ライフサイエンスコーパス: resistance against

1 h different 2'-substituents provided greater resistance against 3'-exonucleases than the correspondin

2 They confer resistance against a broad spectrum of field isolates of

3 lular NAD in transgenic nadC plants enhanced resistance against a diverse range of (a)virulent pathog

4 metabolic defence pathways with relevance to resistance against a hemipteran pest.

5 Li-ion conductivity and a small interfacial resistance against a Li metal anode is a key component i

6 These defects result in defective host resistance against a murine enteropathogen, Citrobacter

7 This series demonstrates no cross-resistance against a panel of Pf strains with mutations

8 all RNA pathways are involved in Arabidopsis resistance against a phloem-feeding insect, the green pe

9 T cell-expressed FURIN is essential for host resistance against a prototypic Th1 pathogen, Toxoplasma

10 e wild-type potato NB-LRR protein Rx confers resistance against a single strain of potato virus X (PV

11 ignificant trend toward increasing microbial resistance against a variety of antibiotics, including c

12 lux pumps that are responsible for bacterial resistance against a variety of antibiotics.

13 um bulbocastanum is a rich source of genetic resistance against a variety of pathogens.

14 increased fungal resistance has an effect on resistance against A. tabida.

15 dian Tubulinosema kingi has an effect on the resistance against A. tabida.

16 FABP1 cDNA transfected cells showed greater resistance against AAP toxicity than vector transfected

17 erate secondary metabolic energy and provide resistance against acid stress.

18 As mutations in pfact and pfugt conveyed resistance against additional unrelated chemical scaffol

19 WhiB4, as key determinants of mycobacterial resistance against AG.

20 tabilization of suspensions and the solution resistance against aggregation.

21 esses the hydrolase AlbD, conferring natural resistance against albicidin.

22 ne serotype results in a transient period of resistance against all serotypes (cross-protection), fol

23 ux system, which plays a significant role in resistance against aminoglycoside antibiotics, is contro

24 ignificant trend toward decreasing microbial resistance against aminoglycosides and imipenem also was

25 per & Nettle's paper exemplifies an emerging resistance against an exclusive focus on deficits in peo

26 al-induced colitis by promoting colonization resistance against an intestinal opportunistic bacterium

27 Resistance against an introduced fish can be through str

28 d the involvement of PLDdelta in penetration resistance against another nonadapted pea powdery mildew

29 t one natural enemy results in a decrease in resistance against another.

30 sm during cellular stress and contributes to resistance against anticancer agents.

31 rf19.4531 (previously named ROA1), increases resistance against antifungal azoles, which was attribut

32 Acquired resistance against antimalarial drugs has further increa

33 ss in harsh environments and contributing to resistance against antimicrobial agents.

34 Resistance against antimicrobial peptides in many Firmic

35 Resistance against antimonial drugs has probably been a

36 aphid (Myzus persicae), indicating enhanced resistance against aphids.

37 Understanding nonhost resistance against ASR may provide an avenue to engineer

38 avenue to engineer soybean to confer durable resistance against ASR.

39 eased parasitoid resistance has an effect on resistance against B. bassiana and T. kingi.

40 c acid (ABA), which has a negative impact on resistance against B. cinerea and P. carotovorum.

41 MCL(-/-) mice showed impaired vaccine resistance against B. dermatitidis infection compared to

42 In addition, CP promotes resistance against bacterial and fungal phytopathogens.

43 genes and signaling pathways, enhancing its resistance against bacterial infection.

44 The recent increase in multidrug resistance against bacterial infections has become a maj

45 kinase signaling pathway that enhances host resistance against bacterial infections.

46 Furthermore, LecRK-I.8 is required for basal resistance against bacterial pathogens, substantiating a

47 To identify the genes involved in nonhost resistance against bacterial pathogens, we developed a v

48 The Xa21 gene confers a broad and persistent resistance against BB.

49 rasitoid Asobara tabida has an effect on the resistance against Beauveria bassiana, an entomopathogen

50 Absence of cross resistance against bedaquiline resistant mutants suggest

51 acteristics of 4 RMD platforms for detecting resistance against beta-lactams in 72 highly resistant i

52 ubspecies enterica serovar Typhi strain with resistance against beta-lactams, cephalosporins (extende

53 Similar to mecA, mecC confers resistance against beta-lactams, leading to the phenotyp

54 Application of exogenous ABA increased basal resistance against Bgh in wild-type plants, but not in H

55 led that PLDdelta is involved in penetration resistance against Bgh, and chemical inhibition of PLDs

56 responses for maintenance of effective basal resistance against Bgh.

