ライフサイエンスコーパス: Magnaporthe

1 l grass species Brachypodium distachyon with Magnaporthe grisea (rice blast), together with modificat

2 Podospora anserina and the pathogenic fungi Magnaporthe grisea and Cryphonectria parasitica, respect

3 t in glycans isolated from the rice pathogen Magnaporthe grisea and from the plant pathogen Botryotin

4 al for the biosynthesis of fungal melanin by Magnaporthe grisea and is a focus of inhibitor design st

5 expression of TAGKO alleles were examined in Magnaporthe grisea and Mycosphaerella graminicola.

6 were constructed for the ascomycete fungus, Magnaporthe grisea and the basidiomycete fungus, Ustilag

7 hydroxy-2-butanone-4-phosphate synthase from Magnaporthe grisea are reported for the E-SO(4)(2-), E-S

8 O39 was previously mapped to chromosome 1 of Magnaporthe grisea between cosegregating markers CH5-120

9 The Magnaporthe grisea BUF1 gene suffers high-frequency muta

10 The filamentous fungus Magnaporthe grisea can cause disease on many species of

11 The blast fungus Magnaporthe grisea causes a serious disease on a wide va

12 The rice blast fungus Magnaporthe grisea causes one of the most damaging disea

13 on alleles of the MPG1 hydrophobin gene from Magnaporthe grisea causes severe defects in development

14 The fungal rice pathogen Magnaporthe grisea contains repetitive DNA sequences cal

15 Mutants of Magnaporthe grisea harboring a defective gene for 1,3, 8

16 Magnaporthe grisea is a fungal pathogen with two mating

17 The rice blast fungus Magnaporthe grisea is a highly destructive plant pathoge

18 Magnaporthe grisea is the most destructive pathogen of r

19 Mutagenesis of Magnaporthe grisea strain 4091-5-8 led to the identifica

20 ene resistance against strains of the fungus Magnaporthe grisea that express avirulent alleles of AVR

21 we show that in the plant pathogenic fungus Magnaporthe grisea trehalose-6-phosphate (T6P) synthase

22 ases of unknown function from the ascomycete Magnaporthe grisea were found to be the closest relative

23 significantly enhanced resistance to fungal (Magnaporthe grisea) and bacterial (Burkholderia glumae)

24 wing challenge with the rice blast pathogen (Magnaporthe grisea) and wheat/barley yellow stripe rusts

25 Rice blast fungus (Magnaporthe grisea) forms a highly specialized infection

26 ense response against the rice blast fungus (Magnaporthe grisea), a large-scale expressed sequence ta

27 When infected with the blast fungus (Magnaporthe grisea), SA-deficient rice exhibits increase

28 a mays), and one from the rice blast fungus (Magnaporthe grisea).

29 erization of ICL1 from the rice blast fungus Magnaporthe grisea, a gene that encodes isocitrate lyase

30 s were found to be present on the conidia of Magnaporthe grisea, and plant surface waxes were found t

31 ine synthases of Mycobacterium tuberculosis, Magnaporthe grisea, Candida albicans, and Schizosaccharo

32 The fungus Magnaporthe grisea, commonly referred to as the rice bla

33 sistant to strains of the rice blast fungus, Magnaporthe grisea, expressing AVR-Pita in a gene-for-ge

34 The rice blast fungus, Magnaporthe grisea, generates enormous turgor pressure w

35 blast disease, caused by the fungal pathogen Magnaporthe grisea, is an excellent model system to stud

36 Magnaporthe grisea, the causal agent of rice blast disea

37 sing metabolite fingerprinting, we show that Magnaporthe grisea, the causal agent of rice blast disea

38 Magnaporthe grisea, the causal agent of rice blast disea

39 d a federated database for genome studies of Magnaporthe grisea, the causal agent of rice blast disea

40 of F. graminearum with the myosin I gene of Magnaporthe grisea, the causal agent of rice blast, also

41 ressorium formation and infectious growth in Magnaporthe grisea, the fungal pathogen responsible for

42 In Magnaporthe grisea, the MST11-MST7-PMK1 MAP kinase (MAPK

43 In the rice (Oryza sativa) blast fungus Magnaporthe grisea, the pathogenicity mitogen-activated

44 r four species (Arabidopsis, rice, grape and Magnaporthe grisea, the rice blast fungus).

