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1  prior to entering meiosis, the fecundity of parthenogenetic A. neomexicana is similar to that of A.
2 ains demonstrate that metaphase I arrest and parthenogenetic activation are not sufficient for terato
3 ncluded that the phenotypes of MI arrest and parthenogenetic activation in LTXBO oocytes are defects
4                Moreover, we demonstrate that parthenogenetic activation of metaphase I-arrested eggs
5                                        After parthenogenetic activation of murine oocytes and interru
6  these results show that metaphase I arrest, parthenogenetic activation of oocytes, and teratoma form
7 cytes led us to explore the role of Nlrp2 in parthenogenetic activation of oocytes.
8 t, the arrest responsible for preventing the parthenogenetic activation of unfertilized eggs.
9 xocytosis in individual mouse eggs following parthenogenetic activation or in vitro fertilization (IV
10           Premature Ca(2+) release can cause parthenogenetic activation prior to fertilization; thus,
11                  Cumulus cells also promoted parthenogenetic activation that occurred in association
12 eiotic maturation and meiosis resumption via parthenogenetic activation were impaired when Emi2 inter
13 d duration of oscillations in aged eggs upon parthenogenetic activation with SrCl2.
14  the metaphase II eggs underwent spontaneous parthenogenetic activation, thus recapitulating the Mos
15 ytes also acquired the ability to respond to parthenogenetic activation, which indicates proper metap
16 nce of MAP kinase activity and can result in parthenogenetic activation.
17 iosis at metaphase I (MI) and in spontaneous parthenogenetic activation.
18 t is necessary, but not sufficient, to cause parthenogenetic activation.
19 s fail to arrest at metaphase II and undergo parthenogenetic activation.
20 stantial impacts upon commonly used means of parthenogenetic activation.
21 a PI3K inhibitor, with or without IL-7 after parthenogenetic activation.
22 oduction has proven to be highly successful, parthenogenetic all-female populations occur frequently
23  the metaphase II plate and persists through parthenogenetic anaphase, but macroH2A is progressively
24  chromatin conformation were also present in parthenogenetic and androgenetic cells and in tissues fr
25 f regions upstream of the coding sequence in parthenogenetic and androgenetic embryonic stem cells.
26                      Adelgids are cyclically parthenogenetic and exhibit multigeneration complex life
27 tent lineages of asexual, all-female clones (parthenogenetic and gynogenetic species) avoid the negat
28                               The species is parthenogenetic and is easy to maintain in the laborator
29 phids, whose reproduction alternates between parthenogenetic and sexual forms: Over the course of a y
30 esearch on the transcriptome of egg cells in parthenogenetic and sexual genotypes.
31 nding of transcriptional differences between parthenogenetic and sexual or non-parthenogenetic eggs c
32 onsistently suggested the occurrence of both parthenogenetic and sexual reproduction in California po
33 ke (Indotyphlops braminus) is the only known parthenogenetic and triploid species within Serpentes.
34 d genes using a cDNA library made from novel parthenogenetic and wild-type fibroblast lines.
35 e-scale genome changes are known to occur in parthenogenetic animals.
36 ructure of Pemphigus bursarius, a cyclically parthenogenetic aphid.
37                    Karyotypes of permanently parthenogenetic aphids of three species of the genus Tra
38 rom fertilization of triploid oocytes from a parthenogenetic Aspidoscelis exsanguis with haploid sper
39  Here, we report the survival of an obligate parthenogenetic bdelloid rotifer, recovered from northea
40 y pluripotent stem cells can be derived from parthenogenetic blastocysts.
41 found there is no tendency for the first two parthenogenetic blastomeres to follow different fates.
42             The mycetomic rickettsiae of two parthenogenetic book lice species are in the spotted fev
43  that is a strict obligatory symbiont of the parthenogenetic booklouse Liposcelis bostrychophila (Pso
44 nimals do not develop normally; they undergo parthenogenetic cell division in the ovary, exhibit abno
45                                  Twenty-nine parthenogenetic clones of three A. pisum biotypes, defin
46                   By using replicated sexual-parthenogenetic comparisons, our study reveals how the a
47                         The majority of pure parthenogenetic concepti have no recognizable axis and e
48 ation of axial development seen in most pure parthenogenetic concepti is a secondary consequence of t
49 as markedly improved in comparison with pure parthenogenetic concepti, with such chimeras attaining a
50 tes emerged as backcrosses of two cyclically parthenogenetic (CP) parental species, D. pulex and D. p
51  introgression events between two cyclically parthenogenetic (CP) species D. pulex and D. pulicaria.
