ライフサイエンスコーパス: nonpathogenic

1 essing HTT with 18 glutamine repeats (YAC18, nonpathogenic).

2 of SAA1.1, suggesting that the native SAA is nonpathogenic.

3 for each variant, suggesting that these are nonpathogenic.

4 gens in healthy and DLE+SLE- subjects may be nonpathogenic.

5 ucleic acid sequences, previously considered nonpathogenic.

6 in the HI neonatal brain but appeared to be nonpathogenic.

7 of neutralizing antibody in animals yet are nonpathogenic.

8 virus is invisible to the immune system and nonpathogenic.

9 5 sequences), are generally considered to be nonpathogenic.

10 es the human pharynx and is considered to be nonpathogenic.

11 or gluconeogenic nutrients could render them nonpathogenic.

12 human flora and are generally assumed to be nonpathogenic.

13 tion and thyroid-stimulating Abs, as well as nonpathogenic Abs detected by ELISA.

14 ed thus far, SPBAANGAS-GAS-GAS is completely nonpathogenic after intracranial infection of mice that

15 s (MNV) is a highly infectious but generally nonpathogenic agent that is commonly found in research m

16 ctinomycetemcomitans and the closely related nonpathogenic Aggregatibacter aphrophilus.

17 o actively maintain immunologic tolerance to nonpathogenic Ags, including commensal bacteria.

18 The tig1 deletion mutant was nonpathogenic and defective in conidiogenesis.

19 AAV vectors are nonpathogenic and elicit minimal inflammatory response.

20 natural SIV hosts in which the infection is nonpathogenic and macrophages are virtually never infect

21 erial efficiency is probed against different nonpathogenic and pathogenic bacteria (Bacillus subtilis

22 on the differences and similarities between nonpathogenic and pathogenic endophytes in terms of host

23 fq affected transcription of genes common to nonpathogenic and pathogenic strains of E. coli as well

24 SNV was nonpathogenic and viremia was not detected despite the f

25 bles comparative studies between pathogenic, nonpathogenic, and elite-controlled infections, to gain

26 enic mechanisms in patients with PV who have nonpathogenic antibodies and show a discrepancy between

27 ail to discriminate platelet-activating from nonpathogenic antibodies.

28 tic lifestyle by acquiring a SUF system from nonpathogenic Archaea to synthesize Fe/S clusters under

29 a natural host for SIV in which infection is nonpathogenic, are less susceptible to SIV infection tha

30 These pathogenic clade B viruses, as well as nonpathogenic arenaviruses of the same clade, use transf

31 Nonpathogenic arenaviruses, closely related to hemorrhag

32 DA5), in sharp contrast to those of 14 other nonpathogenic arenaviruses.

33 elivery of foreign epitopes by a replicating nonpathogenic avian infectious bursal disease virus (IBD

34 ria pseudomallei and the closely related but nonpathogenic B. thailandensis.

35 while in the natural hosts, in which SIV is nonpathogenic, B cells rapidly increase in both lymph no

36 thracis shares many regulatory loci with the nonpathogenic Bacillus species Bacillus subtilis.

37 minescens and Enterococcus faecalis) and two nonpathogenic bacteria (Escherichia coli and Micrococcus

38 awn bordering and roaming behavior on mucoid nonpathogenic bacteria and loss of pathogen avoidance on

39 e, and Xylella fastidiosa T2S also occurs in nonpathogenic bacteria, facilitating symbioses, among ot

40 d to a similar extent by both pathogenic and nonpathogenic bacteria, suggesting that both can induce

41 sion of lysosomes with phagosomes containing nonpathogenic bacteria, uncovering a fundamental differe

42 an the other strains upon infection with the nonpathogenic bacteria.

43 nders them hypersensitive to infections with nonpathogenic bacteria.

44 ts the discrimination between pathogenic and nonpathogenic bacteria.

45 iscriminated the O157:H7 serotype from other nonpathogenic bacteria.

46 l survival in the presence of pathogenic and nonpathogenic bacteria.

47 bling differentiation between pathogenic and nonpathogenic bacteria.

