ライフサイエンスコーパス: hepatitis virus

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

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

3 ol acute infection with the cytopathic mouse hepatitis virus.

4 y presents compared to ALF from conventional hepatitis virus.

5 BV and of woodchucks infected with woodchuck hepatitis virus.

6 that was chronically infected with woodchuck hepatitis virus.

7 A synthesis in a related coronavirus, murine hepatitis virus.

8 fection of p85beta-deficient mice with mouse hepatitis virus.

9 ction by the neurotropic JHM strain of mouse hepatitis virus.

10 irus chikungunya virus and coronavirus mouse hepatitis virus.

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

12 gh-risk etiological challenges, most notably hepatitis virus.

13 ion units of blood are not tested for HIV or hepatitis viruses.

14 nodeficiency virus (HIV) and four species of hepatitis viruses.

15 CV vaccine and future research needs for the hepatitis viruses.

16 They are avian encephalomyelitis virus, duck hepatitis virus 1, duck picornavirus, porcine teschoviru

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

18 sses the recent advances in our knowledge of hepatitis viruses A through G, focusing on the literatur

19 Mouse hepatitis virus, a beta-CoV in group A, uses the galecti

20 irus hemagglutinin and in variants of murine hepatitis virus, a coronavirus.

21 Intracerebral infection of mice with mouse hepatitis virus, a member of the Coronaviridae family, r

22 the role of MDA5 during infection with mouse hepatitis virus, a murine coronavirus used to model vira

23 ity was examined in mice infected with mouse hepatitis virus, a well-described model of virus-induced

24 ly pathogenic neurotropic coronavirus (mouse hepatitis virus A59 strain [MHV-A59]) developed severe e

25 Lpro inhibitors in mice infected with murine hepatitis virus A59, a hepatotropic coronavirus, resulte

26 as helminths, mycobacteria, Plasmodium, and hepatitis viruses affect more than a third of the human

27 urprisingly, two beta-CoVs in group A, mouse hepatitis virus and HKU1, have evolved to use different

28 odchucks chronically infected with woodchuck hepatitis virus and vaccinated with woodchuck hepatitis

29 e estimated risk for transfusion transmitted hepatitis viruses and retroviruses is now vanishingly sm

30 adnaviruses (hepatitis B virus and woodchuck hepatitis virus), and an intron-retaining transcript enc

31 ic enzyme from two CoVs, SARS-CoV and murine hepatitis virus, and its monomeric homologue, XendoU fro

32 n the characterization of several fastidious hepatitis viruses, and we investigated the feasibility o

33 tis aplastic anemia, antibodies to the known hepatitis viruses are absent; the unknown infectious age

34 methylator phenotype and the contribution of hepatitis viruses are poorly understood.

35 's murine encephalomyelitis virus and murine hepatitis virus, are used to induce infectious models of

36 splant recipients commonly are infected with hepatitis viruses, are immunosuppressed, and have other

37 sed from the replicase polyprotein of murine hepatitis virus as fusions with nonstructural protein 2

38 s within the replicase polyprotein of murine hepatitis virus as fusions with nonstructural proteins c

39 d HIV1 and HIV2, as well as of two different hepatitis viruses, attaining results of approximately 87

40 ucks chronically infected with the woodchuck hepatitis virus before and during 30 weeks of therapy wi

41 temperature-sensitive (ts) mutant of Murine hepatitis virus, Bristol ts31 (MHV-Brts31), that defines

42 al nervous system (CNS) by neurotropic mouse hepatitis virus but do not suffice to achieve sterile im

43 ntiviral protein IFN-alpha2 is used to treat hepatitis viruses but has proven rather ineffective agai

44 Infection with hepatitis virus C (HCV) is associated with an increased

45 We found that woodchuck hepatitis virus capsid protein undergoes structural tran

46 Five human hepatitis viruses cause most of the acute and chronic li

47 Analysis of several HBV/woodchuck hepatitis virus chimeras corroborated the findings from

48 Human immunodeficiency virus (HIV) and hepatitis virus coinfection amplify and accelerate hepat

49 We followed 22 910 participants without hepatitis virus coinfection for 114 478 person-years.

50 a monax) chronically infected with woodchuck hepatitis virus contained at least 100,000 clones of >1,

51 n development of HCV sequence databases, the Hepatitis Virus Database (Japan), euHCVdb (France), and

52 ts for lung cancer, and immunodeficiency and hepatitis virus effects for liver cancer.

