Dicer1 and miR-219 Are Required for Normal Oligodendrocyte Differentiation and Myelination
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
These miRs play important roles during myelination.
“In these studies, over-expression of miR-219-5p, miR-338-5p, and miR-338-3p was shown to promote rodent OPC differentiation, indicating that these miRs play important roles during myelination (Lau et al., 2008; Budde et al., 2010; Dugas et al., 2010).”
From Regulation of miRNA 219 and miRNA Clusters 338 and 17-92 in Oligodendrocytes (2012) · cites this paper as Dugas et al., 2010
Over-expression of miR-219-5p, miR-338-5p, and miR-338-3p promotes rodent OPC differentiation.
“In these studies, over-expression of miR-219-5p, miR-338-5p, and miR-338-3p was shown to promote rodent OPC differentiation, indicating that these miRs play important roles during myelination (Lau et al., 2008; Budde et al., 2010; Dugas et al., 2010).”
From Regulation of miRNA 219 and miRNA Clusters 338 and 17-92 in Oligodendrocytes (2012) · cites this paper as Dugas et al., 2010
The miR-338 cluster is expressed in human OLs.
“In summary, we provide the first evidence that miR-338 cluster is expressed in human OLs, as previously demonstrated in rodents (Lau et al., 2008; Dugas et al., 2010; Zhao et al., 2010).”
From Regulation of miRNA 219 and miRNA Clusters 338 and 17-92 in Oligodendrocytes (2012) · cites this paper as Dugas et al., 2010
Expression profiling studies with rodent OLs have reported that several miR species are dramatically regulated during OPC differentiation.
“Expression profiling studies with rodent OLs have reported that several miR species are dramatically regulated during OPC differentiation (Lau et al., 2008; Budde et al., 2010; Dugas et al., 2010).”
From Regulation of miRNA 219 and miRNA Clusters 338 and 17-92 in Oligodendrocytes (2012) · cites this paper as Dugas et al., 2010
Disruptions in miRNA networks involving miR-219-5p, miR-338-5p, and miR-23a/b destabilize myelin maintenance, axonal metabolic support, and cytoskeletal integrity, contributing to early cognitive decline and impaired signal transmission in AD.
“The combined actions of miR-219-5p, miR-338-5p, and miR-23a/b highlight how disruptions in miRNA networks destabilize myelin maintenance, axonal metabolic support, and cytoskeletal integrity, contributing to early cognitive decline and impaired signal transmission in AD (Absalon et al., 2013; Dugas et al., 2010; Li et al., 2018; Lin et al., 2013; Qian et al., 2018).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Dugas et al., 2010
miR-219-5p is the most consistently validated oligodendrocyte-enriched miRNA required for OPC differentiation and expression of mature myelin genes.
“Furthermore, miR-219-5p is the most consistently validated oligodendrocyte-enriched miRNA required for OPC differentiation and expression of mature myelin genes (Dugas et al., 2010).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Dugas et al., 2010
Because miR-219-5p is required for oligodendrocyte maturation and expression of major myelin proteins, its loss impairs myelin maintenance and axonal support while simultaneously promoting tau pathology through de-repression of these kinases.
“Because miR-219-5p is required for oligodendrocyte maturation and expression of major myelin proteins, its loss impairs myelin maintenance and axonal support while simultaneously promoting tau pathology through de-repression of these kinases (Dugas et al., 2010; Li et al., 2018).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Dugas et al., 2010
Restoring miR-219-5p enhances OL differentiation, preserves myelin integrity, and improves cognitive function.
“Restoring miR-219-5p enhances OL differentiation, preserves myelin integrity, and improves cognitive function (Dugas et al., 2010; Li et al., 2018).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Dugas et al., 2010
Oligodendrocyte miRNAs, most prominently miR-219-5p and miR-338-5p, bridge myelin maintenance, OPC maturation, and tau-kinase or APP/BACE1 regulation, linking white-matter degeneration to classical AD pathology.