57 t mouse model of cholera and for V. cholerae resistance against bile salts, perhaps due to environmen

58 e shows an outstanding performance with high resistance against both carbon build-up and sulfur poiso

59 d hypersensitive response, elevated pathogen resistance against both virulent and avirulent pathogens

60 -red enrichment indeed contrastingly affects resistance against Botrytis cinerea between the two spec

61 grafted membranes show much superior fouling resistance against bovine serum albumin (BSA) adsorption

62 being ineffective at conferring colonization resistance against C. albicans.

63 understanding of mechanisms of colonization resistance against C. difficile and novel therapeutic ap

64 sms by which antibiotics reduce colonization resistance against C. difficile are unknown yet importan

65 of these organisms in diarrheal diseases and resistance against C. difficile colonization are warrant

66 piraceae and E. coli strains in colonization resistance against C. difficile in germfree mice.

67 s suggest that full recovery of colonization resistance against C. difficile requires the restoration

68 biota's capability of providing colonization resistance against C. difficile.

69 the gut microbiota can restore colonization resistance against C. difficile.

70 ed from faeces that can restore colonization resistance against C. difficile.

71 solate, could partially restore colonization resistance against C. difficile.

72 obacilli, is vital in promoting colonization resistance against Candida albicans.

73 A cohort nested within the Consortium on Resistance against Carbapenems in Klebsiella pneumoniae

74 bservational studies, CRACKLE (Consortium on Resistance Against Carbapenems in Klebsiella pneumoniae

75 ctamases (MbetaLs) are the main mechanism of resistance against carbapenems.

76 Rapidly emerging resistance against ceftriaxone requires urgent reevaluat

77 in-resident cells, including glial cells, in resistance against cerebral infections remains unknown.

78 mutual interaction causes the physiological resistance against chemotherapy for acute myeloid leukem

79 chlorination is enabled by the films' unique resistance against chlorine degradation.

80 nonhematopoietic and hematopoietic cells in resistance against chronic M. tuberculosis infection in

81 have reported that TLR2 is crucial for host resistance against chronic Mycobacterium tuberculosis in

82 exhibited greatly impaired gut colonization resistance against Citrobacter rodentium.

83 to the variety of bacteria causing it, their resistance against classical antibiotics, the formation

84 species G. arboreum is a natural source for resistance against CLCuD.

85 By using antibiotics to break colonization resistance against Clostridium, Salmonella, and Citrobac

86 ons of commensal bacterial species, provides resistance against colonization and invasion by pathogen

87 n of drug resistance and the degree of cross-resistance against common resistance alleles.

88 l interaction is important for H. influenzae resistance against complement activation and will conseq

89 chanisms of meningococcal immune evasion and resistance against complement increase in response to an

90 In particular, the resistance against complete wetting and the mechanical s

91 ve the potential to circumvent emerging drug resistance against conventional antibiotic treatments.

92 Recent increases in microbial resistance against current drugs has led to a concomitan

93 globally since 2000, reported occurrences of resistance against current therapeutics threaten to reve

94 Resistance against currently used antitubercular therape

95 mode of action will be needed to avoid cross resistance against currently used therapeutic agents.

96 eserves mitochondrial integrity, and confers resistance against cytokine-induced pancreatic beta cell

97 ty binding interaction with IL-6 and provide resistance against degradation by serum endonucleases.

98 With regard to fibril formation kinetics and resistance against denaturants, fibrils formed by full-l

99 ct microbiota development and, consequently, resistance against development of RTIs.

100 idase (NA) of influenza virus correlate with resistance against disease, but the effectiveness of ant

101 We tested enzyme resistance against diverse process-like and operating co

102 hereas subjects harboring D4 have borderline resistance against DM generation (0.68 [0.49-0.94]; P =

103 which could be responsible for the acquired resistance against DNA-damaging agents.

