ライフサイエンスコーパス: Moloney murine leukemia virus

1 ), function as transcriptional activators of Moloney murine leukemia virus.

2 ysis of 639 nucleotides in the gag region of Moloney murine leukemia virus.

3 man immunodeficiency virus type 1 (HIV-1) or Moloney murine leukemia virus.

4 long terminal repeat (LTR) sequences of the Moloney murine leukemia virus.

5 ed by ts1, a temperature-sensitive mutant of Moloney murine leukemia virus.

6 of the dimerization and packaging domain of Moloney murine leukemia virus.

7 tants of Hrs had no effect on the release of Moloney murine leukemia virus.

8 eracting with the capsid (CA) protein of the Moloney murine leukemia virus.

9 elet-derived growth factor (PDGF)-containing Moloney murine leukemia viruses.

10 nregulation of proviral integration site for Moloney murine leukemia virus 1 kinase (PIM-1).

11 e kinase PIM1 (Proviral Integration site for Moloney murine leukemia virus 1) has emerged as a key re

12 pendent kinase proviral integration site for Moloney murine leukemia virus-1 (PIM-1), which in turn r

13 oplasmic domain derived from the amphotropic Moloney murine leukemia virus 4070A GP, revealed about 1

14 Control brains were injected with a Moloney murine leukemia virus, adenovirus, or adeno-asso

15 Reverse transcriptase from Moloney murine leukemia virus and avian myoblastosis vir

16 n cells expressing envelope protein (Env) of Moloney murine leukemia virus and target cells were stud

17 ) genes were generated between the ecotropic Moloney murine leukemia virus and the amphotropic 4070A

18 pseudotyped virus with a genome based on the Moloney murine leukemia virus and the envelope protein o

19 (Pro) primer for (-) strand DNA synthesis of Moloney murine leukemia virus and the first five residue

20 able to gene delivery by wild-type ecotropic Moloney murine leukemia virus and vesicular stomatitis v

21 immunodeficiency virus, HIV type 2 (HIV-2), Moloney murine leukemia virus, and avian myeloblastosis

22 riptases tested (avian myeloblastosis virus, Moloney murine leukemia virus, and human immunodeficienc

23 rotein (GFP)-transducing retroviral vectors, Moloney murine leukemia virus, and lentivirus.

24 -dependent manner and enhanced expression of Moloney murine leukemia virus- and murine embryonic stem

25 ces between XMRV and the intensively studied Moloney murine leukemia virus, architectures of the regu

26 l helper virus, pAM3-IRES-Zeo, that contains Moloney murine leukemia virus as a helper virus and a pi

27 mate lentiviruses and distinct from those of Moloney murine leukemia virus, avian sarcoma leukosis vi

28 evere combined immunodeficiency (SCID-X1), a Moloney murine leukemia virus-based gamma-retrovirus vec

29 atal mice were injected intravenously with a Moloney murine leukemia virus-based retroviral vector (R

30 Moloney murine leukemia virus-based retroviral vector ex

31 Using the Moloney murine leukemia virus-based retroviral vector MF

32 in transduction efficiency by both HIV- and Moloney murine leukemia virus-based retroviral vectors.

33 In this study, we used a Moloney murine leukemia virus-based retrovirus encoding

34 A Moloney murine leukemia virus-based single-replication-c

35 cur between two identical sequences within a Moloney murine leukemia virus-based vector.

36 PD223 cells are able to package Moloney murine leukemia virus-based vectors at a titer o

37 HIV-1 replication than cells transduced with Moloney murine leukemia virus-based vectors expressing T

38 te dehydrogenase (hG6PD) gene transferred by Moloney murine leukemia virus-based vectors into murine

39 Here, we used Moloney murine leukemia virus-based vectors to examine t

40 To address this hypothesis, Moloney murine leukemia virus-based vectors, which were

41 ssive cis-acting DNA sequences identified in Moloney murine leukemia virus but remains sensitive to t

42 retrovirus, MoFe2, or with the parent virus, Moloney murine leukemia virus, caused significant reduct

43 The retrovirus ts1, a mutant of Moloney murine leukemia virus, causes oxidative stress a

44 Harvey sarcoma virus and Moloney murine leukemia virus constructs were used, both

45 e full length, positive-strand genome of the Moloney Murine Leukemia Virus contains a "core encapsida

46 sults also suggest that the leader region of Moloney murine leukemia virus contains inhibitory/regula

47 repeats had been replaced with a duplicated Moloney murine leukemia virus core enhancer.

