ライフサイエンスコーパス: feline immunodeficiency virus

1 y virus, equine infectious anemia virus, and feline immunodeficiency virus.

2 been obtained from animals infected with the feline immunodeficiency virus.

3 us, human immunodeficiency virus type 1, and feline immunodeficiency virus.

4 his model can also explain 3TC resistance in feline immunodeficiency virus and human hepatitis B viru

5 Frameshifting pseudoknots in feline immunodeficiency virus and simian retrovirus have

6 ly inhibit replication of human, simian, and feline immunodeficiency viruses and therefore has broad-

7 tiviruses equine infectious anemia virus and feline immunodeficiency virus, and has no effect on the

8 the dominant selective force acting on this feline immunodeficiency virus as it replicates in a new

9 To address these issues, we used a feline immunodeficiency virus-based (FIV-based) vector.

10 d into the articular joint space a defective feline immunodeficiency virus capable of infecting divid

11 ne was prepared from a pathogenic isolate of feline immunodeficiency virus containing a mutation that

12 s, we evaluated the molecular evolution of a feline immunodeficiency virus derived from a wild cougar

13 ion, delivery of this shRNA by a recombinant feline immunodeficiency virus effectively silenced torsi

14 tant role that CXCR4 plays in infection with feline immunodeficiency virus, expression on PBMC in viv

15 ction with the prototypic Petaluma strain of feline immunodeficiency virus (FIV(PET)) using vaccines

16 GFAP-IL-1betaXAT mice were injected with the feline immunodeficiency virus (FIV) (Cre) vector in the

17 The feline immunodeficiency virus (FIV) accessory factor, Or

18 eline APOBEC3Z3 proteins tested exhibit anti-feline immunodeficiency virus (FIV) activity.

19 on the two pathogenic retroviruses in cats, feline immunodeficiency virus (FIV) and feline leukemia

20 The neurotoxic effects of the feline immunodeficiency virus (FIV) and FIV envelope pro

21 To determine its antiviral activity against feline immunodeficiency virus (FIV) and HIV, the activit

22 Feline immunodeficiency virus (FIV) and human immunodefi

23 ThX and mock-ThX cats were inoculated with feline immunodeficiency virus (FIV) and monitored for th

24 The surface glycoprotein (gp95) of the feline immunodeficiency virus (FIV) binds in a strain-sp

25 an immunodeficiency virus type 2 (HIV-2) and feline immunodeficiency virus (FIV) but not HIV-1.

26 semen from male domestic cats infected with feline immunodeficiency virus (FIV) can transmit virus t

27 Feline immunodeficiency virus (FIV) causes AIDS-like sym

28 Infection with feline immunodeficiency virus (FIV) causes an immunosupp

29 Feline immunodeficiency virus (FIV) causes progressive i

30 The process of feline immunodeficiency virus (FIV) cell entry was exami

31 We have identified feline immunodeficiency virus (FIV) clinical isolates th

32 6-residue multiepitopic synthetic peptide of feline immunodeficiency virus (FIV) comprising immunodom

33 tested the hypothesis that vectors based on feline immunodeficiency virus (FIV) could be used for co

34 Feline immunodeficiency virus (FIV) does not infect huma

35 to provide insights into how hunting shapes feline immunodeficiency virus (FIV) dynamics in puma (Pu

36 combinant soluble CD134 (sCD134) facilitated feline immunodeficiency virus (FIV) entry into CXCR4-pos

37 A heterologous feline immunodeficiency virus (FIV) expression system pe

38 (n = 19) had been chronically infected with feline immunodeficiency virus (FIV) for over 6 years, wh

39 We previously observed feline immunodeficiency virus (FIV) Gag accumulating at

40 omain was identified in the p2 region of the feline immunodeficiency virus (FIV) Gag protein.

