ライフサイエンスコーパス: be resistant to

1 BK5.PRAS40(T246A) mice were resistant to 12-O-tetradecanoylphorbol-13-acetate (

2 dition, an HIF-1alpha Cys(520) serine mutant is resistant to 2-AAPA-induced HIF-1alpha stabilization.

3 amphotericin B, and 7% to echinocandins; 41% were resistant to 2 antifungal classes and 4% were resis

4 ere resistant to 2 antifungal classes and 4% were resistant to 3 classes.

5 we investigated how several strains of HAstV are resistant to a virus-neutralizing monoclonal antibod

6 Moreover, Pml(-/-) animals are resistant to acetaminophen hepatotoxicity or fasting

7 vitro and in vivo Acrolein-modified histones are resistant to acetylation, suggesting that the reduce

8 The tube surface is resistant to adhesion of activated platelets unlike p

9 Unlike subcutaneous WAT, visceral WAT is resistant to adopting a protective thermogenic phenot

10 Mutant mice are resistant to age- and diet-induced weight gain and i

11 lethal phenotype, mice heterozygous for p32 are resistant to age- and high-fat diet-induced ailments

12 None of the surviving V. cholerae colonies are resistant to all three phages.

13 nd by EGFR(L858R/T790M/C797S), a mutant that is resistant to all currently available EGFR TKIs.

14 uggesting that a fraction of virus particles are resistant to antibody neutralization despite high an

15 worldwide currently suffering with epilepsy are resistant to antiepileptic drugs (AEDs).

16 Cancer cells are resistant to apoptosis but "primed for death" by ele

17 of the underlying cause mediating G1 arrest, are resistant to apoptosis induced by the proteasome inh

18 cl-2 family members Bax and Bak are known to be resistant to apoptotic cell death, and previous we ha

19 hils from patients with FMF during remission are resistant to autophagy-mediated NET release, which c

20 lenced cells or SLAMF1(lo) primary CLL cells were resistant to autophagy-activating therapeutic agent

21 ivity against chronic myeloid leukaemia that is resistant to available treatment, although it is asso

22 y, frizzy, spangly, and often fair hair that is resistant to being combed flat.

23 ain-of-function SHP2 mutation (SHP2(D61G/+)) were resistant to bleomycin-induced pulmonary fibrosis.

24 g was projected to result in >5% of isolates being resistant to both B and C within 15 years.

25 Mutant U1060A in 16S Escherichia coli rRNA is resistant to both antibiotics, whereas mutant U1052G

26 that are resistant to isoniazid and one that is resistant to both isoniazid and rifampicin.

27 wed that the semi-arid steppe in north China was resistant to both daytime and nighttime warming, but

28 3, and interestingly M159W, V136E, and L122D were resistant to both isoflurane and TCE activation.

29 ERK activation was resistant to BRAF-V600E inhibition, but responsive t

30 but is effective in killing WCR larvae that are resistant to Bt proteins produced by currently avail

31 DNA cleavage specificity is different and it is resistant to camptothecins (CPTs) and non-CPT Top1 in

32 GO (Spy1) proteins bind and activate Cdk but are resistant to canonical regulatory mechanisms that es

33 The RV-C, unlike other EVs, are resistant to capsid-binding antiviral compounds beca

34 t primary CD4 T cells expressing GPI-scFv X5 were resistant to CCR5 (R5)-, CXCR4 (X4)-, and dual-trop

35 l stages, mouse embryonic stem cells (mESCs) are resistant to cell fate conversion induced by the mel

36 E-cadherin-expressing prostate cancer cells were resistant to cell death by chemotherapeutic drugs b

37 In the current study, a number of isolates were resistant to cephalosporins and fluoroquinolones.

38 a small fraction of cells in the cancer that are resistant to chemotherapy and radiation therapy and

39 LSCs, which are resistant to chemotherapy and serve as reservoirs fo

40 BACKGROUND & AIMS: Cholangiocarcinomas (CCA) are resistant to chemotherapy, so new therapeutic agents

41 re hyperphagic under stressed conditions and are resistant to chemotherapy-induced anorexia and body

42 of cancer-related deaths and is reported to be resistant to chemotherapy caused by tumor-initiating

43 elay of RC, especially if the bladder cancer was resistant to chemotherapy.

