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1  intasome to distinguish it from the greater preintegration complex.
2 f the karyophilic MA into the viral core and preintegration complex.
3 involved in the nuclear translocation of the preintegration complex.
4  infected cells as part of the nucleoprotein/preintegration complex.
5 y gain access to viral proteins of the HIV-1 preintegration complex.
6 n gain access to viral proteins of the HIV-1 preintegration complex.
7  viral DNA integration activity of the HIV-1 preintegration complex.
8 y, and shares properties associated with the preintegration complex.
9 irements for retrograde transport of the MLV preintegration complex.
10 ient to account for its association with the preintegration complex.
11 ransient intermediate within the cytoplasmic preintegration complex.
12  process of nuclear translocation of the HIV preintegration complex.
13 ing infectivity for nuclear targeting of the preintegration complex.
14  plays a role in nuclear import of the viral preintegration complex.
15 ecessary for efficient nuclear import of the preintegration complex.
16 estigate the nuclear import of the HIV-2/SIV preintegration complex.
17 of Vpx in nuclear translocation of the viral preintegration complex.
18  human immunodeficiency virus type I (HIV-I) preintegration complexes.
19 ive intasome structure detected in wild-type preintegration complexes.
20 rganization of Moloney murine leukemia virus preintegration complexes.
21 tegrase and the viral DNA ends in functional preintegration complexes.
22 for such inhibitors in assays using isolated preintegration complexes.
23 diated blockade of productive infection from preintegration complexes.
24 ed in the nuclear localization of retroviral preintegration complexes.
25 icate that HMG I(Y) is associated with MoMLV preintegration complexes.
26 grase (IN) is the catalytic component of the preintegration complex, a large nucleoprotein assembly c
27 etroviral DNA integration is mediated by the preintegration complex, a large nucleoprotein complex de
28 RK1 and -2 appear to phosphorylate the HIV-1 preintegration complex, a step necessary for nuclear tra
29 1 has been implicated in import of the viral preintegration complex across the nuclear pore complex (
30 ulted in a decrease in nuclear import of the preintegration complex and attenuated replication in mac
31 ct capsid; and that interactions between the preintegration complex and LEDGF/p75, and possibly other
32 would facilitate nuclear import of the viral preintegration complex and transduction of quiescent cel
33 pecific antigen (Gag) is associated with the preintegration complex, and mutants of p12 (PM14) show d
34 nscription and nuclear transfer of the viral preintegration complex are observed.
35 tion and subcellular trafficking of subviral preintegration complexes are reported to vary among the
36          Once inside the nucleus, lentiviral preintegration complexes are thought to attach to the ch
37 ssociation of BAF from retroviral DNA within preintegration complexes as monitored by functional assa
38                     Nuclear targeting of the preintegration complex by an IN NLS may prove to be a ge
39  inhibits nuclear targeting of HIV-1-derived preintegration complexes by inactivating the nuclear loc
40 ested HeLa cells, indicating that the mutant preintegration complexes can enter the nuclei of both di
41 alization, participation in transport of the preintegration complex, cation channel activity, oligome
42 itate the study of the roles of IN and other preintegration complex components in preintegration phas
43  operations are executed by individual viral preintegration complexes deep within cells.
44 r DCTN2/p50/dynamitin interacts with the MLV preintegration complex early in infection, suggesting a
45                                              Preintegration complexes extracted from knockout cells m
46                                 Further, the preintegration complexes extracted from the cytoplasm of
47  of sufficient quantities of the cytoplasmic preintegration complexes for biochemical and biophysical
48 , which is equivalent to isolated retrovirus preintegration complexes for full-site integration activ
49 -1) replication is the movement of the viral preintegration complex from the cytoplasm into the nucle
50                                  We prepared preintegration complexes from cells infected with these
51 Vpr regulates nuclear transport of the viral preintegration complex, G(2) cell cycle arrest, and tran
52 ocess by which the avian sarcoma virus (ASV) preintegration complex gains access to target chromatin
53                       Here, we show that the preintegration complex (i.e., the excised transposon) is
54 mbrane, envelope incorporation into virions, preintegration complex import into the nucleus, and nucl
55 port cargoes, the driving force behind HIV-1 preintegration complex import is likely a gradient of th
56 rticipates in nuclear targeting of the viral preintegration complex in nondividing cells and induces
57 py allow three-dimensional analysis of HIV-1 preintegration complexes in the nuclei of infected cells
58 ed with MLV and HIV-1 in vivo and with their preintegration complexes in vitro.