48 ellin-mediated responses and immunity to the nonpathogenic bacterial infection.

49 ome structure and comparing it with those of nonpathogenic bacterial models, we identified some uniqu

50 ron by similar mechanisms, we show that this nonpathogenic bacterium can outcompete and reduce S. Typ

51 erologous expression of the pilB gene in the nonpathogenic bacterium Lactococcus lactis.

52 ivating protein factor (HRF) secreted by the nonpathogenic bacterium Massilia timonae.

53 llei but not present in five closely related nonpathogenic Burkholderia species.

54 t when given by inhalation to mice, S-FLU is nonpathogenic but generates a vigorous T cell response i

55 erican arenaviruses are generally considered nonpathogenic, but some of these viruses have been tenta

56 iated virus (AAV) is widely considered to be nonpathogenic, but the clinical epidemiology of this vir

57 classified six new variants as pathogenic or nonpathogenic by analysis of genetic information from fa

58 m/progenitor cells may be used as alternate, nonpathogenic cell sources for SB patient-specific bladd

59 The nonpathogenic cellular isoform of the human prion protei

60 fection of natural hosts is characterized by nonpathogenic chronic viremia, maintenance of gastrointe

61 dendrobatidis but not by the closely related nonpathogenic chytrid Homolaphlyctis polyrhiza.

62 ficantly increase the number of noncommensal/nonpathogenic clostridial species and provide a key foun

63 We have previously shown that spores of the nonpathogenic clostridial strain C. sporogenes genetical

64 ans to alter the bacterial microbiota during nonpathogenic colonization.

65 In AQP4-expressing cell cultures, the nonpathogenic competing antibodies blocked binding of NM

66 s in the lung control immune responses under nonpathogenic condition is not fully understood.

67 t to their longevity-promoting effects under nonpathogenic conditions.

68 advantage of vesiculation, particularly in a nonpathogenic context, as well as the hurdles that have

69 rom the cell walls of several pathogenic and nonpathogenic Corynebacterium strains directly bound to

70 Thus, nonpathogenic cytosolic proteins appear capable of trans

71 n of sooty mangabeys (SMs) that typically is nonpathogenic despite high viral loads.

72 human primate (NHP) natural hosts is usually nonpathogenic, despite high levels of virus replication.

73 reen monkeys (AGMs) have a remarkably stable nonpathogenic disease course, with levels of immune acti

74 We also found that nonpathogenic E coli gain degrading activity when they a

75 IEC lines with these bacteria compared with nonpathogenic E coli; chitinase activities were measured

76 re sufficient for triggering this event in a nonpathogenic E. coli background.

77 tinguish E. coli O157:H7 from a non-O157:H7, nonpathogenic E. coli by MALDI-TOF-TOF-MS/MS, whereas th

78 ssible to distinguish E. coli O157:H7 from a nonpathogenic E. coli by top-down proteomics of the YahO

79 centrations (10(1) CFU/mL) of pathogenic and nonpathogenic E. coli isolates and (10(0) CFU/mL) E. fae

80 EHEC EDL933 and Sakai strains but absent in nonpathogenic E. coli K-12 and HS strains were subjected

81 Here we show that nonpathogenic E. coli K-12 grown in the presence of 2 mu

82 s; expression of the YbcL variant encoded by nonpathogenic E. coli K-12 strain MG1655 (YbcL(MG)) fail

83 ced by E. coli, is a chemoattractant for the nonpathogenic E. coli RP437 strain.

84 ne of ninety diarrheagenic E. coli and 36/36 nonpathogenic E. coli strains were correctly identified

85 157:H7 was cocultured with phage-susceptible nonpathogenic E. coli.

86 equivalent to Edwardsiella anguillarum Fish-nonpathogenic E. tarda isolates are consistent with E. t

87 n this study, we investigated the effects of nonpathogenic, enteropathogenic, and probiotic bacteria

88 I cells of the lung help tolerate T cells to nonpathogenic environmental Ags.

89 e pathogens of mammals or insects as well as nonpathogenic environmental strains.