41 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) had different patter

42 Feline immunodeficiency virus (FIV) induces a disease st

43 Similar to human immunodeficiency virus, feline immunodeficiency virus (FIV) induces immunodefici

44 In feline immunodeficiency virus (FIV) infected cats, daily

45 Feline immunodeficiency virus (FIV) infection in cats pr

46 s during the acute stage (first 4 months) of feline immunodeficiency virus (FIV) infection in laborat

47 Feline immunodeficiency virus (FIV) infection in the cat

48 A monoclonal antibody, MAb vpg15, inhibits feline immunodeficiency virus (FIV) infection in tissue

49 The acute stage of feline immunodeficiency virus (FIV) infection is charact

50 The acute stage of feline immunodeficiency virus (FIV) infection is charact

51 Disease progression of feline immunodeficiency virus (FIV) infection is charact

52 vestigating the effect of CCR5 expression on feline immunodeficiency virus (FIV) infection must be in

53 cells (Tregs) activated during the course of feline immunodeficiency virus (FIV) infection suppress C

54 Herein we demonstrate that in vitro feline immunodeficiency virus (FIV) infection, but not U

55 rly target cells and tissues in transmucosal feline immunodeficiency virus (FIV) infection, cats were

56 viral replication during the acute stage of feline immunodeficiency virus (FIV) infection.

57 Feline immunodeficiency virus (FIV) infects many species

58 Feline immunodeficiency virus (FIV) infects numerous wil

59 Feline immunodeficiency virus (FIV) is a lentivirus of d

60 Feline immunodeficiency virus (FIV) is a lentivirus that

61 Feline immunodeficiency virus (FIV) is a lentivirus that

62 Feline immunodeficiency virus (FIV) is a lentivirus that

63 Feline immunodeficiency virus (FIV) is a lentivirus whic

64 The orf-A (orf-2) gene of feline immunodeficiency virus (FIV) is a small open read

65 Feline immunodeficiency virus (FIV) is among the most co

66 evelopment of gene delivery vectors based on feline immunodeficiency virus (FIV) is an attractive alt

67 Infection of domestic cats with feline immunodeficiency virus (FIV) is an important mode

68 ogenetic distance from primate lentiviruses, feline immunodeficiency virus (FIV) is becoming the lent

69 of equine infectious anemia virus (EIAV) and feline immunodeficiency virus (FIV) is inhibited by lept

70 The disease induced in cats by feline immunodeficiency virus (FIV) is similar to HIV in

71 Feline immunodeficiency virus (FIV) is similar to human

72 Feline immunodeficiency virus (FIV) is the feline analog

73 ptional elements within the U3 domain of the feline immunodeficiency virus (FIV) long terminal repeat

74 Using the feline immunodeficiency virus (FIV) model of HIV we eval

75 The feline immunodeficiency virus (FIV) model of vertical hu

76 By using the feline immunodeficiency virus (FIV) model, we have docum

77 Previous studies using feline immunodeficiency virus (FIV) molecular clones lac

78 Feline immunodeficiency virus (FIV) naturally infects mu

79 candidates were tested for activity against feline immunodeficiency virus (FIV) on infected CrFK cel

80 Feline immunodeficiency virus (FIV) OrfA is an accessory

81 were evaluated for their incorporation onto feline immunodeficiency virus (FIV) particles, transduct

82 We have used feline immunodeficiency virus (FIV) protease (PR) as a m

83 We used feline immunodeficiency virus (FIV) protease (PR) as a m

84 A novel fluorogenic substrate for continuous feline immunodeficiency virus (FIV) protease (PR) assay

85 The feline immunodeficiency virus (FIV) protease is essentia

86 Feline immunodeficiency virus (FIV) protease is structur

87 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) proteases (PRs).

88 The presence of feline immunodeficiency virus (FIV) proviral DNA, expres

89 A feline immunodeficiency virus (FIV) provirus with a vif

90 ilar to human immunodeficiency virus type 1, feline immunodeficiency virus (FIV) replicates in the th

91 ron (IFN-alpha) induced tetherin and blocked feline immunodeficiency virus (FIV) replication in lymph

92 regulatory properties and ability to support feline immunodeficiency virus (FIV) replication in vitro

93 Mutants of feline immunodeficiency virus (FIV) resistant to (-)-bet

94 Intravaginal inoculation of cats with feline immunodeficiency virus (FIV) results in acute sys

95 ily conserved on both HIV type 1 (HIV-1) and feline immunodeficiency virus (FIV) reverse transcriptas

96 The structure of the putative feline immunodeficiency virus (FIV) ribosomal frameshift

97 We had previously demonstrated that feline immunodeficiency virus (FIV) RNA levels in plasma

98 Feline immunodeficiency virus (FIV) shares with T-cell t

99 The major surface glycoprotein of feline immunodeficiency virus (FIV) specifically binds t

100 A cytopathic variant of feline immunodeficiency virus (FIV) strain PPR emerged a

101 The feline immunodeficiency virus (FIV) targets activated CD

102 t syncytium formation mediated by strains of feline immunodeficiency virus (FIV) that have been selec

103 immunodeficiency virus (HIV) and strains of feline immunodeficiency virus (FIV) that have been selec

104 Variants of feline immunodeficiency virus (FIV) that possess a uniqu

105 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) the least.

