Pages that link to "Q36627034"
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The following pages link to RNA polymerase II is aberrantly phosphorylated and localized to viral replication compartments following herpes simplex virus infection (Q36627034):
Displayed 50 items.
- Herpes simplex virus 1 regulatory protein ICP22 interacts with a new cell cycle-regulated factor and accumulates in a cell cycle-dependent fashion in infected cells. (Q22003919) (← links)
- A novel cellular protein, p60, interacting with both herpes simplex virus 1 regulatory proteins ICP22 and ICP0 is modified in a cell-type-specific manner and Is recruited to the nucleus after infection (Q22009164) (← links)
- Functional anatomy of herpes simplex virus 1 overlapping genes encoding infected-cell protein 22 and US1.5 protein (Q24517275) (← links)
- Association of herpes simplex virus type 1 ICP8 and ICP27 proteins with cellular RNA polymerase II holoenzyme (Q24537648) (← links)
- Lentivirus Tat proteins specifically associate with a cellular protein kinase, TAK, that hyperphosphorylates the carboxyl-terminal domain of the large subunit of RNA polymerase II: candidate for a Tat cofactor (Q24676286) (← links)
- P-TEFb goes viral (Q26741360) (← links)
- Shutoff of Host Gene Expression in Influenza A Virus and Herpesviruses: Similar Mechanisms and Common Themes (Q26752361) (← links)
- Recruitment of cellular recombination and repair proteins to sites of herpes simplex virus type 1 DNA replication is dependent on the composition of viral proteins within prereplicative sites and correlates with the induction of the DNA damage respo (Q33201426) (← links)
- Proteomics of herpes simplex virus replication compartments: association of cellular DNA replication, repair, recombination, and chromatin remodeling proteins with ICP8. (Q33202888) (← links)
- Hsc70 focus formation at the periphery of HSV-1 transcription sites requires ICP27. (Q33317262) (← links)
- A dominant-negative herpesvirus protein inhibits intranuclear targeting of viral proteins: effects on DNA replication and late gene expression (Q33603607) (← links)
- ICP27 phosphorylation site mutants are defective in herpes simplex virus 1 replication and gene expression (Q33648884) (← links)
- Transcription of herpes simplex virus immediate-early and early genes is inhibited by roscovitine, an inhibitor specific for cellular cyclin-dependent kinases (Q33653316) (← links)
- Role of herpes simplex virus 1 immediate early protein ICP22 in viral nuclear egress (Q33744046) (← links)
- Requirement for cellular cyclin-dependent kinases in herpes simplex virus replication and transcription (Q33785061) (← links)
- The PK domain of the large subunit of herpes simplex virus type 2 ribonucleotide reductase (ICP10) is required for immediate-early gene expression and virus growth (Q33785400) (← links)
- Analysis of HCF, the cellular cofactor of VP16, in herpes simplex virus-infected cells (Q33794386) (← links)
- The conserved carboxyl-terminal half of herpes simplex virus type 1 regulatory protein ICP27 is dispensable for viral growth in the presence of compensatory mutations (Q33809511) (← links)
- ICP22 and the UL13 protein kinase are both required for herpes simplex virus-induced modification of the large subunit of RNA polymerase II. (Q33815308) (← links)
- Herpes simplex virus 1 regulatory protein ICP27 undergoes a head-to-tail intramolecular interaction (Q33826787) (← links)
- Posttranslational processing of infected cell protein 22 mediated by viral protein kinases is sensitive to amino acid substitutions at distant sites and can be cell-type specific (Q33827113) (← links)
- RNA polymerase II holoenzyme modifications accompany transcription reprogramming in herpes simplex virus type 1-infected cells (Q33846934) (← links)
- Herpes simplex virus type 1 infection leads to loss of serine-2 phosphorylation on the carboxyl-terminal domain of RNA polymerase II. (Q33930346) (← links)
- Dissection of a novel nuclear localization signal in open reading frame 29 of varicella-zoster virus (Q34045683) (← links)
