ライフサイエンスコーパス: mouse hepatitis virus

1 ted neurotropic coronavirus (rJ2.2 strain of mouse hepatitis virus).

2 ells were highly susceptible to a murine CoV-mouse hepatitis virus.

3 ing infection of p85beta-deficient mice with mouse hepatitis virus.

4 l infection by the neurotropic JHM strain of mouse hepatitis virus.

5 S infection by the neurotropic JHM strain of mouse hepatitis virus.

6 egion of the positive-stranded RNA genome of mouse hepatitis virus.

7 ternative receptor for the mouse coronavirus mouse hepatitis virus.

8 central nervous system by the JHM strain of mouse hepatitis virus.

9 bute to the persistence of the JHM strain of mouse hepatitis virus.

10 alphavirus chikungunya virus and coronavirus mouse hepatitis virus.

11 nucleocapsid protein of a model coronavirus, mouse hepatitis virus.

12 control acute infection with the cytopathic mouse hepatitis virus.

13 Intranasal mouse hepatitis virus-1 (MHV-1) infection of susceptible

14 Mouse hepatitis virus, a beta-CoV in group A, uses the g

15 Intracerebral infection of mice with mouse hepatitis virus, a member of the Coronaviridae fam

16 rmine the role of MDA5 during infection with mouse hepatitis virus, a murine coronavirus used to mode

17 ssibility was examined in mice infected with mouse hepatitis virus, a well-described model of virus-i

18 a mildly pathogenic neurotropic coronavirus (mouse hepatitis virus A59 strain [MHV-A59]) developed se

19 Surprisingly, two beta-CoVs in group A, mouse hepatitis virus and HKU1, have evolved to use diff

20 central nervous system (CNS) by neurotropic mouse hepatitis virus but do not suffice to achieve ster

21 I Ag presentation, H-2d-restricted HIV-1 and mouse hepatitis virus CTL epitopes were linked via vario

22 stem segment mutations on the replication of mouse hepatitis virus defective interfering RNAs.

23 ysis of mice infected with the JHM strain of mouse hepatitis virus demonstrated that, in contrast to

24 Using a neurotropic mouse hepatitis virus encephalomyelitis model, this stud

25 CCL3(-/-) mice infected with mouse hepatitis virus exhibited a significant reduction

26 d of the 3' untranslated region (UTR) of the mouse hepatitis virus genome contains two essential and

27 IP-10(-/-) mice infected with a neurotropic mouse hepatitis virus had an impaired ability to control

28 gnals of the SARS-associated coronavirus and mouse hepatitis virus have evolved to promote optimal fr

29 he pathogenesis of the neurotropic strain of mouse hepatitis virus in Fas-deficient mice suggested th

30 ein, encoded by ORF6, enhanced the growth of mouse hepatitis virus in tissue culture cells and in mic

31 rected against CCL5 to mice with established mouse hepatitis virus-induced demyelination and impaired

32 orates rather than perpetuates JHM strain of mouse hepatitis virus-induced demyelination.

33 To determine functional significance, mouse hepatitis virus-infected mice were treated with an

34 astrocytes during acute encephalomyelitis in mouse hepatitis virus-infected mice, and the majority of

35 Mouse hepatitis virus infection of mice provides a usefu

36 a) in contributing to a Th1 response against mouse hepatitis virus infection of the CNS.

37 infection with the neurotropic JHM strain of mouse hepatitis virus is inhibited in the absence of CD4

38 The MHV-JHM strain of the murine coronavirus mouse hepatitis virus is much more neurovirulent than th

39 Mouse hepatitis virus is used as well studied examplar t

40 For example, C57BL/6 (B6) mice infected with mouse hepatitis virus (JHM strain, JHMV) develop severe

41 ures containing CNS cells were infected with mouse hepatitis virus-JHM, which causes fatal encephalit

42 BL/6 mice with the neurotropic JHM strain of mouse hepatitis virus (JHMV) (a member of the Coronaviri

43 cephalomyelitis induced by the JHM strain of mouse hepatitis virus (JHMV) and sustained during viral

