Regulatory network of miRNA on its target: coordination between transcriptional and post-transcriptional regulation of gene expression

Untitled work

Bartel (2004) · doi:10.1016/s0092-8674(04)00045-5 · Cited by 34,714 · see citing works

MicroRNAs: Target Recognition and Regulatory Functions

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

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 5,094 · see citing works

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 4,896 · see citing works

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 4,355 · see citing works

Prediction of Mammalian MicroRNA Targets

Lewis, B. P., Shih, I.-H., Jones-Rhoades, M. W., Bartel, D. P., & Burge, C. B. (2003) · Cell · doi:10.1016/s0092-8674(03)01018-3 · Cited by 4,333 · see citing works

MicroRNA Targeting Specificity in Mammals: Determinants beyond Seed Pairing

Grimson, A., Farh, K. K.-H., Johnston, W. K., Garrett-Engele, P., Lim, L. P., & Bartel, D. P. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.06.017 · Cited by 3,766 · see citing works

The Transcriptional Landscape of the Mammalian Genome

Carninci, P., Kasukawa, T., Katayama, S., Gough, J., Frith, M. C., Maeda, N., Oyama, R., Ravasi, T., Lenhard, B., Wells, C. A., et al. (2005) · Science · doi:10.1126/science.1112014 · Cited by 3,492 · see citing works

Exportin-5 mediates the nuclear export of pre-microRNAs and short hairpin RNAsPreprint

Yi, R., Qin, Y., Macara, I. G., & Cullen, B. R. (2003) · Genes & Development · doi:10.1101/gad.1158803 · Cited by 3,020 · see citing works

The Microprocessor complex mediates the genesis of microRNAs

Gregory, R. I., Yan, K.-P., Amuthan, G., Chendrimada, T. P., Doratotaj, B., Cooch, N. S., & Shiekhattar, R. (2004) · Nature · doi:10.1038/nature03120 · Cited by 2,724 · see citing works

Nuclear Export of MicroRNA Precursors

Lund, E., Güttinger, S., Calado, Â., Dahlberg, J. E., & Kutay, U. (2003) · Science · doi:10.1126/science.1090599 · Cited by 2,705 · see citing works

Functional siRNAs and miRNAs exhibit strand bias

Khvorova, A., Reynolds, A., & Jayasena, S. D. (2003) · Cell · doi:10.1016/s0092-8674(03)00801-8 · Cited by 2,645 · see citing works

Principles of MicroRNA–Target Recognition

Brennecke, J., Stark, A., Russell, R. B., & Cohen, S. M. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030085 · Cited by 2,384 · see citing works

TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing

Chendrimada, T. P., Gregory, R. I., Kumaraswamy, E., Norman, J. A., Cooch, N. S., Nishikura, K., & Shiekhattar, R. (2005) · Nature · doi:10.1038/nature03868 · Cited by 2,103 · see citing works

Argonaute HITS-CLIP decodes microRNA–mRNA interaction maps

Chi, S. W., Zang, J. B., Mele, A., & Darnell, R. B. (2009) · Nature · doi:10.1038/nature08170 · Cited by 1,791 · see citing works

Human Argonaute2 mediates RNA cleavage targeted by miRNAs and siRNAs

Meister, G., Landthaler, M., Patkaniowska, A., Dorsett, Y., Teng, G., & Tuschl, T. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.07.007 · Cited by 1,718 · see citing works

MicroRNA-Directed Cleavage of <i>HOXB8</i> mRNA

Yekta, S., Shih, I.-H., & Bartel, D. P. (2004) · Science · doi:10.1126/science.1097434 · Cited by 1,702 · see citing works

Antisense Transcription in the Mammalian Transcriptome

Katayama, S., Tomaru, Y., Kasukawa, T., Waki, K., Nakanishi, M., Nakamura, M., Nishida, H., Yap, C.-S., Suzuki, M., Kawai, J., et al. (2005) · Science · doi:10.1126/science.1112009 · Cited by 1,661 · see citing works

MicroRNA-10a binds the 5’UTR of ribosomal protein mRNAs and enhances their translation

Ørom, U. A., Nielsen, F. C., & Lund, A. H. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.05.001 · Cited by 1,384 · see citing works

MicroRNA-373 induces expression of genes with complementary promoter sequences

Place, R. F., Li, L., Pookot, D., Noonan, E. J., & Dahiya, R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707594105 · Cited by 1,231 · see citing works

MicroRNA in Control of Gene Expression: An Overview of Nuclear Functions

Catalanotto, C., Cogoni, C., & Zardo, G. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17101712 · Cited by 1,191 · see citing works

Diversifying microRNA sequence and function

Ameres, S. L., & Zamore, P. D. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3611 · Cited by 1,175 · see citing works

Multivesicular bodies associate with components of miRNA effector complexes and modulate miRNA activity

Gibbings, D., Ciaudo, C., Erhardt, M., & Voinnet, O. (2009) · Nature Cell Biology · doi:10.1038/ncb1929 · Cited by 990 · see citing works

MicroRNA-directed transcriptional gene silencing in mammalian cells

Kim, D. H., Sætrom, P., Snøve, O., & Rossi, J. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808830105 · Cited by 705 · see citing works

A Hexanucleotide Element Directs MicroRNA Nuclear Import

Hwang, H., Wentzel, E. A., & Mendell, J. T. (2007) · Science · doi:10.1126/science.1136235 · Cited by 698 · see citing works

Opposing microRNA families regulate self-renewal in mouse embryonic stem cells

Melton, C. A., Judson, R. L., & Blelloch, R. H. (2010) · Nature · doi:10.1038/nature08725 · Cited by 693 · see citing works

Inhibition of natural antisense transcripts in vivo results in gene-specific transcriptional upregulation

Modarresi, F., Faghihi, M. A., López-Toledano, M. A., Fatemi, R. P., Magistri, M., Brothers, S. P., van der Brug, M. P., & Wahlestedt, C. (2012) · Nature Biotechnology · doi:10.1038/nbt.2158 · Cited by 668 · see citing works

A network-biology perspective of microRNA function and dysfunction in cancer

Bracken, C. P., Scott, H. S., & Goodall, G. J. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.134 · Cited by 668 · see citing works

MicroRNAs, SNPs and Cancer

Vitale, A. V., Tan, H., & Jin, P. (2011) · Journal of Nucleic Acids Investigation · doi:10.4081/jnai.2011.2236 · Cited by 626 · see citing works

MicroRNA Directly Enhances Mitochondrial Translation during Muscle Differentiation