“Oligodendrocyte miRNAs, most prominently miR-219-5p and miR-338-5p, bridge myelin maintenance, OPC maturation, and tau-kinase or APP/BACE1 regulation, linking white-matter degeneration to classical AD pathology (Dugas et al., 2010; Li et al., 2018; Qian et al., 2018).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Dugas et al., 2010
miR-219 and miR-338 are preferentially and abundantly expressed in mature oligodendrocytes.
“Among them, miR-219 and miR-338 are preferentially and abundantly expressed in mature OLs (Dugas et al., 2010; Lau et al., 2008; Zhao et al., 2010).”
From miR-219 Cooperates with miR-338 in Myelination and Promotes Myelin Repair in the CNS (2017) · cites this paper as Dugas et al., 2010
In vitro culture studies suggest miR-219 is critical for OPC differentiation and acts through suppressing expression of OL differentiation inhibitors, including PDGFRα, Sox6, and Zfp238.
“In vitro culture studies suggest that miR-219 is critical for OPC differentiation and acts through suppressing expression of OL differentiation inhibitors, including PDGFRα, Sox6, and Zfp238, predicted by computational algorithms (Dugas et al., 2010; Zhao et al., 2010);”
From miR-219 Cooperates with miR-338 in Myelination and Promotes Myelin Repair in the CNS (2017) · cites this paper as Dugas et al., 2010
miR-219 is mainly expressed in differentiated OL during development and adulthood.
“miR-219 is mainly expressed in differentiated OL during development and adulthood (Dugas et al., 2010; Zhao et al., 2010)”
From miR-219 Cooperates with miR-338 in Myelination and Promotes Myelin Repair in the CNS (2017) · cites this paper as Dugas et al., 2010
PDGFRα is a miR-219 target.
“a miR-219 target PDGFRα (Dugas et al., 2010; Zhao et al., 2010)”
From miR-219 Cooperates with miR-338 in Myelination and Promotes Myelin Repair in the CNS (2017) · cites this paper as Dugas et al., 2010
miR-338-3p induces maturation and differentiation of spinal cord oligodendrocyte precursors by repressing Sox5 and Hes6.
“MiR-338-3p is also expressed in spinal cord oligodendrocytes, where it exerts a related effect, inducing maturation and differentiation of precursors into mature oligodendrocytes by repressing Sox5 and Hes6, two maturation-inhibiting transcription factors [31, 32].”
From MiR-338-3p regulates neuronal maturation and suppresses glioblastoma proliferation. (2017) · cites this paper as [31]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
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 · see citing works
A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing
Landgraf, P., Rusu, M., Sheridan, R., Sewer, A., Iovino, N., Aravin, A., Pfeffer, S., Rice, A., Kamphorst, A. O., Landthaler, M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.04.040 · Cited by 3,626 · see citing works
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129 · see citing works
Self-citationThe bHLH Transcription Factors OLIG2 and OLIG1 Couple Neuronal and Glial Subtype Specification
Zhou, Q., & Anderson, D. J. (2002) · Cell · doi:10.1016/s0092-8674(02)00677-3 · Cited by 1,059 · see citing works
Identification of Dynamically Regulated MicroRNA and mRNA Networks in Developing Oligodendrocytes
Lau, P., Verrier, J. D., Nielsen, J. A., Johnson, K. R., Notterpek, L., & Hudson, L. D. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1932-08.2008 · Cited by 252 · see citing works
Flagged first, then by citations
Research works printed but not linked: 56
- Aoki K Meng G Suzuki K Takashi T Kameoka Y Nakahara K Ishida R Kasai M 1998 RP58 associates with condensed chromatin and mediates a sequence-specific transcriptional repression J Biol Chem 273 26698 26704 9756912