44 infected with the neurotropic JHM strain of mouse hepatitis virus (JHMV) clear infectious virus; nev

45 infected with the neurotropic JHM strain of mouse hepatitis virus (JHMV) develop acute and chronic d

46 ystem (CNS) by the neurotropic JHM strain of mouse hepatitis virus (JHMV) induces an acute encephalom

47 oculation with the neurotropic JHM strain of mouse hepatitis virus (JHMV) into the central nervous sy

48 al nervous system (CNS) by the JHM strain of mouse hepatitis virus (JHMV) is a rodent model of the hu

49 The neurotropic JHM strain of mouse hepatitis virus (JHMV) produces an acute CNS infec

50 Control of neurotropic mouse hepatitis virus (JHMV) requires the collaboration

51 infection with the neurotropic JHM strain of mouse hepatitis virus (JHMV) resulted in an acute enceph

52 mouse CNS with the neurotropic JHM strain of mouse hepatitis virus (JHMV) results in an immune-mediat

53 f the CNS with the neurotropic JHM strain of mouse hepatitis virus (JHMV) was examined.

54 infection with the neurotropic JHM strain of mouse hepatitis virus (JHMV).

55 infection with the neurotropic JHM strain of mouse hepatitis virus (JHMV).

56 tillation with the neurotropic JHM strain of mouse hepatitis virus (JHMV).

57 The 5' 140 nucleotides of the mouse hepatitis virus (MHV) 5' untranslated region (5'UT

58 We used mouse hepatitis virus (MHV) A59 as a model to gain insig

59 The endoribonuclease activity of the mouse hepatitis virus (MHV) A59 Nsp15 was also increased

60 here the outcome of viral encephalomyelitis [mouse hepatitis virus (MHV) A59, Theiler's encephalomyel

61 e that infection with the murine coronavirus mouse hepatitis virus (MHV) activated the NLRP3 inflamma

62 Infection with the murine coronavirus mouse hepatitis virus (MHV) activates the pattern recogn

63 pathogens, including the murine coronavirus mouse hepatitis virus (MHV) and Haemophilus influenzae,

64 wo viruses within the genus Betacoronavirus, mouse hepatitis virus (MHV) and MERS-CoV, encode 2',5'-p

65 of the 5' untranslated regions (5'UTRs) from mouse hepatitis virus (MHV) and severe acute respiratory

66 evere acute respiratory syndrome (SARS)-CoV, mouse hepatitis virus (MHV) and the human CoV OC43 S2 su

67 The subgenomic mRNAs of the coronavirus mouse hepatitis virus (MHV) are composed of a leader seq

68 Receptors for murine coronavirus mouse hepatitis virus (MHV) are members of the murine ca

69 The p28 and p65 proteins of mouse hepatitis virus (MHV) are the most amino-terminal

70 e glycoprotein (S) of the murine coronavirus mouse hepatitis virus (MHV) binds to viral murine CEACAM

71 Some strains of mouse hepatitis virus (MHV) can induce chronic inflammat

72 The neurotropic JHM strain of mouse hepatitis virus (MHV) causes acute encephalitis an

73 Murine coronavirus mouse hepatitis virus (MHV) causes demyelination of the

74 Murine coronavirus mouse hepatitis virus (MHV) causes persistent infection

75 ve interfering (DI) RNA of the JHM strain of mouse hepatitis virus (MHV) consist of three discontinuo

76 2 (SL2) of the 5'-untranslated region of the mouse hepatitis virus (MHV) contains a highly conserved

77 The coronavirus mouse hepatitis virus (MHV) contains a large open readin

78 positive-sense RNA genome of the coronavirus mouse hepatitis virus (MHV) contains sequences that are

79 spike glycoprotein from strain RSA59 (PP) of mouse hepatitis virus (MHV) contains two central, consec

80 ve (ts) mutant helper virus, two coronavirus mouse hepatitis virus (MHV) defective interfering (DI) R

81 Mouse hepatitis virus (MHV) does not induce interferon (

82 ired for clearance of the murine coronavirus mouse hepatitis virus (MHV) during acute infection.