Zhang, X., Zuo, X., Yang, B., Li, Z., Xue, Y., Zhou, Y., Huang, J. S., Zhao, X., Zhou, J., Yan, Y., et al. (2014) · Cell · doi:10.1016/j.cell.2014.05.047 · Cited by 488 · see citing works

New class of microRNA targets containing simultaneous 5′-UTR and 3′-UTR interaction sitesPreprint

Lee, I., Ajay, S. S., Yook, J. I., Kim, H. S., Hong, S. H., Kim, N. H., Dhanasekaran, S. M., Chinnaiyan, A. M., & Athey, B. D. (2009) · Genome Research · doi:10.1101/gr.089367.108 · Cited by 485 · see citing works

The C. elegans microRNA let-7 binds to imperfect let-7 complementary sites from the lin-41 3′UTRPreprint

Vella, M. C., Choi, E.-Y., Lin, S.-Y., Reinert, K. L., & Slack, F. J. (2004) · Genes & Development · doi:10.1101/gad.1165404 · Cited by 442 · see citing works

Stabilization of hepatitis C virus RNA by an Ago2–miR-122 complex

Shimakami, T., Yamane, D., Jangra, R. K., Kempf, B. J., Spaniel, C., Barton, D. J., & Lemon, S. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112263109 · Cited by 398 · see citing works

RNase III enzymes and the initiation of gene silencing

Carmell, M. A., & Hannon, G. J. (2004) · Nature Structural & Molecular Biology · doi:10.1038/nsmb729 · Cited by 393 · see citing works

MicroRNAs activate gene transcription epigenetically as an enhancer trigger

Xiao, M., Li, J., Li, W., Wang, Y., Wu, F., Xi, Y., Zhang, L., Ding, C., Luo, H., Li, Y., et al. (2016) · RNA Biology · doi:10.1080/15476286.2015.1112487 · Cited by 378 · see citing works

RNAi Factors Are Present and Active in Human Cell Nuclei

Gagnon, K. T., Li, L., Chu, Y., Janowski, B. A., & Corey, D. R. (2014) · Cell Reports · doi:10.1016/j.celrep.2013.12.013 · Cited by 367 · see citing works

Bidirectional Transcription Directs Both Transcriptional Gene Activation and Suppression in Human Cells

Morris, K. V., Santoso, S., Turner, A. W., Pastori, C., & Hawkins, P. G. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000258 · Cited by 330 · see citing works

An alternative mode of microRNA target recognition

Chi, S. W., Hannon, G. J., & Darnell, R. B. (2012) · Nature Structural &amp; Molecular Biology · doi:10.1038/nsmb.2230 · Cited by 328 · see citing works

Human box C/D snoRNAs with miRNA like functions: expanding the range of regulatory RNAs

Brameier, M., Herwig, A., Reinhardt, R., Walter, L., & Gruber, J. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq776 · Cited by 300 · see citing works

Upregulation of Cyclin B1 by miRNA and its implications in cancer

Huang, V., Place, R. F., Portnoy, V., Wang, J., Qi, Z., Jia, Z., Yu, A. Y. C., Shuman, M., Yu, J., & Li, L.-C. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr934 · Cited by 288 · see citing works

MicroRNA-135b promotes lung cancer metastasis by regulating multiple targets in the Hippo pathway and LZTS1

Lin, C.-W., Chang, Y., Chang, Y.-C., Lin, J.-C., Chen, C. C., Pan, S., Wu, C., Chen, H.-Y., Yang, S. C., Hong, T.-M., et al. (2013) · Nature Communications · doi:10.1038/ncomms2876 · Cited by 282 · see citing works

Antisense transcripts are targets for activating small RNAs

Schwartz, J. C., Younger, S. T., Nguyen, N.-B., Hardy, D. B., Monia, B. P., Corey, D. R., & Janowski, B. A. (2008) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1444 · Cited by 274 · see citing works

microRNA-9 targets the long non-coding RNA MALAT1 for degradation in the nucleus

Leucci, E., Patella, F., Waage, J., Holmstrøm, K., Lindow, M., Porse, B. T., Kauppinen, S., & Lund, A. H. (2013) · Scientific Reports · doi:10.1038/srep02535 · Cited by 257 · see citing works

Senescence is an endogenous trigger for microRNA-directed transcriptional gene silencing in human cells

Benhamed, M., Herbig, U., Ye, T., Dejean, A., & Bischof, O. (2012) · Nature Cell Biology · doi:10.1038/ncb2443 · Cited by 252 · see citing works

miR-24 Regulates Apoptosis by Targeting the Open Reading Frame (ORF) Region of FAF1 in Cancer Cells

Qin, W., Shi, Y., Zhao, B., Yao, C., Jin, L., Ma, J., & Jin, Y. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009429 · Cited by 248 · see citing works

Promoter RNA links transcriptional regulation of inflammatory pathway genes

Matsui, M., Chu, Y., Zhang, H., Gagnon, K. T., Shaikh, S., Kuchimanchi, S., Manoharan, M., Corey, D. R., & Janowski, B. A. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt777 · Cited by 219 · see citing works

Mouse miRNA-709 directly regulates miRNA-15a/16-1 biogenesis at the posttranscriptional level in the nucleus: evidence for a microRNA hierarchy system

Tang, R., Li, L., Zhu, D., Hou, D., Cao, T., Gu, H., Zhang, J., Chen, J., Zhang, C., & Zen, K. (2011) · Cell Research · doi:10.1038/cr.2011.137 · Cited by 202 · see citing works

Transcriptional gene silencing in mammalian cells by miRNA mimics that target gene promoters

Younger, S. T., & Corey, D. R. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr155 · Cited by 200 · see citing works

A Viral microRNA Down-Regulates Multiple Cell Cycle Genes through mRNA 5′UTRs

Grey, F. E., Tirabassi, R. S., Meyers, H. L., Wu, G., McWeeney, S. K., Hook, L. M., & Nelson, J. A. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000967 · Cited by 200 · see citing works

Transcriptional inhibiton of Hoxd4 expression by miRNA-10a in human breast cancer cells

Tan, Y., Zhang, B., Wu, T., Skogerbø, G., Zhu, X., Guo, X., He, S., & Chen, R. (2009) · BMC Molecular Biology · doi:10.1186/1471-2199-10-12 · Cited by 192 · see citing works

The Whereabouts of microRNA Actions: Cytoplasm and Beyond

Leung, A. K. L. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2015.07.005 · Cited by 192 · see citing works

Understanding microRNA-mediated gene regulatory networks through mathematical modelling

Lai, X., Wolkenhauer, O., & Vera, J. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw550 · Cited by 192 · see citing works

The MicroRNA Biology of the Mammalian Nucleus

Roberts, T. C. (2014) · Molecular Therapy — Nucleic Acids · doi:10.1038/mtna.2014.40 · Cited by 191 · see citing works

