The roles of microRNAs in mouse development

Untitled work

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

The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14

Lee, R. C., Feinbaum, R. L., & Ambros, V. (1993) · Cell · doi:10.1016/0092-8674(93)90529-y · Cited by 12,948 · 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

Natural RNA circles function as efficient microRNA sponges

Hansen, T. B., Jensen, T. I., Clausen, B. H., Bramsen, J. B., Finsen, B., Damgaard, C. K., & Kjems, J. (2013) · Nature · doi:10.1038/nature11993 · Cited by 7,985 · see citing works

Predicting effective microRNA target sites in mammalian mRNAs

Agarwal, V., Bell, G. W., Nam, J.-W., & Bartel, D. P. (2015) · eLife · doi:10.7554/elife.05005 · Cited by 7,318 · see citing works

The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans

Reinhart, B. J., Slack, F. J., Basson, M., Pasquinelli, A. E., Bettinger, J. C., Rougvie, A. E., Horvitz, H. R., & Ruvkun, G. (2000) · Nature · doi:10.1038/35002607 · Cited by 4,989 · see citing works

IL-17 and th17 cells

Korn, T., Bettelli, E., Oukka, M., & Kuchroo, V. K. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132710 · Cited by 4,873 · see citing works

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 · 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

Metazoan MicroRNAs

Bartel, D. P. (2018) · Cell · doi:10.1016/j.cell.2018.03.006 · Cited by 3,751 · see citing works

Identification of tissue-specific microRNAs from mouse

Lagos-Quintana, M., Rauhut, R., Yalcin, A., Meyer, J., Lendeckel, W., & Tuschl, T. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00809-6 · Cited by 2,859 · see citing works

Many roads to maturity: microRNA biogenesis pathways and their regulation

Winter, J. J., Jung, S., Keller, S., Gregory, R. I., & Diederichs, S. (2009) · Nature Cell Biology · doi:10.1038/ncb0309-228 · Cited by 2,646 · see citing works

Dicer is essential for mouse development

Bernstein, E., Kim, S. Y., Carmell, M., Murchison, E., Alcorn, H. L., Li, M. Z., Mills, A., Elledge, S., Anderson, K., & Hannon, G. (2003) · Nature Genetics · doi:10.1038/ng1253 · Cited by 2,100 · see citing works

Towards a molecular understanding of microRNA-mediated gene silencing

Jonas, S., & Izaurralde, E. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3965 · Cited by 1,872 · see citing works

Requirement of <i>bic/microRNA-155</i> for Normal Immune Function

Rodriguez, A., Vigorito, E., Clare, S., Warren, M. V., Couttet, P., Soond, D. R., van Dongen, S., Grocock, R. J., Das, P. P., Miska, E. A., et al. (2007) · Science · doi:10.1126/science.1139253 · Cited by 1,833 · see citing works

Identification of Mammalian microRNA Host Genes and Transcription Units

Rodriguez, A., Griffiths-Jones, S., Ashurst, J. L., & Bradley, A. (2004) · Genome Research · doi:10.1101/gr.2722704 · Cited by 1,732 · 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

Control of Stress-Dependent Cardiac Growth and Gene Expression by a MicroRNA

van Rooij, E., Sutherland, L. B., Qi, X., Richardson, J. A., Hill, J. A., & Olson, E. N. (2007) · Science · doi:10.1126/science.1139089 · Cited by 1,648 · see citing works

Genes and Mechanisms Related to RNA Interference Regulate Expression of the Small Temporal RNAs that Control C. elegans Developmental Timing

Grishok, A., Pasquinelli, A. E., Conte, D., Li, N., Parrish, S., Ha, I., Baillie, D. L., Fire, A., Ruvkun, G., & Mello, C. C. (2001) · Cell · doi:10.1016/s0092-8674(01)00431-7 · Cited by 1,600 · see citing works

The biochemical basis of microRNA targeting efficacy

(2019) · doi:10.1126/science.aav1741 · Cited by 1,570 · see citing works

MicroRNA Expression in Zebrafish Embryonic Development

Wienholds, E., Kloosterman, W. P., Miska, E., Alvarez-Saavedra, E., Berezikov, E., de Bruijn, E., Horvitz, H. R., Kauppinen, S., & Plasterk, R. H. A. (2005) · Science · doi:10.1126/science.1114519 · Cited by 1,551 · see citing works

The evolution of gene regulation by transcription factors and microRNAs

Chen, K., & Rajewsky, N. (2007) · Nature Reviews Genetics · doi:10.1038/nrg1990 · Cited by 1,547 · see citing works

Dicer functions in RNA interference and in synthesis of small RNA involved in developmental timing in <i>C. elegans</i>

Ketting, R. F., Fischer, S. E. J., Bernstein, E., Sijen, T., Hannon, G. J., & Plasterk, R. H. A. (2001) · Genes &amp; Development · doi:10.1101/gad.927801 · Cited by 1,527 · see citing works

Regulation of the Germinal Center Response by MicroRNA-155

Thai, T., Calado, D. P., Casola, S. S., Ansel, K. M., Xiao, C., Xue, Y., Murphy, A. J., Frendewey, D. A., Valenzuela, D. M., Kutok, J. L., et al. (2007) · Science · doi:10.1126/science.1141229 · Cited by 1,477 · see citing works

Distinct Roles for Drosophila Dicer-1 and Dicer-2 in the siRNA/miRNA Silencing Pathways

Lee, Y. S., Nakahara, K., Pham, J. W., Kim, K., He, Z., Sontheimer, E. J., & Carthew, R. W. (2004) · Cell · doi:10.1016/s0092-8674(04)00261-2 · Cited by 1,287 · see citing works

Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes

BASKERVILLE, S., & BARTEL, D. P. (2005) · RNA · doi:10.1261/rna.7240905 · Cited by 1,241 · see citing works

Loss of a mammalian circular RNA locus causes miRNA deregulation and affects brain function

Piwecka, M., Glažar, P., Hernandez-Miranda, L. R., Memczak, S., Wolf, S. A., Rybak-Wolf, A., Filipchyk, A., Klironomos, F., Cerda Jara, C. A., Fenske, P., et al. (2017) · Science · doi:10.1126/science.aam8526 · Cited by 1,210 · see citing works

MicroRNAs Regulate Brain Morphogenesis in Zebrafish

Giraldez, A. J., Cinalli, R. M., Glasner, M. E., Enright, A. J., Thomson, J. M., Baskerville, S., Hammond, S. M., Bartel, D. P., & Schier, A. F. (2005) · Science · doi:10.1126/science.1109020 · Cited by 1,124 · 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

The miR-15a–miR-16-1 cluster controls prostate cancer by targeting multiple oncogenic activities

Bonci, D., Coppola, V., Musumeci, M., Addario, A., Giuffrida, R., Memeo, L., D’Urso, L., Pagliuca, A., Biffoni, M., Labbaye, C., et al. (2008) · Nature Medicine · doi:10.1038/nm.1880 · Cited by 989 · see citing works

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Pinto, D., Delaby, E., Merico, D., Barbosa, M., Merikangas, A., Klei, L., Thiruvahindrapuram, B., Xu, X., Ziman, R., Wang, Z., et al. (2014) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.03.018 · Cited by 969 · see citing works

Distribution of miRNA expression across human tissues

Ludwig, N., Leidinger, P., Becker, K., Backes, C., Fehlmann, T., Pallasch, C., Rheinheimer, S., Meder, B., Stähler, C., Meese, E., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw116 · Cited by 968 · see citing works

miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche

Cheng, L.-C., Pastrana, E., Tavazoie, M., & Doetsch, F. (2009) · Nature Neuroscience · doi:10.1038/nn.2294 · Cited by 865 · see citing works

A majority of m6A residues are in the last exons, allowing the potential for 3′ UTR regulationPreprint

Ke, S., Alemu, E. A., Mertens, C., Gantman, E. C., Fak, J. J., Mele, A., Haripal, B., Zucker-Scharff, I., Moore, M. J., Park, C. Y., et al. (2015) · Genes & Development · doi:10.1101/gad.269415.115 · Cited by 815 · see citing works

MicroRNA function in animal development

Wienholds, E., & Plasterk, R. H. A. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.07.070 · Cited by 811 · 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

