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 monstrate a mechanism that allows for tissue-specific resistance against stress and could aid in the

11 ure studies in associating precise MICs with specific resistance alleles.

12 d and quantified the correlation between age-specific resistance and fitness in the field.

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

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

15 Prevalence of class-specific resistance and resistance-conferring substituti

16 veals a surprisingly complex map of genotype-specific resistance and sensitivity.

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

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

19 We find that multi-drug and antibiotic-specific resistance are acquired through categorically d

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

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

22 In the absence of a specific resistance breakpoint our results suggest a MIC

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

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

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

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

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

28 pathogens and recombinant bacteria carrying specific resistance determinants.

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

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

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

32 The wheat race-specific resistance gene Lr14a encodes an ankyrin-repeat

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

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

35 ntal interfaces related to the occurrence of specific resistance genes (bla(SHV-1) (SHV(238G240E) str

36 esponse to antibiotics (phenotype) or detect specific resistance genes (genotype).

37 Race-specific resistance genes protect the global wheat crop

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

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

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

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

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

43 Here, we show a specific resistance in an Escherichia coli K-12 MG1655 s

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

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

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

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

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

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

50 Including country-specific, age- and sex-specific resistance levels alongside projected demograph

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

52 m 80 to 100%, based on the microorganism and specific resistance marker(s).

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

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

55 ts in vitro and in vivo suggesting that this specific resistance mechanism is unlikely to arise in Mt

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

57 rom the mitochondria into the cytosol, but a specific resistance mechanism to truncated BID-dependent

58 tolerance to antibiotics in the absence of a specific resistance mechanism.

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

60 asses and were selected to address the class-specific resistance mechanisms and determinants that wer

61 suggests fly populations differ in E. muscae-specific resistance mechanisms as well as generic defenc

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

63 pies calls for a better understanding of the specific resistance mechanisms in glioblastoma (GBM) and

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

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

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

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

68 yo Clinic Laboratories not characterized for specific resistance mechanisms, and 128 isolates with CF

69 To address this gap and elucidate species-specific resistance mechanisms, we determined the first

70 onsistent due to poorly understood, pathogen-specific resistance mechanisms.

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

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

73 e relationship between antimicrobial use and specific resistance mechanisms.

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

75 tion experiments failed to identify compound-specific resistance mutations in gag or pol, even though

76 y influence the likelihood of acquisition of specific resistance mutations.

77 on different antibiotics revealed macrolide-specific resistance mutations.

78 arrier function against the passage of ions (specific resistance of approximately 1 MOmega cm(2)) app

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

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

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

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

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

84 nd response mechanisms, (2) identify patient-specific resistance pathways, (3) develop biomarkers for

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

86 and AMR vehicles underlying the expansion of specific resistance phenotypes that coincide with the gr

87 Correlations between strain-specific resistance profiles were largely influenced by

88 hile gyrB RAVs were uncommon and showed drug specific resistance propensity.

89 ailable adjuvants are only effective against specific resistance proteins.

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

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

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

93 Our results provide the first evidence for specific resistance-related traits associated with morta

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

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

96 ilitate an improved understanding of regimen-specific resistance risks and better inform clinical dec

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

98 d 6 was sufficient to limit proliferation in specific resistance settings, RB loss rendered cells com

99 The pathogen-specific resistance signatures and differential abundanc

100 Thus, we identify novel AR3A-specific resistance substitutions and the role of HVR1 i

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

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

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

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

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

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

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

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

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

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

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

112 s and simulations indicate that architecture-specific resistance to compaction and fracture can expla

113 -rich repeat (NLR) protein that confers race-specific resistance to Cs strains.

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

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

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

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

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

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

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

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

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

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

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

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

126 ith other 5-deoxyisoflavonoids, provide race-specific resistance to Phytophthora sojae.

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

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

129 sociated with significant levels of race non-specific resistance to rice blast and sheath blight.

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

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

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

133 al host populations evolve traits conferring specific resistance to viral predators via various defen

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

135 -chip reproduces clinically observed patient-specific resistances to treatment with concurrent chemor

136 Specific resistance was generated both to a plasmacytoma

137 nces in parallel (side-branches), while leaf-specific resistance was independent of plant size.