A mouse locus at which transcription from both DNA strands produces mRNAs complementary at their 3′ ends

Williams, T., & Fried, M. (1986) · Nature · doi:10.1038/322275a0 · Cited by 184 · see citing works

MicroRNAs with a nucleolar location

Politz, J. C. R., Hogan, E. M., & Pederson, T. (2009) · RNA · doi:10.1261/rna.1470409 · Cited by 183 · see citing works

Systematic Analysis of Small RNAs Associated with Human Mitochondria by Deep Sequencing: Detailed Analysis of Mitochondrial Associated miRNA

Sripada, L., Tomar, D., Prajapati, P., Singh, R. K., Singh, A. K., & Singh, R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044873 · Cited by 181 · see citing works

MicroRNA Target Recognition: Insights from Transcriptome-Wide Non-Canonical Interactions

Seok, H., Ham, J., Jang, E.-S., & Chi, S. W. (2016) · Molecules and Cells · doi:10.14348/molcells.2016.0013 · Cited by 159 · see citing works

A Look at Messenger RNP Moving through the Nuclear Pore

Daneholt, B. (1997) · Cell · doi:10.1016/s0092-8674(00)81900-5 · Cited by 149 · see citing works

Importin 8 Regulates the Transport of Mature MicroRNAs into the Cell Nucleus

Wei, Y., Li, L., Wang, D., Zhang, C., & Zen, K. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.c113.541417 · Cited by 147 · see citing works

The IGF2 intronic miR-483 selectively enhances transcription from IGF2 fetal promoters and enhances tumorigenesisPreprint

Liu, M., Roth, A., Yu, M., Morris, R. T., Bersani, F., Rivera, M. N., Lü, J., Shioda, T., Vasudevan, S., Ramaswamy, S., et al. (2013) · Genes & Development · doi:10.1101/gad.224170.113 · Cited by 146 · see citing works

Polycombs and microRNA-223 regulate human granulopoiesis by transcriptional control of target gene expression

Zardo, G., Ciolfi, A., Vian, L., Starnes, L. M., Billi, M., Racanicchi, S., Maresca, C., Fazi, F., Travaglini, L., Noguera, N. I., et al. (2012) · Blood · doi:10.1182/blood-2011-08-371344 · Cited by 145 · see citing works

RISC-target interaction: Cleavage and translational suppression

vandenBerg, A. L., Mols, J., & HAN, J. (2008) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2008.07.005 · Cited by 142 · see citing works

Mechanistic principles of chromatin remodeling guided by siRNAs and miRNAs

González, S., Pisano, D. G., & Serrano, M. (2008) · Cell Cycle · doi:10.4161/cc.7.16.6541 · Cited by 136 · see citing works

Nuclear and cytoplasmic localization of neural stem cell microRNAs.

Jeffries, C. D., Fried, H., & Perkins, D. (2011) · RNA: A publication of the RNA Society · doi:10.1261/rna.2006511 · Cited by 123 · see citing works

A dual inhibition: microRNA-552 suppresses both transcription and translation of cytochrome P450 2E1

Miao, L., Yao, H., Li, C., Pu, M., Yao, X., Yang, H., Qi, X., Ren, J., & Wang, Y. (2016) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2016.02.016 · Cited by 98 · see citing works

Resolving subcellular miRNA trafficking and turnover at single-molecule resolution

Pitchiaya, S., Heinicke, L. A., Park, J. I., Cameron, E. L., & Walter, N. G. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.075 · Cited by 98 · see citing works

MicroRNA-181a modulates gene expression of zinc finger family members by directly targeting their coding regions

Huang, S., Wu, S., Ding, J., Lin, J., Lin, W., Gu, J., & He, X. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq564 · Cited by 90 · see citing works

Hsa-miR-24-3p increases nasopharyngeal carcinoma radiosensitivity by targeting both the 3′UTR and 5′UTR of Jab1/CSN5

Wang, S., Pan, Y., Zhang, R., Xu, T., Wu, W., Zhang, R., Wang, C., Huang, H., Calin, C. A., Yang, H., et al. (2016) · Oncogene · doi:10.1038/onc.2016.147 · Cited by 88 · see citing works

The 3' UTR of FMR1 mRNA is a target of miR-101, miR-129-5p and miR-221: implications for the molecular pathology of FXTAS at the synapse

Zongaro, S., Hukema, R. K., D’Antoni, S., Davidovic, L., Barbry, P., Catania, M. V., Willemsen, R., Mari, B. P., & Bardoni, B. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt044 · Cited by 77 · see citing works

The miR-491-3p/Sp3/ABCB1 axis attenuates multidrug resistance of hepatocellular carcinoma

Zhao, Y., Qi, X., Chen, J., Wei, W., Yu, C., Yan, H., Pu, M., Li, Y., Miao, L., Li, C., et al. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.08.027 · Cited by 77 · see citing works

Combinatorial Action of miRNAs Regulates Transcriptional and Post-Transcriptional Gene Silencing following in vivo PNS Injury

Adilakshmi, T., Sudol, I., & Tapinos, N. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039674 · Cited by 60 · see citing works

The Effects of miR‐20a on p21: Two Mechanisms Blocking Growth Arrest in TGF‐β‐Responsive Colon Carcinoma

Sokolova, V., Fiorino, A., Zoni, E., Crippa, E., Reid, J. F., Gariboldi, M., & Pierotti, M. A. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25051 · Cited by 57 · see citing works

MiR-1254 suppresses HO-1 expression through seed region-dependent silencing and non-seed interaction with TFAP2A transcript to attenuate NSCLC growth

Pu, M., Li, C., Qi, X., Chen, J., Wang, Y., Gao, L., Miao, L., & Ren, J. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006896 · Cited by 47 · see citing works

Nucleocytoplasmic Transport of MicroRNAs and Related Small RNAs

Katahira, J., & Yoneda, Y. (2011) · Traffic · doi:10.1111/j.1600-0854.2011.01211.x · Cited by 44 · see citing works

miR-155 downregulates ErbB2 and suppresses ErbB2-induced malignant transformation of breast epithelial cells

He, X.-H., Zhu, W., Yuan, P., Jiang, S., Li, D., Zhang, H.-W., & Liu, M.-F. (2016) · Oncogene · doi:10.1038/onc.2016.132 · Cited by 43 · see citing works

A multi-omics analysis of the regulatory changes induced by miR-223 in a monocyte/macrophage cell line

