MicroRNAs as Regulators of Differentiation and Cell Fate Decisions

Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs

Lim, L. P., Lau, N. C., Garrett-Engele, P., Grimson, A., Schelter, J. M., Castle, J., Bartel, D. P., Linsley, P. S., & Johnson, J. M. (2005) · Nature · doi:10.1038/nature03315 · Cited by 4,755 · see citing works

MicroRNAs Modulate Hematopoietic Lineage Differentiation

Chen, C.-Z., Li, L., Lodish, H. F., & Bartel, D. P. (2004) · Science · doi:10.1126/science.1091903 · Cited by 3,257 · see citing works

The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation

Chen, J., Mandel, E. M., Thomson, J. M., Wu, Q., Callis, T. E., Hammond, S. M., Conlon, F. L., & Wang, D.-Z. (2005) · Nature Genetics · doi:10.1038/ng1725 · Cited by 2,782 · see citing works

miR-145 and miR-143 regulate smooth muscle cell fate and plasticity

Cordes, K. R., Sheehy, N. T., White, M. P., Berry, E. C., Morton, S. U., Muth, A. N., Lee, T.-H., Miano, J. M., Ivey, K. N., & Srivastava, D. (2009) · Nature · doi:10.1038/nature08195 · Cited by 1,585 · see citing works

Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis

Zhao, Y. B., Samal, E., & Srivastava, D. P. (2005) · Nature · doi:10.1038/nature03817 · Cited by 1,556 · see citing works

Dysregulation of Cardiogenesis, Cardiac Conduction, and Cell Cycle in Mice Lacking miRNA-1-2

Zhao, Y. B., Ransom, J. F., Li, A., Vedantham, V., von Drehle, M., Muth, A. N., Tsuchihashi, T., McManus, M. T., Schwartz, R. J., & Srivastava, D. (2007) · Cell · doi:10.1016/j.cell.2007.03.030 · Cited by 1,418 · see citing works

A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep

Clop, A., Marcq, F., Takeda, H., Pirottin, D., Tordoir, X., Bibé, B., Bouix, J., Caiment, F., Elsen, J.-M., Eychenne, F., et al. (2006) · Nature Genetics · doi:10.1038/ng1810 · Cited by 1,260 · see citing works

DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal

Wang, Y., Medvid, R., Melton, C. A., Jaenisch, R., & Blelloch, R. H. (2007) · Nature Genetics · doi:10.1038/ng1969 · Cited by 1,026 · see citing works

microRNA-133a regulates cardiomyocyte proliferation and suppresses smooth muscle gene expression in the heartPreprint

Liu, N., Bezprozvannaya, S., Williams, A. H., Qi, X., Richardson, J. A., Bassel‐Duby, R., & Olson, E. N. (2008) · Genes & Development · doi:10.1101/gad.1738708 · Cited by 792 · 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

AU-rich-element-mediated upregulation of translation by FXR1 and Argonaute 2

Vasudevan, S., & Steitz, J. A. (2007) · Cell · doi:10.1016/j.cell.2007.01.038 · Cited by 656 · see citing works

MicroRNA Regulation of Cell Lineages in Mouse and Human Embryonic Stem Cells

Ivey, K. N., Muth, A. N., Arnold, J., King, F. W., Yeh, R.-F., Fish, J. E., Hsiao, E. C., Schwartz, R. J., Conklin, B. R., Bernstein, H. S., et al. (2008) · Cell stem cell · doi:10.1016/j.stem.2008.01.016 · Cited by 601 · see citing works

A feedback regulatory loop involving microRNA-9 and nuclear receptor TLX in neural stem cell fate determination

Zhao, C., Sun, G., Li, S., & Shi, Y. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1576 · Cited by 555 · see citing works

A microRNA signature for a BMP2-induced osteoblast lineage commitment program

Li, Z., Hassan, M. Q., Volinia, S., van Wijnen, A. J., Stein, J. L., Croce, C. M., Lian, J. B., & Stein, G. S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804438105 · Cited by 549 · see citing works

Target Protectors Reveal Dampening and Balancing of Nodal Agonist and Antagonist by miR-430

Choi, W.-Y., Giráldez, A. J., & Schier, A. F. (2007) · Science · doi:10.1126/science.1147535 · Cited by 517 · see citing works