104 associated with these subtypes can influence resistance against dolutegravir.

105 ropose different hypotheses to explain their resistance against duplication.

106 apsule, which showed, in addition, increased resistance against early clearance in a mouse model of l

107 The mccF gene confers resistance against endogenous and exogenous McC7 by hydr

108 plicating HLA-DRB1 as a major contributor to resistance against enteric fever, presumably through ant

109 Understanding how the microbiota confers resistance against enteric pathogens and how antibiotics

110 biota plays important roles in digestion and resistance against entero-pathogens.

111 e review how antibiotics reduce colonization resistance against Enterobacteriaceae to pinpoint possib

112 ding a conceptual framework for colonization resistance against Enterobacteriaceae, these mechanistic

113 potlights a molecular mechanism of broad RSV resistance against entry inhibition that may affect the

114 also extends to HCC-827 cells with acquired resistance against Erlotinib, a clinically used inhibito

115 echanism has implications for overcoming the resistance against experimental drugs targeting Ref-1 ac

116 ted with the emergence of S Typhi exhibiting resistance against fluoroquinolones, requiring the trial

117 This contributes to the basal resistance against freezing stress, but also to the furt

118 on from native seed banks, provides enduring resistance against fungal diseases, demonstrating that n

119 kalinization response(6), displayed enhanced resistance against Fusarium.

120 loyed by plants exposed to stress to enhance resistance against future stress episodes with minimal a

121 odification pathway contributes to bacterial resistance against gastrointestinal host defenses and su

122 del(11q), affecting ATM, are associated with resistance against genotoxic chemotherapy (del17p) and p

123 are the (a) history of antibiotic usage and resistance against gonorrhea and the consequences of res

124 NK cells mediate resistance against haematopoietic neoplasms but are gene

125 Mono-acylated anthocyanins showed a higher resistance against heat than di- and non-acylated.

126 Although graft autophagy is essential for resistance against hepatic IRI, its significance in clin

127 nated thujone monoterpenoids associated with resistance against herbivore feeding, particularly ungul

128 that total O-AS levels were associated with resistance against herbivores and pathogens.

129 ited genetic constraints on the evolution of resistance against herbivores in its introduced range, s

130 turn, activates the full defense profile and resistance against herbivores.

131 estication consistently has reduced chemical resistance against herbivorous insects, improving herbiv

132 grown from JA-treated seed showed increased resistance against herbivory by spider mites, caterpilla

133 5 ligands, MIP-1beta (CCL4), increased their resistance against HIV.

134 lementation experiment of hom12 restored the resistance against holomycin.

135 so in membrane barrier function by providing resistance against host antimicrobial stress.

136 IkappaBzeta deficiency also conferred resistance against IL-23-induced psoriasis.

137 owed identification of a mutant line showing resistance against IMIs.

138 aride, which are essential for meningococcal resistance against immune killing.

139 of PPARalpha can ameliorate hepatic insulin resistance against increased ER stress.

140 found that NaCDPK4 and NaCDPK5 affect plant resistance against insects in a JA- and JA-signaling-dep

141 contribute to health, including colonization resistance against intestinal pathogens.

142 ted GTPases that function in cell-autonomous resistance against intracellular pathogens in mice.

143 Here, the biotic resistance against introduced topmouth gudgeon Pseudoras

144 for the maintenance of biodiversity, biotic resistance against introduced weeds, and the success of

145 onal differences in their mode of generating resistance against invading nucleic acids.

146 The microbiota contributes to colonization resistance against invading pathogens by competing for m

147 nity might be augmented benignly to increase resistance against invasive bacteria.

148 ion is essential for hepatic homeostasis and resistance against IR stress in OLTs.

149 represent a new mechanism of acquisition of resistance against JAK inhibitors.

150 Emergence of genetic resistance against kinase inhibitors poses a great chall

151 ficiency of PI3Kgamma significantly enhances resistance against L. mexicana that is associated with a

152 iously shown that IL-23 is required for host resistance against L. monocytogenes and for neutrophil r

153 essential, is insufficient for establishing resistance against lamivudine.

