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1 ing precluded inferences about its ploidy or sexual cycle.
2 cificity is the first defined for a parasite sexual cycle.
3  and is progressively derepressed during the sexual cycle.
4 icating that silencing is induced during the sexual cycle.
5 way squelches transposon activity during the sexual cycle.
6 of which are indicative of cooption into the sexual cycle.
7 t C. lusitaniae undergoes meiosis during its sexual cycle.
8 ous environmental parameters to complete the sexual cycle.
9 and suggest microsporidia may have an extant sexual cycle.
10 al cycle and the lesser known, but puzzling, sexual cycle.
11 tic repertoire that could support a complete sexual cycle.
12 f the conidiophore and an early block in the sexual cycle.
13 h vector competence and part of the parasite sexual cycle.
14 l, C. lusitaniae has been reported to have a sexual cycle.
15 opportunistic fungal pathogen with a defined sexual cycle.
16 gal pathogen in humans, is thought to lack a sexual cycle.
17 the role of these genes in initiation of the sexual cycle.
18 plete meiotic toolkit, possibly indicating a sexual cycle.
19  of genes needed for progression through the sexual cycle.
20 oid organism with an incomplete and atypical sexual cycle.
21  feline-free recapitulation of the T. gondii sexual cycle.
22 duces spores, suggestive of complete meiotic sexual cycles.
23 dormant for thousands of generations between sexual cycles.
24 ly restricted to the prezygotic stage of the sexual cycle and does not interfere with vegetative grow
25                       These discoveries of a sexual cycle and MAT gene function are likely to be of b
26 tilization, and flavor production, while the sexual cycle and other phenotypes related to survival in
27 s a gene expressed preferentially during the sexual cycle and shown to be essential for normal sexual
28 rtant human pathogenic fungus with a defined sexual cycle and well-developed molecular and genetic ap
29 the frequency that yeast lineages experience sexual cycles and hence the opportunity for inbreeding.
30   These include volvocine green algae, where sexual cycles and sex-determining mechanisms have shed l
31                     The organism has a known sexual cycle, and strains of the MATalpha mating type ar
32 dentity and controls progression through the sexual cycle, and we discover that ectopic expression of
33 lead to a new model of how cell fate and the sexual cycle are controlled in C. neoformans.
34 ranscriptional regulators of the asexual and sexual cycle (brlA, abaA and steA) are altered in a delt
35 es is attributed to the circumvention of the sexual cycle by a new mode of transmission-asexual trans
36  detected and altered efficiently during the sexual cycle by a process known as RIP (repeat-induced p
37 on, we now describe conditions under which a sexual cycle can be induced leading to production of mei
38 nia reproduction is mainly clonal, a cryptic sexual cycle capable of producing hybrid genotypes has b
39 stages of Leishmania are capable of having a sexual cycle consistent with a meiotic process like that
40 although SteAp function is restricted to the sexual cycle, cross regulation between the two developme
41                                   During the sexual cycle, delta gna-1 strains are fertile as males.
42 d fertility in homozygous crosses during the sexual cycle; exogenous cAMP has no effect on this pheno
43                                            A sexual cycle for the opportunistic human pathogenic fung
44 ivision is extrapolated to the length of the sexual cycle for this protist, the measure obtained is c
45                                       In the sexual cycle, gna-1(R178C) and gna-1(Q204L) strains are
46                                       Now, a sexual cycle has been discovered in the choanoflagellate
47 pacity to reproduce sexually, even though no sexual cycle has yet been observed.
48 C. neoformans has a defined a-alpha opposite sexual cycle; however, >99% of isolates are of the alpha
49 ance mechanisms and indicate that the annual sexual cycle in aphids may lead to frequent novel genoty
50                    Mating assays confirmed a sexual cycle in Cryptococcus decagattii, demonstrating i
51 vides insight toward the identification of a sexual cycle in Malassezia, with possible implications f
52 ults provide evidence for the existence of a sexual cycle in Microsporidia, and suggest a model for t
53  sequences are frequently mutated during the sexual cycle in Neurospora crassa by a process named rep
54  to functionally replace MatA and drives the sexual cycle in the fungus A. nidulans.