MicroRNA sponges: Progress and possibilities

Ebert, M. S., & Sharp, P. A. (2010) · RNA · doi:10.1261/rna.2414110 · Cited by 762 · see citing works

Mammalian microRNAs: experimental evaluation of novel and previously annotated genes

Chiang, H. R., Schoenfeld, L. W., Ruby, J. G., Auyeung, V. C., Spies, N., Baek, D., Johnston, W. K., Russ, C., Luo, S., Babiarz, J. E., et al. (2010) · Genes &amp; Development · doi:10.1101/gad.1884710 · Cited by 732 · see citing works

Assessing the ceRNA Hypothesis with Quantitative Measurements of miRNA and Target Abundance

Denzler, R., Agarwal, V., Stefano, J., Bartel, D. P., & Stoffel, M. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.03.045 · Cited by 723 · see citing works

Embryonic stem cell–specific microRNAs regulate the G1-S transition and promote rapid proliferation

Wang, Y., Baskerville, S., Shenoy, A., Babiarz, J., Baehner, L., & Blelloch, R. H. (2008) · Nature Genetics · doi:10.1038/ng.250 · Cited by 660 · see citing works

A Network of Noncoding Regulatory RNAs Acts in the Mammalian Brain

Kleaveland, B., Shi, C. Y., Stefano, J., & Bartel, D. P. (2018) · Cell · doi:10.1016/j.cell.2018.05.022 · Cited by 594 · see citing works

The microRNA miR-124 antagonizes the anti-neural REST/SCP1 pathway during embryonic CNS development

Visvanathan, J., Lee, S., Lee, B., Lee, J. W., & Lee, S.-K. (2007) · Genes &amp; Development · doi:10.1101/gad.1519107 · Cited by 579 · see citing works

Mutations that lead to reiterations in the cell lineages of C. elegans.

Chalfie, M., Horvitz, H., & Sulston, J. (1981) · Cell · doi:10.1016/0092-8674(81)90501-8 · Cited by 541 · see citing works

MicroRNA-mediated switching of chromatin-remodelling complexes in neural development

Yoo, A. S., Staahl, B. T., Chen, L., & Crabtree, G. R. (2009) · Nature · doi:10.1038/nature08139 · Cited by 537 · see citing works

The microRNA-producing enzyme Dicer1 is essential for zebrafish development

Wienholds, E., Koudijs, M., van Eeden, F. V., Cuppen, E., & Plasterk, R. (2003) · Nature Genetics · doi:10.1038/ng1251 · Cited by 519 · see citing works

Most Caenorhabditis elegans microRNAs Are Individually Not Essential for Development or Viability

Miska, E. A., Alvarez-Saavedra, E., Abbott, A. L., Lau, N. C., Hellman, A. B., McGonagle, S. M., Bartel, D. P., Ambros, V. R., & Horvitz, H. R. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030215 · Cited by 484 · see citing works

The deep evolution of metazoan microRNAs

Wheeler, B. M., Heimberg, A. M., Moy, V. N., Sperling, E. A., Holstein, T. W., Heber, S., & Peterson, K. J. (2009) · Evolution &amp; Development · doi:10.1111/j.1525-142x.2008.00302.x · Cited by 473 · see citing works

Characterizing Light-Regulated Retinal MicroRNAs Reveals Rapid Turnover as a Common Property of Neuronal MicroRNAs

Krol, J., Busskamp, V., Markiewicz, I., Stadler, M. B., Ribi, S., Richter, J., Duebel, J., Bicker, S., Fehling, H. J., Schübeler, D., et al. (2010) · Cell · doi:10.1016/j.cell.2010.03.039 · Cited by 470 · see citing works

A MicroRNA Imparts Robustness against Environmental Fluctuation during Development

Li, X., Cassidy, J. J., Reinke, C., Fischboeck, S., & Carthew, R. W. (2009) · Cell · doi:10.1016/j.cell.2009.01.058 · Cited by 445 · see citing works

MicroRNA Function Is Globally Suppressed in Mouse Oocytes and Early Embryos

Suh, N., Baehner, L., Moltzahn, F., Melton, C. A., Shenoy, A., Chen, J., & Blelloch, R. H. (2010) · Current Biology · doi:10.1016/j.cub.2009.12.044 · Cited by 435 · see citing works

MicroRNA-responsive 'sensor' transgenes uncover Hox-like and other developmentally regulated patterns of vertebrate microRNA expression

Mansfield, J. H., Harfe, B. D., Nissen, R. M., Obenauer, J. C., Srineel, J., Chaudhuri, A. A., Farzan-Kashani, R., Zuker, M., Pasquinelli, A. E., Ruvkun, G., et al. (2004) · Nature Genetics · doi:10.1038/ng1421 · Cited by 425 · see citing works

MicroRNAs and the advent of vertebrate morphological complexity

Heimberg, A. M., Sempere, L. F., Moy, V. N., Donoghue, P. C. J., & Peterson, K. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712259105 · Cited by 406 · see citing works

MicroRNA-214 protects the mouse heart from ischemic injury by controlling Ca2+ overload and cell death

Aurora, A. B., Mahmoud, A. I., Luo, X., Johnson, B. A., van Rooij, E., Matsuzaki, S., Humphries, K. M., Hill, J. A., Bassel‐Duby, R., Sadek, H. A., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci59327 · Cited by 404 · see citing works

A complex system of small RNAs in the unicellular green alga Chlamydomonas reinhardtiiPreprint

Zhao, T., Li, G., Mi, S., Li, S., Hannon, G. J., Wang, X., & Qi, Y. (2007) · Genes & Development · doi:10.1101/gad.1543507 · Cited by 398 · see citing works

The microRNA miR-196 acts upstream of Hoxb8 and Shh in limb development

Hornstein, E., Mansfield, J. H., Yekta, S., Hu, J. K., Harfe, B. D., McManus, M. T., Baskerville, S., Bartel, D. P., & Tabin, C. J. (2005) · Nature · doi:10.1038/nature04138 · Cited by 392 · see citing works

A microRNA-Hippo pathway that promotes cardiomyocyte proliferation and cardiac regeneration in mice

Tian, Y., Liu, Y., Wang, T., Zhou, N., Kong, J., Chen, L., Snitow, M., Morley, M., Li, D., Petrenko, N., et al. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.3010841 · Cited by 381 · see citing works

The expansion of the metazoan microRNA repertoire

Jana Hertel, A., Lindemeyer, M., Kristin Missal, A., Claudia Fried, A., Andrea Tanzer, A., Christoph Flamm, A., Hofacker, I. L., Stadler, P. F., & 2005, T. S. O. B. C. L. 2. A. (2006) · BMC Genomics · doi:10.1186/1471-2164-7-25 · Cited by 355 · see citing works

Global Analyses of the Effect of Different Cellular Contexts on MicroRNA Targeting

Nam, J., Rissland, O. S., Koppstein, D., Abreu‐Goodger, C., Jan, C. H., Agarwal, V., Yıldırım, M. A., Rodríguez, A., & Bartel, D. P. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.02.013 · Cited by 337 · see citing works

Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta

Sekita, Y., Wagatsuma, H., Nakamura, K., Ono, R., Kagami, M., Wakisaka, N., Hino, T., Suzuki-Migishima, R., Kohda, T., Ogura, A., et al. (2008) · Nature Genetics · doi:10.1038/ng.2007.51 · Cited by 324 · see citing works

The regulation of Hox gene expression during animal development

Mallo, M., & Alonso, C. R. (2013) · Development · doi:10.1242/dev.068346 · Cited by 317 · see citing works

Analysis of intronic and exonic reads in RNA-seq data characterizes transcriptional and post-transcriptional regulation

Gaidatzis, D., Burger, L., Florescu, M., & Stadler, M. B. (2015) · Nature Biotechnology · doi:10.1038/nbt.3269 · Cited by 313 · see citing works

The phylogenetic distribution of metazoan microRNAs: insights into evolutionary complexity and constraint

Sempere, L. F., Cole, C. N., McPeek, M. A., & Peterson, K. J. (2006) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.21118 · Cited by 307 · see citing works

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

Lewis, M. A., Quint, E., Glazier, A. M., Fuchs, H., De Angelis, M. H., Langford, C., van Dongen, S., Abreu-Goodger, C., Piipari, M., Redshaw, N., et al. (2009) · Nature Genetics · doi:10.1038/ng.369 · Cited by 302 · see citing works

