ライフサイエンスコーパス: specific resistance

1 mechanisms associated with Ve-mediated, race-specific resistance.

2 in the establishment of cell death and race-specific resistance.

3 le of BIK1 to basal defense rather than race-specific resistance.

4 hogen-derived effectors and thus confer race-specific resistance.

5 e (SAR) and implicated in expression of race-specific resistance.

6 mediated by RPW8 uses the same mechanisms as specific resistance.

7 lar to those induced by R genes that control specific resistance.

8 these differences endow platelet VWF with a specific resistance against proteolysis by the VWF-cleav

9 ion of transgene-derived RNA, extreme strain-specific resistance against PVX, low and non-uniform GUS

10 lysis estimated subtype frequencies and drug-specific resistance and included a prognostic meta-analy

11 ones are designed to overcome both quinolone-specific resistance and resistance to the coupled agents

12 multilocus sequence types (STs) and for host specific resistance and virulence factors previously ass

13 titution were growth impaired, displayed ATV-specific resistance, and had increased susceptibilities

14 While specific, resistance-bearing mutations at positions 31 a

15 ctive in controlling crop diseases than race-specific resistance because of its broad spectrum and du

16 ease susceptibility) mutation abolishes race-specific resistance conferred by a major subclass of res

17 Thus, specific resistance conferred solely by Pto in N. bentha

18 m them in the absence of antibiotics had the specific resistance-conferring mutations present in the

19 These findings suggest that GraS mediates specific resistance countermeasures to HDPs in immune co

20 the use of recombinant E. coli carrying the specific resistance determinant.

21 pathogens and recombinant bacteria carrying specific resistance determinants.

22 For the United States, state-specific resistance estimates demonstrated an agreement

23 istance and support the hypothesis that host-specific resistance evolved from the recognition and pre

24 therapeutic efficacy of a 6-month program of specific resistance exercise designed to reverse glucoco

25 The race-specific resistance gene Pi-ta has been effectively used

26 olocalized with published NLB QTL and a race-specific resistance gene.

27 Race-specific resistance genes protect the global wheat crop

28 nds of plant species, but some plants harbor specific resistance genes that defend against these pest

29 ve cell death associated with different race-specific resistance genes was unaffected by changes in t

30 erring SNPs, potentially in combination with specific resistance genes, precedes full resistance, we

31 isease, have overcome most of the known race-specific resistance genes.

32 Non-race-specific resistance has been more effective in controlli

33 Thus, NHO1 is deployed for both general and specific resistance in Arabidopsis and targeted by the b

34 providing the first demonstration of aptamer-specific resistance in cell culture.

35 ene-mediated resistance in roots and nonrace-specific resistance in cotyledon tissues.

36 ion of transfected rat ALDH-3 can confer OAP-specific resistance in human MCF-7 cells.

37 Pseudomonas syringae pv tomato triggers race-specific resistance in tomato plants carrying Pto, a res

38 sistance, while the role of NIM1/NPR in race-specific resistance is limited to resistance to P. paras

39 With QTL mapping, the roles of specific resistance loci can be described, race-specific

40 h neocarzinostatin protein alone implicate a specific resistance mechanism in yeast that targets the

41 lated powdery mildew, suggesting that a very specific resistance mechanism is operating in this case.

42 tions raise the possibility for an ABC-DLBCL-specific resistance mechanism that is directed toward 1

43 at can remain effective against the ketolide-specific resistance mechanism.

44 itness of Bt-resistant T. ni depended on the specific resistance mechanisms as well as host plants.

45 tural product antibiotic might be limited by specific resistance mechanisms in some bacteria, such as

46 al peptide sensor system that controls major specific resistance mechanisms of Gram-positive bacteria

47 ecular technology is the direct detection of specific resistance mechanisms that evolve during therap

48 in preclinical models, treatments targeting specific resistance mechanisms to sensitize ICBT-resista

49 ungal species, or the in situ development of specific resistance mechanisms.

