Towards a molecular understanding of microRNA-mediated gene silencing

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

Regulation of microRNA biogenesis

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

Mammalian microRNAs predominantly act to decrease target mRNA levels

Guo, H., Ingolia, N. T., Weissman, J. S., & Bartel, D. P. (2010) · Nature · doi:10.1038/nature09267 · Cited by 3,886

The impact of microRNAs on protein output

Baek, D., Villén, J., Shin, C., Camargo, F. D., Gygi, S. P., & Bartel, D. P. (2008) · Nature · doi:10.1038/nature07242 · Cited by 3,592

Widespread changes in protein synthesis induced by microRNAs

Selbach, M., Schwanhäusser, B., Thierfelder, N., Fang, Z., Khanin, R., & Rajewsky, N. (2008) · Nature · doi:10.1038/nature07228 · Cited by 3,429

The mechanism of eukaryotic translation initiation and principles of its regulation

Jackson, R. J., Hellen, C. U. T., & Pestova, T. V. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2838 · Cited by 2,759

Gene silencing by microRNAs: contributions of translational repression and mRNA decay

Huntzinger, E., & Izaurralde, E. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2936 · Cited by 2,339

A brain-specific microRNA regulates dendritic spine development

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Zebrafish MiR-430 Promotes Deadenylation and Clearance of Maternal mRNAs

Giraldez, A. J., Mishima, Y., Rihel, J., Grocock, R. J., Van Dongen, S., Inoue, K., Enright, A. J., & Schier, A. F. (2006) · Science · doi:10.1126/science.1122689 · Cited by 1,647

Inhibition of Translational Initiation by Let-7 MicroRNA in Human Cells

Pillai, R. S., Bhattacharyya, S. N., Artus-Revel, C. G., Zoller, T., Cougot, N., Basyuk, E. I., Bertrand, É., & Filipowicz, W. (2005) · Science · doi:10.1126/science.1115079 · Cited by 1,489

The Non-coding Side of Medulloblastoma

Laneve, P., & Caffarelli, E. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00275 · Cited by 17

Pancreatic Cancer: Nucleic Acid Drug Discovery and Targeted Therapy

Dai, H., Abdullah, R., Wu, X., Li, F., Ma, Y., Lü, A., & Zhang, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.855474 · Cited by 17

Nonprotein-coding RNAs in Fetal Alcohol Spectrum Disorders

Mahnke, A. H., Salem, N. A., Tseng, A. M., Chung, D. D., & Miranda, R. C. (2018) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.11.024 · Cited by 17

Regulatory roles of vertebrate Nocturnin: insights and remaining mysteries

Hughes, K. L., Abshire, E. T., & Goldstrohm, A. C. (2018) · RNA Biology · doi:10.1080/15476286.2018.1526541 · Cited by 16

Scrotal angiokeratoma (Fordyce): histopathological and ultrastructural findings.

Gioglio, L., Porta, C., Moroni, M., Nastasi, G., & Gangarossa, I. (1992) · PubMed · Cited by 17

Dexamethasone Suppresses Palatal Cell Proliferation through miR-130a-3p

Yoshioka, H., Jun, G., Suzuki, A., & Iwata, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212453 · Cited by 16

Noncoding RNAs in apoptosis: identification and function

Tüncel, Ö., Kara, M., Yaylak, B., Erdoğan, İ., & Akgül, B. (2021) · TURKISH JOURNAL OF BIOLOGY · doi:10.3906/biy-2109-35 · Cited by 16

miR-21-3p and miR-192-5p in patients with type 2 diabetic nephropathy

Akpınar, K., Aslan, D., Fenkçi, S. M., & Caner, V. (2022) · Diagnosis · doi:10.1515/dx-2022-0036 · Cited by 16

MFIDMA: A Multiple Information Integration Model for the Prediction of Drug–miRNA Associations

Guan, Y.-J., Yu, C.-Q., Qiao, Y., Li, L., You, Z., Ren, Z.-H., Li, Y.-C., & Pan, J. (2022) · Biology · doi:10.3390/biology12010041 · Cited by 16

miRNA-Guided Regulation of Mesenchymal Stem Cells Derived from the Umbilical Cord: Paving the Way for Stem-Cell Based Regeneration and Therapy

Thomaidou, A. C., Goulielmaki, M., Tsintarakis, A., Zoumpourlis, P., Toya, M., Christodoulou, I., & Zoumpourlis, V. C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119189 · Cited by 16