53 Using a neurotropic mouse hepatitis virus encephalomyelitis model, this study demo

54 CCL3(-/-) mice infected with mouse hepatitis virus exhibited a significant reduction of vir

55 r results support the hypothesis that murine hepatitis virus ExoN activity is required for resistance

56 he 3' untranslated region (UTR) of the mouse hepatitis virus genome contains two essential and overla

57 (-/-) mice infected with a neurotropic mouse hepatitis virus had an impaired ability to control viral

58 end-stage liver disease (ESLD) secondary to hepatitis viruses has evolved rapidly during the last tw

59 of the SARS-associated coronavirus and mouse hepatitis virus have evolved to promote optimal frameshi

60 e livers chronically infected with woodchuck hepatitis virus, (i) hepadnavirus superinfection and cel

61 g RNA element (WPRE), derived from woodchuck hepatitis virus in combination with an antibody-cytokine

62 ncoded by ORF6, enhanced the growth of mouse hepatitis virus in tissue culture cells and in mice.

63 against CCL5 to mice with established mouse hepatitis virus-induced demyelination and impaired motor

64 opathogenesis, is essential for the study of hepatitis virus-induced liver disease and for therapeuti

65 ined with significant receptor expression in hepatitis virus-infected livers, suggests that IL-29 may

66 us (OR = 9.4; 95% CI = 2.7-32.7) and chronic hepatitis virus infection (OR = 31.2; 95% CI = 6.3-153.2

67 etween heavy alcohol consumption and chronic hepatitis virus infection (OR, 53.9; 95% CI, 7.0-415.7)

68 from cancer worldwide and is associated with hepatitis virus infection in 80% of cases.

69 The role of hepatitis virus infection in glucose homeostasis is unce

70 Mouse hepatitis virus infection of mice provides a useful tool

71 HDV infection is the only chronic human hepatitis virus infection without a therapy approved by

72 In human hepatitis virus infection, ADAR1 has been shown to targe

73 d models were used to estimate the effect of hepatitis virus infection, and adjusted for potential co

74 ividuals that is not attributable to chronic hepatitis virus infection.

75 as similarly observed during acute woodchuck hepatitis virus infection.

76 synergistic interaction between obesity and hepatitis virus infection.

77 r stomatitis virus infection, but not murine hepatitis virus infection.

78 roduction in all viral hepatitis infections: Hepatitis virus infections did not alter NK cell differe

79 d its role in sensing and protecting against hepatitis virus infections is uncertain.

80 A related element from woodchuck hepatitis virus is known as the woodchuck posttranscript

81 V-JHM strain of the murine coronavirus mouse hepatitis virus is much more neurovirulent than the MHV-

82 Mouse hepatitis virus is used as well studied examplar to re-e

83 Coinfection with hepatitis viruses is common in individuals infected with

84 ase, but the intrahepatic immune response to hepatitis viruses is poorly understood because of a lack

85 ample, C57BL/6 (B6) mice infected with mouse hepatitis virus (JHM strain, JHMV) develop severe enceph

86 ontaining CNS cells were infected with mouse hepatitis virus-JHM, which causes fatal encephalitis in

87 ice with the neurotropic JHM strain of mouse hepatitis virus (JHMV) (a member of the Coronaviridae fa

88 omyelitis induced by the JHM strain of mouse hepatitis virus (JHMV) and sustained during viral persis

89 ted with the neurotropic JHM strain of mouse hepatitis virus (JHMV) develop acute and chronic demyeli

90 (CNS) by the neurotropic JHM strain of mouse hepatitis virus (JHMV) induces an acute encephalomyeliti

91 ion with the neurotropic JHM strain of mouse hepatitis virus (JHMV) into the central nervous system (

92 Control of neurotropic mouse hepatitis virus (JHMV) requires the collaboration of CD4

93 ion with the neurotropic JHM strain of mouse hepatitis virus (JHMV) resulted in an acute encephalomye

94 CNS with the neurotropic JHM strain of mouse hepatitis virus (JHMV) results in an immune-mediated dem

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

96 ion with the neurotropic JHM strain of mouse hepatitis virus (JHMV).

97 ion with the neurotropic JHM strain of mouse hepatitis virus (JHMV).

98 ion with the neurotropic JHM strain of mouse hepatitis virus (JHMV).

