MicroRNA

Conserved Seed Pairing, Often Flanked by Adenosines, Indicates that Thousands of Human Genes are MicroRNA Targets

Lewis, B. P., Burge, C. B., & Bartel, D. P. (2005) · Cell · doi:10.1016/j.cell.2004.12.035 · Cited by 11,855 · see citing works

Most mammalian mRNAs are conserved targets of microRNAs

Friedman, R. C., Farh, K. K.-H., Burge, C. B., & Bartel, D. P. (2009) · Genome Research · doi:10.1101/gr.082701.108 · Cited by 8,462 · see citing works

Predicting effective microRNA target sites in mammalian mRNAs

Agarwal, V., Bell, G. W., Nam, J.-W., & Bartel, D. P. (2015) · eLife · doi:10.7554/elife.05005 · Cited by 7,318 · see citing works

Regulation of microRNA biogenesis

Ha, M., & Kim, V. N. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3838 · Cited by 5,462 · see citing works

Real-time quantification of microRNAs by stem-loop RT-PCR

Chen, C. (2005) · Nucleic Acids Research · doi:10.1093/nar/gni178 · Cited by 4,931 · see citing works

MicroRNA therapeutics: towards a new era for the management of cancer and other diseases

Rupaimoole, R., & Slack, F. J. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2016.246 · Cited by 4,741 · see citing works

Silencing of microRNAs in vivo with ‘antagomirs’

Krützfeldt, J., Rajewsky, N., Braich, R., Rajeev, K. G., Tuschl, T., Manoharan, M., & Stoffel, M. (2005) · Nature · doi:10.1038/nature04303 · Cited by 3,949 · see citing works

Human MicroRNA Targets

John, B., Enright, A. J., Aravin, A., Tuschl, T., Sander, C., & Marks, D. S. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020363 · Cited by 3,796 · see citing works

MicroRNA targets in Drosophila

Enright, A. J., John, B., Gaul, U., Tuschl, T., Sander, C., & Marks, D. S. (2003) · Genome Biology · doi:10.1186/gb-2003-5-1-r1 · Cited by 3,597 · see citing works

The MicroRNA Spectrum in 12 Body Fluids

Weber, J. A., Baxter, D. H., Zhang, S., Huang, D. Y. C., Huang, K., Lee, M., Galas, D. J., & Wang, K. (2010) · Clinical Chemistry · doi:10.1373/clinchem.2010.147405 · Cited by 2,754 · see citing works

The microRNA.org resource: targets and expression

Betel, D., Wilson, M. T., Gabow, A. P., Marks, D. S., & Sander, C. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm995 · Cited by 2,490 · see citing works

Towards a molecular understanding of microRNA-mediated gene silencing

Jonas, S., & Izaurralde, E. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3965 · Cited by 1,872 · see citing works

MicroRNA profiling: approaches and considerations

Pritchard, C. C., Cheng, H. H., & Tewari, M. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3198 · Cited by 1,765 · see citing works

Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites

Betel, D., Koppal, A., Agius, P., Sander, C., & Leslie, C. (2010) · Genome Biology · doi:10.1186/gb-2010-11-8-r90 · Cited by 1,592 · see citing works

Facile Means for Quantifying Microrna Expression by Real-Time PCR

Shi, R., & Chiang, V. L. (2005) · BioTechniques · doi:10.2144/000112010 · Cited by 707 · see citing works

MiRNA Biogenesis and Regulation of Diseases: An Overview

Vishnoi, A., & Rani, S. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6524-3_1 · Cited by 694 · see citing works

Identification and consequences of miRNA–target interactions — beyond repression of gene expression

Hausser, J., & Zavolan, M. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3765 · Cited by 620 · see citing works

Expanding the MicroRNA Targeting Code: Functional Sites with Centered Pairing

Shin, C., Nam, J.-W., Farh, K. K.-H., Chiang, H. R., Shkumatava, A., & Bartel, D. P. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.06.005 · Cited by 611 · see citing works

In situ detection of miRNAs in animal embryos using LNA-modified oligonucleotide probes

Kloosterman, W. P., Wienholds, E., de Bruijn, E., Kauppinen, S., & Plasterk, R. H. A. (2006) · Nature Methods · doi:10.1038/nmeth843 · Cited by 540 · see citing works