Small Non-Coding RNAs in Male Reproduction

Olotu, O., Ahmedani, A., & Kotaja, N. (2023) · Seminars in Reproductive Medicine · doi:10.1055/s-0044-1779726 · Cited by 17

The Emerging Role of IGF2BP2 in Cancer Therapy Resistance: From Molecular Mechanism to Future Potential

Li, D., Hu, S., Ye, J., Zhai, C., Liu, J., Wang, Z., Zhou, X., Chen, L., & Zhou, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212150 · Cited by 17

Digital droplet PCR - a prospective technological approach to quantitative profiling of microRNA

Kiseleva, Y. Y., Ptitsyn, K. G., Radko, S. P., Zgoda, V. G., & Archakov, A. I. (2016) · Biomeditsinskaya Khimiya · doi:10.18097/pbmc20166204403 · Cited by 16

Drosophila microRNA modulates viral replication by targeting a homologue of mammalian cJun

Monsanto‐Hearne, V., Asad, S., Sassan Asgari, B., & Johnson, K. N. (2017) · Journal of General Virology · doi:10.1099/jgv.0.000831 · Cited by 18

A high-throughput 3’ UTR reporter screening identifies microRNA interactomes of cancer genes

Peer, G. V., Mets, E., Claeys, S., Punt, I. D., Lefever, S., Ongenaert, M., Rondou, P., Speleman, F., Mestdagh, P., & Vandesompele, J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0194017 · Cited by 16

Global analysis of RNA metabolism using bio-orthogonal labeling coupled with next-generation RNA sequencing

Wolfe, M. B., Goldstrohm, A. C., & Freddolino, L. (2018) · Methods · doi:10.1016/j.ymeth.2018.12.001 · Cited by 15

Differentially expressed microRNAs as diagnostic biomarkers for infected tibial non-union

Dai, Y., Huang, L., Zhang, H., Hong, G., He, Y., Hu, J., & Liu, Y. (2020) · Injury · doi:10.1016/j.injury.2020.09.016 · Cited by 16

MALAT-1: LncRNA ruling miR-182/PIG-C/mesothelin triad in triple negative breast cancer.

Barsoum, F., Awad, A. S., Hussein, N. H., Eissa, R. A., & Tayebi, H. E. E. (2020) · Pathology, Research and Practice · doi:10.1016/j.prp.2020.153274 · Cited by 13

Therapeutic Mechanism of Nucleic Acid Drugs

Liu, L., Gao, H., Guo, C., Liu, T., Li, N., & Qian, Q. (2021) · ChemistrySelect · doi:10.1002/slct.202002901 · Cited by 16

CircGNG4 Promotes the Progression of Prostate Cancer by Sponging miR-223 to Enhance EYA3/c-myc Expression

Xu, S., Lian, Z., Zhang, S., Xu, Y. J., & Zhang, H. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.684125 · Cited by 16

Nematode microRNAs can Individually Regulate Interferon Regulatory Factor 4 and mTOR in Differentiating T Helper 2 Lymphocytes and Modulate Cytokine Production in Macrophages

Soichot, J., Guttmann, N., Rehrauer, H., Joller, N., & Tritten, L. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.909312 · Cited by 17

Identification of MicroRNAs Involved in Growth Arrest and Apoptosis in Hydrogen Peroxide‐Treated Human Hepatocellular Carcinoma Cell Line HepG2

Luo, Y. M., Wen, X., Wang, L., Gao, J., Wang, Z., Zhang, C., Zhang, P., Lu, C., Duan, L.-N., & Tian, Y. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/7530853 · Cited by 16

miR-1247 blocks SOX9–mediated regeneration in alcohol- and fibrosis-associated acute kidney injury in mice

Dreval, K., de Conti, A., Furuya, S., Beland, F. A., Rusyn, I., & Pogribny, I. P. (2017) · Toxicology · doi:10.1016/j.tox.2017.03.004 · Cited by 16

Highly multiplexed single-cell quantitative PCR

VanInsberghe, M. A., Zahn, H., White, A. K., Petriv, O. I., & Hansen, C. L. (2018) · PLoS ONE · doi:10.1371/journal.pone.0191601 · Cited by 16

TNRC6 proteins modulate hepatitis C virus replication by spatially regulating the binding of miR-122/Ago2 complexes to viral RNA

