Towards a molecular understanding of microRNA-mediated gene silencing

Most mammalian mRNAs are conserved targets of microRNAs

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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

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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

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

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Tau/DDX6 interaction increases microRNA activity

Chauderlier, A., Gilles, M., Špolcová, A., Caillierez, R., Chwastyniak, M., Kress, M., Drobecq, H., Bonnefoy, E., Pinet, F., Barbieri-Weill, D., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2018.06.006 · Cited by 26

Exposure of Endothelium to Biomimetic Flow Waveforms Yields Identification of miR-199a-5p as a Potent Regulator of Arteriogenesis

Heuslein, J. L., Gorick, C. M., McDonnell, S. P., Song, J. S., Annex, B. H., & Price, R. J. (2018) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2018.08.001 · Cited by 25

MiR-33b inhibits osteosarcoma cell proliferation through suppression of glycolysis by targeting Lactate Dehydrogenase A (LDHA)

Zheng, X., Xu, C., & Wang, F. (2018) · Cellular and Molecular Biology · doi:10.14715/cmb/2018.64.11.6 · Cited by 25

Neuroprotection with Natural Antioxidants and Nutraceuticals in the Context of Brain Cell Degeneration: The Epigenetic Connection

Carrera, I., Martínez, O., & Cacabelos, R. (2019) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026619666191202155738 · Cited by 25

microRNA expression variation as a potential molecular mechanism contributing to adaptation to hydrogen sulphide

Kelley, J. L., Desvignes, T., McGowan, K. L., Perez, M. A., Arias‐Rodríguez, L., Brown, A. P. C., Culumber, Z. W., & Tobler, M. (2020) · Journal of Evolutionary Biology · doi:10.1111/jeb.13727 · Cited by 25

Pharmacology of heart failure: From basic science to novel therapies

Lother, A., & Hein, L. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.07.004 · Cited by 24

miR-1285-3p is a potential prognostic marker in human osteosarcoma and functions as a tumor suppressor by targeting YAP1

Hu, X., Dai, J., Shang, H., Zhao, Z., & Hao, Y. (2019) · Cancer Biomarkers · doi:10.3233/cbm-180013 · Cited by 24

LINC01977 Promotes Breast Cancer Progression and Chemoresistance to Doxorubicin by Targeting miR-212-3p/GOLM1 Axis

Li, Z., Li, Y., Wang, X., Liang, Y., Luo, D., Han, D., Li, C., Chen, T., Zhang, H., Liu, Y., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.657094 · Cited by 23

CSDE1 attenuates microRNA-mediated silencing of PMEPA1 in melanoma

Kakumani, P. K., Guitart, T., Houle, F., Harvey, L.-M., Goyer, B., Germain, L., Gebauer, F., & Simard, M. J. (2021) · Oncogene · doi:10.1038/s41388-021-01767-9 · Cited by 24

Association between long noncoding RNA taurine‐upregulated gene 1 and microRNA‐377 in vitiligo

Alhelf, M., Rashed, L. A., Ragab, N., & Elmasry, M. F. (2021) · International Journal of Dermatology · doi:10.1111/ijd.15669 · Cited by 24

Silencing of the lncRNA H19 enhances sensitivity to X-ray and carbon-ions through the miR-130a-3p /WNK3 signaling axis in NSCLC cells

Zhao, X., Jin, X., Zhang, Q., Liu, R., Luo, H., Yang, Z., Geng, Y., Feng, S., Li, C., Wang, L., et al. (2021) · Cancer Cell International · doi:10.1186/s12935-021-02268-1 · Cited by 24

Significance of interferon signaling based on mRNA-microRNA integration and plasma protein analyses in critically ill COVID-19 patients

Togami, Y., Matsumoto, H., Yoshimura, J., Matsubara, T., Ebihara, T., Matsuura, H., Mitsuyama, Y., Kojima, T., Ishikawa, M., Sugihara, F., et al. (2022) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2022.07.005 · Cited by 22

miRNAs in anti-cancer drug resistance of non-small cell lung cancer: Recent advances and future potential

Yan, H., Tang, S., Tang, S., Zhang, J., Guo, H., Qin, C., Hu, H., Zhong, C., Li, Y., Zhu, Y., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.949566 · Cited by 24

