The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.
Human ADAR1 Prevents Endogenous RNA from Triggering Translational Shutdown
Open accessAbstract
Type I interferon (IFN) is produced when host sensors detect foreign nucleic acids, but how sensors differentiate self from nonself nucleic acids, such as double-stranded RNA (dsRNA), is incompletely understood. Mutations in ADAR1, an adenosine-to-inosine editing enzyme of dsRNA, cause Aicardi-Goutières syndrome, an autoinflammatory disorder associated with spontaneous interferon production and neurologic sequelae. We generated ADAR1 knockout human cells to explore ADAR1 substrates and function. ADAR1 primarily edited Alu elements in RNA polymerase II (pol II)-transcribed mRNAs, but not putative pol III-transcribed Alus. During the IFN response, ADAR1 blocked translational shutdown by inhibiting hyperactivation of PKR, a dsRNA sensor. ADAR1 dsRNA binding and catalytic activities were required to fully prevent endogenous RNA from activating PKR. Remarkably, ADAR1 knockout neuronal progenitor cells exhibited MDA5 (dsRNA sensor)-dependent spontaneous interferon production, PKR activation, and cell death. Thus, human ADAR1 regulates sensing of self versus nonself RNA, allowing pathogen detection while avoiding autoinflammation.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Major sources of dsRNA, inverted Alu repeats, are normally deaminated by ADAR to reduce their double-stranded character; decreased processing can be sensed by MDA5, resulting in IFN-I activation50, 51, 98.”
From The role of retrotransposable elements in ageing and age-associated diseases (2021) · cites this paper as [50]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506580102 · Cited by 53,625
Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp616 · Cited by 41,364
Salmon provides fast and bias-aware quantification of transcript expression
Patro, R., Duggal, G., Love, M. I., Irizarry, R. A., & Kingsford, C. (2017) · Nature Methods · doi:10.1038/nmeth.4197 · Cited by 12,700
Genome engineering using the CRISPR-Cas9 system
Ran, F. A., Hsu, P. D., Wright, J., Agarwala, V., Scott, D. A., & Zhang, F. (2013) · Nature Protocols · doi:10.1038/nprot.2013.143 · Cited by 11,133
voom: precision weights unlock linear model analysis tools for RNA-seq read counts
Law, C. W., Chen, Y., Shi, W., & Smyth, G. K. (2014) · Genome Biology · doi:10.1186/gb-2014-15-2-r29 · Cited by 6,155
Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling
Chambers, S. M., Fasano, C. A., Papapetrou, E. P., Tomishima, M., Sadelain, M., & Studer, L. (2009) · Nature Biotechnology · doi:10.1038/nbt.1529 · Cited by 3,620
GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists
Eden, E., Navon, R., Steinfeld, I., Lipson, D., & Yakhini, Z. (2009) · BMC Bioinformatics · doi:10.1186/1471-2105-10-48 · Cited by 3,356
Regulation of Translation Initiation in Eukaryotes: Mechanisms and Biological Targets
Sonenberg, N., & Hinnebusch, A. G. (2009) · Cell · doi:10.1016/j.cell.2009.01.042 · Cited by 3,304
Interferon-stimulated genes: A complex web of host defenses
Schneider, W. M., Chevillotte, M. D., & Rice, C. M. (2014) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032713-120231 · Cited by 3,067
