ライフサイエンスコーパス: Newcastle disease

1 mmunization against both avian influenza and Newcastle disease.

2 d widely to protect village chickens against Newcastle disease, due to their decreased dependence on

3 tive vaccination against avian influenza and Newcastle disease in chickens and other poultry.

4 olytic NDV variant that is unlikely to cause Newcastle disease in its avian host, representing an ess

5 An outbreak of Newcastle disease (ND) in poultry was reported in Belize

6 Newcastle disease (ND) is a deadly avian disease worldwi

7 Newcastle disease (ND) is one of the most important dise

8 rains of Newcastle disease virus (NDV) cause Newcastle disease (ND), a devastating disease of poultry

9 icken infectious laryngotracheitis (ILT) and Newcastle disease (ND), two of the most economically imp

10 the response of DCs to virus infection with Newcastle disease virus (NDV) after a 24-hour E2 treatme

11 VLP is composed of the NP and M proteins of Newcastle disease virus (NDV) and a chimeric protein con

12 MuRantes mRNA expression is induced by Newcastle disease virus (NDV) and LPS in the RAW 264.7 m

13 The fusion (F) proteins of Newcastle disease virus (NDV) and Nipah virus (NiV) are

14 he level of IFN-beta protein induced by both Newcastle disease virus (NDV) and Sendai virus infection

15 In this study, we have evaluated Newcastle disease virus (NDV) as a vaccine vector for no

16 c and mucosal immune responses by the use of Newcastle disease virus (NDV) as a vaccine vector.

17 linical development of a mesogenic strain of Newcastle disease virus (NDV) as an oncolytic agent for

18 Newcastle disease virus (NDV) belongs to serotype 1 of t

19 Newcastle disease virus (NDV) can cause severe disease i

20 Virulent strains of Newcastle disease virus (NDV) cause Newcastle disease (N

21 Virus-like particles (VLPs) built on the Newcastle disease virus (NDV) core proteins, NP and M, a

22 h virus-like particles (VLPs) containing the Newcastle disease virus (NDV) core proteins, NP and M, a

23 several paramyxoviruses.IMPORTANCE Oncolytic Newcastle disease virus (NDV) could establish persistent

24 Newcastle disease virus (NDV) edits its P gene by insert

25 Newcastle disease virus (NDV) entry into host cells is m

26 Newcastle disease virus (NDV) expressing HIV-1 BaL gp160

27 respiratory tract based on recombinant avian Newcastle disease virus (NDV) expressing the hemagglutin

28 such a stimulus, we generated a recombinant Newcastle disease virus (NDV) expressing the MV hemagglu

29 iotin-labeled peptides with sequences of the Newcastle disease virus (NDV) F protein heptad repeat 2

30 and 289 in the structure and function of the Newcastle disease virus (NDV) F protein was explored by

31 the basis of the coordinates of the related Newcastle disease virus (NDV) F protein, Valine-94, a de

32 ith those of the parainfluenza virus SV5 and Newcastle disease virus (NDV) F proteins, the structures

33 has been demonstrated that the V protein of Newcastle disease virus (NDV) functions as an alpha/beta

34 The effects of Newcastle disease virus (NDV) fusion (F) glycoprotein cl

35 The sequence and structure of the Newcastle disease virus (NDV) fusion (F) protein are con

36 Newcastle disease virus (NDV) fusion (F) protein directs

37 It has been shown that the L289A-mutated Newcastle disease virus (NDV) fusion (F) protein gains t

38 The synthesis of the Newcastle disease virus (NDV) fusion (F) protein in a ce

39 equences in the transmembrane (TM) domain of Newcastle disease virus (NDV) fusion (F) protein in the

40 The role of N-linked glycosylation of the Newcastle disease virus (NDV) fusion (F) protein in vira

41 To explore the association of the Newcastle disease virus (NDV) fusion (F) protein with ch

42 The Newcastle disease virus (NDV) fusion protein (F) mediate

43 y viral fusion proteins, the sequence of the Newcastle disease virus (NDV) fusion protein has several

44 Naturally occurring strains of Newcastle disease virus (NDV) have shown oncolytic thera

45 The Newcastle disease virus (NDV) hemagglutinin-neuraminidas

46 onstrate that the F-interactive sites on the Newcastle disease virus (NDV) hemagglutinin-neuraminidas

47 To explore the relationships between Newcastle disease virus (NDV) HN and F protein interacti

48 Newcastle disease virus (NDV) HN and HPIV3 HN respond di

49 The stalk region of the Newcastle disease virus (NDV) HN protein has been implic

50 alysis of the three-dimensional structure of Newcastle disease virus (NDV) HN protein revealed the pr

51 e residues in the functional activity of the Newcastle disease virus (NDV) HN protein.