48 ation, followed by reverse transcription via Moloney murine leukemia virus, degradation of chromosoma

49 deletion of sequences in the 3' U3 region of Moloney murine leukemia virus-derived retroviral vectors

50 lular protein that blocks autointegration of Moloney murine leukemia virus DNA, also plays an indirec

51 istones are rapidly loaded onto unintegrated Moloney murine leukemia virus DNAs.

52 erived MLE-15 cells infected with a chimeric Moloney murine leukemia virus driven by the JSRV enhance

53 MEL cells were infected with a Moloney murine leukemia virus encoding the green fluores

54 The trimeric Moloney murine leukemia virus Env protein matures by two

55 l receptor-binding sequence of the ecotropic Moloney murine leukemia virus envelope glycoprotein with

56 acids within the receptor-binding domain of Moloney murine leukemia virus envelope in order to ident

57 we have studied how the protomeric units of Moloney murine leukemia virus envelope protein (Env) are

58 e we report that tryptophan 142 in ecotropic Moloney murine leukemia virus envelope protein is essent

59 Additionally, the MMTV- and Moloney murine leukemia virus envelope proteins coimmuno

60 We have examined the function of Moloney murine leukemia virus envelope proteins with sub

61 Two second-site mutations in Moloney murine leukemia virus envelope surface protein (

62 s between transmembrane proteins (TM) of the Moloney murine leukemia virus envelope using the Sacchar

63 occus nuclease (SN) to the C-terminal end of Moloney murine leukemia virus Gag and demonstrated that

64 trovirus packaging cell lines expressing the Moloney murine leukemia virus gag and pol genes but lack

65 Retroviral genomes encoding a portion of the Moloney murine leukemia virus Gag protein fused to porti

66 In contrast, the wild-type RSV and Moloney murine leukemia virus Gag proteins were complete

67 by eight footprints representing regions of Moloney murine leukemia virus gag, some previously uncha

68 dful" was tested by examining the ability of Moloney murine leukemia virus genomes lengthened by 4, 8

69 coated with the parental wild-type ecotropic Moloney murine leukemia virus glycoprotein through the e

70 es were not detected either to Rev M10 or to Moloney murine leukemia virus gp70 envelope protein.

71 me suppression of the gag gene stop codon in Moloney murine leukemia virus has been studied by UV hyp

72 al analyses of the p12 Gag phosphoprotein of Moloney murine leukemia virus have demonstrated its part

73 Moloney murine leukemia virus-HIV-1 hybrid substrates we

74 nuclear magnetic resonance structure of the Moloney murine leukemia virus IN (M-MLV) C-terminal doma

75 n methylating the 3' long terminal repeat of Moloney murine leukemia virus in vitro.

76 have previously described a mutant RT of the Moloney murine leukemia virus in which F155 was replaced

77 To study the function of the HHCC domain of Moloney murine leukemia virus IN, the first N-terminal 1

78 roduced by the Gag polyproteins of HIV-1 and Moloney murine leukemia virus, indicating that no specif

79 oncogene associated with the progression of Moloney murine leukemia virus-induced T cell lymphomas i

80 viral nucleoprotein complexes isolated from Moloney murine leukemia virus-infected cells exhibit a b

81 receptor-5-positive (Lgr5(+)) and B lymphoma moloney murine leukemia virus insertion region homolog-1

82 The B-lymphoma Moloney murine leukemia virus insertion region-1 protein

83 rabidopsis (Arabidopsis thaliana) B lymphoma Moloney murine leukemia virus insertion region1 homolog

84 B-cell-specific Moloney murine leukemia virus integration site 1 (BMI1)

85 e examine the role of Bmi-1 (B-cell-specific Moloney murine leukemia virus integration site 1) as a r

86 Moloney murine leukemia virus is a prototypical simple r

87 The p12 Gag protein of Moloney murine leukemia virus is a small polypeptide of

88 The envelope (Env) protein of Moloney murine leukemia virus is the primary mediator of

89 igh expression of proviral insertion site of Moloney murine leukemia virus kinases (Pim-1, -2, and -3

