Double-Stranded RNA Sensors and Modulators in Innate Immunity

The HCV Life Cycle: In vitro Tissue Culture Systems and Therapeutic Targets

Gerold, G., & Pietschmann, T. (2014) · Digestive Diseases · doi:10.1159/000360830 · Cited by 4,871

Principles of Nucleic Acid Structure

Neidle, S., & Sanderson, M. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-369507-9.x5001-8 · Cited by 4,519

Biogenesis of small RNAs in animals

Kim, V. N., Han, J., & Siomi, M. C. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2632 · Cited by 2,814

A diverse range of gene products are effectors of the type I interferon antiviral response

Schoggins, J. W., Wilson, S. J., Panis, M., Murphy, M. Y., Jones, C. T., Bieniasz, P. D., & Rice, C. M. (2011) · Nature · doi:10.1038/nature09907 · Cited by 2,412

Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses

Chiappinelli, K. B., Strissel, P. L., Desrichard, A., Li, H., Henke, C., Akman, B., Hein, A., Rote, N. S., Cope, L. M., Snyder, A., et al. (2015) · Cell · doi:10.1016/j.cell.2015.07.011 · Cited by 2,022

DNA-Demethylating Agents Target Colorectal Cancer Cells by Inducing Viral Mimicry by Endogenous Transcripts

Roulois, D., Loo Yau, H., Singhania, R., Wang, Y., Danesh, A., Shen, S. Y., Han, H., Liang, G., Jones, P. A., Pugh, T. J., et al. (2015) · Cell · doi:10.1016/j.cell.2015.07.056 · Cited by 1,527

Identification of host proteins required for HIV infection through a functional genomic screen

Brass, A. L., Dykxhoorn, D. M., Benita, Y., Yan, N., Engelman, A., Xavier, R. J., Lieberman, J., & Elledge, S. J. (2008) · Science · doi:10.1126/science.1152725 · Cited by 1,449

Structure and Mechanism of Helicases and Nucleic Acid Translocases

Singleton, M. R., Dillingham, M. S., & Wigley, D. B. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.052305.115300 · Cited by 1,321

MAVS Forms Functional Prion-like Aggregates to Activate and Propagate Antiviral Innate Immune Response

Hou, F., Sun, L., Zheng, H., Skaug, B. A., Jiang, Q., & Chen, Z. J. (2011) · Cell · doi:10.1016/j.cell.2011.06.041 · Cited by 1,306

Prognostic Immunity and Therapeutic Sensitivity Analyses Based on Differential Genomic Instability-Associated LncRNAs in Left- and Right-Sided Colon Adenocarcinoma

Guo, J., Xia, T.-Y., Deng, S.-H., Xue, W., Cui, B., & Liu, Y. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.668888 · Cited by 9

Epigenetic Regulation of the Non-Coding Genome: Opportunities for Immuno-Oncology

Barrero, M. J. (2020) · Epigenomes · doi:10.3390/epigenomes4030022 · Cited by 10

Proteomic Analysis Uncovers Measles Virus Protein C Interaction With p65–iASPP Protein Complex

Meignié, A., Combredet, C., Santolini, M., Kovács, I. A., Douché, T., Gianetto, Q. G., Eun, H., Matondo, M., Jacob, Y., Grailhe, R., et al. (2021) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2021.100049 · Cited by 9

Activation of Double-Stranded RNA–Activated Protein Kinase in the Dorsal Root Ganglia and Spinal Dorsal Horn Regulates Neuropathic Pain Following Peripheral Nerve Injury in Rats

Zhang, J., Zhang, X., Li, L., Bai, L., Gao, Y., Yang, Y., Wang, L., Qiao, Y., Wang, X., & Xu, J. (2022) · Neurotherapeutics · doi:10.1007/s13311-022-01255-2 · Cited by 10

Move and countermove: the integrated stress response in picorna- and coronavirus-infected cells

Aloise, C., Schipper, J. G., de Groot, R. J., & van Kuppeveld, F. J. M. (2022) · Current Opinion in Immunology · doi:10.1016/j.coi.2022.102254 · Cited by 9

RNA recognition by PKR during DNA virus infection

Zhang, R., & Karijolich, J. J. (2024) · Journal of Medical Virology · doi:10.1002/jmv.29424 · Cited by 9

Biomolecular condensates control and are defined by RNA-RNA interactions that arise in viral replicationPreprint

