ライフサイエンスコーパス: be highly susceptible to

1 Culture-activated HSCs were highly susceptible to 2-AG-induced cell death with

2 th carbonyl carbons of the curcumin molecule are highly susceptible to a nucleophilic attack by the h

3 rference lines with reduced MED21 expression are highly susceptible to A. brassicicola and B. cinerea

4 whole saliva, in contrast to that of serum, is highly susceptible to a variety of physiological and

5 e late phase of the cardiac action potential is highly susceptible to aberrant excitation.

6 In reducing environments, EDB is highly susceptible to abiotic degradation.

7 The HA-Y231H mutant virus was highly susceptible to acid inactivation in vitro and

8 Circuits in the auditory cortex are highly susceptible to acoustic influences during an

9 onsistently, mice defective in cGAS or STING are highly susceptible to acute HSE.

10 ce of DCs, and Flt3L(-/-) mice were found to be highly susceptible to acute toxoplasmosis.

11 usly expressed CAR at the apical surface and was highly susceptible to adenovirus infection.

12 ous and heterozygous Kif3a gene-deleted mice were highly susceptible to aeroallergens from Aspergillu

13 Further, Neil1(-/-) mice are highly susceptible to AFB1-induced HCCs relative to

14 Asthmatic patients are highly susceptible to air pollution and in particula

15 cticola group demonstrated that the isolates were highly susceptible to all drugs tested except clari

16 Consistently, CXCR2(KO) mice were highly susceptible to alveolar bone loss; interesti

17 HBP MAb-binding phenotypes (70% of isolates) were highly susceptible to anti-fHBP v.1 or v.2 bacteric

18 significantly less surface-associated PNAG, was highly susceptible to antibody-independent opsonic k

19 sis showed Chad, Somalia, and South Sudan to be highly susceptible to any outbreak at subnational lev

20 cells stimulated through the T cell receptor are highly susceptible to apoptosis, expanding to smalle

21 l induction of antigen-stimulated Tregs, and is highly susceptible to apoptosis.

22 to wild-type MEF cells, MKK4-null MEF cells were highly susceptible to apoptosis by LY294002, paclit

23 T cells did not accumulate because the cells were highly susceptible to apoptosis.

24 ate that hamsters devoid of functional STAT2 are highly susceptible to as few as 10 PFU of SFTSV, wit

25 ural field conditions showed that the mutant is highly susceptible to attack by an indigenous flea be

26 Nlrp3 or the inflammasome effector caspase-1 were highly susceptible to azoxymethane/dextran sodium s

27 Patients with severe burns are highly susceptible to bacterial infection.

28 Furthermore, Gfi-1(-/-) mice are highly susceptible to bacterial infection.

29 exemplifies this dichotomy: the partnership is highly susceptible to 'bleaching' (stress-induced sym

30 elial cells expressed high levels of VEGFR-2 were highly susceptible to blockade by VEGF Trap.

31 Accordingly, SR-A(-/-) mice were highly susceptible to both Eap(+) and Eap(-) S. aur

32 SKG mice were highly susceptible to both IL-17-mediated T-cell-dr

33 The Arabidopsis mutant wrky33 is highly susceptible to Botrytis cinerea.

34 mutations of the BRCA1 tumor suppressor gene are highly susceptible to breast and ovarian cancer.

35 IL-1beta and IL-18 processing and secretion, were highly susceptible to C. difficile infection.

36 he pathway, develop spontaneous cataract and are highly susceptible to cataract induction by exposure

37 ed pluripotent stem cells have been shown to be highly susceptible to cell death stimuli due to their

38 PD-1(high) SIV-specific CD8+ T cells were highly susceptible to cell death leading to loss of

39 cell transplantation suggests this tumor can be highly susceptible to cellular immunotherapy targeted

40 in the United States; however, these strains were highly susceptible to cephalosporins.

