Cross talk between microRNA and epigenetic regulation in adult neurogenesis

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860

Untitled work

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

DNA methylation patterns and epigenetic memory

Bird, A. (2002) · Genes & Development · doi:10.1101/gad.947102 · Cited by 7,124

Prediction of Mammalian MicroRNA Targets

Lewis, B. P., Shih, I.-H., Jones-Rhoades, M. W., Bartel, D. P., & Burge, C. B. (2003) · Cell · doi:10.1016/s0092-8674(03)01018-3 · Cited by 5,199

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., & Zoghbi, H. Y. (1999) · Nature Genetics · doi:10.1038/13810 · Cited by 4,990

Combinatorial microRNA target predictions

Krek, A., Grün, D., Poy, M. N., Wolf, R., Rosenberg, L., Epstein, E. J., MacMenamin, P., da Piedade, I., Gunsalus, K. C., Stoffel, M., et al. (2005) · Nature Genetics · doi:10.1038/ng1536 · Cited by 4,603

Core Transcriptional Regulatory Circuitry in Human Embryonic Stem Cells

Boyer, L. A., Lee, T. I., Cole, M. F., Johnstone, S. E., Levine, S. S., Zucker, J. P., Guenther, M. G., Kumar, R. M., Murray, H. L., Jenner, R. G., et al. (2005) · Cell · doi:10.1016/j.cell.2005.08.020 · Cited by 4,505

Human MicroRNA Targets

John, B., Enright, A. J., Aravin, A., Tuschl, T., Sander, C., & Marks, D. S. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020363 · Cited by 3,796

The Transcriptional Landscape of the Mammalian Genome

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

Mechanisms and Functional Implications of Adult Neurogenesis

Zhao, C., Deng, W., & Gage, F. H. (2008) · Cell · doi:10.1016/j.cell.2008.01.033 · Cited by 3,007

Effects of microRNA-181b-5p on cognitive deficits in first-episode patients with schizophrenia: Mediated by BCL-2

Gou, M., Pan, S., Tong, J., Zhou, Y., Han, J., Xie, T., Yu, T. Y., Feng, W., Li, Y., Chen, S., et al. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.02.003 · Cited by 19

Adult Neural Stem Cell Regulation by Small Non-coding RNAs: Physiological Significance and Pathological Implications

Penning, A., Tosoni, G., Abiega, O., Bielefeld, P., Gasperini, C., Tonelli, D. D. P., Fitzsimons, C. P., & Salta, E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.781434 · Cited by 23

L-type calcium channels and neuropsychiatric diseases: Insights into genetic risk variant-associated genomic regulation and impact on brain development

Baker, M. R., Lee, A. S., & Rajadhyaksha, A. M. (2023) · Channels · doi:10.1080/19336950.2023.2176984 · Cited by 21

MicroRNA-Mediated Reprogramming of Somatic Cells into Neural Stem Cells or Neurons

Yang, H., Zhang, L., An, J., Zhang, Q., Liu, C., He, B., & Hao, D. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0115-9 · Cited by 19

Polymorphism in schizophrenia risk gene MIR137 is associated with the posterior cingulate Cortex's activation and functional and structural connectivity in healthy controls

Zhang, Z., Yan, T.-J., Wang, Y., Zhang, Q., Zhao, W., Chen, X., Zhai, J., Chen, M., Du, B., Deng, X., et al. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.03.039 · Cited by 19

MiR-138 promotes the migration of cultured chicken embryonic hypothalamic cells by targeting reelin

Kisliouk, T., & Meiri, N. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.02.020 · Cited by 18

Genome-Wide Supported Risk Variants inMIR137,CACNA1C,CSMD1,DRD2, andGRM3Contribute to Schizophrenia Susceptibility in Pakistani Population

Fatima, A., Farooq, M., Abdullah, U., Tariq, M., Mustafa, T., Iqbal, M., Tommerup, N., & Baig, S. M. (2017) · Psychiatry Investigation · doi:10.4306/pi.2017.14.5.687 · Cited by 18

Cell type-specific and cross-population polygenic risk score analyses of MIR137 gene pathway in schizophrenia

Yao, Y., Guo, W., Zhang, S., Yu, H., Yan, H., Zhang, H., Sanders, A. R., Yue, W., & Duan, J. (2021) · iScience · doi:10.1016/j.isci.2021.102785 · Cited by 17