52 study assayed clonal variation in cyclically parthenogenetic Daphnia magna with respect to parasitic
53 entwide samples of two species of cyclically parthenogenetic Daphnia to assess the effect of partial
54 e mechanism of centrosome inheritance during parthenogenetic development has long been an outstanding
55 igin of maternal centrosomes that facilitate parthenogenetic development in Hymenopteran insects.
56 The egg of the aposporous embryo sac follows parthenogenetic development into an embryo; therefore, u
57 cell production (apomeiosis) followed by its parthenogenetic development into offspring that are gene
58  is asexual reproduction as a consequence of parthenogenetic development of a chromosomally unreduced
59                  We herein describe in vitro parthenogenetic development of monkey (Macaca fascicular
60 uble fertilization and imprinting to prevent parthenogenetic development of the endosperm.
61 tophyte (via apospory or diplospory) and the parthenogenetic development of the unreduced egg cell in
62 spring arising from both fertilized eggs and parthenogenetic development were observed to arise from
63     In Sciara, unfertilized embryos initiate parthenogenetic development without centrosomes.
64 e the role of the extraembryonic lineages in parthenogenetic development, we provided them with zygot
65         We show here that transplantation of parthenogenetic dopamine neurons restores motor function
66                      The genetically induced parthenogenetic Drosophila melanogaster eggs exhibit de
67 aneuploidy in larval brains of facultatively parthenogenetic Drosophila.
68  microdissection-based RNA-seq on sexual and parthenogenetic egg cells on the day of anthesis, a de n
69 ranscriptional profiles that distinguish the parthenogenetic egg from its sexual counterpart were ide
70       This outcome is independent of whether parthenogenetic eggs are haploid or diploid.
71 es between parthenogenetic and sexual or non-parthenogenetic eggs can assist with pathway engineering
72 gs, the first 2-cell blastomere to divide in parthenogenetic embryo does not necessarily contribute m
73                   Typical development of the parthenogenetic embryo proper was markedly improved in c
74       No Igf2 expression was detected in the parthenogenetic embryo proper, indicating that imprintin
75                                              Parthenogenetic embryonic stem (ES) cells with two oocyt
76 i transgenic plants results in fewer visible parthenogenetic embryos and a reduction of embryo cell n
77                                        Human parthenogenetic embryos can be obtained following artifi
78 e repetitive Ca2+ transients was observed in parthenogenetic embryos following activation with Sr2+,
79 lowed the loss of macroH2A from pronuclei in parthenogenetic embryos generated by oocyte activation.
80 ecisely the state observed in sperm, even in parthenogenetic embryos lacking a replicating paternal g
81  of a failure to form astral microtubules in parthenogenetic embryos lacking centrosomes.
82         Moreover, the mid-gestation death of parthenogenetic embryos proper despite the presence of z
83                          Previous studies of parthenogenetic embryos revealed severe perturbations of
84 ggest that the derivation of stem cells from parthenogenetic embryos, for the purposes of therapeutic
85 meres in embryos never penetrated by sperm - parthenogenetic embryos.
86 d by analysis of DNA isolated from sperm and parthenogenetic embryos.
87 ugh Wolbachia was found in only one of seven parthenogenetic Encarsia populations examined, the "Enca
88 generated and analysed a collection of human parthenogenetic ES cell lines originating from haploid o
89 mination of an X chromosome in early-passage parthenogenetic ES cells, suggesting that selection agai
90 identification of haploid human cells within parthenogenetic ESC lines.
91 and comparing them with exclusively maternal parthenogenetic ESCs (pESCs) and bi-parental ESCs, estab
92 oding mutations, but significantly more than parthenogenetic ESCs.
93 usively paternal (androgenetic) or maternal (parthenogenetic), exhibit dramatically contrasting patte
94 nvolved in the wing polyphenism described in parthenogenetic females and to investigate the interplay
95                     Fertilization of diploid parthenogenetic females by males of sexual species has p
96 ed from a secondary host plant after several parthenogenetic generations at the same location in two
97 are maintained stably throughout hundreds of parthenogenetic generations in the laboratory.