90 Moloney murine leukemia virus-like particles (M-VLPs) we

91 Second, the Moloney murine leukemia virus long terminal repeat (LTR)

92 tomegalovirus enhancer-promoter fused to the Moloney murine leukemia virus long terminal repeat at th

93 r and enhancer] or an intermediate strength (Moloney murine leukemia virus long terminal repeat) prom

94 ng hybrid duplex substrates derived from the Moloney murine leukemia virus long terminal repeat, we i

95 internal grp78 promoter, in contrast to the Moloney murine leukemia virus long terminal repeat, wher

96 xpression in vivo from vectors driven by the Moloney murine leukemia virus long-terminal repeat (LTR)

97 expressing the antisense RNAs as part of the Moloney murine leukemia virus LTR promoter-directed retr

98 repeat (LTR) was found to be higher than the Moloney murine leukemia virus LTRs in both LNCaP and WPM

99 Moloney murine leukemia virus (M-MLV) replication is res

100 mbinant avian myeloblastosis virus (AMV) and Moloney murine leukemia virus (M-MLV) reverse transcript

101 In the case of the ecotropic Moloney murine leukemia virus (M-MLV), the Nef-like effe

102 substrates and the reverse transcriptases of Moloney murine leukemia virus (M-MuLV) and human immunod

103 t structural studies have suggested that the Moloney murine leukemia virus (M-MuLV) CA protein may as

104 ane-bound arrays of an N-terminal His-tagged Moloney murine leukemia virus (M-MuLV) capsid (CA) prote

105 ly stained, membrane-bound, histidine-tagged Moloney murine leukemia virus (M-MuLV) capsid protein (h

106 The infection of cells with Moloney murine leukemia virus (M-MuLV) causes an increas

107 uctural motifs located in the 5' part of the Moloney murine leukemia virus (M-MuLV) encapsidation dom

108 s shown that gPr80gag facilitates release of Moloney murine leukemia virus (M-MuLV) from cells along

109 The p12 region of the Moloney murine leukemia virus (M-MuLV) Gag protein conta

110 Moloney murine leukemia virus (M-MuLV) IN-IN protein int

111 The nature of Moloney murine leukemia virus (M-MuLV) infection after a

112 wo-end integration reaction catalyzed by the Moloney murine leukemia virus (M-MuLV) integrase (IN) wa

113 Moloney murine leukemia virus (M-MuLV) is a replication-

114 Moloney murine leukemia virus (M-MuLV) is a replication-

115 The enhancer sequences in the Moloney murine leukemia virus (M-MuLV) long terminal rep

116 nces within terminal inverted repeats of the Moloney murine leukemia virus (M-MuLV) LTR were synthesi

117 system that mimics the assembly of immature Moloney murine leukemia virus (M-MuLV) particles to exam

118 were generated within the 3' terminus of the Moloney murine leukemia virus (M-MuLV) pol gene encoding

119 re involved in the specific encapsidation of Moloney murine leukemia virus (M-MuLV) RNA into M-MuLV v

120 By using an RNase H- mutant of Moloney murine leukemia virus (M-MuLV) RT, we demonstrat

121 A chimera between Ty3 and a Neo(r)-marked Moloney murine leukemia virus (M-MuLV) was constructed.

122 The matrix protein (MA) of the Moloney murine leukemia virus (M-MuLV) was found to inte

123 or function of the integrase (IN) protein of Moloney murine leukemia virus (M-MuLV) were investigated

124 an immunodeficiency virus type 1 (HIV-1) and Moloney murine leukemia virus (M-MuLV) were shown to req

125 as constructed by replacing the U3 region of Moloney murine leukemia virus (M-MuLV) with homologous s

126 r gene inactivation during leukemogenesis by Moloney murine leukemia virus (M-MuLV), a genome-wide sc

127 onacutely transforming retroviruses, such as Moloney murine leukemia virus (M-MuLV), differ from tran

128 human immunodeficiency virus type 1 (HIV-1), Moloney murine leukemia virus (M-MuLV), human T-cell leu

129 n immunodeficiency virus, type 1 (HIV-1) and Moloney murine leukemia virus (M-MuLV), we determined th

130 -1 (human immunodeficiency virus type 1) and Moloney murine leukemia virus (M-MuLV), we evaluated how

131 Infection of mice by Moloney murine leukemia virus (M-MuLV), which induces ly

132 Early bone marrow infection of Moloney murine leukemia virus (M-MuLV)-infected mice was

133 mmunodeficiency virus type 1 (HIV-1) and the Moloney murine leukemia virus (M-MuLV).

