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1 n) locus, whereas males are hemizygous (from unfertilized eggs).
2 d is localized to the cortical region of the unfertilized egg.
3 nal protein residing in the cytoplasm of the unfertilized egg.
4 r and reliance on factors inherited from the unfertilized egg.
5 as two- to threefold higher than that in the unfertilized egg.
6 y (LC-MS/MS), we detected 20 steroids within unfertilized eggs.
7 ts, bees and wasps, develop as haploids from unfertilized eggs.
8 rtilized eggs and haploid males develop from unfertilized eggs.
9 ps), workers can produce male offspring from unfertilized eggs.
10 triole-like structures when overexpressed in unfertilized eggs.
11 ed number of eggs laid and a greater rate of unfertilized eggs.
12  in the repression of DNA synthesis found in unfertilized eggs.
13 eggs, as did addition of MKP-3 to lysates of unfertilized eggs.
14              Female meiosis was identical in unfertilized eggs.
15 lei followed by nuclear transplantation into unfertilized eggs.
16 inhibitor PD98059 triggered DNA synthesis in unfertilized eggs.
17 ns each localize to the cortical granules of unfertilized eggs.
18 r of MAPK-dependent CSF arrest in vertebrate unfertilized eggs.
19 icroinjected tyrosine kinase inhibitors into unfertilized eggs.
20 preventing the parthenogenetic activation of unfertilized eggs.
21 develop parthenogenetically as haploids from unfertilized eggs.
22 PgammaS-induced Ca2+ release and pHi rise in unfertilized eggs.
23 using cell-cycle blockade at metaphase II in unfertilized eggs.
24 hat a rare maternal SpHmx mRNA is present in unfertilized eggs.
25 na pellucida (ZP) around growing oocytes and unfertilized eggs.
26 d female provisioning of food in the form of unfertilized eggs.
27  calls of their male partners, feed tadpoles unfertilized eggs.
28                                In vertebrate unfertilized eggs, a special form of meiotic metaphase a
29  abundant maternal transcript present in the unfertilized egg and 2-cell, but not 8-cell, stage embry
30 i (gnu) genes also affect the S-phase in the unfertilized egg and early embryo.
31 transcripts are uniformly distributed in the unfertilized egg and the protein accumulates to similar,
32    Hybridization is strong in female adults, unfertilized eggs and 0-3-h-old embryos, then diminishes
33 iploidy in which males normally develop from unfertilized eggs and are haploid, while females develop
34 ies is hyperphosphorylated relative to YA in unfertilized eggs and embryos.
35 omes incorporated into the nuclear lamina in unfertilized eggs and embryos.
36  Hymenoptera, males develop as haploids from unfertilized eggs and females develop as diploids from f
37                                              Unfertilized eggs and fertilized embryos from Drosophila
38 ome and the corresponding mRNA is present in unfertilized eggs and in early embryos through and up to
39 flurane decreased the numbers of embryos and unfertilized eggs and increased the levels of dead cells
40 how that SpSoxB1 is present at low levels in unfertilized eggs and progressively accumulates during c
41  embryos in the spermatheca, lay damaged and unfertilized eggs, and consequently exhibit dramatically
42 icoid mRNA is stable in retained oocytes, in unfertilized eggs, and during the first 2 h of embryogen
43                       In vertebrate meiosis, unfertilized eggs are arrested in metaphase II by cytost
44 ly uniparental haploid males that arise from unfertilized eggs are capable of reproduction.
45 ential value of growing oocytes, rather than unfertilized eggs, as a source of nuclear reprogramming
46 3) resulted in inactivation of MAP kinase in unfertilized eggs, as did addition of MKP-3 to lysates o
47                   Emi1 is required to arrest unfertilized eggs at metaphase of meiosis II and seems t
48  female pronucleus at the animal pole in the unfertilized egg, becomes associated with the unipolar f
49 ene whose expression peaks in the oocyte and unfertilized egg, begins to decrease gradually after fer
50  The corresponding efflux activity is low in unfertilized eggs but is dramatically upregulated within
51 ant ZP3R/sp56 bound to the zona pellucida of unfertilized eggs but not to 2-cell embryos, indicating
52 rs to the surface of both hemispheres of the unfertilized egg, but not to the surface of the fertiliz
53 andelion that triggers embryo development in unfertilized egg cells.