41 beta1 Integrin-null pancreata were highly susceptible to cerulein-induced acute pancre

42 Fish proteins are highly susceptible to changes during frozen storage,

43 MLF was found to be highly susceptible to changes in temperature.

44 used as natural colorants in foods, but they are highly susceptible to chemical degradation during st

45 reased levels of systemic and fecal IgA, and were highly susceptible to chemical-induced colitis.

46 C/EBPalpha in the hematopoietic compartment are highly susceptible to chemically induced experimenta

47 Mutant embryonic fibroblasts were highly susceptible to chromosome breaks induced by

48 Here, we have shown that Il33-deficient mice are highly susceptible to colitis and CAC.

49 his study, we show that STING-deficient mice are highly susceptible to colitis-associated colorectal

50 on and cancer, and we found Nlrp12(-/-) mice were highly susceptible to colitis and colitis-associate

51 Mice lacking AGR2 were viable but were highly susceptible to colitis, indicating a critica

52 less biomass when dominated by species that are highly susceptible to competition (e.g. Populus spp.

53 in in skeletal muscle results in muscle that is highly susceptible to contraction-induced damage, but

54 ificantly lower levels of specific force and were highly susceptible to contraction-induced injury.

55 the alpha1A subunit of CaV 2.1 channels and are highly susceptible to cortical spreading depression

56 mice expressing the S218L or R192Q mutation are highly susceptible to cortical spreading depression,

57 However, Ugt1(DeltaGI) mice were highly susceptible to CPT-11-induced diarrhea, deve

58 culocyte-binding protein homologue 5 (PfRH5) is highly susceptible to cross-strain neutralizing vacci

59 Coastal and estuarine ecosystems are highly susceptible to crude oil pollution.

60 Although mice are highly susceptible to CVB3 infection when virus is d

61 e, and T1IFN receptor (T1IFNR) knockout mice are highly susceptible to CVB3 infection, succumbing wit

62 ed adoptive cell transplant examination, and were highly susceptible to CVB3 infection during their m

63 progeny at different stages of development, were highly susceptible to CVB3 infection.

64 However, metallic glasses are highly susceptible to cyclic fatigue damage, and pre

65 The mitochondrial genome is highly susceptible to damage by reactive oxygen speci

66 We now show that this plasma protein also is highly susceptible to degradation by hTryptase-beta.

67 gene (HERG) encodes a potassium channel that is highly susceptible to deleterious mutations resulting

68 ingly, a C2 mutant unable to bind 14-3-3zeta is highly susceptible to dephosphorylation.

69 This study showed that these peptides are highly susceptible to destruction in the earliest st

70 eatment, identifies [corrected] patients who are highly susceptible to developing advanced states [co

71 ed by deposition of tau tangles in the brain are highly susceptible to developing arthritis.

72 Female carriers of the Tgkd transgene are highly susceptible to developing teratomas.

73 ice deficient for Nlrp3 or ASC and caspase-1 were highly susceptible to dextran sodium sulfate (DSS)-

74 Lyn(-/-) mice were highly susceptible to dextran sulfate sodium (DSS)

75 Contrary to this, both lines were found to be highly susceptible to diet-induced metabolic disease,

76 T)-deficient C57BL/6J (6J) mice are known to be highly susceptible to diet-induced metabolic disease,

77 omparisons are difficult because the results are highly susceptible to discrepancies due to even mino

78 Subsequently, Nfil3(-/-) mice were highly susceptible to disease when challenged with

79 giving behaviors, mother-infant interactions are highly susceptible to disruption.

80 closporine A (CsA), that inhibit calcineurin are highly susceptible to disseminated fungal infections

81 The lung is highly susceptible to diverse forms of injury, and se

82 In the DMM model, male KO mice were highly susceptible to DMM-induced degenerative chan

83 MS11 recB mutants were found to be highly susceptible to DNA treatments that caused doub

84 Mice null for CD39 were highly susceptible to DSS injury, with heterozygote

85 lack such class-switched memory B cells but are highly susceptible to EBV infection, often developin

86 obases in transfected plasmid DNA substrates are highly susceptible to editing.