134 of the Gag protein p12 block replication of Moloney murine leukemia virus (M-MuLV).

135 we have infected v-Myb transgenic mice with Moloney murine leukemia virus (M-MuLV).

136 Using Moloney murine leukemia virus (MLV) as a tool, we examin

137 cently discovered that the NC protein of the Moloney murine leukemia virus (MLV) can bind with high a

138 We have generated Moloney murine leukemia virus (MLV) envelope derivatives

139 nalyze more than 40 derivatives of ecotropic Moloney murine leukemia virus (MLV) envelope, containing

140 , retrovirus packaging cell lines expressing Moloney murine leukemia virus (MLV) gag and pol genes pr

141 ion of psi (i.e., leader) sequences from the Moloney murine leukemia virus (MLV) genome into the 3' u

142 racterized the structure and function of the Moloney murine leukemia virus (MLV) IN protein in viral

143 identified as a common integration site for Moloney murine leukemia virus (MLV) in rat thymic lympho

144 The roles of cellular proteases in Moloney murine leukemia virus (MLV) infection were inves

145 ansportin 3 protein under conditions whereby Moloney murine leukemia virus (MLV) integrase failed to

146 Moloney murine leukemia virus (MLV) particles contain bo

147 linkages, we digested deproteinized RNA from Moloney murine leukemia virus (MLV) particles with RNase

148 ave probed the nucleoprotein organization of Moloney murine leukemia virus (MLV) pre-integration comp

149 The Moloney murine leukemia virus (MLV) repressor binding si

150 n HIV-1-based lentiviral vector to that by a Moloney murine leukemia virus (MLV) retroviral vector, u

151 ups of synthetic RNA-DNA hybrids with either Moloney murine leukemia virus (MLV) RT or human immunode

152 Moloney murine leukemia virus (MLV) selectively encapsid

153 mmaretroviruses, we engineered a fluorescent Moloney murine leukemia virus (MLV) system consisting of

154 purvalanol A, and methoxy-roscovitine, block Moloney murine leukemia virus (MLV) transcription events

155 mo- and heterodimerization were examined for Moloney murine leukemia virus (MLV) using nondenaturing

156 f human hematopoietic stem cells (HSCs) with Moloney murine leukemia virus (MLV) vectors have been an

157 vity, while infection by the gammaretrovirus Moloney murine leukemia virus (MLV) was unaffected.

158 escribe the properties of the Gag protein of Moloney murine leukemia virus (MLV), a gammaretrovirus.

159 n, with functionally homologous regions from Moloney murine leukemia virus (MLV), a murine retrovirus

160 ins from four different retroviruses: HIV-1, Moloney murine leukemia virus (MLV), Rous sarcoma virus

161 file that may be safer than that of standard Moloney murine leukemia virus (MLV)-derived retroviral v

162 lls are unable to support the replication of Moloney murine leukemia virus (MLV).

163 examined the kinetics of 5'-end joining for Moloney murine leukemia virus (MLV).

164 nd Mason-Pfizer monkey virus (M-PMV) but not Moloney murine leukemia virus (MLV).

165 APOBEC3 (mA3) and human APOBEC3G (hA3G) upon Moloney murine leukemia virus (MLV).

166 retroviral promoters and enhancers from the Moloney Murine Leukemia Virus (MMLV) and the Myeloprolif

167 An RNA kissing loop from the Moloney murine leukemia virus (MMLV) exhibits unusual me

168 Encapsidation of the Moloney murine leukemia virus (MMLV) genome is mediated

169 ed to play a similar preintegrative role for Moloney murine leukemia virus (MMLV) in addition to HIV-

170 ies of the 3' end processing site within the Moloney murine leukemia virus (MMLV) LTR d(TCTTTCATT), a