Aierken, D., Zhang, V., Sealfon, R. S. G., Marecki, J. C., Raney, K. D., Gladfelter, A. S., Joseph, J. A., & Roden, C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.23.630161 · Cited by 9

From genes to traits: Trends in RNA-binding proteins and their role in plant trait development: A review

Rehman, S., Bahadur, S., Xia, W., Runan, C., Ali, M., & Maqbool, Z. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.136753 · Cited by 8

A new type of Caspase-1 upon recognizing bacteria inhibits GSDME-dependent histone modification and NF-κB signaling

Chang, R., Sun, J., Leng, J., Wang, Z., Mu, S., Li, Y., Wang, J., & Song, L. (2025) · Communications Biology · doi:10.1038/s42003-025-08290-7 · Cited by 8

Gene amplification acts as a molecular foothold to facilitate cross-species adaptation and evasion of multiple antiviral pathways

Banerjee, S., Smith, C., Geballe, A. P., Rothenburg, S., Kitzman, J. O., & Brennan, G. (2022) · Virus Evolution · doi:10.1093/ve/veac105 · Cited by 8

ADAR1p110 promotes Enterovirus D68 replication through its deaminase domain and inhibition of PKR pathway

Zhang, K., Wang, S., Chen, T., Tu, Z., Huang, X., Zang, G., Chun, W., Fan, X., Liu, J., Tian, Y., et al. (2022) · Virology Journal · doi:10.1186/s12985-022-01952-6 · Cited by 8

Zebrafish mavs Is Essential for Antiviral Innate Immunity

Ouyang, G., Liao, Q., Fan, S., Cai, X., Wang, J., Liu, X., & Xiao, W. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2200126 · Cited by 8

Protection of eIF2B from inhibitory phosphorylated eIF2: A viral strategy to maintain mRNA translation during the PKR-triggered integrated stress response

Ito, T., Wuerth, J. D., & Weber, F. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105287 · Cited by 9

Prkra dimer senses double-stranded RNAs to dictate global translation efficiency

Lu, T., Ma, P., Fang, H., Chen, A., Xu, J., Kuang, X., Wang, M., Su, L., Wang, S., Zhang, Y., et al. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.04.005 · Cited by 8

Interdependent Transcription of a Natural Sense/Antisense Transcripts Pair (SLC34A1/PFN3)

Zinad, H. S., Sae‐Lee, C., Ariza-Mateos, M., Adamson, G., Khazeem, M. M., Knox, A., Chung, G., Mann, J., & Werner, A. (2022) · Non-Coding RNA · doi:10.3390/ncrna8010019 · Cited by 8

Differential Loss of OAS Genes Indicates Diversification of Antiviral Immunity in Mammals

Eckhart, L., & Sipos, W. (2023) · Vaccines · doi:10.3390/vaccines11020419 · Cited by 8

Coronavirus: a shift in focus away from IFN response and towards other inflammatory targets

Thoutam, A., Breitzig, M., Lockey, R. F., & Kolliputi, N. (2020) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-020-00574-3 · Cited by 8

LinearDesign: Efficient Algorithms for Optimized mRNA Sequence DesignPreprint

Zhang, H., Zhang, L., Li, Z., Liu, K., Liu, B., Mathews, D. H., & Huang, L. (2020) · arXiv (Cornell University) · Cited by 8

Ageing impairs the airway epithelium defence response to SARS-CoV-2Preprint

Capraro, A., Wong, S. L., Adhikari, A., Allan, K. M., Patel, H. R., Zhong, L., Raftery, M. J., Jaffé, A., Yeang, M., Aggarwal, A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.05.437453 · Cited by 9

CellREADR: An ADAR-based RNA sensor-actuator device

Yang, X., Woldemichael, K., Guo, X. D., Zhao, S., Qian, Y., & Huang, Z. J. (2025) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2024.11.027 · Cited by 7

Cellular dsRNA interactome captured by K1 antibody reveals the regulatory map of exogenous RNA sensing

Lim, J., Lee, N., Ju, S., Kim, J., Mun, S., Jeon, M., Lee, S.-H., Lee, S.-H., Ku, J., Kim, S., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-07807-4 · Cited by 7

ADAR1 p150 prevents HSV-1 from triggering PKR/eIF2α-mediated translational arrest and is required for efficient viral replication

Parchure, A., Cesarec, M., Braut, A., Kolman, R., Ivanišević, V., Čunko, M., Bursać, S., de Reuver, R., Begonja, A. J., Rosani, U., et al. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1012452 · Cited by 8

