ライフサイエンスコーパス: endogenous retrovirus

1 sed name for this retrovirus is killer whale endogenous retrovirus.

2 dunni endogenous virus and the Mus musculus endogenous retrovirus.

3 herally expressed superantigen encoded by an endogenous retrovirus.

4 made up of sequences from an apparent human endogenous retrovirus.

5 logy to MMTV and low homology to known human endogenous retrovirus.

6 herally expressed superantigen encoded by an endogenous retrovirus.

7 erm from four fish, suggesting that it is an endogenous retrovirus.

8 in mouse lupus nephritis corresponded to an endogenous retrovirus.

9 orting the hypothesis that TERV is an active endogenous retrovirus.

10 by the long terminal repeat (LTR7) of HERVH endogenous retrovirus.

11 d transcription of HERVH, a primate-specific endogenous retrovirus.

12 mammary tumor virus (MMTV), as well as many endogenous retroviruses.

13 glycoprotein of several exogenous as well as endogenous retroviruses.

14 al repeat (LTR) retroelements, which include endogenous retroviruses.

15 cord" in their hosts' genomes in the form of endogenous retroviruses.

16 aminases that potently inhibit exogenous and endogenous retroviruses.

17 of potent inhibitors for many exogenous and endogenous retroviruses.

18 ved primarily by LINE-1 retrotransposons and endogenous retroviruses.

19 luding DNA transposons, RNA transposons, and endogenous retroviruses.

20 As (ncRNAs) and members of the VL30 class of endogenous retroviruses.

21 e with retrotransposable elements, including endogenous retroviruses.

22 Two such paleoviruses, chimpanzee endogenous retrovirus-1 and -2 (CERV1 and CERV2), are re

23 50 copies of the replication-defective human endogenous retrovirus 9 (ERV-9) and thousands of copies

24 KoRV-A is an endogenous retrovirus-a retrovirus that infects germ cel

25 d nuclear element 1 (LINE-1 or L1) and human endogenous retrovirus, accompanies neoplastic transforma

26 from the LTR retrotransposons of ERV-9 human endogenous retrovirus activated transcription of key ery

27 ion of whether there is a connection between endogenous retrovirus activity and LINE-1 inactivity.

28 minal repeat retrotransposon-like with human endogenous retrovirus and satellite sequences.

29 helial cancer cells through demethylation of endogenous retroviruses and cancer testis antigens.

30 Primate genomes contain a large number of endogenous retroviruses and encode evolutionarily dynami

31 1918 strain of influenza virus and of human endogenous retroviruses and from the restructuring of th

32 Higher expression levels of endogenous retroviruses and genes with high GC content i

33 ce repeats and interspersed repeats, such as endogenous retroviruses and LINE-1 elements.

34 here TRIM28 plays a major role in repressing endogenous retroviruses and long interspersed elements,

35 r interaction of exogenous retroviruses with endogenous retroviruses and may have profound effects on

36 half of the mammalian genome is composed of endogenous retroviruses and other retrotransposable elem

37 Retrotransposons including endogenous retroviruses and their solitary long terminal

38 act that stress can induce the expression of endogenous retroviruses and transposable elements in man

39 e, highlighting the possible risk of porcine endogenous retroviruses and xenotourism.

40 pathogenesis of MS has been linked to human endogenous retroviruses, antiretroviral therapy for HIV

41 The solitary LTRs of ERV-9 human endogenous retrovirus are middle repetitive DNAs associa

42 Although many of the endogenous retroviruses are defective, several contain o

43 Endogenous retroviruses are integral features of vertebr

44 Some endogenous retroviruses are involved in development, whi

45 ow they do, and/or did, replicate.IMPORTANCE Endogenous retroviruses are relics of ancestral virus in

46 RNA defense roles to include the period when endogenous retroviruses are still infectious.

47 Thus, immune strategies that deal with endogenous retroviruses are, by necessity, those of self

48 The retroelements, which include endogenous retroviruses, are the more prominent group in

49 By using endogenous retroviruses as genetic markers, we found tha

50 ontal transfer by infection implicates these endogenous retroviruses as important vehicles for plant

51 is intracellular resistance to exogenous and endogenous retroviruses as well as other mobile genetic

52 clude simple repeats, satellites, LINEs, and endogenous retroviruses as well as transposon fragments.

