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miR-137: A Novel Therapeutic Target for Human Glioma
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“In gliomagenesis, the loss of miR-124-3p, miR-128-3p, and miR-137159 creates an environment conducive to aberrant transcriptional regulation.”
From MiR-128-3p – a gray eminence of the human central nervous system (2024) · cites this paper as [159]
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Cross talk between microRNA and epigenetic regulation in adult neurogenesis
Szulwach, K. E., Li, X., Smrt, R. D., Li, Y., Luo, Y., Lin, L., Santistevan, N. J., Li, W., Zhao, X., & Jin, P. (2010) · Journal of Cell Biology · doi:10.1083/jcb.200908151 · Cited by 493
Self-citationTurturici, G., Tinnirello, R., Sconzo, G., & Geraci, F. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00228.2013 · Cited by 483
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
Malhotra, H., Sheokand, N., Kumar, S., Chauhan, A. S., Kumar, M., Jakhar, P., Boradia, V. M., Raje, C. I., & Raje, M. (2016) · Journal of Biomedical Nanotechnology · doi:10.1166/jbn.2016.2229 · Cited by 114
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Research works printed but not linked: 108
- Morgan, 2015, The epidemiology of glioma in adults: a “state of the science” review, Neuro-oncol., 17, 623, 10.1093/neuonc/nou358 · DOI
- Louis, 2007, The 2007 WHO classification of tumours of the central nervous system, Acta Neuropathol., 114, 97, 10.1007/s00401-007-0243-4 · DOI
- Zhang, 2012, Combined gene expression and protein interaction analysis of dynamic modularity in glioma prognosis, J. Neurooncol., 107, 281, 10.1007/s11060-011-0757-4 · DOI
- Bartel, 2004, MicroRNAs: genomics, biogenesis, mechanism, and function, Cell, 116, 281, 10.1016/S0092-8674(04)00045-5 · DOI
- He, 2004, MicroRNAs: small RNAs with a big role in gene regulation, Nat. Rev. Genet., 5, 522, 10.1038/nrg1379 · DOI · Paper page
- Bier, 2013, MicroRNA-137 is downregulated in glioblastoma and inhibits the stemness of glioma stem cells by targeting RTVP-1, Oncotarget, 4, 665, 10.18632/oncotarget.928 · DOI
- Wright, 2013, Potential Impact of miR-137 and Its Targets in Schizophrenia, Front. Genet., 4, 58, 10.3389/fgene.2013.00058 · DOI
- Smith, 2015, Tumor suppressive microRNA-137 negatively regulates Musashi-1 and colorectal cancer progression, Oncotarget, 6, 12558, 10.18632/oncotarget.3726 · DOI
- Yang, 2015, miR-137 and miR-197 Induce Apoptosis and Suppress Tumorigenicity by Targeting MCL-1 in Multiple Myeloma, Clin. Cancer Res., 21, 2399, 10.1158/1078-0432.CCR-14-1437 · DOI
- Liu, 2014, FoxD3-regulated microRNA-137 suppresses tumour growth and metastasis in human hepatocellular carcinoma by targeting AKT2, Oncotarget, 5, 5113, 10.18632/oncotarget.2089 · DOI
- Yin, 2014, miR-137: a new player in schizophrenia, Int. J. Mol. Sci., 15, 3262, 10.3390/ijms15023262 · DOI
- Soldati, 2013, Dysregulation of REST-regulated coding and non-coding RNAs in a cellular model of Huntington’s disease, J. Neurochem., 124, 418, 10.1111/jnc.12090 · DOI
- Warburton, 2015, Characterization of a REST-Regulated Internal Promoter in the Schizophrenia Genome-Wide Associated Gene MIR137, Schizophr. Bull., 41, 698, 10.1093/schbul/sbu117 · DOI
- Li, 2018, REST, not REST4, is a risk factor associated with radiotherapy plus chemotherapy efficacy in glioma, Drug Des. Devel. Ther., 12, 1363, 10.2147/DDDT.S161602 · DOI