MicroRNA-128 Governs Neuronal Excitability and Motor Behavior in Mice

Tan, C. L., Plotkin, J. L., Venø, M. T., von Schimmelmann, M. J., Feinberg, P. A., Mann, S., Handler, A., Kjems, J., Surmeier, D. J., O’Carroll, D., et al. (2013) · Science · doi:10.1126/science.1244193 · Cited by 301 · see citing works

Many Families of C. elegans MicroRNAs Are Not Essential for Development or Viability

Alvarez-Saavedra, E., & Horvitz, H. R. (2010) · Current Biology · doi:10.1016/j.cub.2009.12.051 · Cited by 295 · see citing works

MicroRNA-9 Regulates Neurogenesis in Mouse Telencephalon by Targeting Multiple Transcription Factors

Shibata, M., Nakao, H., Kiyonari, H., Abe, T., & Aizawa, S. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5085-10.2011 · Cited by 294 · see citing works

Birth and expression evolution of mammalian microRNA genesPreprint

Meunier, J., Lemoine, F., Soumillon, M., Liechti, A., Weier, M., Guschanski, K., Hu, H., Khaitovich, P., & Kaessmann, H. (2012) · Genome Research · doi:10.1101/gr.140269.112 · Cited by 284 · see citing works

MicroRNAs acting in a double-negative feedback loop to control a neuronal cell fate decision

Johnston, R. J., Chang, S., Etchberger, J. F., Ortiz, C. O., & Hobert, O. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505530102 · Cited by 276 · see citing works

Two miRNA clusters, miR-34b/c and miR-449 , are essential for normal brain development, motile ciliogenesis, and spermatogenesis

Wu, J., Bao, J., Kim, M. K., Yuan, S., Tang, C., Zheng, H., Mastick, G. S., Xu, C., & Yan, W. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1407777111 · Cited by 267 · see citing works

Negative regulation of Hif1a expression and TH17 differentiation by the hypoxia-regulated microRNA miR-210

Wang, H., Flach, H., Onizawa, M., Wei, L., McManus, M. T., & Weiss, A. (2014) · Nature Immunology · doi:10.1038/ni.2846 · Cited by 250 · see citing works

Structural Basis for Target-Directed MicroRNA Degradation

Sheu-Gruttadauria, J., Pawlica, P., Klum, S. M., Wang, S., Yario, T. A., Schirle Oakdale, N. T., Steitz, J. A., & MacRae, I. J. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.06.019 · Cited by 246 · see citing works

CRISPR/cas9, a novel genomic tool to knock down microRNA in vitro and in vivo

Chang, H., Yi, B., Ma, R., Zhang, X., Zhao, H., & Xi, Y. (2016) · Scientific Reports · doi:10.1038/srep22312 · Cited by 242 · see citing works

miR-451 protects against erythroid oxidant stress by repressing 14-3-3ζPreprint

Yu, D., dos Santos, C. O., Zhao, G., Jiang, J., Amigo, J. D., Khandros, E., Doré, L. C., Yao, Y., D'Souza, J., Zhang, Z., et al. (2010) · Genes & Development · doi:10.1101/gad.1942110 · Cited by 234 · see citing works

MicroRNA-449 and MicroRNA-34b/c Function Redundantly in Murine Testes by Targeting E2F Transcription Factor-Retinoblastoma Protein (E2F-pRb) Pathway

Bao, J., Li, D., Wang, L., Wu, J., Hu, Y., Wang, Z., Chen, Y., Cao, X., Jiang, C., Yan, W., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.328054 · Cited by 226 · see citing works

The schizophrenia risk gene product miR-137 alters presynaptic plasticity

Siegert, S., Seo, J., Kwon, E. J., Rudenko, A., Cho, S., Wang, W., Flood, Z., Martorell, A. J., Ericsson, M., Mungenast, A. E., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4023 · Cited by 224 · see citing works

miR-34/449 miRNAs are required for motile ciliogenesis by repressing CP110

Song, R., Walentek, P., Sponer, N., Klimke, A., Lee, J. S., Dixon, G., Harland, R., Wan, Y., Lishko, P., Lize, M., et al. (2014) · Nature · doi:10.1038/nature13413 · Cited by 222 · see citing works

Single-cell sequencing of the small-RNA transcriptome

Faridani, O. R., Abdullayev, I., Hagemann-Jensen, M., Schell, J. P., Lanner, F., & Sandberg, R. (2016) · Nature Biotechnology · doi:10.1038/nbt.3701 · Cited by 219 · see citing works

Chromosome 1p21.3 microdeletions comprising <i>DPYD</i> and <i>MIR137</i> are associated with intellectual disability

Willemsen, M. H., Vallès, A., Kirkels, L. A. M. H., Mastebroek, M., Olde Loohuis, N., Kos, A., Wissink-Lindhout, W. M., de Brouwer, A. P. M., Nillesen, W. M., Pfundt, R., et al. (2011) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2011-100294 · Cited by 202 · see citing works

Potent degradation of neuronal miRNAs induced by highly complementary targets

de la Mata, M., Gaidatzis, D., Vitanescu, M., Stadler, M. B., Wentzel, C., Scheiffele, P., Filipowicz, W., & Großhans, H. (2015) · The EMBO Reports · doi:10.15252/embr.201540078 · Cited by 201 · see citing works

Intact p53-Dependent Responses in miR-34–Deficient Mice

Concepcion, C. P., Han, Y.-C., Mu, P., Bonetti, C., Yao, E., D'Andrea, A., Vidigal, J. A., Maughan, W. P., Ogrodowski, P., & Ventura, A. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002797 · Cited by 197 · see citing works

microRNAs in the Same Clusters Evolve to Coordinately Regulate Functionally Related Genes

Wang, Y., Luo, J., Zhang, H., & Lü, J. (2016) · Molecular Biology and Evolution · doi:10.1093/molbev/msw089 · Cited by 187 · see citing works

Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation

Wang, N., Zheng, J., Chen, Z., Yang, L., Dura, B., Kwak, M., Xavier-Ferrucio, J. M., Lu, Y.-C., Zhang, M., Roden, C., et al. (2019) · Nature Communications · doi:10.1038/s41467-018-07981-6 · Cited by 183 · see citing works

MicroRNA Destabilization Enables Dynamic Regulation of the miR-16 Family in Response to Cell-Cycle Changes

Rissland, O. S., Hong, S., & Bartel, D. P. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.08.021 · Cited by 182 · see citing works

Activity-dependent spatially localized miRNA maturation in neuronal dendrites

Sambandan, S., Akbalık, G., Kochen, L., Rinne, J. S., Kahlstatt, J., Glock, C., Tushev, G., Alvarez‐Castelao, B., Heckel, A., & Schuman, E. M. (2017) · Science · doi:10.1126/science.aaf8995 · Cited by 179 · see citing works

miR-219 Cooperates with miR-338 in Myelination and Promotes Myelin Repair in the CNS

Wang, H., Moyano, A. L., Ma, Z., Deng, Y., Lin, Y., Zhao, C., Zhang, L., Jiang, M., He, X., Ma, Z., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.03.001 · Cited by 174 · see citing works

A Resource for the Conditional Ablation of microRNAs in the Mouse

Park, C. Y., Jeker, L. T., Carver-Moore, K., Oh, A., Liu, H. J., Cameron, R., Richards, H. W., Li, Z., Adler, D., Yoshinaga, Y., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.02.008 · Cited by 174 · see citing works

MiR-200b and miR-429 Function in Mouse Ovulation and Are Essential for Female Fertility

Hasuwa, H., Ueda, J., Ikawa, M., & Okabe, M. (2013) · Science · doi:10.1126/science.1237999 · Cited by 173 · see citing works

Regulation of cell-type-specific transcriptomes by microRNA networks during human brain development

Nowakowski, T. J., Rani, N., Golkaram, M., Zhou, H. R., Alvarado, B., Huch, K., West, J. A., Leyrat, A., Pollen, A. A., Kriegstein, A. R., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0265-3 · Cited by 166 · see citing works

Systematic Study of Drosophila MicroRNA Functions Using a Collection of Targeted Knockout Mutations