Self-citationRepbase Update, a database of repetitive elements in eukaryotic genomes
Bao, W., Kojima, K. K., & Kohany, O. (2015) · Mobile DNA · doi:10.1186/s13100-015-0041-9 · Cited by 2,942
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 529
All I's on the RADAR : role of ADAR in gene regulation
Shevchenko, G., & Morris, K. V. (2018) · FEBS Letters · doi:10.1002/1873-3468.13093 · Cited by 67
Bou‐Nader, C., Gordon, J. M., Henderson, F. E., & Zhang, J. (2019) · RNA · doi:10.1261/rna.070169.118 · Cited by 64
Davidson, S., Yu, C., Steiner, A., Ebstein, F., Baker, P. J., Jarur-Chamy, V., Hrovat-Schaale, K., Laohamonthonkul, P., Kong, K., Calleja, D. J., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abi6763 · Cited by 62
The Editor’s I on Disease Development
Jain, M. K., Jantsch, M. F., & Licht, K. (2019) · Trends in Genetics · doi:10.1016/j.tig.2019.09.004 · Cited by 61
Fernández-Torras, A., Duran-Frigola, M., Bertoni, M., Locatelli, M., & Aloy, P. (2022) · Nature Communications · doi:10.1038/s41467-022-33026-0 · Cited by 59
ADAR1 Non-Editing Function in Macrophage Activation and Abdominal Aortic Aneurysm
Cai, D., Sun, C., Murashita, T., Que, X., & Chen, S. (2023) · Circulation Research · doi:10.1161/circresaha.122.321722 · Cited by 59
An Update on Autoinflammatory Diseases: Interferonopathies
Davidson, S., Steiner, A., Harapas, C. R., & Masters, S. L. (2018) · Current Rheumatology Reports · doi:10.1007/s11926-018-0748-y · Cited by 59
The preponderance of nonsynonymous A-to-I RNA editing in coleoids is nonadaptive
Jiang, D., & Zhang, J. (2019) · Nature Communications · doi:10.1038/s41467-019-13275-2 · Cited by 55
Mustelin, T., & Ukadike, K. C. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.593891 · Cited by 55
RNA modifications in cardiovascular health and disease
Gatsiou, A., & Stellos, K. (2022) · Nature Reviews Cardiology · doi:10.1038/s41569-022-00804-8 · Cited by 56
Sun, T., Li, Q., Geisinger, J. M., Hu, S.-B., Fan, B., Su, S., Tsui, W., Guo, H., Ma, J., & Li, J. B. (2025) · Nature Genetics · doi:10.1038/s41588-025-02430-9 · Cited by 55
Self-citationBurgess, H. M., & Mohr, I. (2018) · Journal of Virology · doi:10.1128/jvi.00829-18 · Cited by 54
Stok, J. E., Oosenbrug, T., ter Haar, L. R., Gravekamp, D., Bromley, C. P., Zelenay, S., Sousa, C. R. E., & van der Veen, A. G. (2022) · The EMBO Journal · doi:10.15252/embj.2021109760 · Cited by 53
Rodriguez, S., Şahin, A., Schrank, B. R., Lawati, H. J. A., Costantino, I. M., Benz, E. G., Fard, D., Albers, A. D., Cao, L., Gomez, A. C., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.aaz4699 · Cited by 58
Erdmann, E. A., Mahapatra, A., Mukherjee, P., Yang, B., & Hundley, H. A. (2020) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2020.1856768 · Cited by 52
Investigating the Potential Roles of SINEs in the Human Genome
Zhang, X.-O., Pratt, H., & Weng, Z. (2021) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-111620-100736 · Cited by 55
Dynamic Variations of 3′UTR Length Reprogram the mRNA Regulatory Landscape
Navarro, E., Mallén, A., & Hueso, M. (2021) · Biomedicines · doi:10.3390/biomedicines9111560 · Cited by 55
Adenosine-to-inosine RNA editing in the immune system: friend or foe?