- Bemis, 2008, MicroRNA-137 targets microphthalmia-associated transcription factor in melanoma cell lines, Cancer Res., 68, 1362, 10.1158/0008-5472.CAN-07-2912 · DOI
- Pacheco, 2019, A VNTR Regulates miR-137 Expression Through Novel Alternative Splicing and Contributes to Risk for Schizophrenia, Sci. Rep., 9, 11793, 10.1038/s41598-019-48141-0 · DOI
- Silber, 2008, miR-124 and miR-137 inhibit proliferation of glioblastoma multiforme cells and induce differentiation of brain tumor stem cells, BMC Med., 6, 14, 10.1186/1741-7015-6-14 · DOI · Paper page
- Whitfield, 2002, Identification of genes periodically expressed in the human cell cycle and their expression in tumors, Mol. Biol. Cell, 13, 1977, 10.1091/mbc.02-02-0030 · DOI · Paper page
- Balaguer, 2010, Epigenetic silencing of miR-137 is an early event in colorectal carcinogenesis, Cancer Res., 70, 6609, 10.1158/0008-5472.CAN-10-0622 · DOI
- Guan, 2019, Epigenetic silencing of miR-137 induces resistance to bicalutamide by targeting TRIM24 in prostate cancer cells, Am. J. Transl. Res., 11, 3226
- Qin, 2017, Epigenetic silencing of miR-137 induces drug resistance and chromosomal instability by targeting AURKA in multiple myeloma, Leukemia, 31, 1123, 10.1038/leu.2016.325 · DOI
- Steponaitiene, 2016, Epigenetic silencing of miR-137 is a frequent event in gastric carcinogenesis, Mol. Carcinog., 55, 376, 10.1002/mc.22287 · DOI
- Deng, 2016, miR-137 acts as a tumor suppressor in astrocytoma by targeting RASGRF1, Tumour Biol., 37, 3331, 10.1007/s13277-015-4110-y · DOI
- Sun, 2011, miR-137 forms a regulatory loop with nuclear receptor TLX and LSD1 in neural stem cells, Nat. Commun., 2, 529, 10.1038/ncomms1532 · DOI
- Jiang, 2013, MicroRNA-137 represses Klf4 and Tbx3 during differentiation of mouse embryonic stem cells, Stem Cell Res. (Amst.), 11, 1299, 10.1016/j.scr.2013.09.001 · DOI
- Tarantino, 2010, miRNA 34a, 100, and 137 modulate differentiation of mouse embryonic stem cells, FASEB J., 24, 3255, 10.1096/fj.09-152207 · DOI
- Yu, 2017, Knockdown of long non-coding RNA XIST increases blood-tumor barrier permeability and inhibits glioma angiogenesis by targeting miR-137, Oncogenesis, 6, e303, 10.1038/oncsis.2017.7 · DOI
- Wang, 2017, Long non-coding RNA XIST exerts oncogenic functions in human glioma by targeting miR-137, Am. J. Transl. Res., 9, 1845
- Hao, 2020, Over-expression of long noncoding RNA HOTAIRM1 promotes cell proliferation and invasion in human glioblastoma by up-regulating SP1 via sponging miR-137, Neuroreport, 31, 109, 10.1097/WNR.0000000000001380 · DOI
- Chen, 2020, NCK1-AS1 Increases Drug Resistance of Glioma Cells to Temozolomide by Modulating miR-137/TRIM24, Cancer Biother. Radiopharm., 35, 101
- Du, 2019, miR-137 alleviates doxorubicin resistance in breast cancer through inhibition of epithelial-mesenchymal transition by targeting DUSP4, Cell Death Dis., 10, 922, 10.1038/s41419-019-2164-2 · DOI
- Ying, 2017, MicroRNA-137 inhibits BMP7 to enhance the epithelial-mesenchymal transition of breast cancer cells, Oncotarget, 8, 18348, 10.18632/oncotarget.15442 · DOI
- Han, 2016, miR-137 suppresses the invasion and procedure of EMT of human breast cancer cell line MCF-7 through targeting CtBP1, Hum. Cell, 29, 30, 10.1007/s13577-015-0124-4 · DOI
- Miao, 2019, Overexpression of mircoRNA-137 inhibits cervical cancer cell invasion, migration and epithelial-mesenchymal transition by suppressing the TGF-β/smad pathway via binding to GREM1, Cancer Cell Int., 19, 147, 10.1186/s12935-019-0852-8 · DOI