Li, Y., Wang, L., Rivera-Serrano, E. E., Chen, X., & Lemon, S. M. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz278 · Cited by 16

Transposable elements and miRNA: Regulation of genomic stability and plasticity

Pedersen, I. M., & Zisoulis, D. G. (2016) · Mobile Genetic Elements · doi:10.1080/2159256x.2016.1175537 · Cited by 18

The Complex Landscape of PTEN mRNA RegulationPreprint

Sellars, E., Gabra, M., & Salmena, L. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a036236 · Cited by 16

Current updates regarding biogenesis, functions and dysregulation of microRNAs in cancer: Innovative approaches for detection using CRISPR/Cas13‑based platforms (Review)

Aloliqi, A. A., Alnuqaydan, A. M., Albutti, A., Alharbi, B. F., Rahmani, A. H., & Khan, A. A. (2025) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2025.5531 · Cited by 16

Functional microRNA targeting without seed pairing

Hall, M. H., Wang, P. Y., Pham, T., & Bartel, D. P. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf1018 · Cited by 16

Role of miR-145-5p/ CD40 in the inflammation and apoptosis of HUVECs induced by PM2.5

Xueting, Z., Qi, W., Shi, Y., Li, X., Yin, J., Huo, C., Zhang, R., Zhao, W., Ye, J., Zhou, L., et al. (2021) · Toxicology · doi:10.1016/j.tox.2021.152993 · Cited by 15

The interplay between translational efficiency, poly(A) tails, microRNAs, and neuronal activation

Eisen, T. J., Li, J. J., & Bartel, D. P. (2022) · RNA · doi:10.1261/rna.079046.121 · Cited by 16

Disruption of miR-18a Alters Proliferation, Photoreceptor Replacement Kinetics, Inflammatory Signaling, and Microglia/Macrophage Numbers During Retinal Regeneration in Zebrafish

Magner, E. T., Sandoval-Sanchez, P., Kramer, A. C., Thummel, R., Hitchcock, P. F., & Taylor, S. M. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02783-w · Cited by 15

RNA solutions to treat inborn errors of metabolism

Martínez‐Pizarro, A., & Desviat, L. R. (2022) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2022.07.006 · Cited by 15

A specific type of Argonaute phosphorylation regulates binding to microRNAs during C. elegans development

Huberdeau, M. Q., Shah, V. N., Nahar, S., Neumeier, J., Houle, F., Bruckmann, A., Gypas, F., Nakanishi, K., Großhans, H., Meister, G., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111822 · Cited by 14

Two-motif model illuminates DICER cleavage preferences

Le, C. T., Nguyen, T. D., & Nguyen, T. A. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad1186 · Cited by 15

miR-486-5p protects against rat ischemic kidney injury and prevents the transition to chronic kidney disease and vascular dysfunction

Douvris, A., Viñas, J. L., Gutsol, A. A., Zimpelmann, J., Burger, D. E., & Burns, K. D. (2024) · Clinical Science · doi:10.1042/cs20231752 · Cited by 15

Disruption of pulmonary microvascular endothelial barrier by dysregulated claudin-8 and claudin-4: uncovered mechanisms in porcine reproductive and respiratory syndrome virus infection

Sun, W., Wu, W., Fang, X., Ge, X., Zhang, Y., Han, J., Guo, X., Zhou, L., & Yang, H. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05282-4 · Cited by 15

Biomarkers in Cerebrospinal Fluid for the Diagnosis and Monitoring of Gliomas

Papadimitrakis, D., PERDIKAKIS, M. N., Gargalionis, A. N., & Papavassiliou, A. G. (2024) · Biomolecules · doi:10.3390/biom14070801 · Cited by 15

dFmr1 Plays Roles in Small RNA Pathways of Drosophila melanogaster

Specchia, V., D’Attis, S., Puricella, A., & Bozzetti, M. P. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18051066 · Cited by 15

Pervasive yet nonuniform contributions of Dcp2 and Cnot7 to maternal mRNA clearance in zebrafish

Mishima, Y., & Tomari, Y. (2017) · Genes to Cells · doi:10.1111/gtc.12504 · Cited by 17

Dysregulation of miR-126/Crk protein axis predicts poor prognosis in gastric cancer patients

