Functional interaction between the HCMV IE2 transactivator and the retinoblastoma protein.
about
DNA end-independent activation of DNA-PK mediated via association with the DNA-binding protein C1DAutorepression of the human cytomegalovirus major immediate-early promoter/enhancer at late times of infection is mediated by the recruitment of chromatin remodeling enzymes by IE86Regulation of apoptosis by viral gene productsThe DNA damage response induced by infection with human cytomegalovirus and other virusesA family of Ran binding proteins that includes nucleoporinsCyclin A degradation by primate cytomegalovirus protein pUL21a counters its innate restriction of virus replication.Activation of transcription of the human cytomegalovirus early UL4 promoter by the Ets transcription factor binding element.Effects of human cytomegalovirus major immediate-early proteins in controlling the cell cycle and inhibiting apoptosis: studies with ts13 cellsDisruption of PML subnuclear domains by the acidic IE1 protein of human cytomegalovirus is mediated through interaction with PML and may modulate a RING finger-dependent cryptic transactivator function of PMLInhibition of cell division by the human cytomegalovirus IE86 protein: role of the p53 pathway or cyclin-dependent kinase 1/cyclin B1.Phosphorylation of the human cytomegalovirus 86-kilodalton immediate-early protein IE2.Activation of the mitogen-activated protein kinase p38 by human cytomegalovirus infection through two distinct pathways: a novel mechanism for activation of p38.Covalent modification of the transactivator protein IE2-p86 of human cytomegalovirus by conjugation to the ubiquitin-homologous proteins SUMO-1 and hSMT3b.The human cytomegalovirus IE86 protein can block cell cycle progression after inducing transition into the S phase of permissive cells.Role of human cytomegalovirus immediate-early proteins in cell growth control.Herpesvirus lytic replication and the cell cycle: arresting new developmentsEvaluation of interactions of human cytomegalovirus immediate-early IE2 regulatory protein with small ubiquitin-like modifiers and their conjugation enzyme Ubc9An epistatic relationship between the viral protein kinase UL97 and the UL133-UL138 latency locus during the human cytomegalovirus lytic cycle.An E2F1-mediated DNA damage response contributes to the replication of human cytomegalovirus.Human cytomegalovirus IE1-72 activates ataxia telangiectasia mutated kinase and a p53/p21-mediated growth arrest responseEffect of the human cytomegalovirus IE86 protein on expression of E2F-responsive genes: a DNA microarray analysis.Role of noncovalent SUMO binding by the human cytomegalovirus IE2 transactivator in lytic growth.Low levels of Human Cytomegalovirus Infection in Glioblastoma multiforme associates with patient survival; -a case-control study.Depletion of cellular pre-replication complex factors results in increased human cytomegalovirus DNA replication.The cellular protein MCM3AP is required for inhibition of cellular DNA synthesis by the IE86 protein of human cytomegalovirusAlternative splicing of the human cytomegalovirus major immediate-early genes affects infectious-virus replication and control of cellular cyclin-dependent kinase.Inhibition of cellular DNA synthesis by the human cytomegalovirus IE86 protein is necessary for efficient virus replication.High prevalence of human cytomegalovirus proteins and nucleic acids in primary breast cancer and metastatic sentinel lymph nodes.The salivary secretome of the tsetse fly Glossina pallidipes (Diptera: Glossinidae) infected by salivary gland hypertrophy virus.Cytomegalovirus infection induces high levels of cyclins, phosphorylated Rb, and p53, leading to cell cycle arrest.Activation of the Epstein-Barr virus DNA polymerase promoter by the BRLF1 immediate-early protein is mediated through USF and E2F.The IE2 regulatory protein of human cytomegalovirus induces expression of the human transforming growth factor beta1 gene through an Egr-1 binding site.The human cytomegalovirus IE1-72 protein interacts with the cellular p107 protein and relieves p107-mediated transcriptional repression of an E2F-responsive promoter.The major immediate-early proteins IE1 and IE2 of human cytomegalovirus colocalize with and disrupt PML-associated nuclear bodies at very early times in infected permissive cells.Human cytomegalovirus IE2 86-kilodalton protein binds p53 but does not abrogate G1 checkpoint function.TAF-like functions of human cytomegalovirus immediate-early proteinsHuman cytomegalovirus immediate early interaction with host nuclear structures: definition of an immediate transcript environment.Deficiencies in Cellular Processes Modulated by the Retinoblastoma Protein Do Not Account for Reduced Human Cytomegalovirus Replication in Its AbsenceRole of p16/MTS1, cyclin D1 and RB in primary oral cancer and oral cancer cell linesCell cycle-independent expression of immediate-early gene 3 results in G1 and G2 arrest in murine cytomegalovirus-infected cells.
P2860
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P2860
Functional interaction between the HCMV IE2 transactivator and the retinoblastoma protein.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
1994年學術文章
@zh
1994年學術文章
@zh-hant
name
Functional interaction between ...... nd the retinoblastoma protein.
@en
type
label
Functional interaction between ...... nd the retinoblastoma protein.
@en
prefLabel
Functional interaction between ...... nd the retinoblastoma protein.
@en
P2093
P2860
P1433
P1476
Functional interaction between the HCMV IE2 transactivator and the retinoblastoma protein
@en
P2093
C Hagemeier
G Hayhurst
J Sinclair
T Kouzarides
P2860
P304
P356
10.1002/J.1460-2075.1994.TB06584.X
P407
P577
1994-06-01T00:00:00Z