A novel microRNA targeting HDAC5 regulates osteoblast differentiation in mice and contributes to primary osteoporosis in humans

Li, H., Xie, H., Liu, W., Hu, R., Huang, B., Tan, Y., Liao, E.-Y., Xu, K., Sheng, Z., Zhou, H., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39832 · Cited by 464 · see citing works

Mir-214-Dependent Regulation of the Polycomb Protein Ezh2 in Skeletal Muscle and Embryonic Stem Cells

Juan, A. H., Kumar, R., Marx, J. G., Young, R. A., & Sartorelli, V. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.08.008 · Cited by 350 · see citing works

MicroRNA-9 Coordinates Proliferation and Migration of Human Embryonic Stem Cell-Derived Neural Progenitors

Delaloy, C., Liu, L., Lee, J., Su, H., Shen, F., Yang, G., Young, W. L., Ivey, K. N., & Gao, F. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.02.015 · Cited by 320 · see citing works

MicroRNA-1/206 Targets c-Met and Inhibits Rhabdomyosarcoma Development

Yan, D., Dong, X. D., Chen, X., Wang, L., Lu, C., Wang, J., Qu, J., & Tu, L. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.020511 · Cited by 270 · see citing works

The muscle-specific microRNA miR-206 blocks human rhabdomyosarcoma growth in xenotransplanted mice by promoting myogenic differentiation

Taulli, R., Bersani, F., Foglizzo, V., Linari, A., Vigna, E., Ladanyi, M., Tuschl, T., & Ponzetto, C. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38075 · Cited by 258 · see citing works

MicroRNAs in normal and malignant hematopoiesis

Garzon, R., & Croce, C. M. (2008) · Current Opinion in Hematology · doi:10.1097/moh.0b013e328303e15d · Cited by 245 · see citing works

The miR-430/427/302 Family Controls Mesendodermal Fate Specification via Species-Specific Target Selection

Rosa, A., Spagnoli, F. M., & Brivanlou, A. H. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.02.007 · Cited by 208 · see citing works

MicroRNA Gene Regulatory Pathways in the Establishment and Maintenance of ESC Identity

Martinez, N. J., & Gregory, R. I. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.06.011 · Cited by 152 · see citing works

Circular reasoning: microRNAs and cell-cycle control

Chivukula, R. R., & Mendell, J. T. (2008) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2008.06.008 · Cited by 113 · see citing works

Serum response factor orchestrates nascent sarcomerogenesis and silences the biomineralization gene program in the heart

Niu, Z., Iyer, D., Conway, S. J., Martin, J. F., Ivey, K. N., Srivastava, D., Nordheim, A., & Schwartz, R. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805491105 · Cited by 110 · see citing works

MicroRNA-145 in vascular smooth muscle cell biology: A new therapeutic target for vascular disease

Zhang, C. (2009) · Cell Cycle · doi:10.4161/cc.8.21.9837 · Cited by 94 · see citing works

Untitled work

Krichevsky, A. (2006) · doi:10.1634/stemcells.2005-0441

MicroRNAs as regulatory elements in immune system logic

Mehta, A., & Baltimore, D. (2016) · Nature Reviews Immunology · doi:10.1038/nri.2016.40 · Cited by 704 · see citing works

A microRNA miR-34a-Regulated Bimodal Switch Targets Notch in Colon Cancer Stem Cells

Bu, P., Chen, K., Chen, J. H., Wang, L., Walters, J. N., Shin, Y. J., Goerger, J. P., Sun, J. M., Witherspoon, M., Rakhilin, N., et al. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.03.002 · Cited by 355 · see citing works

Endocytosis and signaling: Cell logistics shape the eukaryotic cell plan

Sigismund, S., Confalonieri, S., Ciliberto, A., Polo, S., Scita, G., & Di Fiore, P. P. (2012) · Physiological Reviews · doi:10.1152/physrev.00005.2011 · Cited by 338 · see citing works

An epigenetic view of plant cells cultured in vitro: Somaclonal variation and beyond

Miguel, C., & Marum, L. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err155 · Cited by 395 · see citing works