45 egion in O-137, a rice pathogenic isolate of Magnaporthe grisea, uncovered a novel gene, designated T

46 Rice blast is caused by the fungus Magnaporthe grisea, which elaborates specialized infecti

47 e economically important rice blast pathogen Magnaporthe grisea, which is required for exocytosis dur

48 ite changes occurring during interactions of Magnaporthe grisea--the cause of rice blast disease--wit

49 chromosome 3 in the plant pathogenic fungus Magnaporthe grisea.

50 elated development of the rice blast fungus, Magnaporthe grisea.

51 visiae, Mkc1 of Candida albicans and Mps1 of Magnaporthe grisea.

52 host infection by the fungal plant pathogen Magnaporthe grisea.

53 ice plants from the fungal disease caused by Magnaporthe grisea.

54 n synthesis in Colletotrichum lagenarium and Magnaporthe grisea.

55 ysis of an mpg1(-) gene disruption mutant in Magnaporthe grisea.

56 ressorium formation in the rice blast fungus Magnaporthe grisea.

57 osons Fot1 of Fusarium oxysporum and Pot2 of Magnaporthe grisea.

58 reted enzyme from the phytopathogenic fungus Magnaporthe grisea.

59 o fungal pathogens, Fusarium graminearum and Magnaporthe grisea.

60 arium moniliforme, Fusarium graminearum, and Magnaporthe grisea.

61 n and infectious growth by the rice pathogen Magnaporthe grisea.

62 ulence was explored in the rice blast fungus Magnaporthe grisea.

63 When the infection-specific MIR1 (Magnaporthe-infection-related gene-1) promoter was used

64 Telomeric restriction fragments in Magnaporthe isolates that infect perennial ryegrass (prg

65 -related genes, are discussed in detail with Magnaporthe oryzae (M. grisea) and Fusarium graminearum

66 rassa [Ncdcl-1 (50.5%); Ncdcl-2 (38.0%)] and Magnaporthe oryzae [MDL-1 (45.6%); MDL-2 (38.0%)], respe

67 stating disease of rice caused by the fungus Magnaporthe oryzae and can result in loss of a third of

68 to world agriculture, but also because both Magnaporthe oryzae and its host are amenable to advanced

69 gal species, including Zymoseptoria tritici, Magnaporthe oryzae and Neurospora crassa, exhibited PAMP

70 resistance against two major rice pathogens: Magnaporthe oryzae and Xanthomonas oryzae.

71 Here, we report that Magnaporthe oryzae CKS1 encodes a cyclin-dependent kinas

72 To cause rice blast disease, the fungus Magnaporthe oryzae develops a pressurized dome-shaped ce

73 ause rice blast disease, the fungal pathogen Magnaporthe oryzae develops a specialized infection stru

74 rice (Oryza sativa) NLR RGA5 recognizes the Magnaporthe oryzae effector AVR-Pia through direct inter

75 explore host factors that interact with the Magnaporthe oryzae effector AVR-Pii.

76 nd to be required for the recognition of the Magnaporthe oryzae effector AVR1-CO39.

77 The rice blast fungus Magnaporthe oryzae elaborates a specialized cell called

78 We demonstrate that Magnaporthe oryzae generates NO during germination and i

79 tant strain of the devastating rice pathogen Magnaporthe oryzae impaired for de novo methionine biosy

80 d development of the important rice pathogen Magnaporthe oryzae in leaf cells.

