Regulation of microRNA biogenesis

MicroRNAs: Target Recognition and Regulatory Functions

Bartel, D. P. (2009) · Cell · doi:10.1016/j.cell.2009.01.002 · Cited by 20,068

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

The nuclear RNase III Drosha initiates microRNA processing

Lee, Y., Ahn, C., Han, J., Choi, H., Kim, J., Yim, J., Lee, J., Provost, P., Rådmark, O., Kim, S., et al. (2003) · Nature · doi:10.1038/nature01957 · Cited by 5,299

miRBase: annotating high confidence microRNAs using deep sequencing data

Kozomara, A., & Griffiths-Jones, S. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1181 · Cited by 5,073

Role for a bidentate ribonuclease in the initiation step of RNA interference

Bernstein, E., Caudy, A. A., Hammond, S. M., & Hannon, G. J. (2001) · Nature · doi:10.1038/35053110 · Cited by 5,018

The widespread regulation of microRNA biogenesis, function and decay

Krol, J., Loedige, I., & Filipowicz, W. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2843 · Cited by 4,672

MicroRNA genes are transcribed by RNA polymerase II

Lee, Y., Kim, M., Han, J., Yeom, K.-H., Lee, S., Baek, S. H., & Kim, V. N. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600385 · Cited by 4,556

Delivery of RNAi Therapeutics to the Airways—From Bench to Bedside

Qiu, Y., Lam, J. K. W., Leung, S. W. S., & Liang, W. (2016) · Molecules · doi:10.3390/molecules21091249 · Cited by 73

Reciprocal regulation of miR-214 and PTEN by high glucose regulates renal glomerular mesangial and proximal tubular epithelial cell hypertrophy and matrix expansion

Bera, A., Das, F., Ghosh‐Choudhury, N., Mariappan, M. M., Kasinath, B. S., & Choudhury, G. G. (2017) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00081.2017 · Cited by 71

NRF2 regulates endothelial glycolysis and proliferation with miR-93 and mediates the effects of oxidized phospholipids on endothelial activation

Linna-Kuosmanen, S., Kansanen, E., Kaikkonen, M. U., Sihvola, V., Pulkkinen, K. H., Jyrkkänen, H.-K., Tuoresmäki, P., Hartikainen, J. E. K., Hippeläinen, M., Kokki, H. J., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx1155 · Cited by 71

G-Quadruplexes influence pri-microRNA processing

Rouleau, S. G., Garant, J., Bolduc, F., Bisaillon, M., & Perreault, J. (2017) · RNA Biology · doi:10.1080/15476286.2017.1405211 · Cited by 72

nc886 is induced by TGF-β and suppresses the microRNA pathway in ovarian cancer

Ahn, J., Lee, H., Lee, J., Lee, Y.-S., Park, J., Kim, S., Hwang, J.-A., Kunkeaw, N., Jung, S. Y., Kim, T. J., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03556-7 · Cited by 71

Molecular mechanism of diabetic cardiomyopathy and modulation of microRNA function by synthetic oligonucleotides

Ghosh, N., & Katare, R. (2018) · Cardiovascular Diabetology · doi:10.1186/s12933-018-0684-1 · Cited by 71

The potential role of miRNAs and exosomes in chemotherapy in ovarian cancer

Alharbi, M. G., Zuñiga, F. A., Elfeky, O. W. M., Guanzon, D., Lai, A., Rice, G. E., Perrin, L. C., Hooper, J. D., & Salomón, C. (2018) · Endocrine Related Cancer · doi:10.1530/erc-18-0019 · Cited by 73

Synthetic small-molecule RNA ligands: future prospects as therapeutic agents

Giorgio, A. D., & Duca, M. (2019) · MedChemComm · doi:10.1039/c9md00195f · Cited by 75

Non-Coding RNAs in Stroke and Neuroprotection

Saugstad, J. A. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00050 · Cited by 71

Role of microRNAs in the regulation of innate immune cells under neuroinflammatory conditions

Cardoso, A. L., Guedes, J. R., & de Lima, M. C. P. (2015) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2015.09.001 · Cited by 71

DICER Inactivation Identifies Pancreatic β-Cell “Disallowed” Genes Targeted by MicroRNAs