44 ond erythrocyte receptor for PvTRAg38, which is resistant to chymotrypsin.

45 tes, 19.2% of Neisseria gonorrhoeae isolates are resistant to ciprofloxacin.

46 A. thaliana gyrase yields active enzyme that is resistant to ciprofloxacin.

47 he viruses, with the exception that mallards were resistant to Ck/Pennsylvania/83 and Ck/Queretaro/95

48 More notably, Mertk(CR) mice, which are resistant to cleavage, showed significantly reduced

49 detected (22%), and 62% and 36% of isolates were resistant to clindamycin and trimethoprim/sulfameth

50 nd and that RAC1-mutant human melanoma cells are resistant to clinical inhibitors of BRAF but are uni

51 miR-34a-deficient mice are resistant to collagen-induced arthritis and interact

52 IRF1-knockout mice were resistant to ConA-induced liver damage, and anti-in

53 athogen-free (SPF) mice, germ-free (GF) mice are resistant to Concanavalin A (ConA)-induced liver inj

54 Furthermore, PGR was resistant to conformational collapse or alpha-helix

55 al-like tumor cell populations in mCRPC that are resistant to conventional and targeted therapies can

56 tion promotes lysis of arterial thrombi that are resistant to conventional approaches such as recombi

57 ent a significant clinical challenge as they are resistant to conventional cancer therapies and play

58 Leukaemia cells that are resistant to conventional therapies are thought to r

59 lation of breast cancer stem-like cells that are resistant to conventional therapies.

60 CANCE STATEMENT Many chronic pain conditions are resistant to conventional therapy.

61 High temperature structural materials must be resistant to cracking and oxidation.

62 heir yield stress is required if they are to be resistant to cracking.

63 , bioassays indicated that field populations were resistant to Cry3Bb1 maize and mCry3A maize, and th

64 tions and disrupts preformed biofilms, which are resistant to current antifungal agents.

65 Leukemia stem cells (LSCs) are resistant to current therapies used to treat chronic

66 rboring BRAF(V600E) and PTEN mutations often are resistant to current therapies, including BRAF inhib

67 origenic glioblastoma stem cells (GSCs) that are resistant to current therapy.

68 Up to one-third of patients are resistant to currently available treatments.

69 development of A. suturalis populations and were resistant to damage caused by plant bug infestation

70 over, glucocorticoid induction of Klf13 mRNA was resistant to de novo protein synthesis inhibition, d

71 /-) mice, WT mice had lower parasitemias and were resistant to death.

72 responsible for the control of eye movement) were resistant to degeneration in endstage SMA mice, as

73 As circular RNAs (circRNAs) are resistant to degradation by exonucleases, their abun

74 Importantly, the conjugates formed are resistant to degradation in plasma and are biologica

75 st proteoliposomes have evolved naturally to be resistant to degradation and provide a supportive env

76 with activated sludge demonstrated that LMG is resistant to degradation and that its human metabolit

77 CP in the kidney, liver, and adipose tissues were resistant to developing high-fat diet-induced obesi

78 ge (BAL) fluid ILC2s from asthmatic patients were resistant to dexamethasone.

79 Dusp6-deficient mice have been shown to be resistant to diet-induced obesity, but the mechanism

80 ed lipid storage and adipose tissue mass and were resistant to diet-induced obesity and insulin resis

81 tently, neither Akt1(-/-) nor Akt2(-/-) mice are resistant to diethylnitrosamine-induced hepatocarcin

82 odimer in human spinal cord homogenates that was resistant to dissociation by boiling, denaturants, o

83 mTOR mutants were resistant to DNA damage-inducible transcript 1-medi

84 The Toxoplasma gondii cyst stage is resistant to drug therapy.

85 e confirmed that this isopeptide replacement is resistant to DUBs and to shaving by proteasome.

