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1  sexual elements, instead of by a process of parthenogenesis".
2 nisms underlying this transition to obligate parthenogenesis.
3  continuously reproduce in the laboratory by parthenogenesis.
4 ary versus communal breeding and facultative parthenogenesis.
5 anging from amphimixis to obligatory mitotic parthenogenesis.
6 ogyne hapla reproduce by facultative meiotic parthenogenesis.
7  with high cyclin B/Cdc2 activity to prevent parthenogenesis.
8 l cleavage, thereby providing conditions for parthenogenesis.
9  of underdominance in the origin of obligate parthenogenesis.
10 some pairing during meiosis in allopolyploid parthenogenesis.
11 andidate genes for the apomictic function of parthenogenesis.
12 hnia pulex typically reproduces via cyclical parthenogenesis.
13                                              Parthenogenesis, a major component of apomixis, commonly
14  Some ant species are capable of thelytokous parthenogenesis, a type of asexual reproduction where fe
15 c generation that reproduces through mitotic parthenogenesis and a dioecious free-living sexually rep
16 esults endorse a key role for PsASGR-BBML in parthenogenesis and a newly discovered role for a member
17 haploid human embryonic stem cells (ESCs) by parthenogenesis and demonstrated their wide differentiat
18  This species reproduces by obligate mitotic parthenogenesis and exhibits a complex pattern of aneupl
19 ith parasitic females reproducing by mitotic parthenogenesis and free-living males and females reprod
20 r; intergenerational clonality in nature via parthenogenesis and gynogenesis; intergenerational hemic
21 sition in plants, also taking recent work on parthenogenesis and haploid induction into consideration
22  fish and offspring ruled out development by parthenogenesis and hermaphroditism, therefore implicati
23 ith a positive character correlation between parthenogenesis and isogamy.
24 atode Strongyloides ratti reproduces by both parthenogenesis and sexual reproduction, but its genetic
25 nheritance are significantly associated with parthenogenesis and that 11 cosegregating markers with u
26  a specific genotype background enabled high parthenogenesis and that full spectrum high-intensity li
27 gg cells before fertilization and can induce parthenogenesis and the production of haploid offspring
28  should be kept together to avoid triggering parthenogenesis and thereby decreasing genetic diversity
29 g induction of reproductive incompatibility, parthenogenesis, and feminization.
30 sed sex ratio, sexual dimorphism, protogyny, parthenogenesis, and oviposition in the pupal case.
31 ated in causing cytoplasmic incompatibility, parthenogenesis, and the feminization of genetic males i
32                                Low levels of parthenogenesis are also observed in this system (about
33  Organisms that reproduce by sperm-dependent parthenogenesis are asexual clones that require sperm of
34 e apomictic taxa suggest that apomeiosis and parthenogenesis are genetically linked, a finding that i
35           This indicates that diplospory and parthenogenesis are unlinked and inherited independently
36 cal support for the negative consequences of parthenogenesis as predicted by theory.
37                                 Induction of parthenogenesis by PsASGR-BBML will be valuable for inst
38 hat the loss of mitotic control resulting in parthenogenesis causes subsequent genome variation withi
39 ution of microbial pathogens, as well as for parthenogenesis, cell fusion events and transitions betw
40 m two different species, and reproduction by parthenogenesis constitutes an effective intrinsic barri
41 t strategies including male killing, induced parthenogenesis, cytoplasmic incompatibility, and femini
42                                  Facultative parthenogenesis enables sexually reproducing organisms t
43 loid that reproduces by facultative, meiotic parthenogenesis, encodes approximately 14,200 genes in a
44                   Dihaploids may result from parthenogenesis, entailing the development of embryos fr
45  including cytoplasmic incompatibility (CI), parthenogenesis, feminization and male killing.
46    Such alterations include the induction of parthenogenesis, feminization, cytoplasmic incompatibili
47 f bacterially infected offspring by inducing parthenogenesis, feminization, male killing, or, most co
48 ation were examined in porcine oocytes after parthenogenesis, fertilization and somatic cell nuclear
49                                  Facultative parthenogenesis (FP) has historically been regarded as r
50                                  Facultative parthenogenesis (FP) is widespread in the animal kingdom
51  of exon 5 (tae) of the gemini gene switches parthenogenesis from arrhenotoky to thelytoky.
52 cally maternal seeds whose embryos derive by parthenogenesis from unreduced egg cells, giving rise to
53 y of workers that reproduce in synchrony via parthenogenesis, giving rise to age-matched cohorts of c
54 , and reptiles are now known to reproduce by parthenogenesis (Greek for 'virgin birth') or its varian
55        The shift from sexual reproduction to parthenogenesis has occurred repeatedly in animals, but
56                     Although sperm-dependent parthenogenesis has some of the disadvantages of sex (re
57 equencing to investigate a suspected case of parthenogenesis in a king cobra (Ophiophagus hannah).
58  results imply evolution of the induction of parthenogenesis in a lineage other than Wolbachia.
59 ate a genetic basis for sporadic facultative parthenogenesis in an animal.