Nakahama, T., & Kawahara, Y. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03466-2 · Cited by 51
Signaling by the integrated stress response kinase PKR is fine-tuned by dynamic clustering
Zappa, F., Muniozguren, N. L., Wilson, M. Z., Costello, M. S., Ponce‐Rojas, J. C., & Acosta‐Alvear, D. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202111100 · Cited by 54
Discrimination Between Self and Non-Self-Nucleic Acids by the Innate Immune System
Kawasaki, T., & Kawai, T. (2018) · International review of cytology · doi:10.1016/bs.ircmb.2018.08.004 · Cited by 52
Endogenous Nucleic Acid Recognition by RIG-I-Like Receptors and cGAS
Lee, J., Chiang, C., & Gack, M. U. (2019) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2019.0015 · Cited by 50
Heraud-Farlow, J. E., & Walkley, C. R. (2020) · Open Biology · doi:10.1098/rsob.200085 · Cited by 50
Targeting ADAR1 with a small molecule for the treatment of prostate cancer
Wang, X., Li, J., Zhu, Y., Shen, H., Ding, J., Zeng, T., Min, W., Liang, S., Huang, L., Shi, Z., et al. (2025) · Nature Cancer · doi:10.1038/s43018-025-00907-4 · Cited by 50
Han, J., An, Ö., Hong, H., Chan, T. H. M., Song, Y., Shen, H., Tang, S. J., Lin, J. S., Ng, V. H. E., Tay, D. J. T., et al. (2020) · Science Advances · doi:10.1126/sciadv.aba5136 · Cited by 49
Santa, P., Garreau, A., Serpas, L., Ferrière, A., Blanco, P., Soni, C., & Sisirak, V. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.629922 · Cited by 56
Inverted Alu repeats: friends or foes in the human transcriptome
Lee, K., Ku, J., Ku, D., & Kim, Y. (2024) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01177-3 · Cited by 48
Wang, L., Sun, Y., Song, X., Wang, Z., Zhang, Y., Zhao, Y., Peng, X., Zhang, X., Li, C., Gao, C., et al. (2021) · Cellular and Molecular Immunology · doi:10.1038/s41423-021-00729-1 · Cited by 48
Barak, M., Porath, H. T., Finkelstein, G., Knisbacher, B. A., Buchumenski, I., Roth, S. H., Levanon, E. Y., & Eisenberg, E. (2020) · Genome biology · doi:10.1186/s13059-020-1937-3 · Cited by 46
RIG-I-like receptors: Molecular mechanism of activation and signaling
Zheng, J., Shi, W., Yang, Z., Chen, J., Qi, A., Yang, Y., Deng, Y., Yang, D., Song, N., Song, B., et al. (2023) · Advances in immunology · doi:10.1016/bs.ai.2023.03.001 · Cited by 46
An internal deletion of ADAR rescued by MAVS deficiency leads to a minute phenotype
Bajad, P., Ebner, F., Amman, F., Szabo, B. R., Kapoor, U., Manjaly, G., Hildebrandt, A., Janisiw, M. P., & Jantsch, M. F. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa025 · Cited by 45
Vogel, O. A., Han, J., Liang, C.-Y., Manicassamy, S., Perez, J. T., & Manicassamy, B. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008842 · Cited by 45
Guillemin, A., Kumar, A., Wencker, M., & Ricci, E. P. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.796012 · Cited by 48
Astrocytes, an active player in Aicardi–Goutières syndrome
Sase, S., Takanohashi, A., Vanderver, A. L., & Almad, A. (2018) · Brain Pathology · doi:10.1111/bpa.12600 · Cited by 45
Protein kinase R and its cellular regulators in cancer: An active player or a surveillant?
Lee, Y. S., Kunkeaw, N., & Lee, Y. (2019) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1558 · Cited by 44
To “Z” or not to “Z”: Z-RNA, self-recognition, and the MDA5 helicase
Herbert, A. G. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009513 · Cited by 44
Luo, J., Gong, L., Yang, Y., Zhang, Y., Liu, Q., Bai, L., Fang, X., Zhang, B., Huang, J., Liu, M., et al. (2023) · Hepatology · doi:10.1097/hep.0000000000000299 · Cited by 43
