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1 ctivity in peroxisomes primarily affects the male gametophyte.
2 e exhibited reduced transmission through the male gametophyte.
3 ontribute to the total RPL10 activity in the male gametophyte.
4 s that show reduced transmission through the male gametophyte.
5 ance in vivo of a specific Rop, rop2, in the male gametophyte.
6  mutated NPG1 is not transmitted through the male gametophyte.
7 nd fem4 mutations affect both the female and male gametophyte.
8 s that SIDECAR POLLEN is indeed expressed in male gametophytes.
9  upregulated in hermaphrodites compared with male gametophytes.
10                                  The fate of male gametophytes after pollen reaches stigmas links pol
11  is essential for the proper function of the male gametophyte, although the synthesis of histidine, l
12 e, we review the evolutionary origins of the male gametophyte among land plants and, in particular, i
13 mately 10% of the genes are expressed in the male gametophyte and approximately 9% in the female game
14 alTase) that is expressed exclusively in the male gametophyte and controls the formation of a pollen-
15 report that MED30 is also essential for both male gametophyte and embryo development in the model pla
16 hat AtPME48 is specifically expressed in the male gametophyte and is the second most expressed PME in
17 iency results in aberrant development of the male gametophyte and sporophyte.
18  alleles were poorly transmitted through the male gametophyte and were lethal in homozygous plants.
19 d extracellular cell-wall matrix surrounding male gametophytes and acts as a natural protector of pol
20        DUO1 is required for cell division in male gametophytes and is a target of microRNA 159 (miR15
21 ctivity is required for guided growth of the male gametophytes and pollen tube-ovule interaction.
22 cifically or preferentially expressed in the male gametophyte, and six genes are highly expressed in
23  patterns, provides a protective barrier for male gametophytes, and serves as a mediator of strong an
24 ts demonstrate that ssSPTs are essential for male gametophytes, are important for FB1 sensitivity, an
25 alysis of transporter genes expressed in the male gametophyte at four developmental stages was conduc
26 ransmission, suggesting a requirement in the male gametophyte, but has no paternal effect on seed dev
27           Transmission frequency through the male gametophyte, but not the female, was lower than exp
28 oid embryo production from in vitro-cultured male gametophytes, but this technique remains poorly und
29 rms) are characterized by pollen tubes (PTs; male gametophytes) carrying two immobile sperm cells tha
30          The intensification of pollen tube (male gametophyte) competition and enhanced maternal sele
31                 An Arabidopsis pollen grain (male gametophyte) consists of three cells: the vegetativ
32  data demonstrate that AtSPP is required for male gametophyte development and pollen maturation in Ar
33  that (1) the delta-subunit is essential for male gametophyte development in Arabidopsis, (2) a distu
34                                              Male gametophyte development is highly sensitive to elev
35 dition, BAM1, BAM2 and BAM3 are required for male gametophyte development, as well as ovule specifica
36                                       During male gametophyte development, the asymmetric mitotic div
37  level of regulation for this transporter in male gametophyte development.
38 of transporters and potential receptors with male gametophyte development.
39 reoisomer of OPDA to produce JA required for male gametophyte development.
40 tic tissues, the young transcriptomes of the male gametophyte displayed greater complexity and divers
41 ull mutant cannot be transmitted through the male gametophyte due to a defect in pollen tube growth.
42 owering plants depends on the fitness of the male gametophyte during fertilization.
43                         Thus, the details of male gametophyte ecology should shape sporophyte reprodu
44                    The haploid pollen grain (male gametophyte) extends a pollen tube that carries two
45 al analyses of insertional mutants affecting male gametophyte function, and should allow detailed gen
46 ese data strongly support a role for rop2 in male gametophyte function, perhaps surprisingly, given t
47 ignaling in vegetative tissue and for normal male gametophyte function.
48 nt T-DNA mutations reveal a role for SEC8 in male gametophyte function.
49 ore than 200 genes have been associated with male gametophyte functions in this species.
50 opoda In conclusion, we provide insight into male gametophyte functions of the most basal angiosperm
51 40) is the main exocyst EXO70 isoform in the male gametophyte, governing the conventional secretory f
52 mone that is required for the development of male gametophytes in the homosporous fern Ceratopteris r
53  protuberance formed by the pollen grain, or male gametophyte, in flowering plants.
54 strated reduced transmission of vcl1 through male gametophytes, indicating that vcl1 was expressive a
55       We propose that the totipotency of the male gametophyte is kept in check by an HDAC-dependent m
56 s microspore embryogenesis system, where the male gametophyte is reprogrammed in vitro to form haploi
57                             TSA treatment of male gametophytes is associated with the hyperacetylatio
58                           The highly reduced male gametophyte of angiosperm plants is a two- or three
59                                          The male gametophyte of Arabidopsis thaliana, which is recal
60 ntaxins from these families is lethal in the male gametophyte of Arabidopsis.
61 precocious translation of transcripts in the male gametophyte of M. vestita.
62 lular mechanism of B chromosome drive in the male gametophyte of rye (Secale cereale).
63 ctures evolved, which genes occur de novo in male gametophytes of angiosperms, and to which extent PT
64 es during the development of both female and male gametophytes of Arabidopsis.
65 tivity with trichostatin A (TSA) in cultured male gametophytes of Brassica napus leads to a large inc
66                                              Male gametophytes of M. polymorpha showed higher levels
67 ion in cell fate determination in developing male gametophytes of M. vestita.
68 ie cell fate determination in the endosporic male gametophytes of the fern, Marsilea vestita.
69                   Interestingly, the haploid male gametophyte or pollen in Arabidopsis, on the other
70             In flowering plants, the haploid male gametophyte or pollen tube (PT) [5] carries two non
71                                     Although male gametophyte performance primarily involves cellular
72 inated development; e.g., development of the male gametophyte pollen depends on the surrounding sporo
73 ends on compatible communication between the male gametophyte (pollen tube) and the maternal tissues
74             In flowering plants, the haploid male gametophytes (pollen grains) are generated in the a
75 oint for sporophytic development controlling male gametophyte production.
76 tion within individual ovules in addition to male gametophyte (sperm) competition and maternal mate c
77 insights into the nature and implications of male gametophyte success.
78 ity depends on the proper development of the male gametophyte, successful pollen germination, tube gr
79                        Pollen grains are the male gametophytes that deliver sperm cells to female gam
80                                  The haploid male gametophyte, the pollen grain, is a terminally diff
81 ical dominance, transition to flowering, and male gametophyte viability.
82 oth kinesins, postmeiotic development of the male gametophyte was severely inhibited.
83 hality in the female gametophyte but not the male gametophyte, which had the redundant LPAT3.