171 (RT) fidelity, we measured the error rate of Moloney murine leukemia virus (MMLV) RT in the presence

172 s in the pE vectors have been taken from the Moloney murine leukemia virus (MMLV) vector pMFG, which

173 ocytes are refractory to gene transfer using Moloney murine leukemia virus (MMLV)-based retroviral ve

174 ansplantation model, the authors evaluated a Moloney murine leukemia virus (MMLV)-based vector encodi

175 In this report, we made use of a chimeric Moloney murine leukemia virus (MMLV)-HIV-1 Gag in which

176 n JSRV and the unrelated murine retroviruses Moloney murine leukemia virus (MMuLV) and mouse mammary

177 Successful integration of Moloney murine leukemia virus (MMuLV)-derived retroviral

178 etherin markedly inhibits the replication of Moloney murine leukemia virus (Mo-MLV) and is required f

179 A Moloney murine leukemia virus (Mo-MLV) Gag-Escherichia c

180 Both the RNase H domain of Moloney murine leukemia virus (Mo-MLV) reverse transcrip

181 A crystallographic study of the Moloney murine leukemia virus (Mo-MLV) RNase H domain wa

182 The use of Moloney murine leukemia virus (Mo-MLV)-based vectors to

183 The capsid (CA) domain of the Moloney murine leukemia virus (Mo-MuLV) Gag protein has

184 be transgenic mice expressing fusions of the Moloney murine leukemia virus (Mo-MuLV) Gag protein to s

185 d the polypurine tract (PPT) sequence in the Moloney murine leukemia virus (Mo-MuLV) genome.

186 Previous studies with Moloney murine leukemia virus (Mo-MuLV) identified two a

187 nuclear localization signals (NLSs) into the Moloney murine leukemia virus (Mo-MuLV) integrase (IN) p

188 B1/DNMT3A/DNMT3L complex to newly integrated Moloney murine leukemia virus (Mo-MuLV) proviral DNA.

189 ed in which the U3 region of T-lymphomagenic Moloney murine leukemia virus (Mo-MuLV) was replaced by

190 1), simian immunodeficiency virus (SIV), and Moloney murine leukemia virus (Mo-MuLV), for the presenc

191 Recombinant Moloney murine leukemia virus (Mo-MuLV)-based retrovirus

192 This agent is a Moloney murine leukemia virus (Mo-MuLV)-based virus that

193 The core site in the Moloney murine leukemia virus (Moloney MLV) enhancer was

194 tion of a novel domain in the Gag protein of Moloney murine leukemia virus (MoLV) that is important f

195 an immunodeficiency virus type I (HIV-1) and Moloney murine leukemia virus (MoMLV) capsid proteins we

196 an immunodeficiency virus type 1 (HIV-1) and Moloney murine leukemia virus (MoMLV) cDNA.

197 es, whereas the prototypical gammaretrovirus Moloney murine leukemia virus (MoMLV) favors strong enha

198 Moloney murine leukemia virus (MoMLV) Gag utilizes its l

199 1), feline immunodeficiency virus (FIV), and Moloney murine leukemia virus (MoMLV) integrases were st

200 Retroviral reverse transcriptase (RT) of Moloney murine leukemia virus (MoMLV) is expressed in th

201 n factor (BAF) blocks the autointegration of Moloney murine leukemia virus (MoMLV) PICs in vitro.

202 To examine the role of this domain in Moloney murine leukemia virus (MoMLV) replication, we an

203 The Moloney murine leukemia virus (MoMLV) ribonucleoprotein

204 polymerase, but not the RNase H function of Moloney Murine Leukemia Virus (MoMLV) RT and also inhibi

205 ays which show that tetherin does not affect Moloney murine leukemia virus (MoMLV) spread, and only m

206 he HIV-1 vector was also more efficient than Moloney murine leukemia virus (MoMLV) vectors for transd

207 nd particle ultrastructure highly similar to Moloney murine leukemia virus (MoMLV), another gammaretr

208 xamine the early events in the life cycle of Moloney murine leukemia virus (MoMLV), we analyzed the i

209 lope protein (Env) can be used to pseudotype Moloney murine leukemia virus (MoMLV)-based retrovirus v

210 This is in contrast to a Moloney murine leukemia virus (MoMLV)-based retrovirus v

211 Previous studies have suggested that Moloney murine leukemia virus (MoMLV)-based vectors pseu

212 Moloney murine leukemia virus (MoMLV)-derived vectors re

213 erization linkage structure in the genome of Moloney murine leukemia virus (MoMLV).