Hsc70-4: An unanticipated mediator of dsRNA internalization in Drosophila

Fletcher, S. J., Bardossy, E. S., Tomé-Poderti, L., Moss, T. J., Mongelli, V. C., Frangeul, L., Blanc, H., Verdier, Y., Vinh, J., Mukherjee, S., et al. (2025) · Science Advances · doi:10.1126/sciadv.adv1286 · Cited by 7

Double-Stranded RNA Enhances Matrix Metalloproteinase-1 and -13 Expressions through TLR3-Dependent Activation of Transglutaminase 2 in Dermal Fibroblasts

Hong, A.-Y., Lee, S., Lee, K. B., Shin, J., Jeong, E. M., & Kim, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052709 · Cited by 7

Transcriptome-wide identification of single-stranded RNA binding proteins

Zhao, R., Fang, X., Mai, Z., Chen, X., Mo, J., Lin, Y., Xiao, R., Bao, X., Weng, X., & Zhou, X. (2023) · Chemical Science · doi:10.1039/d3sc00957b · Cited by 7

The Role of RNA Sensors in Regulating Innate Immunity to Gammaherpesviral Infections

Zhang, H., Sandhu, P., & Damania, B. (2023) · Cells · doi:10.3390/cells12121650 · Cited by 7

Targeting Myeloid Differentiation Primary Response Protein 88 (MyD88) and Galectin-3 to Develop Broad-Spectrum Host-Mediated Therapeutics against SARS-CoV-2

Saikh, K. U., Anam, K., Sultana, H., Ahmed, R., Kumar, S., Srinivasan, S., & Ahmed, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158421 · Cited by 7

RNA editing regulates host immune response and T cell homeostasis in SARS-CoV-2 infection

Huang, M., Mark, A., Pham, J., Vera, K., Saravia-Butler, A. M., Beheshti, A., Jiang, Q.-F., & Fisch, K. M. (2024) · PLoS ONE · doi:10.1371/journal.pone.0307450 · Cited by 10

Analysis of transcriptomic responses to SARS-CoV-2 reveals plausible defective pathways responsible for increased susceptibility to infection and complications and helps to develop fast-track repositioning of drugs against COVID-19

deAndrés‐Galiana, E. J., Fernández‐Martínez, J. L., Álvarez-Machancoses, Ó., Bea, G., Galmarini, C. M., & Kloczkowski, A. (2022) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2022.106029 · Cited by 7

Oncolytic Rodent Protoparvoviruses Evade a TLR- and RLR-Independent Antiviral Response in Transformed Cells

Angelova, A. L., Pierrard, K., Detje, C. N., Santiago, E., Grewenig, A., Nüesch, J. P. F., Kalinke, U., Ungerechts, G., Rommelaere, J., & Daeffler, L. (2023) · Pathogens · doi:10.3390/pathogens12040607 · Cited by 6

Cellular Stress Responses against Coronavirus Infection: A Means of the Innate Antiviral Defense

Yoo, J. (2023) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2307.07038 · Cited by 7

NSUN5 Facilitates Viral RNA Recognition by RIG-I Receptor

Sun, B., Zeng, H., Liang, J., Zhang, L., Hu, H., Wang, Q., Meng, W., Li, C., Ye, F., Wang, C., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1901455 · Cited by 7

A truncated SARS-CoV-2 nucleocapsid protein enhances virus fitness by evading antiviral responsesPreprint

Mulloy, R. P., Evseev, D., Bui-Marinos, M. P., Sharlin, N., & Corcoran, J. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.15.638421 · Cited by 7

Research progress on immune mechanism and control strategy of dsRNA impurities in mRNA vaccine

Liu, X., Hu, C., He, Q., Bai, Y., Zhang, X., Fu, Z., Ma, X., Xu, M., Liang, Z., & Mao, Q. (2025) · Expert Review of Vaccines · doi:10.1080/14760584.2025.2510335 · Cited by 6

Nucleic acid-protein condensates in innate immunity

Loucas, G., Locker, N., & Parker, R. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.09.014 · Cited by 7

Interferon-Based Therapeutics in Cancer Therapy: Past, Present, and Future

Vorona, K., Ryapolova, A., Sokolova, O., Karabelsky, A. V., Ivanov, R. A., Reshetnikov, V. V., & Minskaia, E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311679 · Cited by 7