IMPs: an RNA-binding protein family that provides a link between stem cell maintenance in normal development and cancer

Degrauwe, N., Suvà, M.-L., Janiszewska, M., Riggi, N., & Stamenkovic, I. (2016) · Genes & Development · doi:10.1101/gad.287540.116 · Cited by 324 · see citing works

Coordinated regulation of neuronal mRNA steady-state levels through developmentally controlled intron retention

Yap, K., Lim, Z. Q., Khandelia, P., Friedman, B., & Makeyev, E. V. (2012) · Genes & Development · doi:10.1101/gad.188037.112 · Cited by 286 · see citing works

microRNAs as Developmental RegulatorsPreprint

Ivey, K. N., & Srivastava, D. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008144 · Cited by 251 · see citing works

Hepatocellular Carcinoma Cell-Secreted Exosomal MicroRNA-210 Promotes Angiogenesis In Vitro and In Vivo

Lin, X.-J., Fang, J., Yang, X.-J., Zhang, C., Yuan, Y., Zheng, L., & Zhuang, S. (2018) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2018.02.014 · Cited by 225 · see citing works

Modulation of microRNA expression in human T-cell development: targeting of NOTCH3 by miR-150

Ghisi, M., Corradin, A., Basso, K., Frasson, C., Serafin, V., Mukherjee, S., Mussolin, L., Ruggero, K., Bonanno, L., Guffanti, A., et al. (2011) · Blood · doi:10.1182/blood-2010-12-326629 · Cited by 221 · see citing works

MiR-137: an important player in neural development and neoplastic transformation

Mahmoudi, E., & Cairns, M. J. (2017) · Molecular Psychiatry · doi:10.1038/mp.2016.150 · Cited by 198 · see citing works

In Vivo Activation of a Conserved MicroRNA Program Induces Mammalian Heart Regeneration

Aguirre, A., Montserrat, N., Zacchigna, S., Nivet, E., Hishida, T., Krause, M. N., Kurian, L., Ocampo, A., Vazquez-Ferrer, E., Rodrı́guez-Esteban, C., et al. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.10.003 · Cited by 196 · see citing works

Identification of miRNAs associated with the follicular–luteal transition in the ruminant ovary

McBride, D., Carré, W., Sontakke, S. D., Hogg, C. O., Law, A., Donadeu, F. X., & Clinton, M. (2012) · Reproduction · doi:10.1530/rep-12-0025 · Cited by 198 · see citing works

Expression of miR-1, miR-133a, miR-133b and miR-206 increases during development of human skeletal muscle

Koutsoulidou, A., Mastroyiannopoulos, N. P., Furling, D., Uney, J. B., & Phylactou, L. A. (2011) · BMC Developmental Biology · doi:10.1186/1471-213x-11-34 · Cited by 187 · see citing works

Epigenetic Modifications and Head and Neck Cancer: Implications for Tumor Progression and Resistance to Therapy

CASTILHO, R. M., SQUARIZE, C. H., & Almeida, L. O. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071506 · Cited by 185 · see citing works

The shift in the balance between osteoblastogenesis and adipogenesis of mesenchymal stem cells mediated by glucocorticoid receptor

Han, L., Wang, B., Wang, R., Gong, S., Chen, G., & Xu, W. (2019) · Stem Cell Research & Therapy · doi:10.1186/s13287-019-1498-0 · Cited by 172 · see citing works

miR-17-5p and miR-106a are involved in the balance between osteogenic and adipogenic differentiation of adipose-derived mesenchymal stem cells

Li, H., Li, T., Wang, S., Wei, J., Fan, J., Li, J., Han, Q., Liao, L., Shao, C., & Zhao, R. C. (2012) · Stem Cell Research · doi:10.1016/j.scr.2012.11.007 · Cited by 171 · see citing works

miR‐21 modulates the ERK–MAPK signaling pathway by regulating SPRY2 expression during human mesenchymal stem cell differentiation

Yang, M., Bian, C., Li, J., Du, Z., Zhou, H., Yang, Z., & Zhao, R. C. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24479 · Cited by 170 · see citing works

MicroRNA as Type I Interferon-Regulated Transcripts and Modulators of the Innate Immune Response

Forster, S. C., Tate, M. D., & Hertzog, P. J. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00334 · Cited by 169 · see citing works