Regulatory mechanisms of microRNA expression

Gulyaeva, L. F., & Kushlinskiy, N. E. (2016) · Journal of Translational Medicine · doi:10.1186/s12967-016-0893-x · Cited by 464 · see citing works

Practical Aspects of microRNA Target Prediction

Witkos, T. M., Kościańska, E., & Krzyżosiak, W. J. (2011) · Current Molecular Medicine · doi:10.2174/156652411794859250 · Cited by 463 · see citing works

Methodological challenges in utilizing mi<scp>RNA</scp>s as circulating biomarkers

Moldovan, L., Batte, K. E., Trgovcich, J., Wisler, J., Marsh, C. B., & Piper, M. (2014) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12236 · Cited by 436 · see citing works

Chemical modification and design of anti-miRNA oligonucleotides

Lennox, K. A., & Behlke, M. A. (2011) · Gene Therapy · doi:10.1038/gt.2011.100 · Cited by 432 · see citing works

Specific and sensitive quantitative RT-PCR of miRNAs with DNA primers

Balcells, I., Cirera, S., & Busk, P. K. (2011) · BMC Biotechnology · doi:10.1186/1472-6750-11-70 · Cited by 310 · see citing works

Targeting non-coding RNAs with the CRISPR/Cas9 system in human cell lines

Ho, T.-T., Zhou, N., Huang, J., Koirala, P., Xu, M., Fung, R., Wu, F., & Mo, Y. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1198 · Cited by 244 · see citing works

Importance of RNA isolation methods for analysis of exosomal RNA: Evaluation of different methods

Eldh, M., Lötvall, J. O., Malmhäll, C., & Ekström, K. M. (2012) · Molecular Immunology · doi:10.1016/j.molimm.2012.02.001 · Cited by 227 · see citing works

Diagnostic, functional, and therapeutic roles of microRNA in allergic diseases

Lu, T. X., & Rothenberg, M. E. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.04.039 · Cited by 221 · see citing works

Short Structured RNAs with Low GC Content Are Selectively Lost during Extraction from a Small Number of Cells

Kim, Y. K., Yeo, J., Kim, B., Ha, M., & Kim, V. N. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.05.036 · Cited by 221 · see citing works

Transfection of microRNA Mimics Should Be Used with Caution

Jin, H. Y., González-Martín, A., Miletic, A. V., Lai, M., Knight, S., Sabouri-Ghomi, M., Head, S. R., Macauley, M. S., Rickert, R. C., & Xiao, C. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00340 · Cited by 194 · see citing works

Lentivirus-mediated antagomir expression for specific inhibition of miRNA function

Scherr, M., Venturini, L., Battmer, K., Schaller-Schoenitz, M., Schaefer, D., Dallmann, I., Ganser, A., & Eder, M. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm971 · Cited by 190 · see citing works

A Resource for the Conditional Ablation of microRNAs in the Mouse

Park, C. Y., Jeker, L. T., Carver-Moore, K., Oh, A., Liu, H. J., Cameron, R., Richards, H. W., Li, Z., Adler, D., Yoshinaga, Y., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.02.008 · Cited by 174 · see citing works

On Measuring miRNAs after Transient Transfection of Mimics or Antisense Inhibitors

Thomson, D. W., Bracken, C. P., Szubert, J. M., & Goodall, G. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055214 · Cited by 118 · see citing works

Specificity and functionality of microRNA inhibitors

Robertson, B., Dalby, A. B., Karpilow, J. M., Khvorova, A., Leake, D., & Vermeulen, A. (2010) · Silence · doi:10.1186/1758-907x-1-10 · Cited by 79 · see citing works

VEGF controls lung Th2 inflammation via the miR-1–Mpl (myeloproliferative leukemia virus oncogene)–P-selectin axis

Takyar, S. S., Vasavada, H. H., Zhang, J., Ahangari, F., Niu, N., Liu, Q., Lee, C. G., Cohn, L. E., & Elias, J. A. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20121200 · Cited by 67 · see citing works

MicroRNAs in Allergic Disease

Dissanayake, E., & Inoue, Y. (2016) · Current Allergy and Asthma Reports · doi:10.1007/s11882-016-0648-z · Cited by 64 · see citing works