83 tep toward understanding the function of the mouse hepatitis virus (MHV) E protein, we carried out cl

84 on with the recombinant JHM (RJHM) strain of mouse hepatitis virus (MHV) elicits a weak CD8(+) T-cell

85 e replicase gene (gene 1) of the coronavirus mouse hepatitis virus (MHV) encodes two co-amino-termina

86 We used experimental evolution of mouse hepatitis virus (MHV) encoding a cellular AKAP7 ph

87 Various strains of mouse hepatitis virus (MHV) exhibit different pathogenic

88 Most strains of murine coronavirus mouse hepatitis virus (MHV) express a cleavable spike gl

89 Using the recombinant murine coronavirus mouse hepatitis virus (MHV) expressing the T cell-chemoa

90 While the 5' cis-acting sequence of mouse hepatitis virus (MHV) for genomic RNA replication

91 Murine coronavirus mouse hepatitis virus (MHV) gene 1 encodes several nonst

92 ithin the 3'-terminal 166 nucleotides of the mouse hepatitis virus (MHV) genome and assessed their fu

93 The mouse hepatitis virus (MHV) genome's 3' untranslated reg

94 The 3'-end of mouse hepatitis virus (MHV) genomic RNA contains a recog

95 ream of the leader at the 5' terminus of the mouse hepatitis virus (MHV) genomic RNA, contains a sequ

96 ction of murine astrocytoma (DBT) cells with mouse hepatitis virus (MHV) has been established.

97 Previous work with the prototype coronavirus mouse hepatitis virus (MHV) has shown that a major deter

98 Many strains of the murine coronavirus mouse hepatitis virus (MHV) have distinct, S-dependent o

99 Previous studies have demonstrated that mouse hepatitis virus (MHV) hepatotropism is determined

100 o the nonessential gene 4 of the coronavirus mouse hepatitis virus (MHV) in order to test the applica

101 constructed mutants of the model coronavirus mouse hepatitis virus (MHV) in which all or part of the

102 , we constructed a mutant of the coronavirus mouse hepatitis virus (MHV) in which the ectodomain of t

103 of 17Cl-1 cells with the murine coronavirus mouse hepatitis virus (MHV) induced caspase-dependent ap

104 The murine coronavirus mouse hepatitis virus (MHV) induced the expression of ty

105 The coronavirus mouse hepatitis virus (MHV) induces a minimal type I int

106 induced demyelination, including coronavirus mouse hepatitis virus (MHV) infection in mice.

107 Thus, during mouse hepatitis virus (MHV) infection, hepatitis, which

108 encephalomyelitis virus (TMEV) infection and mouse hepatitis virus (MHV) infection.

109 Mouse hepatitis virus (MHV) is a 31-kb positive-strand R

110 Mouse hepatitis virus (MHV) is a murine betacoronavirus

111 The M protein of mouse hepatitis virus (MHV) is an integral membrane prot

112 RNA synthesis by the prototype coronavirus mouse hepatitis virus (MHV) is carried out by a replicas

113 processing of the replicase gene product of mouse hepatitis virus (MHV) is essential for viral repli

114 The 3C-like proteinase (3CLpro) of mouse hepatitis virus (MHV) is predicted to cleave at le

115 Mouse hepatitis virus (MHV) isolates JHM.WU and JHM.SD p

116 binds specifically to the plus strand of the mouse hepatitis virus (MHV) leader RNA.