53 these results indicate that Gag proteins of endogenous retroviruses can coassemble with HIV-1 Gag an

54 It has been reported that endogenous retroviruses can contaminate human cell lines

55 Endogenous retroviruses comprise millions of discrete ge

56 Endogenous retroviruses constitute a significant genomic

57 litary long terminal repeats (LTRs) of ERV-9 endogenous retrovirus contain the U3, R, and U5 regions

58 Endogenous retroviruses contribute in myriad ways to the

59 Importantly, the richness and complexity of endogenous retrovirus data can be used to understand how

60 iviruses clustered as sister taxa to several endogenous retroviruses derived from rodents and insecti

61 ival, >140 days) without evidence of porcine endogenous retrovirus dissemination.

62 nd subclasses of repetitive elements (LINEs, endogenous retroviruses, DNA transposons, simple repeats

63 hermore, in addition to the single ecotropic endogenous retrovirus (eERV) located on chromosome 11 (E

64 sses expression of intracisternal-A particle endogenous retrovirus elements and B2 short interspersed

65 YD5 cancer cells was associated with LTR and endogenous retrovirus elements and decreased H4K20me3.

66 We also found a significant excess of endogenous retrovirus elements in human-specific hypomet

67 t was localized to an inverted pair of human endogenous retrovirus elements within the large, flankin

68 g subset, which is known to be responsive to endogenous retrovirus-encoded superantigens.

69 A family of endogenous retroviruses (enJSRV) closely related to Jaag

70 ep genome harbors approximately 20 copies of endogenous retroviruses (enJSRVs) closely related to the

71 Actively replicating endogenous retroviruses entered the human genome million

72 e coding sequence appears to be made from an endogenous retrovirus envelope gene.

73 Here, we uncover a full-length endogenous retrovirus envelope protein, dubbed HEMO [hum

74 or extracting phylogenetic signal from large endogenous retrovirus (ERV) datasets by collapsing infor

75 Endogenous retrovirus (ERV) elements have been shown to

76 Endogenous retrovirus (ERV) families are derived from th

77 Upregulation of hypermethylated endogenous retrovirus (ERV) genes accompanies the respon

78 We mapped thousands of endogenous retrovirus (ERV) germline integrants in highl

79 We report that LTR class I endogenous retrovirus (ERV) retroelements impact conside

80 pe 2 (TI-2) antigens causes up-regulation of endogenous retrovirus (ERV) RNAs in antigen-specific mou

81 The Fv1 virus resistance gene is a coopted endogenous retrovirus (ERV) sequence related to the gag

82 nterspersed nuclear elements (LINEs) and the endogenous retrovirus (ERV) superfamily.

83 hile half of these are biallelic and include endogenous retrovirus (ERV) targets, the rest show monoa

84 ed expression of bidirectionally transcribed endogenous retrovirus (ERV) transcripts, increased cytos

85 g terminal repeat (LTR)-retrotransposons, or endogenous retroviruses (ERV), account for most novel in

86 nactivation, and activation and silencing of endogenous retroviruses (ERV).

87 The human endogenous retrovirus ERV3 possesses an open reading fra

88 Endogenous retroviruses (ERVs) are abundant in mammalian

89 Endogenous retroviruses (ERVs) are fixed and abundant in

90 Endogenous retroviruses (ERVs) are proposed as a molecul

91 Endogenous retroviruses (ERVs) are remnants of ancient r

92 Endogenous retroviruses (ERVs) are the remnants of ancie

93 Endogenous retroviruses (ERVs) are vertically transmitte

94 Endogenous retroviruses (ERVs) are widespread in vertebr

95 Endogenous retroviruses (ERVs) comprise 6-8% of the huma

96 Endogenous retroviruses (ERVs) constitute a substantial

97 Endogenous retroviruses (ERVs) differ from typical retro

98 Endogenous retroviruses (ERVs) have contributed to more

99 Repression of endogenous retroviruses (ERVs) in mammals involves sever

100 LVs) exist in mice as infectious viruses and endogenous retroviruses (ERVs) inserted into mouse chrom

101 Endogenous retroviruses (ERVs) occupy extensive regions

102 Endogenous retroviruses (ERVs) of these 2 gammaretroviru

103 s-specific enhancers are highly enriched for endogenous retroviruses (ERVs) on a genome-wide level.

