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1 ly by developing an embryo from a fertilized egg cell.
2 h MCM7 is expressed at a higher level in the egg cell.
3 e female tissues to eventually fertilize the egg cell.
4 ained within a pollen tube, to fertilize the egg cell.
5  that bias their segregation into the future egg cell.
6 bryo sac before fertilization, including the egg cell.
7  B chromosomes preferentially fertilizes the egg cell.
8 ne where the germ plasm will form within the egg cell.
9  triggers embryo development in unfertilized egg cells.
10 ly) may occur in either reduced or unreduced egg cells.
11  BABYBOOM1 (BBM1) parthenogenetic trigger in egg cells.
12  as germline stem cells transition to become egg cells.
13 tiation, leading to the absence of sperm and egg cells.
14  embryonic precursors of gametes - sperm and egg cells.
15 aintaining the genomic integrity of immature eggs cells.
16 ead across heterochromatic regions, while in egg cells, 24-nt siRNAs were concentrated at a smaller n
17 he embryo sac before cellularization, in the egg cell after cellularization, in the zygote/embryo imm
18 y the pollen tube cell to the egg apparatus (egg cell and accessory synergid cells).
19                              It produces the egg cell and central cell (which give rise to the embryo
20        It is the structure that produces the egg cell and central cell which, following fertilization
21 uce two highly dimorphic female gametes, the egg cell and central cell.
22  that transcriptome abundance doubles in the egg cell and increases approximately 1.6-fold in the cen
23        In contrast, Fie2 is expressed in the egg cell and more intensively in the central cell simila
24 mbers that are specifically expressed in the egg cell and redundantly control gamete fusion during do
25                                          The egg cell and sperm cell transcriptomes reveal major diff
26 es: twice during double fertilization of the egg cell and the central cell and once during female gam
27                  Double fertilization of the egg cell and the central cell by two sperm cells, result
28 ing plants, two distinct female gametes, the egg cell and the central cell, are fertilized to produce
29 structure consisting of four cell types: one egg cell and two synergids, one central cell, and three
30 les, the dominant PAR allele is expressed in egg cells and has a miniature inverted-repeat transposab
31 ive organs, the final differentiation of the egg cell, and the progression of canal cells into a cell
32 s, one gene was expressed exclusively in the egg cell, and three genes were expressed strongly in mul
33 ls are the embryonic precursors to sperm and egg cells, and their development is regulated by multipl
34 rays to study environmental toxicity in tiny eggs, cells, and neonates, whereas localization in large
35 extremely small-mass-limited samples such as eggs, cells, and tiny organisms.
36 of the archegonium, the canal cells, and the egg cell are also sites of auxin responsiveness and are
37 e of growth but have a difficult journey, as egg cells are buried within the ovary of the carpel.
38 BOOM-like (PsASGR-BBML) gene is expressed in egg cells before fertilization and can induce parthenoge
39 s one sperm cell successfully fuses with the egg cell but the second sperm cell fails to fuse with th
40 g in triploid apomicts that produce triploid egg cells but largely nonfunctional pollen.
41                          Fertilization of an egg cell by more than one sperm cell can produce viable
42  propose occasional fertilization of diploid egg cells by haploid pollen, resulting in triploid apomi
43  combined with the expression of BBM1 in the egg cell, clonal progeny can be obtained that retain gen
44 bundance is central cell, synergid cell, and egg cell, consistent with their cell size variation.
45  we propose a mathematical model of the frog egg cell cycle including effects of unreplicated DNA on
46    Here, we report that in the early Xenopus egg cell cycles, phosphorylation of endogenous cdc25C Se
47         We found that CHH methylation in the egg cell depends on DOMAINS REARRANGED METHYLASE 2 (DRM2
48 idence that age may cause a breakdown in the egg cell division machinery.
49 rophyte generation and, upon maturation, the egg cell establishes a quiescent state that is maintaine
50 ybrid of rice by inducing MiMe mutations and egg cell expression of BBM1 in a single step.
51 of embryo sac abnormalities, including extra egg cells, extra polar nuclei, and extra synergids.
52  which specifies central cells and restricts egg cell fate.
53 d-enriched sperm cell (S(ua)) fuses with the egg cell, forming the zygote and embryo.