Feng, R., Sah, B. K., Beeharry, M. K., Yuan, F., Su, L., Jin, X., Yan, M., Liu, B., Li, C., & Zhu, Z. (2017) · Cancer Biomarkers · doi:10.3233/cbm-170472 · Cited by 17

microRNA-19a protects osteoblasts from dexamethasone via targeting TSC1

Liu, G., Chen, F., Ji, F., Fei, H., Xie, Y., & Wang, S. (2017) · Oncotarget · doi:10.18632/oncotarget.23326 · Cited by 15

Focused screening reveals functional effects of microRNAs differentially expressed in colorectal cancer

Sastre, D., Baiochi, J. F., Lima, I. M. D. S., de Souza, F. C., Corveloni, A. C., Thomé, C. H., Faça, V. M., Schiavinato, J. L. D. S., Covas, D. T., & Panepucci, R. A. (2019) · BMC Cancer · doi:10.1186/s12885-019-6468-5 · Cited by 15

From the Argonauts Mythological Sailors to the Argonautes RNA-Silencing Navigators: Their Emerging Roles in Human-Cell Pathologies

Pantazopoulou, V. I., Georgiou, S., Kakoulidis, P., Giannakopoulou, S. N., Tseleni, S., Stravopodis, D. J., & Anastasiadou, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114007 · Cited by 18

Circ_0001490/miR-579-3p/FSTL1 axis modulates the survival of mycobacteria and the viability, apoptosis and inflammatory response in Mycobacterium tuberculosis-infected macrophages

Deng, Q., Huang, J., Yan, J., Mao, E., Chen, H., & Wang, C. (2021) · Tuberculosis · doi:10.1016/j.tube.2021.102123 · Cited by 16

Porcine Reproductive and Respiratory Syndrome Virus Evades Antiviral Innate Immunity via MicroRNAs Regulation

Zhang, X., & Feng, W.-H. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.804264 · Cited by 15

In vivo validation of metastasis-regulating microRNA-766 in human triple-negative breast cancer cells

Oh, K., & Lee, D. (2017) · Laboratory Animal Research · doi:10.5625/lar.2017.33.3.256 · Cited by 15

Early microRNA indicators of PPARα pathway activation in the liver

Chorley, B. N., Carswell, G. K., Nelson, G. M., Bhat, V. S., & Wood, C. E. (2020) · Toxicology Reports · doi:10.1016/j.toxrep.2020.06.006 · Cited by 15

Long Non-coding RNA AFAP1-AS1 Facilitates Prostate Cancer Progression by Regulating miR-15b/IGF1R Axis

Liu, B., Jiang, H., Yuan, T., Zhou, W., Xiang, Z., Jiang, Q.-Q., & Wu, D. (2021) · Current Pharmaceutical Design · doi:10.2174/1381612827666210612052317 · Cited by 15

The E3 ubiquitin ligase mechanism specifying targeted microRNA degradation

Farnung, J., Slobodyanyuk, E., Wang, P. Y., Blodgett, L. W., Lin, D. H., von Gronau, S., Schulman, B. A., & Bartel, D. P. (2026) · Nature · doi:10.1038/s41586-026-10232-0 · Cited by 14

Highly Sensitive Detection and Intracellular Imaging of Micrornas Based on Target-Triggered Cascade Catalytic Hairpin Assembly

Li, L., Fang, X., Le, J., Zheng, Y., Tan, X., Jiang, Z., Li, H., Xu, J., & Xu, H. Y. (2022) · Talanta · doi:10.1016/j.talanta.2022.123753 · Cited by 14

Casein kinase 1 and 2 phosphorylate Argonaute proteins to regulate miRNA‐mediated gene silencing

Shah, V. N., Neumeier, J., Huberdeau, M. Q., Zeitler, D. M., Bruckmann, A., Meister, G., & Simard, M. J. (2023) · EMBO Reports · doi:10.15252/embr.202357250 · Cited by 14

ExplORRNet: An interactive web tool to explore stage-wise miRNA expression profiles and their interactions with mRNA and lncRNA in human breast and gynecological cancers

Lawarde, A., Rahmani, E. S., Nath, A., Lavõgina, D., Jaal, J., Salumets, A., & Modhukur, V. (2023) · Non-coding RNA Research · doi:10.1016/j.ncrna.2023.10.006 · Cited by 14

CiRS-7 Enhances the Liquid-liquid Phase Separation of miRISC and Promotes DNA Damage Repair