M’Baya-Moutoula, E., Louvet, L., Molinié, R., Guerrera, I. C., Cerutti, C., Fourdinier, O., Nourry, V., Gutierrez, L., Morlière, P., Mesnard, F., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.05.010 · Cited by 41 · see citing works

miR-196b-Mediated Translation Regulation of Mouse Insulin2 via the 5′UTR

Panda, A. C., Sahu, I., Kulkarni, S. D., Martindale, J. L., Abdelmohsen, K., Vindu, A., Joseph, J., Gorospe, M., & Seshadri, V. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101084 · Cited by 38 · see citing works

Transcriptional regulation by miRNA mimics that target sequences downstream of gene termini

Younger, S. T., & Corey, D. R. (2011) · Molecular BioSystems · doi:10.1039/c1mb05090g · Cited by 32 · see citing works

Dual inhibition of PCDH9 expression by miR-215-5p up-regulation in gliomas

Wang, C., Chen, Q., Li, S., Li, S., Zhao, Z., Gao, H., Wang, X., Li, B., Zhang, W., Yuan, Y., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.14396 · Cited by 32 · see citing works

The dual-inhibitory effect of miR-338-5p on the multidrug resistance and cell growth of hepatocellular carcinoma

Zhao, Y., Chen, J., Wei, W., Qi, X., Li, C., & Ren, J. (2018) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-017-0003-4 · Cited by 28 · see citing works

Integrated microRNA and mRNA network analysis of the human myometrial transcriptome in the transition from quiescence to labor†,‡

Ackerman, W. E., Buhimschi, I. A., Brubaker, D. K., Maxwell, S., Rood, K. M., Chance, M. R., Jing, H., Mesiano, S. A., & Buhimschi, C. S. (2018) · Biology of Reproduction · doi:10.1093/biolre/ioy040 · Cited by 16 · see citing works

Understanding the molecular mechanisms for the enhanced phytoremediation of heavy metals through plant growth promoting rhizobacteria: A review

Ravi, M. S., Karthik, C., Kadirvelu, K., Arulselvi, P. I., Shanmugasundaram, T., Bruno, L. B., & Rajkumar, M. (2019) · Journal of Environmental Management · doi:10.1016/j.jenvman.2019.109779 · Cited by 461 · see citing works

Trials and Tribulations of MicroRNA Therapeutics

Seyhan, A. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031469 · Cited by 381 · see citing works

The roles of miRNA, lncRNA and circRNA in the development of osteoporosis

Yang, Y., Yujiao, W., Wang, F., Linhui, Y., Guo, Z., Zhichen, W., Zirui, W., & Wang, S. (2020) · Biological Research · doi:10.1186/s40659-020-00309-z · Cited by 284 · see citing works

miRTarBase 2025: updates to the collection of experimentally validated microRNA–target interactions

Cui, S., Yu, S., Huang, H., Lin, Y.-C.-D., Huang, Y., Zhang, B., Xiao, J., Zuo, H., Wang, J., Li, G., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1072 · Cited by 275 · see citing works

Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential

Yuan, M., Yang, B., Rothschild, G., Mann, J. J., Sanford, L. D., Tang, X., Huang, C., Wang, C., & Zhang, W. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01519-z · Cited by 246 · see citing works

Human Long Noncoding RNA Interactome: Detection, Characterization and Function

Kazimierczyk, M., Kasprowicz, M. K., Kasprzyk, M. E., & Wrzesiński, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21031027 · Cited by 204 · see citing works

Tumor‐derived exosomal miR‐19b‐3p facilitates M2 macrophage polarization and exosomal LINC00273 secretion to promote lung adenocarcinoma metastasis via Hippo pathway

Chen, J., Zhang, K., Zhi, Y., Wu, Y., Chen, B., Bai, J., & Wang, X. (2021) · Clinical and Translational Medicine · doi:10.1002/ctm2.478 · Cited by 206 · see citing works

Competing Endogenous RNAs, Non-Coding RNAs and Diseases: An Intertwined Story

Ala, U. (2020) · Cells · doi:10.3390/cells9071574 · Cited by 204 · see citing works

Hypoxia induced exosomal circRNA promotes metastasis of Colorectal Cancer via targeting GEF-H1/RhoA axis

Yang, H., Zhang, H., Yang, Y., Wang, X., Deng, T., Liu, R., Ning, T., Bai, M., Li, H., Zhu, K., et al. (2020) · Theranostics · doi:10.7150/thno.44419 · Cited by 196 · see citing works

Regulatory RNAs in Heart Failure

Gomes, C. P. C., Schroen, B. L. M., Kuster, G. M., Robinson, E. L., Ford, K. L., Squire, I. B., Heymans, S. R. B., Martelli, F., Emanueli, C., Devaux, Y., et al. (2020) · Circulation · doi:10.1161/circulationaha.119.042474 · Cited by 189 · 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

RNA-based scaffolds for bone regeneration: application and mechanisms of mRNA, miRNA and siRNA

Leng, Q., Chen, L., & Lv, Y. (2020) · Theranostics · doi:10.7150/thno.42640 · Cited by 146 · see citing works

MicroRNA as an Important Target for Anticancer Drug Development

Fu, Z., Wang, L., Li, S., Chen, F., Au-Yeung, K. K.-W., & Shi, C. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.736323 · Cited by 133 · see citing works

Long noncoding RNA lncRNA354 functions as a competing endogenous RNA of miR160b to regulate ARF genes in response to salt stress in upland cotton

Zhang, X., Shen, J. X., Xu, Q., Dong, J., Song, L., Wang, W., & Shen, F. (2021) · Plant Cell & Environment · doi:10.1111/pce.14133 · Cited by 125 · see citing works

Upregulation of Circular RNA CircNFIB Attenuates Cardiac Fibrosis by Sponging miR-433

Zhu, Y., Pan, W. Q., Yang, T., Meng, X., Jiang, Z., Tao, L., & Wang, L. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00564 · Cited by 118 · see citing works

Diabetes mellitus promotes susceptibility to periodontitis—novel insight into the molecular mechanisms

Zhao, M., Xie, Y., Gao, W., Li, C., Ye, Q., & Li, Y. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1192625 · Cited by 111 · see citing works

The Role of microRNAs in Metabolic Syndrome-Related Oxidative Stress

Włodarski, A., Strycharz, J., Wróblewski, A. M., Kasznicki, J., Drzewoski, J., & Śliwińska, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186902 · Cited by 99 · see citing works

Recent advances in nanomaterial-based electrochemical and optical sensing platforms for microRNA assays

Wang, Y., He, L., Huang, K., Chen, Y., Wang, S., Liu, Z., & Li, D. (2019) · The Analyst · doi:10.1039/c9an00081j · Cited by 97 · see citing works