90 he vapA gene and enhances the persistence of nonpathogenic Escherichia coli in macrophages.

91 ls expressed MD-2/TLR4 and hyperresponded to nonpathogenic Escherichia coli or LPS with reactive oxyg

92 he function of SgrS is well-characterized in nonpathogenic Escherichia coli, where it was originally

93 s quickly succumb to infection with normally nonpathogenic Escherichia coli.

94 e maternal gastrointestinal tract, including nonpathogenic Escherichia coli.

95 mortality, indicating that the infection is nonpathogenic even when acquired early in life.

96 , and Japanese encephalitis viruses, and the nonpathogenic flaviviruses normally persist in a natural

97 Nonpathogenic foliar fungi (i.e. endophytes and epiphyte

98 hereas the Delta-peptide-Fc of an ebolavirus nonpathogenic for humans (Reston virus) and that of an e

99 of RESTV infection, suggesting that RESTV is nonpathogenic for humans.

100 humans and animals and have been considered nonpathogenic for humans.

101 ains but absent in Listeria species that are nonpathogenic for humans.

102 fever in Asian macaques but is thought to be nonpathogenic for humans.

103 ils to divert the autoantibody response to a nonpathogenic form.

104 than the average for other cyanobacteria and nonpathogenic, free-living bacteria.

105 deoxyanthocyanidins when challenged with the nonpathogenic fungus Cochliobolus heterostrophus.

106 RGPs are bactericidal against pathogenic and nonpathogenic Gram-positive bacteria, but not normal flo

107 as also observed in response to priming with nonpathogenic Gram-positive Listeria innocua.

108 In contrast, the Gn tail of the nonpathogenic hantavirus Prospect Hill virus (PHV) faile

109 thelial cells in response to VEGF, while the nonpathogenic hantaviruses Prospect Hill and Tula have n

110 These findings fundamentally distinguish nonpathogenic hantaviruses, PHV and TULV, and demonstrat

111 The G1 tails of pathogenic, but not nonpathogenic, hantaviruses contain intervening hydrophi

112 induced high levels of type 1 IFN, while the nonpathogenic HIV-R3B showed no significant induction in

113 B. megaterium is a commercially available, nonpathogenic host for the biotechnological production o

114 ically reduced in BAK1(Y610F) plants and the nonpathogenic hrpA mutant of Pseudomonas syringae was ab

115 Little is known in relation to the seemingly nonpathogenic HTLV-3 and HTLV-4 viruses, and studies of

116 In all, our results demonstrate that nonpathogenic HTT can indeed influence synaptic protein

117 fered significantly from those seen with the nonpathogenic human T. phagedenis strain.

118 the mutant huntingtin protein, the role that nonpathogenic huntingtin (HTT) plays in synaptic functio

119 ophil elastase inhibitor, and aquaporumab, a nonpathogenic IgG that competes with NMO-IgG for aquapor

120 hogenic in tomato (Solanum lycopersicum) yet nonpathogenic in Arabidopsis.

121 t, as opposed to most other fungi, which are nonpathogenic in D. melanogaster (e.g., Aspergillus fumi

122 which was chosen because it is likely to be nonpathogenic in human subjects.

123 veloped single-stranded DNA viruses that are nonpathogenic in humans but have potential utility as ca

124 tic acid bacteria were previously considered nonpathogenic in humans.

125 mian immunodeficiency virus (SIVagm) that is nonpathogenic in its host.

126 se data suggest that despite being generally nonpathogenic in its natural host, SIV infection selects

127 this recombinant virus vaccine candidate was nonpathogenic in mice when given by either the intramusc

128 Myxoma virus is nonpathogenic in mice, whereas systemic infection with v

129 wever, it is not known why most microbes are nonpathogenic in most plant species.