MicroRNAs modulate neuroinflammation after intracerebral hemorrhage: Prospects for new therapy

Xia, S., Zheng, Y., Yan, F., & Chen, G. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.945860 · Cited by 24

Matrix reconstruction with reliable neighbors for predicting potential MiRNA–disease associations

Feng, H., Jin, D., Li, J., Li, Y., Zou, Q., & Liu, T. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac571 · Cited by 24

Non-Coding RNAs Modulating Estrogen Signaling and Response to Endocrine Therapy in Breast Cancer

Treeck, O., Haerteis, S., & Ortmann, O. (2023) · Cancers · doi:10.3390/cancers15061632 · Cited by 24

Transfer RNA: From pioneering crystallographic studies to contemporary tRNA biology

Fernández-Millán, P., Schelcher, C., Chihade, J. W., Masquida, B., Giegé, P., & Sauter, C. (2016) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2016.03.005 · Cited by 24

A survey of software tools for microRNA discovery and characterization using RNA-seq

Bortolomeazzi, M., Gaffo, E., & Bortoluzzi, S. (2017) · Briefings in Bioinformatics · doi:10.1093/bib/bbx148 · Cited by 25

Cartilage MicroRNA Dysregulation During the Onset and Progression of Mouse Osteoarthritis Is Independent of Aggrecanolysis and Overlaps With Candidates From End‐Stage Human Disease

Kung, L. H. W., Ravi, V., Rowley, L., Angelucci, C., Fosang, A., Bell, K. M., Little, C. B., & Bateman, J. F. (2017) · Arthritis & Rheumatology · doi:10.1002/art.40378 · Cited by 24

MicroRNA profiling of dogs with transitional cell carcinoma of the bladder using blood and urine samples

Kent, M. S., Zwingenberger, A. L., Westropp, J. L., Barrett, L. E., Durbin-Johnson, B. P., Ghosh, P., & Vinall, R. L. (2017) · BMC Veterinary Research · doi:10.1186/s12917-017-1259-1 · Cited by 24

Epigenetic mechanisms in amyotrophic lateral sclerosis: A short review

Dolinar, A., Ravnik‐Glavač, M., & Glavač, D. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.03.005 · Cited by 25

A potential role of extended simple sequence repeats in competing endogenous RNA crosstalk

Witkos, T. M., Krzyżosiak, W. J., Fiszer, A., & Kościańska, E. (2018) · RNA Biology · doi:10.1080/15476286.2018.1536593 · Cited by 24

microRNA-7 inhibition protects human osteoblasts from dexamethasone via activation of epidermal growth factor receptor signaling

Fan, J., Liu, W., Zhu, X., Cui, S., Cui, Z., & Zhao, J. (2019) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-019-03575-y · Cited by 24

Tissue-Specific miRNAs Regulate the Development of Thoracic Aortic Aneurysm: The Emerging Role of KLF4 Network

Gasiulė, S., Stankevičius, V., Patamsytė, V., Ražanskas, R., Žukovas, G., Kapustina, Ž., Žaliaduonytė, D., Benetis, R., Lesauskaitė, V., & Vilkaitis, G. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101609 · Cited by 24

The Oncogenic Kaposi’s Sarcoma-Associated Herpesvirus Encodes a Mimic of the Tumor-Suppressive miR-15/16 miRNA Family

Morrison, K., Manzano, M., Chung, K., Schipma, M. J., Bartom, E. T., & Gottwein, E. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.005 · Cited by 24

Role of the RNA-binding protein Bicaudal-C1 and interacting factors in cystic kidney diseases

Rothé, B., Gagnieux, C., Leal-Esteban, L. C., & Constam, D. B. (2019) · Cellular Signalling · doi:10.1016/j.cellsig.2019.109499 · Cited by 26

miR24‐2 accelerates progression of liver cancer cells by activating Pim1 through tri‐methylation of Histone H3 on the ninth lysine

Yang, Y., Song, S., Meng, Q., Wang, L., Li, X., Xie, S., Chen, Y., Jiang, X., Wang, C., Lu, Y., et al. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15030 · Cited by 24

