OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

E3 ubiquitin ligases, the powerful modulator of innate antiviral immunity
Yi Zheng, Chengjiang Gao
Cellular Immunology (2019) Vol. 340, pp. 103915-103915
Closed Access | Times Cited: 43

Showing 1-25 of 43 citing articles:

Comparative Structure and Function Analysis of the RIG-I-Like Receptors: RIG-I and MDA5
Morgan Brisse, Hinh Ly
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 306

USP18 positively regulates innate antiviral immunity by promoting K63-linked polyubiquitination of MAVS
Jinxiu Hou, Lulu Han, Ze Zhao, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 84

TBK1, a central kinase in innate immune sensing of nucleic acids and beyond
Ruyuan Zhou, Qian Zhang, Pinglong Xu
Acta Biochimica et Biophysica Sinica (2020) Vol. 52, Iss. 7, pp. 757-767
Open Access | Times Cited: 78

Potential Inhibitors Targeting Papain-Like Protease of SARS-CoV-2: Two Birds With One Stone
Haihai Jiang, Peiyao Yang, Jin Zhang
Frontiers in Chemistry (2022) Vol. 10
Open Access | Times Cited: 43

Epigenetic Control of Innate Immunity: Consequences of Acute Respiratory Virus Infection
Rivka Bella Lefkowitz, Clare M. Miller, Juan David Martinez-Caballero, et al.
Viruses (2024) Vol. 16, Iss. 2, pp. 197-197
Open Access | Times Cited: 10

Structural analysis of RIG-I-like receptors reveals ancient rules of engagement between diverse RNA helicases and TRIM ubiquitin ligases
Kazuki Kato, Sadeem Ahmad, Zixiang Zhu, et al.
Molecular Cell (2020) Vol. 81, Iss. 3, pp. 599-613.e8
Open Access | Times Cited: 69

HERC5 and the ISGylation Pathway: Critical Modulators of the Antiviral Immune Response
Nicholas A. Mathieu, Ermela Paparisto, Stephen D. Barr, et al.
Viruses (2021) Vol. 13, Iss. 6, pp. 1102-1102
Open Access | Times Cited: 45

The Dual Role of the Innate Immune System in the Effectiveness of mRNA Therapeutics
Аlbert R. Muslimov, Valeriy Tereshchenko, Daniil Shevyrev, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 19, pp. 14820-14820
Open Access | Times Cited: 19

Stress granule-localized USP8 potentiates cGAS-mediated type I interferonopathies through deubiquitination of DDX3X
Xuejing Zhang, Lulu Han, Jinxiu Hou, et al.
Cell Reports (2024) Vol. 43, Iss. 6, pp. 114248-114248
Open Access | Times Cited: 7

Phase Separation: The Robust Modulator of Innate Antiviral Signaling and SARS-CoV-2 Infection
Yi Zheng, Chengjiang Gao
Pathogens (2023) Vol. 12, Iss. 2, pp. 243-243
Open Access | Times Cited: 15

PRV-encoded UL13 protein kinase acts as an antagonist of innate immunity by targeting IRF3-signaling pathways
Lin Lv, Mingzhu Cao, Juan Bai, et al.
Veterinary Microbiology (2020) Vol. 250, pp. 108860-108860
Closed Access | Times Cited: 33

RING finger protein 13 protects against nonalcoholic steatohepatitis by targeting STING-relayed signaling pathways
Zhibin Lin, Peijun Yang, Yufeng Hu, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 12

Emerging Roles of TRIM56 in Antiviral Innate Immunity
Dang Wang, Kui Li
Viruses (2025) Vol. 17, Iss. 1, pp. 72-72
Open Access

IDR-driven TOLLIP condensates antagonize the innate antiviral immunity by promoting the deSUMOylation of MAVS
Jinxiu Hou, Shengnan Zheng, Xuejing Zhang, et al.
Cell Reports (2025) Vol. 44, Iss. 3, pp. 115348-115348
Open Access

RNF149 modulates the type I IFN innate antiviral immune responses through degrading IRF3
Mengyun Wu, Jiamin Cai, Guodong Qiao, et al.
PLoS Pathogens (2025) Vol. 21, Iss. 4, pp. e1013051-e1013051
Open Access

Molecular analyses of the gill symbiosis of the bathymodiolin mussel Gigantidas platifrons
Hao Wang, Huan Zhang, Zhaoshan Zhong, et al.
iScience (2020) Vol. 24, Iss. 1, pp. 101894-101894
Open Access | Times Cited: 31

Zebrafish F-box Protein fbxo3 Negatively Regulates Antiviral Response through Promoting K27-Linked Polyubiquitination of the Transcription Factors irf3 and irf7
Zhi Li, Sijia Fan, Jing Wang, et al.
The Journal of Immunology (2020) Vol. 205, Iss. 7, pp. 1897-1908
Open Access | Times Cited: 28

Zebrafish otud6b Negatively Regulates Antiviral Responses by Suppressing K63-Linked Ubiquitination of irf3 and irf7
Ziwen Zhou, Xiaolian Cai, Junji Zhu, et al.
The Journal of Immunology (2021) Vol. 207, Iss. 1, pp. 244-256
Open Access | Times Cited: 24

Fine-tuning of antiviral innate immunity by ubiquitination
Yi Zheng, Chengjiang Gao
Advances in immunology (2019), pp. 95-128
Closed Access | Times Cited: 29

Novel insights into stress-induced susceptibility to influenza: corticosterone impacts interferon-β responses by Mfn2-mediated ubiquitin degradation of MAVS
Zhuo Luo, Lifang Liu, Yingnan Jiang, et al.
Signal Transduction and Targeted Therapy (2020) Vol. 5, Iss. 1
Open Access | Times Cited: 27

Human Beta Papillomavirus Type 8 E1 and E2 Proteins Suppress the Activation of the RIG-I-Like Receptor MDA5
Stephanie Rattay, Martin Hufbauer, Christian Hagen, et al.
Viruses (2022) Vol. 14, Iss. 7, pp. 1361-1361
Open Access | Times Cited: 12

E3 ubiquitin ligase ANKIB1 attenuates antiviral immune responses by promoting K48-linked polyubiquitination of MAVS
Wei Liu, Cui Yuan, Buwen Fu, et al.
Cell Reports (2024) Vol. 43, Iss. 9, pp. 114687-114687
Open Access | Times Cited: 2

The Ubiquitin Sensor and Adaptor Protein p62 Mediates Signal Transduction of a Viral Oncogenic Pathway
Ling Wang, Mary E. A. Howell, Ayrianna Sparks-Wallace, et al.
mBio (2021) Vol. 12, Iss. 5
Open Access | Times Cited: 13

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