130 to our understanding of why SIV infection is nonpathogenic in sooty mangabeys while it is pathogenic

131 munodeficiency viruses (SIVs), are virtually nonpathogenic in their natural hosts remains a fundament

132 mmunodeficiency viruses (SIVs) are generally nonpathogenic in their natural hosts, dramatic increases

133 thogenic (in pig-tailed macaques [PTMs]) and nonpathogenic (in African green monkeys [AGMs]) SIVsab i

134 than in HIV-1-infected humans and results in nonpathogenic infection associated with low SIV viremia.

135 conformational epitope recognition, with the nonpathogenic infection being characterized by an evolut

136 epends on the establishment of a persistent, nonpathogenic infection in the mosquito vector.

137 In contrast, during nonpathogenic infection with SIV from African green monk

138 an green monkeys infected with SIVsab9315BR (nonpathogenic infection).

139 rological and immunological features of this nonpathogenic infection.

140 the early immune response in pathogenic and nonpathogenic infections identified here may be importan

141 erous differences between the pathogenic and nonpathogenic infections with regard to dynamics of the

142 ponses did not differ between pathogenic and nonpathogenic infections, with the exception of the conf

143 re and even lethal disease to subclinical or nonpathogenic infections.

144 In the nonpathogenic isolate P. syringae 508 the genomic region

145 effector orthologues was confirmed for other nonpathogenic isolates.

146 t of Escherichia coli pathogenic O157:H7 and nonpathogenic K12 strains in water-saturated Quincy sand

147 A with the LF82 chiA gene, but not chiA from nonpathogenic (K12) E coli, increased adhesion.

148 genic (L. monocytogenes and L. ivanovii) and nonpathogenic (L. welshimeri, L. innocua, L. seeligeri,

149 and aggregative adherence on nonadherent and nonpathogenic laboratory E. coli strains.

150 to study the immunologic contributions to a nonpathogenic lentiviral disease outcome.

151 Thus, lessons from pathogenic and nonpathogenic lentivirus infections provide insight into

152 strategies to restrict viral replication to nonpathogenic levels.

153 or the pathogenic lineage 1 Texas-HC2002 and nonpathogenic lineage 2 Madagascar-AnMg798 strains.

154 split pathogenic strains from environmental, nonpathogenic lineages.

155 the genetic relatedness among pathogenic and nonpathogenic Listeria species.

156 ence for the presence of functional SecA2 in nonpathogenic Listeria.

157 was similar to that of other pathogenic and nonpathogenic lymphotropic SIVs.

158 ilar genes were used for both pathogenic and nonpathogenic mAbs.

159 inocytes treated with pathogenic compared to nonpathogenic mAbs.

160 egion 3 (H-CDR3) of most pathogenic, but not nonpathogenic, mAbs shared an amino acid consensus seque

161 ycomembrane of Corynebacterium glutamicum, a nonpathogenic member of the Corynebacteriales order.

162 e secA2 gene and its genetic organization in nonpathogenic members of the genus Listeria.

163 ld arenaviruses contains both pathogenic and nonpathogenic members, whose surface glycoproteins (GPs)

164 ses comprise a large group of pathogenic and nonpathogenic members.

165 n to seek differences between pathogenic and nonpathogenic microbes and the role that the host plays

166 ole of species interactions among indigenous nonpathogenic microbes in developing and maintaining dis

167 sed immune response to pathogens compared to nonpathogenic microbes is poorly understood.

168 discriminate between pathogenic microbes and nonpathogenic microbes to control inflammation.

169 issue damage and infection by pathogenic and nonpathogenic microbes.

170 llow colonization by potentially beneficial, nonpathogenic microbes.

171 enic mutations in 34 probands and 7 probable nonpathogenic missense mutations in 9 probands.

172 VUS in the DBD of BRCA2 using 18 established nonpathogenic missense variants and all 13 established p

173 p, derived from the fusion glycoprotein of a nonpathogenic model arenavirus, which demonstrates antiv

174 athogenic Mycobacterium tuberculosis and the nonpathogenic model mycobacterium Mycobacterium smegmati

175 of HU (Hlp) in Mycobacterium smegmatis, the nonpathogenic model of Mycobacterium tuberculosis.