52 tion, mutations in a conserved domain in the Newcastle disease virus (NDV) HN stalk result in a sharp

53 porated into progeny Sendai virions, whereas Newcastle disease virus (NDV) HN was not.

54 e second receptor-binding site identified in Newcastle disease virus (NDV) HN.

55 morbidity-mortality event involving virulent Newcastle disease virus (NDV) in wild double-crested cor

56 Upon newcastle disease virus (NDV) infection, bone marrow-der

57 We show that, in addition to Newcastle disease virus (NDV) infection, vesicular stoma

58 hemagglutinin-neuraminidase (HN) protein of Newcastle disease virus (NDV) is a multifunctional prote

59 Newcastle disease virus (NDV) is a negative-sense RNA vi

60 Newcastle disease virus (NDV) is a negative-strand RNA v

61 hemagglutinin-neuraminidase (HN) protein of Newcastle disease virus (NDV) is an important determinan

62 Newcastle disease virus (NDV) is an oncolytic virus bein

63 The characteristics of three virulent Newcastle disease virus (NDV) isolates from this outbrea

64 However, VLPs composed of the Newcastle disease virus (NDV) nucleocapsid and membrane

65 The disease is caused by Newcastle disease virus (NDV) or avian paramyxovirus typ

66 A Newcastle disease virus (NDV) outbreak in chickens was r

67 hemagglutinin-neuraminidase (HN) protein of Newcastle disease virus (NDV) plays a crucial role in th

68 We generated a recombinant Newcastle disease virus (NDV) possessing a two-segmented

69 In the present study, we generated Newcastle disease virus (NDV) recombinants expressing gl

70 In the present study, we generated Newcastle disease virus (NDV) recombinants, based on the

71 tinin-neuraminidase (HN) cytoplasmic tail in Newcastle disease virus (NDV) replication and pathogenic

72 The promotion of membrane fusion by Newcastle disease virus (NDV) requires an interaction be

73 Ps) released from avian cells expressing the Newcastle disease virus (NDV) strain AV proteins NP, M,

74 The complete genome sequence of an African Newcastle disease virus (NDV) strain isolated from a chi

75 Newcastle disease virus (NDV) strains are classified as

76 onomic losses, but little is known about the Newcastle disease virus (NDV) strains circulating in Afr

77 Naturally occurring Newcastle disease virus (NDV) strains vary greatly in vi

78 Naturally occurring Newcastle disease virus (NDV) strains vary greatly in vi

79 Eight highly virulent Newcastle disease virus (NDV) strains were isolated from

80 ystallographic structure of an HN dimer from Newcastle disease virus (NDV) suggests that a single sit

81 We have generated a recombinant Newcastle disease virus (NDV) that expresses the green f

82 A complete cDNA clone of the Newcastle disease virus (NDV) vaccine strain Hitchner B1

83 Thermostable Newcastle disease virus (NDV) vaccines have been used wi

84 he present study, we generated a recombinant Newcastle disease virus (NDV) vectoring the fusion (F) p

85 Newcastle disease virus (NDV) was isolated from an outbr

86 the membrane cytoskeleton in the assembly of Newcastle disease virus (NDV) were investigated.

87 ression of the fusion glycoprotein of RSV by Newcastle disease virus (NDV) would stimulate a more rob

88 xpression, replication, and pathogenicity of Newcastle disease virus (NDV), a green fluorescent prote

89 Newcastle disease virus (NDV), a member of the family Pa

90 Pteropus vampyrus bat kidney (PVK) cells to Newcastle disease virus (NDV), an avian paramyxovirus kn

91 We evaluated Newcastle disease virus (NDV), an avian paramyxovirus th

92 To address this issue, we evaluated Newcastle disease virus (NDV), an avian paramyxovirus th

93 We previously engineered Newcastle disease virus (NDV), an avian paramyxovirus, a

94 Newcastle disease virus (NDV), an avian paramyxovirus, i

95 Newcastle disease virus (NDV), an avian paramyxovirus, i

96 Newcastle disease virus (NDV), an avian paramyxovirus, i

97 Newcastle disease virus (NDV), an avian paramyxovirus, i

98 Newcastle disease virus (NDV), an avian paramyxovirus, i

99 the F proteins of SV5 (W3A and WR isolates), Newcastle disease virus (NDV), and human parainfluenza v