LKB1 Down-Modulation by miR-17 Identifies Patients With NSCLC Having Worse Prognosis Eligible for Energy-Stress–Based Treatments

Borzi, C., Ganzinelli, M., Caiola, E., Colombo, M., Centonze, G., Boeri, M., Signorelli, D., Caleca, L., Rulli, E., Busico, A., et al. (2021) · Journal of Thoracic Oncology · doi:10.1016/j.jtho.2021.04.005 · Cited by 24

The role of microRNAs in the development and progression of chemical-associated cancers

Pogribny, I. P., Beland, F. A., & Rusyn, I. (2015) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2015.11.013 · Cited by 23

Cas9-mediated excision of proximal DNaseI/H3K4me3 signatures confers robust silencing of microRNA and long non-coding RNA genes

Janga, H., Aznaourova, M., Boldt, F., Damm, K., Grünweller, A., & Schulte, L. N. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193066 · Cited by 22

The development of a sensitive fluorescent protein-based transcript reporter for high throughput screening of negative modulators of lncRNAs

Zeng, Z., Huang, B., Huang, S., Zhang, R., Yan, S., Yu, X., Shu, Y., Zhao, C., Lei, J., Zhang, W., et al. (2018) · Genes & Diseases · doi:10.1016/j.gendis.2018.02.001 · Cited by 23

Tumor necrosis factor-alpha suppresses the invasion of HTR-8/SVneo trophoblast cells through microRNA-145-5p-mediated downregulation of Cyr61

Wen, Z., Chen, Y., Yu, L., Yu, J., & Li, M. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.08.005 · Cited by 25

A conserved miRNA-183 cluster regulates the innate antiviral response

Singaravelu, R., Ahmed, N., Quan, C., Srinivasan, P., Ablenas, C. J., Roy, D. G., & Pezacki, J. P. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010858 · Cited by 23

Epigenetics of osteoarthritis: Histones and TGF-β1

He, J., Cao, W., Azeem, I., & Shao, Z. (2020) · Clinica Chimica Acta · doi:10.1016/j.cca.2020.08.011 · Cited by 23

Downregulation of circFASTKD1 ameliorates myocardial infarction by promoting angiogenesis

Gao, W., Hu, X., Zhang, Q., Yang, L., Lv, X., Chen, S., Wu, P., Duan, D., Lang, Y., Ning, M., et al. (2020) · Aging · doi:10.18632/aging.202305 · Cited by 23

Evaluation of exosomal miRNAs as potential diagnostic biomarkers for acute myocardial infarction using next-generation sequencing

Guo, M. L., Li, R., Yang, L., Zhu, Q., Han, M., Chen, Z., Ruan, F., Yuan, Y., Liu, Z., Huang, B., et al. (2021) · Annals of Translational Medicine · doi:10.21037/atm-20-2337 · Cited by 23

Construction of Competitive Endogenous RNA Network and Verification of 3-Key LncRNA Signature Associated With Distant Metastasis and Poor Prognosis in Patients With Clear Cell Renal Cell Carcinoma

Su, Y., Zhang, T., Tang, J., Zhang, L., Fan, S., Zhou, J., & Liang, C. Y. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.640150 · Cited by 23

In Silico Identification of miRNA–lncRNA Interactions in Male Reproductive Disorder Associated with COVID-19 Infection

Sabetian, S., Castiglioni, I., Jahromi, B. N., Mousavi, P., & Cava, C. (2021) · Cells · doi:10.3390/cells10061480 · Cited by 23

Long non-coding RNA LINC01559 serves as a competing endogenous RNA accelerating triple-negative breast cancer progression

Yang, X., Yang, Y., Qian, X., Xu, X., & Lv, P. (2021) · Biomedical Journal · doi:10.1016/j.bj.2021.05.002 · Cited by 23

Regulation of human UDP-glycosyltransferase (UGT) genes by miRNAs

Hu, D. G., Mackenzie, P. I., Hulin, J.-A., McKinnon, R. A., & Meech, R. (2022) · Drug Metabolism Reviews · doi:10.1080/03602532.2022.2048846 · Cited by 23

Pan-cancer analysis of microRNA expression profiles highlights microRNAs enriched in normal body cells as effective suppressors of multiple tumor types: A study based on TCGA database