86 C57BL/6 mice deficient in GM-CSF are resistant to EAE induced by immunization with myelin

87 Mice expressing RORgammat(M) were resistant to EAE associated with defective TH17 dif

88 riant of RAGE (RAGE splice variant 4), which is resistant to ectodomain shedding, inhibited RAGE liga

89 ne (m(6)A) facilitates mRNA translation that is resistant to eIF4F inactivation.

90 ents discharged home after treatment failure were resistant to eight or more drugs.

91 hway occurs frequently in breast cancer that is resistant to endocrine therapy.

92 Of interest, VE-cadherin mutants that are resistant to endocytosis are similarly resistant to

93 AMCase was resistant to endogenous pepsin C digestion and remai

94 The respiration-moisture relationship was resistant to environmental change in field common ga

95 nkages, particularly from prokaryotes, which are resistant to enzymatic or chemical release, could al

96 und foot it forms an (S)-stereocenter, which is resistant to enzymatic hydrolysis.

97 However, the rise of fungi that are resistant to existing antifungal agents poses a subs

98 cancer in adolescents and young adults that is resistant to existing treatments.

99 o LDL or extracellular PCSK9, the LDLR-R410S was resistant to exogenous PCSK9-mediated degradation in

100 nsfer of WT platelets to CD40-KO mice, which are resistant to experimental cerebral malaria, partiall

101 ripheral IFN-gamma(+) gammadelta T cells and were resistant to experimental cerebral malaria.

102 d by associative learning, has been shown to be resistant to extinction.

103 While memory B-cells from cirrhotic patients were resistant to Fas-mediated apoptosis ex vivo, Toll-l

104 ce in the proportion of tested isolates that were resistant to fluconazole between the fluconazole an

105 sing stringent break points, 93% of isolates were resistant to fluconazole, 35% to amphotericin B, an

106 -derived tetracycline-like viridicatumtoxins are resistant to fungal biotransformation, providing che

107 ADAMTS10 is resistant to furin cleavage, however we show that ADA

108 accumulate in the GTP-bound conformation and are resistant to GAP-mediated GTP hydrolysis.

109 strongly inhibited growth of CC, whereas SC was resistant to growth inhibition, and this was coupled

110 Blood isolates were more likely to be resistant to >/=1 agent for serotypes Enteritidis, Ja

111 A total of 26% of isolates were resistant to >/=3 antibiotic classes.

112 ich Mst1/Mst2 heterodimers are not possible, are resistant to H-ras-mediated transformation and maint

113 The alpha-Gal IgE epitopes were resistant to heat denaturation.

114 ce, but mice lacking either NE or C/EBPalpha are resistant to HFD-induced myelopoiesis.

115 steroid receptor RNA activator (SRA) (SRAKO) are resistant to high fat diet-induced obesity with a ph

116 BALB/c mice are known to be resistant to high fat diet (HFD)-induced obesity, how

117 Mice transfused with these red blood cells are resistant to highly lethal doses of BoNT/A.

118 indicates that subsets of cellular proteins are resistant to host shutoff and continue to be synthes

119 S3-G4 conjugates were resistant to hydrolysis by H1N1 neuraminidase.

120 ice display increased energy expenditure and are resistant to hypothermia and obesity.

121 AI mutants deficient in nucleic acid binding are resistant to IAV-triggered necroptosis and apoptosis

122 This sample was resistant to ibrutinib-mediated inhibition of NF-kap

123 Further, ADAM10(DC)(-/-) mice are resistant to IgE-mediated anaphylaxis.

124 findings suggest that R. pseudoacacia growth is resistant to increased drought frequency because it e

125 mmation in imiquimod-induced dermatitis, and were resistant to induction of experimental autoimmune e