54                                   In Xenopus egg cell-free extracts, Xkid and Xklp1 are essential for
55 n mitotic chromosome condensation in Xenopus egg cell-free extracts.
56 en penetrates this matrix and fuses with the egg cell, generating a zygote.
57 when double fertilization precedes maternal (egg cell) genome loss.
58 yos derive by parthenogenesis from unreduced egg cells, giving rise to clonal offspring.
59                Consistent with a role in the egg cell, heterozygous mcm7 mutants resulted in frequent
60 h and/or maintain the quiescent state of the egg cell in the absence of fertilization.
61 s, causing their preferential segregation to egg cells in a process known as meiotic drive.
62 omosome segregation during the production of egg cells in humans are becoming clearer.
63  for future research on the transcriptome of egg cells in parthenogenetic and sexual genotypes.
64 ogous expression of dandelion PAR in lettuce egg cells induced haploid embryo-like structures in the
65 parthenogenetic development of the unreduced egg cell into an embryo.
66  extended [Ca2+]cyto transient solely in the egg cell is correlated with successful fertilization.
67              Successful fertilization of the egg cell is not blocked in the glc mutant, suggesting th
68 ongly modified after fertilization, that the egg cell is primed to activate the translational machine
69            Ectopic expression of BBM1 in the egg cell is sufficient for parthenogenesis, which indica
70 t from animal genomes [11-13], can induce an egg cell-like transcriptome in sporophytic cells of A. t
71 s have not produced phenotypes affecting the egg cell, likely due to genetic redundancy and/or cross-
72  through which the sperm passes to reach the egg cell membrane.
73  thought to mediate fusion between sperm and egg cell membranes.
74 after in vivo fertilization of G. barbadense egg cells (n = 26).
75 that Fie1 is neither expressed in the sperm, egg cell nor central cell before fertilization.
76 distributions of small RNAs in the sperm and egg cells of rice.
77 -based RNA-seq on sexual and parthenogenetic egg cells on the day of anthesis, a de novo transcriptom
78                                   Later, the egg cell plays a central role in specifying accessory ce
79                                    Thus, the egg cell probably remained unfertilized in aborted lre-5
80 n) is characterized by meiotically unreduced egg cell production (apomeiosis) followed by its parthen
81             It is the structure within which egg cell production and fertilization take place.
82 viruses with decreased neutralizing antibody egg/cell ratio.
83  of the zygote siRNA loci do not overlap any egg cell siRNA loci.
84                 However, only few genes with egg cell-specific expression or defects have been identi
85    These findings may account for the unique egg cell specification characteristic of angiosperms and
86 xin has been found to mediate patterning and egg cell specification.
87                           We isolated living egg cells, sperm cells and pollen vegetative cells from
88 c acid chains derived from the S. purpuratus egg cell surface complex inhibited fertilization; the no
89 ated glycopeptide fraction isolated from the egg cell surface complex of another species of sea urchi
90 in synergids, specialized cells flanking the egg cell that attract pollen tubes and degenerate upon p
91 diploids, so that the plant produces diploid egg cells that can develop without fertilization, but ha
92 vered by the pollen tube (PT) fuses with the egg cell to form the zygote, whereas the second unites w
93 female gametophyte typically consists of one egg cell, two synergid cells, one central cell, and thre
94 force generation on the membrane of starfish egg cells, undergo spontaneous braiding dynamics.
95 indle size is positively correlated with the egg cell volume.
96 novo transcriptome for the Cenchrus ciliaris egg cells was created, transcriptional profiles that dis
97  the normality and holistic integrity of the egg cell, was one of its purest adherents.
98         Beginning with the activation of the egg cell, we summarize and discuss the process of matern
99 o sac embedded within the ovule contains the egg cell, whereas the pollen grain contains two sperm ce
100  polyspermy can selectively polyploidize the egg cell, while rendering the genome size of the ploidy-
101 chanisms plants use to prevent the fusion of egg cells with multiple sperm cells.
102 bility to initiate embryo formation from the egg cell without fertilization, also can be valuable in
103 rough the production and fusion of sperm and egg cells, yet little is known about the ancestry of ani

 
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