ライフサイエンスコーパス: nonpathogenic

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

2 5 sequences), are generally considered to be nonpathogenic.

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

4 or gluconeogenic nutrients could render them nonpathogenic.

5 human flora and are generally assumed to be nonpathogenic.

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

7 for each variant, suggesting that these are nonpathogenic.

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

9 ucleic acid sequences, previously considered nonpathogenic.

10 thogen, whereas adeno-associated viruses are nonpathogenic.

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

12 nment that has historically been regarded as nonpathogenic.

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

14 FD rich in saturated fats and cholesterol to nonpathogenic (African green monkeys) and pathogenic (pi

15 mimicked in animal models via injection of a nonpathogenic agent poly(I:C) during pregnancy.

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

17 ctinomycetemcomitans and the closely related nonpathogenic Aggregatibacter aphrophilus.

18 Herpesvirus of turkeys (HVT) is a nonpathogenic alphaherpesvirus of turkeys and chickens t

19 of the disease; and inoculation of both the nonpathogenic ALV-E and SB-1 escalates it to much higher

20 exogenous ALV infection; inoculation of the nonpathogenic ALV-E or MDV-2 (SB-1) boosts the incidence

21 e of experimental evidence on the potency of nonpathogenic ALV-E, MDV-2, and ALV-E plus MDV-2 in boos

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

23 AAV vectors are nonpathogenic and elicit minimal inflammatory response.

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

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

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

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

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

29 mic to certain regions of Brazil and exhibit nonpathogenic anti-DSG1 antibodies.

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

31 ail to discriminate platelet-activating from nonpathogenic antibodies.

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

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

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

35 Nonpathogenic arenaviruses, closely related to hemorrhag

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

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

38 mune cells to B. anthracis PGA and PGAs from nonpathogenic B. subtilis subsp. chungkookjang and B. li

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

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

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

42 entirely of d-isomer glutamic acid, whereas nonpathogenic Bacillus species produce mixed d-, l-isome

43 tively by innate immune cells than PGAs from nonpathogenic Bacillus species, resulting in failure to

44 Ectopic production of PLY endowed the nonpathogenic Bacillus subtilis with the ability to trig

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

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

47 Using the tools of synthetic biology, nonpathogenic bacteria can be designed to sense and resp

48 mmox granular sludge and previously in other nonpathogenic bacteria pointed out that sialic acids and

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

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

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

52 bling differentiation between pathogenic and nonpathogenic bacteria.

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

54 nders them hypersensitive to infections with nonpathogenic bacteria.

55 ts the discrimination between pathogenic and nonpathogenic bacteria.

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

57 ts key co-factor HPr, have been performed in nonpathogenic bacteria.

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

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

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

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

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

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

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

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

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

67 The nonpathogenic cellular isoform of the human prion protei

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

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

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

71 ans to alter the bacterial microbiota during nonpathogenic colonization.

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

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

74 repressed by HOS15 under both pathogenic and nonpathogenic conditions but by HDA9 only under infectio

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

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

77 Thus, nonpathogenic cytosolic proteins appear capable of trans

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

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

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

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

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

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

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

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

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

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

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

89 rvival, whereas corresponding mutants in the nonpathogenic E. coli K-12 strain MG1655 displayed signi

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

91 Controlled expressions of this operon in nonpathogenic E. coli strains led to efficient assembly

92 157:H7 was cocultured with phage-susceptible nonpathogenic E. coli.

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

94 ates the potential of using algal viruses as nonpathogenic, easy to culture, and readily available su

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

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

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

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

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

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

101 e maternal gastrointestinal tract, including nonpathogenic Escherichia coli.

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

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

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

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

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

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

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

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

110 irus," which has long been thought to be the nonpathogenic form of JCV.

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

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

113 deoxyanthocyanidins when challenged with the nonpathogenic fungus Cochliobolus heterostrophus.

114 t may be that healthy women are colonized by nonpathogenic Gardnerella species, whereas virulent stra

115 man patient exomes aim to filter out as many nonpathogenic genetic variants (NPVs) as possible, witho

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

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

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

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

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

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

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

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

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

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

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

127 member of the New World mammarenaviruses, is nonpathogenic in humans but able to provide protection a

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

129 tic acid bacteria were previously considered nonpathogenic in humans.

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

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

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

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

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

135 he formation of infection structures and was nonpathogenic in planta, which was partially recovered b

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

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

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

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

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

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

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

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

144 rological and immunological features of this nonpathogenic infection.

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

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

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

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

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

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

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

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

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

154 strategies to restrict viral replication to nonpathogenic levels.

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

156 split pathogenic strains from environmental, nonpathogenic lineages.

157 the genetic relatedness among pathogenic and nonpathogenic Listeria species.

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

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

160 1 and Dsg3/Dsc3 beads, respectively, whereas nonpathogenic mAbs did not.

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

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

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

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

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

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

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

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

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

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

171 llow colonization by potentially beneficial, nonpathogenic microbes.

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

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

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

175 athogenic Mycobacterium tuberculosis and the nonpathogenic model mycobacterium Mycobacterium smegmati

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

187 Notably, nonpathogenic Mycobacterium smegmatis did not increase M

188 enic Mycobacterium abscessus, as well as the nonpathogenic Mycobacterium smegmatis, results in hypers

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

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

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

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

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

194 e singular divergence that could explain its nonpathogenic nature.

195 Nonpathogenic Neisseria strains (Neisseria cinerea and N

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

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

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

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

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

203 Infection with a nonpathogenic oral bacterial species, Streptococcus miti

204 sis, and yet the role of the SOS response in nonpathogenic organisms and in physiological settings re

205 n cross-reactive with similar pathogenic and nonpathogenic organisms.

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 Vaccines that induce nonpathogenic protective immunity may soon be available,

215 Understanding the function of the nonpathogenic PrP(C) monomer is an important objective.

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

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

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

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

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

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

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

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

229 iler breeder flocks, in combination with the nonpathogenic SB-1 on LL-like lymphoma incidences in bot

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

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

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

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

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

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

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

241 In contrast, nonpathogenic SIV infection of SM evidenced preservation

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

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

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

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

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

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

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

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

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

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

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

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

254 ition from the ancestral tetrapolar state in nonpathogenic species to a bipolar mating system in path

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

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

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

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

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

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

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

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

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

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

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

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

267 There is a need to identify nonpathogenic surrogates for adenovirus for the water tr

268 sistance alleles also affect colonisation by nonpathogenic symbionts.

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

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

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

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

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

274 e differentially expressed in pathogenic and nonpathogenic Th17 cells.

275 heterogeneity fostering both pathogenic and nonpathogenic, tissue-protective functions.

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

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

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

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

280 Nonpathogenic TSHR Abs (ELISA) were enhanced in transgen

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

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

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

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

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

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

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

288 ed as pathogenic/likely pathogenic and 21 as nonpathogenic (variant of uncertain significance/benign)

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

290 ion substructure and admixture, inclusion of nonpathogenic variants, as well as allelic and locus het

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 lovirus vectors.IMPORTANCE Baculoviruses are nonpathogenic viruses that infect mammals, which, among

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

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