126 CD163 knockout (KO) pigs are resistant to infection with genotype 2 (type 2) porc

127 Since immunocompetent mice are resistant to infection with S. stercoralis, we hypot

128 Mice were also found to be resistant to infection with the rodent malaria Plasmo

129 to fibrin contributes to clot stability and is resistant to inhibition by antithrombin/heparin while

130 Furthermore, MNP-based nanosystems are resistant to inhibitory factors present in body flui

131 Importantly, ISD treated podocytes were resistant to injury-induced loss of transepithelial

132 mping studies revealed that ECSHIP2(Delta/+) was resistant to insulin-stimulated glucose uptake in ad

133 Olfactory and spatial memory are resistant to interference from the addition of a mem

134 We found that Th-MYCN/Trp53(KI/KI) tumors were resistant to ionizing radiation (IR), as expected.

135 losis clinical isolates, including four that are resistant to isoniazid and one that is resistant to

136 of clinically relevant A. baumannii strains are resistant to killing by normal human serum (NHS), an

137 d amplitudes of their speed tuning functions are resistant to large changes in spatial frequency.

138 ddition, the growing prevalence of UPEC that are resistant to last-line antibiotic treatments, and mo

139 ave lower adenovirus titers in the lung, and are resistant to lethal herpes simplex virus-1 infection

140 lar and cytokine-based lung inflammation and were resistant to lethal influenza virus infection.

141 d IFN-beta (IFN-alpha/beta) in the serum and were resistant to lethal plasmodium yoelii YM infection.

142 ion and chemotaxis, and TIPE2-deficient mice were resistant to leukocyte-mediated neural inflammation

143 Spx1 was resistant to limited proteinase K digestion, but was

144 ng cause of hospital-acquired infections and is resistant to many antibiotics.

145 comprise an important clinical subtype that is resistant to many standard of care chemotherapeutics

146 ative in glioblastoma (GBM) tumor cells that is resistant to mechanistic target of rapamycin (mTOR) i

147 Cish(-/-) mice were resistant to melanoma, prostate and breast cancer m

148 putative ubiquitin-acceptor lysine residues are resistant to MG-induced degradation.

149 Chromatinized genomic DNA is resistant to MjAgo degradation, and recombinant histo

150 Additionally, Cd300lf(-/-) mice are resistant to MNoV infection.

151 nd suggest a mechanism for why some memories are resistant to modification.

152 Carbapenem-resistant Enterobacteriaceae are resistant to most beta-lactam antibiotics due to the

153 ors of apoptosis because without them a cell is resistant to most apoptotic stimuli.

154 lus sp. LC231, a cave bacterial isolate that is resistant to most clinically used antibiotics.

155 Although the OctaKO cells were resistant to most apoptotic stimuli tested, they un

156 larming increase of pathogenic bacteria that are resistant to multiple antibiotics is now recognized

157 These Klebsiella strains are resistant to multiple antibiotics, tend to colonize

158 y plants, both in nature and in agriculture, are resistant to multiple diseases.

159 ectivity of viruses harboring mutant PR that are resistant to multiple PR inhibitors or mutant Gag pr

160 s in a localized ligand radical species that is resistant to N coupling of the nitrides and is stable

161 cell lines and primary tumors that otherwise were resistant to native IL-21 treatment.

162 ize authentic filoviruses, which appeared to be resistant to neutralization.

163 -section within the microcolony 3D structure were resistant to neutralization (vs. upper and peripher

164 genetically diverse strains of A. baumannii are resistant to NHS killing.

165 T cells, do not bind anti-HLA antibodies and are resistant to NK-mediated lysis.

166 igh levels of HLA-I because of copy gain and was resistant to NK cell killing.

167 LTP is dependent upon APP since APP-KO mice were resistant to oAbeta- and oTau-induced defects in sp

168 GLUT4 promoter (i.e., transgenic [TG] mice) are resistant to obesity-induced insulin resistance.

169 inistered a sclerostin-neutralizing antibody are resistant to obesogenic diet-induced disturbances in

170 ta to generate a mutant IgE-Fc fragment that is resistant to omalizumab binding.