Martínez-Sánchez, A., Nguyen‐Tu, M., & Rutter, G. A. (2015) · Molecular Endocrinology · doi:10.1210/me.2015-1059 · Cited by 73

MicroRNA-specific regulatory mechanisms in atherosclerosis

Nazari-Jahantigh, M., Egea, V., Schober, A., & Weber, C. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2014.10.021 · Cited by 72

MicroRNA-378-mediated suppression of Runx1 alleviates the aggressive phenotype of triple-negative MDA-MB-231 human breast cancer cells

Browne, G., Dragon, J. A., Hong, D., Messier, T., Gordon, J. A. R., Farina, N. H., Boyd, J. R., VanOudenhove, J., Perez, A. W., Zaidi, S. K., et al. (2016) · Tumor Biology · doi:10.1007/s13277-015-4710-6 · Cited by 70

Pharma-Nutritional Properties of Olive Oil Phenols. Transfer of New Findings to Human Nutrition

Crespo, M. C., Tomé‐Carneiro, J., Dávalos, A., & Visioli, F. (2018) · Foods · doi:10.3390/foods7060090 · Cited by 72

Emerging role of extracellular vesicles in the respiratory system

Holtzman, J., & Lee, H. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-0450-9 · Cited by 70

Circ-PRKDC Contributes to 5-Fluorouracil Resistance of Colorectal Cancer Cells by Regulating miR-375/FOXM1 Axis and Wnt/β-Catenin Pathway

Chen, H., Pei, L., Xie, P., & Guo, G. (2020) · OncoTargets and Therapy · doi:10.2147/ott.s253468 · Cited by 70

Sulforaphane as a potential remedy against cancer: Comprehensive mechanistic review

Ul‐Haq, I., Khan, S., Awan, K. A., & Iqbal, M. J. (2021) · Journal of Food Biochemistry · doi:10.1111/jfbc.13886 · Cited by 70

Three dysregulated microRNAs in serum as novel biomarkers for gastric cancer screening

Wang, H., Wang, L., Wu, Z., Sun, R., Jin, H., Ma, J., Liu, L., Ling, R., Yi, J., Wang, L., et al. (2014) · Medical Oncology · doi:10.1007/s12032-014-0298-8 · Cited by 70

Upregulation of Mir-21 Levels in the Vitreous Humor Is Associated with Development of Proliferative Vitreoretinal Disease

Usui‐Ouchi, A., Ouchi, Y., KIYOKAWA, M., Sakuma, T., Ito, R., & Ebihara, N. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158043 · Cited by 71

Pseudomonas aeruginosa infection augments inflammation through miR-301b repression of c-Myb-mediated immune activation and infiltration

Li, X., He, S., Li, R., Zhou, X., Zhang, S., Yu, M., Ye, Y., Wang, Y., Huang, C., & Wu, M. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.132 · Cited by 70

miR-206 regulates 5-FU resistance by targeting Bcl-2 in colon cancer cells

Meng, X., & Fu, R. (2018) · OncoTargets and Therapy · doi:10.2147/ott.s159093 · Cited by 70

Pivotal regulators of tissue homeostasis and cancer: macrophages

Chen, Y., & Zhang, X. (2017) · Experimental Hematology and Oncology · doi:10.1186/s40164-017-0083-4 · Cited by 72

Microprocessor depends on hemin to recognize the apical loop of primary microRNA

Nguyen, T. A., Park, J., Dang, T. L., Choi, Y.-G., & Kim, V. N. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky248 · Cited by 72

IsomiRs: Expanding the miRNA repression toolbox beyond the seed

Bofill-De Ros, X., Yang, A., & Gu, S. (2020) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2019.03.005 · Cited by 71

Current and Future Trends in Molecular Biomarkers for Diagnostic, Prognostic, and Predictive Purposes in Non-Melanoma Skin Cancer

Νikolouzakis, Τ. Κ., Falzone, L., Lasithiotakis, K. G., Krüger‐Krasagakis, S., Kalogeraki, A. M., Sifaki, M., Spandidos, D. A., Chrysos, E., Tsatsakis, A. M., & Tsiaoussis, J. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9092868 · Cited by 71

Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update

Schätzl, T., Kaiser, L., & Deigner, H. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-01760-1 · Cited by 70

