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

5 ate immunity and confers robust and reliable resistance against a major poplar pathogen, Septoria mus

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

7 serial viral passages were applied to select resistance against a newly developed isoxazole-conjugate

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

9 n infection leading to transiently increased resistance against a second infection.

10 al microbiota, thereby reducing colonization resistance against a wide range of antibiotic-resistant

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

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

13 tabilization of suspensions and the solution resistance against aggregation.

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

15 in the causal parasites have led to onset of resistance against all commercial antimalarial drugs.

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

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

18 tures dictate bacterial propensity to evolve resistance against AMPs.

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

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

21 lity of the Env trimer and to neutralization resistance against antibodies.

22 The bad prognosis, high rate of relapse and resistance against anticancer drugs have been associated

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

24 Acquired resistance against antimalarial drugs has further increa

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

26 Resistance against antimicrobial peptides in many Firmic

27 Resistance against antimonial drugs has probably been a

28 most notable mechanisms of exosome-mediated resistance against antitumor immunity and we discuss how

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

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

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

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

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

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

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

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

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

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

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

40 Absence of cross resistance against bedaquiline resistant mutants suggest

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

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

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

44 cells and basophils are central to acquired resistance against blood-feeding arthropods which, in tu

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

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

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

48 mmensal microbiota in mediating colonization resistance against C. difficile have associated CDI with

49 rsodiol, may be able to restore colonization resistance against C. difficile in vivo However, the mec

50 ich ursodiol is able to restore colonization resistance against C. difficile remains unknown.

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

52 polyphenols led to the loss of colonization resistance against C. difficile.

53 SHP2 signaling was recently linked to drug resistance against cancer medications such as MEK and BR

54 atients were selected from the Consortium on Resistance Against Carbapenems in Klebsiella and Other E

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

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

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

58 Rapidly emerging resistance against ceftriaxone requires urgent reevaluat

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

60 Our work indicates that evolution of resistance against certain AMPs, such as tachyplesin II

61 immune responses, which provide far greater resistance against challenge with nontyphoidal serovar S

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

63 ciated with increased cell proliferation and resistance against chemotherapy.

64 phytochemical diversity better explain plant resistance against chewing and sap-feeding herbivores th

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

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

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

68 exhibited greatly impaired gut colonization resistance against Citrobacter rodentium.

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

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

71 cribe their ability to reverse existing drug resistance against clinically relevant antibiotics.

72 exa-acyl disaccharides significantly augment resistance against clinically relevant Gram-negative and

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

74 This microbiome might provide resistance against colonization by bacteria that promote

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

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

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

78 While resistance against conventional antimicrobials rapidly e

79 suggesting that escape pathways that confer resistance against conventional CD4-based inhibitors are

80 to other S. thermophilus strains it provided resistance against cos-type (Sfi21dt1virus genus) phages

81 gest that genome modifications indeed afford resistance against CRISPR systems.

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

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

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

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

86 ruses, demonstrating a powerful form of host resistance against deadly primate lentiviruses.

87 lar matrix-that provide shape and mechanical resistance against deformation is assumed to dominate ti

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

89 plications in genome editing for novel plant resistance against devastating HLB.

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

91 ance genes and had a high level of stem rust resistance against different races.

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

93 organic matrix, providing potentially higher resistance against dissolution in more corrosive waters.

94 -rich repeat immune receptors (NLRs) provide resistance against diverse pathogens.

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

96 associated with these subtypes can influence resistance against dolutegravir.

97 sphorylation at serine-70 (S70pBcl2) confers resistance against drug-induced apoptosis.

98 ctive EGFR mutations eventually develop drug resistance against EGFR tyrosine-kinase inhibitors; ther

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

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

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

102 tics of [Nle(15)]MG11 showed either improved resistance against enzymatic degradation or a significan

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

104 ysbiosis using a mouse model of colonization resistance against Escherichia coli.

105 are restricted by mutations associated with resistance against ESCs.