176 Macrophages also encounter nonpathogenic molecules that cluster receptors weakly an

177 In contrast, nonpathogenic Mopeia virus, which is a genetic relative

178 pe and IL-10(-/-) mice monoassociated with a nonpathogenic, murine isolate of Escherichia coli (NC101

179 llular bacterium Legionella pneumophila or a nonpathogenic mutant of L. pneumophila.

180 seudomonas syringae pv tomato DC3000 and the nonpathogenic mutant strain DC3000hrpA- allowed us to es

181 e primary difference between the rod-shaped, nonpathogenic mutants and the helix-shaped, pathogenic s

182 eins are not simply virulence factors, since nonpathogenic mycobacteria also express and secrete thes

183 lieved to be utilized by both pathogenic and nonpathogenic mycobacteria for iron acquisition in both

184 d MmpL11 are conserved across pathogenic and nonpathogenic mycobacteria, a feature consistent with an

185 ocus that is conserved across pathogenic and nonpathogenic mycobacteria.

186 y one of them alone is sufficient to allow a nonpathogenic mycobacterial species to proliferate.

187 The addition of M. leprae DNA enhanced nonpathogenic Mycobacterium bovis bacillus Calmette-Guer

188 ivity that is not found in its ortholog from nonpathogenic Mycobacterium smegmatis.

189 chemical profiles of selected pathogenic and nonpathogenic Naegleria in vitro using an untargeted met

190 Despite its nonpathogenic nature in vivo, SAA2.2 spontaneously forms

191 We hypothesized that the nonpathogenic nature of AAV plays a critical role in ind

192 ations in natural hosts, thus confirming the nonpathogenic nature of SIV infection in the wild.

193 e singular divergence that could explain its nonpathogenic nature.

194 Nonpathogenic Neisseria strains (Neisseria cinerea and N

195 opic virus variant and those infected with a nonpathogenic neurotropic virus variant both succumbed t

196 GPC processing of a panel of pathogenic and nonpathogenic New World arenaviruses, suggesting that GP

197 The EndoS-treated, nonpathogenic NMO-IgG competitively displaced pathogenic

198 ) or mutant L. monocytogenes strains, or its nonpathogenic noninvasive relative Listeria innocua, or

199 " hTSHR A-subunit protein recognized only by nonpathogenic (not pathogenic) TSHR Abs.

200 host to distinguish pathogenic microbes from nonpathogenic ones and to subsequently activate multiple

201 ruses are distinguished from closely related nonpathogenic ones by their additional ability to utiliz

202 in the mammalian nervous system, but whether nonpathogenic ones spread is unknown.

203 They are usually regarded as nonpathogenic or even mutualistic, but whether plants re

204 f the Huntingtin (Htt) protein with either a nonpathogenic or pathogenic polyglutamine repeat (Htt-10

205 Infection with a nonpathogenic oral bacterial species, Streptococcus miti

206 can suppress inflammation after exposure to nonpathogenic organisms.

207 nic PCV2 cloned into the genomic backbone of nonpathogenic PCV1 is attenuated in pigs but elicits pro

208 Its morphological similarity to nonpathogenic Penicillium species delayed the diagnosis

209 he cleavages that generate the pathogenic or nonpathogenic peptide fragments.

210 iruses (SFV) has been documented, leading to nonpathogenic persistent infections.

211 teractions may provide key insights into the nonpathogenic phenotype of SIVagm, we developed a mucosa

212 Swapping of the LCMV Z NTD into the nonpathogenic Pichinde virus (PICV) genome does not affe

213 cine circovirus-1 (PCV1), a highly prevalent nonpathogenic pig virus, which has not been shown to be

214 s is a common feature of both pathogenic and nonpathogenic primate lentivirus infections and support

215 Vaccines that induce nonpathogenic protective immunity may soon be available,

216 Two nonpathogenic PS1 mutations, P433L and L435R, caused ess

217 man huntingtin encoding pathogenic (Q138) or nonpathogenic (Q15) proteins, allowing in vivo imaging o

218 We generated nonpathogenic recombinant monoclonal anti-AQP4 antibodie

219 mutant strain of Mycobacterium smegmatis, a nonpathogenic relative of M. tuberculosis, which either