Epigenetic modifications from arsenic exposure: A comprehensive review

Chakraborty, A., Ghosh, S., Biswas, B., Pramanik, S., Nriagu, J. O., & Bhowmick, S. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.151218 · Cited by 69

Matrix metalloproteinases in rheumatoid arthritis and osteoarthritis: a state of the art review

Pulik, Ł., Łęgosz, P., & Motyl, G. (2023) · Reumatologia/Rheumatology · doi:10.5114/reum/168503 · Cited by 71

High-Resolution Mapping of RNA Polymerases Identifies Mechanisms of Sensitivity and Resistance to BET Inhibitors in t(8;21) AML

Zhao, Y., Liu, Q., Acharya, P., Stengel, K. R., Sheng, Q., Zhou, X., Kwak, H., Fischer, M. A., Bradner, J. E., Strickland, S. A., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.032 · Cited by 71

Wnt-signalling pathways and microRNAs network in carcinogenesis: experimental and bioinformatics approaches

Onyido, E. K., Sweeney, E., & Nateri, A. S. (2016) · Molecular Cancer · doi:10.1186/s12943-016-0541-3 · Cited by 69

MiR-148a the epigenetic regulator of bone homeostasis is increased in plasma of osteoporotic postmenopausal women

Bedene, A., Mencej-Bedrač, S., Ješe, L., Marc, J., Vrtačnik, P., Preželj, J., Kocjan, T., Kranjc, T., & Ostanek, B. (2016) · Wiener klinische Wochenschrift · doi:10.1007/s00508-016-1141-3 · Cited by 69

Photoactive Hybrid AuNR‐Pt@Ag2S Core–Satellite Nanostructures for Near‐Infrared Quantitive Cell Imaging

Qu, A., Xu, L., Sun, M., Liu, L., Kuang, H., & Xu, C. (2017) · Advanced Functional Materials · doi:10.1002/adfm.201703408 · Cited by 69

Epigenetic mechanisms underlying nervous system diseases

Qureshi, I., & Mehler, M. F. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63233-3.00005-1 · Cited by 70

miR-26 suppresses adipocyte progenitor differentiation and fat production by targeting Fbxl19Preprint

Acharya, A., Berry, D. C., Zhang, H., Jiang, Y., Jones, B. T., Hammer, R. E., Graff, J. M., & Mendell, J. T. (2019) · Genes & Development · doi:10.1101/gad.328955.119 · Cited by 69

Regulating microRNA expression: at the heart of diabetes mellitus and the mitochondrion

Hathaway, Q. A., Pinti, M. V., Durr, A. J., Waris, S. A., Shepherd, D. L., & Hollander, J. M. (2017) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00520.2017 · Cited by 69

Differential and unique patterns of synaptic miRNA expression in dorsolateral prefrontal cortex of depressed subjects

Yoshino, Y., Roy, B., & Dwivedi, Y. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-00861-y · Cited by 70

DICER1‐associated embryonal rhabdomyosarcoma and adenosarcoma of the gynecologic tract: Pathology, molecular genetics, and indications for molecular testing

Apellániz-Ruiz, M., McCluggage, W. G., & Foulkes, W. D. (2020) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22913 · Cited by 68

Pathomechanisms and therapeutic opportunities in radiation-induced heart disease: from bench to bedside

Sárközy, M., Varga, Z., Gáspár, R., Szűcs, G., Kovács, M. G., Kovács, Z. Z. A., László, A., Kahán, Z., & Csont, T. (2021) · Clinical Research in Cardiology · doi:10.1007/s00392-021-01809-y · Cited by 72

Non-Coding RNAs in Legumes: Their Emerging Roles in Regulating Biotic/Abiotic Stress Responses and Plant Growth and Development

Jha, U. C., Nayyar, H., Mantri, N. L., & Siddique, K. H. M. (2021) · Cells · doi:10.3390/cells10071674 · Cited by 68

PABPC1——mRNA stability, protein translation and tumorigenesis

Qi, Y., Wang, M., & Jiang, Q. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.1025291 · Cited by 72

Crosstalk between miRNAs and DNA Methylation in Cancer

Saviana, M., Le, P., Micalo, L., Morales, D. D. V., Romano, G., Acunzo, M., Li, H. Y., & Nana-Sinkam, P. S. (2023) · Genes · doi:10.3390/genes14051075 · Cited by 72