171 ive against several influenza A viruses that are resistant to one or both classes of Food and Drug Ad

172 ates revealed that only four of the isolates were resistant to one or more antibiotics.

173 % of HIV-1 isolates, including 16 of 20 that were resistant to other members of its class.

174 GSB were resistant to oxygen and showed a low affinity to su

175 ll isolates were beta-lactamase positive and were resistant to penicillin, tetracycline, and ciproflo

176 Parasites with esterase mutations are resistant to pepstatin esters and to an open source

177 transfer), and cells harboring this mutation are resistant to peptidyl-transferase inhibitors (e.g.,

178 tiffness and hardness comparable to diamond, is resistant to perforation with a diamond indenter and

179 receptor 9 (TLR9)-deficient (TLR9(-/-)) mice are resistant to periodontitis, a disease characterized

180 ant breeders have developed crop plants that are resistant to pests, but the continual evolution of p

181 the substrates of oculomotor control, often is resistant to pharmacotherapy.

182 one or in combination with onion leaf lectin are resistant to Phenacoccus solenopsis (cotton mealybug

183 , the prosurvival phenotype of patient cells was resistant to phosphoinositide 3-kinase inhibition.

184 ic alterations, mesenchymal-like tumor cells are resistant to PI3K and MAPK pathway inhibitors, sugge

185 ssing a constitutively activated form of AKT were resistant to PI3Kdelta inhibition, suggesting that

186 tiple substrains of the 129 mouse background are resistant to pigmentation locus-negative (pgm(-)) Ye

187 Cys42Ser PKGIalpha knock-in (KI) mice, which are resistant to PKGIalpha oxidation, have diastolic dys

188 ith reversions detected in tumor-derived DNA were resistant to platin- or poly ADP ribose polymerase

189 These materials are resistant to poisoning by small reactive gases (CO a

190 t pandemic O1 Vibrio cholerae biotype El Tor is resistant to polymyxins, whereas a previous pandemic

191 sgenes containing natural or synthetic PATCs are resistant to position effect variegation and stochas

192 ommon phase in high-silica igneous rocks and is resistant to post-eruptive alteration, thus offering

193 requires an isoprenylatable CaaX motif that is resistant to post-isoprenylation events.

194 ssemble in to noninfectious nanocapsids that are resistant to proteolytic/acidic mucosal delivery con

195 portunity to develop production animals that are resistant to PRRS, the costliest viral disease to ev

196 Remarkably, dominant jaz2Deltajas mutants are resistant to Pseudomonas syringae but retain unalter

197 Unexpectedly, some VHL-mutant ccRCCs were resistant to PT2399.

198 ly populated regions in Malawi, An. funestus is resistant to pyrethroids, carbamates, and organochlor

199 at determining whether the infected strains were resistant to quinolone can be performed simultaneou

200 Conversely, among patients who were resistant to R-CHOP, basal DLBCL mutations did not

201 that Rs-cps transgenic N. benthamiana plants were resistant to R. similis and the transcription level

202 sive CD4 T cells engineered with GPI-scFv X5 are resistant to R5-, X4-, or dual-tropic virus infectio

203 mor cells initiate and sustain tumor growth, are resistant to radiation and drugs, and bear specific

204 Cardiomyocytes are resistant to radiation.

205 produced higher levels of the Dxr substrate were resistant to RCB-185.

206 ifferentiated HSPCs and that quiescent HSPCs are resistant to reactivation by histone deacetylase inh

207 Notably, cured mice were resistant to rechallenge not only by WEHI-164 cells

208 LS-3DCHIm is resistant to reduction, is unreactive toward weakly a

209 questration of metals as sulfides that could be resistant to reoxidation.

210 as a model for culture of other viruses that are resistant to replication in conventional cell cultur

211 fixed dysfunctional state in which the cells are resistant to reprogramming.

212 nscriptionally >100-fold upon Dicer loss and is resistant to resilencing by complete restoration of m

213 memories created with 10 tone-shock pairings are resistant to retrieval-dependent memory destabilizat

214 nal studies of essential noncoding RNAs that are resistant to RNAi and RNase H-based degradation.