- Dong, 2016, MiR-137 and miR-34a directly target Snail and inhibit EMT, invasion and sphere-forming ability of ovarian cancer cells, J. Exp. Clin. Cancer Res., 35, 132, 10.1186/s13046-016-0415-y · DOI
- Wang, 2018, Knockdown of LncRNA-XIST Suppresses Proliferation and TGF-β1-Induced EMT in NSCLC Through the Notch-1 Pathway by Regulation of miR-137, Genet. Test. Mol. Biomarkers, 22, 333, 10.1089/gtmb.2018.0026 · DOI
- Chang, 2017, Upregulation of microRNA-137 expression by Slug promotes tumor invasion and metastasis of non-small cell lung cancer cells through suppression of TFAP2C, Cancer Lett., 402, 190, 10.1016/j.canlet.2017.06.002 · DOI
- Liu, 2014, MiR-137 regulates epithelial-mesenchymal transition in gastrointestinal stromal tumor, Tumour Biol., 35, 9131, 10.1007/s13277-014-2177-5 · DOI
- Chen, 2012, miR-137 is frequently down-regulated in glioblastoma and is a negative regulator of Cox-2, Eur. J. Cancer, 48, 3104, 10.1016/j.ejca.2012.02.007 · DOI
- Koshkin, 2014, Profile of microRNA expression in brain tumors of different malignancy, Bull. Exp. Biol. Med., 157, 794, 10.1007/s10517-014-2669-8 · DOI
- Koshkin, 2014, Analysis of expression of microRNAs and genes involved in the control of key signaling mechanisms that support or inhibit development of brain tumors of different grades, Clin. Chim. Acta, 430, 55, 10.1016/j.cca.2014.01.001 · DOI · Paper page
- Visani, 2014, Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I-III, Mol. Oncol., 8, 417, 10.1016/j.molonc.2013.12.010 · DOI
- Liang, 2016, Downregulation of miR-137 and miR-6500-3p promotes cell proliferation in pediatric high-grade gliomas, Oncotarget, 7, 19723, 10.18632/oncotarget.7736 · DOI
- Tamim, 2014, Genomic analyses reveal broad impact of miR-137 on genes associated with malignant transformation and neuronal differentiation in glioblastoma cells, PLoS ONE, 9, e85591, 10.1371/journal.pone.0085591 · DOI
- Bhaskaran, 2019, The functional synergism of microRNA clustering provides therapeutically relevant epigenetic interference in glioblastoma, Nat. Commun., 10, 422, 10.1038/s41467-019-08390-z · DOI · Paper page
- Channakkar, 2020, MiRNA-137-mediated modulation of mitochondrial dynamics regulates human neural stem cell fate, Stem Cells, 38, 683, 10.1002/stem.3155 · DOI
- Schouten, 2015, MicroRNA-124 and -137 cooperativity controls caspase-3 activity through BCL2L13 in hippocampal neural stem cells, Sci. Rep., 5, 12448, 10.1038/srep12448 · DOI
- Sun, 2013, Overexpressed miRNA-137 inhibits human glioma cells growth by targeting Rac1, Cancer Biother. Radiopharm., 28, 327
- Luo, 2018, miR-137 regulates ferroptosis by targeting glutamine transporter SLC1A5 in melanoma, Cell Death Differ., 25, 1457, 10.1038/s41418-017-0053-8 · DOI · Paper page
- van Geldermalsen, 2016, ASCT2/SLC1A5 controls glutamine uptake and tumour growth in triple-negative basal-like breast cancer, Oncogene, 35, 3201, 10.1038/onc.2015.381 · DOI
- Chakrabarti, 2015, Direct transfection of miR-137 mimics is more effective than DNA demethylation of miR-137 promoter to augment anti-tumor mechanisms of delphinidin in human glioblastoma U87MG and LN18 cells, Gene, 573, 141, 10.1016/j.gene.2015.07.034 · DOI
- Li, 2017, miR-137 acts as a tumor suppressor via inhibiting CXCL12 in human glioblastoma, Oncotarget, 8, 101262, 10.18632/oncotarget.20589 · DOI
- Zhang, 2017, MicroRNA-137 inhibits growth of glioblastoma through EGFR suppression, Am. J. Transl. Res., 9, 1492
- Su, 2015, Stanniocalcin-1, a new biomarker of glioma progression, is associated with prognosis of patients, Tumour Biol., 36, 6333, 10.1007/s13277-015-3319-0 · DOI