The Role of microRNA in the Inflammatory Response of Wound Healing

Jiang, Y., Xu, X. Z., Xiao, L., Wang, L., & Qiang, S. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.852419 · Cited by 93 · see citing works

miR-615-3p promotes the epithelial-mesenchymal transition and metastasis of breast cancer by targeting PICK1/TGFBRI axis

Lei, B., Wang, D., Zhang, M., Deng, Y., Jiang, H., & Li, Y. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01571-5 · Cited by 85 · see citing works

miRNAs; a novel strategy for the treatment of COVID‐19

Ying, H., Ebrahimi, M., Keivan, M., Khoshnam, S. E., Salahi, S., & Farzaneh, M. (2021) · Cell Biology International · doi:10.1002/cbin.11653 · Cited by 84 · see citing works

Exosome-Encapsulated microRNA-127-3p Released from Bone Marrow-Derived Mesenchymal Stem Cells Alleviates Osteoarthritis Through Regulating CDH11-Mediated Wnt/β-Catenin Pathway

Dong, J., Li, L., Fang, X., & Zang, M. (2021) · Journal of Pain Research · doi:10.2147/jpr.s291472 · Cited by 82 · see citing works

Long Noncoding RNA EBLN3P Promotes the Progression of Liver Cancer via Alteration of microRNA-144-3p/DOCK4 Signal

Li, H., Wang, M., Zhou, H., Lu, S., & Zhang, B. (2020) · Cancer Management and Research · doi:10.2147/cmar.s261976 · Cited by 68 · see citing works

Recent insights into the microRNA-dependent modulation of gliomas from pathogenesis to diagnosis and treatment

Mafi, A., Rahmati, A., Aghdam, Z. B., Salami, R., Salami, M., Vakili, O., & Aghadavod, E. (2022) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-022-00354-4 · Cited by 66 · see citing works

miR-276 and miR-182013-5p modulate insect metamorphosis and reproduction via dually regulating juvenile hormone acid methyltransferase

Song, J., Li, W., Gao, L., Yan, Q., Zhang, X., Liu, M., & Zhou, S. (2024) · Communications Biology · doi:10.1038/s42003-024-07285-0 · Cited by 65 · see citing works

Nuclear miRNAs: Gene Regulation Activities

Billi, M., Marinis, E. D., Gentile, M., Nervi, C., & Grignani, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25116066 · Cited by 65 · see citing works

Gene autoregulation by 3’ UTR-derived bacterial small RNAs

Hoyos, M., Huber, M., Förstner, K. U., & Papenfort, K. (2020) · eLife · doi:10.7554/elife.58836 · Cited by 61 · see citing works

Applications of nanotechnologies for miRNA-based cancer therapeutics: current advances and future perspectives

Bravo-Vázquez, L. A., Méndez-García, A., Rodríguez, A. L., Sahare, P., Pathak, S., Banerjee, A., Duttaroy, A. K., & Paul, S. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1208547 · Cited by 59 · see citing works

Circulating microRNAs as Potential Biomarkers in Pancreatic Cancer—Advances and Challenges

Seyhan, A. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713340 · Cited by 60 · see citing works

Advances in the discovery of microRNA-based anticancer therapeutics: latest tools and developments

To, K. K. W., Fong, W., Tong, C. W. S., Wu, M., Yan, W., & Cho, W. C. S. (2019) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2020.1690449 · Cited by 57 · see citing works

Noncoding RNAs: Master Regulator of Fibroblast to Myofibroblast Transition in Fibrosis

Zhang, H., Zhou, Y., Wen, D., & Wang, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021801 · Cited by 57 · see citing works

Determinants of Functional MicroRNA Targeting

Hwang, H., Chang, H. R., & Baek, D. (2023) · Molecules and Cells · doi:10.14348/molcells.2023.2157 · Cited by 55 · see citing works

Exosomes: From Potential Culprits to New Therapeutic Promise in the Setting of Cardiac Fibrosis

Tikhomirov, R., Reilly-O’Donnell, B., Catapano, F., Faggian, G. G., Gorelik, J., Martelli, F., & Emanueli, C. (2020) · Cells · doi:10.3390/cells9030592 · Cited by 56 · see citing works

Advances in the regulation of plant development and stress response by miR167

Liu, X., Huang, S., & Xie, H. (2021) · Frontiers in Bioscience-Landmark · doi:10.52586/4974 · Cited by 50 · see citing works

Non-coding RNAs in lung cancer: molecular mechanisms and clinical applications

Liu, Y., Ding, W., Wang, J., Ao, X., & Xue, J. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1256537 · Cited by 52 · see citing works

Exosome–transmitted microRNA‐133b inhibited bladder cancer proliferation by upregulating dual‐specificity protein phosphatase 1

Cai, X., Qu, L., Yang, J., Xu, J., Sun, L., Wei, X., Qu, X., Bai, T., Guo, Z., & Zhu, Y. (2020) · Cancer Medicine · doi:10.1002/cam4.3263 · Cited by 52 · see citing works

MicroRNA-575 regulates development of gastric cancer by targeting PTEN

Wang, Y., Xu, F., Zhang, P., Wang, P., Wei, Y., Wu, C., & Cheng, S. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.108716 · Cited by 51 · see citing works

MiR-149-3p promotes the cisplatin resistance and EMT in ovarian cancer through downregulating TIMP2 and CDKN1A

Wang, J., & Liu, L. (2021) · Journal of Ovarian Research · doi:10.1186/s13048-021-00919-5 · Cited by 51 · see citing works

Well-Aligned Track-Accelerated Tripedal DNA Walker for Photoelectrochemical Recognition of Dual-miRNAs Based on Molecular Logic Gates

Yang, H. Y., Shen, H., Qileng, A., Cui, G., Liang, Z., Liu, Y., & Liu, W. (2023) · Analytical Chemistry · doi:10.1021/acs.analchem.3c00027 · Cited by 50 · see citing works

Identification of key Genes and Pathways Associated With Thermal Stress in Peripheral Blood Mononuclear Cells of Holstein Dairy Cattle

Fang, H., Kang, L., Abbas, Z., Hu, L., Chen, Y., Tan, X., Wang, Y., & Xu, Q. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.662080 · Cited by 50 · see citing works

The Biogenesis of miRNAs and Their Role in the Development of Amyotrophic Lateral Sclerosis

Liu, J., Zhou, F., Guan, Y., Meng, F., Zhao, Z., Su, Q., Bao, W., Wang, X., Zhao, J., Huo, Z., et al. (2022) · Cells · doi:10.3390/cells11030572 · Cited by 49 · see citing works

ath-miR164c influences plant responses to the combined stress of drought and bacterial infection by regulating proline metabolism