87 demonstrate that the acridine C9-N9 linkage is highly susceptible to electrophilic and nucleophilic

88 , mice expressing the human-elk chimeric PrP were highly susceptible to elk and deer CWD prions but w

89 MDA5-knockout mice are highly susceptible to EMCV infection and develop sig

90 established, and immunocompromised patients are highly susceptible to emergence of antiviral drug re

91 Here, we show that mice deficient in MKP-1 were highly susceptible to endotoxic shock in vivo, asso

92 Freshwater habitats are highly susceptible to environmental change and exhib

93 present with any overt viral phenotype, but are highly susceptible to environmental mycobacteria and

94 with complete or IMF-specific Tpl2 ablation are highly susceptible to epithelial injury-induced coli

95 LP), which is caused by mutations in SH2D1A, are highly susceptible to Epstein-Barr virus (EBV) infec

96 ge amount of proteins during ER stress, they are highly susceptible to ER stress-associated cell deat

97 e that TRIF(-/-) but not MyD88(-/-) neonates are highly susceptible to Escherichia coli peritonitis a

98 deficient (il25-/-) mice and found that they are highly susceptible to experimental autoimmune enceph

99 F-kappaB activation threshold and these mice are highly susceptible to experimental colitis.

100 Moreover, these mice were highly susceptible to experimental triggers of coli

101 Tropical and sub-tropical South America are highly susceptible to extreme droughts.

102 ion and daughter ion fragmentation patterns are highly susceptible to false negative findings, and t

103 nctional landscape of noncoding regions, but is highly susceptible to false discovery and misinterpre

104 Wild-type and Casp1(-/-) mice were highly susceptible to fatal ehrlichiosis, had overw

105 ice, which cannot recruit PMNs to the lungs, were highly susceptible to fatal P. aeruginosa lung infe

106 vels of FcgammaRIIb among B cell subsets and are highly susceptible to FcgammaRIIb-mediated apoptosis

107 rt a high diversity of larger predators that are highly susceptible to fluctuations in prey biomass.

108 es in a bovine kidney cell line (LF-BK) that is highly susceptible to FMDV infection and then isolate

109 Among the DPRs, poly(GA) is highly susceptible to form cytoplasmic inclusions, wh

110 identified specific areas in the heart that were highly susceptible to forming extrasystolic foci, a

111 it is easy to grow and maintain in the lab, is highly susceptible to gene inhibition using RNAi and

112 Dysf, MKO, and FER muscles were highly susceptible to glycerol exposure in vitro, d

113 defense against infection as anxa2(-/-) mice were highly susceptible to Gram-negative bacteria-induce

114 igenic explanation of why middle-aged adults were highly susceptible to H1N1 viruses during the 2013-

115 Mice lacking CYLD (CYLD-/-) were highly susceptible to hepatocellular damage, inflam

116 enced in NaAGO8 expression grew normally but were highly susceptible to herbivore attack.

117 d5 exposure or expanded by rAd5 vaccination, are highly susceptible to HIV in vitro and are preferent

118 We found that the circulating pTfh cells are highly susceptible to HIV infection and that in HIV-

119 gut mucosal fetal and infant CD4(+) T cells were highly susceptible to HIV-1 without any prestimulat

120 binding affinity and kinetic instability and were highly susceptible to HLA-DM-mediated peptide excha

121 serve that mice with a deficiency of miR-155 are highly susceptible to HSE with a majority of animals

122 RPE cells are highly susceptible to HSV-2 entry and replication.

123 t the constitutively low expression of Prdx4 is highly susceptible to hyperoxidation in the presence

124 esults demonstrate that B7-deficient T cells are highly susceptible to immune suppression by WT Tregs

125 read beliefs that any merozoite antigen that is highly susceptible to immune attack would be subject

126 oral infection, i.p. infected CD73(-/-) mice were highly susceptible to immune-mediated pathology, wi

127 Indolent NHL is highly susceptible to immunologic graft-versus-lympho

128 imary site for systemic glucose disposal and is highly susceptible to impaired insulin action by elev

129 his function is unclear because the proteins are highly susceptible to inactivation by H(2)O(2).

