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1  reverse transcriptase activity typical of a gammaretrovirus.
2 ull-length viral genome with that of another gammaretrovirus.
3  in mice by MoFe2-MuLV, a unique recombinant gammaretrovirus.
4 nfected with murine leukemia virus (MuLV), a gammaretrovirus.
5 ld support infection of a pseudotyped modern gammaretrovirus.
6 in of Moloney murine leukemia virus (MLV), a gammaretrovirus.
7 6.9% nucleotide identity to the killer whale gammaretrovirus.
8 loney murine leukemia virus (MoMLV), another gammaretrovirus.
9 portant reservoirs of exogenous KoRV-related gammaretroviruses.
10 ntified as invariant among highly infectious gammaretroviruses.
11  by the polytropic host range group of mouse gammaretroviruses.
12  not previously reported for mouse ecotropic gammaretroviruses.
13 ning proteins similar to receptors for other gammaretroviruses.
14 se and RNase H domains groups ARTgagpol with gammaretroviruses.
15 ation near transcriptional start sites, like gammaretroviruses.
16 e residues are also conserved in the RSEs of gammaretroviruses.
17 entry mediated by Env proteins of delta- and gammaretroviruses.
18 roducer cells are superinfected with certain gammaretroviruses.
19 ions for the selection of antivirals against gammaretroviruses.
20 e LTR associated with increased pathology in gammaretroviruses.
21 sh endogenous retrovirus (ZFERV) between the Gammaretrovirus and Epsilonretrovirus genera.
22  postentry determinant of the host range for gammaretroviruses and lentiviruses and, more recently, s
23 onal relationships between the SUs of type C gammaretroviruses and lentiviruses.
24 stem to evaluate the in vivo spread of these gammaretroviruses and their disease potential in their n
25 nonprimate lentiviruses, a Betaretrovirus, a Gammaretrovirus, and the Alpharetrovirus Rous sarcoma vi
26                             Class I includes gammaretroviruses, and class II includes lentiviruses an
27 entiviruses, spumaviruses, betaretroviruses, gammaretroviruses, and other elements containing reverse
28  (Yescarta and Kymriah), and Strimvelis (the gammaretrovirus approved for adenosine deaminase-severe
29 NA transcripts, and RNA export mechanisms of gammaretroviruses are poorly characterized.
30                                    Beta- and gammaretroviruses are two types of simple retroviruses t
31                     Lentiviruses, unlike the gammaretroviruses, are able to infect nondividing cells
32 sequences and baboon endogenous virus type C gammaretrovirus (BaEV) sequences were induced by AzaC, w
33 rom adult killer whales and detected a novel gammaretrovirus by degenerate PCR.
34                  Nonspecific inactivation of gammaretroviruses by serum factors appears insufficient
35 mate lentiviruses are distinguished from the gammaretroviruses by their ability to infect nondividing
36           The 5'-untranslated regions of all gammaretroviruses contain a conserved "double-hairpin mo
37        The surface glycoprotein (SU) of most gammaretroviruses contains a conserved histidine at its
38         Here we report on a novel endogenous gammaretrovirus (CrERVgamma; for cervid endogenous gamma
39                                          For gammaretroviruses, CV-N inhibited entry mediated by some
40 rk, a series of INs from the Betaretrovirus, Gammaretrovirus, Deltaretrovirus, Spumavirus and Lentivi
41             Recently, a new endogenous koala gammaretrovirus, designated KoRV, was isolated from koal
42 o predicted nucleosome positions showed that gammaretroviruses direct integration into outward-facing
43  virus-related virus (XMRV) is a novel human gammaretrovirus discovered in association with human pro
44                              The env gene of gammaretroviruses encodes a glycoprotein conserved among
45                         We suggest that this gammaretrovirus entered the delphinoid ancestor's genome
46                   Here we show that pairs of gammaretrovirus envelope proteins (from Friend virus and
47 e been elucidated, with the exception of the gammaretrovirus family.
48 ine leukemia virus-related virus (XMRV) is a gammaretrovirus found in association with human prostate
49 tion, and from recent cross-species jumps of gammaretroviruses from rodents to primates and marsupial
50 est relatives of CrERVgamma being endogenous gammaretroviruses from sheep and pig.
51 virus, spumaretrovirus, alpharetrovirus, and gammaretrovirus genera, no members of the deltaretroviru
52 d identification of a previously undescribed gammaretrovirus genome, xenotropic murine leukemia virus
53 istribution, origin, and transmission of the Gammaretrovirus genus and associated class I ERVs.