- Nuclear translocation and carboxyl-terminal domain phosphorylation of RNA polymerase II delineate the two phases of zygotic gene activation in mammalian embryos (Q34250244) (← links)
- Mapping of functional regions in the amino-terminal portion of the herpes simplex virus ICP27 regulatory protein: importance of the leucine-rich nuclear export signal and RGG Box RNA-binding domain (Q34359278) (← links)
- ICP27 interacts with the C-terminal domain of RNA polymerase II and facilitates its recruitment to herpes simplex virus 1 transcription sites, where it undergoes proteasomal degradation during infection (Q34545620) (← links)
- The ICP22 protein selectively modifies the transcription of different kinetic classes of pseudorabies virus genes. (Q34566922) (← links)
- Heat-shock inactivation of the TFIIH-associated kinase and change in the phosphorylation sites on the C-terminal domain of RNA polymerase II. (Q34626147) (← links)
- Schizophrenia susceptibility genes directly implicated in the life cycles of pathogens: cytomegalovirus, influenza, herpes simplex, rubella, and Toxoplasma gondii. (Q34786420) (← links)
- Herpesviral replication compartments move and coalesce at nuclear speckles to enhance export of viral late mRNA. (Q35008429) (← links)
- HSV-1 Cgal+ infection promotes quaking RNA binding protein production and induces nuclear-cytoplasmic shuttling of quaking I-5 isoform in human hepatoma cells (Q35026933) (← links)
- Inhibition of cdk9 during herpes simplex virus 1 infection impedes viral transcription (Q35036881) (← links)
- Herpes simplex virus virion host shutoff protein: immune evasion mediated by a viral RNase? (Q35543196) (← links)
- Intracellular localization of the herpes simplex virus type 1 major transcriptional regulatory protein, ICP4, is affected by ICP27 (Q35828561) (← links)
- Herpes simplex virus immediate-early protein ICP22 is required for viral modification of host RNA polymerase II and establishment of the normal viral transcription program (Q35845807) (← links)
- Functional interactions between herpes simplex virus immediate-early proteins during infection: gene expression as a consequence of ICP27 and different domains of ICP4 (Q35845959) (← links)
- Herpes simplex virus immediate-early protein ICP22 triggers loss of serine 2-phosphorylated RNA polymerase II (Q35857527) (← links)
- Identification and characterization of a filament-associated protein encoded by Amsacta moorei entomopoxvirus (Q35859700) (← links)
- Repression of the alpha0 gene by ICP4 during a productive herpes simplex virus infection (Q35861084) (← links)
- Overexpression of the herpes simplex virus type 1 immediate-early regulatory protein, ICP27, is responsible for the aberrant localization of ICP0 and mutant forms of ICP4 in ICP4 mutant virus-infected cells (Q35866195) (← links)
- Attenuation of DNA-dependent protein kinase activity and its catalytic subunit by the herpes simplex virus type 1 transactivator ICP0. (Q35871672) (← links)
- Association of herpes simplex virus regulatory protein ICP22 with transcriptional complexes containing EAP, ICP4, RNA polymerase II, and viral DNA requires posttranslational modification by the U(L)13 proteinkinase. (Q35876535) (← links)
- Repression of host RNA polymerase II transcription by herpes simplex virus type 1 (Q35878134) (← links)
- Mutational analysis of the herpes simplex virus type 1 ICP0 C3HC4 zinc ring finger reveals a requirement for ICP0 in the expression of the essential alpha27 gene. (Q35898699) (← links)
- Casein kinase II specifically nucleotidylylates in vitro the amino acid sequence of the protein encoded by the alpha 22 gene of herpes simplex virus 1. (Q35944280) (← links)
- Mitotic transcription repression in vivo in the absence of nucleosomal chromatin condensation (Q36342523) (← links)
- Transcription-dependent redistribution of the large subunit of RNA polymerase II to discrete nuclear domains (Q36382489) (← links)
- The full-length protein encoded by human cytomegalovirus gene UL117 is required for the proper maturation of viral replication compartments (Q36498138) (← links)
- Probing the nuclear import signal and nuclear transport molecular determinants of PRV ICP22 (Q36503728) (← links)