Gupta, A., Patil, M., Qamar, A., & Senthil‐Kumar, M. (2020) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2020.103998 · Cited by 47 · see citing works

The PI3K/AKT/mTOR signaling pathway in breast cancer: Review of clinical trials and latest advances

Khorasani, A. B. S., Hafezi, N., Sanaei, M., Jafari‐Raddani, F., Pourbagheri‐Sigaroodi, A., & Bashash, D. (2024) · Cell Biochemistry and Function · doi:10.1002/cbf.3998 · Cited by 45 · see citing works

Decoding TDP-43: the molecular chameleon of neurodegenerative diseases

Zeng, J., Luo, C., Jiang, Y., Hu, T., Lin, B., Xie, Y., Lan, J. X., & Miao, J. (2024) · Acta Neuropathologica Communications · doi:10.1186/s40478-024-01914-9 · Cited by 49 · see citing works

Unraveling the Role of MicroRNAs in Mycobacterium tuberculosis Infection and Disease: Advances and Pitfalls

Ruiz-Tagle, C., Naves, R. F., & Balcells, M. E. (2019) · Infection and Immunity · doi:10.1128/iai.00649-19 · Cited by 46 · see citing works

Extracellular MicroRNAs as Intercellular Mediators and Noninvasive Biomarkers of Cancer

Ortíz-Quintero, B. (2020) · Cancers · doi:10.3390/cancers12113455 · Cited by 47 · see citing works

LncRNA EBLN3P promotes the progression of osteosarcoma through modifying the miR-224-5p/Rab10 signaling axis

Dai, S., Li, N., Zhou, M., Yuan, Y., Yue, D., Li, T., & Zhang, X. (2021) · Scientific Reports · doi:10.1038/s41598-021-81641-6 · Cited by 42 · see citing works

Inhibition of miR-135a-5p attenuates vascular smooth muscle cell proliferation and vascular remodeling in hypertensive rats

Ye, C., Tong, Y., Wu, N., Wan, G.-W., Zheng, F., Chen, J., Lei, J., Zhou, H., Chen, A., Wang, J., et al. (2021) · Acta Pharmacologica Sinica · doi:10.1038/s41401-020-00608-x · Cited by 42 · see citing works

Alternative Splicing of Pre-mRNA in the Control of Immune Activity

Su, Z., & Huang, D. (2021) · Genes · doi:10.3390/genes12040574 · Cited by 43 · see citing works

Complete loss of miR-200 family induces EMT associated cellular senescence in gastric cancer

Yu, L., Cao, C., Li, X., Zhang, M., Gu, Q., Gao, H., Balic, J., Xu, D.-G., Zhang, L., Ying, L., et al. (2021) · Oncogene · doi:10.1038/s41388-021-02067-y · Cited by 37 · see citing works

The Pathological Role of miRNAs in Endometriosis

Begum, M. I. A., Lin, C., Hong, S., & Chae, H. (2023) · Biomedicines · doi:10.3390/biomedicines11113087 · Cited by 40 · see citing works

Addressing Alzheimer’s Disease (AD) Neuropathology Using Anti-microRNA (AM) Strategies

Jaber, V. R., Zhao, Y., Sharfman, N. M., Li, W., & Lukiw, W. J. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1632-0 · Cited by 39 · see citing works

DRP1 contributes to head and neck cancer progression and induces glycolysis through modulated FOXM1/MMP12 axis

Huang, T.-L., Chang, C.-R., Chien, C., Huang, G.-K., Chen, Y.-F., Su, L., Tsai, H.-T., Lin, Y.-S., Fang, F.-M., & Chen, C.-H. (2022) · Molecular Oncology · doi:10.1002/1878-0261.13212 · Cited by 37 · see citing works

Non-coding RNA delivery for bone tissue engineering: Progress, challenges, and potential solutions

Guan, S., Zhang, Z., & Wu, J. (2022) · iScience · doi:10.1016/j.isci.2022.104807 · Cited by 39 · see citing works

Clinical relevance of circulating non-coding RNAs in metabolic diseases: Emphasis on obesity, diabetes, cardiovascular diseases and metabolic syndrome

Dandare, A., Khan, M. J., Naeem, A., & Liaquat, A. (2022) · Genes & Diseases · doi:10.1016/j.gendis.2022.05.022 · Cited by 38 · see citing works

Athlete’s Heart Revisited: Historical, Clinical, and Molecular Perspectives

Hsieh, P. N., Shen, S., Chukwurah, M. I., Churchill, T. W., Stewart, K. M., Chung, E. H., Weiner, R. B., Li, H., & Guseh, J. S. (2025) · Circulation Research · doi:10.1161/circresaha.125.325638 · Cited by 37 · see citing works

MiR-876-5p regulates gastric cancer cell proliferation, apoptosis and migration through targeting WNT5A and MITF

Xu, Z., Yu, Z., Tan, Q., Cheng, W., Tang, Q., Wang, L., & Hong, Y. (2019) · Bioscience Reports · doi:10.1042/bsr20190066 · Cited by 37 · see citing works

Role of long non-coding RNA H19 in the development of osteoporosis

Chen, S., Liu, D., Zhou, Z., & Qin, S. (2021) · Molecular Medicine · doi:10.1186/s10020-021-00386-0 · Cited by 37 · see citing works

Interference Reduction Biosensing Strategy for Highly Sensitive microRNA Detection

Chen, F., Li, G., Chun, W., Wang, L., Ko, C.-N., Ma, D., & Leung, C. (2022) · Analytical Chemistry · doi:10.1021/acs.analchem.2c00138 · Cited by 37 · see citing works

Long non‐coding RNA NORAD functions as a microRNA‐204‐5p sponge to repress the progression of Parkinson's disease in vitro by increasing the solute carrier family 5 member 3 expression

Zhou, S., Zhang, D., Guo, J., Chen, Z., Chen, Y., & Zhang, J. (2020) · IUBMB Life · doi:10.1002/iub.2344 · Cited by 36 · see citing works

Non-coding RNAs in breast cancer: Implications for programmed cell death

Luo, Y., Tang, W., Xiang, S., Feng, J., & Zu, X. (2022) · Cancer Letters · doi:10.1016/j.canlet.2022.215929 · Cited by 35 · see citing works

Nondigestible stachyose binds membranous HSP90β on small intestinal epithelium to regulate the exosomal miRNAs: A new function and mechanism

Li, T., Liu, Y., Duan, T., Guo, C., Liu, B., Fu, X., Wang, L., Wang, X., Dong, X., Wang, C., et al. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.10.012 · Cited by 34 · see citing works