99 we demonstrate that NHC inhibits both murine hepatitis virus (MHV) (50% effective concentration [EC(5

100 The 5' 140 nucleotides of the mouse hepatitis virus (MHV) 5' untranslated region (5'UTR) are

101 We used mouse hepatitis virus (MHV) A59 as a model to gain insight int

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

103 he outcome of viral encephalomyelitis [mouse hepatitis virus (MHV) A59, Theiler's encephalomyelitis v

104 infection with the murine coronavirus mouse hepatitis virus (MHV) activated the NLRP3 inflammasome a

105 Infection with the murine coronavirus mouse hepatitis virus (MHV) activates the pattern recognition

106 uses within the genus Betacoronavirus, mouse hepatitis virus (MHV) and MERS-CoV, encode 2',5'-phospho

107 -D; four nucleotide substitutions) in murine hepatitis virus (MHV) and severe acute respiratory syndr

108 5' untranslated regions (5'UTRs) from mouse hepatitis virus (MHV) and severe acute respiratory syndr

109 Murine hepatitis virus (MHV) and severe acute respiratory syndr

110 acute respiratory syndrome (SARS)-CoV, mouse hepatitis virus (MHV) and the human CoV OC43 S2 subunits

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

112 Some strains of mouse hepatitis virus (MHV) can induce chronic inflammatory de

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

114 Murine coronavirus mouse hepatitis virus (MHV) causes persistent infection of the

115 ) of the 5'-untranslated region of the mouse hepatitis virus (MHV) contains a highly conserved pental

116 glycoprotein from strain RSA59 (PP) of mouse hepatitis virus (MHV) contains two central, consecutive

117 Mouse hepatitis virus (MHV) does not induce interferon (IFN) p

118 or clearance of the murine coronavirus mouse hepatitis virus (MHV) during acute infection.

119 h the recombinant JHM (RJHM) strain of mouse hepatitis virus (MHV) elicits a weak CD8(+) T-cell respo

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

121 Overall, our data suggest murine hepatitis virus (MHV) ExoN activity is required for resi

122 Most strains of murine coronavirus mouse hepatitis virus (MHV) express a cleavable spike glycopro

123 ing the recombinant murine coronavirus mouse hepatitis virus (MHV) expressing the T cell-chemoattract

124 Murine coronavirus mouse hepatitis virus (MHV) gene 1 encodes several nonstructur

125 The mouse hepatitis virus (MHV) genome's 3' untranslated region co

126 Murine hepatitis virus (MHV) has long served as a model system

127 us work with the prototype coronavirus mouse hepatitis virus (MHV) has shown that a major determinant

128 Many strains of the murine coronavirus mouse hepatitis virus (MHV) have distinct, S-dependent organ a

129 revious studies have demonstrated that mouse hepatitis virus (MHV) hepatotropism is determined largel

130 We have used several strains of murine hepatitis virus (MHV) in cell culture and in vivo in mou

131 ucted mutants of the model coronavirus mouse hepatitis virus (MHV) in which all or part of the M prot

132 nts of a severely defective mutant of murine hepatitis virus (MHV) in which the N gene was replaced w

133 The murine coronavirus mouse hepatitis virus (MHV) induced the expression of type I i

134 The coronavirus mouse hepatitis virus (MHV) induces a minimal type I interfero

135 determine the requirement of nsp4 for murine hepatitis virus (MHV) infection in culture, engineered d

136 Murine hepatitis virus (MHV) infection provides a model system

137 Thus, during mouse hepatitis virus (MHV) infection, hepatitis, which damage

138 function in the context of a related murine hepatitis virus (MHV) infection.

139 e replacements were engineered into a murine hepatitis virus (MHV) infectious clone in place of conse

140 Mouse hepatitis virus (MHV) is a murine betacoronavirus (m-CoV

141 synthesis by the prototype coronavirus mouse hepatitis virus (MHV) is carried out by a replicase-tran

142 Mouse hepatitis virus (MHV) isolates JHM.WU and JHM.SD promote

143 ive roles of specific ISGs against the mouse hepatitis virus (MHV) members of the coronaviruses are l

144 Mouse hepatitis virus (MHV) neurotropism varies by strain: MHV

145 monstrated that the murine coronavirus mouse hepatitis virus (MHV) nonstructural protein 2 (ns2) is a

146 We modeled the CoV murine hepatitis virus (MHV) nsp12-RdRp structure and superimpo

147 Here, we engineered mutations in murine hepatitis virus (MHV) nsp14 N7-MTase at residues D330 an

148 ween the endoribonuclease activity of murine hepatitis virus (MHV) Nsp15 (mNsp15) and its role in vir