214 Retroviral vectors based on the Moloney murine leukemia virus (MoMuLV) are currently the

215 The ts1 mutant of the Moloney murine leukemia virus (MoMuLV) causes neurodegen

216 ents for host proteins in the integration of Moloney murine leukemia virus (MoMuLV) cDNA in vitro.

217 To investigate receptor-mediated Moloney murine leukemia virus (MoMuLV) entry, the green

218 The cytoplasmic tail of the immature Moloney murine leukemia virus (MoMuLV) envelope protein

219 We have generated mutants of the Moloney murine leukemia virus (MoMuLV) envelope protein

220 Recent studies with small fragments of the Moloney murine leukemia virus (MoMuLV) genome suggested

221 Retroviral vectors based on the Moloney murine leukemia virus (MoMuLV) have shown incons

222 The ts1 mutant of Moloney murine leukemia virus (MoMuLV) induces a neurode

223 The envelope (Env) protein of Moloney murine leukemia virus (MoMuLV) is a homotrimeric

224 ll surface reporter under the control of the Moloney murine leukemia virus (MoMuLV) long terminal rep

225 For Moloney murine leukemia virus (MoMuLV), the envelope pro

226 n with gibbon-ape leukemia virus pseudotyped Moloney murine leukemia virus (MoMuLV)-based retrovirus

227 ropathogenic temperature-sensitive mutant of Moloney murine leukemia virus (MoMuLV-ts1), results in m

228 Moloney murine leukemia virus (MuLV) preferentially capt

229 rmation from scarce, femtomole quantities of Moloney murine leukemia virus (MuLV) RNA inside authenti

230 free Mg(2+) (~0.25 mM) and is comparable to Moloney murine leukemia virus (MuLV) RT fidelity.

231 In the gammaretroviruses, typified by Moloney murine leukemia virus (MuLV), gag and pol are in

232 e-deficient (PR-) and mature, wild-type (WT) Moloney murine leukemia virus (MuLV).

233 rized the effects of three such compounds on Moloney murine leukemia virus (MuLV).

234 Moloney murine leukemia virus mutants His 34-->Cys (CCCC

235 Moreover, Moloney murine leukemia virus NC, which contains a singl

236 We find that Moloney murine leukemia virus nucleocapsid protein reduc

237 irus type 1 nucleocapsid protein and for the moloney murine leukemia virus nucleocapsid zinc knuckle

238 R-region sequences from Moloney murine leukemia virus or feline leukemia virus d

239 able of producing high titers of recombinant Moloney murine leukemia virus particles that have incorp

240 The provirus integration site for Moloney murine leukemia virus (Pim) 1 kinase is an oncog

241 Proviral integration site for Moloney murine leukemia virus (Pim) kinases are serine/t

242 onine-specific proviral integration site for Moloney murine leukemia virus (PIM) kinases PIM1 and PIM

243 tated sequences both within and flanking the Moloney murine leukemia virus polypurine tract (PPT) and

244 R to probe the nucleoprotein organization of Moloney murine leukemia virus preintegration complexes.

245 For Moloney murine leukemia virus, primer removal at the RNA

246 e TGF-beta1 under the control of the CMV and Moloney murine leukemia virus promoters significantly in

247 le of forming heterodimeric species with the Moloney murine leukemia virus Psi domain.

248 nal structure of the double hairpin from the Moloney murine leukemia virus ([Psi(CD)](2), 132 nt, 42.

249 Homology requirements for Moloney murine leukemia virus recombination were address

250 elops in mice infected with ts1, a mutant of Moloney murine leukemia virus, resembles human AIDS.