54                                The mammalian gammaretroviruses gibbon ape leukemia virus (GALV) and f
55  shares 78% nucleotide identity with another gammaretrovirus, gibbon ape leukemia virus (GALV).
56      Like the primate lentivirus Nef and the gammaretrovirus glycoGag, the accessory protein from EIA
57 ein does not assemble in heteromers with the gammaretrovirus glycoproteins tested and does not affect
58 iently forms pseudotyped particles with many gammaretrovirus glycoproteins, such as Friend murine leu
59 urine leukemia virus-related virus (XMRV), a gammaretrovirus, has been isolated from human prostate c
60                                        While gammaretroviruses have well-characterized oncogenic effe
61                          A close relative of gammaretroviruses, HERV-T, circulated in primates for 25
62            These include the Hervey pteropid gammaretrovirus (HPG), identified in the scat of the Aus
63 viral mechanism of 5-aza-C between HIV-1 and gammaretroviruses - i.e., murine leukemia virus (MuLV) a
64 ia virus-related virus (XMRV) is a new human gammaretrovirus identified in prostate cancer tissue fro
65 p of koala retrovirus-related (KoRV-related) gammaretroviruses in Australian and Asian bats.
66 etrovirus (CrERVgamma; for cervid endogenous gammaretrovirus) in the mule deer (Odocoileus hemionus)
67 served cis-acting element in the pol gene of gammaretroviruses, including murine leukemia virus (MLV)
68 g) is an accessory protein expressed by most gammaretroviruses, including murine leukemia virus (MLV)
69                                          All gammaretroviruses, including murine leukemia viruses (Mu
70  basal promoter elements compared with other gammaretroviruses, including the presence of enhancer-li
71                                              Gammaretroviruses, including the subgroups A, B, and C o
72 d lymphoid progenitors in the bone marrow of gammaretrovirus-infected animals and thereby contribute
73 quence, which reveals many past epidemics of gammaretrovirus infection, and from recent cross-species
74 likely arose in conjunction with exposure to gammaretrovirus infections and coevolutionary adaptation
75  intermediately inhibited Betaretrovirus and Gammaretrovirus infections yet was basically ineffective
76 genome displays a rich fossil record of past gammaretrovirus infections, yet no current epidemic is e
77                                   The KoRV-A gammaretrovirus infects the soma and germline and is swe
78      These results document the diversity in gammaretroviruses isolated from globally distributedMuss
79 s gPr80gag is evolutionarily conserved among gammaretroviruses, its mechanism of action has been uncl
80 d in human prostate cancers and is the first gammaretrovirus known to infect humans.
81                    Although the endogenizing gammaretrovirus koala endogenous retrovirus (KoRV) was i
82 rovirus, Deltaretrovirus, Epsilonretrovirus, Gammaretrovirus, Lentivirus, and Spumavirus.
83  stem/progenitor cells compared to analogous gammaretrovirus/lentivirus vectors carrying the same enh
84  preference for nongenic regions compared to gammaretrovirus/lentivirus vectors.
85 er preference for nongenic integrations than gammaretroviruses/lentiviruses and preferential integrat
86 ial copackaging of homodimers in the case of gammaretroviruses, like murine leukemia virus (MLV), led
87 ine leukemia virus-related virus (XMRV) is a gammaretrovirus linked to prostate carcinoma and chronic
88   Infection with a recombinant murine-feline gammaretrovirus, MoFe2, or with the parent virus, Molone
89 ed HIV-1 infectivity, while infection by the gammaretrovirus Moloney murine leukemia virus (MLV) was
90 es of active genes, whereas the prototypical gammaretrovirus Moloney murine leukemia virus (MoMLV) fa
91 gh efficiency on virus replication using the gammaretrovirus MuLV as a model system.
92 that for cells chronically infected with the gammaretrovirus murine leukemia virus in which receptor
93 nodeficiency virus, and has no effect on the gammaretrovirus murine leukemia virus.