104 Epsilon-like retroviruses have become endogenous retroviruses (ERVs) on several occasions, int

105 Endogenous retroviruses (ERVs) represent ancestral seque

106 Endogenous retroviruses (ERVs) represent genomic fossils

107 Endogenous retroviruses (ERVs) result from germ line inf

108 llions of years, accumulating in the form of endogenous retroviruses (ERVs) that account for nearly o

109 These exogenous MLVs derive from endogenous retroviruses (ERVs) that were acquired by the

110 a viruses (MLVs) recombine with nonecotropic endogenous retroviruses (ERVs) to produce polytropic MLV

111 The life cycle of endogenous retroviruses (ERVs), also called long termina

112 ratory and gastrointestinal tracts, and also endogenous retroviruses (ERVs), comprising a substantial

113 Transposable elements, including endogenous retroviruses (ERVs), constitute a large fract

114 s typically contain hundreds of thousands of endogenous retroviruses (ERVs), derived from ancient ret

115 ian genomes include a considerable number of endogenous retroviruses (ERVs), relics of ancestral infe

116 Endogenous retroviruses (ERVs), the majority of which ex

117 Endogenous retroviruses (ERVs), the remnants of retrovir

118 Unlike individual families of endogenous retroviruses (ERVs), they have remained activ

119 A of their host by entering the germ line as endogenous retroviruses (ERVs), where they lose their in

120 ng comparison to the distribution of chicken endogenous retroviruses (ERVs).

121 About 8% of the human genome is made up of endogenous retroviruses (ERVs).

122 ng a large-scale phylogenomic approach using endogenous retroviruses (ERVs).

123 portion of vertebrate genomes are made up of endogenous retroviruses (ERVs).

124 s the expression of exogenous proviruses and endogenous retroviruses (ERVs).

125 ied and mapped putative EREs (a total of 111 endogenous retroviruses [ERVs] and 488 solo long termina

126 Syncytin-1, the envelope gene of the human Endogenous Retrovirus ERVW-1, is one of the most importa

127 nrecognized example of a naturally occurring endogenous retrovirus expressing a dominant negative Gag

128 e identified 18 candidates belonging to five endogenous retrovirus families, with one gene displaying

129 is closely related to but distinct from the endogenous retrovirus family defined by the Mus dunni en

130 ining LINE-1 activity, we have identified an endogenous retrovirus family differentially amplified in

131 it (Oryctolagus cuniculus) and belongs to an endogenous retrovirus family found in rabbits.

132 ysTR represent recent amplifications of this endogenous retrovirus family to unprecedented levels.

133 This family of human endogenous retroviruses first entered the primate genome

134 eages of basal amphibian and fish foamy-like endogenous retroviruses (FLERVs).

135 s K (HERV-K)108--a betaretrovirus-like human endogenous retrovirus--for intersubunit bonding and foun

136 The resurrection of endogenous retroviruses from inactive molecular fossils

137 ion on the expression and release of porcine endogenous retroviruses from primary endothelial cells i

138 the mammalian radiation, specific groups of endogenous retroviruses generally remain active for comp

139 es, but also in the mobilization of complete endogenous retrovirus genomes via pseudotyping within ex

140 Elevated transcript expression of the endogenous retrovirus group HERV-K (HML-2) is seen in ma

141 Here, we report that human endogenous retrovirus group K (HERV-K) (HML-2) proviruse

142 Recent studies suggest that human endogenous retrovirus group K (HERV-K) provirus expressi

143 V-5 should now be denoted RERV-H (for rabbit endogenous retrovirus H).

144 g that human retrovirus 5 is actually rabbit endogenous retrovirus H.

145 ion in trans, and that an infectious pool of endogenous retroviruses has persisted within the primate

146 Endogenous retroviruses have colonized approximately 10%

147 Endogenous retroviruses have shaped the evolution of mam

148 s cervicolor isolate M813 and Mus spicilegus endogenous retrovirus HEMV.

149 ess transcripts derived from the novel human endogenous retrovirus HERV-E (named CT-RCC HERV-E).

150 se findings demonstrate that elements of the endogenous retrovirus HERV-K (HML-2) can be found in the

151 Our study reveals that upregulation of the endogenous retrovirus HERV-K could both initiate and sus

152 belonged to the long form that contains the endogenous retrovirus HERV-K(C4).