RNA signaling in cellular plasticity during homeostasis and regeneration

Nagaraj, A. C., Ahi, E. P., Änkö, M., & Kaslin, J. (2026) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2026.102478 · Cited by 6

The organization of double-stranded RNA in the chikungunya virus replication organelle

Laurent, T., & Carlson, L. A. (2023) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0011404 · Cited by 6

Characterization of tumor microenvironment and tumor immunology based on the double-stranded RNA-binding protein related genes in cervical cancer

Li, J., Wan, C., Li, X., Quan, C., Li, X., & Wu, X. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04505-9 · Cited by 7

Detection of Double-Stranded RNA Intermediates During SARS-CoV-2 Infections of Syrian Golden Hamsters with Monoclonal Antibodies and Its Implications for Histopathological Evaluation of In Vivo Studies

Beythien, G., de le Roi, M., Stanelle‐Bertram, S., Armando, F., Heydemann, L., Rosiak, M., Becker, S., Lamers, M. M., Kaiser, F. K., Haagmans, B. L., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252111425 · Cited by 6

Molecular basis of autoimmune disease protection by MDA5 variants

Singh, R., Joiner, J. D., del Valle, A. H., Zwaagstra, M., Jobe, I., Ferguson, B. J., van Kuppeveld, F. J. M., & Modis, Y. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115754 · Cited by 9

Co-Regulation of Protein Coding Genes by Transcription Factor and Long Non-Coding RNA in SARS-CoV-2 Infected Cells: An In Silico Analysis

Saha, C., Laha, S., Chatterjee, R., & Bhattacharyya, N. P. (2021) · Non-Coding RNA · doi:10.3390/ncrna7040074 · Cited by 6

Detecting Z-RNA and Z-DNA in Mammalian Cells

Yin, C., Zhang, T., & Balachandran, S. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3084-6_19 · Cited by 5

The entanglement of DNA damage and pattern recognition receptor signaling

Ha, C. T., Tageldein, M. M., & Harding, S. M. (2023) · DNA repair · doi:10.1016/j.dnarep.2023.103595 · Cited by 6

Editorial: Community series in antiviral innate immune sensing, regulation, and viral immune evasion: volume II

Wang, L., & Xing, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1341193 · Cited by 6

DHX15 and Rig-I Coordinate Apoptosis and Innate Immune Signaling by Antiviral RNase L

Ramnani, B., Devale, T., Manivannan, P., Haridas, A., & Malathi, K. (2024) · Viruses · doi:10.3390/v16121913 · Cited by 5

Breaking through barrier: The emerging role of nucleic acids-based drug delivery in stroke

Yin, G., Zheng, Y., Li, M., Wu, G., & Luo, Y. (2025) · Progress in Materials Science · doi:10.1016/j.pmatsci.2025.101436 · Cited by 5

Characterization of dsRNA binding proteins through solubility analysis identifies ZNF385A as a dsRNA homeostasis regulator

Jiang, N., Yang, H.-K., Lei, Y., Qin, W., Xiong, H., Chen, K.-B., Mei, K.-R., Li, G., Mu, X., & Chen, R.-B. (2025) · Nature Communications · doi:10.1038/s41467-025-58704-7 · Cited by 4

DHX34 deficiency triggers tumor-intrinsic immunity via a dsRNA-mediated type I interferon pathway activation in HCC

Zhang, S., Huang, L., Li, Z., Wang, Q., Liu, N., Zhang, C., Liu, X., Zhang, C., He, G., Sun, J., et al. (2025) · Neoplasia · doi:10.1016/j.neo.2025.101198 · Cited by 5

Effect of berberine on herpes simplex keratitis through the dimerization of eukaryotic translation initiation factor 2-alpha kinase 2

Lin, J., Wang, H., Wei, X., Qin, L., Xing, S., Wang, X., Li, Y., Yi, Y., Huang, W., Tan, R., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.157112 · Cited by 5

Molecular mechanism of MDA5 nucleation and filament formation by LGP2

Kurihara, N., Isayama, Y., Zhang, J., Yamashita, T., Awaji, K., Ito, Y., Yoshizaki, A., Kouwaki, T., Oshiumi, H., Nishimasu, H., et al. (2026) · Molecular Cell · doi:10.1016/j.molcel.2025.12.019 · Cited by 7

A Comparison of Conserved Features in the Human Coronavirus Family Shows That Studies of Viruses Less Pathogenic than SARS-CoV-2, Such as HCoV-OC43, Are Good Model Systems for Elucidating Basic Mechanisms of Infection and Replication in Standard Laboratories