94 virus (FeLV) is a common naturally occurring gammaretrovirus of domestic cats that is associated with
95 than 100 patients with ADA-SCID who received gammaretrovirus- or lentivirus-mediated autologous hemat
96 ine leukemia virus-related virus (XMRV) is a gammaretrovirus originally identified in a subset of pro
97    CrERVgamma forms a distinct branch of the gammaretrovirus phylogeny, with the closest relatives of
98             The koala retrovirus (KoRV) is a gammaretrovirus present in both captive and wild koala c
99 Vs) are part of a larger group of pathogenic gammaretroviruses present across phylogenetically divers
100                                              Gammaretroviruses produce spliced Env mRNAs and unsplice
101 ine leukemia virus-related virus (XMRV) is a gammaretrovirus recently isolated from human prostate ca
102 s due to a nonpermissive variant of the XPR1 gammaretrovirus receptor, a resistance that also limits
103 rovides a plausible explanation for why most gammaretrovirus recombinants, although relatively rare,
104                                        These gammaretroviruses rely on the XPR1 receptor for entry, a
105 e mutation into feline and murine infectious gammaretroviruses resulted in a similar Env dysfunction.
106  are similar and reveal common principles of gammaretrovirus RNA genome packaging.
107 NA, but not RNA, containing novel endogenous gammaretrovirus sequences was detected in the JEV vaccin
108 cted as important overlooked facilitators of gammaretrovirus spread across diverse mammalian hosts.
109    Endogenous retroviruses (ERVs) of these 2 gammaretrovirus subtypes are largely segregated in diffe
110 on with FeLV.IMPORTANCE Domestic exposure to gammaretroviruses such as feline leukemia viruses (FeLVs
111 der of magnitude more frequently than simple gammaretroviruses such as murine leukemia virus and sple
112                                              Gammaretroviruses, such as murine leukemia virus (MLV),
113 sequence connecting the CA and NC domains in gammaretroviruses, such as murine leukemia virus (MLV),
114                                 For numerous gammaretroviruses, such as the gibbon ape leukemia virus
115                               Members of the gammaretroviruses--such as murine leukemia viruses (MLVs
116 ent articles have reported the presence of a gammaretrovirus, termed "XMRV" (xenotropic murine leukem
117 urine leukemia virus-related virus (XMRV), a gammaretrovirus that can infect human cells.
118 emia virus (FeLV) is a naturally transmitted gammaretrovirus that infects domestic cats.
119                                              Gammaretroviruses that enter cells via binding to a surf
120  viruses (XMVs and PMVs) are closely related gammaretroviruses that use the XPR1 receptor for entry.
121 dify the MLV CA to resemble those from other gammaretroviruses, the deletion mutants produced virions
122 mized HIV-1 Gag-Pol and envelope proteins of gammaretroviruses; these producer cells could make up to
123              The data obtained indicate that gammaretroviruses tolerate a substantial excess of viral
124                                       In the gammaretroviruses, typified by Moloney murine leukemia v
125           Thus, our results demonstrate that gammaretroviruses use NXF1 for the cytoplasmic accumulat
126 ing that two essentially unrelated beta- and gammaretroviruses use similar mechanisms to escape inhib
127 tion with cells transduced with an identical gammaretrovirus vector backbone expressing methylguanine
128                    Strong viral enhancers in gammaretrovirus vectors have caused cellular proto-oncog
129 mmunodeficiency virus type 1 (HIV-1) and the gammaretroviruses was previously reported, with the form
130 rine leukaemia virus-related virus (XMRV), a gammaretrovirus, was discovered in prostate cancer tumou
131              To extend this investigation to gammaretroviruses, we engineered a fluorescent Moloney m
132             In addition, we found that these gammaretroviruses were strongly (X-MLV) or partially (XM
133 ukemia virus (FeLV) is a member of the genus Gammaretrovirus, which causes malignant diseases in cats
134        KoRV represents a unique example of a gammaretrovirus whose envelope has evolved to allow for
135            Feline leukemia virus (FeLV) is a gammaretrovirus with horizontally transmitted and endoge
136  experimental evidence that XMRV is indeed a gammaretrovirus with protein composition and particle ul
137 versifying selection were detected among the gammaretroviruses with concentration in the env gene acr
138 monstrated only for nontransmissible variant gammaretroviruses with recombinant and mutant envelope g
139 matitis Indiana virus (VSV), lentiviruses or gammaretroviruses with their envelope proteins replaced
140                                      A novel gammaretrovirus, xenotropic murine leukemia virus-relate
141 CFS patients, we identified DNA from a human gammaretrovirus, xenotropic murine leukemia virus-relate
142 l. reported an association between the human gammaretrovirus XMRV and chronic fatigue syndrome.

 
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