153 The human endogenous retroviruses HERV-K113 and HERV-K115 are full

154 In addition, human endogenous retrovirus (hERV) envelope RNAs were present

155 A member of the human endogenous retrovirus (HERV) family termed HERV-W encode

156 B virus, GB virus C, anellovirus, and human endogenous retrovirus (HERV) reads.

157 interspersed nuclear element (LINE) or human endogenous retrovirus (HERV) repeats as a cause of delet

158 antigen were found to be derived from human endogenous retrovirus (HERV) type E and were expressed i

159 ne proteins 1 and 2A), transactivate a human endogenous retrovirus (HERV), HERV-K18, in infected B ly

160 and C-terminally truncated version of human endogenous retrovirus (HERV)-K10 protease were expressed

161 cloned an EBV-associated superantigen, human endogenous retrovirus (HERV)-K18 envelope protein (Env).

162 equences necessary for transduction of human endogenous retrovirus (HERV)-Kcon, a consensus of the HE

163 Human endogenous retrovirus (HERV)-specific T cell responses i

164 Expression of a human endogenous retrovirus (HERV-K) was determined in autopsy

165 Human endogenous retroviruses (HERV) make up 8% of the human g

166 Indeed, one endogenous retrovirus [HERV-K(HML-2)], which has replica

167 y reported finding the RNA of a type K human endogenous retrovirus, HERV-K (HML-2), at high titers in

168 anscriptionally activates the env gene of an endogenous retrovirus, HERV-K18, that possesses SAg acti

169 ctivates a superantigen encoded by the human endogenous retrovirus, HERV-K18.

170 Of all the endogenous retroviruses, HERV-K viruses are the most int

171 Human endogenous retroviruses (HERVs) are a potential source o

172 Human endogenous retroviruses (HERVs) are the remnants of anci

173 Though most human endogenous retroviruses (HERVs) are thought to be irrele

174 Human endogenous retroviruses (HERVs) are viruses that have co

175 n genome sequence contains many thousands of endogenous retroviruses (HERVs) but all are defective, c

176 e forces directing the accumulation of human endogenous retroviruses (HERVs) by comparing de novo HER

177 Human endogenous retroviruses (HERVs) comprise approximately 8

178 Human endogenous retroviruses (HERVs) comprise up to 8% of the

179 The fate of most human endogenous retroviruses (HERVs) has been to undergo reco

180 Human endogenous retroviruses (HERVs) make up 8% of the human

181 Human endogenous retroviruses (HERVs) make up 8% of the human

182 Human endogenous retroviruses (HERVs) make up 8% of the human

183 Human endogenous retroviruses (HERVs) result from ancestral in

184 One lineage of human endogenous retroviruses (HERVs), HERV-K(HML2), is upregu

185 Human endogenous retroviruses (HERVs), which are remnants of a

186 Human endogenous retroviruses (HERVs), which are remnants of p

187 ent of the human genome is composed of human endogenous retroviruses (HERVs), which are thought to be

188 Human endogenous retroviruses (HERVs), which make up approxima

189 te surrounding cancers associated with human endogenous retroviruses (HERVs).

190 e human-tropic replication-competent porcine endogenous retroviruses (HTRC PERVs), using in vitro coc

191 Since Hili also inhibited the movement of an endogenous retrovirus (IAP), our finding shed new light

192 However, DNA walking identified a murine endogenous retrovirus (IAPLTR1: ERVK) insertion in exon

193 copy number and distribution of the kangaroo endogenous retrovirus in the Macropus genus.

194 iverse gene cluster in which insertion of an endogenous retrovirus in the ninth intron of C4, termed

195 FeLV-A by mutation and/or recombination with endogenous retroviruses in domestic cats, resulting in a

196 lating evidence suggests potential roles for endogenous retroviruses in early life events, which may

197 Here, we describe the first endogenous retroviruses in humans for which both the ful

198 tions, based on the appearance of particular endogenous retroviruses in primate genomes.

199 for investigating the presence of inducible, endogenous retroviruses in the AGM-derived Vero cell lin

200 nd also of most members of the vast array of endogenous retroviruses in the genome.