Manjunath, L., Oh, S., Ortega, P., Bouin, A., Bournique, E., Sanchez, A., Martensen, P. M., Auerbach, A. A., Becker, J. T., Seldin, M. M., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36445-9 · Cited by 42
RNA editing in cancer impacts mRNA abundance in immune response pathways
Chan, T. W., Fu, T., Bahn, J. H., Jun, H.-I., Lee, J., Quinones-Valdez, G., Cheng, C., & Xiao, X. G. (2020) · Genome biology · doi:10.1186/s13059-020-02171-4 · Cited by 42
In search of critical dsRNA targets of ADAR1
Levanon, E. Y., Cohen‐Fultheim, R., & Eisenberg, E. (2023) · Trends in Genetics · doi:10.1016/j.tig.2023.12.002 · Cited by 41
Zheng, R., Dunlap, M., Bobkov, G. O. M., Gonzalez‐Figueroa, C., Patel, K. J., Lyu, J., Harvey, S. E., Chan, T. W., Quinones-Valdez, G., Choudhury, M., et al. (2024) · Molecular Cell · doi:10.1016/j.molcel.2024.05.004 · Cited by 44
Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features
Piccoli, C., Bronner, N., Gavazzi, F., Dubbs, H. A., Simone, M. D., GIORGIS, V. D., Orcesi, S., Fazzi, E. M., Galli, J., Masnada, S., et al. (2020) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2020.10.012 · Cited by 41
8-Azaadenosine and 8-Chloroadenosine are not Selective Inhibitors of ADAR
Cottrell, K. A., Torres, L. S., Dizon, M. G., & Weber, J. D. (2021) · Cancer Research Communications · doi:10.1158/2767-9764.crc-21-0027 · Cited by 41
Unified mechanisms for self-RNA recognition by RIG-I Singleton-Merten syndrome variants
Lässig, C., Lammens, K., López, J. L. G., Michalski, S., Fettscher, O., & Hopfner, K. (2018) · eLife · doi:10.7554/elife.38958 · Cited by 40
Induction of Viral Mimicry Upon Loss of DHX9 and ADAR1 in Breast Cancer Cells
Cottrell, K. A., Ryu, S., Pierce, J. R., Torres, L. S., Bohlin, H. E., Schab, A. M., & Weber, J. D. (2024) · Cancer Research Communications · doi:10.1158/2767-9764.crc-23-0488 · Cited by 39
Deficiency for SAMHD1 activates MDA5 in a cGAS/STING-dependent manner
Schumann, T., Ramon, S. C., Schubert, N., Mayo, M. A., Hega, M., Maser, K. I., Ada, S.-R., Sydow, L., Hajikazemi, M., Badstübner, M., et al. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20220829 · Cited by 41
Making sense of IL‐6 signalling cues in pathophysiology
Millrine, D., Jenkins, R. L., Hughes, S. T. O., & Jones, S. A. (2021) · FEBS Letters · doi:10.1002/1873-3468.14201 · Cited by 39
Yuan, J., Li, X., Bao, H., Wang, J.-L., Zhao, Y., & Chen, S. (2023) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-023-02727-9 · Cited by 38
Rivera, M., Zhang, H., Pham, J., Isquith, J. M., Zhou, Q. J., Balaian, L., Šášik, R., Enlund, S., Mark, A., Ma, W., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113704 · Cited by 38
An ADAR1 dsRBD3-PKR kinase domain interaction on dsRNA inhibits PKR activation
Sinigaglia, K., Cherian, A., Du, Q., Lacovich, V., Vukić, D., Melicherová, J., Linhartova, P., Zerad, L., Stejskal, S., Malı́k, R., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114618 · Cited by 38
Cytosolic nucleic acid sensing as driver of critical illness: mechanisms and advances in therapy
Chen, Z., Behrendt, R., Wild, L., Schlee, M., & Bode, C. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02174-2 · Cited by 44
A mark of disease: how mRNA modifications shape genetic and acquired pathologies
Destefanis, E., Avşar, G., Groza, P., Romitelli, A., Torrini, S., Pir, P., Conticello, S. G., Aguiló, F., & Dassi, E. (2020) · RNA · doi:10.1261/rna.077271.120 · Cited by 38
Lodi, L., Melki, I., Bondet, V., Seabra, L., Rice, G., Carter, E., Lepelley, A., Martin-Niclós, M. J., Al‐Adba, B., Bader‐Meunier, B., et al. (2021) · Journal of Clinical Immunology · doi:10.1007/s10875-020-00952-x · Cited by 38
An I for an A: Dynamic Regulation of Adenosine Deamination-Mediated RNA Editing