Role of miRNAs in Brain Development

Sharma, H., Kaushik, M., Goswami, P. K., Sreevani, S., Chakraborty, A., Ashique, S., & Pal, R. (2024) · MicroRNA · doi:10.2174/0122115366287127240322054519 · Cited by 33 · see citing works

miR-34a-5p regulates PINK1-mediated mitophagy via multiple modes

Tai, Y., Pu, M., Yuan, L., Guo, H., Qiao, J., Lu, H., Wang, G., Chen, J., Qi, X., Tao, Z., et al. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119415 · Cited by 33 · see citing works

An ultrasensitive solid-state ECL biosensor based on synergistic effect between Zn-NGQDs and porphyrin-based MOF as “on-off-on” platform

Dai, C., Gan, Y., Qin, J., Ma, L., Liu, Q., Huang, L., Yang, Z., Zang, G., & Zhu, S. (2023) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2023.113322 · Cited by 32 · see citing works

Identification of potential biomarkers in dengue via integrated bioinformatic analysis

Xie, L., Yin, X., Bi, J., Luo, H., Cao, X., Ma, Y., Liu, Y., Su, J., Lin, G.-L., & Guo, X. (2021) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0009633 · Cited by 32 · see citing works

Foldback-crRNA-Enhanced CRISPR/Cas13a System (FCECas13a) Enables Direct Detection of Ultrashort sncRNA

Chen, Y., Zhang, Y., Luo, S., Yang, X., Liu, C., Zhang, Q., Liu, Y., & Zhang, X. (2023) · Analytical Chemistry · doi:10.1021/acs.analchem.3c02687 · Cited by 31 · see citing works

CircHIPK3/miR-876-5p/PIK3R1 axis regulates regulation proliferation, migration, invasion, and glutaminolysis in gastric cancer cells

Li, Q., Tian, Y., Liang, Y., & Li, C. (2020) · Cancer Cell International · doi:10.1186/s12935-020-01455-w · Cited by 31 · see citing works

HIF1α-SP1 interaction disrupts the circ-0001875/miR-31-5p/SP1 regulatory loop under a hypoxic microenvironment and promotes non-small cell lung cancer progression

Wu, D., Chen, T., Zhao, X., Huang, D., Huang, J., Huang, Y., Huang, Q., Liang, Z., Chen, C., Chen, M., et al. (2022) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-022-02336-y · Cited by 31 · see citing works

Regulating miRNAs Expression by Resveratrol: Novel Insights based on Molecular Mechanism and Strategies for Cancer Therapy

Keshavarzmotamed, A., Mousavi, V., Masihipour, N., Rahmati, A., Dehmordi, R. M., Ghezelbash, B., Alimohammadi, M., & Mafi, A. (2023) · Current Molecular Pharmacology · doi:10.2174/0118761429249717230920113227 · Cited by 30 · see citing works

The Role of MicroRNAs in the Pathophysiology of Osteoarthritis

Szala, D., Kopańska, M., Trojniak, J., Jabłoński, J., Hanf-Osetek, D., Snela, S., & Zawlik, I. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126352 · Cited by 32 · see citing works

MicroRNA-22 in female malignancies: Focusing on breast, cervical, and ovarian cancers

Nejati‐Koshki, K., Alivand, M. R., & Arabzadeh, A. (2021) · Pathology - Research and Practice · doi:10.1016/j.prp.2021.153452 · Cited by 30 · see citing works

hsa-miR-7-5p suppresses proliferation, migration and promotes apoptosis in hepatocellular carcinoma cell lines by inhibiting SPC24 expression

Wang, Y., Yang, H., Zhang, G., Luo, C., Zhang, S., Luo, R., & Deng, B. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.05.020 · Cited by 30 · see citing works

LncRNA DHRS4-AS1 ameliorates hepatocellular carcinoma by suppressing proliferation and promoting apoptosis via miR-522-3p/SOCS5 axis

Zhou, Y., Li, K., Zou, X., Hua, Z., Wang, H., Bian, W., Wang, H., Chen, F., & Dai, T. (2021) · Bioengineered · doi:10.1080/21655979.2021.1994719 · Cited by 30 · see citing works

Mapping the function of MicroRNAs as a critical regulator of tumor-immune cell communication in breast cancer and potential treatment strategies

Manap, A. S. A., Wisham, A. A., Wong, F. W., Najmi, H. R. A., Ng, Z. F., & Diba, R. S. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1390704 · Cited by 29 · see citing works

New PCSK9 inhibitor miR-552-3p reduces LDL-C via enhancing LDLR in high fat diet-fed mice

Ma, N., Fan, L., Dong, Y., Xu, X., Yu, C., Chen, J., & Ren, J. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105562 · Cited by 29 · see citing works

Role of microRNAs in Obesity-Related Kidney Disease

Caus, M., Eritja, À., & Božić, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111416 · Cited by 29 · see citing works

MicroRNA and Alternative mRNA Splicing Events in Cancer Drug Response/Resistance: Potent Therapeutic Targets

Marima, R. M., Francies, F. Z., Hull, R., Molefi, T., Oyomno, M., Khanyile, R., Mbatha, S. Z., Mabongo, M., Bates, D. O., & Dlamini, Z. (2021) · Biomedicines · doi:10.3390/biomedicines9121818 · Cited by 29 · see citing works

Emerging roles of noncoding RNAs in human cancers

Wu, S., Wu, Y., Deng, S., Lei, X., & Yang, X. (2023) · Discover Oncology · doi:10.1007/s12672-023-00728-w · Cited by 29 · see citing works

Insight into the surface discharge cold plasma efficient inactivation of Pseudomonas fluorescens in water based on exogenous reactive oxygen and nitrogen species: Synergistic mechanism and energy benefits

Ni, J., Ding, C., Zhang, J., Fang, X.-M., & Xiao, H. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.134984 · Cited by 28 · see citing works

miR-3065-3p promotes stemness and metastasis by targeting CRLF1 in colorectal cancer

Li, Y., Xun, J., Wang, B., Ma, Y., Zhang, L., Yang, L., Gao, R., Guan, J., Liu, T., Gao, H., et al. (2021) · Journal of Translational Medicine · doi:10.1186/s12967-021-03102-y · Cited by 27 · see citing works

Knockdown of long non-coding RNA CDKN2B-AS1 suppresses the progression of breast cancer by miR-122-5p/STK39 axis

Qin, S., Ning, M., Liu, Q., Ding, X., Wang, Y., & Liu, Q. (2021) · Bioengineered · doi:10.1080/21655979.2021.1962685 · Cited by 28 · see citing works

Long non-coding RNA PCA3 inhibits lipid accumulation and atherosclerosis through the miR-140-5p/RFX7/ABCA1 axis