130 ils), 82% are tide-dominated, and almost 49% are highly susceptible to increases in flooding frequenc

131 function, developed electric remodeling, and were highly susceptible to inducible arrhythmias.

132 ndings indicate that human endothelial cells are highly susceptible to infection by dengue virus (typ

133 type siderophores, and lipocalin 2(-/-) mice are highly susceptible to infection by Escherichia coli

134 how that both rhesus and cynomolgus macaques are highly susceptible to infection by lineages of Zika

135 Homozygotes are highly susceptible to infection by Listeria monocyto

136 r histocompatibility complex (MHC) class II, are highly susceptible to infection by type A influenza

137 nts in neonatal intensive care units (NICUs) are highly susceptible to infection due to the immaturit

138 We conclude that HCE cell cultures are highly susceptible to infection whereas the cultured

139 es and monocyte-derived macrophages in vitro are highly susceptible to infection with HIV-1 R5 tropic

140 cell-mediated immunity, newborns and infants are highly susceptible to infection with intracellular p

141 that mice lacking a functional STAT1 pathway are highly susceptible to infection with LASV and develo

142 rac2(-/-) larvae are highly susceptible to infection with Pseudomonas aer

143 n lymph nodes have elevated CCR5 expression, are highly susceptible to infection with R5-tropic virus

144 NC93B1 as well as functional endosomal TLRs, are highly susceptible to infection with Trypanosoma cru

145 ) mice display lower levels of Th1 cells and are highly susceptible to infection, but can be rescued

146 nt flies, those with an inactive period gene are highly susceptible to infection, whereas mutants wit

147 Newborn infants are highly susceptible to infection.

148 Newborns are highly susceptible to infection.

149 omoter-GFP transgenic mice (actin-GFP NPSCs) were highly susceptible to infection with a recombinant

150 here that cultured chicken and duck myotubes were highly susceptible to infection with both low- and

151 Consequently, such cells were highly susceptible to infection with DNA viruses in

152 /99) (H3N2) virus, we found that guinea pigs were highly susceptible to infection with the unadapted

153 G96 mice were highly susceptible to infection, and disease appear

154 ly, IL-1R1(-/-) and IL-1alpha/beta(-/-) mice were highly susceptible to infection.

155 the 5HT2a receptor (5HT2aR) for JC virus and were highly susceptible to infection.

156 Burn patients are highly susceptible to infections due to increased ex

157 Patients undergoing chemotherapy for cancer are highly susceptible to influenza virus infection.

158 We report that RSV is highly susceptible to inhibition by human APOBEC3G, A

159 t to the alpha7 nAChR, the alpha7beta2 nAChR is highly susceptible to inhibition by the volatile anes

160 apoB:1000, (i) apoB:996 and apoB:996 + 4Ala were highly susceptible to intracellular degradation, (i

161 CBA/J mice were highly susceptible to intratracheal (i.t.) Cryptoco

162 hese patients can develop severe colitis and are highly susceptible to invasive fungal infection.

163 Hematopoietic stem cells (HSCs) are highly susceptible to ionizing radiation-mediated de

164 planting CD73-deficient inbred hearts, which are highly susceptible to ischemia-reperfusion injury, r

165 Affected hepatocytes are known to be highly susceptible to ischemic insults, responding to

166 oclonal antibodies (MAbs), MAb I and MAb II, are highly susceptible to isomerization due to the prese

167 e to persist in mice, and, most importantly, is highly susceptible to killing by antibiotics, showing

168 While M. tuberculosis is highly susceptible to killing by vitamin C, other Gra

169 ficient for TLR3, -7, and -9 (Tlr3/7/9(-/-)) are highly susceptible to L. major infection.

170 t although CD40 and CD40L knockout (KO) mice are highly susceptible to L. major, treatment with rIL-1

171 es showed that C5aR1(-/-) and C3aR(-/-) mice are highly susceptible to L. monocytogenes infection as

172 ottlenose dolphins (Tursiops truncatus) have been highly susceptible to large-scale unusual mortality

173 the C57BL/6 (resistant) genetic background, are highly susceptible to Leishmania major infection.