Insulin-Like Growth Factor-1 Receptor Is Regulated by microRNA-133 during Skeletal Myogenesis

Huang, M., Xu, H. M., Xie, S., Zhou, H., & Qu, L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0029173 · Cited by 165 · see citing works

Dynamic expression of tRNA‐derived small RNAs define cellular states

Gopinath, S. K., Yim, D., Lakshmanan, V., Tirumalai, V., Koh, J. L. Y., Park, J. E., Cheong, J. K., Low, J.-L., Lim, M. J., Sze, S. K., et al. (2019) · EMBO Reports · doi:10.15252/embr.201947789 · Cited by 164 · see citing works

let-7 Enhances Osteogenesis and Bone Formation While Repressing Adipogenesis of Human Stromal/Mesenchymal Stem Cells by Regulating HMGA2

Wei, J., Li, H., Wang, S., Li, T., Fan, J., Liang, X., Li, J., Han, Q., Zhu, L., Fan, L., et al. (2014) · Stem Cells and Development · doi:10.1089/scd.2013.0600 · Cited by 164 · see citing works

Comparative miRNA Expression Profiles in Individuals with Latent and Active Tuberculosis

Wang, C., Yang, S., Sun, G., Tang, X., Lu, S., Neyrolles, O., & Gao, Q. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025832 · Cited by 157 · see citing works

MicroRNA delivery for regenerative medicine

Peng, B., Chen, Y., & Leong, K. W. (2015) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2015.05.014 · Cited by 158 · see citing works

MicroRNA Gene Regulatory Pathways in the Establishment and Maintenance of ESC Identity

Martinez, N. J., & Gregory, R. I. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.06.011 · Cited by 152 · see citing works

LNA-mediated anti–miR-155 silencing in low-grade B-cell lymphomas

Zhang, Y., Roccaro, A. M., Rombaoa, C. P., Flores, L., Obad, S., Fernandes, S. M., Sacco, A., Liu, Y., Ngo, H. T., Quang, P., et al. (2012) · Blood · doi:10.1182/blood-2012-02-410647 · Cited by 152 · see citing works

The Bone Marrow-Derived Stromal Cells: Commitment and Regulation of Adipogenesis

Tencerova, M., & Kassem, M. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00127 · Cited by 149 · see citing works

CircRNA-vgll3 promotes osteogenic differentiation of adipose-derived mesenchymal stem cells via modulating miRNA-dependent integrin α5 expression

Zhang, D., Ni, N., Wang, Y., Tang, Z., Gao, H., Ju, Y., Sun, N., He, X., Gu, P., & Fan, X. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-0600-6 · Cited by 149 · see citing works

MicroRNAs and Stem Cells

Heinrich, E.-M., & Dimmeler, S. (2012) · Circulation Research · doi:10.1161/circresaha.111.243394 · Cited by 146 · see citing works

Vesiculated Long Non-Coding RNAs: Offshore Packages Deciphering Trans-Regulation between Cells, Cancer Progression and Resistance to Therapies

Fatima, F., & Nawaz, M. (2017) · Non-Coding RNA · doi:10.3390/ncrna3010010 · Cited by 144 · see citing works

miR-133a Enhances the Protective Capacity of Cardiac Progenitors Cells after Myocardial Infarction

Izarra, A., Moscoso, I., Levent, E., Cañón, S., Cerrada, I., Díez‐Juan, A., Blanca, V., Nuñez-Gil, I. J., Valiente, Í., Ruiz‐Saurí, A., et al. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.10.010 · Cited by 141 · see citing works

MicroRNA: Dynamic Regulators of Macrophage Polarization and Plasticity

Self-Fordham, J., Naqvi, A. R., Uttamani, J. R., Kulkarni, V., & Nares, S. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01062 · Cited by 140 · see citing works

In vitro culture: an epigenetic challenge for plants

Us-Camas, R. Y., Rivera-Solís, G., Duarte-Aké, F., & De‐la‐Peña, C. (2014) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-014-0482-8 · Cited by 138 · see citing works

MicroRNA-205 controls neonatal expansion of skin stem cells by modulating the PI(3)K pathway