Vesely, C., & Jantsch, M. F. (2021) · Genes · doi:10.3390/genes12071026 · Cited by 37
How RNA modifications regulate the antiviral response
Thompson, M. G., Sacco, M. T., & Horner, S. M. (2021) · Immunological Reviews · doi:10.1111/imr.13020 · Cited by 37
ADAR1 links R-loop homeostasis to ATR activation in replication stress response
Zhang, B., Li, Y., Zhang, J., Wang, Y., Liang, C., Lü, T., Zhang, C., Liu, L., Qin, Y. F., He, J., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad839 · Cited by 37
ADAR1 Facilitates KSHV Lytic Reactivation by Modulating the RLR-Dependent Signaling Pathway
Zhang, H., Ni, G., & Damania, B. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107564 · Cited by 37
Cesaro, T., Hayashi, Y., Borghese, F., Vertommen, D., Wavreil, F., & Michiels, T. (2021) · Scientific Reports · doi:10.1038/s41598-021-88610-z · Cited by 36
Lin, W., Luo, Y., Wu, J. J., Zhang, H., Jin, G., Guo, C., Zhou, H., Liang, H., & Xu, X. (2023) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2023-007402 · Cited by 36
ADAR1-Dependent RNA Editing Promotes MET and iPSC Reprogramming by Alleviating ER Stress
Guallar, D., Fuentes-Iglesias, A., Souto, Y., Ameneiro, C., Freire-Agulleiro, Ó., Pardavila, J. Á., Escudero, A., Garcia‐Outeiral, V., Moreira, T., Sáenz, C., et al. (2020) · Cell stem cell · doi:10.1016/j.stem.2020.04.016 · Cited by 36
The Emerging Role of RNA Modifications in the Regulation of Antiviral Innate Immunity
Tong, J., Zhang, W., Chen, Y., Yuan, Q., Qin, N.-N., & Qu, G. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.845625 · Cited by 37
Small Hero with Great Powers: Vaccinia Virus E3 Protein and Evasion of the Type I IFN Response
Szczerba, M., Subramanian, S., Trainor, K., McCaughan, M., Kibler, K. V., & Jacobs, B. L. (2022) · Biomedicines · doi:10.3390/biomedicines10020235 · Cited by 37
Patel, A. J., Warda, S., Mååg, J. L. V., Misra, R., Miranda-Román, M. A., Pachai, M. R., Lee, C. J., Li, D., Wang, N., Bayshtok, G., et al. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-21-1671 · Cited by 36
DUSP11-mediated control of 5′-triphosphate RNA regulates RIG-I sensitivityPreprint
Choi, J. H., Burke, J. M., Szymanik, K. H., Nepal, U., Battenhouse, A. M., Lau, J. T., Stark, A., Lam, V. L., & Sullivan, C. S. (2020) · Genes & Development · doi:10.1101/gad.340604.120 · Cited by 37
ADAR1 affects HCV infection by modulating innate immune response
Pujantell, M., Franco, S., Galván‐Femenía, I., Badía, R., Castellví, M., García-Vidal, E., Clotet, B., de Cid, R., Tural, C., Martı́nez, M. Á., et al. (2018) · Antiviral Research · doi:10.1016/j.antiviral.2018.05.012 · Cited by 35
Qadir, A. S., Stults, A. M., Murmann, A. E., & Peter, M. E. (2020) · Scientific Reports · doi:10.1038/s41598-020-58211-3 · Cited by 35
Endogenous retroelements as alarms for disruptions to cellular homeostasis
Lindholm, H. T., Chen, R. E., & Carvalho, D. D. D. (2022) · Trends in cancer · doi:10.1016/j.trecan.2022.09.001 · Cited by 34
Intracellular RNA Sensing in Mammalian Cells: Role in Stress Response and Cancer Therapies
Khodarev, N. N. (2018) · International review of cytology · doi:10.1016/bs.ircmb.2018.08.005 · Cited by 34
Evidence of Aberrant Immune Response by Endogenous Double‐Stranded RNAs: Attack from Within
Kim, S., Ku, Y., Ku, J., & Kim, Y. (2019) · BioEssays · doi:10.1002/bies.201900023 · Cited by 34
Filament-like Assemblies of Intracellular Nucleic Acid Sensors: Commonalities and Differences
Cadena, C., & Hur, S. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.09.023 · Cited by 34
Bravo, J. I., Nozownik, S., Danthi, P. S., & Benayoun, B. A. (2020) · Development · doi:10.1242/dev.175786 · Cited by 36