MicroRNA In Situ Hybridization

Nielsen, B. S. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-427-8_5 · Cited by 63 · see citing works

MicroRNA in Chronic Rhinosinusitis and Allergic Rhinitis

Zhang, X., Zhang, Y., & Liu, Z. (2014) · Current Allergy and Asthma Reports · doi:10.1007/s11882-013-0415-3 · Cited by 53 · see citing works

Passenger strand loading in overexpression experiments using microRNA mimics

Søkilde, R., Newie, I., Persson, H., Borg, Å., & Rovira, C. (2015) · RNA Biology · doi:10.1080/15476286.2015.1020270 · Cited by 50 · see citing works

Validation of a multiplex reverse transcription and pre-amplification method using TaqMan® MicroRNA assays

Carré, J. L., Lamon, S., & Léger, B. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00413 · Cited by 34 · see citing works

MicroRNA in United Airway Diseases

Liu, Z., Zhang, X.-H., Callejas, F. D. B., & Mullol, J. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17050716 · Cited by 33 · see citing works

Functional Screening Identifies Human miRNAs that Modulate Adenovirus Propagation in Prostate Cancer Cells

Hodzic, J., Sie, D., Vermeulen, A., & van Beusechem, V. W. (2017) · Human Gene Therapy · doi:10.1089/hum.2016.143 · Cited by 28 · see citing works

Functional Analysis of microRNA in Multiple Myeloma

Martino, M. T. D., Amodio, N., Tassone, P., & Tagliaferri, P. (2015) · Methods in molecular biology · doi:10.1007/7651_2015_250 · Cited by 18 · see citing works

Lentiviral Overexpression of miRNAs

Zöllner, H., Hahn, S. A., & Maghnouj, A. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-703-7_15 · Cited by 14 · see citing works

GPX4: The hub of lipid oxidation, ferroptosis, disease and treatment

Liu, Y., Wan, Y., Jiang, Y., Zhang, L., & Cheng, W. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.188890 · Cited by 536 · see citing works

GPX4, ferroptosis, and diseases

Zhang, W., Liu, Y., Yan, L., Zhu, C., & Zou, Z. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116512 · Cited by 447 · see citing works

Oxidative Stress and Inflammation in Osteoporosis: Molecular Mechanisms Involved and the Relationship with microRNAs

Iantomasi, T., Romagnoli, C., Palmini, G., Donati, S., Falsetti, I., Miglietta, F., Aurilia, C., Marini, F., Giusti, F., & Brandi, M. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043772 · Cited by 395 · see citing works

CircRNA hsa_circRNA_104348 promotes hepatocellular carcinoma progression through modulating miR-187-3p/RTKN2 axis and activating Wnt/β-catenin pathway

Huang, G., Liang, M., Liu, H., Huang, J., Li, P., Wang, C., Zhang, Y., Lin, Y., & Jiang, X. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03276-1 · Cited by 325 · see citing works

Recent advances in exosome-mediated nucleic acid delivery for cancer therapy

Zhang, Y., Liu, Q., Zhang, X., Huang, H., Tang, S., Chai, Y., Xu, Z., Li, M., Chen, X., Liu, J., et al. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01472-z · Cited by 306 · see citing works

The Role of Exosomes and Exosomal MicroRNA in Cardiovascular Disease

Zheng, D., Huo, M., Li, B., Wang, W., Piao, H., Wang, Y., Zhu, Z., Li, D., Wang, T., & Liu, K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.616161 · Cited by 251 · see citing works

Pyroptosis and ferroptosis induced by mixed lineage kinase 3 (MLK3) signaling in cardiomyocytes are essential for myocardial fibrosis in response to pressure overload

Wang, J., Deng, B., Liu, Q., Huang, Y., Chen, W., Li, J., Zhou, Z., Zhang, L., Liang, B., He, J., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02777-3 · Cited by 223 · see citing works

miR-182-5p and miR-378a-3p regulate ferroptosis in I/R-induced renal injury

Ding, C., Ding, X., Zheng, J., Wang, B., Yang, L., Xiang, H., Dou, M., Qiao, Y., Tian, P., & Xue, W. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03135-z · Cited by 213 · see citing works

Noncoding RNAs regulate alternative splicing in Cancer

Liu, Y., Liu, X., Lin, C., Jia, X., Zhu, H., Song, J. H., & Zhang, Y. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01798-2 · Cited by 183 · see citing works