Wang, Y., Feng, L.-L., Shi, J., Chen, W.-Y., Bie, S.-Y., Bai, S.-M., Zeng, G.-D., Wang, R., Zheng, J., Wan, X., et al. (2023) · Nucleus · doi:10.1080/19491034.2023.2293599 · Cited by 14

Crosstalk between m6A modification and non-coding RNAs in HCC

Qiu, Z., Yuan, X., Wang, X., & Liu, S. (2024) · Cellular Signalling · doi:10.1016/j.cellsig.2024.111076 · Cited by 14

miRNA-Mediated Mechanisms in the Generation of Effective and Safe Oncolytic Viruses

Toropko, M., Chuvpilo, S. A., & Karabelsky, A. V. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16080986 · Cited by 14

In search for an ideal marker of endometrial receptivity: from histology to comprehensive molecular genetics-based approaches

Kibanov, M. V., Makhmudova, G. M., & Gokhberg, Y. A. (2019) · Almanac of Clinical Medicine · doi:10.18786/2072-0505-2019-47-005 · Cited by 14

Communication Is Key: 5′–3′ Interactions that Regulate mRNA Translation and Turnover

Fakim, H., & Fabian, M. R. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-31434-7_6 · Cited by 14

Cardiac fibroblast miR‐27a may function as an endogenous anti‐fibrotic by negatively regulating Early Growth Response Protein 3 (EGR3)

Teng, L., Huang, Y., Guo, J., Li, B., Jin, L., Ma, L., Wang, Y., Ye, C., & Chen, Q. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15814 · Cited by 14

Construction and validation of a three-microRNA signature as prognostic biomarker in patients with hepatocellular carcinoma

Zhang, X., Ma, L., Zhai, L., Chen, D., Li, Y., Shang, Z., Zhang, Z., Gao, Y., Yang, W. P., Li, Y., et al. (2021) · International Journal of Medical Sciences · doi:10.7150/ijms.49126 · Cited by 14

Expression Regulation, Protein Chemistry and Functional Biology of the Guanine-Rich Sequence Binding Factor 1 (GRSF1)

Dumoulin, B., Ufer, C., Kühn, H., & Sofi, S. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.166922 · Cited by 14

miR-934 promotes breast cancer metastasis by regulation of PTEN and epithelial–mesenchymal transition

Lu, Y., Hu, X., & Yang, X. (2021) · Tissue and Cell · doi:10.1016/j.tice.2021.101581 · Cited by 14

Sox6, A Potential Target for MicroRNAs in Cardiometabolic Disease

Saleem, M., Rahman, S., Elijovich, F., Laffer, C. L., Ertuğlu, L. A., Masenga, S. K., & Kirabo, A. (2022) · Current Hypertension Reports · doi:10.1007/s11906-022-01175-8 · Cited by 14

Elevated Expression of miR-200c/141 in MDA-MB-231 Cells Suppresses MXRA8 Levels and Impairs Breast Cancer Growth and Metastasis In Vivo

Simpson, K. E., Watson, K. L. M., & Moorehead, R. A. (2022) · Genes · doi:10.3390/genes13040691 · Cited by 13

Mature microRNA-binding protein QKI promotes microRNA-mediated gene silencing

Min, K., Jo, M. H., Song, M., Lee, J. W., Shim, M. J., Kim, K., Park, H. B., Ha, S., Mun, H., Polash, A., et al. (2024) · RNA Biology · doi:10.1080/15476286.2024.2314846 · Cited by 14

Mitochondrial translation factors reflect coordination between organelles and cytoplasmic translation via mTOR signaling: Implication in disease

Cao, X., & Qin, Y. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.04.010 · Cited by 15

Hypothesis: Exosomal microRNAs as potential biomarkers for schizophrenia

Raghavan, V., Bhomia, M., Torres, I., Jain, S., & Wang, K. (2017) · Medical Hypotheses · doi:10.1016/j.mehy.2017.04.003 · Cited by 14

The PICK1 Ca2+ sensor modulates N-methyl-d-aspartate (NMDA) receptor-dependent microRNA-mediated translational repression in neurons

Rajgor, D., Fiuza, M., Parkinson, G. T., & Hanley, J. G. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.776302 · Cited by 14

The DEAD-box RNA-binding protein DDX6 regulates parental RNA decay for cellular reprogramming to pluripotency

