Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

The PARP1-Siah1 Axis Controls HIV-1 Transcription and Expression of Siah1 Substrates
Dan Yu, Rongdiao Liu, Geng Yang, et al.
Cell Reports (2018) Vol. 23, Iss. 13, pp. 3741-3749
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

The Enigmatic Function of PARP1: From PARylation Activity to PAR Readers
Tatiana Kamaletdinova, Zahra Fanaei‐Kahrani, Zhao‐Qi Wang
Cells (2019) Vol. 8, Iss. 12, pp. 1625-1625
Open Access | Times Cited: 133
Poly(ADP-ribosylation) of P-TEFb by PARP1 disrupts phase separation to inhibit global transcription after DNA damage
Huanyi Fu, Rongdiao Liu, Zixuan Jia, et al.
Nature Cell Biology (2022) Vol. 24, Iss. 4, pp. 513-525
Open Access | Times Cited: 52
Structure-guided drug design identifies a BRD4-selective small molecule that suppresses HIV
Qingli Niu, Zhiqing Liu, Edrous Alamer, et al.
Journal of Clinical Investigation (2019) Vol. 129, Iss. 8, pp. 3361-3373
Open Access | Times Cited: 69
Reiterative Enrichment and Authentication of CRISPRi Targets (REACT) identifies the proteasome as a key contributor to HIV-1 latency
Zichong Li, Jun Wu, Leonard Chávez, et al.
PLoS Pathogens (2019) Vol. 15, Iss. 1, pp. e1007498-e1007498
Open Access | Times Cited: 52
Poly(ADP-ribose)-dependent ubiquitination and its clinical implications
Christina A. Vivelo, Vinay Ayyappan, Anthony K. L. Leung
Biochemical Pharmacology (2019) Vol. 167, pp. 3-12
Open Access | Times Cited: 40
Zinc finger proteins in the host-virus interplay: multifaceted functions based on their nucleic acid-binding property
Guanming Wang, Chunfu Zheng
FEMS Microbiology Reviews (2020) Vol. 45, Iss. 3
Closed Access | Times Cited: 38
Africa-specific human genetic variation near CHD1L associates with HIV-1 load
Paul J. McLaren, Immacolata Porreca, Gennaro Iaconis, et al.
Nature (2023) Vol. 620, Iss. 7976, pp. 1025-1030
Closed Access | Times Cited: 11
Transcriptional impacts of substance use disorder and HIV on human ventral midbrain neurons and microglia
A. Wilson, Michelle M. Jacobs, Tova Y. Lambert, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
NF-κB-Driven HIV-1 Gene Expression in Human Cells Is Independent of Poly(ADP-ribose) polymerase-1 Function.
Denisse A. Gutiérrez, Manuel Llano
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
NAD+-consuming enzymes in immune defense against viral infection
Jialin Shang, Michael R. Smith, Ananya Anmangandla, et al.
Biochemical Journal (2021) Vol. 478, Iss. 23, pp. 4071-4092
Open Access | Times Cited: 27
Histone deacetylase inhibitors induce complex host responses that contribute to differential potencies of these compounds in HIV reactivation
Nadejda Beliakova‐Bethell, Amey Mukim, Cory White, et al.
Journal of Biological Chemistry (2019) Vol. 294, Iss. 14, pp. 5576-5589
Open Access | Times Cited: 25
DBC1, p300, HDAC3, and Siah1 coordinately regulate ELL stability and function for expression of its target genes
Subham Basu, Mahesh Barad, Dipika Yadav, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 12, pp. 6509-6520
Open Access | Times Cited: 22
Siah1 in cancer and nervous system diseases (Review)
Hui Zhang, Jie Wang, Yidong Ge, et al.
Oncology Reports (2021) Vol. 47, Iss. 2
Open Access | Times Cited: 19
NAD+ Degrading Enzymes, Evidence for Roles During Infection
Arnold Tan, Craig Doig
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 18
Circ-CCNB1 Modulates Trophoblast Proliferation and Invasion in Spontaneous Abortion by Regulating miR-223/SIAH1 axis
Mengyu Jing, Laidi Xie, Xi Chen, et al.
Endocrinology (2022) Vol. 163, Iss. 8
Open Access | Times Cited: 12
Chronic HIV Transcription, Translation, and Persistent Inflammation
Jonathan M. Kilroy, Andrew A. Leal, Andrew J. Henderson
Viruses (2024) Vol. 16, Iss. 5, pp. 751-751
Open Access | Times Cited: 2
Phosphorylation Targets of DNA-PK and Their Role in HIV-1 Replication
Andrey Anisenko, Marina Kan, Olga Shadrina, et al.
Cells (2020) Vol. 9, Iss. 8, pp. 1907-1907
Open Access | Times Cited: 17
Fine tuning of the transcription juggernaut: A sweet and sour saga of acetylation and ubiquitination
Avik K. Ghosh, Poushali Chakraborty, Debabrata Biswas
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2023) Vol. 1866, Iss. 3, pp. 194944-194944
Closed Access | Times Cited: 6
Design, synthesis and biological evaluation of methylenehydrazine-1-carboxamide derivatives with (5-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)-1H-indole scaffold: Novel potential CDK9 inhibitors
Hongyu Hu, Jun Wu, Mingtao Ao, et al.
Bioorganic Chemistry (2020) Vol. 102, pp. 104064-104064
Closed Access | Times Cited: 16
Host cell factors stimulate HIV-1 transcription by antagonizing substrate-binding function of Siah1 ubiquitin ligase to stabilize transcription elongation factor ELL2
Jun Wu, Yuhua Xue, Xiang Gao, et al.
Nucleic Acids Research (2020)
Open Access | Times Cited: 15
ADP‐ribosylation in evasion, promotion and exacerbation of immune responses
Maria Manuela Rosado, Claudio Pioli
Immunology (2021) Vol. 164, Iss. 1, pp. 15-30
Open Access | Times Cited: 14
miRNA-149 targets PARP-2 in endometrial epithelial and stromal cells to regulate the trophoblast attachment process
Upendra Kumar Soni, Sangappa B. Chadchan, Rakesh Kumar Gupta, et al.
Molecular Human Reproduction (2021) Vol. 27, Iss. 6
Closed Access | Times Cited: 12
Inhibition of the Super Elongation Complex Suppresses Herpes Simplex Virus Immediate Early Gene Expression, Lytic Infection, and Reactivation from Latency
Roberto Alfonso, Jesse H. Arbuckle, Jodi L. Vogel, et al.
mBio (2020) Vol. 11, Iss. 3
Open Access | Times Cited: 12
PARP1 Might Substitute HSF1 to Reactivate Latent HIV-1 by Binding to Heat Shock Element
Xinfeng Xu, Yingtong Lin, Xiaoyun Zeng, et al.
Cells (2022) Vol. 11, Iss. 15, pp. 2331-2331
Open Access | Times Cited: 8
Poly (ADP-ribose) polymerase-1 regulates HIV-1 replication in human CD4+ T cells
Zachary Martinez, Denisse A. Gutiérrez, Carlos A. Valenzuela, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Page 1 - Next Page

Scroll to top