Diagnostic and mechanistic roles of MicroRNAs in neurodevelopmental & neurodegenerative disorders

Khoodoruth, M. A. S., Khoodoruth, W. N. C., Uroos, M., Alabdulla, M., Khan, Y. S., & Mohammad, F. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106717 · Cited by 21

Regulation of Adult Neurogenesis by Non-coding RNAs: Implications for Substance Use Disorders

Oliver, R. J., & Mandyam, C. D. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00849 · Cited by 18

Proteins in DNA methylation and their role in neural stem cell proliferation and differentiation

Sun, J., Yang, J., Miao, X., Loh, H. H., Pei, D., & Zheng, H. (2021) · Cell Regeneration · doi:10.1186/s13619-020-00070-4 · Cited by 19

Functional implications of hippocampal adult neurogenesis in intellectual disabilities

Pons‐Espinal, M., de Lagrán, M. M., & Dierssen, M. (2013) · Amino Acids · doi:10.1007/s00726-013-1489-x · Cited by 18

Methods of reactivation and reprogramming of neural stem cells for neural repair

Tian, Z., Zhao, Q., Biswas, S., & Deng, W. (2017) · Methods · doi:10.1016/j.ymeth.2017.08.014 · Cited by 18

MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions

Tucci, A., Ciaccio, C., Scuvera, G., Esposito, S., & Milani, D. (2016) · Molecular Cytogenetics · doi:10.1186/s13039-016-0289-x · Cited by 16

miR-137 downregulates c-kit expression in acute myeloid leukemia

Hu, Y., Dong, X., Chu, G., Lai, G., Zhang, B., Wang, L., & Zhao, Y. (2017) · Leukemia Research · doi:10.1016/j.leukres.2017.01.028 · Cited by 16

Exploring the biological role of postzygotic and germinal de novo mutations in ASD

Alonso-González, A., Calaza, M., Amigo, J., González‐Peñas, J., Martínez-Regueiro, R., Fernández‐Prieto, M., Parellada, M., Arango, C., Rodriguez‐Fontenla, C., & Carracedo, Á. (2021) · Scientific Reports · doi:10.1038/s41598-020-79412-w · Cited by 16

Maintenance of Positional Identity of Neural Progenitors in the Embryonic and Postnatal Telencephalon

Delgado, R. N., & Lim, D. A. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00373 · Cited by 18

A role for miR-19 in the migration of adult-born neurons and schizophrenia

Han, J., & Gage, F. H. (2016) · Neurogenesis · doi:10.1080/23262133.2016.1251873 · Cited by 17

RYBP modulates embryonic neurogenesis involving the Notch signaling pathway in a PRC1-independent pattern

Li, Q., Chen, J., Liang, F., Zhang, J., Qu, W., Huang, X., Cheng, X., Zhao, X., Yang, Z.-J., Xu, S., et al. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.10.013 · Cited by 15

microRNA-dependent regulation of gene expression in GABAergic interneurons

Kołosowska, K., Schratt, G. M., & Winterer, J. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1188574 · Cited by 16

Therapeutic potential of NOX inhibitors in neuropsychiatric disorders

Kaur, P., Khan, H., Grewal, A. K., Dua, K., & Singh, T. G. (2023) · Psychopharmacology · doi:10.1007/s00213-023-06424-5 · Cited by 15

Epigenetic regulation in adult neural stem cells

Shi, J., Wang, Z., Wang, Z., Shao, G., & Li, X. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1331074 · Cited by 17

Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants

Kelly, S., Morris, D. W., Mothersill, O., Rose, E. J., Fahey, C., O'Brien, C. L., O’Hanlon, E., Gill, M., Corvin, A. P., & Donohoe, G. J. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.05.002 · Cited by 15

Direct reprogramming of terminally differentiated cells into neurons: A novel and promising strategy for Alzheimer's disease treatment

Yavarpour‐Bali, H., Ghasemi‐Kasman, M., & Shojaei, A. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109820 · Cited by 15

The role of noncoding RNAs and sirtuins in cancer drug resistance

Zahedipour, F., Jamialahmadi, K., & Karimi, G. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173094 · Cited by 15