- Sakata, 2019, MicroRNA regulating stanniocalcin-1 is a metastasis and dissemination promoting factor in glioblastoma, J. Neurooncol., 142, 241, 10.1007/s11060-019-03113-2 · DOI
- Sun, 2015, MiR-137 inhibits proliferation and angiogenesis of human glioblastoma cells by targeting EZH2, J. Neurooncol., 122, 481, 10.1007/s11060-015-1753-x · DOI
- Li, 2018, Stanniocalcin-1 augments stem-like traits of glioblastoma cells through binding and activating NOTCH1, Cancer Lett., 416, 66, 10.1016/j.canlet.2017.11.033 · DOI
- Velasco, 2019, Antagonism between the RNA-binding protein Musashi1 and miR-137 and its potential impact on neurogenesis and glioblastoma development, RNA, 25, 768, 10.1261/rna.069211.118 · DOI
- Kwon, 2013, Validation of schizophrenia-associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR-137 targets, Mol. Psychiatry, 18, 11, 10.1038/mp.2011.170 · DOI · Paper page
- Ji, 2018, FOXK1 promotes cell growth through activating wnt/beta-catenin pathway and emerges as a novel target of miR-137 in glioma, Am. J. Transl. Res., 10, 1784
- Li, 2013, MIR-137 suppresses growth and invasion, is downregulated in oligodendroglial tumors and targets CSE1L, Brain Pathol., 23, 426, 10.1111/bpa.12015 · DOI
- Wang, 2016, PTP4A3 is a target for inhibition of cell proliferatin, migration and invasion through Akt/mTOR signaling pathway in glioblastoma under the regulation of miR-137, Brain Res., 1646, 441, 10.1016/j.brainres.2016.06.026 · DOI
- Takwi, 2014, miR-137 regulates the constitutive androstane receptor and modulates doxorubicin sensitivity in parental and doxorubicin-resistant neuroblastoma cells, Oncogene, 33, 3717, 10.1038/onc.2013.330 · DOI
- Giunti, 2019, A microRNA profile of pediatric glioblastoma: The role of NUCKS1 upregulation, Mol. Clin. Oncol., 10, 331
- Ciechomska, 2020, Histone Modifying Enzymes and Chromatin Modifiers in Glioma Pathobiology and Therapy Responses, Adv. Exp. Med. Biol., 1202, 259, 10.1007/978-3-030-30651-9_13 · DOI
- Maleszewska, 2015, ). Deregulation of histone-modifying enzymes and chromatin structure modifiers contributes to glioma development, Future Oncol., 11, 2587, 10.2217/fon.15.171 · DOI
- Li, 2015, Quantitative nuclear proteomics identifies that miR-137-mediated EZH2 reduction regulates resveratrol-induced apoptosis of neuroblastoma cells, Mol. Cell Proteomics., 14, 316, 10.1074/mcp.M114.041905 · DOI
- Vire, 2006, The Polycomb group protein EZH2 directly controls DNA methylation, Nature., 439, 871, 10.1038/nature04431 · DOI · Paper page
- Pereira, 2010, ). Ezh2, the histone methyltransferase of PRC2, regulates the balance between self-renewal and differentiation in the cerebral cortex, Proc. Natl. Acad. Sci. USA., 107, 15957, 10.1073/pnas.1002530107 · DOI
- Hwang, 2014, Distinct and separable roles for EZH2 in neurogenic astroglia, Elife., 3, e02439, 10.7554/eLife.02439 · DOI
- Zhang, 2015, TRIM24 promotes glioma progression and enhances chemoresistance through activation of the PI3K/Akt signaling pathway, Oncogene., 34, 600, 10.1038/onc.2013.593 · DOI
- Lv, 2017, Histone Acetyltransferase KAT6A Upregulates PI3K/AKT Signaling through TRIM24 Binding, Cancer Res., 77, 6190, 10.1158/0008-5472.CAN-17-1388 · DOI
- Wood, 2008, Centromere-associated protein E: a motor that puts the brakes on the mitotic checkpoint, Clin Cancer Res., 14, 7588, 10.1158/1078-0432.CCR-07-4443 · DOI
- Sharma, 2015, NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability, Nucleic Acids Res., 43, 9817
