ライフサイエンスコーパス: endogenous retrovirus

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

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

3 dunni endogenous virus and the Mus musculus endogenous retrovirus.

4 herally expressed superantigen encoded by an endogenous retrovirus.

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

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

7 permissive to other FeLV subgroups or feline endogenous retrovirus.

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

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

10 e with retrotransposable elements, including endogenous retroviruses.

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

12 RIG-I and MDA5, and a release of a subset of endogenous retroviruses.

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

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

15 aminases that potently inhibit exogenous and endogenous retroviruses.

16 of potent inhibitors for many exogenous and endogenous retroviruses.

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

18 elated with upregulation of nearby genes and endogenous retroviruses.

19 glycoprotein of several exogenous as well as endogenous retroviruses.

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

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

22 50 copies of the replication-defective human endogenous retrovirus 9 (ERV-9) and thousands of copies

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

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

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

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

27 e might relate to the selective targeting of endogenous retroviruses adjacent to Th1 enhancers.

28 -forming intergenic transcripts enriched for endogenous retroviruses, Alu and LINE-1 elements.

29 t phylogenetic analysis of a pericentromeric endogenous retrovirus amplified by PCR revealed possible

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

31 cell-stage (2C) transcripts, including MERVL endogenous retrovirus and Zscan4 cluster genes.

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

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

34 1918 strain of influenza virus and of human endogenous retroviruses and from the restructuring of th

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

36 thousands of transposable elements including endogenous retroviruses and latent cancer testis antigen

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

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

39 Endogenous retroviruses and long terminal repeat (LTR) r

40 Together, endogenous retroviruses and LTR retrotransposons represe

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

42 n that may have allowed a large diversity of endogenous retroviruses and other endogenous viral eleme

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

44 Retrotransposons including endogenous retroviruses and their solitary long terminal

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

46 ssociated with cell-intrinsic suppression of endogenous retroviruses and type I IFN signaling, and in

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

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

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

50 Desilenced endogenous retroviruses are associated with human autoim

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

52 Endogenous retroviruses are integral features of vertebr

53 Some endogenous retroviruses are involved in development, whi

54 Endogenous retroviruses are most significantly enriched

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

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

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

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

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

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

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

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

63 Endogenous retroviruses comprise millions of discrete ge

64 Endogenous retroviruses constitute a significant genomic

65 Endogenous retroviruses contribute in myriad ways to the

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

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

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

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

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

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

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

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

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

75 o the silencing of developmentally regulated endogenous retrovirus elements.

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

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

78 Actively replicating endogenous retroviruses entered the human genome million

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

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

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

82 Endogenous retrovirus (ERV) elements have been shown to

83 Here we identify six endogenous retrovirus (ERV) families with AML-associated

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

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

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

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

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

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

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

91 Elevated endogenous retrovirus (ERV) transcription and anti-ERV a

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

93 s genomic region, significantly derepressing endogenous retrovirus (ERV)3-1, with promoter demethylat

94 Endogenous retroviruses (ERV) are found throughout verte

95 nd humans, their roles in the restriction of endogenous retroviruses (ERV) have been limited to in vi

96 Among them, endogenous retroviruses (ERV) represent sequences that c

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

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

99 High levels of endogenous retrovirus (ERV1) expression were linked to a

100 The human endogenous retrovirus ERV3 possesses an open reading fra

101 Endogenous retroviruses (ERVs) are abundant in mammalian

102 Endogenous retroviruses (ERVs) are fixed and abundant in

103 Although endogenous retroviruses (ERVs) are known to harbor cis-r

104 Endogenous retroviruses (ERVs) are proposed as a molecul

105 Endogenous retroviruses (ERVs) are remnants of ancient r

106 Endogenous retroviruses (ERVs) are the remnants of ancie

107 Endogenous retroviruses (ERVs) are vertically transmitte

108 Endogenous retroviruses (ERVs) are widespread in vertebr

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

110 Endogenous retroviruses (ERVs) constitute a substantial

111 Endogenous retroviruses (ERVs) differ from typical retro

112 Endogenous retroviruses (ERVs) have contributed to more

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

114 Here, we show that endogenous retroviruses (ERVs) influence species-specifi

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

116 Endogenous retroviruses (ERVs) occupy extensive regions

117 Endogenous retroviruses (ERVs) of domestic cats (ERV-DCs

118 Endogenous retroviruses (ERVs) of these 2 gammaretroviru

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

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

121 Endogenous retroviruses (ERVs) represent ancestral seque

122 Endogenous retroviruses (ERVs) represent genomic fossils

123 Endogenous retroviruses (ERVs) result from germ line inf

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

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

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

127 In the case of endogenous retroviruses (ERVs), a TE subclass, experimen

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

129 ly applicable to other LTR retrotransposons, endogenous retroviruses (ERVs), and exogenous retrovirus