174 We showed that AHNAK1-deficient mice were highly susceptible to Leishmania major infection.

175 We also show that mice lacking Ask1 are highly susceptible to lethal bacterial infection owi

176 ired type I IFN production, Trim14(-/-) mice are highly susceptible to lethal HSV-1 infection.

177 with these observations, the Atf6(-/-) mice were highly susceptible to lethal bacterial infections c

178 (Atg16L1(HM)), which have reduced autophagy, were highly susceptible to lethality in both sepsis and

179 nt with the observation that RDH12-null mice are highly susceptible to light-induced retinal apoptosi

180 e mice were resistant to endotoxin shock but were highly susceptible to Listeria monocytogenes.

181 robust innate immune response, Pxr(-/-) mice were highly susceptible to Lm infection.

182 in IMT behaviour, this suggests that the IMT is highly susceptible to local changes in, for example,

183 In addition, LRG47-deficient mice are highly susceptible to LPS, but not TLR2 ligand-induc

184 rticoid receptor (GR) in DCs (GR(CD11c-cre)) were highly susceptible to LPS-induced septic shock, evi

185 Both CD4(+) T(H) subsets are highly susceptible to lysis by NK cells after activa

186 rn sheep (Ovis canadensis) (BHS), since they are highly susceptible to M. haemolytica infection.

187 different length scales and on top of that, is highly susceptible to many external stimuli, which ca

188 results of conventional phenotypic methods, are highly susceptible to methicillin-like antibiotics a

189 ve previously shown that diabetic db/db mice are highly susceptible to methionine choline-deficient d

190 In A/J and C3H/HeJ mice, which are highly susceptible to MHV-1-induced disease, we demo

191 ea that multiple structural elements of PDE6 are highly susceptible to misfolding during heterologous

192 Using this approach, we show that FRAP data are highly susceptible to misinterpretation.

193 y monocytes and THP-1 cells treated with Vpr are highly susceptible to mitochondrial depolarization,

194 Some primary cells have been shown to be highly susceptible to most strains of FMD virus (FMDV

195 treptococcus agalactiae isolates (n = 1,056) were highly susceptible to most antimicrobials, although

196 Roughly one in three individuals is highly susceptible to motion sickness and yet the und

197 Annexin1-deficient mice were highly susceptible to Mtb infection and showed an i

198 hibitors with larger groups at this position were highly susceptible to mutations at Arg155, Ala156,

199 cluding MHC class I and beta2 microglobulin, were highly susceptible to mycolactone treatment, indica

200 l-2 and Deltadcl-1/Deltadcl-2 mutant strains were highly susceptible to mycovirus infection, with CHV

201 was compromised in the wrky33 mutant, which is highly susceptible to necrotrophic pathogens.

202 ent through the inhibitory network as CCKBCs are highly susceptible to neuromodulation by local and s

203 type II PRRSV field isolate (PRRSV-01) that is highly susceptible to neutralization and induces an a

204 AtFAAH overexpressors also were highly susceptible to non-host pathogens P. syringa

205 HLA-DQ8 transgenic mice were highly susceptible to oMG.

206 he human IL-3 receptor alpha and beta chains were highly susceptible to oncogenic transformation by e

207 activation molecule-associated protein (SAP) are highly susceptible to one specific viral pathogen, t

208 mice deficient in NLRC4 or the IL-1 receptor were highly susceptible to orogastric but not intraperit

209 (CAST) mouse, a wild-derived inbred strain, is highly susceptible to orthopoxvirus infection by intr

210 0% inducible clindamycin resistance rate but were highly susceptible to other tested agents.

211 term memory, in which a given stimulus trace is highly susceptible to "overwriting" by a subsequent s

212 However, this amino acid is highly susceptible to oxidation, resulting in a mixtu

213 is a four-stranded G-rich DNA structure that is highly susceptible to oxidation.