Wang, D., Zhang, Z., O’Loughlin, E., Wang, L., Fan, X., Lai, E. C., & Yi, R. (2013) · Nature Cell Biology · doi:10.1038/ncb2827 · Cited by 139 · see citing works

The functions of microRNAs in pluripotency and reprogramming

Leonardo, T. R., Schultheisz, H. L., Loring, J. F., & Laurent, L. C. (2012) · Nature Cell Biology · doi:10.1038/ncb2613 · Cited by 134 · see citing works

The RNA Binding Protein IMP2 Preserves Glioblastoma Stem Cells by Preventing let-7 Target Gene Silencing

Degrauwe, N., Schlumpf, T. B., Janiszewska, M., Martin, P., Cauderay, A., Provero, P., Riggi, N., Suvà, M.-L., Paro, R., & Stamenkovic, I. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.04.086 · Cited by 136 · see citing works

Tissue inhibitor of metalloproteinase-1 (TIMP-1) regulates mesenchymal stem cells through let-7f microRNA and Wnt/β-catenin signaling

Egea, V., Stefan Zahler, A., Rieth, N., Neth, P., Popp, T., Kehe, K., Jochum, M., & Ries, C. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1115083109 · Cited by 135 · see citing works

miRNA-128 Suppresses Prostate Cancer by Inhibiting BMI-1 to Inhibit Tumor-Initiating Cells

Jin, M., Zhang, T., Liu, C., Badeaux, M. A., Liu, B., Liu, R., Jeter, C. R., Chen, X., Vlassov, A. V., & Tang, D. G. (2014) · Cancer Research · doi:10.1158/0008-5472.can-14-0404 · Cited by 135 · see citing works

microRNA regulation of Wnt signaling pathways in development and disease

Song, J. L., Nigam, P., Tektas, S. S., & Selva, E. M. (2015) · Cellular Signalling · doi:10.1016/j.cellsig.2015.03.018 · Cited by 131 · see citing works

Total RNA extraction from tissues for microRNA and target gene expression analysis: not all kits are created equal

Brown, R. A. M., Epis, M. R., Horsham, J. L., Kabir, T. D., Richardson, K. L., & Leedman, P. J. (2018) · BMC Biotechnology · doi:10.1186/s12896-018-0421-6 · Cited by 132 · see citing works

miR-101-2, miR-125b-2 and miR-451a act as potential tumor suppressors in gastric cancer through regulation of the PI3K/AKT/mTOR pathway

Riquelme, I., Tapia, Ó., Leal, P., Sandoval, A., Varga, M. G., Letelier, P. J., Buchegger, K., Bizama, C., Espinoza, J. A., Peek, R. M., et al. (2015) · Cellular Oncology · doi:10.1007/s13402-015-0247-3 · Cited by 131 · see citing works

Assessment of RT-qPCR Normalization Strategies for Accurate Quantification of Extracellular microRNAs in Murine Serum

Roberts, T. C., Coenen-Stass, A. M. L., & Wood, M. J. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089237 · Cited by 128 · see citing works

MicroRNA-26a targets ten eleven translocation enzymes and is regulated during pancreatic cell differentiation

Fu, X., Jin, L., Wang, X., Luo, A., Hu, J., Zheng, X., Tsark, W. M. K., Riggs, A. D., Ku, H. T., & Huang, W. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1317397110 · Cited by 127 · see citing works

MiR-2 family regulates insect metamorphosis by controlling the juvenile hormone signaling pathway

Lozano-Fernández, J., Montañez, R., & Bellés, X. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418522112 · Cited by 123 · see citing works

MicroRNA expression profiling identifies miR-328 regulates cancer stem cell-like SP cells in colorectal cancer

Xu, X., Xu, Q., Tong, J., Zhu, M., Nie, F., Chen, X., Xiao, S., & Ran, Z. H. (2012) · British Journal of Cancer · doi:10.1038/bjc.2012.88 · Cited by 123 · see citing works

MicroRNA miR-124 Controls the Choice between Neuronal and Astrocyte Differentiation by Fine-tuning Ezh2 Expression

Neo, W. H., Yap, K., Lee, S. H., Looi, L., Khandelia, P., Neo, S. X., Makeyev, E. V., & Su, I.-H. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.525493 · Cited by 122 · see citing works

