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1 y (hisn1a hisn1b) exhibited a combination of gametophytic and embryonic lethality in heterozygotes.
2  homozygotes could not be identified, due to gametophytic and embryonic lethality.
3           Synchronized communication between gametophytic and sporophytic tissue is crucial for succe
4 same individual genes were expressed both in gametophytic and sporophytic tissues, although under dif
5 mal development of either the sporophytic or gametophytic anther tissues.
6                                           In gametophytic apomicts of the aposporous type, each cell
7    Asexual seed production (agamospermy) via gametophytic apomixis in flowering plants typically invo
8                                              Gametophytic apomixis in Pennisetum squamulatum and Cenc
9                                              Gametophytic apomixis is a way of asexual plant reproduc
10                                              Gametophytic apomixis is asexual reproduction as a conse
11  it is coupled with parthenogenesis to yield gametophytic apomixis via apospory or diplospory.
12 uires maternal gene activity in the haploid (gametophytic) as well as diploid (sporophytic) tissues o
13 tial for cytokinesis in both sporophytic and gametophytic cell types.
14    Remarkably, we uncover new sets of female gametophytic cell-specific transcripts with predicted bi
15 es are typically sex-specific, e.g., gametic/gametophytic competition typically occurs among sperm/po
16 rocal crosses indicated a significant female gametophytic contribution to this mutant phenotype.
17 action domains and their requirement in male gametophytic cytokinesis.
18 -of-function mutation in PAPS1 causes a male gametophytic defect, whereas a weak allele leads to redu
19 UMP1a and UMP1b isoforms displaying a strong gametophytic defect.
20 one of these, termed PAPS1, result in a male gametophytic defect.
21 e mutants in Arabidopsis XPO1A and XPO1B are gametophytic defective.
22 ackground causes serious growth retardation, gametophytic defects and premature cell death in develop
23        Homozygous nrpd2 mutants have neither gametophytic defects nor embryo lethality, although adul
24 utants for ATPd could not be obtained due to gametophytic defects, while heterozygotes possess no vis
25                                       Female gametophytic development and early embryonic development
26 urrently, the genes and pathways involved in gametophytic development and function in flowering plant
27 t the HSFB2a locus influences vegetative and gametophytic development in Arabidopsis.
28 y of these transposition events occur during gametophytic development.
29 patible crossing 'anomalies' suggest that a 'gametophytic element' may influence the outcome of cross
30 e used to evaluate the possibility of female gametophytic expression for any gene in the ATH1 array,
31 1/+ mutants and VAL_RNAi lines, we find that GAMETOPHYTIC FACTOR 2 (GFA2), which is required for syne
32                                          Two gametophytic factors are sufficient for pollen compatibi
33 fic conflict over reinforcement inspired by "gametophytic factors", which act as PMPZ barriers among
34 eles pointed to a dual role, sporophytic and gametophytic, for the gene on the male side.
35 th bryophytes and tracheophytes, the haploid gametophytic generation is inferred to be ancestrally fr
36 d that hypomethylation in the female or male gametophytic generation was sufficient to influence F(1)
37 e Arabidopsis genome require analysis of the gametophytic generation, since approximately 10% of the
38 (FM) is crucial for the establishment of the gametophytic generation, the mechanisms that determine t
39 entiate into a multicellular gamete-forming "gametophytic generation." Different populations of helpe
40 cle includes diploid sporophytic and haploid gametophytic generations.
41 s that delete or disrupt genes essential for gametophytic growth and development.
42 eraction of products contributed by both the gametophytic (haploid) and sporophytic (diploid) genomes
43  and P450 mutant phenotypes, indicating that gametophytic homocastasterone biosynthesis is affected i
44 established mechanisms, that is, homomorphic gametophytic, homomorphic sporophytic or heteromorphic S
45                                The two-locus gametophytic incompatibility system in perennial ryegras
46                            We show that male gametophytic kokopelli (kpl) mutants display frequent si
47 the Columbia ecotype but sidecar pollen is a gametophytic lethal in the Landsberg erecta ecotype.
48 ever, the stt3a-1 stt3b-1 double mutation is gametophytic lethal.
49 emoval of any of these components results in gametophytic lethality due to pollen defects, demonstrat
50 of AtGPAT9 demonstrates both male and female gametophytic lethality phenotypes, consistent with the r
51           Our results identify two essential gametophytic loci required for progression through diffe
52 t regulates cell proliferation by exerting a gametophytic maternal control during seed development.
53                 The characterization of many gametophytic maternal effect (GME) mutants affecting see
54                                          The gametophytic maternal effect mutant medea (mea) shows ab
55 s with both sporophytic maternal effects and gametophytic maternal effects have been identified.
56                                      A novel gametophytic maternal-effect mutant defective in early e
57 d insight into the dynamic regulation of the gametophytic meristem and its evolution.
58 s are major products of both sporophytic and gametophytic metabolism during pollen development.
59                              Apparently, the gametophytic microspore oil-body oleosins share common e
60 inations of backcross and F2 lines suggest a gametophytic mode of restoration, and indicate that enha
61              The Arabidopsis thaliana female gametophytic mutant glauce (glc) can exhibit embryo deve
62  applications including a genetic screen for gametophytic mutants and methods for investigating gene
63 ophytic mutation, to our knowledge the first gametophytic mutation in Arabidopsis that affects early
64 opteris, it is difficult to assess whether a gametophytic mutation is dominant or recessive or to det
65      To our knowledge, scp is the first male gametophytic mutation to be described in Arabidopsis.
66 trad analysis to show that raring-to-go is a gametophytic mutation, to our knowledge the first gameto
67  and gum mutants correspond to male-specific gametophytic mutations that also reduce pollen fitness.