Mini but mighty: micro RNA s in the pathobiology of periodontal disease

Kebschull, M., & Papapanou, P. N. (2015) · Periodontology 2000 · doi:10.1111/prd.12095 · Cited by 69

Dicer interacts with SIRT7 and regulates H3K18 deacetylation in response to DNA damaging agents

Zhang, P.-Y., Li, G., Deng, Z., Liu, L., Chen, L., Tang, J., Wang, Y.-Q., Cao, S.-T., Fang, Y., Wen, F., et al. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1504 · Cited by 69

Cajal bodies and their role in plant stress and disease responses

Love, A. J., Yu, C., Petukhova, N. V., Kalinina, N. O., Chen, J., & Taliansky, M. E. (2016) · RNA Biology · doi:10.1080/15476286.2016.1243650 · Cited by 68

Non-Coding RNAs: New Players in Skin Wound Healing

Herter, E. K., & Xu, N. (2017) · Advances in Wound Care · doi:10.1089/wound.2016.0711 · Cited by 69

miR-455-3p Alleviates Hepatic Stellate Cell Activation and Liver Fibrosis by Suppressing HSF1 Expression

Song, W., Wang, Q., Zhou, H., Qiu, J., Li, C., Shi, C., Zhou, S., Liu, R., & Lü, L. (2019) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2019.05.001 · Cited by 67

Structure of the Dicer-2–R2D2 heterodimer bound to a small RNA duplex

Yamaguchi, S., Naganuma, M., Nishizawa, T., Kusakizako, T., Tomari, Y., Nishimasu, H., & Nureki, O. (2022) · Nature · doi:10.1038/s41586-022-04790-2 · Cited by 71

Mitochondrial miRNAs (MitomiRs): Their potential roles in breast and other cancers

Ertürk, E., Onur, O. E., Akgün, O., Tuna, G., Yıldız, Y., & Arı, F. (2022) · Mitochondrion · doi:10.1016/j.mito.2022.08.002 · Cited by 67

MicroRNAs are important regulators of drug resistance in colorectal cancer

Zhang, Y., & Wang, J. (2017) · Biological Chemistry · doi:10.1515/hsz-2016-0308 · Cited by 68

Overexpression of miR-206 ameliorates chronic constriction injury-induced neuropathic pain in rats via the MEK/ERK pathway by targeting brain-derived neurotrophic factor

Sun, W., Zhang, L., & Li, R. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2016.12.047 · Cited by 67

miR-708-5p: a microRNA with emerging roles in cancer

Monteleone, N. J., & Lutz, C. S. (2017) · Oncotarget · doi:10.18632/oncotarget.19772 · Cited by 69

Fishing Into the MicroRNA Transcriptome

Herkenhoff, M. E., de Oliveira, A. C., Nachtigall, P. G., Costa, J. M., Campos, V. F., Hilsdorf, A. W. S., & Pinhal, D. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00088 · Cited by 67

The RNA-binding protein ARPP21 controls dendritic branching by functionally opposing the miRNA it hosts

Rehfeld, F., Maticzka, D., Grosser, S., Knauff, P., Eravci, M., Vida, I., Backofen, R., & Wulczyn, F. G. (2018) · Nature Communications · doi:10.1038/s41467-018-03681-3 · Cited by 74

MiR-205 promotes motility of ovarian cancer cells via targeting ZEB1

Niu, K., Shen, W., Zhang, Y., Zhao, Y. Y., & Lu, Y. (2015) · Gene · doi:10.1016/j.gene.2015.08.017 · Cited by 66

Micro RNA s (mi RNA s) in the control of HF development and cycling: the next frontiers in hair research

Andl, T., & Botchkareva, N. V. (2015) · Experimental Dermatology · doi:10.1111/exd.12785 · Cited by 67

MicroRNA and Metastasis

Ma, L. (2016) · Advances in cancer research · doi:10.1016/bs.acr.2016.07.004 · Cited by 69

Cancer-Derived Extracellular Vesicle-Associated MicroRNAs in Intercellular Communication: One Cell’s Trash Is Another Cell’s Treasure

Mills, J., Capece, M., Cocucci, E., Tessari, A., & Palmieri, D. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246109 · Cited by 68

Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics

Cuciniello, R., Filosa, S., & Crispi, S. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-02193-1 · Cited by 68

Cancer-related hypercalcemia and potential treatments

Almuradova, E., & Çiçin, İ. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1039490 · Cited by 66

Circulating MicroRNA and Long Noncoding RNA as Biomarkers of Cardiovascular Diseases

Shi, Q., & Yang, X. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25174 · Cited by 66

RNA silencing movement in plants

Mermigka, G., Verret, F., & Kalantidis, K. (2015) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12423 · Cited by 68

Discovery of a Small-Molecule Inhibitor of Protein–MicroRNA Interaction Using Binding Assay with a Site-Specifically Labeled Lin28

Lim, D., Byun, W. G., Koo, J. Y., Park, H., & Park, S. B. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b06965 · Cited by 66

Epigenetic disruption of miR-130a promotes prostate cancer by targeting SEC23B and DEPDC1

Ramalho-Carvalho, J., Martins, J. B., Cekaite, L., Sveen, A., Torres-Ferreira, J., Graça, I. C. R., Costa‐Pinheiro, P., Eilertsen, I. A., Antunes, L., Oliveira, J., et al. (2016) · Cancer Letters · doi:10.1016/j.canlet.2016.10.028 · Cited by 66

miR-146a-5p plays an essential role in the aberrant epithelial–fibroblast cross-talk in COPD

Osei, E. T., Florez‐Sampedro, L., Tasena, H., Faiz, A., Noordhoek, J. A., Timens, W., Postma, D. S., Hackett, T., Heijink, I. H., & Brandsma, C. (2017) · European Respiratory Journal · doi:10.1183/13993003.02538-2016 · Cited by 67

Nuclear export of RNA: Different sizes, shapes and functions

Williams, T. D., Ngo, L. H., & Wickramasinghe, V. O. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.08.054 · Cited by 69

Mirnovo: genome-free prediction of microRNAs from small RNA sequencing data and single-cells using decision forests

Vitsios, D., Kentepozidou, E., Quintais, L. T., Benito‐Gutiérrez, È., van Dongen, S., Davis, M. P. A., & Enright, A. J. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx836 · Cited by 66

Heme enables proper positioning of Drosha and DGCR8 on primary microRNAs

Partin, A. C., Ngo, T. D., Herrell, E., Jeong, B., Hon, G. C., & Nam, Y. (2017) · Nature Communications · doi:10.1038/s41467-017-01713-y · Cited by 68

Unveiling the non-repair face of the Base Excision Repair pathway in RNA processing: A missing link between DNA repair and gene expression?

Antoniali, G., Malfatti, M. C., & Tell, G. (2017) · DNA repair · doi:10.1016/j.dnarep.2017.06.008 · Cited by 66

Regulation of miRNA Biogenesis and Histone Modification by K63-Polyubiquitinated DDX17 Controls Cancer Stem-like Features

Kao, S.-H., Cheng, W., Wang, Y.-T., Wu, H.-T., Yeh, H.-Y., Chen, Y., Tsai, M., & Wu, K. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-2376 · Cited by 65

Mismatched and wobble base pairs govern primary microRNA processing by human Microprocessor

Li, S., Nguyen, T. D., Nguyen, T. A., & Nguyen, T. A. (2020) · Nature Communications · doi:10.1038/s41467-020-15674-2 · Cited by 67

Icariin alleviates rheumatoid arthritis via regulating miR-223-3p/NLRP3 signalling axis

Wu, Z., Luo, J. F., Shi, X., Zhang, S.-X., Zhu, X., & Guo, J. (2020) · Autoimmunity · doi:10.1080/08916934.2020.1836488 · Cited by 65

Role of Virus-Induced Host Cell Epigenetic Changes in Cancer

Pietropaolo, V., Prezioso, C., & Moens, U. L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158346 · Cited by 65

The role of exosomal miRNA in nonalcoholic fatty liver disease

Mahmoudi, A., Butler, A., Jamialahmadi, T., & Sahebkar, A. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30699 · Cited by 56