50 e relationship between antimicrobial use and specific resistance mechanisms.

51 rsonalized ICBT strategies that target tumor-specific resistance mechanisms.

52 cost and that this cost is determined by the specific resistance mutation and strain genetic backgrou

53 on different antibiotics revealed macrolide-specific resistance mutations.

54 Race-specific resistance of cowpea to Striga involves a coile

55 These data demonstrate a durable and specific resistance of human thymocytes to apoptosis ind

56 ghtly to the Rps1-k allele that confers race-specific resistance of soybean to the the fungal pathoge

57 ed as major populations during failure; only specific resistance pathways (Y143R-Q148H/R-N155H) assoc

58 methods with studies revealing biomarkers of specific resistance pathways and pharmacologic approache

59 rategy should be adapted relative to country-specific resistance patterns.

60 BON1 is a negative regulator of a haplotype-specific Resistance (R) gene SNC1.

61 Cultivar-specific resistance (R) genes mediate a highly localized

62 re dispensable for immunity mediated by race-specific resistance (R) genes, highlighting fundamental

63 virulence gene products are required for the specific resistance response as long as the avirulence g

64 sis RIN4, and the ability to trigger an RPS2-specific resistance response.

65 ion of basal resistance (hrpA mutants), gene-specific resistance (RPM1-specified interactions) and su

66 were isolated previously, revealing a virus-specific resistance system in the phloem.

67 plant innate immunity system provides highly specific resistance, there is emerging evidence to suppo

68 Recessive strain-specific resistance to a number of plant viruses in the

69 Plants with specific resistance to a single class of herbicides have

70 lites by Arabidopsis thaliana confers tissue-specific resistance to a wide range of bacterial pathoge

71 rential glycosylation, platelet-VWF exhibits specific resistance to ADAMTS13 proteolysis.

72 earing I50L with those bearing I50V revealed specific resistance to ATV and amprenavir, respectively,

73 on for xa5, a recessive gene conferring race-specific resistance to bacterial blight in rice.

74 lmonary tuberculosis and suggest that strain-specific resistance to BCG-induced protective immunity m

75 ription factor in rice that confers non-race-specific resistance to blast.

76 stance gene confers Rar1-dependent, AvrMla13-specific resistance to Blumeria graminis f. sp. hordei (

77 These findings demonstrate disease-specific resistance to Fas-mediated death signaling in p

78 RFO3 confers specific resistance to FOM and provides no resistance to

79 should focus on secreted protein antigens in specific resistance to infection and have increased our

80 anslational flexibility as well as cell type-specific resistance to inhibition of cap-dependent trans

81 LXRalpha in transgenic mice confers a female-specific resistance to lithocholic acid (LCA)-induced he

82 in otherwise nonrestricting cells conferred specific resistance to N-MLV infection, indicating that

83 ibroblasts, overexpression of YB-1 confers a specific resistance to oncogenic cellular transformation

84 R-2) led to a loss of HR cell death and race-specific resistance to P. sojae and also to a loss of is

85 monas syringae pv glycinea) mediates species-specific resistance to P. syringae expressing the avirul

86 Pto kinase of tomato, which is required for specific resistance to P. syringae strains expressing av

87 ant disease resistance (R) genes confer race-specific resistance to pathogens and are genetically def

88 We analyzed strain-specific resistance to PG9 using sequence and structural

89 alleles confer agronomically important race-specific resistance to powdery mildew (Blumeria graminis

90 hirsutum var. glabratum that exhibits avrPto-specific resistance to Pst.

91 sease resistance (R) gene Pto specifies race-specific resistance to the bacterial pathogen Pseudomona

92 otein, Sr33, which is responsible for strain-specific resistance to the wheat stem rust pathogen, Puc

93 tecture, does not develop high-level biofilm-specific resistance to three different classes of antibi

94 of the Flv(r) allele that confers flavivirus-specific resistance to virus-induced disease in mice by

95 Specific resistance was generated both to a plasmacytoma