Zhao, Z.-W., Zhang, M., Liao, L.-X., Zou, J., Wang, G., Wan, X.-J., Zhou, L., Li, H., Qin, Y., Yu, X.-H., et al. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2021.158904 · Cited by 27 · see citing works

MicroRNA-214 enriched exosomes from human cerebral endothelial cells (hCEC) sensitize hepatocellular carcinoma to anti-cancer drugs

Semaan, L., Zeng, Q., Lü, Y., Zhang, Y., Zreik, M. M., Chamseddine, M. B., Chopp, M., Zhang, Z. G., & Moonka, D. (2021) · Oncotarget · doi:10.18632/oncotarget.27879 · Cited by 27 · see citing works

The Extensive Regulation of MicroRNA in Immune Thrombocytopenia

Zhao, Y., Cui, S., Wang, Y., & Xu, R. (2022) · Clinical and Applied Thrombosis/Hemostasis · doi:10.1177/10760296221093595 · Cited by 27 · see citing works

The Influence of Host miRNA Binding to RNA Within RNA Viruses on Virus Multiplication

Lei, L., Cheng, A., Wang, M., & Jia, R. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.802149 · Cited by 26 · see citing works

Circ_0079593 facilitates proliferation, metastasis, glucose metabolism and inhibits apoptosis in melanoma by regulating the miR-516b/GRM3 axis

Lu, J.-J., & Li, Y. (2020) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-020-03875-8 · Cited by 26 · see citing works

BMAL1 attenuates intracerebral hemorrhage-induced secondary brain injury in rats by regulating the Nrf2 signaling pathway

Gong, Y. Q., Zhang, G., Li, B., Cao, C., Cao, D., Li, X., Li, H., Ye, M., Shen, H., & Chen, G. (2021) · Annals of Translational Medicine · doi:10.21037/atm-21-1863 · Cited by 26 · see citing works

GARP as a Therapeutic Target for the Modulation of Regulatory T Cells in Cancer and Autoimmunity

Zimmer, N., Trzeciak, E. R., Graefen, B., Satoh, K., & Tuettenberg, A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.928450 · Cited by 26 · see citing works

Downregulation of microRNA-224-3p Hampers Retinoblastoma Progression via Activation of the Hippo-YAP Signaling Pathway by Increasing LATS2

Song, L., Huang, Y., Zhang, X., Han, S., Hou, M., & Li, H. (2020) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.61.3.32 · Cited by 26 · see citing works

IL‐17 Affects the Progression, Metastasis, and Recurrence of Laryngeal Cancer via the Inhibition of Apoptosis through Activation of the PI3K/AKT/FAS/FASL Pathways

Song, Y., Yang, M., Zhang, H., Sun, Y., Tao, Y., Li, H., Zhang, J., Li, Y., & Yang, J. (2020) · Journal of Immunology Research · doi:10.1155/2020/2953191 · Cited by 25 · see citing works

LncRNA LINC00355 promotes EMT and metastasis of bladder cancer cells through the miR-424-5p/HMGA2 axis

Li, W.-J., Li, G., Liu, Z.-W., Chen, Z., & Pu, R. (2021) · Neoplasma · doi:10.4149/neo_2021_210427n574 · Cited by 25 · see citing works

MicroRNA-376b-3p Promotes Porcine Reproductive and Respiratory Syndrome Virus Replication by Targeting Viral Restriction Factor TRIM22

Chen, J., Zhao, S., Cui, Z., Li, W., Xu, P., Liu, H., Miao, X., Chen, Y., Han, F., Zhang, H., et al. (2021) · Journal of Virology · doi:10.1128/jvi.01597-21 · Cited by 25 · see citing works

Alterations of Phenylpropanoid Biosynthesis Lead to the Natural Formation of Pinkish-Skinned and White-Fleshed Strawberry (Fragaria × ananassa)

Jiang, L., Yue, M., Liu, Y., Ye, Y., Zhang, Y., Lin, Y., Wang, X., Chen, Q., & Tang, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137375 · Cited by 25 · see citing works

miRNA Studies in Glaucoma: A Comprehensive Review of Current Knowledge and Future Perspectives

Dobrzycka, M., Sulewska, A., Biecek, P., Charkiewicz, R., Karabowicz, P., Charkiewicz, A. E., Gołaszewska, K., Milewska, P., Michalska‐Falkowska, A., Nowak, K., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914699 · Cited by 25 · see citing works

MiR-133a-3p Relieves the Oxidative Stress Induced Trophoblast Cell Apoptosis Through the BACH1/Nrf2/HO-1 Signaling Pathway

Guo, H., Wang, Y., Jia, W., & Liu, L. (2021) · Physiological Research · doi:10.33549/physiolres.934506 · Cited by 24 · see citing works

GATA1 regulates the microRNA‑328‑3p/PIM1 axis via circular RNA ITGB1 to promote renal ischemia/reperfusion injury in HK‑2 cells

Gao, Y., Xu, W., Guo, C., & Huang, T. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5156 · Cited by 24 · see citing works

Long Non-coding RNA MINCR Regulates miR-876-5p/GSPT1 Axis to Aggravate Glioma Progression

Li, Z., Xie, X., Fan, X., & Li, X. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03029-8 · Cited by 23 · see citing works

MicroRNA-Mediated Gene Regulation of Secondary Metabolism in Plants

Jiang, S., Cui, J., & Li, X. (2021) · Critical Reviews in Plant Sciences · doi:10.1080/07352689.2022.2031674 · Cited by 23 · see citing works

Exosomal and Non-Exosomal MicroRNAs: New Kids on the Block for Cancer Therapy

Syed, S. N., & Brüne, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094493 · Cited by 24 · see citing works

Biogenesis and mechanisms of microRNA‐mediated gene regulation

Rani, V., & Sengar, R. S. (2022) · Biotechnology and Bioengineering · doi:10.1002/bit.28029 · Cited by 172 · see citing works

microRNA(interference) networks are embedded in the gene regulatory networks

Pitto, L., Ripoli, A., Cremisi, F., & Rainaldi, G. (2008) · Cell Cycle · doi:10.4161/cc.7.16.6455 · Cited by 25 · see citing works

miRNA goes nuclear

Huang, V., & Li, L. (2012) · RNA Biology · doi:10.4161/rna.19354 · Cited by 70 · see citing works

Interconnection of MicroRNA and Transcription Factor-Mediated Regulatory Networks

Yiming, Z. (2019) · doi:10.1201/9780429067143-8

Paradigm shift: microRNAs interact with target gene promoters to cause transcriptional gene activation or silencing

Sarkar, N., & Kumar, A. (2024) · Experimental Cell Research · doi:10.1016/j.yexcr.2024.114372 · Cited by 22 · see citing works