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

107 lanin within its cell wall for infection and resistance against external stresses such as exposure to

108 m-resistance-related metabolites and affects resistance against F. graminearum in maize seedling root

109 a mechanical dashpot, producing significant resistance against fast motions but minimal resistance a

110 can be edited, if non-functional, to enhance resistance against FHB.

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

112 ssing chickpea resumes its ability to confer resistance against Foc1 after application of 26S proteas

113 WRKY40 isoform in chickpea fails to provide resistance against Foc1.

114 We investigated the development of resistance against four antibodies to the spike protein

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

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

117 plant wastes) was found to mediate systemic resistance against Fusarium crown rot and to simultaneou

118 re identified that could contribute to maize resistance against Fusarium graminearum and other fungal

119 ntrasting chickpea genotypes with respect to resistance against Fusarium oxysporum f. sp. ciceri Race

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

121 ess response in yeast, which is required for resistance against future stressful conditions.

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

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

124 Nanobody (Nb)-mediated resistance against GFLV has been created recently, and s

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

126 NK cells mediate resistance against haematopoietic neoplasms but are gene

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

128 nder phloem specific promoters which confers resistance against hemipteran insects.

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

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

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

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

133 croenvironment, paradoxically promoting host resistance against HIV acquisition.

134 netic recombinant inbred lines (epiRILs) for resistance against Hyaloperonospora arabidopsidis (Hpa).

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

136 tial for GMO-free development of new genetic resistance against important crop pathogens.

137 IL-17A each efficiently overturned neonatal resistance against infection.

138 ry bile acids, and facilitating colonization resistance against intestinal pathogens.

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

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

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

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

143 Resistance against its infestation in sunflower is commo

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

145 gene pyramiding that confers broad-spectrum resistance against lepidopteran (Helicoverpa armigera an

146 The emergence of bacterial resistance against life-saving medicines has forced the

147 Hilpda depletion reduced resistance against lipid overload and increased producti

148 ith the 11-strain mixture enhances both host resistance against Listeria monocytogenes infection and

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

150 technologies for engineering durable disease resistance against major pathogens of poplar and other p

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

152 MPORTANCE B cells play critical role in host resistance against many respiratory viral infections.

153 hree non-synonymous mutations with increased resistance against mecillinam or piperacillin-tazobactam

154 nto verjuice, a product that shows intrinsic resistance against microbial growth and significant anti

155 To overcome resistance against microtubule stabilizing agents such a

156 ible organisms and conferring high levels of resistance against MLS(B) in vitro.

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

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

159 entify genomic regions associated with blast resistance against MoT isolates in Bolivia and Banglades

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

161 that activates downstream genes to increase resistance against multiple classes of antibiotics.

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

163 risingly, tcer-1 mutants exhibit exceptional resistance against multiple stressors, including infecti

164 zation and type 1 immunity are essential for resistance against murine sarcomas and selected human tu

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

166 ution of Toll-like receptor 2 (TLR2) to host resistance against Mycobacterium tuberculosis HN878, a c

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

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

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

170 to Pseudomonas syringae but retain unaltered resistance against necrotrophs.

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

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

173 n drug combinations where the development of resistance against one drug leads to collateral sensitiv

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

175 methodology was developed to quantify wines resistance against oxidation.

176 ing how it might be possible to change wines resistance against oxidation.

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

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

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

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

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

182 otential for protecting crops by engineering resistance against parasitic plants.

183 s containing heritable symbionts that confer resistance against parasitism.

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

185 and plays crucial roles in establishing host resistance against pathogens and in regulating innate im

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

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

188 Crop plant resistance against pathogens is governed by dynamic mole

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

190 photosynthesis, growth and reproduction, and resistance against pathogens, epibionts and grazers.

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

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

193 , which functions in conferring colonization resistance against pathogens.

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

195 host immune response facilitate colonization resistance against pathogens.

196 miRNAs contribute to plant resistance against pathogens.

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

198 mol m(-2) s(-1), 2 days) was associated with resistance against Penicillium digitatum, the main posth

199 provides S. thermophilus SMQ-301 with strong resistance against phage DT1.