149 magnetic resonance (NMR) structure of mouse hepatitis virus (MHV) nsp3a and show, using isothermal t

150 en shown previously that mutations in murine hepatitis virus (MHV) nsp4 loop 1 that alter nsp4 glycos

151 everse genetic mutagenesis of the CoV murine hepatitis virus (MHV) nsp5, we identified a new temperat

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

153 Murine hepatitis virus (MHV) PLP2 and orthologs recognize and c

154 Infection of the CNS with the mouse hepatitis virus (MHV) provides a unique model situation

155 Mouse hepatitis virus (MHV) replicase products nsp3, nsp4, and

156 Mouse hepatitis virus (MHV) replication in actively growing DB

157 proteins and their processing during murine hepatitis virus (MHV) replication.

158 cultured cells with murine coronavirus mouse hepatitis virus (MHV) resulted in activation of the mito

159 t infection of rat oligodendrocytes by mouse hepatitis virus (MHV) resulted in apoptosis, which is ca

160 ) A1 has previously been shown to bind mouse hepatitis virus (MHV) RNA at the 3' end of both plus and

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

162 Mouse hepatitis virus (MHV) RNA synthesis is mediated by a vir

163 The 3' cis-acting element for mouse hepatitis virus (MHV) RNA synthesis resides entirely wit

164 The Murine hepatitis virus (MHV) strain A59 ns2 protein is a 30-kDa

165 important for clearance of neurotropic mouse hepatitis virus (MHV) strain A59, although their possibl

166 The murine coronavirus, mouse hepatitis virus (MHV) strain A59, causes acute encephali

167 temperature-sensitive (TS) mutants of murine hepatitis virus (MHV) strain A59, proposes that an inter

168 C57BL/6 (B6) mice infected with mouse hepatitis virus (MHV) strain JHM develop a clinically ev

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

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

171 Sequencing and reversion analysis of murine hepatitis virus (MHV) temperature-sensitive (ts) viruses

172 previously generated E gene mutants of mouse hepatitis virus (MHV) that had marked defects in viral g

173 urrent studies, neurotropic strains of mouse hepatitis virus (MHV) that induce meningitis, encephalit

174 usly generated E gene point mutants of mouse hepatitis virus (MHV) that were defective in growth and

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

176 at infection by the murine coronavirus mouse hepatitis virus (MHV) triggers the proximal UPR transduc

177 Mouse hepatitis virus (MHV) uses its N-terminal domain (NTD) o

178 The mouse hepatitis virus (MHV) variant MHV/BHK can infect hamster

179 We previously described mouse hepatitis virus (MHV) variant V51 derived from a persist

180 Antibodies directed against mouse hepatitis virus (MHV) virions and against the putative R

181 kaging signal (PS) for the coronavirus mouse hepatitis virus (MHV) was originally identified as an el

182 Mouse hepatitis virus (MHV) was used as a model to study the i

183 hR is activated in cells infected with mouse hepatitis virus (MHV), a coronavirus (CoV), and contribu

184 In previous work with the coronavirus mouse hepatitis virus (MHV), a highly defective M protein muta

185 everal PARPs following infection with murine hepatitis virus (MHV), a model coronavirus.

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

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

188 stion, we used the rJHM strain (rJ) of mouse hepatitis virus (MHV), a neurotropic coronavirus that ca

189 erminal domain (NTD) of N protein from mouse hepatitis virus (MHV), a virus most closely related to S

190 d by the prototypical Betacoronavirus, mouse hepatitis virus (MHV), and by Middle East respiratory sy

191 The murine coronavirus, mouse hepatitis virus (MHV), causes acute hepatitis in its nat

192 vely, including the murine coronavirus mouse hepatitis virus (MHV), Haemophilus influenzae, Neisseria

193 For the prototype coronavirus mouse hepatitis virus (MHV), it has previously been establishe

194 pe of a highly neurovirulent strain of mouse hepatitis virus (MHV), JHM, is thought to be essential f

195 In murine hepatitis virus (MHV), nsps 1, 2, and 3 are processed by

196 nfected with a prototypic coronavirus, mouse hepatitis virus (MHV), resulting in the expression of se

197 Infection of mice with mouse hepatitis virus (MHV), strain JHM, results in acute and

198 ed virus entry and cell-cell fusion of mouse hepatitis virus (MHV), suggesting the importance of lipi

199 For the coronavirus mouse hepatitis virus (MHV), the first proteolytic processing

200 In mouse hepatitis virus (MHV), the NTD binds the transcriptional

201 y, we exploited the model coronavirus, mouse hepatitis virus (MHV), to investigate the genotype and p