100 cular stomatitis virus (VSV), Sindbis virus, Newcastle disease virus (NDV), and Sendai virus (SeV), w

101 of the H5 and H7 hemagglutinin subtypes, and Newcastle disease virus (NDV), are important pathogens i

102 Paramyxoviruses, such as Newcastle disease virus (NDV), assemble in and bud from

103 es such as avian metapneumovirus (aMPV), and Newcastle disease virus (NDV), human pathogens such as h

104 Here we find that intratumoral therapy with Newcastle disease virus (NDV), in addition to the activa

105 yxovirus 1 (APMV-1) RNA, also referred to as Newcastle disease virus (NDV), in clinical samples from

106 When infected with Newcastle Disease Virus (NDV), NOD2 expression in DCs wa

107 For Newcastle disease virus (NDV), one bifunctional site (si

108 Virulent and moderately virulent strains of Newcastle disease virus (NDV), representing avian paramy

109 DCs showed a reduced type I IFN response to Newcastle disease virus (NDV), Sendai virus (SeV), and S

110 For many paramyxoviruses, including Newcastle disease virus (NDV), syncytium formation requi

111 ns (UTRs) in replication and pathogenesis of Newcastle disease virus (NDV), we generated recombinant

112 is hypothesis, L929 cells were infected with Newcastle disease virus (NDV), which led to the inductio

113 Cells infected with a Newcastle disease virus (NDV)-expressing VP35 redistribu

114 Newcastle disease virus (NDV)-induced membrane fusion re

115 Newcastle disease virus (NDV)-induced membrane fusion re

116 e effects of lipopolysaccharide (LPS) on the Newcastle disease virus (NDV)-mediated induction of cyto

117 In this study, we show that Newcastle disease virus (NDV)-vectored H7 (NDV-H7) and N

118 e of preexisting immunity in humans, such as Newcastle disease virus (NDV).

119 r IRF phosphorylation in cells infected with Newcastle disease virus (NDV).

120 ion with vectored vaccine, using recombinant Newcastle disease virus (rNDV) expressing glycoprotein D

121 A recombinant Newcastle disease virus (rNDV) expressing simian immunod

122 Recombinant Newcastle disease virus (rNDV) stands out as a vaccine v

123 me this obstacle, we generated a recombinant Newcastle disease virus (rNDV)-vectored experimental nor

124 Isolates from the 2002-2003 virulent Newcastle disease virus (v-NDV) outbreak in southern Cal

125 One year after a virulent Newcastle disease virus (vNDV) outbreak in Pakistan, the

126 Newcastle disease virus [NDV (avian paramyxovirus type 1

127 modulate fusion (numbering according to the Newcastle disease virus [NDV] F protein sequence).

128 We found that matrix proteins purified from Newcastle disease virus adsorb on a phospholipid bilayer

129 d RNA viruses that have dsRNA intermediates, Newcastle disease virus and Sendai virus, and a DNA viru

130 Newcastle disease virus and vesicular stomatitis virus (

131 In this study, we found Newcastle disease virus and vesicular stomatitis virus r

132 Newcastle disease virus assembles in plasma membrane dom

133 Here, we present a recombinant Newcastle disease virus expressing a North American line

134 ns for the ability to rescue the growth of a Newcastle disease virus expressing green fluorescent pro

135 mutational analysis of the HR1 domain of the Newcastle disease virus fusion protein, focusing on the

136 This model uses the Newcastle disease virus hemagglutinin-neuraminidase prot

137 on of HN of parainfluenza virus 5 (PIV5) and Newcastle disease virus HN abolishes cell-cell fusion, w

138 Here, we report the structure of the Newcastle disease virus HN ectodomain, revealing dimers

139 embrane fusion, we characterized a series of Newcastle disease virus HN proteins whose surface residu

140 ith functionally active "headless" mumps and Newcastle disease virus HN proteins, provide insights in

141 Mutations of the Newcastle disease virus HN stalk region have been shown

142 e second receptor-binding site identified in Newcastle disease virus HN.

143 ose to the second binding site identified in Newcastle disease virus HN.