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

201 Thus, plant PGIPs not only confer resistance against phytopathogens, but may also aid in d

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

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

204 Here, we describe a role for PCS in disease resistance against plant pathogenic fungi.

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

206 insights into RPW8.2-activated, EHM-focused resistance against powdery mildew.

207 we found that neutrophils are essential for resistance against primary 3-methylcholantrene-induced c

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

209 nucleopeptides exhibit excellent proteolytic resistance against proteinase K.

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

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

212 t MDA5/MAVS signaling was essential for host resistance against pulmonary Aspergillus fumigatus chall

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

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

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

216 ting the balance between CD8 T cell-mediated resistance against respiratory viral infection and memor

217 he EDTEE motif might have evolved to mediate resistance against retroviruses that use Nef-like protei

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

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

220 either community alone, confers colonization resistance against S. Enteritidis in neonatal chicks, ph

221 de in poplar leaves was sufficient to confer resistance against S. musiva.

222 ysogenized by phages carrying genes encoding resistance against secondary infections, such as those u

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

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

225 ng enzyme of R. solani gives a high level of resistance against sheath blight disease of rice.

226 f utilizing RNA interference (RNAi)-mediated resistance against sheath blight disease, we identified

227 resistance against fast motions but minimal resistance against slow motions, allowing for the integr

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

229 us and Prochlorococcus and compared modes of resistance against specialist and generalist cyanophages

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

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

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

233 ins and their B-chains displayed significant resistance against stress-induced fibrillation, particul

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

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

236 indicates that antibodies are essential for resistance against systemic Salmonella infections and ca

237 age experiments were performed to select for resistance against telaprevir.

238 P. aeruginosa displayed enhanced antibiotic resistance against tetracycline through increased expres

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

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

241 Both cell lines display cross-resistance against the chemotherapeutic drug docetaxel d

242 drives face a major obstacle in the form of resistance against the drive.

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

244 potential to allow for some level of biotic resistance against the effects of M. rubra on plant comm

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

246 e evaluated whether bacterial H(2)S provides resistance against the immune response, using two bacter

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

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

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

250 n, several issues were flagged such as cross-resistance against the multidrug-resistant K1 strain, in

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

252 rexpression of OsPT8 suppresses rice disease resistance against the pathogens Magnaporthe oryzae and

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

254 Soil inoculation consistently induced resistance against the thrips Frankliniella occidentalis

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

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

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

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

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

260 ntibiotics is the concomitant development of resistance against them.

261 marks of cancers is their ability to develop resistance against therapeutic agents.

262 Treated protein isolates showed more resistance against thermal degradation than native prote

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

264 range of soil bacteria confer no detectable resistance against these AMPs when introduced into nativ

265 Resistance against these drugs could be explained by inh

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

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

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

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

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

271 However, emergence of resistance against this drug is inevitable, and it has b

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

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

274 failed to develop transgenerational acquired resistance against this pathogen.

275 er effects or immunological or environmental resistance against this type outside Asia.

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

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

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

279 d has been associated with genes that confer resistance against toxoplasmosis in humans.

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

281 vaccination exhibited significantly enhanced resistance against tuberculosis.

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

283 ne the ability of influenza virus to develop resistance against UV-4B, mouse-adapted influenza virus

284 61A) mice was accompanied by increased viral resistance against vaccinia virus and influenza B virus

285 7 and BRAF(V600E) reduced the development of resistance against Vemurafenib.

286 host to balance tissue tolerance and immune resistance against viral and bacterial challenges.

287 ernal immune defense mechanisms that mediate resistance against viral infections and discuss the rang

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

289 y in ETI conferred by some TNLs and in basal resistance against virulent pathogens.

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

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

292 id-induced SnRK2 activity and regulate plant resistance against water deficit.

293 indings support improving acylsugar-mediated resistance against WFT by breeding tomatoes exuding grea

294 rious biotic stresses through enhanced plant resistance against wide range of herbivores.

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

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

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

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

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

300 revealed that EC958 employs both evasion and resistance against zinc toxicity, enabling its dissemina