215 HIV-1 RNA from infected DBR1 knockdown cells was resistant to RNase R that degrades linear RNAs but n

216 while hyperphosphorylated cdc24 mutants that were resistant to scaffold stimulation displayed a defic

217 VAMP8(-/-) acini are resistant to secretory inhibition by supramaximal CC

218 in locomotor activity and spatial memory and were resistant to seizure induction.

219 In general, the enzyme was resistant to several metal ions and reagents.

220 y expressed RHBDL2 and that a subset of them is resistant to shedding by cell surface metalloprotease

221 Moreover, while their ability to self-renew was resistant to SHH inhibitors, as has been previously

222 Furthermore, the VIR165-dependent viruses were resistant to soluble CD4-induced Env destabilizatio

223 f Staphylococcus aureus or staph, because it is resistant to some commonly used antibiotics.

224 hermore, cells expressing mutant Fyn (C448A) were resistant to SSL-induced apoptosis.

225 lls in which Fyn expression was knocked down were resistant to SSL-induced apoptosis.

226 d tumors often contain hypoxic regions which are resistant to standard chemotherapy and radiotherapy.

227 Furthermore, this severe asthma is resistant to steroids and characterized by mixed TH2

228 c-Rel-deficient mice are resistant to streptozotocin-induced diabetes, a drug

229 The resultant tumor-free mice were resistant to subsequent challenge with CT26, indica

230 Autoimmune diseases feature T cells that are resistant to suppression by Tregs, whereas in cancer

231 vity (TRPM7(KR) ), are not hyperallergic and are resistant to systemic magnesium (Mg(2+) ) deprivatio

232 strogen, progesterone and HER2 receptors and is resistant to targeted and hormone therapies.

233 ve against the parasite, they need to either be resistant to TbMTAP-mediated cleavage, which is the c

234 yers involves cell-to-cell transmission that is resistant to tetherin but that virion dissemination v

235 es, but not proximal nerves or dorsal roots, is resistant to tetrodotoxin and that, in mice, this eff

236 de of the dipeptide d-Hot horizontal lineTap is resistant to TFA and thus can serve as a bioorthogona

237 o analysis reveals that CD4(+) T(Pam3) cells are resistant to TGF-beta-mediated gene expression throu

238 xp3 expression, became more suppressive, and were resistant to Th17 skewing in vitro.

239 d in vivo In addition many rotavirus strains are resistant to the actions of different IFN types.

240 However, a number of bacterial pathogens are resistant to the antimicrobial activities of macroph

241 that nTregs, unlike Teffs (CD3(+)FOXP3(-)), are resistant to the antiproliferative effects of AzaC.

242 In cells that are resistant to the combined therapy, PAKs regulate JNK

243 Myeloid cells, unlike lymphocytes, are resistant to the cytopathic effects of HIV.

244 Accordingly, Vav.G9a(-/-) mice are resistant to the development of allergic lung inflam

245 Mice devoid of Smad7 specifically in DCs are resistant to the development of experimental autoimm

246 Strong evidence now shows that CML LSCs are resistant to the effects of TKIs and persist in all

247 ol and PC/phosphatidylethanolamine ratio and are resistant to the hepatitis and fibrosis normally ind

248 (+)/PIK3CA(H1047R) transgenic mammary tumors are resistant to the HER2 antibodies trastuzumab and per

249 We report here that nascent HSCs are resistant to the JAK2V617F mutation and show no decr

250 Lastly, mice deficient in PP5 are resistant to the negative effects of rosiglitazone o

251 Lactococcus lactis, we isolated mutants that are resistant to the PG hydrolase lysozyme.

252 ins of human astrovirus serotype 2 (HAstV-2) are resistant to the potent HAstV-2-neutralizing monoclo

253 or predisposing gene for autoimmune disease, are resistant to the suppressive effects of TGFbeta.

