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1 uence homology between vaccine immunogen and endogenous virus.
2 , in turn, promote the cellular co-option of endogenous viruses.
3 e range of vertebrates as both exogenous and endogenous viruses.
7 s retrovirus family defined by the Mus dunni endogenous virus and the Mus musculus endogenous retrovi
8 ed for activation of and recombination among endogenous viruses and could have resulted in generation
9 ses: feline endogenous virus (RD114), baboon endogenous virus, and avian reticuloendotheliosis virus.
10 ls conferred susceptibility to RD114, baboon endogenous virus, and the type D simian retroviruses.
12 e discovery of the widespread recruitment of endogenous viruses as regulatory elements for immune gen
14 the feline endogenous virus (RD114), baboon endogenous virus (BaEV), human endogenous virus type W (
15 able to efficiently process and present both endogenous virus epitopes and exogenous myelin epitopes
17 of the core protein of a 4-million-year-old endogenous virus from the chimpanzee genome and show tha
20 examine the multitude of ways through which endogenous viruses have influenced, for better or worse,
21 netic mismatch between vaccine immunogen and endogenous virus; however, these commonly failed to reco
22 apitulates late expression patterns from the endogenous virus, implicating specific cis-active sequen
23 ses and determine T-cell cross-reactivity to endogenous virus in patients with chronic HCV infection.
24 se findings demonstrate that the presence of endogenous viruses in source animals needs to be careful
25 to the env gene of MMTV but not to the known endogenous viruses, in 38% of human breast cancers exami
26 FN-gamma production decreases in response to endogenous, virus-induced IFN-alpha and during IFN-alpha
28 c innate immune system activation, driven by endogenous virus-like nucleic acids and potentially modi
35 uses, Coronaviruses, Flavivriuses and in two endogenous viruses of the yeast Saccharomyces cerevisiae
37 ting enzyme (ICE)-like proteases, stimulated endogenous virus production in activated PBMCs derived f
41 udotyped with the envelope protein of feline endogenous virus (RD114) than with conventional amphotro
42 oup of retroviruses that includes the feline endogenous virus (RD114), baboon endogenous virus (BaEV)
43 e receptor with three type C viruses: feline endogenous virus (RD114), baboon endogenous virus, and a
45 t of restimulating CAR(+) CTLs through their endogenous virus-specific T-cell antigen receptor (TcR)
46 opic virus results in pseudotyping of intact endogenous viruses that have not undergone recombination
47 he identification of a novel family of avian endogenous viruses that include env coding sequences tha
48 -env sequences defined a new family of avian endogenous viruses that we designated the ev/J family.
49 netic mismatch between vaccine immunogen and endogenous virus; this highlights the major challenge of
50 in regulating the unwarranted expression of endogenous viruses through the RNA interference pathway.
51 D betaretrovirus (SERV) sequences and baboon endogenous virus type C gammaretrovirus (BaEV) sequences
52 D114), baboon endogenous virus (BaEV), human endogenous virus type W (HERV-W), and type D primate ret
53 including spleen necrosis virus, and baboon endogenous virus, use a common cell-surface receptor for
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