81 The rice blast fungus Magnaporthe oryzae infects plants with a specialized cel

82 The rice blast fungus Magnaporthe oryzae is a model for studying fungal-plant

83 The fungus Magnaporthe oryzae is a serious pathogen of rice and oth

84 Magnaporthe oryzae is the causal agent of rice blast dis

85 Magnaporthe oryzae is the most damaging fungal pathogen

86 The blast fungus Magnaporthe oryzae is the most devastating pathogen of c

87 he crystal structure of the DBD of PCG2, the Magnaporthe oryzae orthologue of MBP1, bound to MCB-DNA.

88 Here, we show that the rice blast fungus Magnaporthe oryzae overcomes this first line of plant de

89 Here we report that the rice blast fungus Magnaporthe oryzae possesses two distinct secretion syst

90 effector AvrPiz-t from the rice blast fungus Magnaporthe oryzae preferentially accumulates in the spe

91 truction by the hemibiotrophic rice pathogen Magnaporthe oryzae requires plant defence suppression to

92 hic invasive hyphae (IH) of the blast fungus Magnaporthe oryzae secrete effectors to alter host defen

93 The rice blast fungus Magnaporthe oryzae spreads in rice biotrophically early

94 were inoculated with the race IB49 of Magnaporthe oryzae that recognizes Pi-ta.

95 Various surface signals are recognized by Magnaporthe oryzae to activate the Pmk1 MAP kinase that

96 and development of pathogenic fungi such as Magnaporthe oryzae which causes rice blast.

97 llb shows enhanced resistance to rice blast (Magnaporthe oryzae) and bacterial blight (Xanthomonas or

98 mentous fungi such as the rice blast fungus (Magnaporthe oryzae) remains unclear.

99 n developed for use in the rice blast fungus Magnaporthe oryzae, allowing rapid generation of transfo

100 h corresponds to MAP kinase kinase kinase in Magnaporthe oryzae, and urate oxidase (designated ClUras

101 Magnaporthe oryzae, the causal agent of blast disease, i

102 In Magnaporthe oryzae, the Mst11-Mst7-Pmk1 MAP kinase pathw

103 ing in pathogenesis of the rice blast fungus Magnaporthe oryzae, we identified MoGlo3 as an ArfGAP pr

104 sease is caused by the hemibiotrophic fungus Magnaporthe oryzae, which invades living plant cells usi

105 formation, was validated in the hemibiotroph Magnaporthe oryzae.

106 cterized MoVrp1 as the yeast Vrp1 homolog in Magnaporthe oryzae.

107 ressorium formation plays a critical role in Magnaporthe oryzae.

108 hetic system involving the rice blast fungus Magnaporthe oryzae.

109 coding gene (ETFDH) in the rice blast fungus Magnaporthe oryzae.

110 ppressorium formation and plant infection in Magnaporthe oryzae.

111 otein kinase C is essential for viability of Magnaporthe oryzae.

112 ogenesis in a model plant pathogenic fungus, Magnaporthe oryzae.

113 r the development of infection structures in Magnaporthe oryzae.

114 ction after infection by the fungal pathogen Magnaporthe oryzae.

115 tion is a key step in the infection cycle of Magnaporthe oryzae.

116 criptome sequencing of the rice blast fungus Magnaporthe oryzae.

117 st due to infection by the rice blast fungus Magnaporthe oryzae.

118 chromosome ends of the rice blast pathogen, Magnaporthe oryzae.

119 at control two fungal CFI protein classes in Magnaporthe oryzae: Rbp35/CfI25 complex and Hrp1.

120 Magnaporthe poae, a fungal pathogen of Kentucky bluegras

121 trated the evolutionary relationship between Magnaporthe species and the influence of host differenti

122 we compared genome sequence of 6 isolates of Magnaporthe species obtained from three different host p

123 ergence are host adaptability mechanisms for Magnaporthe species, and this coevolution processes is g

124 entified an asymmetric selection pressure on Magnaporthe species.

125 o filamentous fungi, but homologous genes in Magnaporthe, Ustilago, Aspergillus, Fusarium, Epichloe,