RNA regulatory mechanisms that control antiviral innate immunity
Gokhale, N. S., Smith, J. R., Gelder, R. D. V., & Savan, R. (2021) · Immunological Reviews · doi:10.1111/imr.13019 · Cited by 34
A phenolic small molecule inhibitor of RNase L prevents cell death from ADAR1 deficiency
Daou, S., Talukdar, M., Tang, J., Dong, B., Banerjee, S., Li, Y., Duffy, N. M., Ogunjimi, A. A., Gaughan, C., Jha, B. K., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2006883117 · Cited by 33
Zhang, J., Li, Y., Zhang, J., Liu, L., Chen, Y., Yang, X., Liao, X., He, M., Jia, Z., Fan, J., et al. (2023) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2023.07.006 · Cited by 32
Wang, Q., Lin, Z., Wang, Z., Ye, L., Xian, M., Xiao, L., Pan, S., Bi, E., Huang, Y.-H., Qian, J., et al. (2021) · Blood · doi:10.1182/blood.2020009856 · Cited by 32
McDonald, J. I., Diab, N., Arthofer, E., Hadley, M. M., Kanholm, T., Rentia, U., Gomez, S., Yu, A. Y. C., Grundy, E. E., Cox, O. L., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-4243 · Cited by 35
Lepelley, A., Wai, T., & Crow, Y. J. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.729763 · Cited by 33
The Role of Nucleic Acid Sensing in Controlling Microbial and Autoimmune Disorders
Matz, K. M., Guzman, R. M., & Goodman, A. G. (2018) · International review of cytology · doi:10.1016/bs.ircmb.2018.08.002 · Cited by 32
Dawn of Epitranscriptomic Medicine
Gatsiou, A., & Stellos, K. (2018) · Circulation Genomic and Precision Medicine · doi:10.1161/circgen.118.001927 · Cited by 31
Dauber, B., Saffran, H. A., & Smiley, J. R. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1008111 · Cited by 31
Innate Viral Sensor MDA5 and Coxsackievirus Interplay in Type 1 Diabetes Development
Blum, S. I., & Tse, H. M. (2020) · Microorganisms · doi:10.3390/microorganisms8070993 · Cited by 31
Tossberg, J. T., Heinrich, R. M., Farley, V. M., Crooke, P. S., & Aune, T. M. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000384 · Cited by 31
Rabaan, A. A., Mutair, A. S. A., Alhumaid, S., Garout, M. A., Alsubki, R. A., Alshahrani, F. S., Alfouzan, W. A., Alestad, J. H., Alsaleh, A. E., Al-Mozaini, M., et al. (2022) · Medicina · doi:10.3390/medicina58050680 · Cited by 34
RNA Editing and Retrotransposons in Neurology
Krestel, H. E., & Meier, J. C. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00163 · Cited by 32
Yu, Q., del Valle, A. H., Singh, R., & Modis, Y. (2021) · Nature Communications · doi:10.1038/s41467-021-27062-5 · Cited by 30
Zhang, Q., Xiu, B., Zhang, L.-Y., Chen, M., Chi, W., Li, L., Guo, R., Xue, J., Yang, B., Huang, X., et al. (2022) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2022-004666 · Cited by 31
Vlachogiannis, N. I., Verrou, K., Stellos, K., Sfikakis, P. P., & Paraskevis, D. N. (2021) · Clinical Immunology · doi:10.1016/j.clim.2021.108699 · Cited by 30
Seek and hide: the manipulating interplay of measles virus with the innate immune system
Ayasoufi, K., & Pfaller, C. K. (2020) · Current Opinion in Virology · doi:10.1016/j.coviro.2020.03.001 · Cited by 30
The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules
Chiang, D. C., Li, Y., & Ng, S. K. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.625504 · Cited by 30
The effects of RNA editing in cancer tissue at different stages in carcinogenesis
Kurkowiak, M., Arcimowicz, Ł., Chruściel, E., Urban‐Wójciuk, Z., Papak, I., Keegan, L. P., O’Connell, M. A., Kowalski, J., Hupp, T. R., & Marek-Trzonkowska, N. M. (2021) · RNA Biology · doi:10.1080/15476286.2021.1877024 · Cited by 29