Moradi, S., Kamal, A., Es, H. A., Farhadi, F., Ebrahimi, M., Chitsaz, H., Sharifi‐Zarchi, A., & Baharvand, H. (2022) · PLoS ONE · doi:10.1371/journal.pone.0267291 · Cited by 24

Target binding triggers hierarchical phosphorylation of human Argonaute-2 to promote target release

Bibel, B., Elkayam, E., Silletti, S., Komives, E. A., & Joshua‐Tor, L. (2022) · eLife · doi:10.7554/elife.76908 · Cited by 22

The epigenetic basis of evolution

Spadafora, C. (2023) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2023.01.005 · Cited by 24

Control of RNA degradation in cell fate decision

Deng, M., Wang, X., Xiong, Z. Q., & Tang, P. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1164546 · Cited by 23

Induction of exportin-5 expression during melanoma development supports the cellular behavior of human malignant melanoma cells

Ott, C., Linck-Paulus, L., Kremmer, E., Meister, G., & Bosserhoff, A. (2016) · Oncotarget · doi:10.18632/oncotarget.11410 · Cited by 23

A continuum of mRNP complexes in embryonic microRNA-mediated silencing

Wu, E., Vashisht, A. A., Chapat, C., Flamand, M. N., Cohen, E., Sarov, M., Tabach, Y., Sonenberg, N., Wohlschlegel, J. A., & Duchaîne, T. F. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw872 · Cited by 23

MicroRNA-22-3p as a novel regulator and therapeutic target for autoimmune diseases

Wang, B., Yao, Q., Xu, D., & Zhang, J. (2017) · International Reviews of Immunology · doi:10.1080/08830185.2017.1281272 · Cited by 22

Combination of ginsenoside Rb1 and Rd protects the retina against bright light-induced degeneration

Bian, M., Du, X., Wang, P., Cui, J., Xu, J., Gu, J., Zhang, T., & Chen, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-06471-x · Cited by 23

Systematic review regulatory principles of non-coding RNAs in cardiovascular diseases

Li, Y., Huo, C., Pan, T., Li, X., Jin, X., Li, X., Chen, J., Zhang, J., Guo, Z., Xu, J., et al. (2017) · Briefings in Bioinformatics · doi:10.1093/bib/bbx095 · Cited by 23

The Requirement for GW182 Scaffolding Protein Depends on Whether Argonaute Is Mediating Translation, Transcription, or Splicing

Liu, J., Liu, Z., & Corey, D. R. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00602 · Cited by 23

microRNA-4500 inhibits human glioma cell progression by targeting IGF2BP1

Li, Z., Xue, M., Zhu, B., Yue, C., Chen, M., & Qin, H. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.04.058 · Cited by 23

The relevance of the non-invasive biomarkers lncRNA GAS5/miR-21 ceRNA regulatory network in the early identification of diabetes and diabetic nephropathy

Sun, H. Y., Chen, T., Li, X., Zhu, Y., Zhang, S., He, P., Peng, Y., & Fan, Q. (2023) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-023-01179-7 · Cited by 22

Influence of RNA circularity on Target RNA-Directed MicroRNA Degradation

Wightman, F. F., Lukin, J., Giusti, S. A., Soutschek, M., Bragado, L., Pozzi, B., Pierelli, M. L., González, P., Fededa, J. P., Schratt, G. M., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae094 · Cited by 24

Clinical evaluation of microRNA-145 expression in renal cell carcinoma: a promising molecular marker for discriminating and staging the clear cell histological subtype

Papadopoulos, E. I., Petraki, C. D., Gregorakis, A., Fragoulis, E. G., & Scorilas, A. (2016) · Biological Chemistry · doi:10.1515/hsz-2015-0284 · Cited by 21

The coupled and uncoupled mechanisms by which trans-acting factors regulate mRNA stability and translation

Fukao, A., & Fujiwara, T. (2016) · The Journal of Biochemistry · doi:10.1093/jb/mvw086 · Cited by 22

TIMP-1 downregulation modulates miR-125a-5p expression and triggers the apoptotic pathway