Alteration of twinfilin1 expression underlies opioid withdrawal-induced remodeling of actin cytoskeleton at synapses and formation of aversive memory

Wang, Y., Yu, C. F., Wu, W.-W., Ju, Y., Liu, Y., Xu, C., Long, J.-D., Zan, G., Wei, X., Zhang, L., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01111-3 · Cited by 15

Effect of propofol on microRNA expression in rat primary embryonic neural stem cells

Fan, J., Zhou, Q., Qin, Z., & Tao, T. (2016) · BMC Anesthesiology · doi:10.1186/s12871-016-0259-1 · Cited by 15

A NOTCH1/LSD1/BMP2 co-regulatory network mediated by miR-137 negatively regulates osteogenesis of human adipose-derived stem cells

Fan, C., Ma, X., Wang, Y., Lv, L., Zhu, Y., Liu, H., & Liu, Y. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02495-3 · Cited by 15

Path from schizophrenia genomics to biology: gene regulation and perturbation in neurons derived from induced pluripotent stem cells and genome editing

Duan, J. (2015) · Neuroscience Bulletin · doi:10.1007/s12264-014-1488-2 · Cited by 14

Can Adult Neural Stem Cells Create New Brains? Plasticity in the Adult Mammalian Neurogenic Niches

Kazanis, I. (2011) · The Neuroscientist · doi:10.1177/1073858410390379 · Cited by 14

The role of hippocampal niche exosomes in rat hippocampal neurogenesis after fimbria–fornix transection

Cheng, X., Li, W., Zhao, R., Li, H., Qin, J., Tian, M., Zhang, X., & Jin, G. (2021) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.015561 · Cited by 13

Lupus nephritis: The regulatory interplay between epigenetic and MicroRNAs

Xu, N., Liu, J., & Li, X. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.925416 · Cited by 13

Mitochondrial regulation of adult hippocampal neurogenesis: Insights into neurological function and neurodevelopmental disorders

Bonzano, S., Dallorto, E., Bovetti, S., Studer, M., & Marchis, S. D. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106604 · Cited by 16

Experimental validation of candidate schizophrenia gene CALN1 as a target for microRNA-137

Xia, S., Zhou, X., Wang, T., Zhang, Q., Li, Q., Liu, Y., Xing, Q., Wang, L., He, L., & Zhao, X. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.07.001 · Cited by 13

Epigenetic modulation during hippocampal development (Review)

Fan, S., Sun, A., & Liu, L. (2018) · Biomedical Reports · doi:10.3892/br.2018.1160 · Cited by 14

Epigenetic mechanisms in Alzheimer's disease

Balázs, R. (2014) · Degenerative Neurological and Neuromuscular Disease · doi:10.2147/dnnd.s37341 · Cited by 15

Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals

Albizzati, E., Florio, E., Miramondi, F., Sormonta, I., Landsberger, N., & Frasca, A. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.823060 · Cited by 12

Epigenetic Regulation of the Hippocampus, with Special Reference to Radiation Exposure

Saw, G., & Tang, F. R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249514 · Cited by 13

NAD+ Modulates the Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells via Akt Signaling Pathway

Huang, X., Guo, H., Cheng, X., Zhang, J., Qu, W., Ding, Q., Sun, Q., Shu, Q., & Li, X. (2022) · Cells · doi:10.3390/cells11081283 · Cited by 12

MicroRNA-650 Regulates the Pathogenesis of Alzheimer’s Disease Through Targeting Cyclin-Dependent Kinase 5

Li, L., Liu, X., Cheng, X., Li, Y., Gearing, M., Levey, A. I., Huang, X., Li, Y., Jin, P., & Li, X. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03224-y · Cited by 12

MicroRNA’s impact on neurotransmitter and neuropeptide systems: small but mighty mediators of anxiety

Martinetz, S. (2016) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-016-1814-9 · Cited by 12

miR-762 regulates the proliferation and differentiation of retinal progenitor cells by targeting NPDC1

Gao, H., Ni, N., Zhang, D., Wang, Y., Tang, Z., Sun, N., Ju, Y., Dai, X., Zhang, Y., Liu, Y., et al. (2020) · Cell Cycle · doi:10.1080/15384101.2020.1777805 · Cited by 12