98            Daphnia pulex were exposed for 50 parthenogenetic generations to environmentally realistic
99  androgenetic (AG: two paternal genomes) and parthenogenetic (GG/PG: two maternal genomes) cells [3,4
100 ot demethylate the second maternal genome in parthenogenetic, gynogenetic and triploid digynic embryo
101 ale development and the production of viable parthenogenetic haploid embryos.
102                           Here, we show that parthenogenetic haploid ESCs at high passage have robust
103 lization success of male gametes produced by parthenogenetic hermaphrodites and (iii) potential eggs
104  optimal levels of male gamete production by parthenogenetic hermaphrodites through natural selection
105                       In certain situations, parthenogenetic hermaphrodites with an intermediate leve
106 sexual in their female function (henceforth "parthenogenetic hermaphrodites") are treated as variable
107 al cases, with increases in (i) frequency of parthenogenetic hermaphrodites, (ii) fertilization succe
108 or levels of male gamete output exists among parthenogenetic hermaphrodites, this raises the possibil
109 er capita egg loss of sexual individuals and parthenogenetic hermaphrodites, we partition the cost in
110  upon the relative male gamete output of the parthenogenetic hermaphrodites.
111 in real time during early development in the parthenogenetic hymenopteran Nasonia vitripennis.
112         We detected Rickettsia in all of the parthenogenetic individuals we checked but not in any Ar
113 ce to GM crops in diploid, haplodiploid, and parthenogenetic insect pests.
114 ops will likely soon target haplodiploid and parthenogenetic insects.
115 cterized by possession of complex cyclically parthenogenetic life cycles and the ability to induce a
116  the transition from a haplodiploid cyclical parthenogenetic life history to parthenogenetic paedogen
117  conditions that allow the generation of new parthenogenetic lineages are currently well understood.
118         It has been proposed that vertebrate parthenogenetic lineages arise from hybridisation betwee
119 have been due to the existence of obligately parthenogenetic lineages living on the secondary host or
120                      NSCs were isolated from parthenogenetic lizard embryos, rendered unresponsive to
121 ve-lethal gametophytic selection against the parthenogenetic locus and univalent inheritance of the r
122                                Production of parthenogenetic male offspring occurs through environmen
123  accumulation between four life stages for a parthenogenetic mayfly (Neocloeon triangulifer).
124                                              Parthenogenetic MEFs reach a lower saturation density, s
125 cells (ESCs) have recently been derived from parthenogenetic mouse embryos and offer new possibilitie
126 lls have been observed in egg cylinder stage parthenogenetic mouse embryos, most cells in surviving e
127 esentational difference analysis (Me-RDA) to parthenogenetic mouse embryos, to identify differentiall
128                            The genome of the parthenogenetic nematode Diploscapter pachys gives clues
129    Here we report the genome sequence of the parthenogenetic nematode Diploscapter pachys with only o
130 ternally inherited in two species of asexual parthenogenetic nematodes and identified two different s
131                               Thus, in these parthenogenetic nematodes, centrioles are maternally-inh
132 er, we precisely estimated heterozygosity in parthenogenetic offspring and found appreciable retained
133   Our findings challenge the assumption that parthenogenetic offspring are near genetic replicas of t
134 philids, we compared sexually reproduced and parthenogenetic offspring from an engineered facultative
135 re we use genetic fingerprinting to identify parthenogenetic offspring produced by two female Komodo
136 auses subsequent genome variation within the parthenogenetic offspring.
137 an Daphnia pulex species complex, obligately parthenogenetic (OP) isolates emerged as backcrosses of
138           Despite the presence of obligately parthenogenetic (OP) lineages derived from sexual ancest
139    Aphids that are anholocyclic (permanently parthenogenetic) or are monoecious (non-host-alternating
140 ving complete maternal UPD consistent with a parthenogenetic origin.
141 ts in a species of beetle that reproduces by parthenogenetic paedogenesis, without the production of
142 oid cyclical parthenogenetic life history to parthenogenetic paedogenesis.
143 ies to manage resistance in haplodiploid and parthenogenetic pests are urgently needed.
144 lity of GM crops that target haplodiploid or parthenogenetic pests will require careful consideration
145 e evolution of resistance in haplodiploid or parthenogenetic pests.