154 M) , sigma(W) and sigma(X) all contribute to resistance against lantibiotics.

155 Hilpda depletion reduced resistance against lipid overload and increased producti

156 Akt/beta-catenin/Foxo1 signaling, leading to resistance against liver ischemia/reperfusion (IR) damag

157 fic HAX-1 overexpression was associated with resistance against loss of mitochondrial membrane potent

158 intestinal microbiota provides colonization resistance against many orally acquired pathogens, and a

159 ultimate strength, and (iii) a growth of the resistance against material fatigue.

160 Crystalline beads displayed superior resistance against matrix leaching in HNO(3).

161 proteins have been indicated as mediators of resistance against metabolic stress.

162 To overcome resistance against microtubule stabilizing agents such a

163 romic repeats-CRISPR associated), to provide resistance against mobile invaders, such as viruses and

164 ding to the ubiquitous problem of increasing resistance against most of the currently available antim

165 ding to the ubiquitous problem of increasing resistance against most of the currently available antim

166 zymes were generalists, conferring increased resistance against most of the examined beta-lactams.

167 mutant overexpressing cancer cells acquired resistance against multiple anticancer drugs, thus sugge

168 ing that this immune receptor is involved in resistance against multiple fungal pathogens.

169 ons in the kinase domain of MPS1 that confer resistance against multiple inhibitors.

170 (Pinus monticola), in providing canola with resistance against multiple phytopathogenic fungi.

171 owing influenza virus infection and improved resistance against mutagen/inflammation-induced colorect

172 died the roles of CG and NE in the pulmonary resistance against Mycobacterium bovis bacillus Calmette

173 h with a lung migratory phase, affected host resistance against Mycobacterium tuberculosis infection

174 n various biological conditions and improved resistance against NaCN digestion.

175 e and signaling metabolites known to mediate resistance against native herbivores.

176 Providing resistance against natural enemies appears to be a parti

177 Plant resistance against necrotrophic pathogens with a broad h

178 to Pseudomonas syringae but retain unaltered resistance against necrotrophs.

179 However, the emergence of viral resistance against NRTIs is a major threat to their ther

180 tability and are likely molecular origins of resistance against nucleases.

181 olutionary level, suggests that evolution of resistance against one class of natural enemies is large

182 the form of a trade-off, when an increase in resistance against one natural enemy results in a decrea

183 ch induces apoptosis and reverses multi-drug resistance against ovarian cancer cells through downregu

184 ted characteristics (HDL particle oxidation, resistance against oxidative modification, main lipid an

185 the nervous system led to an increase in the resistance against oxidative stress and starvation, but

186 Pneumococcal proteins involved in the resistance against oxidative stress are present in all s

187 tion of cells with heparanase enhanced their resistance against oxidative stress- or growth factor st

188 that the Nlrp3 inflammasome is essential for resistance against P. brasiliensis because it orchestrat

189 A strong constitutive resistance against P. brassicae caterpillars in combinat

190 homozygous HbSS erythrocytes, contributes to resistance against P. falciparum.

191 the role of the DMNT biosynthetic pathway in resistance against P. irregulare.

192 immunity, we test for the existence of cross-resistance against parasites and pathogens, at both a ph

193 ells are innate lymphoid cells which mediate resistance against pathogens and contribute to the activ

194 To confer resistance against pathogens and pests in plants, typica

195 inal tract microbiota, reducing colonization resistance against pathogens including Clostridium diffi

196 wheat and rye that are associated with plant resistance against pathogens, and recent studies have em

197 st agronomically important traits, including resistance against pathogens, are governed by quantitati

198 robiota and consequently reduce colonization resistance against pathogens, including Clostridium diff

199 uggested to play an important role in innate resistance against pathogens, regulation of inflammation

200 host immune response facilitate colonization resistance against pathogens.

201 malexin, a phytoalexin that confers enhanced resistance against pathogens.

202 ese studies reveal a role for NLRP12 in host resistance against pathogens.

203 n additional role for NRT2.1 linked to plant resistance against pathogens.