Epigenetic profiles in polyglutamine disorders

Liu, H., Tang, T.-S., & Guo, C. (2017) · Epigenomics · doi:10.2217/epi-2017-0089 · Cited by 12

Xenogenic Neural Stem Cell‐Derived Extracellular Nanovesicles Modulate Human Mesenchymal Stem Cell Fate and Reconstruct Metabolomic Structure

Derkuş, B., Işık, M., Eylem, C. C., Ergin, İ., Camci, C. B., Bilgin, S., Elbüken, Ç., Arslan, Y. E., Akkulak, M., Adalı, O., et al. (2022) · Advanced Biology · doi:10.1002/adbi.202101317 · Cited by 12

Bromodomain-Containing Protein 9 Regulates Signaling Pathways and Reprograms the Epigenome in Immortalized Human Uterine Fibroid Cells

Yang, Q., Vafaei, S., Falahati, A., Khosh, A., Bariani, M. V., Omran, M. M., Bai, T., Siblini, H., Ali, M. K., He, C., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020905 · Cited by 11

Neural stem cell heterogeneity in adult hippocampus

Liang, Z., Jin, N., & Guo, W. (2025) · Cell Regeneration · doi:10.1186/s13619-025-00222-4 · Cited by 12

‘Traffic light rules’: Chromatin states direct miRNA-mediated network motifs running by integrating epigenome and regulatome

Zhao, H., Zhang, G., Pang, L., Lan, Y., Wang, L., Yu, F., Hu, J. R., Li, F., Zhao, T., Xiao, Y., et al. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.04.008 · Cited by 11

Impact of Gestational Haloperidol Exposure on miR-137-3p and Nr3c1 mRNA Expression in Hippocampus of Offspring Mice

Yoshino, Y., Kumon, H., Shimokawa, T., Yano, H., Ochi, S., Funahashi, Y., Iga, J., Matsuda, S., Tanaka, J., & Ueno, S. (2022) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyac044 · Cited by 11

MeCP2 Caught Moonlighting as a Suppressor of MicroRNA Processing

Woo, J., & Kim, V. N. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.02.015 · Cited by 11

Noncoding RNA in the transcriptional landscape of human neural progenitor cell differentiation

Hecht, P. M., Ballesteros‐Yáñez, I., Grepo, N., Knowles, J. A., & Campbell, D. B. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00392 · Cited by 11

Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma

Brečević, L., Rinčić, M., Krsnik, Ž., Sedmak, G., Hamid, A. B., Kosyakova, N., Galić, I., Liehr, T., & Borovečki, F. (2015) · Translational Neuroscience · doi:10.1515/tnsci-2015-0007 · Cited by 11

Prevention of transgenerational transmission of disease susceptibility through perinatal intervention

Nemoto, T., & Sagawa, N. (2023) · Endocrine Journal · doi:10.1507/endocrj.ej23-0381 · Cited by 11

Outline of Epigenetics

Paul, B., & Tollefsbol, T. O. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-417114-5.00002-4 · Cited by 10

The Multifarious Hippocampal Functions of MicroRNA-137

Kos, A., Aschrafi, A., & Kasri, N. N. (2015) · The Neuroscientist · doi:10.1177/1073858415608356 · Cited by 10

Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 14–18, 2012

Anderson‐Schmidt, H., Beltcheva, O., Brandon, M. D., Byrne, E. M., Chater‐Diehl, E., Duncan, L. E., Gonzalez, S., Hannon, E. J., Kantojärvi, K., Karagiannidis, I., et al. (2013) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32132 · Cited by 9

MiR-3099 is Overexpressed in Differentiating 46c Mouse Embryonic Stem Cells upon Neural Induction.

Abidin, S. Z., Abbaspourbabaei, M., Ntimi, C. M., Siew, W.-H., Pike-See, C., Rosli, R., Nordin, N., & Ling, K. (2014) · Europe PMC (PubMed Central) · Cited by 10

Evaluating Neurotrophin Signaling Using MicroRNA Perilymph Profiling in Cochlear Implant Patients With and Without Residual Hearing

Shew, M. A., Wichova, H., Warnecke, A., Lenarz, T., & Staecker, H. (2021) · Otology & Neurotology · doi:10.1097/mao.0000000000003182 · Cited by 10

Mina53 demethylates histone H4 arginine 3 asymmetric dimethylation to regulate neural stem/progenitor cell identity

