes and prevents DNA replication between the
31 le phenotype characterized by the absence of mature oocytes and the presence of trapped, immature ooc
32 distinct functions of OMA-1 and OMA-2 in the maturing oocyte and 1-cell embryo, ensuring a normal ooc
35 ns, OMA-1 and OMA-2, express specifically in maturing oocytes and function redundantly in oocyte matu
37 h accompanies cytoplasmic polyadenylation in maturing oocytes and in in vitro activated oocyte lysate
38 croH2A is associated with the chromosomes of mature oocytes, and abundant macroH2A is present in the
39 nation, during repair of radiation damage in mature oocytes, and in proliferating somatic cells, wher
40 on of cyclin B1 requires factors specific to mature oocytes, and that to overcome arrest at MII, Ca2+
41 et the high-energy demands of embryogenesis, mature oocytes are furnished with vast amounts of mitoch
43 anslocation of cortical granules in in vitro-matured oocytes begins with the movement of the germinal
44 us p27kip1 in vitro to lysates of hormonally matured oocytes blocked the enzymatic activity of the ac
45 on of antibodies to either Mad1 or Mad2 into maturing oocytes blocks the establishment of CSF arrest
47 opus oocytes and translational activation in mature oocytes, but the protein that binds to the TCS an
50 with gonadotropins allowed the generation of mature oocytes capable of undergoing early embryonic dev
52 uniraptor, the position and number of AN in mature oocytes correspond to the position and number of
54 n Drosophila oogenesis, the development of a mature oocyte depends on having properly developed ring
55 n vivo, intact bull sperm microinjected into mature oocytes do not undergo disassembly of the PT.
56 actor (MPF), prevented GVBD, indicating that maturing oocytes eventually need to elevate their MPF le
59 uperovulation is to obtain maximum number of mature oocytes/follicles within a particular size range.
60 belonging to the phylum Nemertea, the ER of maturing oocytes forms numerous distinct clusters that a
61 d the PLU and GNU activating subunits in the mature oocyte, GNU is phosphorylated at Cyclin B/CDK1sit
65 se data demonstrate the sensitivity of mouse maturing oocytes in vivo to maternal protein undernutrit
67 ecal valve, a critical step for the entry of mature oocytes into the spermatheca for fertilization.
68 n contraction that is required for expelling mature oocytes into the spermatheca where fertilization
71 rates and marine invertebrates begins when a mature oocyte is fertilized, resulting in a rise in intr
74 n immature oocytes (germinal vesicle stage), matured oocytes (metaphase II eggs) and 2-cell stage emb
75 ion at two key stages of bovine development, matured oocytes (MII) and 8-cell-stage embryos, constitu
79 ecipitation analysis of soluble keratin from matured oocytes revealed the presence of type I and type
80 erved novel phenotypes in these precociously maturing oocytes, such as chromosome coalescence, aberra
81 ed chromosome scattering in Colcemid-treated mature oocytes, suggesting a role in mediating chromosom
84 Genetically, Tgkd teratomas originate from mature oocytes that have completed meiosis I, suggesting
86 they can neither be initiated nor erased in mature oocytes; these properties are unique to the devel
87 ortant role in early development by enabling mature oocytes to generate a normal calcium response.
88 During Drosophila oogenesis, RCs connect the maturing oocyte to nurse cells supporting its growth.
90 g functions posttranscriptionally already in mature oocytes via Wnt/stabilization of proteins (STOP)
92 [5], or retention of bcd at the anterior in mature oocytes, which can remain dormant for weeks befor
93 a mutant frequency induced by irradiation of mature oocytes with 5 Gy increases approximately twofold
95 also describes the stage specific growth of maturing oocytes within the ovary and permits the presen
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