Viral apoptosis is induced by IRF-3-mediated activation of Bax
about
Intracellular events and cell fate in filovirus infectionIRF7: activation, regulation, modification and functionFunction and regulation of retinoic acid-inducible gene-IdsRNA-activation of TLR3 and RLR signaling: gene induction-dependent and independent effectsInterplay between Inflammation and Cellular Stress Triggered by Flaviviridae VirusesNorovirus regulation of the innate immune response and apoptosis occurs via the product of the alternative open reading frame 4Structural basis of RNA recognition and activation by innate immune receptor RIG-IDifferential Protein Distribution between the Nucleus and Mitochondria: Implications in AgingA drug screening method based on the autophagy pathway and studies of the mechanism of evodiamine against influenza A virusInduction of interferon-stimulated genes by IRF3 promotes replication of Toxoplasma gondiiThe transcription factor IRF3 triggers "defensive suicide" necrosis in response to viral and bacterial pathogensThe influenza A virus protein PB1-F2: killing two birds with one stone?A TRIF-independent branch of TLR3 signaling.RIG-I enhanced interferon independent apoptosis upon Junin virus infection.Interplay between innate immunity and negative-strand RNA viruses: towards a rational modelThe ISG56/IFIT1 gene family.Sendai virus pathogenesis in mice is prevented by Ifit2 and exacerbated by interferon.Porcine sapovirus replication is restricted by the type I interferon response in cell culture.Distinct roles for the NF-kappa B RelA subunit during antiviral innate immune responses.The IRF-3/Bax-mediated apoptotic pathway, activated by viral cytoplasmic RNA and DNA, inhibits virus replication.The proapoptotic Bcl-2 protein Bax plays an important role in the pathogenesis of reovirus encephalitisPhosphatidylinositol 3-kinase signaling delays sendai virus-induced apoptosis by preventing XIAP degradation.The pestivirus N terminal protease N(pro) redistributes to mitochondria and peroxisomes suggesting new sites for regulation of IRF3 by N(pro.).Transfected poly(I:C) activates different dsRNA receptors, leading to apoptosis or immunoadjuvant response in androgen-independent prostate cancer cellsIRF3 polymorphisms induce different innate anti-Theiler's virus immune responses in RAW264.7 macrophages.The ribonucleotide reductase R1 subunits of herpes simplex virus 1 and 2 protect cells against poly(I · C)-induced apoptosisCell death regulation during influenza A virus infection by matrix (M1) protein: a model of viral control over the cellular survival pathwayInterferon regulatory transcription factor 3 protects mice from uterine horn pathology during Chlamydia muridarum genital infectionCaspase-8-mediated cleavage inhibits IRF-3 protein by facilitating its proteasome-mediated degradationTom70 mediates Sendai virus-induced apoptosis on mitochondria.TLR3 engagement induces IRF-3-dependent apoptosis in androgen-sensitive prostate cancer cells and inhibits tumour growth in vivo.The Fox and the Rabbits-Environmental Variables and Population Genetics (1) Replication Problems in Association Studies and the Untapped Power of GWAS (2) Vitamin A Deficiency, Herpes Simplex Reactivation and Other Causes of Alzheimer's DiseaseLymphocytic Choriomeningitis Virus Differentially Affects the Virus-Induced Type I Interferon Response and Mitochondrial Apoptosis Mediated by RIG-I/MAVS.RNase L Cleavage Products Promote Switch from Autophagy to Apoptosis by Caspase-Mediated Cleavage of Beclin-1.Genetic Variation of Goat Interferon Regulatory Factor 3 Gene and Its Implication in Goat Evolution.EGFR kinase activity is required for TLR4 signaling and the septic shock response.IPS-1 differentially induces TRAIL, BCL2, BIRC3 and PRKCE in type I interferons-dependent and -independent anticancer activity.Role of interferon regulatory factor 3-mediated apoptosis in the establishment and maintenance of persistent infection by Sendai virusTLR3, TRIF, and caspase 8 determine double-stranded RNA-induced epithelial cell death and survival in vivoActivation of the innate signaling molecule MAVS by bunyavirus infection upregulates the adaptor protein SARM1, leading to neuronal death.