117 rotective roles of specific ISGs against the mouse hepatitis virus (MHV) members of the coronaviruses

118 Mouse hepatitis virus (MHV) neurotropism varies by strai

119 ave demonstrated that the murine coronavirus mouse hepatitis virus (MHV) nonstructural protein 2 (ns2

120 uclear magnetic resonance (NMR) structure of mouse hepatitis virus (MHV) nsp3a and show, using isothe

121 In the prototype coronavirus mouse hepatitis virus (MHV) packaging selectivity is bro

122 The coronavirus mouse hepatitis virus (MHV) performs RNA replication on

123 Murine coronavirus mouse hepatitis virus (MHV) produces a genome-length mRN

124 Infection of the CNS with the mouse hepatitis virus (MHV) provides a unique model situ

125 Mouse hepatitis virus (MHV) receptor, the receptor for t

126 Mouse hepatitis virus (MHV) replicase products nsp3, nsp

127 Mouse hepatitis virus (MHV) replication in actively grow

128 on of cultured cells with murine coronavirus mouse hepatitis virus (MHV) resulted in activation of th

129 ed that infection of rat oligodendrocytes by mouse hepatitis virus (MHV) resulted in apoptosis, which

130 Intracranial infection of C57BL/6 mice with mouse hepatitis virus (MHV) results in an acute encephal

131 Intracerebral infection of mice with mouse hepatitis virus (MHV) results in an acute encephal

132 (hnRNP) A1 has previously been shown to bind mouse hepatitis virus (MHV) RNA at the 3' end of both pl

133 The 3'-untranslated region (3'-UTR) of mouse hepatitis virus (MHV) RNA regulates the replicatio

134 shown to function as regulatory factors for mouse hepatitis virus (MHV) RNA synthesis as a result of

135 Mouse hepatitis virus (MHV) RNA synthesis is mediated by

136 The 3' cis-acting element for mouse hepatitis virus (MHV) RNA synthesis resides entire

137 Mouse hepatitis virus (MHV) RNA transcription is regulat

138 e leader RNA and intergenic (IG) sequence of mouse hepatitis virus (MHV) RNA.

139 accumulation kinetics of murine coronavirus mouse hepatitis virus (MHV) RNAs early in infection by u

140 The mouse hepatitis virus (MHV) spike glycoprotein, S, has b

141 Persistent infection with mouse hepatitis virus (MHV) strain A59 in murine DBT (de

142 s are important for clearance of neurotropic mouse hepatitis virus (MHV) strain A59, although their p

143 The murine coronavirus, mouse hepatitis virus (MHV) strain A59, causes acute enc

144 C57BL/6 (B6) mice infected with mouse hepatitis virus (MHV) strain JHM develop a clinica

145 Mice infected with mouse hepatitis virus (MHV) strain JHM develop primary d

146 We observed that the nonfusogenic mouse hepatitis virus (MHV) strain MHV-2 reached a titer

147 We demonstrate that MHV-A59, a mouse hepatitis virus (MHV) strain that causes brain and

148 Mouse hepatitis virus (MHV) strains (MHV-A59, MHV-JHM, a

149 erfering (DI) RNAs of the murine coronavirus mouse hepatitis virus (MHV) suggest that a 69-nucleotide

150 have previously generated E gene mutants of mouse hepatitis virus (MHV) that had marked defects in v

151 the current studies, neurotropic strains of mouse hepatitis virus (MHV) that induce meningitis, ence

152 previously generated E gene point mutants of mouse hepatitis virus (MHV) that were defective in growt

153 s, we previously generated E gene mutants of mouse hepatitis virus (MHV) that were defective in viral

154 The coronavirus mouse hepatitis virus (MHV) translates its replicase gen

155 ort that infection by the murine coronavirus mouse hepatitis virus (MHV) triggers the proximal UPR tr

156 Mouse hepatitis virus (MHV) uses its N-terminal domain (

157 The mouse hepatitis virus (MHV) variant MHV/BHK can infect h

158 We previously described mouse hepatitis virus (MHV) variant V51 derived from a p

159 Antibodies directed against mouse hepatitis virus (MHV) virions and against the puta

160 ic packaging signal (PS) for the coronavirus mouse hepatitis virus (MHV) was originally identified as

161 Mouse hepatitis virus (MHV) was used as a model to study

162 that AhR is activated in cells infected with mouse hepatitis virus (MHV), a coronavirus (CoV), and co

163 In previous work with the coronavirus mouse hepatitis virus (MHV), a highly defective M protei

164 Mouse hepatitis virus (MHV), a member of the Coronavirid

165 The primary cellular receptor for mouse hepatitis virus (MHV), a murine coronavirus, is MH

166 rms of murine CEACAM1 serve as receptors for mouse hepatitis virus (MHV), a murine coronavirus.