Breaking the mold with RNA—a “RNAissance” of life science

Jones, C. H., Androsavich, J. R., So, N., Jenkins, M. P., MacCormack, D., Prigodich, A. E., Welch, V., True, J. M., & Dolsten, M. (2024) · npj Genomic Medicine · doi:10.1038/s41525-023-00387-4 · Cited by 70

Epigenetic mechanisms and therapeutic targets of chemotherapy resistance in epithelial ovarian cancer

Borley, J., & Brown, R. E. (2015) · Annals of Medicine · doi:10.3109/07853890.2015.1043140 · Cited by 67

MicroRNAs and oncolytic viruses

Ruiz, A. J., & Russell, S. J. (2015) · Current Opinion in Virology · doi:10.1016/j.coviro.2015.03.007 · Cited by 66

MicroRNA MIR21 (miR-21) and PTGS2 Expression in Colorectal Cancer and Patient Survival

Mima, K., Nishihara, R., Yang, J., Dou, R., Masugi, Y., Shi, Y. X., da Silva, A., Cao, Y., Song, M., Nowak, J. A., et al. (2016) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-15-2173 · Cited by 65

Argonaute 2-dependent Regulation of Gene Expression by Single-stranded miRNA Mimics

Matsui, M., Prakash, T. P., & Corey, D. R. (2016) · Molecular Therapy · doi:10.1038/mt.2016.39 · Cited by 65

Rbfox proteins regulate microRNA biogenesis by sequence-specific binding to their precursors and target downstream Dicer

Chen, Y., Zubović, L., Yang, F., Godin, K. S., Pavelitz, T., Castellanos, J., Macchi, P., & Varani, G. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw177 · Cited by 66

Role of circulating microRNAs in liver diseases

Loosen, S. H., Schueller, F., Trautwein, C., Roy, S., & Roderburg, C. (2017) · World Journal of Hepatology · doi:10.4254/wjh.v9.i12.586 · Cited by 65

Splicing factors as regulators of miRNA biogenesis – links to human disease

Ratnadiwakara, M., Mohenska, M., & Änkö, M. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.10.008 · Cited by 65

Structural Differences between Pri-miRNA Paralogs Promote Alternative Drosha Cleavage and Expand Target Repertoires

Ros, X. B., Kasprzak, W. K., Bhandari, Y. R., Fan, L., Cavanaugh, Q., Jiang, M., Dai, L., Yang, A., Shao, T., Shapiro, B. A., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.054 · Cited by 68

A non-canonical landscape of the microRNA system

Cipolla, G. A. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00337 · Cited by 64

Super enhancers at the miR-146a and miR-155 genes contribute to self-regulation of inflammation

Duan, Q., Mao, X., Xiao, Y., Liu, Z., Wang, Y., Zhou, H., Zhou, Z., Cai, J., Xia, K., Zhu, Q., et al. (2016) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2016.02.004 · Cited by 64

Plant microRNAs: Front line players against invading pathogens

Islam, W., Qasim, M. U., Noman, A., Adnan, M., Tayyab, M., Farooq, T. H., Huang, W., & Wang, L. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.03.008 · Cited by 64

Non-coding RNAs and epithelial mesenchymal transition in cancer: molecular mechanisms and clinical implications

Khanbabaei, H., Ebrahimi, S., García‐Rodríguez, J. L., Ghasemi, Z., Pourghadamyari, H., Mohammadi, M., & Kristensen, L. S. (2022) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-022-02488-x · Cited by 67

miRNAs: biological and clinical determinants in epilepsy

Alsharafi, W. A., Xiao, B., Abuhamed, M. M., & Luo, Z. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00059 · Cited by 65

A Non-canonical RNA Silencing Pathway Promotes mRNA Degradation in Basal Fungi

Trieu, T. A., Calo, S., Nicolás, F. E., Vila, A., Moxon, S., Dalmay, T., Torres‐Martínez, S., Garre, V., & Ruiz‐Vázquez, R. M. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005168 · Cited by 64

The Role of microRNAs in Bovine Infection and Immunity

Lawless, N., Végh, P., O’Farrelly, C., & Lynn, D. J. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00611 · Cited by 64

Involvement and Clinical Aspects of MicroRNA in Osteosarcoma

Kumar, R., Boro, A., & Fuchs, B. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17060877 · Cited by 64

MicroRNAs and Cardiovascular Disease in Diabetes Mellitus

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