- Cheong, 2016, Identification of NUCKS1 as a putative oncogene and immunodiagnostic marker of hepatocellular carcinoma, Gene, 584, 47, 10.1016/j.gene.2016.03.006 · DOI
- Kikuchi, 2013, Identification of NUCKS1 as a colorectal cancer prognostic marker through integrated expression and copy number analysis, Int. J. Cancer, 132, 2295, 10.1002/ijc.27911 · DOI
- Gao, 2017, Wnt/β-catenin signaling pathway inhibits the proliferation and apoptosis of U87 glioma cells via different mechanisms, PLoS One, 12, e0181346, 10.1371/journal.pone.0181346 · DOI
- Gu, 2014, TCTP promotes glioma cell proliferation in vitro and in vivo via enhanced beta-catenin/TCF-4 transcription, Neuro Oncol., 16, 217, 10.1093/neuonc/not194 · DOI
- Fortin Ensign, 2013, Implications of Rho GTPase Signaling in Glioma Cell Invasion and Tumor Progression, Front. Oncol., 3, 241, 10.3389/fonc.2013.00241 · DOI
- Savitch, 2006, Increased fibroblast growth factor-inducible 14 expression levels promote glioma cell invasion via Rac1 and nuclear factor-kappaB and correlate with poor patient outcome, Cancer Res., 66, 9535, 10.1158/0008-5472.CAN-06-0418 · DOI
- Chan, 2008, The guanine nucleotide exchange factors trio, Ect2, and Vav3 mediate the invasive behavior of glioblastoma, Am. J. Pathol., 173, 1828, 10.2353/ajpath.2008.080043 · DOI
- Innocenti, 1999, CDC25(Mm)/Ras-GRF1 regulates both Ras and Rac signaling pathways, FEBS Lett., 460, 357, 10.1016/S0014-5793(99)01374-5 · DOI
- Kiyono, 1999, G protein beta gamma subunit-dependent Rac-guanine nucleotide exchange activity of Ras-GRF1/CDC25(Mm), Proc. Natl. Acad. Sci. U S A, 96, 4826, 10.1073/pnas.96.9.4826 · DOI
- Li, 2016, Circulating microRNA-137 is a potential biomarker for human glioblastoma, Eur. Rev. Med. Pharmacol. Sci., 20, 3599
- Riemenschneider, 2010, MGMT promoter methylation in malignant gliomas, Target Oncol., 5, 161, 10.1007/s11523-010-0153-6 · DOI
- Kozaki, 2008, Exploration of tumor-suppressive microRNAs silenced by DNA hypermethylation in oral cancer, Cancer Res., 68, 2094, 10.1158/0008-5472.CAN-07-5194 · DOI
- Sun, 2019, miR-137 mediates the functional link between c-Myc and EZH2 that regulates cisplatin resistance in ovarian cancer, Oncogene., 38, 564, 10.1038/s41388-018-0459-x · DOI
- Ma, 2019, LncRNA DSCAM-AS1 acts as a sponge of miR-137 to enhance Tamoxifen resistance in breast cancer, J. Cell. Physiol., 234, 2880, 10.1002/jcp.27105 · DOI
- Cheng, 2019, Knockdown Of lncRNA NCK-AS1 Regulates Cisplatin Resistance Through Modulating miR-137 In Osteosarcoma Cells, Onco Targets Ther., 12, 11057, 10.2147/OTT.S228199 · DOI
- Zhu, 2013, MiR-137 restoration sensitizes multidrug-resistant MCF-7/ADM cells to anticancer agents by targeting YB-1, Acta Biochim. Biophys. Sin. (Shanghai)., 45, 80, 10.1093/abbs/gms099 · DOI
- Mazzoleni, 2010, Epidermal growth factor receptor expression identifies functionally and molecularly distinct tumor-initiating cells in human glioblastoma multiforme and is required for gliomagenesis, Cancer Res., 70, 7500, 10.1158/0008-5472.CAN-10-2353 · DOI
- Tunca, 2012, Olea europaea leaf extract alters microRNA expression in human glioblastoma cells., J. Cancer Res. Clin. Oncol., 138, 1831, 10.1007/s00432-012-1261-8 · DOI
- Al-Nedawi, 2008, Intercellular transfer of the oncogenic receptor EGFRvIII by microvesicles derived from tumour cells, Nat. Cell Biol., 10, 619, 10.1038/ncb1725 · DOI
- Skog, 2008, Glioblastoma microvesicles transport RNA and proteins that promote tumour growth and provide diagnostic biomarkers, Nat. Cell Biol., 10, 1470, 10.1038/ncb1800 · DOI · Paper page