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

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

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

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

134 from integrated retroviral elements, termed endogenous retroviruses (ERVs), that comprise ~8% of the

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

136 Endogenous retroviruses (ERVs), the remnants of retrovir

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

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

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

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

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

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

143 sed of ancient retroviral sequences known as endogenous retroviruses (ERVs).

144 ately 8% of the human genome is derived from endogenous retroviruses (ERVs).

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

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

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

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

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

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

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

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

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

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

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

156 The resurrection of endogenous retroviruses from inactive molecular fossils

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

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

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

160 p W member 1, envelope (ERVW1) and SYNCYTIN2/endogenous retrovirus group FRD member 1, envelope (ERVF

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

162 s-like 2 (HML-2) is the most recently active endogenous retrovirus group in humans, and the only grou

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

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

165 ogenous retrovirally encoded genes SYNCYTIN1/endogenous retrovirus group W member 1, envelope (ERVW1)

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

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

168 Capture of retroviral envelope genes from endogenous retroviruses has played a role in the evoluti

169 Endogenous retroviruses have colonized approximately 10%

170 Endogenous retroviruses have proved to be a reliable gen

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

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

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

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

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

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

177 Characterization of Human Endogenous Retrovirus (HERV) expression within the trans

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

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

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

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

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

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

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

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

186 Human endogenous retroviruses (HERV) form a substantial part o

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

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

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

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

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

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

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

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

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

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

197 Human endogenous retroviruses (HERVs) comprise approximately 8

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

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

200 Human endogenous retroviruses (HERVs) result from ancestral in

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

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

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

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

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

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

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

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

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

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

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

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

213 cessfully captured the expression profile of endogenous retroviruses in single cells.

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

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

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

217 The endogenous retroviruses infect and are integrated into t

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

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

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

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

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

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

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

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

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

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

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

229 n=11, 41%), human pegivirus (n=1, 4%), human endogenous retrovirus K (n=27, 100%), and anellovirus (n

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

231 arditis (n=2) and GCM (n=13) contained human endogenous retrovirus K.

232 that non-canonical imprints are localized to endogenous retrovirus-K (ERVK) long terminal repeats (LT

233 Human endogenous retrovirus-K (HERV-K) human mouse mammary tum

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

235 6% identity with macaque), as well as simian endogenous retrovirus-K Gag and Env, induced polyfunctio

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

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

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

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

240 nscription of 2C-like markers such as murine endogenous retrovirus-like elements (MERVL) and Zscan4.

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

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

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

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

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

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

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

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

249 gnized as a key part of individual cells (as endogenous retroviruses or persistent infection) and mul

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

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

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

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

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

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

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

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

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

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

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

263 well as by the risk of transmitting porcine endogenous retroviruses (PERVs).

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

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

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

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

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

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

270 a novel approach termed cellular labeling of endogenous retrovirus replication (CLEVR), which reports

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

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

273 te-specific endogenous retrotransposon human endogenous retrovirus subfamily H (HERV-H) in creating t

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

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

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

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

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

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

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

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

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

283 Expression of the human endogenous retrovirus type K (HERV-K) has been associate

284 Human Endogenous Retrovirus type K (HERV-K) is the only HERV k

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

286 Expression of the Human Endogenous Retrovirus Type K (HERV-K), the youngest and

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

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

289 We have previously demonstrated that human endogenous retrovirus type W (HERV-W) negatively affects

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

291 The mobilization of endogenous retroviruses upon infection with an exogenous

292 anscriptase-encoding elements like LINE-1 or endogenous retroviruses via a process termed retrocopyin

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

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

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

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

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

298 s the most recently acquired family of human endogenous retroviruses, with many proviruses less than

299 ow that this spreading death is caused by an endogenous retrovirus within the glia, which leads to DN

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