60 gical mechanisms associated with thelytokous parthenogenesis in ants and suggests the decay of chromo
61 ied in D. mercatorum that causes facultative parthenogenesis in D. melanogaster results in aneuploidy
62  if this is a general feature of facultative parthenogenesis in drosophilids, we compared sexually re
63 e genetic mechanisms giving rise to obligate parthenogenesis in eukaryotes remain understudied.
64 d to be the cytogenetic mechanism underlying parthenogenesis in M. smithii.
65 daptations and genetic mechanisms underlying parthenogenesis in reptilian species, challenging tradit
66 ermore, phylogenetic patterns of facultative parthenogenesis in snakes and a sex-linked color mutatio
67 ts terminal fusion as a mechanism underlying parthenogenesis in snakes.
68 sophila mercatorum could lead to facultative parthenogenesis in the non-parthenogenetic species Droso
69  of a desaturase, Desat2, caused facultative parthenogenesis in the non-parthenogenetic species that
70 n research on the significance of vertebrate parthenogenesis in the wild.
71 no apparent barriers for Wolbachia to induce parthenogenesis in these non-native backgrounds.
72 at maternally inherited microorganisms cause parthenogenesis in these wasps.
73 fertilized eggs highlights the prevalence of parthenogenesis in whitespotted bamboo sharks and poses
74 mination in the Hymenoptera is arrhenotokous parthenogenesis, in which diploid females develop from f
75                                              Parthenogenesis-inducing (PI) Wolbachia belong to a clas
76 ental stages of the host: male feminization; parthenogenesis induction; male killing; and cytoplasmic
77                                      Whereas parthenogenesis is a common mode of reproduction in lowe
78                                     Obligate parthenogenesis is found in only 0.1% of the vertebrate
79                                              Parthenogenesis is the biological phenomenon by which em
80         Asexual reproduction via thelytokous parthenogenesis is widespread in the Hymenoptera, but it
81 ts of a single meiosis (automixis or meiotic parthenogenesis) is found in diverse groups of plant, an
82 g cytoplasmic incompatibility, feminization, parthenogenesis, male killing, parasitoid defense, and p
83 fect host reproduction through feminisation, parthenogenesis, male-killing, cytoplasmic incompatibili
84 to term or survived in the wild, facultative parthenogenesis might have adaptive significance [1].
85 xual lettuce to complement dandelion LOSS OF PARTHENOGENESIS mutants.
86 y host, Populus nigra, are interspersed with parthenogenesis on a range of secondary hosts.
87 is a secondary consequence of the effects of parthenogenesis on the trophectoderm and primitive endod
88  known to cause cytoplasmic incompatibility, parthenogenesis, or feminization in various insect speci
89                                       Female parthenogenesis, or thelytoky, is particularly common in
90                         We have isolated the PARTHENOGENESIS (PAR) gene from apomictic dandelion that
91 (ES) cells generated via nuclear transfer or parthenogenesis (pES cells) are a potential source of hi
92 CI), male killing (MK), and the induction of parthenogenesis (PI).
93 s of animal populations with sperm-dependent parthenogenesis (pseudogamy or gynogenesis), based on th
94                                              Parthenogenesis rate for inseminated females was 0.71%.
95 es and population genomic data, we show that parthenogenesis results in an extreme reduction of heter
96 such as chromosomal inversions and apomictic parthenogenesis that physically restrict recombination i
97 our data support a mechanism for facultative parthenogenesis that removes all heterozygosity in a sin
98                                  Facultative parthenogenesis - the ability of sexually reproducing sp
99 Smith and David Shuker introduce facultative parthenogenesis, the ability of organisms to alternate b
100 ved from nucellar cells of the ovary and, by parthenogenesis, the development of the unreduced egg in
101                                              Parthenogenesis, the production of offspring without fer
102                  Investigating the origin of parthenogenesis through interspecific hybridization can
103  PsASGR-BBML will be valuable for installing parthenogenesis to synthesize apomixis in crops and will
104 lants is rare except when it is coupled with parthenogenesis to yield gametophytic apomixis via aposp
105 exual reproduction can resort to facultative parthenogenesis under extenuating circumstances that iso
106        Patterns of appearance of thelytokous parthenogenesis were inconsistent with a single locus, e
107 w transcription factors in promoting natural parthenogenesis were suggested.
108  of reproduction among ants is arrhenotokous parthenogenesis where unfertilized eggs give rise to hap
109 on of BBM1 in the egg cell is sufficient for parthenogenesis, which indicates that a single wild-type
110 . violaceum is analogous to forms of meiotic parthenogenesis with first division restitution (i.e. au
111       Daphnia normally reproduce by cyclical parthenogenesis, with offspring sex being determined by
112 pecies Eucypris virens exhibits geographical parthenogenesis, with rare sexual populations in souther
113 aid eggs that hatched from fertilization and parthenogenesis within the same clutch.
114                 With this mechanism, meiotic parthenogenesis would be expected to result in rapid gen
115 s true, it is reasonable to hypothesize that parthenogenesis would be found most often at low populat
116 high-intensity light supplementation boosted parthenogenesis, yielding hundreds of haploid seeds per

 
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