Zhou, L., Zhao, X., Sun, J., Zou, K., Huang, X., Yu, L., Wu, M.-X., Wang, Y., Li, X.-K., & Yi, W. (2024) · Nature Communications · doi:10.1038/s41467-024-54680-6 · Cited by 9

Cellular senescence, neuroinflammation, and microRNAs: Possible interactions driving aging and neurodegeneration in the hippocampal neurogenic niche

Polzer, O., Kinloch, E., & Fitzsimons, C. P. (2025) · Aging Brain · doi:10.1016/j.nbas.2025.100141 · Cited by 10

High-Throughput Sequencing-Based Mapping of Cytosine Modifications

Bernstein, A. I., & Jin, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801080-8.00003-x · Cited by 9

Loss of MicroRNA-137 Impairs the Homeostasis of Potassium in Neurons via KCC2

Mi, T., Sun, X., Wang, Z., Wang, Y., He, X., Liu, C., Zhang, S.-F., Du, H., Liu, C.-M., & Teng, Z. (2020) · Experimental Neurobiology · doi:10.5607/en19072 · Cited by 9

No association between the rs10503253 polymorphism in the CSMD1 gene and schizophrenia in a Han Chinese population

Liu, Y., Cheng, Z., Wang, J., Jin, C., Yuan, J., Wang, G., Zhang, F., & Zhao, X. (2016) · BMC Psychiatry · doi:10.1186/s12888-016-0923-5 · Cited by 9

Crosstalk between MicroRNAs and Autophagy in Adult Neurogenesis: Implications for Neurodegenerative Disorders

Pircs, K., Petri, R., & Jakobsson, J. (2017) · Brain Plasticity · doi:10.3233/bpl-180066 · Cited by 8

Information Processes

Knoflacher, M. (2024) · Springer eBooks · doi:10.1007/978-3-662-69423-7_6 · Cited by 9

Rbm24/Notch1 signaling regulates adult neurogenesis in the subventricular zone and mediates Parkinson-associated olfactory dysfunction

Wang, K., Liu, X., Liu, S.-F., Wang, X., Wei, Y.-H., Zhu, J., Liu, J., Xu, X. Q., & Wen, L. (2024) · Theranostics · doi:10.7150/thno.96045 · Cited by 9

It takes two to tango: Widening our understanding of the onset of schizophrenia from a neuro-angiogenic perspective

Casas, B. S., Arancibia‐Altamirano, D., Rosa, F. A.-L., Garrido-Jara, D., Maksaev, V., Pérez-Monje, D., & Palma, V. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.946706 · Cited by 9

The Role of miR-137 in Neurodegenerative Disorders

Bodai, L., Borosta, R., Ferencz, Á., Kovács, M., & Zsindely, N. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137229 · Cited by 11

Dendrites in Autism Spectrum Disorders

Martínez‐Cerdeño, V., Maezawa, I., & Jin, L. (2016) · Springer eBooks · doi:10.1007/978-4-431-56050-0_20 · Cited by 8

Heterogeneity of Stem Cells in the Hippocampus

Tosun, M., Semerci, F., & Maletić‐Savatić, M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-24108-7_2 · Cited by 9

miR-17 regulates the proliferation and differentiation of retinal progenitor cells by targeting CHMP1A

Sun, N., Zhang, D., Ni, N., Tang, Z., Gao, H., Ju, Y., Dai, X., Wang, J., Gu, P., & Ji, J. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.11.108 · Cited by 8

MeCP2 loss‐of‐function dysregulates microRNAs regionally and disrupts excitatory/inhibitory synaptic transmission balance

Horvath, P. M., Piazza, M. K., Kavalali, E. T., & Monteggia, L. M. (2022) · Hippocampus · doi:10.1002/hipo.23455 · Cited by 10

Comparison of miRNA transcriptome of exosomes in three categories of somatic cells with derived iPSCs

Yu, C., Zhang, M., Xiong, Y., Wang, Q., Wang, Y., Wu, S.-L., Hussain, S., Wang, Y., Zhang, Z., Rao, N., et al. (2023) · Scientific Data · doi:10.1038/s41597-023-02493-5 · Cited by 7