Ghoshal-Gupta, S., Kutiyanawalla, A., Lee, B. R., Ojha, J., Nurani, A., Mondal, A. K., Kolhe, R. B., Rojiani, A. M., & Rojiani, M. V. (2018) · Oncotarget · doi:10.18632/oncotarget.23832 · Cited by 21

Dissimilar Appearances Are Deceptive–Common microRNAs and Therapeutic Strategies in Liver Cancer and Melanoma

Linck-Paulus, L., Hellerbrand, C., Bosserhoff, A., & Dietrich, P. (2020) · Cells · doi:10.3390/cells9010114 · Cited by 24

miR-4458 inhibits the epithelial–mesenchymal transition of hepatocellular carcinoma cells by suppressing the TGF-β signaling pathway via targeting TGFBR1

Zhang, Y., Shi, K., Liu, H., Chen, W., Luo, Y., Wei, X., & Wu, Z. (2020) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmaa029 · Cited by 22

miR‐223‐3p Inhibits Antigen Endocytosis and Presentation and Promotes the Tolerogenic Potential of Dendritic Cells through Targeting Mannose Receptor Signaling and Rhob

Tang, H., Lai, Y., Zheng, J., Jiang, H., & Xu, G. (2020) · Journal of Immunology Research · doi:10.1155/2020/1379458 · Cited by 24

miR‑101‑3p sensitizes lung adenocarcinoma cells to irradiation via targeting BIRC5

Meng, X., Sun, Y., Liu, S., & Mu, Y. (2021) · Oncology Letters · doi:10.3892/ol.2021.12543 · Cited by 22

Roles of Non-Coding RNAs in Cervical Cancer Metastasis

Cheng, T., & Huang, S. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.646192 · Cited by 22

Simvastatin regulates the proliferation, apoptosis, migration and invasion of human acute myeloid leukemia cells via miR-19a-3p/HIF-1α axis

Tian, H., Qiang, T., Wang, J., Li, J., & Li, B. (2021) · Bioengineered · doi:10.1080/21655979.2021.1999552 · Cited by 22

Network Approaches to Study Endogenous RNA Competition and Its Impact on Tissue-Specific microRNA Functions

Marques, T. M., & Gama‐Carvalho, M. (2022) · Biomolecules · doi:10.3390/biom12020332 · Cited by 23

PSRR: A Web Server for Predicting the Regulation of miRNAs Expression by Small Molecules

Yu, F., Li, B., Sun, J., Qi, J., Wilde, R. L. D., la Roche, L. A. T.-D., Li, C., Ahmad, S., Shi, W., Li, X., et al. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.817294 · Cited by 22

MiR-148a deletion protects from bone loss in physiological and estrogen-deficient mice by targeting NRP1

Pan, B., Zheng, L., Liu, S., Fang, J., Lou, C., Hu, X., Ye, L., Lai, H., Gao, J., Zhang, Y., et al. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-01261-5 · Cited by 27

MicroRNAs as Biomarkers for Coronary Artery Disease Related to Type 2 Diabetes Mellitus—From Pathogenesis to Potential Clinical Application

Szydełko, J., & Matyjaszek-Matuszek, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010616 · Cited by 19

Message Transmission Between Adipocyte and Macrophage in Obesity

Engin, A. B. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-63657-8_9 · Cited by 22

Post-transcriptional gene silencing activity of human GIGYF2

Kryszke, M.-H., Adjeriou, B., Liang, F., Chen, H., & Dautry, F. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.05.022 · Cited by 22

Comparative study of joint bioinformatics analysis of underlying potential of ‘neurimmiR’, miR-212-3P/miR-132-3P, being involved in epilepsy and its emerging role in human cancer

Xia, L., Li, D., Lin, C., Ou, S., Li, X., & Pan, S. (2017) · Oncotarget · doi:10.18632/oncotarget.16541 · Cited by 22

A Tiny RNA that Packs a Big Punch: The Critical Role of a Viral miR-155 Ortholog in Lymphomagenesis in Marek’s Disease

Zhuang, G., Sun, A., Teng, M., & Luo, J. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01169 · Cited by 22

Valproic acid exposure decreases the mRNA stability of Bcl-2 via up-regulating miR-34a in the cerebellum of rat

Dai, X., Yin, Y., & Qin, L. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.08.018 · Cited by 23