Heffner, A. L., & Rouault, T. A. (2025) · Viruses · doi:10.3390/v17020256 · Cited by 5

Advances in the evasion of innate immunity by fish viruses: A glance at RLRs and cGAS-STING signaling pathways

Liu, R., & Shan, S. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.740197 · Cited by 5

Mining the Unmapped Reads in Bovine RNA-Seq Data Reveals the Prevalence of Bovine Herpes Virus-6 in European Dairy Cows and the Associated Changes in Their Phenotype and Leucocyte Transcriptome

Buggiotti, L., Cheng, Z., & Wathes, D. C. (2020) · Viruses · doi:10.3390/v12121451 · Cited by 5

Live imaging of neolymphangiogenesis identifies acute antimetastatic roles of dsRNA mimics

Olmeda, D., Cerezo‐Wallis, D., Mucientes, C., Calvo, T. G., Cañón, E., Alonso‐Curbelo, D., Ibarz, N., Muñoz, J., Rodríguez‐­Peralto, J. L., Ortiz-Romero, P. L., et al. (2021) · EMBO Molecular Medicine · doi:10.15252/emmm.202012924 · Cited by 5

Endogenous Retroviruses Augment Amphibian (Xenopus laevis) Tadpole Antiviral Protection

Kalia, N., Hauser, K. A., Burton, S., Hossainey, M. R. H., Zelle, M., Horb, M. E., & Grayfer, L. (2022) · Journal of Virology · doi:10.1128/jvi.00634-22 · Cited by 5

LINE-associated cryptic splicing induces dsRNA-mediated interferon response and tumor immunityPreprint

Zheng, R., Dunlap, M., Lyu, J., Gonzalez‐Figueroa, C., Bobkov, G. O. M., Harvey, S. E., Chan, T. W., Quinones-Valdez, G., Choudhury, M., Vuong, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.23.529804 · Cited by 5

Insights into Noncanonical and Diversified Functions of ABCF1: From Health to Disease

Duan, J., Saini, P., & Fong, Y. W. (2025) · Journal of Molecular Biology · doi:10.1016/j.jmb.2025.169286 · Cited by 4

Transcriptomics analysis highlights potential ways in human pathogenesis in Leishmania braziliensis infected with the viral endosymbiont LRV1

Felipin, K. P., Paloschi, M. V., Silva, M. D. S., Ikenohuchi, Y. J., Santana, H. M., Setúbal, S. D. S., Rego, C. M. A., Lopes, J. A., Boeno, C. N., Serrath, S. N., et al. (2024) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0012126 · Cited by 4

Bacteriophage derived dsRNA induces polarized activation of alveolar macrophages from Balb/c and C57Bl/6 mice in vitro in sex- and age-dependent manner

DOVHYI, R., Dvukhriadkina, A., Ostrovska, K., Rudyk, M. P., Verhovcova, I., Vaivode, K., Pjanova, D., Остапченко, Л. І., & Skivka, L. M. (2025) · Cellular Immunology · doi:10.1016/j.cellimm.2025.104916 · Cited by 4

Argonaute 2 inhibits RIG-I signaling via competition for viral RNA binding

Liu, H., Liao, Y., Yu, F., Li, L. N.-S., Zhang, Y., Zhu, L., Xie, G., Liu, J., Liu, S., Deng, S., et al. (2025) · iScience · doi:10.1016/j.isci.2025.113391 · Cited by 4

RNA is a pro-apoptotic target of cisplatin in cancer cell lines and C. elegans

Rose, F., Köberle, B., Honnen, S., Bay, C., Burhenne, J., Weiß, J., Haefeli, W. E., & Theile, D. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116450 · Cited by 4

Identification of common genes and pathways between type 2 diabetes and COVID-19

Wang, Y., Li, K., Mo, S., Yao, P., Zeng, J., Lu, S., & Qin, S. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2024.1249501 · Cited by 4

Chinese Medicine for Treatment of COVID-19: A Review of Potential Pharmacological Components and Mechanisms

Xu, Q., Yu, D., Fan, X., Cui, H., Dai, Q., Zhong, X.-Y., Zhang, X., Zhao, C., You, L., & Shang, H. (2024) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-024-3909-z · Cited by 5