Chen, Y., Song, S., Weng, R., Verma, P., Kugler, J., Buescher, M., Rouam, S. L., & Cohen, S. M. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.11.029 · Cited by 152 · see citing works

Loss of motoneuron-specific microRNA-218 causes systemic neuromuscular failure

Amin, N. D., Bai, G., Klug, J. R., Bonanomi, D., Pankratz, M. T., Gifford, W. D., Hinckley, C. A., Sternfeld, M. J., Driscoll, S. P., Dominguez, B., et al. (2015) · Science · doi:10.1126/science.aad2509 · Cited by 146 · see citing works

miR-133a Regulates Adipocyte Browning In Vivo

Liu, W., Bi, P., Shan, T., Yang, X., Yin, H., Wang, Y.-X., Liu, N., Rudnicki, M. A., & Kuang, S. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003626 · Cited by 144 · see citing works

Evidence for a microRNA expansion in the bilaterian ancestor

Prochnik, S. E., Rokhsar, D. S., & Aboobaker, A. A. (2006) · Development Genes and Evolution · doi:10.1007/s00427-006-0116-1 · Cited by 142 · 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

Partial loss of psychiatric risk gene Mir137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a

Cheng, Y., Wang, Z., Tan, W., Wang, X., Li, Y., Bai, B., Li, Y., Zhang, S.-F., Yan, H., Chen, Z.-L., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0261-7 · Cited by 136 · see citing works

Highly Complementary Target RNAs Promote Release of Guide RNAs from Human Argonaute2

De, N., Young, L. E., Lau, P., Meisner-Kober, N. C., Morrissey, D. V., & MacRae, I. J. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.04.001 · Cited by 131 · see citing works

Widespread context dependency of microRNA-mediated regulationPreprint

Erhard, F., Haas, J., Lieber, D., Malterer, G., Jaśkiewicz, Ł., Zavolan, M., Dölken, L., & Zimmer, R. (2014) · Genome Research · doi:10.1101/gr.166702.113 · Cited by 129 · see citing works

The effect of cellular context on miR-155-mediated gene regulation in four major immune cell types

Hsin, J.-P., Lu, Y., Loeb, G. B., Leslie, C. S., & Rudensky, A. Y. (2018) · Nature Immunology · doi:10.1038/s41590-018-0208-x · Cited by 126 · see citing works

miR-1/133a Clusters Cooperatively Specify the Cardiomyogenic Lineage by Adjustment of Myocardin Levels during Embryonic Heart Development

Wystub-Lis, K., Besser, J., Bachmann, A., Boettger, T., & Braun, T. W. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003793 · Cited by 123 · see citing works

The landscape of miRNA editing in animals and its impact on miRNA biogenesis and targetingPreprint

Li, L., Song, Y., Shi, X., Liu, J. F., Xiong, S., Chen, W., Fu, Q., Huang, Z., Gu, N., & Zhang, R. (2017) · Genome Research · doi:10.1101/gr.224386.117 · Cited by 111 · see citing works

An allelic series of miR-17∼92–mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron

Han, Y.-C., Vidigal, J. A., Mu, P., Yao, E. S., Singh, I., González, A. J., Concepcion, C. P., Bonetti, C., Ogrodowski, P., Carver, B. S., et al. (2015) · Nature Genetics · doi:10.1038/ng.3321 · Cited by 109 · see citing works

A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

Duan, J., Shi, J., Fiorentino, A., Leites, C., Chen, X., Moy, W., Chen, J., Alexandrov, B. S., Usheva, A., S, D. H. B., et al. (2014) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.11.001 · Cited by 104 · see citing works

Induced miR‐99a expression represses Mtor cooperatively with miR‐150 to promote regulatory T‐cell differentiation

Warth, S. C., Hoefig, K. P., Hiekel, A., Schallenberg, S., Jovanovic, K., Klein, L., Kretschmer, K., Ansel, K. M., & Heissmeyer, V. (2015) · The EMBO Journal · doi:10.15252/embj.201489589 · Cited by 99 · see citing works

miR-302 Is Required for Timing of Neural Differentiation, Neural Tube Closure, and Embryonic Viability

Parchem, R. J., Moore, N., Fish, J. L., Parchem, J. G., Braga, T. T., Shenoy, A., Oldham, M. C., Rubenstein, J. L. R., Schneider, R. A., & Blelloch, R. H. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.06.074 · Cited by 97 · see citing works

3′ Uridylation Confers miRNAs with Non-canonical Target Repertoires

Yang, A., Ros, X. B., Shao, T., Jiang, M., Li, K., Villanueva, P., Dai, L., & Gu, S. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.05.014 · Cited by 97 · see citing works

An Early Developmental Role for miRNAs in the Maintenance of Extraembryonic Stem Cells in the Mouse Embryo

Spruce, T., Pernaute, B., Gregorio, A. D., Cobb, B. S., Merkenschlager, M., Manzanares, M., & Rodríguez, T. A. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.07.014 · Cited by 88 · see citing works

The relationship between the evolution of microRNA targets and the length of their UTRs

Cheng, C., Bhardwaj, N., & Gerstein, M. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-431 · Cited by 85 · see citing works

miR-29a maintains mouse hematopoietic stem cell self-renewal by regulating Dnmt3a

Hu, W., Dooley, J., Chung, S. S., Chandramohan, D., Cimmino, L., Mukherjee, S., Mason, C. E., Strooper, B. D., Liston, A., & Park, C. Y. (2015) · Blood · doi:10.1182/blood-2014-06-585273 · Cited by 83 · see citing works

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

Kurata, J. S., & Lin, R.-J. (2018) · RNA · doi:10.1261/rna.066282.118 · Cited by 82 · see citing works

A trans-homologue interaction between reciprocally imprinted miR-127 and Rtl1 regulates placenta development

Ito, M., Sferruzzi-Perri, A. N., Edwards, C. A., Aðalsteinsson, B. Þ., Allen, S. E., Loo, T.-H., Kitazawa, M., Kaneko‐Ishino, T., Ishino, F., Stewart, C. L., et al. (2015) · Development · doi:10.1242/dev.121996 · Cited by 80 · see citing works

Multifaceted roles of miR-1s in repressing the fetal gene program in the heart

Wei, Y., Peng, S., Wu, M., Sachidanandam, R., Tu, Z., Zhang, S., Falce, C., Sobie, E. A., Lebeche, D., & Zhao, Y. B. (2014) · Cell Research · doi:10.1038/cr.2014.12 · Cited by 72 · see citing works

miR-122 removal in the liver activates imprinted microRNAs and enables more effective microRNA-mediated gene repression

Valdmanis, P. N., Kim, H. K., Chu, K. C., Zhang, F., Xu, J., Munding, E. M., Shen, J. Y., & Kay, M. A. (2018) · Nature Communications · doi:10.1038/s41467-018-07786-7 · Cited by 72 · see citing works

Decoupling the impact of microRNAs on translational repression versus RNA degradation in embryonic stem cells

Freimer, J. W., Hu, T., & Blelloch, R. (2018) · eLife · doi:10.7554/elife.38014 · Cited by 69 · see citing works

Outside the coding genome, mammalian microRNAs confer structural and functional complexity

Olive, V., Minella, A. C., & He, L. (2015) · Science Signaling · doi:10.1126/scisignal.2005813 · Cited by 65 · see citing works

Non-canonical targets destabilize microRNAs in human Argonautes

Park, J. H., Shin, S., & Shin, C. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx029 · Cited by 61 · see citing works

MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development

Fededa, J. P., Esk, C., Mierzwa, B. E., Stanytė, R., Yuan, S., Zheng, H., Ebnet, K., Yan, W., Knoblich, J. A., & Gerlich, D. W. (2016) · The EMBO Journal · doi:10.15252/embj.201694056 · Cited by 60 · see citing works

Regulation of gene expression by miR-144/451 during mouse erythropoiesis

Xu, P., Palmer, L. E., Lechauve, C., Zhao, G., Yao, Y., Luan, J. Y., Vourekas, A., Tan, H., Peng, J., Schuetz, J. D., et al. (2019) · Blood · doi:10.1182/blood.2018854604 · Cited by 56 · see citing works

Large scale chromosomal mapping of human microRNA structural clusters

Mathelier, A., & Carbone, A. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt112 · Cited by 53 · see citing works