251 Neonatal infection of these mice with Moloney murine leukemia virus resulted in accelerated tu

252 with ts1, the neuropathogenic mutant of the Moloney murine leukemia virus, results in motor neuronal

253 Inhibitor resistance of several commercial Moloney murine leukemia virus reverse transcriptase (MML

254 an effort to increase the thermostability of Moloney Murine Leukemia Virus reverse transcriptase (MML

255 n which the host, the N-terminal fragment of Moloney murine leukemia virus reverse transcriptase (MML

256 Both Moloney murine leukemia virus reverse transcriptase and

257 with the Superscript II version of RNase H- Moloney murine leukemia virus reverse transcriptase at 5

258 A resolution of an N-terminal fragment from Moloney murine leukemia virus reverse transcriptase comp

259 A 157-amino-acid fragment of Moloney murine leukemia virus reverse transcriptase enco

260 Previous results indicated that Moloney murine leukemia virus reverse transcriptase is c

261 restored by adding back a truncated form of Moloney murine leukemia virus reverse transcriptase lack

262 Template switching rates of Moloney murine leukemia virus reverse transcriptase muta

263 ed on the ability of the RNase H activity of Moloney murine leukemia virus reverse transcriptase to c

264 The refined structure determination of Moloney murine leukemia virus reverse transcriptase, a s

265 , including D114A and R116A substitutions in Moloney murine leukemia virus reverse transcriptase, are

266 conserved residues in the fingers domain of Moloney murine leukemia virus reverse transcriptase, res

267 member of the highly conserved LPQG motif in Moloney murine leukemia virus reverse transcriptase, we

268 t includes the fingers and palm domains from Moloney murine leukemia virus reverse transcriptase.

269 of mutations affecting the RNase H domain of Moloney murine leukemia virus reverse transcriptase.

270 n of human immunodeficiency virus type 1 and Moloney murine leukemia virus reverse transcriptases wit

271 ng model hybrid substrates and the HIV-1 and Moloney murine leukemia virus reverse transcriptases, we

272 to complete a single round of intracellular Moloney murine leukemia virus reverse transcription appr

273 The first strong stop template switch during Moloney murine leukemia virus reverse transcription was

274 These compounds also inhibit Moloney murine leukemia virus RT but not the Klenow frag

275 Avian myeloblastosis and Moloney murine leukemia virus RTs also bound more stably

276 ddition, PARP-1-deficient MEFs infected with Moloney murine leukemia virus showed no decrease in viru

277 1 (fti-1) (feline leukemia virus) and Ahi-1 (Moloney murine leukemia virus) shows that these display

278 transcriptase-associated RNase H activity of Moloney murine leukemia virus specifically cleaves withi

279 ts1 is a temperature-sensitive mutant of Moloney murine leukemia virus that causes hind-limb para

280 he generation of retroviral vectors based on Moloney murine leukemia virus that specifically transduc

281 eviously, we have shown that, in the case of Moloney murine leukemia virus, the U3 region of the LTR

282 In Moloney murine leukemia virus, three stem-loops are impo

283 The Moloney murine leukemia virus TM envelope protein, p15E,

284 ic HTLV-1 with a replaced envelope gene from Moloney murine leukemia virus to allow HTLV-1 to fuse wi

285 substitutions were introduced into the NC of Moloney murine leukemia virus to examine further its rol

286 We used Moloney murine leukemia virus to induce lymphomas in p27

287 s on the neurovirulent viruses FrCas(NC) and Moloney murine leukemia virus ts1 indicate that the nasc

288 The recent development of a pseudotyped Moloney murine leukemia virus vector that contains the G

289 and (hTRAIL), into a cell line that packages Moloney murine leukemia virus vectors.

290 Replicating Moloney murine leukemia virus viral production was great

291 e Hsp70 was not detected in association with Moloney murine leukemia virus virions.

292 onlentiviral MAs and does not associate with Moloney murine leukemia virus virions.

293 TM cleavage in Moloney murine leukemia virus was inhibited by amprenavi

294 ting residues in the nucleocapsid protein of Moloney murine leukemia virus was investigated by introd

295 r-promoter of the 3' long terminal repeat of Moloney murine leukemia virus with a synthetic tetracycl

296 study, we tested replication properties for Moloney murine leukemia viruses with targeted mutations

297 tion of p10, the nucleocapsid protein of the Moloney murine leukemia virus, with nucleic acids.

298 We also determined whether the wild type Moloney murine leukemia virus (wt-MoMuLV) and one of its