55 opportunistic fungal pathogen with a defined sexual cycle in which the alpha allele of the mating typ
56 enomics have aided progress in understanding sexual cycles in less-studied taxa including ulvophyte,
57 ultiple phenotypes during the vegetative and sexual cycles in N. crassa.
58 exually, and indicate a role for specialized sexual cycles in the survival and adaptation of pathogen
59                                            A sexual cycle involving haploid cells of a and alpha mati
60                             It has a defined sexual cycle involving haploid cells of alpha and a mati
61 opportunistic fungal pathogen with a defined sexual cycle involving mating between haploid MATa and M
62                   The organism has a defined sexual cycle involving mating between haploid MATalpha a
63 is a pathogenic basidiomycete with a defined sexual cycle involving mating between haploid yeast cell
64 rate that C. lusitaniae is haploid and has a sexual cycle involving mating between MATa and MATalpha
65 ii can occur in any warm-blooded mammal, the sexual cycle is restricted to the feline intestine.
66 ly throughout the year and what drives human sexual cycles is a long-standing question.
67  human pathogen, has been thought to have no sexual cycle, it normally possesses mating-type-like ort
68    Additionally, in an approach to uncover a sexual cycle, Malassezia furfur strains were engineered
69 ng, which were highly induced throughout the sexual cycle of C. lusitaniae.
70 gna-2 is expressed during the vegetative and sexual cycle of N. crassa in both A and a mating types.
71                                          The sexual cycle of Plasmodium is required for transmission
72                                Moreover, the sexual cycle of the closest living relatives of animals,
73 Here we explore Hei10's roles throughout the sexual cycle of the fungus Sordaria with respect to loca
74 ia species may provide useful models for the sexual cycles of Candida species.
75 es exhibits altruism during both asexual and sexual cycles of its life history, and recent studies ha
76 siae and C. lusitaniae, and that a concerted sexual cycle operates in C. lusitaniae that is more remi
77 curs through an outcrossing/heterothallic a- sexual cycle or an inbreeding/homothallic - unisexual ma
78 is, Dictyostelium discoideum development and sexual cycles, Plasmodium falciparum infection, and the
79 ther or not the fungus undergoes an obligate sexual cycle, produces resting spores in affected inflor
80 en identified that corresponds to the master sexual cycle regulators a1, alpha1, and alpha2 of the Sa
81 hich is critical for genome stability across sexual cycles-relies on homologous recombination initiat
82 e of mating type genes during a self-fertile sexual cycle remain largely unknown.
83 enetic analyses, and the discovery of extant sexual cycles reveal an on-going revolution in the under
84               Profiling of the C. lusitaniae sexual cycle revealed that gene expression patterns duri
85                             By contrast, the sexual cycle showed both temporal delay and quantitative
86                  However, the development of sexual cycle-specific Hulle cells is unaffected.
87                            We report a novel sexual-cycle-specific gene-silencing system in the genet
88 ow that vaginal odour intensity differs with sexual cycle stage suggesting that odour might play a ro
89 s is a basidiomycetous fungus with a defined sexual cycle that has been linked to differentiation and
90 genome polymorphisms revealed evidence for a sexual cycle that may provide genetic diversity to allev
91                              However, in the sexual cycle, the [Het-s] prion causes meiotic drive fav
92      However, instead of the classic a-alpha sexual cycle, the majority outbreak clone appears to hav
93          G. lamblia) are not known to have a sexual cycle; these protists may be an early-diverging l
94 s differed was the ability to go through the sexual cycle to generate mature spores and viable mutant
95 t and break the species barrier to allow the sexual cycle to occur in mice.
96                 The identified heterothallic sexual cycle was used for strain development purposes, g
97                 Mutants fail to complete the sexual cycle, which normally coincides with peak MTA1 ex