106 We compared feline immunodeficiency virus (FIV) to other restricted

107 ssion in arthritic joints of mice, using the feline immunodeficiency virus (FIV) vector, which is cap

108 The ability of feline immunodeficiency virus (FIV) vectors to transfer

109 V), bovine immunodeficiency virus (BIV), and feline immunodeficiency virus (FIV) Vif appear specific

110 Stable expression of feline immunodeficiency virus (FIV) Vif-green fluorescen

111 Vertical transmission of feline immunodeficiency virus (FIV) was studied in cats

112 y RNA ligands for reverse transcriptase from feline immunodeficiency virus (FIV) were isolated from a

113 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) were prepared to exa

114 binant Vif derived from the 34TF10 strain of feline immunodeficiency virus (FIV) were used to assess

115 we generated a defective mutant provirus of feline immunodeficiency virus (FIV) with an in-frame del

116 Feline immunodeficiency virus (FIV), a lentivirus, cause

117 ore than 20 feline species test positive for feline immunodeficiency virus (FIV), a lineage of lentiv

118 d from the pathogenic GL8 molecular clone of feline immunodeficiency virus (FIV), a range of viral va

119 xamined the brains of cats infected with the feline immunodeficiency virus (FIV), an animal model of

120 human immunodeficiency virus type 1 (HIV-1), feline immunodeficiency virus (FIV), and equine infectio

121 l leukemia virus type 1 (HTLV-1), HIV-1, and feline immunodeficiency virus (FIV), and have been postu

122 Human immunodeficiency virus type 1 (HIV-1), feline immunodeficiency virus (FIV), and Moloney murine

123 BIV), equine infectious anemia virus (EIAV), feline immunodeficiency virus (FIV), and Rous sarcoma vi

124 cells and cell lines did not restrict HIV-1, feline immunodeficiency virus (FIV), equine infectious a

125 Feline immunodeficiency virus (FIV), like other members

126 tes for three species groups of lentiviruses-feline immunodeficiency virus (FIV), simian immunodefici

127 of CD134 is the primary binding receptor for feline immunodeficiency virus (FIV), targeting the virus

128 (fCD134) is the primary binding receptor for feline immunodeficiency virus (FIV), targeting the virus

129 f human acquired immune deficiency syndrome, feline immunodeficiency virus (FIV), was used to model m

130 For the rapid genetic analysis of feline immunodeficiency virus (FIV), we developed a hete

131 For unknown reasons, the feline immunodeficiency virus (FIV), which infects both

132 r efficiency and tissue or cell tropism of a feline immunodeficiency virus (FIV)-based lentiviral vec

133 Feline immunodeficiency virus (FIV)-based lentiviral vec

134 natural lung tropism; however, pseudotyping feline immunodeficiency virus (FIV)-based lentiviral vec

135 pression following a single application of a feline immunodeficiency virus (FIV)-based lentivirus vec

136 epatoma cells following gene transfer with a feline immunodeficiency virus (FIV)-based lentivirus vec

137 arget these apical receptors, we pseudotyped feline immunodeficiency virus (FIV)-based vectors by usi

138 When recombinant feline immunodeficiency virus (FIV)-based vectors expres

139 We investigated the efficacy of feline immunodeficiency virus (FIV)-based vectors in tar

140 gical signals' alterations, we have used the feline immunodeficiency virus (FIV)-derived gp120 and ev

141 influence of the protease inhibitor TL-3 on feline immunodeficiency virus (FIV)-induced central nerv

142 We analyzed antibody responses in sera from feline immunodeficiency virus (FIV)-infected and uninfec

143 and immunodeficiency is a characteristic of feline immunodeficiency virus (FIV)-infected cats, it is

144 s were mucosally challenged with 10(2)-10(6) feline immunodeficiency virus (FIV)-infected T cells.

145 lymphocytes that suppress the replication of feline immunodeficiency virus (FIV).

146 ferent cell tropisms for molecular clones of feline immunodeficiency virus (FIV).

147 ld cat following experimental infection with feline immunodeficiency virus (FIV).