Inhibition of epigenetic regulator UHRF1 attenuates renal fibrosis and retains transcription factor Krüppel-like factor 15 expression

Gu, Y., Lv, S., Huang, X., Wang, J., Wang, Y., Zhang, H., Shen, Z., Chen, J., Zhu, C. G., Zhang, D., et al. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02549-y · Cited by 7

Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states

González‐Peñas, J., Amigo, J., Santomé, L., Sobrino, B., Brenlla, J., Agra, S., Paz, E., Páramo, M., Carracedo, Á., Arrojo, M., et al. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.03.029 · Cited by 7

Rs1625579 polymorphism in the MIR137 gene is associated with the risk of schizophrenia: updated meta-analysis

Liu, Y.-P., Meng, J.-H., Wu, X., Xu, F., Xia, X., Zhang, X., Liu, Y., Yao, J., & Wang, B. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134535 · Cited by 7

miR-17∼92 exerts stage-specific effects in adult V-SVZ neural stem cell lineages

Favaloro, F., DeLeo, A. M., Delgado, A. C., & Doetsch, F. K. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111773 · Cited by 7

3D genome-selected microRNAs to improve Alzheimer's disease prediction

Li, K., Chi, R., Liu, L., Feng, M., Su, K., Li, X., He, G., & Shi, Y. Y. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1059492 · Cited by 7

Site-blocking antisense oligonucleotides as a mechanism to fine-tune MeCP2 expression

Vanderplow, A. M., Dodis, G. E., Rhee, Y., Cikowski, J., Gonzalez, S., Smith, M. L., & Gogliotti, R. G. (2024) · RNA · doi:10.1261/rna.080220.124 · Cited by 6

MicroRNA-mediated regulation of proliferation, lineage differentiation, and apoptosis in neural stem cells

Lee, Y., Boschian, C., & Ko, K. (2025) · RNA Biology · doi:10.1080/15476286.2025.2558631 · Cited by 7

MeCP2 regulates telencephalic development in human cerebral organoids

Tenreiro, M. F., Mohana-Borges, R., Sánchez-Sánchez, S. M., Dias, Â. R. M., Blanch, R., & Muotri, A. R. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116670 · Cited by 8

Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy

Castells, A. A., Balada, R., Tristán‐Noguero, A., O’Callaghan, M., Cortès‐Saladelafont, E., Pascual‐Alonso, A., García‐Cazorla, À., Armstrong, J., & Alcántara, S. (2021) · Biomedicines · doi:10.3390/biomedicines9020148 · Cited by 6

The potential role of miRNAs in the pathogenesis of schizophrenia – A focus on signaling pathways interplay

Zaki, M. B., Abulsoud, A. I., Ashraf, A., Abdelmaksoud, N. M., Sallam, A.-A. M., Aly, S. H., El-Tokhy, F. S., Rashad, A. A., El‐Dakroury, W. A., Mageed, S. S. A., et al. (2024) · Pathology - Research and Practice · doi:10.1016/j.prp.2024.155102 · Cited by 6

The Genetics of Schizophrenia

Samson, J. N., & Wong, A. H. C. (2015) · Royal Society of Chemistry eBooks · doi:10.1039/9781782622499-00001 · Cited by 6

MicroRNA-Based Separation of Cortico-Fugal Projection Neuron-Like Cells Derived From Embryonic Stem Cells

Sunohara, T., Morizane, A., Matsuura, S., Miyamoto, S., Saito, H., & Takahashi, J. B. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01141 · Cited by 6

Distinct Mirna Expression Patterns of Extracellular Vesicles Derived From 4 Types of Mesenchymal Stem Cells

Zhou, Y., Yamamoto, Y., Ochiya, T., Xiao, Z., & Itaya, T. (2018) · Journal of Stem Cell Research & Therapy · doi:10.4172/2157-7633.1000415 · Cited by 6

miR-137 regulates PTP61F, affecting insulin signaling, metabolic homeostasis, and starvation resistance in Drosophila

Saedi, H., Waro, G., Giacchetta, L., & Tsunoda, S. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2319475121 · Cited by 5

The exo‐microRNA (miRNA) signaling pathways in pathogenesis and treatment of stroke diseases: Emphasize on mesenchymal stem cells (MSCs)

