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2 ering 100% of the genome; contributions from xenotropic and polytropic ERVs differentially alter the
5 rential susceptibilities of mouse strains to xenotropic and polytropic murine leukemia viruses (X-MLV
12 onsistent with observed interference between xenotropic and polytropic viruses in some cell types.
15 shown that B10 xenotropic virus 1 (Bxv1), a xenotropic endogenous murine leukemia virus (MuLV), is p
16 these resistance genes control expression of xenotropic env glycoprotein that interferes with exogeno
17 La cell RNA that conferred susceptibility to xenotropic envelope protein binding and virus infection
18 ed to divide with KGF, high-titer ampho- and xenotropic enveloped vectors preferentially infected cel
19 Six MLVs show close relationships to a small xenotropic ERV subgroup largely confined to the inbred m
20 cells, displayed either no or extremely weak xenotropic helper activity toward MuLV-based retrovector
21 y polytropic/MCF and also by closely related xenotropic MLV has been mapped to Rmc1 on mouse chromoso
23 stablishes infectivity by MCF MLV as well as xenotropic MLV, which do not infect laboratory mice.
24 with unique U3 structures demonstrated that xenotropic MLV-related proviruses were present only in M
25 Murine leukemia viruses (MLVs), including xenotropic-MLV-related virus (XMRV), have been controver
29 atures of phylogenetic intermediates linking xenotropic MLVs to the polytropic and modified polytropi
30 ly poorly conserved even among ecotropic and xenotropic MLVs, it was also fully sufficient for the re
32 mouse strains carry endogenous copies of the xenotropic mouse leukemia viruses (X-MLVs), named for th
33 nce M. castaneus contains multiple copies of xenotropic MuLV env genes, we suggest that these resista
35 Rmc1, the gene encoding the receptor for MCF/xenotropic MuLVs, suggesting that resistance is mediated
38 ) receptor variant nonpermissive to XMRV and xenotropic murine leukemia virus (X-MLV) infection, sugg
39 leukemia viruses (MLVs), most notably XMRV [xenotropic murine leukemia virus (X-MLV)-related virus--
40 s, including murine leukemia virus (MLV) and xenotropic murine leukemia virus (XMRV), named the CAE (
41 nes for the RD114 cat endogenous retrovirus, xenotropic murine leukemia virus, and type C feline leuk
42 of PERV-C (a virus without human tropism) by xenotropic murine leukemia virus, rather than to de novo
52 re are questions regarding the prevalence of xenotropic murine leukemia virus-related virus (XMRV) in
62 immunodeficiency virus type-1 (HIV-1) and of xenotropic murine leukemia virus-related virus (XMRV), a
63 kemia virus (MLV)-based retroviral vector or xenotropic murine leukemia virus-related virus (XMRV), a
66 identified DNA from a human gammaretrovirus, xenotropic murine leukemia virus-related virus (XMRV), i
67 eviously undescribed gammaretrovirus genome, xenotropic murine leukemia virus-related virus (XMRV), i
69 ral analysis of authentic genomic RNA of the xenotropic murine leukemia virus-related virus (XMRV).
70 lls infected with the human retrovirus XMRV (xenotropic murine leukemia virus-related virus) can indu
72 resence of a gammaretrovirus, termed "XMRV" (xenotropic murine leukemia virus-related virus) in prost
75 rting to show that a retrovirus called XMRV (xenotropic murine leukemia virus-related virus) was pres
76 present in many copies in the mouse genome, xenotropic murine leukemia viruses cannot infect cells f
78 fatigue syndrome (CFS) harbor a retrovirus, xenotropic murine leukemia-related virus (XMRV), in bloo
79 lies the development of prostate cancer, and xenotropic murine leukemia-related virus is a candidate
80 ogic characterization of a novel retrovirus, xenotropic murine leukemia-related virus, isolated and c
82 infected by NZB-XMV(New Zealand Black mouse xenotropic murine virus)-enveloped vectors, expressing a
85 l G-protein-coupled receptor (GPCR) and that xenotropic or polytropic retrovirus binding can disrupt
86 ent receptors for cell entry: the ecotropic, xenotropic, polytropic, amphotropic, 10A1, and Mus dunni
87 ry strains contain proviral env genes of the xenotropic/polytropic subgroup of mouse leukemia viruses
88 ity toward MuLV-based retrovectors, although xenotropic retrovirus sequences and transcripts were det
89 ctors, expressing an envelope derived from a xenotropic retrovirus that, like XMRV, employs Xpr1 as a
90 oblasts only if the RBD was deleted from the xenotropic viral envelope and the soluble RBD from ecotr
93 lope proteins (from Friend virus and GALV or xenotropic viruses) assemble into heteromers when coexpr
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