167 lpha/beta IFN (IFN-alpha/beta) receptor with mouse hepatitis virus (MHV), a murine coronavirus.

168 is question, we used the rJHM strain (rJ) of mouse hepatitis virus (MHV), a neurotropic coronavirus t

169 he N-terminal domain (NTD) of N protein from mouse hepatitis virus (MHV), a virus most closely relate

170 a Sarbecovirus, and the packaging signal of mouse hepatitis virus (MHV), an Embecovirus, which is a

171 encoded by the prototypical Betacoronavirus, mouse hepatitis virus (MHV), and by Middle East respirat

172 The murine coronavirus, mouse hepatitis virus (MHV), causes acute hepatitis in i

173 spectively, including the murine coronavirus mouse hepatitis virus (MHV), Haemophilus influenzae, Nei

174 For the prototype coronavirus mouse hepatitis virus (MHV), heterogeneous nuclear ribon

175 For the prototype coronavirus mouse hepatitis virus (MHV), it has previously been esta

176 The murine coronavirus, mouse hepatitis virus (MHV), JHM strain, induces a bipha

177 epitope of a highly neurovirulent strain of mouse hepatitis virus (MHV), JHM, is thought to be essen

178 This gene is referred to as "I" for mouse hepatitis virus (MHV), ORF9b for severe acute resp

179 ells infected with a prototypic coronavirus, mouse hepatitis virus (MHV), resulting in the expression

180 Demyelination induced by mouse hepatitis virus (MHV), strain JHM, is in large par

181 Infection of mice with mouse hepatitis virus (MHV), strain JHM, results in acut

182 nhibited virus entry and cell-cell fusion of mouse hepatitis virus (MHV), suggesting the importance o

183 For the coronavirus mouse hepatitis virus (MHV), the first proteolytic proce

184 In mouse hepatitis virus (MHV), the NTD binds the transcrip

185 s study, we exploited the model coronavirus, mouse hepatitis virus (MHV), to investigate the genotype

186 we report genetic analysis of a ts strain of mouse hepatitis virus (MHV), tsNC11, focusing on the rol

187 ns in the N protein of the model coronavirus mouse hepatitis virus (MHV), we constructed mutants in w

188 ions of N protein domains in the coronavirus mouse hepatitis virus (MHV), we replaced the MHV N gene

189 terfering (DI) RNA of the murine coronavirus mouse hepatitis virus (MHV), when introduced into MHV-in

190 tory syndrome coronavirus 2 (SARS-CoV-2) and mouse hepatitis virus (MHV)-A59 and identified conserved

191 ocalization and expression is altered due to mouse hepatitis virus (MHV)-A59 infection both in vivo a

192 a group of mutants of the murine coronavirus mouse hepatitis virus (MHV)-A59, isolated from persisten

193 Mouse hepatitis virus (MHV)-infected cells contain full-

194 In this study, mouse hepatitis virus (MHV)-infected cells were fraction

195 togen-activated protein kinases (MAPKs) in a mouse hepatitis virus (MHV)-infected macrophage-derived

196 in response to intracerebral infection with mouse hepatitis virus (MHV).

197 terpart in the prototype group 2 coronavirus mouse hepatitis virus (MHV).

198 icacy against a member of the Coronaviridae, Mouse hepatitis virus (MHV).

199 on (3' UTR) of the genome of the coronavirus mouse hepatitis virus (MHV).

200 curs within the CNS following infection with mouse hepatitis virus (MHV).