Farahmand, Y., Nabiuni, M., Mastanabad, M. V., Sheibani, M., Mahmood, B. S., Obayes, A. M., Asadi, F., & Davallou, R. (2024) · Cell Biochemistry and Function · doi:10.1002/cbf.3917 · Cited by 5

Generation and transcriptomic characterization of MIR137 knockout miniature pig model for neurodevelopmental disorders

Xu, S., Wang, J., Mao, K., Jiao, D., Zhu, L., Zhao, H., Sun, Y., Feng, J., Lai, Y., Peng, R., et al. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01268-8 · Cited by 5

The relevance of polycomb group proteins to the development of psychiatric disorders

Peedicayil, J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.927833 · Cited by 5

Regulatory networks between Polycomb complexes and non-coding RNAs in the central nervous system

Xu, Y., Liu, P., Shyh‐Chang, N., Teng, Z., & Liu, C. (2019) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjz058 · Cited by 5

Transcription Factors of Direct Neuronal Reprogramming in Ontogenesis and Ex Vivo

Samoilova, E. M., Викторович, Б. В., & Baklaushev, V. P. (2021) · Molecular Biology · doi:10.1134/s0026893321040087 · Cited by 5

Epigenetics: major regulators of embryonic neurogenesis

Shen, T., Ji, F., & Jiao, J. (2015) · 中国科学通报：英文版 · doi:10.1007/s11434-015-0871-3 · Cited by 4

Brain, Behavior and the Journey Towards Neuroepigenetic Therapeutics

Wani, A. L., & Shadab, G. G. H. A. (2019) · Epigenomics · doi:10.2217/epi-2018-0014 · Cited by 4

Транскрипционные факторы прямого пронейронального репрограммирования в онтогенезе и ex vivo

Samoilova, E. M., Викторович, Б. В., & Baklaushev, V. P. (2021) · Molecular Biology · doi:10.31857/s0026898421050086 · Cited by 4

Stress response abnormalities transgenerationally inherited via miR-23 downregulation are restored by a methyl modulator during the lactation period

Nemoto, T., Morita, Y., & Kakinuma, Y. (2023) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174423000363 · Cited by 4

Autismo y epigenética: Un modelo de explicación para la comprensión de la génesis en los trastornos del espectro autista

Arberas, C. L., & Ruggieri, V. L. (2013) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 4

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. (2017) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.09.595 · Cited by 3

Two Thalamic Regions Screened Using Laser Capture Microdissection with Whole Human Genome Microarray in Schizophrenia Postmortem Samples

Bakshi, K. P., & Kemether, E. M. (2020) · Schizophrenia Research and Treatment · doi:10.1155/2020/5176834 · Cited by 4

A miR-137-related biological pathway of risk for Schizophrenia is associated with human brain emotion processingPreprint

Pergola, G., Rampino, A., Carlo, P. D., Marakhovskaia, A., Quarto, T., Fazio, L., Papalino, M., Torretta, S., Amoroso, N., Castro, M. N., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.03.230227 · Cited by 4

Prediction of Alzheimer's Disease Based on 3D Genome Selected circRNA

Chi, R., Li, K.-C., Su, K., Liu, L., Feng, M., Zhang, X., Wang, J., Li, X., He, G. Q., & Shi, Y. (2024) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2024.52 · Cited by 3

JCB: Article 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. (2013)

MicroRNAs and Epigenetics in Adult Neurogenesis

Wakabayashi, T., Hidaka, R., Fujimaki, S., Asashima, M., & Kuwabara, T. (2014) · Advances in genetics · doi:10.1016/b978-0-12-800222-3.00002-4 · Cited by 51

Role of miRNAs and epigenetics in neural stem cell fate determination

Lopez‐Ramirez, M. A., & Nicoli, S. (2013) · Epigenetics · doi:10.4161/epi.27536 · Cited by 48

Crosstalk between microRNA and Epigenetic Regulation in Stem Cells

Szulwach, K. E., Chang, S., & Jin, P. (2009) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-04298-0_7

An epigenetic feedback regulatory loop involving microRNA-195 and MBD1 governs neural stem cell differentiation. PLoS One 2013

Liu, C., Teng, Z.-Q., Mcquate, A. L., Christ, C. C., Von, S. J., Reyes, M. D., Polich, E. D., Xing, Y., Li, Y., Guo, W., et al. (2016)