54 in B1 and B2 protein levels were high in the unfertilized egg, declined upon fertilization, and reacc
55                                  In Nasonia, unfertilized eggs develop as haploid males while fertili
56 g recessive zygotic lethal mutations because unfertilized eggs develop as males while fertilized eggs
57 hree steps of BER in zebrafish extracts from unfertilized eggs, embryos at different developmental st
58 evealed a major 1.5 kb CG12108 transcript in unfertilized eggs, embryos, larvae, pupae, adult head an
59 rmation of large endolysosomal structures in unfertilized eggs ensures that lysosomes remain dormant
60                  The total lipid fraction in unfertilized egg exhibits 0.8 pmole PIP2 per egg and thi
61 ion mean hatching success (usually < 10%) of unfertilized eggs from females of typically sexually rep
62  ants is arrhenotokous parthenogenesis where unfertilized eggs give rise to haploid males and fertili
63       In each case, the animal region of the unfertilized egg has the intrinsic ability to form apica
64                                Incubation of unfertilized eggs in the Ca(2+) ionophore A23187 led to
65                                Incubation of unfertilized eggs in the MEK inhibitor U0126 (0.5 microM
66  factor, required for metaphase II arrest of unfertilized eggs in vertebrates.
67  accumulation of RNA and abundant protein in unfertilized eggs; in embryos, the endogenous I-2 protei
68 e for species-restricted binding of sperm to unfertilized eggs, inducing sperm to undergo acrosomal e
69 yc transgene, the methylation pattern in the unfertilized egg is maintained by the early mouse embryo
70                Dead cells, ROS, embryos, and unfertilized eggs laid by hermaphrodites were measured b
71      Ins(1,4,5)P3 increases 3.2-fold from an unfertilized egg level of 0.13 pmole per egg (0.29 micro
72 pts as preferentially expressed in the mouse unfertilized egg libraries.
73                                              Unfertilized egg lysates were treated with U0126 to inac
74                                In vertebrate unfertilized eggs, metaphase arrest in Meiosis II is med
75 he spe-27 gene are self-sterile, laying only unfertilized eggs; mutant males are fertile.
76 ondria are asymmetrically distributed in the unfertilized egg of Strongylocentrotus purpuratus, and t
77 g in nucleoplasmic extracts derived from the unfertilized eggs of Xenopus laevis.
78 r in eggs at 1 min postfertilization than in unfertilized eggs or in 20-min-postfertilized eggs.
79 s, entailing the development of embryos from unfertilized eggs, or genome elimination, entailing miss
80          Microinjection of these nuclei into unfertilized eggs produces viable embryos that can be sc
81 cific stage of development, to an enucleated unfertilized egg, provided an opportunity to investigate
82 iploid Hymenoptera, haploid males arise from unfertilized eggs, receiving a single set of maternal ch
83 y the transplantation of somatic nuclei into unfertilized eggs requires a dramatic remodeling of chro
84 uggest that Irf6 translated in the oocyte or unfertilized egg suffices for early development.
85 oncentration near the plasma membrane in the unfertilized egg that is augmented significantly near th
86 onspecific and heterospecific males produced unfertilized eggs that underwent spontaneous development
87 ese findings provide strong evidence that in unfertilized eggs the egg receptor for sperm exists as p
88                                           In unfertilized eggs, the asters migrated inwards and two o
89 sociated with the zygotic nucleus and, as in unfertilized eggs, they rapidly degenerated.Conclusions:
90  times, with mothers of some species feeding unfertilized eggs to their developing offspring until ta
91                In haplodiploid reproduction, unfertilized eggs typically develop into uniparental hap
92 capable of stimulating Ca(2+) release in the unfertilized egg via PLCgamma, as at fertilization.
93                       To increase the pH(i), unfertilized eggs were injected with zwitterionic buffer
94 riments in which molecules on the surface of unfertilized eggs were labeled with biotin and traced af
95  was reduced in a dose-dependent manner when unfertilized eggs were preincubated with recombinant ZP3
96 ession and activity of the enzyme in normal, unfertilized eggs, which likely provide the protein to n
97 ase kinase) are phosphorylated and active in unfertilized eggs while both are dephosphorylated and in
98                                 Treatment of unfertilized eggs with crude collagenase resulted in pro
99 e is present primarily in the nucleus of the unfertilized egg, with some of the phosphorylated form i
100         Transplantation of these nuclei into unfertilized eggs yields hundreds of normal, diploid emb