68 romeres, easily distinguish sporophytic from gametophytic mutations, and accurately assess crossover
69 cytoplasm, male fertility is determined by a gametophytic, nuclear restoration-of-fertility gene.
70  allele of sidecar pollen shows differential gametophytic penetrance and variable expressivity in dif
71 ue to haploid purifying selection during the gametophytic phase of the life cycle.
72 In angiosperms, the transition to the female gametophytic phase relies on the specification of premei
73 splayed no phenotypic alterations during its gametophytic phase, it failed to develop sporophytes, in
74 ween the diploid sporophytic and the haploid gametophytic phases.
75  an important role in consolidating the male gametophytic ploidy consistency.
76  of the SMC5/6 complex in the maintenance of gametophytic ploidy in Arabidopsis.
77  a relatively recent consensus that hornwort gametophytic pores ('HGPs' - our term) are not homologou
78  homologues, namely the two-celled epidermal gametophytic pores of hornworts (typically referred to a
79 , so that accumulation of maternally derived gametophytic protein is likely to be responsible for the
80 e microspores of the tetrad, and also play a gametophytic role later in pollen grain maturation.
81 s for allo- or autotetraploid species with a gametophytic S-Z SI system.
82 d, which indicate the possible presence of a gametophytic SC locus.
83 plained by a combination of recessive-lethal gametophytic selection against the parthenogenetic locus
84 as much more influence on genes subjected to gametophytic selection than on genes solely under sporop
85 ents, such as meiotic drive in F1 parents or gametophytic selection, contributed to TRD.
86                                         With gametophytic selection, low frequencies of double reduct
87 the presence of another SC locus, exhibiting gametophytic selection, segregating in this population a
88                         Wild cherry exhibits gametophytic self-incompatibility (GSI) and vegetative r
89 ription of the breakdown of S-RNase-mediated gametophytic self-incompatibility (GSI) in a polyploid s
90 se and F-box proteins) are essential for the gametophytic self-incompatibility (GSI) specific recogni
91 ymorphism at the S locus that determines the gametophytic self-incompatibility (GSI) system in the pi
92 xamined were heterozygous, as expected under gametophytic self-incompatibility (GSI).
93                                              Gametophytic self-incompatibility (SI) possessed by the
94 y species of Prunus display an S-RNase-based gametophytic self-incompatibility (SI), controlled by a
95 mbers also include the S-RNases, involved in gametophytic self-incompatibility in plants.
96 systems of balancing selection such as plant gametophytic self-incompatibility loci.
97 ions of allelic diversity at the RNase-based gametophytic self-incompatibility locus in the Rosaceae.
98                                          The gametophytic self-incompatibility mechanism enables the
99 sent in natural populations are designed for gametophytic self-incompatibility systems (GSI) in which
100 ework for investigating the evolution of the gametophytic self-incompatibility systems in other famil
101 rasus) exhibits a genotype-dependent loss of gametophytic self-incompatibility that is caused by the
102  investigate protein-protein interactions in gametophytic self-incompatibility, we used a yeast two-h
103                        One such mechanism is gametophytic self-incompatibility, which allows the fema
104 favoured a novel mechanism co-occurring with gametophytic self-incompatibility.
105                                    Moreover, gametophytic selfing affects the relative influence of d
106                                 We find that gametophytic selfing increases the range of epistasis un
107 velopmental stages, our results suggest that gametophytic selfing may have greater significance for f
108 We consider two different life cycles: under gametophytic selfing, a given proportion of fertilizatio
109 hree different mating systems, one of which, gametophytic selfing, is an extreme form of inbreeding o
110  of fern species studied show a capacity for gametophytic selfing, producing sporophytes from both is
111                    The observation that some gametophytic sex-determining mutants have phenotypic eff
112 ants and the mechanisms regulating bryophyte gametophytic shoot development are largely unknown.
113 eral branching evolved by convergence in the gametophytic shoot of mosses and primed its diversificat
114                              We show that in gametophytic shoots of Physcomitrella, lateral branches
115                  We have found that treating gametophytic shoots of the moss Physcomitrella patens wi
116 ber in populations of a tetraploid herb with gametophytic SI (GSI) spanning a range of effective popu
117                                              Gametophytic SI is well characterized for Solanaceae and
118 resent functional alleles under single-locus gametophytic SI.
119       About half of these mutations are male gametophytic-specific mutations, while the others also a
120                                       Mutual gametophytic sterility was overcome by complementation w
121  pollen viability, involves a novel two-gene gametophytic system, wherein genes designated Rf3 and Rf
122 itrella patens results in a shared defect in gametophytic tip cell growth.
123       Protoplasts, isolated from filamentous gametophytic tissue, regenerate directly into filamentou
124          The steroid profile of maternal and gametophytic tissues of wild-type (WT) and adxr ovules r
125 toring GSNOR expression in maternal, but not gametophytic tissues, or increasing auxin efflux substra
126 ssed in the sporophytic tapetal cells and in gametophytic tissues, they are regulated differentially
127 Arabidopsis ENOD-like proteins accumulate in gametophytic tissues, whereas in both floral and vegetat
128 ess tolerance while TTL2 is involved in male gametophytic transmission.
129 ossing, wind-pollinated species exhibiting a gametophytic two-locus system of self-incompatibility (S
130  show a regulatory function of miR171 at the gametophytic vegetative growth stage and targeted deleti
131 ormation of multiple apical meristems at the gametophytic vegetative stage in response to elevated Pp

 
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