201 AXX-SETDB1-KAP1-HDAC1 complex that represses endogenous retroviruses independently of ATRX and H3.3 i

202 The endogenous retroviruses infect and are integrated into t

203 retroviruses on HIV-1 replication.IMPORTANCE Endogenous retroviruses inhabit big portions of our geno

204 rrectly processed mRNA from genes mutated by endogenous retrovirus insertions into introns, including

205 The release of porcine endogenous retroviruses into the supernatant was monitor

206 ry long terminal repeat (LTR) of ERV-9 human endogenous retrovirus is located upstream of the HS5 sit

207 find that the repression of specific murine endogenous retroviruses is dependent on DAXX, but not on

208 find that the appearance of new families of endogenous retroviruses is strongly predictive of the ap

209 ility of retrotransposons and replication of endogenous retroviruses, is most likely to prevent the d

210 Here we show that RNA from human endogenous retrovirus K (HERV-K) (HML-2), a relatively r

211 functional studies have implicated the human endogenous retrovirus K (HERV-K) dUTPase located within

212 ated SAMHD1 to increased expression of human endogenous retrovirus K (HERV-K) in PAH versus control l

213 Human endogenous retrovirus K (HERV-K) is the most intact retr

214 eotidohydrolase (dUTPase) encoded by a human endogenous retrovirus K (HERV-K) may be a candidate gene

215 proteins of JSRV and MMTV, as well as human endogenous retrovirus K (HERV-K)108--a betaretrovirus-li

216 orted HERV-K(HML2) elements (HERV-K is human endogenous retrovirus K).

217 onses to all Ags, and Ab responses to simian endogenous retrovirus-K Env.

218 6% identity with macaque), as well as simian endogenous retrovirus-K Gag and Env, induced polyfunctio

219 95% homologous to MMTV but only 57% to human endogenous retrovirus K10 in 3.5 kb of the gag and pol g

220 onuclear cells (PBMCs) were tested for human endogenous retrovirus-K18 (HERV-K18) env transcripts usi

221 omic structure and evolution of the kangaroo endogenous retrovirus (KERV) in the marsupial genus Macr

222 hough the endogenizing gammaretrovirus koala endogenous retrovirus (KoRV) was isolated from these koa

223 Both murine endogenous retrovirus-L (MuERV-L) and intracisternal A p

224 The unique insertion sites of endogenous retroviruses, like those of other transposabl

225 quence from an intracisternal A particle (an endogenous retrovirus-like sequence) and one had capture

226 ely spliced, exon due to the insertion of an endogenous retrovirus-like sequence.

227 ors CD28, CTLA4, and ICOS, and a HERV-H type endogenous retrovirus located 366 bp downstream of ICOS

228 w that an LTR retrotransposon of ERV-9 human endogenous retrovirus located 40-70 kb upstream of the h

229 ing into the long terminal repeat of a human endogenous retrovirus located between the last two exons

230 e results indicated that multiple, inducible endogenous retrovirus loci are present in the AGM genome

231 Retrotransposons, mainly LINEs, SINEs, and endogenous retroviruses, make up roughly 40% of the mamm

232 ian wild mouse species Mus caroli harbors an endogenous retrovirus (McERV) that is closely related to

233 In the absence of KDM1A, the murine endogenous retrovirus MuERV-L/MERVL becomes overexpresse

234 ents, a yeast retrotransposon, Ty1, a murine endogenous retrovirus, MusD, and a lentivirus, human imm

235 indicate that amplification of the kangaroo endogenous retrovirus occurred in a lineage-specific fas

236 e chimeras between JSRV and the JSRV-related endogenous retroviruses of sheep (enJSRVs) and assessed

237 nging to the Betaretrovirus genus shows that endogenous retroviruses of this family are more broadly

238 way for further studies on the influence of endogenous retroviruses on HIV-1 replication.IMPORTANCE

239 t and inflammatory tissues sometimes express endogenous retroviruses or their proteins.

240 ets of filtered supernatants, indicated that endogenous retrovirus particles related to simian endoge

241 tion is available on transmission of porcine endogenous retrovirus (PERV) after xenotransplantation a

242 e replication- competent humantropic porcine endogenous retrovirus (PERV) has prompted studies on the

243 We document the presence of porcine endogenous retrovirus (PERV) in plasma samples of pigs a

244 In particular, the transmission of porcine endogenous retrovirus (PERV) is a major concern.

245 Porcine endogenous retrovirus (PERV) is a potential pathogen in

246 Porcine endogenous retrovirus (PERV) is considered one of the ma

247 of determinants of human tropism of porcine endogenous retrovirus (PERV) is critical to understandin

248 We investigated the sensitivity of porcine endogenous retrovirus (PERV) produced from Gal-null and

249 In this study, porcine endogenous retrovirus (PERV) was produced in a porcine c

250 Porcine endogenous retrovirus (PERV), porcine cytomegalovirus (P

251 However, all pigs contain the porcine endogenous retrovirus (PERV), raising concerns regarding

252 inevitably resulting in exposure to porcine endogenous retrovirus (PERV).