204 vels of wear abrasion and substrate adhesion resistance against pencil hardness, dry/wet scribed tape

205 in orange antisense (AS) fruits, leading to resistance against Penicillium digitatum infection.

206 we show that anteiso-BCFAs enhance bacterial resistance against phagosomal killing in macrophages.

207 yrhizi resistance gene CcRpp1 (Cajanus cajan Resistance against Phakopsora pachyrhizi 1) from pigeonp

208 opically expressing AdVPE exhibited enhanced resistance against Phytophthora parasitica var. nicotian

209 aphid (phloem feeder) differentially induce resistance against Pieris brassicae caterpillars in Arab

210 ic Duffy-null blood group-believed to confer resistance against Plasmodium vivax infection-was recent

211 is involved in defense signaling in nonhost resistance against powdery mildew fungi and put PLDdelta

212 itical function in mediating direct chemical resistance against predation.

213 cer tumors leads to the rapid development of resistance against promising EGFR tyrosine kinase inhibi

214 nucleopeptides exhibit excellent proteolytic resistance against proteinase K.

215 fferences endow platelet VWF with a specific resistance against proteolysis by the VWF-cleaving prote

216 NCODING RNA1 (ELENA1), as a factor enhancing resistance against Pseudomonas syringe pv tomato DC3000.

217 ed in ABA tolerance and contributes to plant resistance against PstDC3000.

218 (RVRp13 and RVRp22) were selected, and their resistance against random mutation was shown in cultured

219 pathway represent a first line of Salmonella resistance against reactive oxygen and nitrogen species

220 tion with Toxoplasma gondii induces a potent resistance against reinfection, and IFN-gamma production

221 roduce overlap-length-dependent "brake-like" resistance against relative microtubule sliding in both

222 s affecting microbiota stability and thereby resistance against respiratory tract infections (RTIs) o

223 ates oxidative stress responses and provides resistance against ROS, thereby contributing to the surv

224 how leukemic cells could acquire the serious resistance against RUNX1-inhibition therapies and also w

225 ect defenses induced by ZmPep3 contribute to resistance against S. exigua through significant reducti

226 ate immunity, playing a nonredundant role in resistance against selected microbes and in the regulati

227 mocyte densities, proPhenoloxidase activity, resistance against Serratia marcescens), and for the lif

228 almonella typhimurium, clones with increased resistance against seven different beta-lactam antibioti

229 ood predictors and contributors to QTL-based resistance against several devastating rice diseases.

230 species and demonstrated that it can confer resistance against Smb.

231 tide or dinucleotide incorporation increases resistance against snake venom phosphodiesterase.

232 expected to provide broader and more durable resistance against soybean aphids compared with cultivar

233 at makes the strongest known contribution to resistance against soybean cyst nematode (SCN), Heterode

234 rhg1-b allele of soybean is widely used for resistance against soybean cyst nematode (SCN), the most

235 s that are involved both in virulence and in resistance against specific in vitro stresses, thereby r

236 as the mechanisms, that govern colonization resistance against specific pathogens.

237 Our results show that their chemostability (resistance against spontaneous decomposition forming iso

238 sion library protein products that increased resistance against streptomycin and kanamycin.

239 of the mechanism of unique, broad RSV cross-resistance against structurally distinct entry inhibitor

240 tivator of defense, thus leading to enhanced resistance against subsequent infections.

241 ting a protective response that may underlie resistance against such death.

242 ammaR confers approximately 140-fold greater resistance against systemic vascular leakage-associated

243 nduced total phenolics, and for constitutive resistance against T. pityocampa in bioassays, (ii) no e

244 ll invasion, transendothelial migration, and resistance against TGF-beta.

245 Importantly, Hib and Hif resistance against the bactericidal effect of human seru

246 is SDE5 is required to generate an effective resistance against the biotrophic bacteria Pseudomonas s

247 powdery mildew resistance locus A12-mediated resistance against the biotrophic powdery mildew fungus

248 cterial membrane may contribute to bacterial resistance against the drug.