201 gitis virus (LCMV), vaccinia virus (VV), and mouse hepatitis virus (MHV).

202 in cells infected with a murine coronavirus, mouse hepatitis virus (MHV).

203 and replication of a cytoplasmic RNA virus, mouse hepatitis virus (MHV).

204 n cells infected with the murine coronavirus mouse hepatitis virus (MHV).

205 piratory syndrome coronavirus (SARS-CoV) and mouse hepatitis virus (MHV).

206 espiratory syndrome CoV, and the murine CoV, mouse hepatitis virus (MHV).

207 ase inhibitor in a coronavirus model system, mouse hepatitis virus (MHV).

208 trol of in vivo infection by the coronavirus mouse hepatitis virus (MHV).

209 ralized the infectivity of the A59 strain of mouse hepatitis virus (MHV-A59) in a concentration-depen

210 Specifically, murine beta-coronavirus, mouse hepatitis virus (MHV-A59) inoculation in the mouse

211 N did not serve as a functional receptor for mouse hepatitis virus (MHV-A59), which is in serogroup I

212 ainst a neurotropic murine beta-coronavirus, mouse hepatitis virus (MHV-A59).

213 inst other embecoviruses, including HKU1 and mouse hepatitis virus (MHV-A59).

214 infection with the neurotropic strain JHM of mouse hepatitis virus (MHV-JHM).

215 n of C57BL/6 mice with the V5A13.1 strain of mouse hepatitis virus (MHV-V5A13.1) results in an acute

216 Mouse hepatitis virus (MHV; murine coronavirus) causes m

217 Recombinant mouse hepatitis viruses (MHV) differing only in the spik

218 uced into a heterologous murine coronavirus (mouse hepatitis virus [MHV]) but is not essential for op

219 mice with a recombinant murine coronavirus (mouse hepatitis virus [MHV]) expressing the T-cell chemo

220 vation of RNase L during murine coronavirus (mouse hepatitis virus [MHV]) infection of myeloid cells

221 Murine coronavirus (mouse hepatitis virus [MHV]) nonstructural protein 2 (ns

222 infected with the neurotropic JHMV strain of mouse hepatitis virus mount potent regional CTL response

223 udied the interaction between coronaviruses (mouse hepatitis virus) of different neurovirulences with

224 Early during clearance of the JHM strain of mouse hepatitis virus, only few virus-specific Ab-secret

225 ce show reduced inflammasome activation upon mouse hepatitis virus or rotavirus infection, and in ste

226 utralization is critical for maintaining JHM mouse hepatitis virus persistence within the central ner

227 cellular immunity in controlling neurotropic mouse hepatitis virus persistence within the CNS were de

228 The neurotropic coronavirus JHM strain of mouse hepatitis virus persists in oligodendroglia despit

229 tem (CNS) with the neurotropic JHM strain of mouse hepatitis virus produces acute and chronic demyeli

230 Infection by the neurotropic JHM strain of mouse hepatitis virus produces an acute demyelinating en

231 Mouse hepatitis virus receptor (MHVR) is a murine biliar

232 Detection of the mouse hepatitis virus receptor within the central nervou

233 we found that proteasome inhibitors blocked mouse hepatitis virus replication at an early step in th

234 binant CXCL10-expressing murine coronavirus (mouse hepatitis virus) resulted in protection from disea

235 most neurotropic strains of the coronavirus mouse hepatitis virus results in an immune response-medi

236 tion of the neuroattenuated OBLV60 strain of mouse hepatitis virus results in infection of mitral neu

237 vel 2 conditions, we constructed recombinant mouse hepatitis viruses (rMHVs) (rMHV strain A59) that e

238 on activation gene 2(-/-) mice with only non-mouse hepatitis virus-specific T cells, we show that CD8

239 al (i.n.) infection of A/J mice with the CoV mouse hepatitis virus strain 1 (MHV-1) induces an acute

240 here investigation into the genetic basis of mouse hepatitis virus strain 1 (MHV-1) pneumovirulence.