253 Porcine endogenous retroviruses (PERV) can infect human cell lin

254 that demonstrate the transmission of porcine endogenous retroviruses (PERV) from porcine cells to hum

255 he potential risk of transmission of porcine endogenous retroviruses (PERV) from xenogeneic donors in

256 Porcine endogenous retroviruses (PERV) have been shown to infect

257 Replication-competent porcine endogenous retroviruses (PERVs) are either human cell tr

258 The pig genome contains porcine endogenous retroviruses (PERVs) capable of infecting hum

259 isk of cross-species transmission of porcine endogenous retroviruses (PERVs) has impeded the clinical

260 The potential transmission of porcine endogenous retroviruses (PERVs) has raised concern in th

261 understand the replication of these porcine endogenous retroviruses (PERVs) in cells of different ty

262 Interestingly, porcine endogenous retroviruses (PERVs) of all three host-range

263 y concerns about the transmission of porcine endogenous retroviruses (PERVs) to humans.

264 complete proviral structure of the kangaroo endogenous retrovirus, phylogenetic relationship among r

265 n, the potential for transmission of porcine endogenous retroviruses, porcine cytomegalovirus, and po

266 Therefore, human endogenous retroviruses potentially play a role in multi

267 we did find a 3,600-bp region of XMRV in an endogenous retrovirus present in NIH/3T3 cells.

268 monkey species, there has been no report of endogenous retroviruses produced from African green monk

269 ely to be the most common mechanism by which endogenous retroviruses proliferate in their hosts.

270 trovirus vectors pseudotyped with the feline endogenous retrovirus (RD114) envelope protein produced

271 impact of a group of LTRs from the mammalian endogenous retrovirus-related ERVL retrotransposon class

272 ssential for SETDB1's enzymatic activity and endogenous retrovirus silencing in murine embryonic stem

273 neages and strongly inducing MuERV-L (MERVL) endogenous retroviruses, similar to what is seen with fe

274 Porcine cells express endogenous retroviruses, some of which are infectious fo

275 The replication of porcine endogenous retrovirus subgroup A (PERV-A) and PERV-B in

276 n RNA transcripts, especially for some human endogenous retroviruses, such as LINE-1 and Alu retrotra

277 ated from long terminal repeats derived from endogenous retroviruses, suggesting this foreign sequenc

278 -defective retrovirus, here named tetraonine endogenous retrovirus (TERV), from Bonasa umbellus (ruff

279 closely related to those of polytropic mouse endogenous retroviruses than to those of XMRVs and were

280 Syncytins are envelope genes from endogenous retroviruses that have been captured during e

281 eractions with a wide variety of viruses and endogenous retroviruses that predate the origin of prima

282 tion and loss of env is the trait that leads endogenous retroviruses to becoming genomic superspreade

283 A human endogenous retrovirus type E (HERV-E) was recently found

284 ctivates the overall expression of the human endogenous retrovirus type K (HERV-K) (HML-2), we used n

285 Human endogenous retrovirus type K (HERV-K) proviruses are sca

286 , mouse mammary tumor virus (MMTV) and human endogenous retrovirus type K, encode analogous factors (

287 Recent studies showed that human endogenous retrovirus type W (HERV-W) contributes signif

288 The human endogenous retrovirus type W (HERV-W) family includes pr

289 ctions is attributed to members of the human endogenous retrovirus type-K (HERV-K) (HML-2) family.

290 The mobilization of endogenous retroviruses upon infection with an exogenous

291 nsert deletion through recombination with an endogenous retrovirus was also observed.

292 No porcine endogenous retrovirus was detected in SJPL cells, and in

293 by the antisense strand of the HRES-1 human endogenous retrovirus was isolated from peripheral blood

294 scripts derived from ancient transposons and endogenous retroviruses were also upregulated.

295 combination rate correlates with fixation of endogenous retroviruses, whereas the local recombination

296 because of the expression of closely related endogenous retroviruses, which are not present in humans

297 Also, interactions between human endogenous retroviruses, which likely do not replicate,

298 gnition of a self Ag, encoded by a defective endogenous retrovirus, whose expression is confined to t

299 clade, we identified the envelope gene of an endogenous retrovirus with all the features of a Syncyti

300 rse transcriptase places SSSV with zebrafish endogenous retrovirus (ZFERV) between the Gammaretroviru