220 luding C. immitis and C. posadasii; a close, nonpathogenic relative, Uncinocarpus reesii; and a more

221 to skew the immune system towards beneficial nonpathogenic responses by selectively priming protectiv

222 Vectors derived from foamy virus, a nonpathogenic retrovirus, show higher preference for non

223 Foamy viruses are a ubiquitous family of nonpathogenic retroviruses that have potential as gene t

224 Systemic resistance induced in plants by nonpathogenic rhizobacteria is typically effective again

225 of patients; HR, 1.96; 95% CI, 0.92-4.18) or nonpathogenic risk variants (6.6% of patients; HR, 1.36;

226 his hypothesis, we deleted the trg gene from nonpathogenic Salmonella.

227 -sensing (QS) system and a GFP reporter into nonpathogenic Salmonella.

228 mpact of interrupting O-mannosylation in the nonpathogenic saprophyte Mycobacterium smegmatis and in

229 pportunistic pathogen, B. thailandensis is a nonpathogenic saprophyte, and B. mallei is a host-restri

230 saccharide (CPS) antigens were isolated from nonpathogenic, select-agent-excluded strains of B. pseud

231 ents: p.L1201R and p.R1300Q likely represent nonpathogenic sequence variants, whereas the p.R2107H su

232 Taken together, we identified a nonpathogenic signature of intestinal homeostatic Th17 c

233 These data suggest that, similar to nonpathogenic simian immunodeficiency virus (SIV) infect

234 ficiency virus (HIV) infection of humans and nonpathogenic simian immunodeficiency virus (SIV) infect

235 Studies of natural, nonpathogenic simian immunodeficiency virus (SIV) infect

236 compartment of the gut is well-maintained in nonpathogenic simian immunodeficiency virus infection as

237 cation of Bacillus globigii, a spore forming nonpathogenic simulant of Bacillus anthracis.

238 Adeno-associated virus (AAV) is a nonpathogenic single-stranded human parvovirus which usu

239 n in Asian macaques, its role in maintaining nonpathogenic SIV infection in natural hosts such as soo

240 IV infection and absent during the course of nonpathogenic SIV infection in natural nonhuman primate

241 elp account for the nonprogressive nature of nonpathogenic SIV infection in sooty mangabeys.

242 rhesus and pigtailed macaques (PTMs) and in nonpathogenic SIV infection of African green monkeys (AG

243 hese data demonstrate an association between nonpathogenic SIV infection of SM and a reduced monocyte

244 In contrast, nonpathogenic SIV infection of SM evidenced preservation

245 Although the nonpathogenic SIV infection of SMs induces the same patt

246 ic SIV infection of rhesus macaques (RM) and nonpathogenic SIV infection of sooty mangabeys (SM).

247 A key feature differentiating nonpathogenic SIV infection of sooty mangabeys (SMs) fro

248 In contrast, during nonpathogenic SIV infection of sooty mangabeys (SMs), ne

249 hogenic SIV infection of rhesus macaques and nonpathogenic SIV infection of sooty mangabeys.

250 Our data suggest that, in nonpathogenic SIV infection, NK cells migrate into folli

251 uch as African green monkeys (AGMs), sustain nonpathogenic SIV infections and rarely vertically trans

252 AGMs), the natural SIV host species, sustain nonpathogenic SIV infections, rarely transmit the virus

253 ty and maturation between the pathogenic and nonpathogenic SIV infections, we identified a major diff

254 Pathogenic, but not nonpathogenic, SIV infection was associated with signifi

255 isms, the overwhelming majority of which are nonpathogenic, some are responsible for food spoilage, a

256 However, OMVs also benefit nonpathogenic species by delivering degradative enzymes

257 GP from Reston ebolavirus, a nonpathogenic species in humans, showed a phenotype simi

258 ority of these proteins are conserved in the nonpathogenic species Leptospira biflexa, and proteins i

259 ization of the secA2 locus in pathogenic and nonpathogenic species.