Extracellular vesicles derived from M1 macrophages deliver miR-146a-5p and miR-146b-5p to suppress trophoblast migration and invasion by targeting TRAF6 in recurrent spontaneous abortion

Ding, J., Zhang, Y., Cai, X., Zhang, Y., Yan, S., Wang, J., Zhang, S., Yin, T., Yang, C., & Yang, J. (2021) · Theranostics · doi:10.7150/thno.58731 · Cited by 170 · see citing works

Mononuclear phagocyte system blockade using extracellular vesicles modified with CD47 on membrane surface for myocardial infarction reperfusion injury treatment

Wei, Z., Chen, Z., Zhao, Y., Fan, F., Xiong, W., Song, S., Yin, Y., Hu, J., Yang, K., Yang, L., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121000 · Cited by 163 · see citing works

Landscape of small nucleic acid therapeutics: moving from the bench to the clinic as next-generation medicines

Liu, M., Wang, Y., Zhang, Y.-B., Hu, D., Tang, L., Zhou, B., & Yang, L. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02112-8 · Cited by 174 · see citing works

Therapeutic delivery of microRNA-125a-5p oligonucleotides improves recovery from myocardial ischemia/reperfusion injury in mice and swine

Gao, L., Qiu, F., Cao, H., Li, H., Dai, G., Ma, T., Gong, Y., Luo, W., Zhu, D., Qiu, Z., et al. (2023) · Theranostics · doi:10.7150/thno.73568 · Cited by 145 · see citing works

The role of miRNAs in colorectal cancer progression and chemoradiotherapy

Zhang, N., Hu, X., Du, Y., & Du, J. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.111099 · Cited by 145 · see citing works

Extracellular vesicles: Emerging tools as therapeutic agent carriers

Liu, S., Wu, X., Chandra, S., Lyon, C. J., Ning, B., Jiang, L., Fan, J., & Hu, Y. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.05.002 · Cited by 146 · see citing works

Targeting epigenetic regulators as a promising avenue to overcome cancer therapy resistance

Song, J., Yang, P. X., Chen, C., Ding, W., Tillement, O., Bai, H., & Zhang, S. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02266-z · Cited by 145 · see citing works

Metal–organic frameworks (MOFs) as host materials for the enhanced delivery of biomacromolecular therapeutics

Tong, P., Zhu, L. Z., Zang, Y., Li, J. X., He, X., & James, T. D. (2021) · Chemical Communications · doi:10.1039/d1cc05157a · Cited by 126 · see citing works

Human umbilical cord mesenchymal stem cells derived exosome shuttling mir-129-5p attenuates inflammatory bowel disease by inhibiting ferroptosis

Wei, Z., Hang, S., Ocansey, D. K. W., Zhang, Z., Wang, B., Zhang, X., & Mao, F. (2023) · Journal of Nanobiotechnology · doi:10.1186/s12951-023-01951-x · Cited by 119 · see citing works

Target c-Myc to treat pancreatic cancer

Ala, M. (2022) · Cancer Biology & Therapy · doi:10.1080/15384047.2021.2017223 · Cited by 119 · see citing works

Metformin induces ferroptosis by targeting miR-324-3p/GPX4 axis in breast cancer

Hou, Y.-F., Cai, S., Yu, S., & Lin, H. (2021) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmaa180 · Cited by 116 · see citing works

Regulation of lung epithelial cell senescence in smoking-induced COPD/emphysema by microR-125a-5p via Sp1 mediation of SIRT1/HIF-1a

Wu, H., Ma, H., Wang, L., Zhang, H., Lu, L., Xiao, T., Cheng, C., Wang, P., Yang, Y., Wu, M., et al. (2021) · International Journal of Biological Sciences · doi:10.7150/ijbs.65861 · Cited by 116 · see citing works

MiRNAs and Cancer: Key Link in Diagnosis and Therapy

Shi, Y., Liu, Z., Lin, Q., Luo, Q., Cen, Y., Li, J., Fang, X., & Gong, C. (2021) · Genes · doi:10.3390/genes12081289 · Cited by 115 · see citing works

Berberine for gastric cancer prevention and treatment: Multi-step actions on the Correa’s cascade underlie its therapeutic effects

