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1 uence homology between vaccine immunogen and endogenous virus.
2 anded cells to produce replication-competent endogenous virus.
3 e range of vertebrates as both exogenous and endogenous viruses.
4 , in turn, promote the cellular co-option of endogenous viruses.
5 egions, as well as transposable elements and endogenous viruses.
7 overy indicates a protective capacity of the endogenous virus against the exogenous form, either via
10 s retrovirus family defined by the Mus dunni endogenous virus and the Mus musculus endogenous retrovi
11 ed for activation of and recombination among endogenous viruses and could have resulted in generation
12 ses: feline endogenous virus (RD114), baboon endogenous virus, and avian reticuloendotheliosis virus.
13 ls conferred susceptibility to RD114, baboon endogenous virus, and the type D simian retroviruses.
16 e discovery of the widespread recruitment of endogenous viruses as regulatory elements for immune gen
18 the feline endogenous virus (RD114), baboon endogenous virus (BaEV), human endogenous virus type W (
19 ies noted a negative association between the endogenous virus copy number and exogenous virus infecti
20 parasitoid wasp that harbors a domesticated endogenous virus (DEV) and parasitizes host insects like
21 able to efficiently process and present both endogenous virus epitopes and exogenous myelin epitopes
23 of the core protein of a 4-million-year-old endogenous virus from the chimpanzee genome and show tha
26 examine the multitude of ways through which endogenous viruses have influenced, for better or worse,
27 netic mismatch between vaccine immunogen and endogenous virus; however, these commonly failed to reco
28 apitulates late expression patterns from the endogenous virus, implicating specific cis-active sequen
29 ses and determine T-cell cross-reactivity to endogenous virus in patients with chronic HCV infection.
32 se findings demonstrate that the presence of endogenous viruses in source animals needs to be careful
33 to the env gene of MMTV but not to the known endogenous viruses, in 38% of human breast cancers exami
34 FN-gamma production decreases in response to endogenous, virus-induced IFN-alpha and during IFN-alpha
35 have emerged as one of the oldest groups of endogenous viruses infecting vertebrates (>=419 million
37 c innate immune system activation, driven by endogenous virus-like nucleic acids and potentially modi
44 uses, Coronaviruses, Flavivriuses and in two endogenous viruses of the yeast Saccharomyces cerevisiae
46 ting enzyme (ICE)-like proteases, stimulated endogenous virus production in activated PBMCs derived f
50 udotyped with the envelope protein of feline endogenous virus (RD114) than with conventional amphotro
51 oup of retroviruses that includes the feline endogenous virus (RD114), baboon endogenous virus (BaEV)
52 e receptor with three type C viruses: feline endogenous virus (RD114), baboon endogenous virus, and a
54 t of restimulating CAR(+) CTLs through their endogenous virus-specific T-cell antigen receptor (TcR)
55 opic virus results in pseudotyping of intact endogenous viruses that have not undergone recombination
56 he identification of a novel family of avian endogenous viruses that include env coding sequences tha
57 -env sequences defined a new family of avian endogenous viruses that we designated the ev/J family.
58 netic mismatch between vaccine immunogen and endogenous virus; this highlights the major challenge of
59 in regulating the unwarranted expression of endogenous viruses through the RNA interference pathway.
60 D betaretrovirus (SERV) sequences and baboon endogenous virus type C gammaretrovirus (BaEV) sequences
61 D114), baboon endogenous virus (BaEV), human endogenous virus type W (HERV-W), and type D primate ret
62 including spleen necrosis virus, and baboon endogenous virus, use a common cell-surface receptor for
64 been implicated in cancer and disclose human endogenous viruses whose expression is associated with p