MicroRNA 375 Mediates Palmitate-Induced Enteric Neuronal Damage and High-Fat Diet-Induced Delayed Intestinal Transit in Mice

Nezami, B. G., Mwangi, S. M., Lee, J. E., Jeppsson, S., Anitha, M., Yarandi, S., Farris, A. B., & Srinivasan, S. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.10.053 · Cited by 121 · see citing works

Redox regulation of cell state and fate

Lee, B. W. L., Ghode, P. B., & Ong, D. S. T. (2018) · Redox Biology · doi:10.1016/j.redox.2018.11.014 · Cited by 120 · see citing works

MicroRNAs Modulate Schwann Cell Response to Nerve Injury by Reinforcing Transcriptional Silencing of Dedifferentiation-Related Genes

Viader, A., Chang, L., Fahrner, T. J., Nagarajan, R., & Milbrandt, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3931-11.2011 · Cited by 119 · see citing works

A Versatile Method to Design Stem-Loop Primer-Based Quantitative PCR Assays for Detecting Small Regulatory RNA Molecules

Czimmerer, Z., Hulvely, J., Simándi, Z., Várallyay, É., Havelda, Z., Szabo, E., Varga, A., Dezsö, B., Balogh, M. G., Horváth, A., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055168 · Cited by 117 · see citing works

Hsa-miR-326 targets CCND1 and inhibits non-small cell lung cancer development

Sun, C., Huang, C., Li, S., Yang, C., Xi, Y., Wang, L., Zhang, F., Fu, Y., & Li, D. (2016) · Oncotarget · doi:10.18632/oncotarget.7071 · Cited by 118 · see citing works

FOXP1 circular RNA sustains mesenchymal stem cell identity via microRNA inhibition

Cherubini, A., Barilani, M., Rossi, R. L., Jalal, M., Rusconi, F., Buono, G., Ragni, E., Cantarella, G., Simpson, H., Péault, B., et al. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz199 · Cited by 116 · see citing works

Non-coding RNAs in Mesenchymal Stem Cell-Derived Extracellular Vesicles: Deciphering Regulatory Roles in Stem Cell Potency, Inflammatory Resolve, and Tissue Regeneration

Fatima, F., Ekström, K. M., Nazarenko, I. A., Maugeri, M., Valadi, H., Hill, A. F., Camussi, G., & Nawaz, M. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00161 · Cited by 116 · see citing works

MicroRNA-145 Regulates Neural Stem Cell Differentiation Through the Sox2–Lin28/let-7 Signaling Pathway

Morgado, A. L., Rodrigues, C. M. P., & Solá, S. (2016) · Stem Cells · doi:10.1002/stem.2309 · Cited by 107 · see citing works

microRNAs: key triggers of neuronal cell fate

Meza‐Sosa, K. F., Pedraza‐Alva, G., & Pérez-Martínez, L. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00175 · Cited by 104 · see citing works

Conserved chromosomal functions of RNA interference

Gutbrod, M. J., & Martienssen, R. A. (2020) · Nature Reviews Genetics · doi:10.1038/s41576-019-0203-6 · Cited by 100 · see citing works

miR-145 and miR-143 Regulate Odontoblast Differentiation through Targeting Klf4 and Osx Genes in a Feedback Loop

Liu, H., Lin, H., Zhang, L., Sun, Q., Yuan, G., Zhang, L., Chen, S., & Chen, Z. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.433730 · Cited by 102 · see citing works

microRNA‐124 Regulates Cardiomyocyte Differentiation of Bone Marrow‐Derived Mesenchymal Stem Cells Via Targeting STAT3 Signaling

Cai, B., Li, J., Wang, J., Luo, X., Ai, J., Liu, Y., Wang, N., Liang, H., Zhang, M., Chen, N., et al. (2012) · Stem Cells · doi:10.1002/stem.1154 · Cited by 101 · see citing works

A Novel YY1-miR-1 Regulatory Circuit in Skeletal Myogenesis Revealed by Genome-Wide Prediction of YY1-miRNA Network

Lu, L., Zhou, L., Chen, E. Z., Sun, K., Jiang, P., Wang, L., Su, X., Sun, H., & Wang, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0027596 · Cited by 101 · see citing works