The Expansion of Animal MicroRNA Families Revisited

Jana Hertel, A., & Stadler, P. F. (2015) · Life · doi:10.3390/life5010905 · Cited by 53 · see citing works

MSDD: a manually curated database of experimentally supported associations among miRNAs, SNPs and human diseases

Yue, M., Zhou, D., Zhi, H., Wang, P., Zhang, Y., Guo, M., Guo, M., Li, X., Wang, Y., Zhang, Y., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx1035 · Cited by 48 · see citing works

RNA-Binding Proteins in the Regulation of miRNA Activity: A Focus on Neuronal Functions

Loffreda, A., Rigamonti, A., Barabino, S. M. L., & Lenzken, S. C. (2015) · Biomolecules · doi:10.3390/biom5042363 · Cited by 41 · see citing works

In vivo mutagenesis of miRNA gene families using a scalable multiplexed CRISPR/Cas9 nuclease system

Narayanan, A., Hill-Terán, G., Moro, A., Ristori, E., Kasper, D. M., Roden, C., Lü, J., & Nicoli, S. (2016) · Scientific Reports · doi:10.1038/srep32386 · Cited by 39 · see citing works

Disruption of the MicroRNA 137 Primary Transcript Results in Early Embryonic Lethality in Mice

Crowley, J. J., Collins, A. L., Lee, R. J., Nonneman, R. J., Farrell, M. S., Ancalade, N., Mugford, J. W., Agster, K. L., Nikolova, V. D., Moy, S. S., et al. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.05.022 · Cited by 33 · see citing works

miR-322 stabilizes MEK1 expression to inhibit RAF/MEK/ERK pathway activation in cartilage

Bluhm, B., Ehlen, H. W. A., Holzer, T., Georgieva, V. S., Heilig, J., Pitzler, L., Etich, J., Borteçen, T., Frie, C., Probst, K., et al. (2017) · Development · doi:10.1242/dev.148429 · Cited by 32 · see citing works

The eutheria-specific miR-290 cluster modulates placental growth and maternal-fetal transport

Paikari, A., Belair, C. D., Saw, D., & Blelloch, R. H. (2017) · Development · doi:10.1242/dev.151654 · Cited by 31 · see citing works

Nanoscale imaging reveals miRNA-mediated control of functional states of dendritic spines

Park, I., Kim, H. J., Kim, Y., Hwang, H. S., Kasai, H., Kim, J., & Park, J. W. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1819374116 · Cited by 31 · see citing works

Creating Lineage Trajectory Maps Via Integration of Single‐Cell RNA‐Sequencing and Lineage Tracing

Fletcher, R. B., Das, D., & Ngai, J. (2018) · BioEssays · doi:10.1002/bies.201800056 · Cited by 24 · see citing works

Termination of cell-type specification gene programs by the miR-183 cluster determines the population sizes of low-threshold mechanosensitive neurons

Peng, C., Furlan, A., Zhang, M.-D., Su, J., Lübke, M., Lönnerberg, P., Abdo, H., Sontheimer, J., Sundström, E., & Ernfors, P. (2018) · Development · doi:10.1242/dev.165613 · Cited by 11 · see citing works

Comment on “microRNAs in the Same Clusters Evolve to Coordinately Regulate Functionally Related Genes”

Marco, A. D. (2019) · Molecular Biology and Evolution · doi:10.1093/molbev/msz120 · Cited by 5 · see citing works

Classical and noncanonical functions of miRNAs in cancers

Dragomir, M. P., Knutsen, E., & Călin, G. A. (2021) · Trends in Genetics · doi:10.1016/j.tig.2021.10.002 · Cited by 194 · see citing works

MirGeneDB 2.1: toward a complete sampling of all major animal phyla

Fromm, B., Høye, E., Domanska, D., Zhong, X., Aparicio-Puerta, E., Ovchinnikov, V., Umu, S. U., Chabot, P. J., Kang, W., Aslanzadeh, M., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkab1101 · Cited by 167 · 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

Motif-Aware miRNA-Disease Association Prediction via Hierarchical Attention Network

Zhao, B.-W., He, Y.-Z., Su, X., Yang, Y., Li, G., Huang, Y., Hu, P., You, Z., & Hu, L. (2024) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2024.3383591 · Cited by 61 · see citing works

A plant immune protein enables broad antitumor response by rescuing microRNA deficiency

Qi, Y., Ding, L., Zhang, S., Yao, S., Ong, J., Li, Y., Wu, H., & Du, P. (2022) · Cell · doi:10.1016/j.cell.2022.04.030 · Cited by 57 · see citing works

Roles of MicroRNAs in Disease Biology

Suzuki, H. I. (2023) · JMA Journal · doi:10.31662/jmaj.2023-0009 · Cited by 58 · see citing works

Cytoplasmic mRNA decay and quality control machineries in eukaryotes

Dowdle, M. E., & Lykke‐Andersen, J. (2025) · Nature Reviews Genetics · doi:10.1038/s41576-024-00810-1 · Cited by 46 · see citing works

DNA Logic Circuits for Multiple Tumor Cells Identification Using Intracellular MicroRNA Molecular Bispecific Recognition

Yang, Q., Yang, F., Dai, W., Meng, X., Wei, W., Cheng, Y., Dong, J., Lu, H., & Dong, H. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202101130 · Cited by 46 · see citing works

Scalable and deep profiling of mRNA targets for individual microRNAs with chimeric eCLIP

Manakov, S. A., Shishkin, A. A., Yee, B. A., Shen, K. A., Cox, D. C., Park, S. S., Foster, H. M., Chapman, K. B., Yeo, G. W., & Van Nostrand, E. L. (2022) · doi:10.1101/2022.02.13.480296 · Cited by 43 · see citing works

MicroRNAs and their delivery in diabetic fibrosis

Wonnacott, A., Denby, L., Coward, R. J., Fraser, D. J., & Bowen, T. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.114045 · Cited by 43 · see citing works

The RNA m6A landscape of mouse oocytes and preimplantation embryos

Wang, Y., Li, Y., Skuland, T., Zhou, C., Li, A., Hashim, A., Jermstad, I., Khan, S., Dalen, K. T., Greggains, G. D., et al. (2023) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-00969-x · Cited by 41 · see citing works

Spatially Resolved, Error‐Robust Multiplexed MicroRNA Profiling in Single Living Cells

Wei, W., Dai, W., Yang, F., Lu, H., Zhang, K., Xing, Y., Meng, X., Zhou, L., Zhang, Y., Yang, Q., et al. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202116909 · Cited by 39 · see citing works

Nuclear localization of Argonaute 2 is affected by cell density and may relieve repression by microRNAs

Johnson, K. C., Kilikevičius, A., Hofman, C. R., Hu, J., Liu, Y., Aguilar, S., Graswich, J., Han, Y., Wang, T., Westcott, J. M., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad1155 · Cited by 31 · 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

MicroRNAs as Indicators into the Causes and Consequences of Whole-Genome Duplication Events

Peterson, K. J., Beavan, A. J. S., Chabot, P. J., McPeek, M. A., Pisani, D., Fromm, B., & Simakov, O. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab344 · Cited by 31 · see citing works

Exosome-like vesicles encapsulated with specific microRNAs accelerate burn wound healing and ameliorate scarring

Lei, Z., Chen, X., Chen, K., Liu, P., Ao, M., Gan, L., & Yu, L. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-025-03337-7 · Cited by 28 · see citing works

Spatiotemporal regulation of maternal mRNAs during vertebrate oocyte meiotic maturation

Jiang, Y.-W., Adhikari, D., Li, C.-J., & Zhou, X. (2023) · Biological Reviews of The Cambridge Philosophical Society · doi:10.1111/brv.12937 · Cited by 30 · see citing works

MicroRNA-mediated gene regulation and the resilience of multicellular animals

Ambros, V. (2024) · Postępy Biochemii · doi:10.18388/pb.2021_515 · Cited by 27 · see citing works

Molecular Mechanisms Involved in the Regulation of Neurodevelopment by miR-124

Gu, X., Xu, X., Jia, C., Wang, J., Zhang, J., Gao, Q., & Chen, J. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03271-5 · Cited by 27 · see citing works