P2860
Q22305521-42805FBF-D195-4C94-992A-CA6EB3FA9BDDQ24299740-4743F166-53B4-4D35-A309-A68032DA24E4Q24632537-451B3A65-27B7-4052-9B18-96F0B43A4A0EQ26864048-3838B5DB-D0A1-48E9-BC07-CD21E569633CQ26970803-6E4C704E-B9A0-401F-9B00-3D0E35590A16Q27348186-387CEEF7-E627-4022-BB98-13C9F945C435Q27674465-9EDBE420-262F-4DA1-9387-1C89822F3A60Q28075214-C9D6DCC7-7644-45CE-AD71-AAEF9E018E7BQ28482183-808AEF16-FAD6-4A01-A9A3-AC5999B62DA4Q28545027-65201776-A731-48F7-B8DB-480B6D3A3F1FQ28594137-FF6B830A-93EE-4B85-A6E3-0AF8580F230AQ30407763-A92DA550-37BD-45A4-B49B-FFBB60816ECFQ30519445-5031E4A7-F278-4FA0-9078-12638D0A8D7EQ33740309-4B507C0E-1BAA-42F3-B3E7-1D64C5FDA78BQ34212787-F6D6567A-B14F-4C6E-AEC7-5A2783BCCCDAQ34492459-01340447-6F86-497D-8918-8ED43E268F0DQ34594056-A54FC66C-5340-43DE-BE75-86D3892D9FA1Q34720811-87298A61-FF2E-46A7-B9AA-4B6C07197451Q34742996-19DECEA1-67E6-4CD8-A8E2-FA7D00667B7FQ35076557-494CD05B-92A8-470E-B6F0-D143703AB5B8Q35076581-FB982A65-E969-405D-AABF-55723C218490Q35076629-66E8DF53-4EE9-438C-854F-C41B04F38718Q35097600-6A580CE2-EE72-491B-BE46-EE4FAB3C908EQ35126624-C4E0C513-F3DC-413B-8F2E-57129E30AB7BQ35186448-7D00F73A-6D02-4C1E-B84E-0BF82B2899FEQ35193001-AB8BA8A1-CAEA-4B1D-AEF8-9B65ED2160FEQ35269835-66B0FD0D-21D1-4187-A0A0-56A49E3E5F33Q35272894-F1D12362-7006-40CE-B048-33D8DD0DB10DQ35311960-3A406D83-25B5-4FD5-AFB2-244E7FF16D93Q35488097-4B56E83E-4CFC-4CCE-956B-C6458D7538CEQ35531400-E7BB8392-DB01-4D5B-8BEE-F04F5BA588FCQ35687324-805F7FD1-0CEE-4AD8-9299-F4EE8D72E70EQ35760477-AFE01B82-C4B4-472D-81C2-BB3524551690Q36088492-41D90556-EFA9-47B6-878D-8DEB13D54196Q36123848-C2E16AE3-2393-48C3-BF6F-705BFE202673Q36270871-681F2DEB-6512-4144-9BDD-818C74D6AE5FQ36346936-5BFE0542-F508-4B16-BFC2-C67749F0CAEBQ36506888-CB3E45E2-CA56-41A4-8C40-DD3131A8188CQ36551987-E59BBECF-067F-4C7E-BDC1-A00A4D0BB26BQ36664718-A3ABF78A-B5D2-4FDC-B074-EBBE768A1320
P2860
Viral apoptosis is induced by IRF-3-mediated activation of Bax
description
2010 nî lūn-bûn
@nan
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@ast
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@en
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@en-gb
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@nl
type
label
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@ast
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@en
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@en-gb
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@nl
prefLabel
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@ast
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@en
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@en-gb
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@nl
P2093
P2860
P921
P3181
P356
P1433
P1476
Viral apoptosis is induced by IRF-3-mediated activation of Bax
@en
P2093
Avanti Desai
Ganes C Sen
Kevin Smith
Kristi L Peters
Michifumi Yamashita
Saurabh Chattopadhyay
P2860
P304
P3181
P356
10.1038/EMBOJ.2010.50
P407
P577
2010-04-01T00:00:00Z