59 tations demonstrate that in vivo, within the preintegration complex, IN performs a central role in co
60           Vpr mediates nuclear import of the preintegration complex, induces host cell apoptosis, and
61 peat, participation in the nuclear import of preintegration complexes, induction of G2 arrest, and in
62              BAF also facilitates retroviral preintegration complex insertion into target DNA in vitr
63 rmitting the translocation of the retroviral preintegration complex into the nucleus and enabling int
64 ription, DNA synthesis, and translocation of preintegration complex into the nucleus in cord and adul
65                         The transport of the preintegration complex into the nucleus is cell cycle-in
66   A model in which TRN-SR2 imports the viral preintegration complex into the nucleus is supported by
67 ls depends critically on import of the viral preintegration complex into the nucleus.
68 ng the role of integrase in transport of the preintegration complex into the nucleus.
69                       The transport of virus preintegration complexes into the nucleus in primary mac
70  cells such as macrophages because the viral preintegration complex is able to actively traverse the
71  and GLFG Nups and that nuclear entry of the preintegration complex is further promoted by nuclear lo
72  that the impairment of nuclear transport of preintegration complexes is responsible for the restrict
73 lex in retrovirus-infected cells, termed the preintegration complex, is responsible for the concerted
74  us to analyze the structure and function of preintegration complexes isolated from cells infected wi
75 Previous transposon-mediated footprinting of preintegration complexes isolated from infected cells re
76 outhern blotting of S1 nuclease-digested FIV preintegration complexes isolated from infected cells, w
77 tions between a gypsy provirus and the gypsy preintegration complex may also participate in the proce
78 NA flap does not play a major role in either preintegration complex nuclear import or HIV-1 replicati
79                            We found that the preintegration complex of murine leukemia virus (MLV) in
80  These ruptures are sufficient to enable the preintegration complexes of invading virions to enter th
81 reverse transcription, nuclear import of the preintegration complex, or viral DNA integration, sugges
82                                          The preintegration complex (PIC) containing the viral DNA, t
83 ne breakdown during cell division, the HIV-1 preintegration complex (PIC) enters the nucleus by trave
84 uired for nuclear translocation of the viral preintegration complex (PIC) in quiescent cells.
85  human immunodeficiency virus type 1 (HIV-1) preintegration complex (PIC) is essential for the produc
86 eficiency virus type 1 (HIV-1) infection and preintegration complex (PIC) nuclear import.
87  reverse transcription is a component of the preintegration complex (PIC) that also contains the vira
88 ion, the retroviral genome is contained in a preintegration complex (PIC) that mediates its integrati
89      However, integration requires the viral preintegration complex (PIC) to overcome the structural
90 LV) p12, encoded within Gag, binds the viral preintegration complex (PIC) to the mitotic chromatin.
91 gate the role of Vpr in docking of the HIV-1 preintegration complex (PIC) to the nuclear pore complex
92      Retroviral integration is mediated by a preintegration complex (PIC) which contains the viral DN
93 rse transcription complex and later with the preintegration complex (PIC), allowing it to reach and e
94 kemia virus (MLV) Gag is associated with the preintegration complex (PIC), and mutants of p12 (PM14)
95 ffects of CPSF6 on the activity of the HIV-1 preintegration complex (PIC)-the sub-viral machinery tha
96 by a large nucleoprotein complex, termed the preintegration complex (PIC).
97 integrated into chromosomal hot spots by the preintegration complex (PIC).
98 IN) is implicated in nuclear import of HIV-1 preintegration complex (PIC).
99 ells due to the active nuclear import of its preintegration complex (PIC).
100 g in an inability to form a functional viral preintegration complex (PIC).