Liu, Q., Tang, J., Chen, S., Hu, S., Shen, C., Xiang, J., Chen, N., Wang, J., Ma, X., Zhang, Y., et al. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106440 · Cited by 111 · see citing works

CircPVT1 contributes to chemotherapy resistance of lung adenocarcinoma through miR-145-5p/ABCC1 axis

Zheng, F., & Xu, R. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.109828 · Cited by 110 · see citing works

Designing strategies of small-molecule compounds for modulating non-coding RNAs in cancer therapy

Zhao, R., Fu, J., Zhu, L., Chen, Y., & Liu, B. (2022) · Journal of Hematology & Oncology · doi:10.1186/s13045-022-01230-6 · Cited by 109 · see citing works

The Progress and Promise of RNA Medicine─An Arsenal of Targeted Treatments

Sasso, J. M., Ambrose, B. J. B., Tenchov, R., Datta, R. S., Basel, M. T., DeLong, R. K., & Zhou, Q. A. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c00024 · Cited by 104 · see citing works

Early Biomarkers of Neurodegenerative and Neurovascular Disorders in Diabetes

Gąsecka, A., Siwik, D., Gajewska, M., Jaguszewski, M. J., Mazurek, T., Filipiak, K. J., Postula, M. A., & Eyileten, C. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9092807 · Cited by 103 · see citing works

MiR-27a-3p Promotes Non-Small Cell Lung Cancer Through SLC7A11-Mediated-Ferroptosis

Lu, X., Kang, N., Ling, X.-X., Pan, M., Du, W., & Gao, S. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.759346 · Cited by 103 · see citing works

Updated review of advances in microRNAs and complex diseases: experimental results, databases, webservers and data fusion

Li, H., Zhang, L., & Chen, X. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac397 · Cited by 101 · see citing works

Exosomal microRNA-22-3p alleviates cerebral ischemic injury by modulating KDM6B/BMP2/BMF axis

Zhang, Y., Liu, J., Su, M., Wang, X., & Xie, C. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-02091-x · Cited by 100 · see citing works

Infrared Plasmonic Biosensor with Tetrahedral DNA Nanostructure as Carriers for Label‐Free and Ultrasensitive Detection of miR‐155

Hui, X., Yang, C., Li, D., He, X., Huang, H., Zhou, H., Chen, M., Lee, C., & Mu, X. (2021) · Advanced Science · doi:10.1002/advs.202100583 · Cited by 99 · see citing works

MicroRNA‐351 eases insulin resistance and liver gluconeogenesis via the PI3K/AKT pathway by inhibiting FLOT2 in mice of gestational diabetes mellitus

Chen, S., Liu, X., & Peng, Y. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14079 · Cited by 97 · see citing works

Hypoxic preconditioning rejuvenates mesenchymal stem cells and enhances neuroprotection following intracerebral hemorrhage via the miR-326-mediated autophagy

Liu, J., He, J., Ge, L., Xiao, H., Huang, Y., Zeng, L., Jiang, Z., Lü, M., & Hu, Z. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02480-w · Cited by 97 · see citing works

Recent Advances and Challenges in Gene Delivery Mediated by Polyester-Based Nanoparticles

Piperno, A., Sciortino, M. T., Giusto, E., Montesi, M., Panseri, S., & Scala, A. (2021) · International Journal of Nanomedicine · doi:10.2147/ijn.s321329 · Cited by 97 · see citing works

Recent advances in lean NAFLD

Xu, R., Pan, J., Zhou, W., Ji, G., & Dang, Y. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113331 · Cited by 97 · see citing works

Blood biomarkers for assessment of mitochondrial dysfunction: An expert review

Hubens, W. H. G., Vallbona-Garcia, A., de Coo, I. F. M., van Tienen, F. H. J., Webers, C. A. B., Smeets, H. J. M., & Gorgels, T. G. M. F. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.10.008 · Cited by 94 · see citing works

ALKBH5 promotes lung fibroblast activation and silica-induced pulmonary fibrosis through miR-320a-3p and FOXM1

Sun, W., Li, Y., Ma, D., Liu, Y., Xu, Q., Cheng, D., Li, G., & Ni, C. (2022) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-022-00329-5 · Cited by 93 · see citing works