MicroRNA-1: Diverse role of a small player in multiple cancers

Κhan, P., Ebenezer, N. S., Siddiqui, J. A., Maurya, S. K., Lakshmanan, I., Salgia, R., Batra, S. K., & Nasser, M. W. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.05.020 · Cited by 26 · see citing works

Comparative Analysis of microRNA Binding Site Distribution and microRNA-Mediated Gene Expression Repression of Oncogenes and Tumor Suppressor Genes

Tian, S., Wang, J., Zhang, F., & Wang, D. (2022) · Genes · doi:10.3390/genes13030481 · Cited by 23 · see citing works

The epigenetic basis of evolution

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

MicroRNA-126: A key regulator of angiogenesis, inflammation, and tumorigenesis — Exploring its multifaceted functions in vascular health and cancer

Woźniak, O., Mierzejewski, B., & Brzóska, E. (2025) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2025.167984 · Cited by 21 · see citing works

LncRNA H19 sponges miR-103-3p to promote the high phosphorus-induced osteoblast phenotypic transition of vascular smooth muscle cells by upregulating Runx2

Zhou, W., Feng, Q., Cheng, M., Zhang, D., Jin, J., Zhang, S., Bai, Y., & Xu, J. (2021) · Cellular Signalling · doi:10.1016/j.cellsig.2021.110220 · Cited by 21 · see citing works

Multiplexed Organelles Portrait Barcodes for Subcellular MicroRNA Array Detection in Living Cells

Wei, W., Lu, H., Dai, W., Zheng, X. S., & Dong, H. (2022) · ACS Nano · doi:10.1021/acsnano.2c06252 · Cited by 21 · see citing works

Stimuli-responsive probes for amplification-based imaging of miRNAs in living cells

Wei, R., Wang, K., Liu, X., Shi, M., Pan, W., Li, N., & Tang, B. (2023) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2023.115584 · Cited by 21 · see citing works

The Emerging Roles of Exosomal miRNAs in Breast Cancer Progression and Potential Clinical Applications

Li, J., He, D., Bi, Y., & Liu, S. (2023) · Breast Cancer Targets and Therapy · doi:10.2147/bctt.s432750 · Cited by 21 · see citing works

Dynamics of miRNA accumulation duringC. eleganslarval development

Nahar, S., Moya, L. J. M., Brunner, J., Hendriks, G., Towbin, B. D., Hauser, Y. P., Brancati, G., Gaidatzis, D., & Großhans, H. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae115 · Cited by 20 · see citing works

G1/S restriction point coordinates phasic gene expression and cell differentiation

DeVeale, B., Liu, L., Boileau, R. M., Swindlehurst-Chan, J., Marsh, B., Freimer, J. W., Abate, A. R., & Blelloch, R. H. (2022) · Nature Communications · doi:10.1038/s41467-022-31101-0 · Cited by 20 · see citing works

MicroRNA-183/96/182 cluster in immunity and autoimmunity

Wang, Z., Dai, R., & Ahmed, S. A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1134634 · Cited by 19 · see citing works

Nuclear microRNA-mediated transcriptional control determines adult microglial homeostasis and brain function

Zhu, L., Mao, K., Liu, L., Xu, S., Zeng, M., Fu, Y., Huang, J., Li, T., Gao, G., Teng, Z., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113964 · Cited by 18 · see citing works

Convergent and divergent evolution of microRNA ‐mediated regulation in metazoans

Wang, Y., Tang, X., & Lü, J. (2023) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.13033 · Cited by 21 · see citing works

MicroRNAs: A Link between Mammary Gland Development and Breast Cancer

Wu, D., Thompson, L. U., & Comelli, E. M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415978 · Cited by 17 · see citing works

Gene-editing technology, from macromolecule therapeutics to organ transplantation: Applications, limitations, and prospective uses

Harisa, G. I., Faris, T. M., Sherif, A. Y., Alzhrani, R. F., Alanazi, S. A., Kohaf, N. A., & Alanazi, F. K. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.127055 · Cited by 17 · see citing works

miRNA Changes in Retinal Ganglion Cells after Optic Nerve Crush and Glaucomatous Damage

Mead, B., Kerr, A., Nakaya, N., & Tomarev, S. I. (2021) · Cells · doi:10.3390/cells10071564 · Cited by 17 · see citing works

Critical role of cellular microRNAs in virus infection: Decades of progress

Han, Y., Zhang, G., Lv, X., & Ren, L. (2025) · Animals and zoonoses. · doi:10.1016/j.azn.2025.01.002 · Cited by 16 · see citing works

Application of the neuropeptide NPVF to enhance angiogenesis and osteogenesis in bone regeneration

Yu, H., Wang, Y., Gao, J., Gao, Y., Zhong, C., & Chen, Y. (2023) · Communications Biology · doi:10.1038/s42003-023-04567-x · Cited by 16 · see citing works

An atlas of small non-coding RNAs in human preimplantation development

Russell, S. J., Zhao, C., Biondic, S., Menezes, K., Hagemann-Jensen, M., Librach, C. L., & Sophie Petropoulos, A. (2024) · Nature Communications · doi:10.1038/s41467-024-52943-w · Cited by 17 · see citing works

ceRNA network mediated by lncRNA-miRNA-mRNA of Pelteobagrus fulvidraco plays a dual function of immunity and lipid metabolism in response to Aeromonas veronii infection

Peng, Y., Han, B., Zhang, K., Tang, P., Zhang, Y., Ji, J., Yin, S., & Ning, X. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.739475 · Cited by 15 · see citing works

Sequence Requirements for miR-424-5p Regulating and Function in Cancers

Xuan, J., Liu, Y., Zeng, X., & Wang, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23074037 · Cited by 15 · see citing works

Global and precise identification of functional miRNA targets in mESCs by integrative analysis

Schaefer, M., Nabih, A., Spies, D., Hermes, V., Bodak, M., Wischnewski, H., Stalder, P., Ngondo, R. P., Liechti, L. A., Sajic, T., et al. (2022) · EMBO Reports · doi:10.15252/embr.202254762 · Cited by 15 · see citing works

Overexpression of miR-1306-5p, miR-3195, and miR-3914 Inhibits Ameloblast Differentiation through Suppression of Genes Associated with Human Amelogenesis Imperfecta

Yoshioka, H., Wang, Y., Suzuki, A., Shayegh, M., Gajera, M. V., Zhao, Z., & Iwata, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042202 · Cited by 14 · see citing works

A transient transcriptional activation governs unpolarized-to-polarized morphogenesis during embryo implantation

Lyu, X., Cui, Y., Kong, Y., Yang, M., Shen, H., Liao, S., Li, S., An, C., Wang, H., Zhang, Z., et al. (2024) · Molecular Cell · doi:10.1016/j.molcel.2024.06.005 · Cited by 13 · see citing works

MicroRNAs in diabetic macroangiopathy

Rao, G., Peng, B.-Q., Zhang, G., Fu, X., Tian, J., & Tian, Y. (2024) · Cardiovascular Diabetology · doi:10.1186/s12933-024-02405-w · Cited by 13 · see citing works

The RNA m6A landscape during human oocyte-to-embryo transition

Li, Y., Wang, Y., Cengiz, A., Jin, K.-X., Castroviejo, B. C., Lin, X., Indahl, M., Zuo, R.-J., Skuland, T., Fosslie, M., et al. (2025) · The EMBO Journal · doi:10.1038/s44318-025-00474-5 · Cited by 13 · see citing works

Functions and applications of RNA interference and small regulatory RNAs

Feng, X., & Guang, S. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024196 · Cited by 12 · see citing works

AGO1 regulates pericentromeric regions in mouse embryonic stem cells

Müller, M., Fäh, T., Schaefer, M., Hermes, V., Luitz, J., Stalder, P., Arora, R., Ngondo, R. P., & Ciaudo, C. (2022) · Life Science Alliance · doi:10.26508/lsa.202101277 · Cited by 12 · see citing works

Endothelial miR-196b-5p regulates angiogenesis via the hypoxia/miR-196b-5p/HMGA2/HIF1α loop

Ren, R., Ma, K., Jiang, Y., Chen, J., Kou, Y., Ge, Z., Chen, Z., Wei, X., & Yu, L. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00309.2022 · Cited by 11 · see citing works

The miR-144/Hmgn2 regulatory axis orchestrates chromatin organization during erythropoiesis