260 However, during coculture with the nonpathogenic strain E. coli C600, PA2 produced Stx2a le

261 scherichia coli O157:H7 and one non-O157:H7, nonpathogenic strain of E. coli have been identified by

262 te to attenuation of the naturally occurring nonpathogenic strain of West Nile virus (WNV), the Kunji

263 Acinetobacter NAD metabolism using a model (nonpathogenic) strain Acinetobacter baylyi sp. ADP1.

264 tion with HR-eliciting, disease-forming, and nonpathogenic strains and also with flagellin (flg22).

265 om the pathogenic viruses, with entry of the nonpathogenic strains being TfR1 independent.

266 Although QseC and QseE are present in nonpathogenic strains of E. coli, EHEC exploits these ki

267 d susceptibility of Hsp70-depleted plants to nonpathogenic strains of P. syringae supports a defense-

268 Expression of MAM7 on nonpathogenic strains produced a tool that can be used t

269 with various degrees of virulence (including nonpathogenic strains) have been described in different

270 In contrast to Ecoli nonpathogenic strains, pathogenic Ecoli strains predomin

271 genes associated with primary metabolism in nonpathogenic Streptomyces species have been recruited a

272 ucleus in response to various pathogenic and nonpathogenic stresses, leading to an inhibition of mRNA

273 In cells infected with the nonpathogenic Tacaribe virus or the attenuated Candid#1

274 sequences are more common in pathogenic than nonpathogenic taxa and are associated with changes in pa

275 Nonpathogenic TC-derived virus N13R10 (cloned as a bacte

276 autoimmunity in mice are distinguished from nonpathogenic Th17 cells by a unique transcriptional sig

277 Subpopulations of pathogenic or nonpathogenic Th17 cells were reported to develop when p

278 e differentially expressed in pathogenic and nonpathogenic Th17 cells.

279 In contrast, HAZV is nonpathogenic to humans and thus represents an excellent

280 irus (REBOV) is the only Ebola virus that is nonpathogenic to humans despite the fact that REBOV can

281 cies, of which Reston ebolavirus is uniquely nonpathogenic to humans.

282 e variation in a diversity of pathogenic and nonpathogenic treponemes.

283 Cs but were unaltered in ECs infected by the nonpathogenic Tula hantavirus (TULV).

284 with the previous tomographic studies of the nonpathogenic Tula hantavirus indicates a common structu

285 In contrast, cells comparably infected with nonpathogenic Tula virus (TULV) failed to recruit platel

286 es virus (ANDV) and Hantaan virus (HTNV) and nonpathogenic Tula virus (TULV) hantaviruses.

287 In contrast to infection of cells with nonpathogenic Tula virus (TULV), we observed that exposu

288 These findings indicate that the nonpathogenic TULV Gn-T regulates IFN induction but acco

289 otoxic, and they can be either pathogenic or nonpathogenic upon adoptive transfer in the model of aut

290 R, T17M, P23A, P23H, P23L, and C110Y; or the nonpathogenic variants F220L and A299S.

291 pectedly developed TSHR Abs, but only of the nonpathogenic variety detected by ELISA.

292 changes in the entry glycoproteins of these nonpathogenic viruses may allow human transmission.

293 sing closely related pairs of pathogenic and nonpathogenic viruses, we investigated the determinants

294 y gram-negative species, both pathogenic and nonpathogenic, where it supports the delivery of a varie

295 and infection in these animals is generally nonpathogenic, whereas infection of nonnatural hosts, su

296 isolated as a contaminant of PK-15 cells, is nonpathogenic, whereas porcine circovirus type 2 (PCV2)

297 olates, SylvioX10/4 (SYL, virulent) and TCC (nonpathogenic), which represent mphi stimulation and inf

298 apgp1 and Deltapgp2 mutants were essentially nonpathogenic, while all strains with a curved or helica

299 ction of the pathogen in the presence of the nonpathogenic wild strain showed that the antibody fragm

300 Chimeras of nonpathogenic wtSOD1YFP and G85R SOD1CFP also exhibited