Retrospective analysis of clustered neuroinflammatory and neurodegenerative diseases in captive lions in the early 1970s

de le Roi, M., Nägler, I., Rubbenstroth, D., Beer, M., Höper, D. W., Barth, S., Fayyad, A. F., Puff, C., Baumgärtner, W., & Wohlsein, P. (2025) · Veterinary Pathology · doi:10.1177/03009858251335280 · Cited by 4

Primate-specific retrotransposons and the evolution of circadian networks in the human brain

Li, M., & Larsen, P. A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.049 · Cited by 5

Computational Investigation of Bending Properties of RNA AUUCU, CCUG, CAG, and CUG Repeat Expansions Associated With Neuromuscular Disorders

Taghavi, A., & Yildirim, I. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.830161 · Cited by 5

p120-catenin promotes innate antiviral immunity through stabilizing TBK1-IRF3 complex

Wu, H. M., Yan, X., Zhao, L., Li, X., Li, X., Zhang, Y., Gu, C., Yang, F., Yan, J., Lou, Y., et al. (2023) · Molecular Immunology · doi:10.1016/j.molimm.2023.03.013 · Cited by 4

Differential regulation of ATP hydrolysis of RIG-I-like receptors by transactivation response RNA-binding protein

Chunhaphinyokul, B., Emi, H., Miyamoto, M., & Komuro, A. (2023) · Bioscience Reports · doi:10.1042/bsr20222152 · Cited by 4

Modulation of the replication of positive-sense RNA viruses by the natural plant metabolite xanthohumol and its derivatives

Marongiu, L., Burkard, M., Helling, T., Biendl, M., & Venturelli, S. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2275169 · Cited by 4

RNA-seq reveals role of cell-cycle regulating genes in the pathogenicity of a field very virulent infectious bursal disease virus

Chen, J., Wang, W., Li, S., Wang, Z., Zuo, W., Nong, T., Li, Y., Liu, H., Wei, P., & He, X. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1334586 · Cited by 4

RNA editing in mesothelioma: a look forward

Hariharan, A., Sun, S., Wipplinger, M., & Felley‐Bosco, E. (2020) · Open Biology · doi:10.1098/rsob.200112 · Cited by 4

SARS-CoV-2 and autoimmune rheumatic diseases

Stoilov, N. R., & Boyadzhieva, V. V. (2021) · Rheumatology (Bulgaria) · doi:10.35465/28.4.2020.pp36-44 · Cited by 4

Ubiquitin ligase RIPLET mediates polyubiquitination of RIG-I and LGP2 and regulates the innate immune responses to SARS-CoV-2 infectionPreprint

Kouwaki, T., Nishimura, T., Wang, G., Nakagawa, R., & Oshiumi, H. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.25.428042 · Cited by 4

Nucleic acid nanomaterials: Mechanisms and strategies for regulating innate immune activation

Zou, K., Liu, Y., Tang, L., Wang, Y., Wang, J., & Song, J. (2025) · Nano Today · doi:10.1016/j.nantod.2025.102897 · Cited by 3

pH denaturation of dsRNA: A novel approach to mRNA purification

Puc, J., Mencin, N., Krušič, A., Nett, E., Perković, M., Sahin, U., Štrancar, A., & Sekirnik, R. (2026) · Separation and Purification Technology · doi:10.1016/j.seppur.2026.136864 · Cited by 3

ADAR1: a central regulator of dsRNA sensing in host-virus interactions

Liu, C., & Choi, Y. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1756517 · Cited by 5

MDA5 generates compact ribonucleoprotein complexes via ATP-dependent double-stranded RNA unwinding

Quack, S., Maity, S., America, P. P. B., Klein, M., del Valle, A. H., Singh, R., Joiner, J. D., Rashid, Z. M., Smitskamp, Q., Rivas, P., et al. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag274 · Cited by 3

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The current landscape of mRNA therapy and the strategies for mRNA purification and dsRNA removal

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Caring for patients with rare diseases during the COVID-19 pandemic

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Multiscale network analysis identifies potential receptors for SARS‐CoV ‐2 and reveals their tissue‐specific and age‐dependent expression

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The Magic and Mystery of TRIM65 in Diseases

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Sensores de ARN de cadena doble en la inmunidad innata

García Japón, B. (2021) · idUS (Universidad de Sevilla)

Sensing of double-stranded RNA in human cells: molecular mechanisms and cellular consequences

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dsRNA Sensing During Viral Infection: Lessons from Plants, Worms, Insects, and Mammals

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