Kretov, D. A., Folkes, L., Mora-Martin, A., Walawalkar, I. A., Imrat, Syedah, N., Vanuytsel, K., Moxon, S., Murphy, G. J., & Cifuentes, D. (2024) · Nature Communications · doi:10.1038/s41467-024-47982-2 · Cited by 10 · see citing works

Bidirectional Interplay Among Non-Coding RNAs, the Microbiome, and the Host During Development and Diseases

Nai, S., Song, J., Su, W., & Liu, X. (2025) · Genes · doi:10.3390/genes16020208 · Cited by 11 · see citing works

A Compilation of the Diverse miRNA Functions in Caenorhabditis elegans and Drosophila melanogaster Development

Quesnelle, D. C., Bendena, W. G., & Chin-Sang, I. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24086963 · Cited by 9 · see citing works

Fatty Acid Desaturation Is Suppressed in Mir-26a/b Knockout Goat Mammary Epithelial Cells by Upregulating INSIG1

Zhu, L., Jiao, H., Gao, W., Huang, L., Shi, C., Zhang, F., Wu, J., & Luo, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210028 · Cited by 9 · see citing works

PUMILIO competes with AUF1 to control DICER1 RNA levels and miRNA processing

Rajasekaran, S., Khan, E., Ching, S. R., Khan, M. U., Siddiqui, J., Gradia, D. F., Lin, C., Bouley, S. J., Mercadante, D. L., Manning, A. L., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac499 · Cited by 9 · see citing works

Impacts of circulating microRNAs in exercise-induced vascular remodeling

Guilder, G. P. V., Preston, C. C., Munce, T. A., & Faustino, R. S. (2021) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00894.2020 · Cited by 8 · see citing works

MILNP: Plant lncRNA–miRNA Interaction Prediction Based on Improved Linear Neighborhood Similarity and Label Propagation

Cai, L., Gao, M., Ren, X., Fu, X., Xu, J., Wang, P., & Chen, Y. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.861886 · Cited by 8 · see citing works

Mime-seq 2.0: a method to sequence microRNAs from specific mouse cell types

Mandlbauer, A., Sun, Q., Popitsch, N. P., Schwickert, T. A., Spanova, M., Wang, J., Ameres, S. L., Busslinger, M., & Cochella, L. (2024) · The EMBO Journal · doi:10.1038/s44318-024-00102-8 · Cited by 7 · see citing works

Functional mapping of microRNA promoters with dCas9 fused to transcriptional regulators

Kumar, P., Courtes, M., Lemmers, C., Digarcher, A. L., Coku, I., Monteil, A., Hong, C. C., Varrault, A., Liu, R., Wang, L., et al. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1147222 · Cited by 8 · see citing works

miR-373-3p promotes aerobic glycolysis in colon cancer cells by targeting MFN2

Wang, Y., Lun, J., Zhang, Y., Yu, M., Liu, X., Guo, J., Zhang, H., Qiu, W., & Fang, J. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024090 · Cited by 7 · see citing works

MicroRNA regulation of enteric nervous system development and disease

Holland, A. M., Jehoul, R., Vranken, J., Wohl, S. G., & Boesmans, W. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.02.004 · Cited by 7 · see citing works

Polyphyllin I suppressed the apoptosis of intervertebral disc nucleus pulposus cells induced by IL-1β by miR-503-5p/Bcl-2 axis

Yuan, L., Miao, H., Heng, D., Zhang, F., Lou, Z., & Li, X. (2023) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-023-03947-7 · Cited by 7 · see citing works

Evidence for Functional Roles of MicroRNAs in Lineage Specification During Mouse and Human Preimplantation Development

Biondic, S., & Sophie Petropoulos, A. (2023) · The Yale Journal of Biology and Medicine · doi:10.59249/fosi4358 · Cited by 7 · see citing works

Therapeutic potential of microRNAs in neurological disorders: mechanisms, biomarkers, and emerging therapeutic strategies

Pal, S., & Mandal, S. (2025) · Exploration of Neuroprotective Therapy · doi:10.37349/ent.2025.1004111 · Cited by 8 · see citing works

Effects of Low and High Maternal Protein Intake on Fetal Skeletal Muscle miRNAome in Sheep

Akyüz, B., Sohel, M. M. H., Konca, Y., Arslan, K., Gürbulak, K., Abay, M., Kali̇ber, M., White, S. N., & Çınar, M. U. (2024) · Animals · doi:10.3390/ani14111594 · Cited by 6 · see citing works

Simultaneous detection of multiple microRNAs based on fluorescence resonance energy transfer under a single excitation wavelength

Liu, L., He, J. H., Wu, X. Q., Liu, J. J., Lv, W. Y., Huang, C. Z., Liu, H., & Li, C. M. (2024) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2024.124788 · Cited by 6 · see citing works

Dynamic Nanostructure‐Based DNA Logic Gates for Cancer Diagnosis and Therapy

Bi, S., Yang, R., Ju, H., & Liu, Y. (2024) · ChemBioChem · doi:10.1002/cbic.202400754 · Cited by 6 · see citing works

Identification of miRNAs of Strongyloides stercoralis L1 and iL3 larvae isolated from human stool

Pomari, E., Malerba, G., Veschetti, L., Franceschi, A., Tor, L. M. D., Deiana, M., Degani, M., Mistretta, M., Patuzzo, C., Ragusa, A., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-14185-y · Cited by 6 · see citing works

Role of microRNAs in embryo–endometrial interactions: biological functions and clinical applications

Qi, S., Kodithuwakku, S., Pang, R. T., Chiu, P. C. N., Tang, M. Y., & Lee, K.-F. (2023) · Reproductive and Developmental Medicine · doi:10.1097/rd9.0000000000000073 · Cited by 6 · see citing works

Prolactin receptor potentiates chemotherapy through miRNAs ‐induced G6PD / TKT inhibition in pancreatic cancer

Liao, Y., Huang, P.-Q., Pan, H., Gai, Y., Zhan, Y., Li, S., & Nie, H. (2024) · The FASEB Journal · doi:10.1096/fj.202302287rr · Cited by 5 · see citing works

Nanotechnological approaches in topical RNAi therapy for skin diseases

da Silva, U. J., Morais, M. F., Pereira, J. V. D. A., & Bentley, M. V. L. B. (2025) · Academia Biology · doi:10.20935/acadbiol7599 · Cited by 5 · see citing works

Advances in Genetic Polymorphisms

Abdelmoula, N. B., & Abdelmoula, B. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.1001553 · Cited by 5 · see citing works

Plagl1 and Lrrc58 control mammalian body size by triggering target-directed microRNA degradation of miR-322 and miR-503Preprint

LaVigne, C. A., Han, J., Zhang, H., Cho, S., Kim, M., Sethia, K., Evers, B. M., Acharya, A., Chang, T.-C., & Mendell, J. T. (2025) · Genes & Development · doi:10.1101/gad.353138.125 · Cited by 5 · see citing works

High-Throughput Sequencing to Investigate the Expression and Potential Role of Differentially Expressed microRNAs in Myocardial Cells after Ischemia-Reperfusion Injury

Li, S., Lv, D., Lü, Y., Zhang, Y., & Jia, Y. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2901038 · Cited by 4 · see citing works

The miR-290 and miR-302 clusters are essential for reprogramming of fibroblasts to induced pluripotent stem cells

Ye, J., Boileau, R. M., Parchem, R. J., Judson‐Torres, R. L., & Blelloch, R. H. (2025) · Stem Cells · doi:10.1093/stmcls/sxae080 · Cited by 4 · see citing works

miRNA-GABA influences female Aedes aegypti reproduction by modulating midgut homeostasis

Cao, J., & Lin, L. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115776 · Cited by 4 · see citing works

Comprehensive analysis of peripheral blood non-coding RNAs identifies a diagnostic panel for fungal infection after transplantation

Yang, A., Chen, H., Lin, J., Han, M., Yuan, X., Zhang, T., Nian, Q., Peng, M., Li, D., Wu, C., et al. (2022) · Bioengineered · doi:10.1080/21655979.2022.2032963 · Cited by 4 · see citing works

Spatially Resolved, Error‐Robust Multiplexed MicroRNA Profiling in Single Living Cells