MicroRNAs in infectious diseases: potential diagnostic biomarkers and therapeutic targets

Kimura, M., Kothari, S. P., Gohir, W., Camargo, J. F., & Husain, S. (2023) · Clinical Microbiology Reviews · doi:10.1128/cmr.00015-23 · Cited by 97 · see citing works

Lipid Lowering Therapy: An Era Beyond Statins

Abdul‐Rahman, T., Bukhari, S. M. A., Cantu‐Herrera, E., Awuah, W. A., Lawrence, J. A., de Andrade, H., Patel, N., Shah, R. M., Shaikh, R., Capriles, C. A. A., et al. (2022) · Current Problems in Cardiology · doi:10.1016/j.cpcardiol.2022.101342 · Cited by 91 · see citing works

Biomarkers in Breast Cancer: An Old Story with a New End

Alves, L. N. R., Meira, D. D., Merigueti, L. P., Casotti, M. C., Ventorim, D. P., Almeida, J. F. F., de Sousa, V. P., Sant’Ana, M. C., da Cruz, R. G. C., Louro, L. S., et al. (2023) · Genes · doi:10.3390/genes14071364 · Cited by 90 · see citing works

Müller Glia-Mediated Retinal Regeneration

Gao, H., Luodan, A., Huang, X., Chen, X., & Xu, H. (2021) · Molecular Neurobiology · doi:10.1007/s12035-020-02274-w · Cited by 83 · see citing works

Endothelial progenitor cell-derived exosomes promote anti-inflammatory macrophages via SOCS3/JAK2/STAT3 axis and improve the outcome of spinal cord injury

Yuan, F., Peng, W., Yang, Y., Xu, J., Liu, Y., Xie, Y., Huang, T., Shi, C., Ding, Y., Li, C., et al. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02833-7 · Cited by 86 · see citing works

MicroRNA in extracellular vesicles regulates inflammation through macrophages under hypoxia

Li, Y., Tan, J., Miao, Y., & Zhang, Q. (2021) · Cell Death Discovery · doi:10.1038/s41420-021-00670-2 · Cited by 82 · see citing works

Frailty biomarkers under the perspective of geroscience: A narrative review

Gonçalves, R. S. D. S. A., Maciel, Á. C. C., Rolland, Y., Vellas, B. J., & Barreto, P. D. S. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101737 · Cited by 85 · see citing works

miR-205: A Potential Biomedicine for Cancer Therapy

Chauhan, N., Dhasmana, A., Jaggi, M., Chauhan, S. C., & Yallapu, M. M. (2020) · Cells · doi:10.3390/cells9091957 · Cited by 82 · see citing works

Autophagy in Age-Related Macular Degeneration: A Regulatory Mechanism of Oxidative Stress

Zhang, Z.-Y., Bao, X.-L., Cong, Y.-Y., Fan, B., & Li, G. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/2896036 · Cited by 80 · see citing works

Targeting epigenetic regulators for inflammation: Mechanisms and intervention therapy

Zhang, S., Meng, Y., Zhou, L., Qiu, L., Wang, H., Su, D., Zhang, B., Chan, K. M., & Han, J. (2022) · MedComm · doi:10.1002/mco2.173 · Cited by 82 · see citing works

HDAC3 protects against atherosclerosis through inhibition of inflammation via the microRNA-19b/PPARγ/NF-κB axis

Wang, J., Xu, X., Li, P., Zhang, B., & Zhang, J. (2021) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2021.02.013 · Cited by 79 · see citing works

The Applications of Gold Nanoparticles in the Diagnosis and Treatment of Gastrointestinal Cancer

Yang, Z., Wang, D., Zhang, C., Liu, H., Hao, M., Kan, S., Liu, D., & Liu, W. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2021.819329 · Cited by 80 · see citing works

Bone marrow mesenchymal stem cell-derived exosomal miR-21a-5p alleviates renal fibrosis by attenuating glycolysis by targeting PFKM

Xu, S., Cheuk, Y. C., Jia, Y., Chen, T., Chen, J., Luo, Y., Cao, Y., Guo, J., Dong, L., Zhang, Y., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05305-7 · Cited by 81 · see citing works

Targeting CLDN18.2 in cancers of the gastrointestinal tract: new drugs and new indications

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