254 embryonic fibroblasts deficient in Bax/Bak1 are resistant to the third major form of cell death asso

255 further demonstrate that tumor cells, which are resistant to the toxin when grown in vitro, become h

256 The LREX' prostate cancer model is resistant to the antiandrogen enzalutamide via activa

257 LPH2 is localized to the plant cell cytosol, is resistant to the classic serine/threonine phosphatase

258 alternative pathway for virus spread, which is resistant to the host humoral immune response.

259 Homeostatic Treg cell proliferation is resistant to the inhibitory effect of rapamycin and F

260 ve malignancy associated with infection that is resistant to the majority of chemotherapeutic drugs.

261 nce that restores the essential function and is resistant to the nuclease.

262 contrast, the parental virus expressing sGP was resistant to the MAb.

263 ient who had an activating EGFR mutation but was resistant to the TKI gefitinib.

264 MCF7-Y537S cells were resistant to the anti-estrogen tamoxifen and fulves

265 Furthermore, these viruses were resistant to the drug erlotinib, which targets epid

266 d elevated numbers of pulmonary NK cells yet were resistant to the induction of allergic inflammation

267 Mice deficient for CaV3.1 were resistant to the induction of experimental autoimmu

268 inhibitors, we generated mutant viruses that were resistant to the inhibitory effects of Z-d-Phe-l-Ph

269 13 366 (51.1%) of 26 174 bacterial isolates were resistant to the Malawian first-line antibiotics am

270 ions into an ataxin 7 transgene such that it is resistant to their effect.

271 It is resistant to thermal/chemical stress, and it binds to

272 ntrols of the same sex, indicating that they were resistant to thermal effects.

273 cy of antifungal agents; however, fungi that are resistant to these treatments are regularly isolated

274 In contrast, spirochaete hooks are resistant to these treatments, and several lines of

275 nsive fibrosis, whereas IL-13 deficient mice were resistant to these changes.

276 First, eel NCCbeta is resistant to thiazides.

277 and may select for transmitted viruses that are resistant to this IFN-mediated inhibition.

278 econsolidation updating, strong memories can be resistant to this approach.

279 e the virulence of MRSA despite the pathogen being resistant to this drug.

280 The copepod is resistant to this toxic alga, but little is known abo

281 , which inherit mutations present in GSC and are resistant to traditional antiangiogenic therapies.

282 n addiction, particularly in individuals who are resistant to traditional therapies.

283 Because it is resistant to traditional groundwater treatments, reme

284 mising efficacy, but many pancreatic cancers are resistant to TRAIL therapy.

285 ngly, a small subgroup of nucleosome changes is resistant to transcriptional inhibition.

286 defective for antitumor immune responses and are resistant to treatment with anti-PD-1.

287 oms only partially, with 30%-40% of patients being resistant to treatment.

288 uced by catecholamine injections, TG animals were resistant to triggered ventricular arrhythmias.

289 mechanism by which certain species appear to be resistant to TSEs is critical.

290 In contrast, >30% of the C-CAP was resistant to TTX in distal peripheral branches of mo

291 cific homozygous or heterozygous Arid1a loss were resistant to tumor initiation while ARID1A overexpr

292 However, they are resistant to tumorigenesis, and most normal cells is

293 ratings within hours of dosing patients who are resistant to typical antidepressants.

294 Mice with p53 knock out (p53-KO) were resistant to VAN induced AKI, indicated by the anal

295 ablation of HCC, hepatic veins and arteries were resistant to vessel occlusion compared with portal

296 ion, our results indicated that some neurons are resistant to virus-mediated cell death and provide a

297 on in the p110delta gene (p110delta(D910A) ) are resistant to VL, due in part to impaired regulatory

298 In addition, Cs2PdBr6 is resistant to water, in contrast to lead-halide perovs

299 report that TLR8-deficient (Tlr8(-/-)) mice were resistant to WNV infection compared with wild-type

300 lant Nicotiana benthamiana has been shown to be resistant to Xanthomonas and Pseudomonas due to an im