Wei, W., Dai, W., Yang, F., Lu, H., Zhang, K., Xing, Y., Meng, X., Zhou, L., Zhang, Y., Yang, Q., et al. (2022) · Angewandte Chemie · doi:10.1002/ange.202116909 · Cited by 4 · see citing works

The Role of microRNAs in the Gonocyte Theory as Target of Malignancy: Looking for Potential Diagnostic Biomarkers

García-Andrade, F., Vigueras‐Villaseñor, R. M., Chávez‐Saldaña, M., Rojas‐Castañeda, J. C., Bahena, I., Aréchaga-Ocampo, E., Díaz‐Chávez, J., & Landero‐Huerta, D. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810526 · Cited by 4 · see citing works

An atlas of expression quantitative trait loci of microRNAs in longissimus muscle of eight-way crossbred pigs

Zhong, L., Zheng, M., Huang, Y., Jiang, T., Yang, B. J., Huang, L., & Ma, J. (2023) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2023.02.007 · Cited by 4 · see citing works

Early expression onset of tissue-specific effector genes during the specification process in sea urchin embryos

Yamakawa, S., Yamazaki, A. K., Morino, Y., & Wada, H. (2023) · EvoDevo · doi:10.1186/s13227-023-00210-2 · Cited by 4 · see citing works

Multiple Genetic Polymorphisms within microRNA Targets and Homologous microRNA-Binding Sites: Two More Factors Influencing microRNA-Mediated Regulation of Gene Expression

Giurgiu, M., Kaltenbach, R. F. I., Ahrend, F., Weeks, S., Clifton, H., Bouldo, M. G., Voloshin, V., Zhong, J., Harden, S., & Kofman, A. V. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.1002250 · Cited by 4 · see citing works

DDX6 interacts with DDX3X to repress translation in microRNA-mediated silencing

Lu, Y., Meng, T., Su, H. H., Tu, Y., Wang, J.-P., Kuroda, M., & Wang, X. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf868 · Cited by 3 · see citing works

A Rapid Evolving microRNA Cluster Rewires Its Target Regulatory Networks in Drosophila

Lyu, Y., Liufu, Z., Xiao, J., & Tang, T. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.760530 · Cited by 3 · see citing works

G-Quadruplexes Regulate miRNA Biogenesis in Live Zebrafish Embryos

Steeman, T. J., Weiner, A. M. J., David, A. P., Binolfi, A., Calcaterra, N. B., & Armas, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054828 · Cited by 3 · see citing works

miR-195b is required for proper cellular homeostasis in the elderly

Muñoz-Gallardo, M. D. M., García‐Padilla, C., Vicente‐García, C., Carvajal, J. J., Arenega, A., & Franco, D. (2024) · Scientific Reports · doi:10.1038/s41598-024-51256-8 · Cited by 3 · see citing works

MEF2C Directly Interacts with Pre-miRNAs and Distinct RNPs to Post-Transcriptionally Regulate miR-23a-miR-27a-miR-24-2 microRNA Cluster Member Expression

Lozano-Velasco, E., García‐Padilla, C., Carmona-García, M., Gonzalez-Diaz, A., Arequipa-Rendon, A., Aránega, A. E., & Franco, D. (2024) · Non-Coding RNA · doi:10.3390/ncrna10030032 · Cited by 3 · see citing works

lncRNA MEG3 Promotes PDK4/GSK-3β/β-Catenin Axis in MEFs by Targeting miR-532-5p

Yang, Y., Deng, Y., Yao, X., Luo, H., He, W.-G., Cao, X.-L., Chen, R., He, B., Jiang, H., & Wang, J. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/3563663 · Cited by 3 · see citing works

Emerging role of interaction between m6A and main ncRNAs in gastrointestinal (GI) cancers

Xu, Y., Yu, X., Guo, W., & He, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1129298 · Cited by 3 · see citing works

Analysis of mRNA Dynamics Using RNA Sequencing Data

Alkallas, R., & Najafabadi, H. S. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2409-8_9 · Cited by 2 · see citing works

Global discovery, expression pattern, and regulatory role of miRNA-like RNAs in Ascosphaera apis infecting the Asian honeybee larvae

Liu, X., Geng, S., Ye, D., Xu, W., Zheng, Y., Wang, F., Lei, J., Wu, Y., Jiang, H., Hu, Y. C., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1551625 · Cited by 2 · see citing works

miR-203 facilitates timely cell fate transitions via epigenetic modulation during early embryogenesis

González‐Martínez, J., Sánchez-Belmonte, A., Ayala, E., Escobar, B., Gómez, J., Garcia-Diaz, A., Nogueira, E., Muñoz, J., Melati, A., Brandauer, A., et al. (2026) · Science Advances · doi:10.1126/sciadv.adr1776 · Cited by 2 · see citing works

CLASHub is an integrated database and analytical platform for microRNA-target interactions

Li, L., Sheng, P., Hiers, N. M., Li, T., Grimme, A. L., Wang, Y., Traugot, C. M., D'Agati, O. M., & Xie, M. (2026) · Nature Communications · doi:10.1038/s41467-026-72902-x · Cited by 2 · see citing works

Computational Methods for Identifying MicroRNA-Gene Regulatory Modules

Liu, Y. (2022) · Springer handbooks of computational statistics · doi:10.1007/978-3-662-65902-1_10 · Cited by 2 · see citing works

Overexpression of miR ‐155 Modulates Interferon Response and Inhibits Viral Replication of IHNV and IPNV in EPC Cells

Abdellaoui, N., Park, I. W., Choi, S., Kim, M., & Kim, M. S. (2025) · Journal of Fish Diseases · doi:10.1111/jfd.14092 · Cited by 2 · see citing works

Creating and maintaining a high-confidence microRNA repository for crop research: A brief review and re-examination of the current crop microRNA registries

Meng, Y., Ma, X., Li, J., & Shao, C. (2022) · Journal of Plant Physiology · doi:10.1016/j.jplph.2022.153636 · Cited by 2 · see citing works

Point Mutation in Prkra Alters miRNA Expression During Embryonic External Ear Development

Liu, W., Lin, L., Yang, Q., Jin, S., & Jiang, H. (2022) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000008837 · Cited by 2 · see citing works

MiR92b-3p synthetic analogue impairs zebrafish embryonic development, leading to ocular defects, decreased movement and hatching rate, and increased mortality

Kranert, K., Woźny, M., Podlasz, P., Wa̧sowicz, K., & Brzuzan, P. (2022) · Journal of Applied Genetics · doi:10.1007/s13353-022-00732-w · Cited by 2 · see citing works

Differential Regulation Analysis Quantifies Mirna Regulatory Roles and Context-Specific TargetsPreprint

Ning, B., Spira, T., Beane, J., & Lenburg, M. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.24.501303 · Cited by 2 · see citing works

Non-Linear Relationship between MiRNA Regulatory Activity and Binding Site Counts on Target mRNAs

Tian, S., Zhao, Z., Ren, B., & Wang, D. (2024) · Data · doi:10.3390/data9100111 · Cited by 1 · see citing works

The Primary Role of Noncoding RNA in the Pathogenesis of Cancer

Shah, A. (2025) · Genes · doi:10.3390/genes16070771 · Cited by 1 · see citing works

Chain-based precision amplification biosensor for microRNA detection based on dCas13a system and iridium complex

Zhang, Y., Chen, Z., Wei, S., Zhang, Y., Liu, Y., Li, D., Wang, J., Gao, Q., Li, D., Zhang, H., et al. (2025) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2025.138881 · Cited by 1 · see citing works

A framework for understanding the roles of miRNAs in animal development

Alberti, C., & Cochella, L. (2017) · Development · doi:10.1242/dev.146613 · Cited by 150 · see citing works

MicroRNAs in mammalian development

Lee, C.-T., Risom, T., & Strauss, W. M. (2006) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20072 · Cited by 71 · see citing works

miRNA dynamics in development: orchestrators of gene expression and cell fate

Vasudevan, V., Segonds, M. W., & Simard, M. J. (2026) · Transcription · doi:10.1080/21541264.2026.2643027

MicroRNAs in mammalian development and tumorigenesis

O'Rourke, J. R., Swanson, M. S., & Harfe, B. D. (2006) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20071 · Cited by 45 · see citing works

Analysis of microRNA knockouts in mice

Park, C. Y., Choi, Y. S., & McManus, M. T. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq367 · Cited by 209 · see citing works