148 of viral mRNAs produced in cells infected by feline immunodeficiency virus (FIV).

149 ell line protect cats against challenge with feline immunodeficiency virus (FIV).

150 es in the production of infectious HIV-1 and feline immunodeficiency virus (FIV).

151 d cat (not herein) with complications due to feline immunodeficiency virus (FIV).

152 f many viruses, including strains of HIV and feline immunodeficiency virus (FIV).

153 nonuclear cell (PBMC) subsets in response to feline immunodeficiency virus (FIV).

154 suppresses the infectivity of vif-defective feline immunodeficiency virus (FIV).

155 The feline immunodeficiency virus (FIV)/cat system was used

156 An infectious chimeric feline immunodeficiency virus (FIV)/HIV strain carrying

157 immunity to infection can be induced against feline immunodeficiency virus (FIV); however, protection

158 ase (IN) mutants for a non-human lentivirus (feline immunodeficiency virus [FIV]) and analyzed both t

159 Feline lentiviral (feline immunodeficiency virus [FIV]) encapsidation has n

160 onprimate lentiviral genomic RNAs (HIV-1 and feline immunodeficiency virus [FIV]) vis-a-vis their Gag

161 , we demonstrate that a fast-evolving virus (feline immunodeficiency virus, FIV) can reveal details o

162 transmission pathways for three subtypes of feline immunodeficiency virus (FIVPle ) in African lions

163 DGF/p75-dependent disparity was observed for feline immunodeficiency virus IN.

164 tranasal insulin treatment of experimentally feline immunodeficiency virus-infected animals resulted

165 This investigation of feline immunodeficiency virus infection in bobcats and p

166 IDS, and their homologues may play a role in feline immunodeficiency virus infection.

167 s of MLV integrase and truncated variants of feline immunodeficiency virus integrase, suggesting that

168 (HIV-2), simian immunodeficiency virus, and feline immunodeficiency virus integrases.

169 ian immunodeficiency virus, puma lentivirus, feline immunodeficiency virus, Jembrana disease virus, v

170 The earliest experiments were in the cat/feline immunodeficiency virus model, followed a decade l

171 A full-length feline immunodeficiency virus NCSU1 (FIV-NCSU1) genome (

172 Lion lentivirus (LLV; also known as feline immunodeficiency virus of lion, Panthera leo [FIV

173 d with feline lentiviruses (puma lentivirus, feline immunodeficiency virus Pco [FIV-Pco], referred to

174 structures of complexes of a D30N mutant of feline immunodeficiency virus protease (FIV PR) complexe

175 is a protease inhibitor developed using the feline immunodeficiency virus protease as a model.

176 es in success when targeting HIV-1 protease, feline immunodeficiency virus protease, and HIV-1 integr

177 S3' subsite binding specificities of HIV and feline immunodeficiency virus proteases (FIV) proteases

178 l cross-species transmission of a subtype of feline immunodeficiency virus, puma lentivirus A (PLVA),

179 TRIMCyp transgenic cat lymphocytes resisted feline immunodeficiency virus replication.

180 e similarities to the export signal found in feline immunodeficiency virus Rev protein.

181 of cells productively infected with HIV-1 or feline immunodeficiency virus revealed dramatic patterns

182 nus of tRNA(Lys,3) and the U5-IR loop of the feline immunodeficiency virus RNA genome suggests a nove

183 Except for the feline immunodeficiency virus, sequences similar to the

184 of HIV, infection of neonatal cats with the feline immunodeficiency virus, showed development of per

185 enetic diversity, and molecular evolution of feline immunodeficiency virus specific to cougars (FIVpc

186 used to compare the nucleotide sequences of feline immunodeficiency virus strains isolated from Texa

187 eported previously for functional binding of feline immunodeficiency virus SU to its coreceptor CD134

188 zed a highly pathogenic molecular isolate of feline immunodeficiency virus subtype C (FIV-C) CABCpady

189 of cellular receptors for human, simian, and feline immunodeficiency viruses that are tropic for lymp

190 Finally, replacing nucleotides of the feline immunodeficiency virus U5-IR loop with the (A)(4)

191 A feline immunodeficiency virus vector encoding both full-

192 , we report that human DC-SIGN also captures feline immunodeficiency virus via high-affinity (1 nM),

193 CV-N potently blocked infection by feline immunodeficiency virus, which utilizes the chemok