101                                   Retrovirus preintegration complexes (PIC) in virus-infected cells c
102                                   Retrovirus preintegration complexes (PIC) purified from virus-infec
103 N) into the host genome occurs via assembled preintegration complexes (PIC).
104 ecular-weight nucleoprotein complexes termed preintegration complexes (PIC).
105                                        These preintegration complexes (PICs) can direct integration o
106 ion, it is possible to lyse cells and obtain preintegration complexes (PICs) capable of integrating t
107 etroviral integration in vivo is mediated by preintegration complexes (PICs) derived from infectious
108 sessed the integration activity of the HIV-1 preintegration complexes (PICs) extracted from acutely i
109                                 Accordingly, preintegration complexes (PICs) extracted from TREX1-ove
110 r of viral factors that are present in HIV-1 preintegration complexes (PICs) have been assigned funct
111 proteins and examined their association with preintegration complexes (PICs) in infected cells.
112 own to aid the nuclear localization of viral preintegration complexes (PICs) in infected cells.
113 t protein is important for function of HIV-1 preintegration complexes (PICs) in vitro.
114 arly reduced the efficiency with which HIV-1 preintegration complexes (PICs) integrated into a target
115 are actively dividing, and nuclear import of preintegration complexes (PICs) is not required for infe
116 upled with the biochemical analysis of HIV-1 preintegration complexes (PICs) isolated from acutely in
117 A nonspecifically and is a host component of preintegration complexes (PICs) isolated from cells infe
118 rted that HMG I(Y) cofractionates with HIV-1 preintegration complexes (PICs) isolated from freshly in
119  vitro on purified integrase and on subviral preintegration complexes (PICs) isolated from lymphoid c
120                                              Preintegration complexes (PICs) mediate retroviral integ
121 ave established an assay for the function of preintegration complexes (PICs) of human immunodeficienc
122             In vitro integration assays with preintegration complexes (PICs) showed that endogenous L
123                                              Preintegration complexes (PICs) stripped of BAF lose the
124  and U5 ends of viral cDNA or by using viral preintegration complexes (PICs) that form during virus i
125 t factors to facilitate the passage of their preintegration complexes (PICs) through nuclear pore com
126 growth factor (LEDGF/p75) tethers lentiviral preintegration complexes (PICs) to chromatin and is esse
127  Retroviral integration is mediated by viral preintegration complexes (PICs), and human immunodeficie
128  human immunodeficiency virus type 1 (HIV-1) preintegration complexes (PICs), the large nucleoprotein
129 interaction stimulates the activity of HIV-1 preintegration complexes (PICs).
130  integrases (INs) function in the context of preintegration complexes (PICs).
131 ll cycle arrest, apoptosis, translocation of preintegration complex, potentiation of glucocorticoid a
132 ns in mitotic nuclear reassembly, retroviral preintegration complex stability, and transcriptional re
133 ome during maturation, and uncoat to release preintegration complexes that archive a double-stranded
134 s with the ability to mature into functional preintegration complexes that can proceed to provirus es
135 v1 gene product and a component of the viral preintegration complex, the capsid protein CA.
136 rocess of nuclear translocation of the viral preintegration complex, thus facilitating HIV-1 replicat
137  and LEDGF/p75 in the targeting of the viral preintegration complex to gene-dense regions of chromati
138 ociate from the viral membrane to direct the preintegration complex to the host-cell nucleus.
139 gnal that promotes localization of the viral preintegration complex to the nucleus of non-dividing ce
140  transcription but prior to migration of the preintegration complex to the nucleus.
141 hitecture remain intact upon delivery of the preintegration complex to the nucleus.
142  a cellular factor that binds IN and tethers preintegration complexes to chromatin before integration
143 g that binds HIV-1 capsid and connects HIV-1 preintegration complexes to intranuclear trafficking pat
144 ey molecular interactions that specify HIV-1 preintegration complex trafficking to active chromatin.
145     Cell fractionation showed that the viral preintegration complex was present in a form that could
146  reverse transcription and nuclear import of preintegration complexes, we found that memory, but not
147                                              Preintegration complexes were partially purified from ce
148 rase-binding domain interacts with the viral preintegration complex, whereas the N-terminal PWWP doma
149 chromosome, can suffice to connect the HIV-1 preintegration complex with the cell nuclear import mach

 
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