- Yu, 2018, Delivery of MGMT mRNA to glioma cells by reactive astrocyte-derived exosomes confers a temozolomide resistance phenotype, Cancer Lett., 433, 210, 10.1016/j.canlet.2018.06.041 · DOI
- Lang, 2017, Glioma cells enhance angiogenesis and inhibit endothelial cell apoptosis through the release of exosomes that contain long non-coding RNA CCAT2, Oncol. Rep., 38, 785, 10.3892/or.2017.5742 · DOI
- Li, 2013, Glioma microvesicles carry selectively packaged coding and non-coding RNAs which alter gene expression in recipient cells, RNA Biol., 10, 1333, 10.4161/rna.25281 · DOI
- Salido-Guadarrama, 2014, MicroRNAs transported by exosomes in body fluids as mediators of intercellular communication in cancer, Onco Targets Ther., 7, 1327
- Akers, 2013, MiR-21 in the extracellular vesicles (EVs) of cerebrospinal fluid (CSF): a platform for glioblastoma biomarker development, PLoS One, 8, e78115, 10.1371/journal.pone.0078115 · DOI
- Wei, 2018, Serum Exosomal miR-223 Serves as a Potential Diagnostic and Prognostic Biomarker for Dementia, Neuroscience, 379, 167, 10.1016/j.neuroscience.2018.03.016 · DOI · Paper page
- Jiang, 2019, Serum secreted miR-137-containing exosomes affects oxidative stress of neurons by regulating OXR1 in Parkinson’s disease, Brain Res., 1722, 146331, 10.1016/j.brainres.2019.146331 · DOI
- Wood, 2011, Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes.:, Nat. Biotechnol., 29, 341, 10.1038/nbt.1807 · DOI · Paper page
- Hood, 2016, Post isolation modification of exosomes for nanomedicine applications, Nanomedicine (Lond), 11, 1745, 10.2217/nnm-2016-0102 · DOI
- Rupert, 2017, Methods for the physical characterization and quantification of extracellular vesicles in biological samples, Biochim. Biophys. Acta Gen. Subj., 1861, 3164, 10.1016/j.bbagen.2016.07.028 · DOI
- Zhuang, 2010, A novel nanoparticle drug delivery system: the anti-inflammatory activity of curcumin is enhanced when encapsulated in exosomes, Mol. Ther., 18, 1606, 10.1038/mt.2010.105 · DOI
- Zhuang, 2011, Treatment of brain inflammatory diseases by delivering exosome encapsulated anti-inflammatory drugs from the nasal region to the brain, Mol Ther., 19, 1769, 10.1038/mt.2011.164 · DOI · Paper page
- Ahmed, 2015, Exosome-mediated delivery of the intrinsic C-terminus domain of PTEN protects it from proteasomal degradation and ablates tumorigenesis, Mol Ther., 23, 255, 10.1038/mt.2014.202 · DOI
- Wei, 2018, Exosomal transfer of miR-151a enhances chemosensitivity to temozolomide in drug-resistant glioblastoma, Cancer Lett., 436, 10, 10.1016/j.canlet.2018.08.004 · DOI
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MiR-128-3p – a gray eminence of the human central nervous system
Kiel, K., Król, S. K., Bronisz, A., & Godlewski, J. (2024) · Molecular Therapy Nucleic Acids · doi:10.1016/j.omtn.2024.102141 · Cited by 15
Metadata
- Authors
- Wang, Y., Chen, R., Zhou, X., Guo, R., Yin, J., Li, Y., & Ma, G.
- ORCID
- Ma, Guoda
- Venue
- Molecular Therapy Nucleic Acids
- Publisher
- Elsevier BV
- Published
- 2020-09
- Volume
- 21
- Pages
- 614-622
- ISSN
- 2162-2531
- PMC
- PMC7393316
- Cited by
- 40
- References
- 4
- Language
- en
- Licence
- Funders
- National Natural Science Foundation of China (81571157, 81670252, 81770034, 81873649)
- Applied Basic Research Foundation of Yunnan Province (2019A1515011306, 2019A1515011424, 2020A1515010240)
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