202 ort genetic analysis of a ts strain of mouse hepatitis virus (MHV), tsNC11, focusing on the role of m

203 the N protein of the model coronavirus mouse hepatitis virus (MHV), we constructed mutants in which e

204 f N protein domains in the coronavirus mouse hepatitis virus (MHV), we replaced the MHV N gene with i

205 ation and expression is altered due to mouse hepatitis virus (MHV)-A59 infection both in vivo and in

206 activated protein kinases (MAPKs) in a mouse hepatitis virus (MHV)-infected macrophage-derived J774.1

207 f in vivo infection by the coronavirus mouse hepatitis virus (MHV).

208 eases replication fidelity of the CoV murine hepatitis virus (MHV).

209 sponse to intracerebral infection with mouse hepatitis virus (MHV).

210 t in the prototype group 2 coronavirus mouse hepatitis virus (MHV).

211 nfection by the enveloped coronavirus murine hepatitis virus (MHV).

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

213 UTR) of the genome of the coronavirus mouse hepatitis virus (MHV).

214 ry syndrome coronavirus (SARS-CoV) and mouse hepatitis virus (MHV).

215 tory syndrome CoV, and the murine CoV, mouse hepatitis virus (MHV).

216 hibitor in a coronavirus model system, mouse hepatitis virus (MHV).

217 titution mutations into the genome of murine hepatitis virus (MHV-A59) containing ExoN activity [ExoN

218 Mouse hepatitis virus (MHV; murine coronavirus) causes meningo

219 nto a heterologous murine coronavirus (mouse hepatitis virus [MHV]) but is not essential for optimal

220 with a recombinant murine coronavirus (mouse hepatitis virus [MHV]) expressing the T-cell chemoattrac

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

222 Murine coronavirus (mouse hepatitis virus [MHV]) nonstructural protein 2 (ns2) is

223 Restricted analyses among hepatitis virus-negative subjects, nondrinkers, nondiabe

224 In this report, we show that the murine hepatitis virus nsp2 sequence was tolerated in ORF1b wit

225 the interaction between coronaviruses (mouse hepatitis virus) of different neurovirulences with prima

226 Regarding hepatitis viruses, one-third of the patients had been te

227 during clearance of the JHM strain of mouse hepatitis virus, only few virus-specific Ab-secreting ce

228 zation is critical for maintaining JHM mouse hepatitis virus persistence within the central nervous s

229 neurotropic coronavirus JHM strain of mouse hepatitis virus persists in oligodendroglia despite the

230 us-mouse phenylalanine hydroxylase-woodchuck hepatitis virus post-transcriptional response element (r

231 The woodchuck hepatitis virus posttranscriptional regulatory element (

232 s sc counterpart, which lacked the woodchuck hepatitis virus posttranscriptional regulatory element (

233 NS) with the neurotropic JHM strain of mouse hepatitis virus produces acute and chronic demyelination

234 Detection of the mouse hepatitis virus receptor within the central nervous syst

235 duced high titer viremia and acute resolving hepatitis; viruses recovered from both animals lacked th

236 und that proteasome inhibitors blocked mouse hepatitis virus replication at an early step in the vira

237 trypsinogen activation in pancreatitis, and hepatitis virus replication.

238 CXCL10-expressing murine coronavirus (mouse hepatitis virus) resulted in protection from disease and

239 The identification of hepatitis virus specific signatures provides a foundatio

240 ligation of T cells in vitro with the murine hepatitis virus spike protein, a natural ligand for the

241 Combining risk-score tertile levels and hepatitis virus status to stratify participants was more

242 ped using accessible variables combined with hepatitis virus status, which allows selection of asympt

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

244 nvestigation into the genetic basis of mouse hepatitis virus strain 1 (MHV-1) pneumovirulence.

245 ne coronaviruses expressing wild-type murine hepatitis virus strain 4 (MHV-4) or MHV-A59 spike glycop

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

247 The murine hepatitis virus strain A59 (MHV-A59) model produces foca

248 Previous work showed that mouse hepatitis virus strain A59 (MHV-A59) with a mutated cata

249 cently established for the coronavirus mouse hepatitis virus strain A59 (MHV-A59), in which cDNA frag

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

251 Mouse hepatitis virus strain A59 infection of mice is a useful

252 tranasal infection with the gliatropic mouse hepatitis virus strain A59.