144 d receptor binding site of the paramyxovirus Newcastle disease virus in its function and its relation

145 le NF-kappaB activity, both Sendai virus and Newcastle disease virus infection led to robust IFN-beta

146 N expression in response to Sendai virus and Newcastle disease virus infection.

147 ther stimuli, such as lipopolysaccharide and Newcastle disease virus infection.

148 on of interferon beta mRNA 27-fold following Newcastle disease virus infection.

149 As with any other RNA virus, Newcastle disease virus is expected to evolve naturally;

150 opathological characterization of a virulent Newcastle disease virus isolate (NDV-Peru/08) obtained f

151 ed to mimic sites that are found in virulent Newcastle disease virus isolates and to contain 4 or 5 b

152 Eight Newcastle disease virus isolates from Pakistan were sequ

153 Fifteen Newcastle disease virus isolates were recovered only fro

154 hemagglutinin-neuraminidase (HN) protein of Newcastle disease virus mediates attachment to sialic ac

155 r ordered assembly and release of infectious Newcastle disease virus particles.

156 or Streptococcus, but not Vibrio cholerae or Newcastle disease virus sialidase.

157 Overexpression of Lgp2 inhibits SV and Newcastle disease virus signaling to IFN-stimulated regu

158 rs by about 2.5-fold, and neuraminidase from Newcastle disease virus typically increased infectivity

159 the growth of a highly IFN-sensitive virus (Newcastle disease virus) in the presence of IFN, suggest

160 aramyxovirus 1 (APMV-1; a group encompassing Newcastle disease virus), which is a highly contagious p

161 ells infected with a heterologous RNA virus (Newcastle disease virus).

162 omography to show that the matrix protein of Newcastle disease virus, a paramyxovirus and relative of

163 mutation is demonstrated in the F protein of Newcastle disease virus, a paramyxovirus of a different

164 nduced by all IL-33-inducing agonists except Newcastle disease virus, a RIG-I agonist that induced ex

165 from non-target viruses such as H6N2, H9N2, Newcastle disease virus, and infectious bronchitis virus

166 efficacy: vaccinia, measles, mumps, viruses, Newcastle disease virus, and reovirus.

167 ense RNA viruses (influenza viruses A and B, Newcastle disease virus, and vesicular stomatitis virus)

168 simplex virus type-1 (HSV-1), Sendai virus, Newcastle disease virus, and vesicular stomatitis virus.

169 PV701, a replication-competent strain of Newcastle disease virus, causes regression of tumor xeno

170 paramyxoviruses measles virus, mumps virus, Newcastle disease virus, human parainfluenza virus 3, an

171 DCs) by negative-strand RNA viruses, such as Newcastle disease virus, leads to the induction of the I

172 ed against CPE resulting from infection with Newcastle disease virus, Sendai virus, canine distemper

173 We report here that for Newcastle disease virus, the HN receptor avidity is incr

174 y this network, we studied DCs infected with Newcastle disease virus, which is able to stimulate inna

175 in primary human dendritic cells infected by Newcastle disease virus, with copy numbers varying from

176 nd tumor necrosis factor alpha (TNFalpha) in Newcastle disease virus-infected Irf5(-)(/)(-) mice.

177 not type I interferon gene transcription in Newcastle disease virus-infected peritoneal macrophages.

178 Quantitative RT-PCR analysis on Newcastle disease virus-infected primary DCs from 130 in

179 ing a control or fusion protein derived from Newcastle disease virus.

180 idase (HN) glycoprotein of the paramyxovirus Newcastle disease virus.

181 onse to HSV-1, but not to Sendai virus or to Newcastle disease virus.

182 d to rescue replication of the IFN-sensitive Newcastle disease virus.

183 nts similar to the one for cells infected by Newcastle disease virus.

184 Low-virulence Newcastle disease viruses (loNDV) are frequently recover

185 Using reverse genetics, three recombinant Newcastle disease viruses (rNDVs) were engineered, each

186 packaging revealed a majority of infectious Newcastle disease viruses contain one functional genome.

187 Newcastle disease viruses isolated from Hong Kong live b

188 ession after infection with either Sendai or Newcastle disease viruses or after engagement of the Tol

189 W proteins) were expressed from recombinant Newcastle disease viruses, and the responses of infected

190 Using recombinant influenza and Newcastle disease viruses, with or without the NS1 gene