A DGCR8-Independent Stable MicroRNA Expression Strategy Reveals Important Functions of miR-290 and miR-183–182 Families in Mouse Embryonic Stem Cells

Wang, X., Hao, J., Guo, W., Liao, L., Huang, S.-Y., Guo, X., Bao, X., Esteban, M. A., & Wang, Y. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.08.027 · Cited by 22

New roles for nuclear EGFR in regulating the stability and translation of mRNAs associated with VEGF signaling

Dittmann, K., Mayer, C., Czemmel, S., Huber, S. M., & Rodemann, H. P. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189087 · Cited by 22

Expression of Alternative Ago2 Isoform Associated with Loss of microRNA-Driven Translational Repression in Mouse Oocytes

Freimer, J. W., Krishnakumar, R., Cook, M. S., & Blelloch, R. H. (2018) · Current Biology · doi:10.1016/j.cub.2017.11.067 · Cited by 24

Lamins in Lung Cancer: Biomarkers and Key Factors for Disease Progression through miR-9 Regulation?

Guinde, J., Frankel, D., Perrin, S., Delecourt, V., Lévy, N., Barlési, F., Astoul, P. J., Roll, P., & Kaspi, É. (2018) · Cells · doi:10.3390/cells7070078 · Cited by 22

Differential Inhibition of Target Gene Expression by Human microRNAs

Li, P., Chen, Y., Juma, C. A., Yang, C., Huang, J., Zhang, X., & Zeng, Y. (2019) · Cells · doi:10.3390/cells8080791 · Cited by 22

WBNPMD: weighted bipartite network projection for microRNA-disease association prediction

Xie, G., Fan, Z., Sun, Y., Wu, C., & Ma, L. (2019) · Journal of Translational Medicine · doi:10.1186/s12967-019-2063-4 · Cited by 22

Integrated analysis of directly captured microRNA targets reveals the impact of microRNAs on mammalian transcriptome

Bjerke, G. A., & Yi, R. (2020) · RNA · doi:10.1261/rna.073635.119 · Cited by 22

Coordinated AR and microRNA regulation in prostate cancer

Eringyte, I., Losada, J. N. Z., Powell, S. M., Bevan, C. L., & Fletcher, C. E. (2020) · Asian journal of urology · doi:10.1016/j.ajur.2020.06.003 · Cited by 24

miRNALoc: predicting miRNA subcellular localizations based on principal component scores of physico-chemical properties and pseudo compositions of di-nucleotides

Meher, P. K., Satpathy, S., & Rao, A. R. (2020) · Scientific Reports · doi:10.1038/s41598-020-71381-4 · Cited by 22

Could MicroRNAs Be Useful Tools to Improve the Diagnosis and Treatment of Rare Gynecological Cancers? A Brief Overview

Fiore, R. D., Suleiman, S., Pentimalli, F., O’Toole, S. A., O’Leary, J. J., Ward, M. P., Conlon, N. T., Sabol, M., Ozretić, P., Erson-Bensan, A. E., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22083822 · Cited by 22

LncRNA PVT1 Regulates High Glucose-Induced Viability, Oxidative Stress, Fibrosis, and Inflammation in Diabetic Nephropathy via miR-325-3p/Snail1 Axis

Qin, B., & Cao, X. (2021) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s303151 · Cited by 22

Astrocyte Activation Markers

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Muscle allele-specific expression QTLs may affect meat quality traits in Bos indicus

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Under the Radar: Strategies Used by Helicobacter pylori to Evade Host Responses

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Epigenetic Regulations of Perineural Invasion in Head and Neck Squamous Cell Carcinoma

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P-bodies directly regulate MARF1-mediated mRNA decay in human cells

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This Week in Science

(2011) · Science · doi:10.1126/science.2011.331.6017.twis

Mechanistic Insights into MicroRNA-Mediated Gene SilencingPreprint

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miRNA-mediated gene silencing by translational repression followed by mRNA deadenylation and decay

Djuranovic, S., Nahvi, A., & Green, R. (2012) · Science · doi:10.1126/science.1215691 · Cited by 811

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

Kinetic analysis reveals successive steps leading to miRNA‐mediated silencing in mammalian cells

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