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

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

255 Mouse hepatitis virus strain JHM causes a chronic demyelinatin

256 Mice infected with mouse hepatitis virus strain JHM develop an inflammatory demye

257 The coronavirus, mouse hepatitis virus strain JHM, causes acute and chronic neu

258 ected with the neurotropic coronavirus mouse hepatitis virus strain JHM.

259 fections, including mice infected with mouse hepatitis virus strain JHM.

260 e to high-fat diet-caused obesity and murine hepatitis virus strain-3 (MHV-3)-induced fulminant hepat

261 Mice infected with the coronavirus mouse hepatitis virus, strain JHM (JHM) develop a disease that

262 infected with the murine coronavirus, mouse hepatitis virus, strain JHM (MHV) develop an immune-medi

263 ce infected with attenuated strains of mouse hepatitis virus, strain JHM, develop a chronic infection

264 cognized in C57BL/6 mice infected with mouse hepatitis virus, strain JHM, or lymphocytic choriomening

265 epatitis virus and vaccinated with woodchuck hepatitis virus surface antigen could be induced to reco

266 s are likely to be related to differences in hepatitis viruses that are most prevalent in a populatio

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

268 Intranasal mouse hepatitis virus type 1 (MHV-1) infection of mice induces

269 recently been shown that cell entry of mouse hepatitis virus type 2 (MHV-2) is mediated through endoc

270 From a public health perspective, hepatitis virus vaccination programs and efforts to both

271 y of PLPs from SARS-CoV, MERS-CoV, and mouse hepatitis virus was evaluated against seven ISG15s origi

272 importance of the CD (SWWSFNPETNNL) in mouse hepatitis virus was investigated with a panel of mutant

273 s mice infected with the JHM strain of mouse hepatitis virus, which exhibit CTL escape variants with

274 he cis-acting element found in the woodchuck hepatitis virus (WHV) (the WHV posttranscriptional regul

275 onically infected with HBV-related woodchuck hepatitis virus (WHV) and already developed HCCs were us

276 her animal hepadnaviruses, such as woodchuck hepatitis virus (WHV) and duck hepatitis B virus (DHBV).

277 ed that the X-deficient mutants of woodchuck hepatitis virus (WHV) are not completely replication def

278 odchucks chronically infected with woodchuck hepatitis virus (WHV) are superinfected with HDV, they p

279 Woodchucks infected at birth with woodchuck hepatitis virus (WHV) cleared viremia and developed anti

280 Integrations of woodchuck hepatitis virus (WHV) DNA and rearrangements of the N-my

281 ucks chronically infected with the woodchuck hepatitis virus (WHV) elicited differential T-cell respo

282 odchucks chronically infected with woodchuck hepatitis virus (WHV) induces a transient decline in vir

283 atal woodchucks with self-limiting woodchuck hepatitis virus (WHV) infection to those woodchucks prog

284 issue from woodchucks with chronic woodchuck hepatitis virus (WHV) infection was assayed for randomly

285 ed (resolved) and chronic neonatal woodchuck hepatitis virus (WHV) infection.

286 over during clearance of transient woodchuck hepatitis virus (WHV) infections.

287 Woodchuck hepatitis virus (WHV) is prone to aberrant assembly in v

288 (Marmota monax) infected with the woodchuck hepatitis virus (WHV) represent the best animal model fo

289 en the immunogenicity of an analog woodchuck hepatitis virus (WHV) surface antigen (WHsAg) pDNA vacci

290 ting the ability of the virions of woodchuck hepatitis virus (WHV) to induce productive acute infecti

291 Woodchuck hepatitis virus (WHV), a close relative of human hepatit

292 monax) is naturally infected with woodchuck hepatitis virus (WHV), a hepadnavirus closely related to

293 odchucks chronically infected with woodchuck hepatitis virus (WHV), a hepadnavirus closely related to

294 n an estimated 240 million people; woodchuck hepatitis virus (WHV), an HBV homologue, has been an imp

295 from X/c-myc bitransgenic mice and woodchuck hepatitis virus (WHV)-infected woodchucks.

296 emonstrated for HBV or HBV-related woodchuck hepatitis virus (WHV).

297 rmota monax ) harbors a DNA virus (Woodchuck hepatitis virus [WHV]) that is similar in structure and

298 e (M) protein of the model coronavirus mouse hepatitis virus with its counterpart from a heterologous

299 ation of the neurotropic JHM strain of mouse hepatitis virus within the central nervous system is con

300 tional regulatory element from the woodchuck hepatitis virus (WPRE).