146 the derivation of uniparental cells, such as parthenogenetic (PG) ES cell lines from disease allele-f
147 vidence was found for a distinct, cyclically parthenogenetic population that exploited Lactuca sativa
148                          Its sperm-dependent parthenogenetic populations are reproductive parasites o
149  element is most likely active in cyclically parthenogenetic populations but is, for the most part, i
150 hought to be obligately asexual because only parthenogenetic populations have been collected from wid
151 clude that (1) there is genetic variation in parthenogenetic populations of F. candida, and (2) this
152          Pokey, in obligately and cyclically parthenogenetic populations of the cladoceran crustacean
153                                      Using a parthenogenetic primate embryonic stem cell line, we hav
154                                              Parthenogenetic pronuclei drift centripetally and assemb
155 y-array analysis to estimate outcrossing and parthenogenetic rates for two tychoparthenogenetic popul
156           In most aphid species, facultative parthenogenetic reproduction allows rapid growth and for
157 Results indicate that substantial amounts of parthenogenetic reproduction are occurring in these natu
158 ed that the females retain the capability of parthenogenetic reproduction characteristic of their tri
159  transmitted and associated with thelytokous parthenogenetic reproduction in Encarsia, a genus of par
160                For decades, only thelytokous parthenogenetic reproduction was documented in L. bostry
161                          When animals evolve parthenogenetic reproduction, information about the sexu
162 how that heterozygous M. hapla females, upon parthenogenetic reproduction, produce progeny that segre
163 ely 1 in 10,000 animal species is capable of parthenogenetic reproduction, the evolutionary causes an
164 ganisms to switch between sexual and asexual parthenogenetic reproduction.
165  be genetically homogeneous because of their parthenogenetic reproduction.
166 alifornia are believed to have predominantly parthenogenetic reproduction.
167 ghted divergence between mitotic and meiotic parthenogenetic RKN species and probable interspecific h
168 clonal and genetic structure of the cyclical parthenogenetic rotifer Brachionus plicatilis by followi
169      Although it is unknown if either of the parthenogenetic snakes would have been carried to term o
170             We now show that in the obligate parthenogenetic species A. neomexicana the vast majority
171 hermaphroditic species are not uncommon, and parthenogenetic species are also known.
172                                              Parthenogenetic species did not show increased transposa
173 ad to facultative parthenogenesis in the non-parthenogenetic species Drosophila melanogaster.
174 rence genomes for five independently evolved parthenogenetic species in the stick insect genus Timema
175 sence, origin, and function of centrioles in parthenogenetic species is unknown.
176                                              Parthenogenetic species of whiptail lizards in the genus
177                                    Moreover, parthenogenetic species often maintain a certain level o
178 aused facultative parthenogenesis in the non-parthenogenetic species that was enhanced by increased e
179 nce for less effective positive selection in parthenogenetic species, suggesting that sex is ubiquito
180 high degree of fixed heterozygosity in these parthenogenetic species, supporting the view that they o
181 ciated with the lack of genetic diversity in parthenogenetic species.
182 luating the safety and tolerability of human parthenogenetic stem cell derived neural stem cells ISC-
183 olleagues show that cardiomyocytes made from parthenogenetic stem cells (PSCs) and deployed as engine
184       Here we hypothesized that nonembryonic parthenogenetic stem cells (PSCs) can be directed toward
185 hese data provide proof for the concept that parthenogenetic stem cells are a suitable source of func
186  sexual strain was most closely related to a parthenogenetic strain in Illinois.
187 tic offspring from an engineered facultative parthenogenetic strain of D. melanogaster.
188 nced the genomes of sexually reproducing and parthenogenetic strains of Drosophila mercatorum and ide
189 strain with the Hawaii sexual strain and the parthenogenetic strains of L. bostrychophila.
190                               The sexual and parthenogenetic strains show some differences in eye mor
191                                   Completely parthenogenetic Trichogramma wasps can be rendered perma
192  ectopically expressing the BABYBOOM1 (BBM1) parthenogenetic trigger in egg cells.
193 in development, with chimeras generated with parthenogenetic (two maternal chromosomes) or androgenet
194 nces with twice the number of chromosomes in parthenogenetic versus sexual species, a mechanism that
195        Coccophagine species may be sexual or parthenogenetic; we discuss reproductive modes and the i

 
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