The Human Papillomavirus E6 Oncoprotein Targets USP15 and TRIM25 To Suppress RIG-I-Mediated Innate Immune Signaling

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Manipulation of the innate immune response by human papillomaviruses

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Evasion of host immune defenses by human papillomavirus

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RIG-I-Mediated STING Upregulation Restricts Herpes Simplex Virus 1 Infection

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High-Risk Human Papillomavirus E7 Proteins Target PTPN14 for Degradation

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TRIM25 blockade by RNA interference inhibited migration and invasion of gastric cancer cells through TGF-β signaling

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Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway

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CRISPR/Cas9-Mediated Genome Editing of Herpesviruses Limits Productive and Latent Infections

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Pathogenesis of human papillomavirus-associated mucosal disease

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TRIM25 has a dual function in the p53/Mdm2 circuit

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DNA tumor virus oncogenes antagonize the cGAS-STING DNA-sensing pathway

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Genus Beta Human Papillomavirus E6 Proteins Vary in Their Effects on the Transactivation of p53 Target Genes

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Antiviral immunity via RIG-I-mediated recognition of RNA bearing 5′-diphosphates

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Structural basis for ubiquitin-mediated antiviral signal activation by RIG-I

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The Ubiquitin-Specific Protease USP15 Promotes RIG-I-Mediated Antiviral Signaling by Deubiquitylating TRIM25

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HPV16-E7 Expression in Squamous Epithelium Creates a Local Immune Suppressive Environment via CCL2- and CCL5- Mediated Recruitment of Mast Cells

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Cytosolic Sensing of Viruses

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Papillomavirus E6 oncoproteins

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Human Papillomavirus (HPV) Upregulates the Cellular Deubiquitinase UCHL1 to Suppress the Keratinocyte's Innate Immune Response

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Ubiquitin-Induced Oligomerization of the RNA Sensors RIG-I and MDA5 Activates Antiviral Innate Immune Response

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Activation of Cap-Dependent Translation by Mucosal Human Papillomavirus E6 Proteins Is Dependent on the Integrity of the LXXLL Binding Motif

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Comprehensive Analysis of Host Cellular Interactions with Human Papillomavirus E6 Proteins Identifies New E6 Binding Partners and Reflects Viral Diversity

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Systematic identification of interactions between host cell proteins and E7 oncoproteins from diverse human papillomaviruses

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High-Risk Human Papillomaviruses Repress Constitutive Kappa Interferon Transcription via E6 To Prevent Pathogen Recognition Receptor and Antiviral-Gene Expression

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Human Papillomavirus Deregulates the Response of a Cellular Network Comprising of Chemotactic and Proinflammatory Genes

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Cross-Neutralization Potential of Native Human Papillomavirus N-Terminal L2 Epitopes

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Differentiation-Dependent Interpentameric Disulfide Bond Stabilizes Native Human Papillomavirus Type 16

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Pattern Recognition Receptors and Inflammation

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Phosphorylation-Mediated Negative Regulation of RIG-I Antiviral Activity

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RNA Polymerase III Detects Cytosolic DNA and Induces Type I Interferons through the RIG-I Pathway

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Human Papillomaviruses and the Interferon Response

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The Ubiquitin-Specific Peptidase USP15 Regulates Human Papillomavirus Type 16 E6 Protein Stability

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Tissue-Spanning Redox Gradient-Dependent Assembly of Native Human Papillomavirus Type 16 Virions

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RIG-I-dependent sensing of poly(dA:dT) through the induction of an RNA polymerase III–transcribed RNA intermediate

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Herpes simplex virus infection is sensed by both Toll-like receptors and retinoic acid-inducible gene- like receptors, which synergize to induce type I interferon production

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Roles of RIG-I N-terminal tandem CARD and splice variant in TRIM25-mediated antiviral signal transduction

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