Kami, D., Kitani, T., Nakamura, A., Wakui, N., Onoguchi‐Mizutani, R., Ohue, M., Kametani, F., Akimitsu, N., & Gojo, S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0203708 · Cited by 13

HRPK-1, a conserved KH-domain protein, modulates microRNA activity during Caenorhabditis elegans development

Li, L., Veksler‐Lublinsky, I., & Zinovyeva, A. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008067 · Cited by 14

Small Non-Coding RNAs in Leukemia

Balatti, V., & Croce, C. M. (2022) · Cancers · doi:10.3390/cancers14030509 · Cited by 14

Down-regulated serum miR-126 is associated with aggressive progression and poor prognosis of gastric cancer

Feng, R., Beeharry, M. K., Lu, S., Sah, B. K., Yuan, F., Yan, M., Liu, B., Li, C., & Zhu, Z. (2018) · Cancer Biomarkers · doi:10.3233/cbm-171099 · Cited by 13

Shedding light on microRNA function via microscopy-based screening

Lopes, I. R., Silva, R. J., Caramelo, I., Eulálio, A., & Mano, M. (2018) · Methods · doi:10.1016/j.ymeth.2018.09.011 · Cited by 14

MicroRNA-Mediated Regulation of Vascular Endothelium: From Pro-Inflammation to Atherosclerosis

Silva, V. R., Azar, A., Gonçalves, E. R., Nascimento, T. C. D. M., Buchaim, R. L., Buchaim, D. V., Oliveira, F. A., Nassar, C. C., Camargo, T. M., Caboclo, R. F., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26135919 · Cited by 13

Advances in Pathophysiology and Novel Therapeutic Strategies for Coronary No-Reflow Phenomenon

Borzuta, H., Kociemba, W., Bochenek, O., Jarowicz, M., & Wsół, A. (2025) · Biomedicines · doi:10.3390/biomedicines13071716 · Cited by 13

miRNA in the Progression of Diabetic Kidney Disease: New Insight

Zou, Z., Zhou, N., & Zhang, C. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms27010420 · Cited by 14

The Noncoding Side of Cardiac Differentiation and Regeneration

Pagano, F., Calicchio, A., Picchio, V., & Ballarino, M. (2020) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x15666200123120249 · Cited by 12

Circ_0138960 knockdown alleviates lipopolysaccharide-induced inflammatory response and injury in human dental pulp cells by targeting miR-545-5p/MYD88 axis in pulpitis

Liang, C., Wu, W., He, X., Xue, F., & Feng, D. (2022) · Journal of Dental Sciences · doi:10.1016/j.jds.2022.06.012 · Cited by 13

A conserved domain of Drosophila RNA-binding protein Pumilio interacts with multiple CCR4–NOT deadenylase complex subunits to repress target mRNAs

Haugen, R. J., Arvola, R. M., Connacher, R. P., Roden, R., & Goldstrohm, A. C. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102270 · Cited by 12

Cancer Stem Cells—The Insight into Non-Coding RNAs

Bryl, R., Piwócka, O., Kawka, E., Mozdziak, P. E., Kempisty, B., & Knopik-Skrocka, A. (2022) · Cells · doi:10.3390/cells11223699 · Cited by 14

Identification of long non-coding RNA and circular RNA associated networks in cellular stress responses

Li, X., Li, J., Shan, G., & Wang, X. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1097571 · Cited by 13

Noncanonical functions of microRNAs in the nucleus

Gu, J., Li, Y., Tian, Y., Zhang, Y., Cheng, Y., & Tang, Y. (2023) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2023268 · Cited by 13

miRNA-Mediated Fine Regulation of TLR-Induced M1 Polarization

Rumpel, N., Riechert, G., & Schumann, J. E. (2024) · Cells · doi:10.3390/cells13080701 · Cited by 13

Research Progress on miRNAs and Artificial miRNAs in Insect and Disease Resistance and Breeding in Plants

ZengFeng, M., Wang, J., & Li, C. (2024) · Genes · doi:10.3390/genes15091200 · Cited by 13

Split activator ligation assay: A CRISPR/Cas12a-enabled biosensor for the genotyping of cancer-associated miRNA single-nucleotide polymorphisms

Jin, X., Feng, S., Lv, W., Shen, D., & Li, B. (2025) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2025.138134 · Cited by 13

FXR1a-associated microRNP: A driver of specialized non-canonical translation in quiescent conditions

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