214 Telomeres are highly susceptible to oxidative DNA damage, which if

215 Old mice were highly susceptible to oxidative stress following hi

216 ce exhibit a hyperinflammatory phenotype and are highly susceptible to P. gingivalis-induced periodon

217 Humans and other mammals are highly susceptible to permanent hearing and balance

218 DHA is highly susceptible to peroxidation, which yields an a

219 ucture and function of photosystem II (PSII) are highly susceptible to photo-oxidative damage induced

220 Furthermore, Sirt1 knock-out mice were highly susceptible to PM-induced lung coagulation a

221 mice improves survival, treml-1(-/-) animals are highly susceptible to polymicrobial infection.

222 ent study, we demonstrate that diabetic mice are highly susceptible to polymicrobial sepsis due to re

223 n the lungs of patients with cystic fibrosis is highly susceptible to polymicrobial infections by opp

224 Thus, IgA(-/-) mice are highly susceptible to primary pulmonary LVS infectio

225 origenesis did not occur, transgenic animals were highly susceptible to progestin/7,12-dimethylbenz(a

226 strated that the inner third of TRPML3's TM5 is highly susceptible to proline-based kinks.

227 In addition, Cnm produced by DeltapgfS was highly susceptible to proteinase K degradation, in c

228 molecules that are not bound to microtubules are highly susceptible to proteolysis and turned over im

229 sequencing revealed that all three fibulins are highly susceptible to proteolysis within the N-termi

230 A subset of surface-exposed proteins were highly susceptible to proteolysis when intact bacte

231 we demonstrated that serpinb1-deficient mice are highly susceptible to pulmonary bacterial and viral

232 aeruginosa Here, we demonstrate that CF mice are highly susceptible to pulmonary infections with S. a

233 We found that MyD88-/- mice were highly susceptible to pulmonary challenge with B. m

234 , whereas rabbit PMNs, like those of humans, are highly susceptible to PVL-induced cytolysis.

235 le to show that suburban raccoon populations are highly susceptible to rabies outbreaks, that the ris

236 We infer that E. coli is highly susceptible to radiation-induced ROS because i

237 es following infection, and many individuals are highly susceptible to reinfection.

238 to less soluble TcO(2).nH(2)O, but the oxide is highly susceptible to reoxidation.

239 Cells deficient in FAK are highly susceptible to RNA virus infection and attenu

240 Consequently, HDAC6 knockout mice were highly susceptible to RNA virus infections compared

241 The translocon mRNA should be highly susceptible to RNase E cleavage because of its

242 and IFN-I receptor 1 (Ifnar1)-deficient mice are highly susceptible to S. pyogenes infection.

243 The GLM, however, appears to be highly susceptible to sampling bias compared with the

244 respiratory syndrome coronavirus (SARS-CoV), were highly susceptible to SARS-CoV infection, which res

245 lmark of diabetic nephropathy, and podocytes are highly susceptible to saturated FFAs but not to prot

246 at asthmatic mice, unlike nonasthmatic mice, were highly susceptible to secondary heterologous virus

247 These septic patients are highly susceptible to "secondary" infections with in

248 oV strains may select for some variants that are highly susceptible to select MAbs that bind to RBDs.

249 The elderly host is highly susceptible to severe disease and treatment fa

250 terferon receptor knockout (IFNAR(-/-)) mice were highly susceptible to SFTSV infection, and all mice

251 We conclude that piglets are highly susceptible to shigellosis, providing a usefu

252 ence that cytokinetically quiescent MM cells are highly susceptible to simultaneous Chk1 and MEK1/2 i

253 ating that mice lacking this ISG15 E1 enzyme were highly susceptible to Sindbis virus infection.

254 epidermal-specific C/EBPalpha knockout mice were highly susceptible to skin tumor development involv

255 the Brazilian P. falciparum 7G8 line, but it is highly susceptible to some African P. falciparum stra

256 XMRV RT is highly susceptible to some nucleoside RT inhibitors,

257 Importantly, Bub1 hypomorphic mice are highly susceptible to spontaneous tumors, whereas Bu

258 highly exposed we anticipate that they would be highly susceptible to spontaneous DNA damage.