The phenotype of the most common human ADAR1p150 Zα mutation P193A in mice is partially penetrant
Liang, Z., Chalk, A. M., Taylor, S., Goradia, A., Heraud-Farlow, J. E., & Walkley, C. R. (2023) · EMBO Reports · doi:10.15252/embr.202255835 · Cited by 30
Camilli, S., Lockey, R. F., & Kolliputi, N. (2023) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-023-01135-2 · Cited by 29
PACT prevents aberrant activation of PKR by endogenous dsRNA without sequestration
Ahmad, S., Zou, T., Hwang, J., Zhao, L., Wang, X., Davydenko, A., Buchumenski, I., Zhuang, P., Fishbein, A. R., Capcha-Rodriguez, D., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58433-x · Cited by 29
Sun, S., Frontini, F., Qi, W., Hariharan, A., Ronner, M., Wipplinger, M., Blanquart, C., Rehrauer, H., Fonteneau, J., & Felley‐Bosco, E. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.03.004 · Cited by 30
Interplay between RNA interference and transposable elements in mammals
Cornec, A., & Poirier, E. Z. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1212086 · Cited by 29
RNA-Guided Adenosine Deaminases: Advances and Challenges for Therapeutic RNA Editing
Chen, G., Katrekar, D., & Mali, P. (2019) · Biochemistry · doi:10.1021/acs.biochem.9b00046 · Cited by 28
Datta, R., Adamska, J. Z., Bhate, A., & Li, J. B. (2023) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1817 · Cited by 29
RNA sensing induced by chromosome missegregation augments anti-tumor immunity
Sasaki, N., Homme, M., Murayama, T., Osaki, T., Tenma, T., An, T., Takegami, Y., Tani, T., Gedeon, P. C., Kobayashi, Y., et al. (2024) · Molecular Cell · doi:10.1016/j.molcel.2024.11.025 · Cited by 31
Neurodegenerative diseases have genetic hallmarks of autoinflammatory disease
Richards, R. I., Robertson, S. A., & Kastner, D. L. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy139 · Cited by 27
Zhuang, T., Yi, X., Chen, J., Kang, P., Chen, X., Chen, J., Cui, T., Chang, Y., Ye, Z., Ni, Q., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2665-z · Cited by 29
RNA Editing in Neurological and Neurodegenerative Disorders
Cruz, P. H. C., & Kawahara, Y. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0787-9_18 · Cited by 27
Metadata
- Authors
- Chung, H., Calis, J. J. A., Wu, X., Sun, T., Yu, Y., Sarbanes, S. L., Dao Thi, V. L., Shilvock, A. R., Hoffmann, H.-H., Rosenberg, B. R., & Rice, C. M.
- Affiliations
- Rockefeller University (US)
- Corresponding author
- Rice, Charles M.
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2018-02
- Volume
- 172
- Issue
- 4
- Pages
- 811-824.e14
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC5831367
- OpenAlex
- W2784970793
- Cited by
- 538
- References
- 55
- Citations by year
- 2026: 53 · 2025: 69 · 2024: 67 · 2023: 71 · 2022: 64 · 2021: 74 · 2020: 60 · 2019: 44 · 2018: 36
- FWCI
- 19.03
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIAID/NIH (R01-AI091707, F32AI114211)
- John C. Whitehead Presidential Fellowship
- Netherlands Organization for Scientific Research
- Helmsley postdoctoral fellowship
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- ADAR1, Aicardi-Goutières syndrome, type I interferon, dsRNA sensing, PKR, MDA5, Alu elements, RNA editing, autoinflammation, neural progenitor cells, cell death, RNA polymerase II transcripts
- MeSH terms
- Interferon-Induced Helicase, IFIH1, Adenosine Deaminase, Humans, Inflammation, Nervous System Malformations, RNA Polymerase II, RNA, Double-Stranded, Protein Biosynthesis, RNA-Binding Proteins, Cell Death, eIF-2 Kinase, Alu Elements, Autoimmune Diseases of the Nervous System, Gene Knockout Techniques, HEK293 Cells, Neural Stem Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review