241 ially induced in primary mouse astrocytes by mouse hepatitis virus strain A59 (MHV-A59) and MHV-2.

242 The 21.7-kb replicase locus of mouse hepatitis virus strain A59 (MHV-A59) encodes sever

243 Mouse hepatitis virus strain A59 (MHV-A59) produces meni

244 Previous work showed that mouse hepatitis virus strain A59 (MHV-A59) with a mutate

245 ersistently infected with murine coronavirus mouse hepatitis virus strain A59 (MHV-A59), expression o

246 was recently established for the coronavirus mouse hepatitis virus strain A59 (MHV-A59), in which cDN

247 infectious cDNA of the group II coronavirus mouse hepatitis virus strain A59 (MHV-A59).

248 se data suggest that clearance of infectious mouse hepatitis virus strain A59 from the CNS requires A

249 Mouse hepatitis virus strain A59 infection of mice is a

250 hether B cells are important for controlling mouse hepatitis virus strain A59 infection, we infected

251 Intracerebral inoculation with mouse hepatitis virus strain A59 results in viral replic

252 ing intranasal infection with the gliatropic mouse hepatitis virus strain A59.

253 Replication of the neurotropic mouse hepatitis virus strain JHM (JHMV) is controlled pr

254 Mouse hepatitis virus strain JHM (MHV-JHM) causes acute

255 ce infected with the neurotropic coronavirus mouse hepatitis virus strain JHM (MHV-JHM) develop a chr

256 Mice infected with mouse hepatitis virus strain JHM (MHV-JHM) develop a chr

257 C57BL/6 mice infected with mouse hepatitis virus strain JHM (MHV-JHM) develop a chr

258 ons, C57BL/6 mice persistently infected with mouse hepatitis virus strain JHM (MHV-JHM) develop clini

259 Mouse hepatitis virus strain JHM causes a chronic demyel

260 Mice infected with mouse hepatitis virus strain JHM develop an inflammatory

261 The coronavirus, mouse hepatitis virus strain JHM, causes acute and chron

262 ce infected with the neurotropic coronavirus mouse hepatitis virus strain JHM.

263 nic infections, including mice infected with mouse hepatitis virus strain JHM.

264 urine beta coronavirus (mCoV) infection with mouse hepatitis virus strain-A59 (MHV-A59).

265 Mice infected with the coronavirus mouse hepatitis virus, strain JHM (JHM) develop a diseas

266 Mice infected with the murine coronavirus, mouse hepatitis virus, strain JHM (MHV) develop an immun

267 C57BI/6 mice infected with mouse hepatitis virus, strain JHM (MHV-JHM) develop a ch

268 Mice infected with attenuated strains of mouse hepatitis virus, strain JHM, develop a chronic inf

269 pes recognized in C57BL/6 mice infected with mouse hepatitis virus, strain JHM, or lymphocytic chorio

270 e selected in mice chronically infected with mouse hepatitis virus, strain JHM.

271 Cs are readily infected by another strain of mouse hepatitis virus, the A59 strain (MHV-A59).

272 Intranasal mouse hepatitis virus type 1 (MHV-1) infection of mice i

273 t has recently been shown that cell entry of mouse hepatitis virus type 2 (MHV-2) is mediated through

274 ctivity of PLPs from SARS-CoV, MERS-CoV, and mouse hepatitis virus was evaluated against seven ISG15s

275 The importance of the CD (SWWSFNPETNNL) in mouse hepatitis virus was investigated with a panel of m

276 al and sublethal infections with neurotropic mouse hepatitis virus was investigated.

277 nonpathogenic (V-2) variant of a neurotropic mouse hepatitis virus, which differ in the ability to pe

278 well as mice infected with the JHM strain of mouse hepatitis virus, which exhibit CTL escape variants

279 embrane (M) protein of the model coronavirus mouse hepatitis virus with its counterpart from a hetero

280 Replication of the neurotropic JHM strain of mouse hepatitis virus within the central nervous system