ライフサイエンスコーパス: sexual cycle

1 ing precluded inferences about its ploidy or sexual cycle.

2 plete meiotic toolkit, possibly indicating a 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 of genes needed for progression through the sexual cycle.

19 duces spores, suggestive of complete meiotic sexual cycles.

20 ly restricted to the prezygotic stage of the sexual cycle and does not interfere with vegetative grow

21 These discoveries of a sexual cycle and MAT gene function are likely to be of b

22 tilization, and flavor production, while the sexual cycle and other phenotypes related to survival in

23 s a gene expressed preferentially during the sexual cycle and shown to be essential for normal sexual

24 rtant human pathogenic fungus with a defined sexual cycle and well-developed molecular and genetic ap

25 the frequency that yeast lineages experience sexual cycles and hence the opportunity for inbreeding.

26 The organism has a known sexual cycle, and strains of the MATalpha mating type ar

27 dentity and controls progression through the sexual cycle, and we discover that ectopic expression of

28 lead to a new model of how cell fate and the sexual cycle are controlled in C. neoformans.

29 ranscriptional regulators of the asexual and sexual cycle (brlA, abaA and steA) are altered in a delt

30 es is attributed to the circumvention of the sexual cycle by a new mode of transmission-asexual trans

31 detected and altered efficiently during the sexual cycle by a process known as RIP (repeat-induced p

32 on, we now describe conditions under which a sexual cycle can be induced leading to production of mei

33 stages of Leishmania are capable of having a sexual cycle consistent with a meiotic process like that

34 although SteAp function is restricted to the sexual cycle, cross regulation between the two developme

35 During the sexual cycle, delta gna-1 strains are fertile as males.

36 d fertility in homozygous crosses during the sexual cycle; exogenous cAMP has no effect on this pheno

37 ivision is extrapolated to the length of the sexual cycle for this protist, the measure obtained is c

38 In the sexual cycle, gna-1(R178C) and gna-1(Q204L) strains are

39 Now, a sexual cycle has been discovered in the choanoflagellate

40 C. neoformans has a defined a-alpha opposite sexual cycle; however, >99% of isolates are of the alpha

41 ance mechanisms and indicate that the annual sexual cycle in aphids may lead to frequent novel genoty

42 sequences are frequently mutated during the sexual cycle in Neurospora crassa by a process named rep

43 to functionally replace MatA and drives the sexual cycle in the fungus A. nidulans.

44 opportunistic fungal pathogen with a defined sexual cycle in which the alpha allele of the mating typ

45 ultiple phenotypes during the vegetative and sexual cycles in N. crassa.

46 exually, and indicate a role for specialized sexual cycles in the survival and adaptation of pathogen

47 A sexual cycle involving haploid cells of a and alpha mati

48 It has a defined sexual cycle involving haploid cells of alpha and a mati

49 opportunistic fungal pathogen with a defined sexual cycle involving mating between haploid MATa and M

50 The organism has a defined sexual cycle involving mating between haploid MATalpha a

51 is a pathogenic basidiomycete with a defined sexual cycle involving mating between haploid yeast cell

52 rate that C. lusitaniae is haploid and has a sexual cycle involving mating between MATa and MATalpha

53 ly throughout the year and what drives human sexual cycles is a long-standing question.

54 human pathogen, has been thought to have no sexual cycle, it normally possesses mating-type-like ort

55 ng, which were highly induced throughout the sexual cycle of C. lusitaniae.

56 gna-2 is expressed during the vegetative and sexual cycle of N. crassa in both A and a mating types.

57 The sexual cycle of Plasmodium is required for transmission

58 Moreover, the sexual cycle of the closest living relatives of animals,

59 Here we explore Hei10's roles throughout the sexual cycle of the fungus Sordaria with respect to loca

60 ia species may provide useful models for the sexual cycles of Candida species.

61 es exhibits altruism during both asexual and sexual cycles of its life history, and recent studies ha

62 siae and C. lusitaniae, and that a concerted sexual cycle operates in C. lusitaniae that is more remi

63 curs through an outcrossing/heterothallic a- sexual cycle or an inbreeding/homothallic - unisexual ma

64 ther or not the fungus undergoes an obligate sexual cycle, produces resting spores in affected inflor

65 en identified that corresponds to the master sexual cycle regulators a1, alpha1, and alpha2 of the Sa

66 e of mating type genes during a self-fertile sexual cycle remain largely unknown.

67 enetic analyses, and the discovery of extant sexual cycles reveal an on-going revolution in the under

68 Profiling of the C. lusitaniae sexual cycle revealed that gene expression patterns duri

69 By contrast, the sexual cycle showed both temporal delay and quantitative

70 However, the development of sexual cycle-specific Hulle cells is unaffected.

71 We report a novel sexual-cycle-specific gene-silencing system in the genet

72 s is a basidiomycetous fungus with a defined sexual cycle that has been linked to differentiation and

73 genome polymorphisms revealed evidence for a sexual cycle that may provide genetic diversity to allev

74 However, in the sexual cycle, the [Het-s] prion causes meiotic drive fav

75 However, instead of the classic a-alpha sexual cycle, the majority outbreak clone appears to hav

76 G. lamblia) are not known to have a sexual cycle; these protists may be an early-diverging l

77 s differed was the ability to go through the sexual cycle to generate mature spores and viable mutant

78 The identified heterothallic sexual cycle was used for strain development purposes, g