249 The pho1 mutant also showed an increased resistance against the generalist herbivore Spodoptera l

250 This immune response participates to resistance against the hemibiotrophic bacterium Pseudomo

251 ase-VI.2 (LecRK-VI.2) contributes to disease resistance against the hemibiotrophic Pseudomonas syring

252 Innate immune responses are crucial for host resistance against the infection, however the molecules

253 e-stranded RNA killer virus and confers cell resistance against the killer virus.

254 and whether they participate in LBL-elicited resistance against the most important postharvest pathog

255 s thaliana) leaves, ATP pretreatment induced resistance against the necrotrophic fungus, Botrytis cin

256 emies is largely independent of evolution of resistance against the other.

257 CT1 transcript alone is sufficient to confer resistance against the pathogen.

258 gut microbiota and subsequently colonization resistance against the pathogen.

259 Disruption of IGMT5 function increases resistance against the root-knot nematode Meloidogyne ja

260 ntify a role for accessory protein 3a in the resistance against the type I IFN response.

261 ng MKP1 displays enhanced PAMP responses and resistance against the virulent bacterium Pseudomonas sy

262 r PRMT5 function results in enhanced disease resistance against the virulent oomycete pathogen Hyalop

263 aphids [9] and ants [10, 11] manipulate wind resistance against their legs and thorax.

264 Plasmodium falciparum malaria, but clinical resistance against them has already been reported.

265 ntibiotics is the concomitant development of resistance against them.

266 opt other secondary structures, and provided resistance against thermal unfolding.

267 However, resistance against these agents, both de novo and acquir

268 Resistance against these compounds is widespread, and th

269 al development, we sought to investigate how resistance against these inhibitors may arise so that mi

270 monas syringae pathogens and is required for resistance against these pathogens.

271 of action of cationic AMPs and the bacterial resistance against these peptides.

272 cently discovered EGFR-C797S mutation causes resistance against third-generation EGFR inhibitors.

273 Resistance against this class was induced and revealed o

274 asite populations that exhibited significant resistance against this compound class.

275 hile signaling pathways leading to the basal resistance against this fungus are well described, the r

276 estinal commensal species that, by enhancing resistance against this pathogen, represent potential pr

277 in the development of genetic engineering of resistance against this pathogen.

278 failed to develop transgenerational acquired resistance against this pathogen.

279 binding site has been linked to the acquired resistance against those first generation therapeutics.

280 enerates selective pressure that may lead to resistance against to the administered drug, and may als

281 e-strand breaks, thereby conferring cellular resistance against Top2 poisons.

282 elial cells provides both passive and active resistance against transcellular tunnel formation, servi

283 eterozygous APOL1 G1 and G2 alleles increase resistance against Trypanosoma that cause African sleepi

284 vaccination exhibited significantly enhanced resistance against tuberculosis.

285 , loss of Cdk1 in the liver confers complete resistance against tumorigenesis induced by activated Ra

286 ADS26-down-regulated plants exhibit enhanced resistance against two major rice pathogens: Magnaporthe

287 61A) mice was accompanied by increased viral resistance against vaccinia virus and influenza B virus

288 longevity is often correlated with increased resistance against various stressors.

289 GD3 was detected in ALL cells that developed resistance against vincristine or nilotinib, drugs with

290 conclusion, this report supports that plant resistance against viral infections can be achieved by t

291 have been advantageous by providing natural resistance against viral pathogens that exploited the al

292 rom a wild-derived mouse strain that confers resistance against virulent parasites by interference wi

293 However, the MSRB8 gene does not influence resistance against virulent Pst or P. syringae pv. macul

294 nd Clostridium bolteae restores colonization resistance against VRE and clears VRE from the intestine

295 ct 4-hydroxynonenal (4HNE), is important for resistance against wound infection in Drosophila muscle.

296 binding leucine-rich repeat protein, confers resistance against X. oryzae isolates by recognizing mul

297 s identified as a major component of nonhost resistance against Xanthomonas citri subsp. citri (Xcc)

298 both AtrbohD and ICS1 contribute to nonhost resistance against Xcc, our results reveal an epigenetic

299 evisiae and is involved in the phenomenon of resistance against xenobiotics, which are clinically rel

300 nts and complemented strains were tested for resistance against zinc stress, intracellular zinc accum