Differentiation therapy for hepatocellular carcinoma: Multifaceted effects of miR‐148a on tumor growth and phenotype and liver fibrosis

Jung, K. H., Zhang, J., Zhou, C., Shen, H., Gagea, M., Rodriguez‐Aguayo, C., Lopez‐Berestein, G., Sood, A. K., & Beretta, L. (2015) · Hepatology · doi:10.1002/hep.28367 · Cited by 101 · see citing works

Strontium-incorporated mesoporous bioactive glass scaffolds stimulating in vitro proliferation and differentiation of bone marrow stromal cells and in vivo regeneration of osteoporotic bone defects

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Tristability in Cancer-Associated MicroRNA-TF Chimera Toggle Switch

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MicroRNA-205 functions as a tumor suppressor in human glioblastoma cells by targeting VEGF-A

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MicroRNAs: A Puzzling Tool in Cancer Diagnostics and Therapy

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Bone marrow mesenchymal stem cells for post‐myocardial infarction cardiac repair: microRNAs as novel regulators

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Multifaceted roles of pericytes in central nervous system homeostasis and disease

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MicroRNA-7: A miRNA with expanding roles in development and disease

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PBX3 is targeted by multiple miRNAs and is essential for liver tumour-initiating cells

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Micro-RNA-34a Contributes to the Impaired Function of Bone Marrow-Derived Mononuclear Cells From Patients With Cardiovascular Disease

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Dynamics of miRNA transcriptome during gonadal development of zebrafish

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Non-coding landscapes of colorectal cancer

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MicroRNA-34a Modulates Neural Stem Cell Differentiation by Regulating Expression of Synaptic and Autophagic Proteins

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MicroRNA-focused CRISPR-Cas9 library screen reveals fitness-associated miRNAs

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MicroRNA Regulation in Extreme Environments: Differential Expression of MicroRNAs in the Intertidal Snail Littorina Littorea During Extended Periods of Freezing and Anoxia

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Induction of Cellular Senescence by Doxorubicin Is Associated with Upregulated miR-375 and Induction of Autophagy in K562 Cells

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Deep Sequencing Reveals Novel MicroRNAs and Regulation of MicroRNA Expression during Cell Senescence

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miR-216a inhibits osteosarcoma cell proliferation, invasion and metastasis by targeting CDK14

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MiR‐214 is an important regulator of the musculoskeletal metabolism and disease

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microRNA Control of Mouse and Human Pluripotent Stem Cell Behavior

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Dclk1 facilitates intestinal tumor growth via enhancing pluripotency and epithelial mesenchymal transition

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Differential Expression of Mature MicroRNAs Involved in Muscle Maintenance of Hibernating Little Brown Bats, Myotis Lucifugus : A Model of Muscle Atrophy Resistance

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Rapid and widespread suppression of self-renewal by microRNA-203 during epidermal differentiation

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Untitled work

(2013) · doi:10.18632/aging.100540

miR-34a: a new player in the regulation of T cell function by modulation of NF-κB signaling

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miR-146a-5p circuitry uncouples cell proliferation and migration, but not differentiation, in human mesenchymal stem cells

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Circulating small noncoding RNAs as biomarkers of aging

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MicroRNA-Based Promotion of Human Neuronal Differentiation and Subtype Specification

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GNAI1 Suppresses Tumor Cell Migration and Invasion and is Post-Transcriptionally Regulated by Mir-320a/c/d in Hepatocellular Carcinoma.

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The role of microRNAs in cell fate determination of mesenchymal stem cells : balancing adipogenesis and osteogenesis

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miR‐372 and miR‐373 enhance the stemness of colorectal cancer cells by repressing differentiation signaling pathways

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The conserved miR-8/miR-200 microRNA family and their role in invertebrate and vertebrate neurogenesis

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MicroRNA Regulation of Stem Cell Fate

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MicroRNA helps set cell fate

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Regulation of microRNA function in somatic stem cell proliferation and differentiation

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MicroRNA Regulation of Cell Lineages in Mouse and Human Embryonic Stem Cells

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MicroRNAs: Modulators of Cell Identity, and their Applications in Tissue Engineering

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