259 e rare genetic disease, Fanconi anemia (FA), are highly susceptible to squamous cell carcinomas arisi

260 ural symmetry and interlayer coupling, which are highly susceptible to stacking.

261 However, MSD measurements are highly susceptible to static error introduced by noi

262 The starchless pgm mutant is highly susceptible to submergence and also fails to i

263 not those deficient in either protein alone, were highly susceptible to subthreshold carcinogen expos

264 ptor or lacking the ability to secrete IL-17 are highly susceptible to systemic candidiasis, but we f

265 y, the triple TLR7/TLR9/TLR11-deficient mice are highly susceptible to T. gondii infection, recapitul

266 TCRbeta(-/-) mice were highly susceptible to T cell-mediated colitis, wher

267 source of mutation for nuclear genomes that is highly susceptible to temperature fluctuations that a

268 In addition, fetal NK cells were highly susceptible to TGF-beta-mediated suppression

269 completely quenched, even at interfaces that are highly susceptible to the effect, by insertion of a

270 prediction that sediment dwelling organisms are highly susceptible to the effects of ZnO NPs and sho

271 The F. novicida mutant was highly susceptible to the cationic antimicrobial pep

272 MMP-2(-/-) mice were highly susceptible to the development of colitis in

273 et(-/-) mice, but not wild-type BALB/c mice, were highly susceptible to the development of experiment

274 unohistopathology revealed that C57BL/6 mice were highly susceptible to the disease following intrana

275 Mice deficient in both TLR2 and TLR4 were highly susceptible to the intracellular bacterial p

276 ty of a few fluorophores, e.g., fluorescein, were highly susceptible to the intracellular environment

277 pression of rat nonclassic MHC class I C/E16 were highly susceptible to the killing by the CD8alphaal

278 ting molecule itself, their electronic state is highly susceptible to thermal fluctuations.

279 single molecule fluorescence dye Cy3, which is highly susceptible to this destructive pathway.

280 circulating IgG complexes in their blood and are highly susceptible to thrombotic events.

281 S) Toll-like receptors TLR3, TLR7, and TLR9, are highly susceptible to Toxoplasma gondii infection.

282 Here, we show that TRIM21 knockout mice were highly susceptible to Toxoplasma infection, exhibit

283 r postnatal expansion phase when these cells are highly susceptible to transformation.

284 apolipoprotein E -deficient (ApoE(-/-)) mice are highly susceptible to tuberculosis and that their su

285 PERA/Ei (PE) mice are highly susceptible to tumor induction by polyoma vir

286 owed that mice lacking beta(2)-microglobulin are highly susceptible to tumors induced by mouse polyom

287 We show here that C331A nNOS is highly susceptible to ubiquitination by a purified sy

288 wever, we found that K14 HPV49 E6/E7-Tg mice were highly susceptible to upper digestive tract carcino

289 While these mice were highly susceptible to UV-induced skin carcinogenesi

290 CKOalpha mice were highly susceptible to UVB-induced SCCs and exhibite

291 w that AZ-521 human gastric epithelial cells are highly susceptible to VacA-induced cell death.

292 e adhesin required for erythrocyte invasion, is highly susceptible to vaccine-inducible strain-transc

293 treptococcus pneumoniae isolates (n = 3,373) were highly susceptible to vancomycin (100%), linezolid

294 maize (Zea mays), particular genomic regions are highly susceptible to variation introduced by differ

295 Cells with the knockdown of tlr13 are highly susceptible to vesicular stomatitis virus inf

296 and pediatric Mandarin-speaking CI patients are highly susceptible to whispered speech, due to the l

297 db/db mice were highly susceptible to WNV disease, exhibited increa

298 nd found that CD22 knockout (Cd22(-/-)) mice were highly susceptible to WNV infection and had increas

299 murine Sp2 in epidermal basal keratinocytes were highly susceptible to wound- and carcinogen-induced

300 We demonstrate that primary human SCs were highly susceptible to ZIKV compared to the closely