- Assanah M Lochhead R Ogden A Bruce J Goldman J Canoll P 2006 Glial progenitors in adult white matter are driven to form malignant gliomas by platelet-derived growth factor-expressing retroviruses J Neurosci 26 6781 6790 16793885 PMC6673823
- Assanah MC Bruce JN Suzuki SO Chen A Goldman JE Canoll P 2009 PDGF stimulates the massive expansion of glial progenitors in the neonatal forebrain Glia 19533602
- Barres BA Lazar MA Raff MC 1994a A novel role for thyroid hormone, glucocorticoids and retinoic acid in timing oligodendrocyte development Development 120 1097 1108 8026323
- Barres BA Raff MC 1994 Control of oligodendrocyte number in the developing rat optic nerve Neuron 12 935 942 8185952
- Barres BA Schmid R Sendnter M Raff MC 1993 Multiple extracellular signals are required for long-term oligodendrocyte survival Development 118 283 295 8375338
- Bartel DP 2004 MicroRNAs: genomics, biogenesis, mechanism, and function Cell 116 281 297 14744438
- Bartel DP 2009 MicroRNAs: target recognition and regulatory functions Cell 136 215 233 19167326 PMC3794896
- Baumann N Pham-Dinh D 2001 Biology of oligodendrocyte and myelin in the mammalian central nervous system Physiol Rev 81 871 927 11274346
- Bernstein E Kim SY Carmell MA Murchison EP Alcorn H Li MZ Mills AA Elledge SJ Anderson KV Hannon GJ 2003 Dicer is essential for mouse development Nat Genet 35 215 217 14528307
- Besnard F Perraud F Sensenbrenner M Labourdette G 1987 Platelet-derived growth factor is a mitogen for glial but not for neuronal rat brain cells in vitro Neurosci Lett 73 287 292 3561869
- Buttitta LA Edgar BA 2007 Mechanisms controlling cell cycle exit upon terminal differentiation Curr Opin Cell Biol 19 697 704 18035529 PMC2700000
- Calver AR Hall AC Yu WP Walsh FS Heath JK Betsholtz C Richardson WD 1998 Oligodendrocyte population dynamics and the role of PDGF in vivo Neuron 20 869 882 9620692
- Carleton M Cleary MA Linsley PS 2007 MicroRNAs and cell cycle regulation Cell cycle (Georgetown, Tex 6 2127 2132 17786041
- Casaccia-Bonnefil P Liu A 2003 Relationship between cell cycle molecules and onset of oligodendrocyte differentiation Journal of neuroscience research 72 1 11 12645074
- Chen Y Stevens B Chang J Milbrandt J Barres BA Hell JW 2008 NS21: re-defined and modified supplement B27 for neuronal cultures J Neurosci Methods 171 239 247 18471889 PMC2678682
- Cheng HY Papp JW Varlamova O Dziema H Russell B Curfman JP Nakazawa T Shimizu K Okamura H Impey S Obrietan K 2007 microRNA modulation of circadian-clock period and entrainment Neuron 54 813 829 17553428 PMC2590749
- Cuellar TL Davis TH Nelson PT Loeb GB Harfe BD Ullian E McManus MT 2008 Dicer loss in striatal neurons produces behavioral and neuroanatomical phenotypes in the absence of neurodegeneration Proc Natl Acad Sci U S A 105 5614 5619 18385371 PMC2291142
- Davis TH Cuellar TL Koch SM Barker AJ Harfe BD McManus MT Ullian EM 2008 Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus J Neurosci 28 4322 4330 18434510 PMC3844796
- Dugas JC Tai YC Speed TP Ngai J Barres BA 2006 Functional Genomic Analysis of Oligodendrocyte Differentiation J Neurosci 26 10967 10983 17065439 PMC6674672
- Durand B Raff M 2000 A cell-intrinsic timer that operates during oligodendrocyte development Bioessays 22 64 71 10649292
- Emery B Agalliu D Cahoy JD Watkins TA Dugas JC Mulinyawe SB Ibrahim A Ligon KL Rowitch DH Barres BA 2009 Identification of Myelin-gene Regulatory Factor as a Critical Transcriptional Regulator Required for CNS Myelination Cell In Press PMC2757090 19596243
- Ferretti E De Smaele E Po A Di Marcotullio L Tosi E Espinola MS Di Rocco C Riccardi R Giangaspero F Farcomeni A 2009 MicroRNA profiling in human medulloblastoma Int J Cancer 124 568 577 18973228
- Georges SA Biery MC Kim SY Schelter JM Guo J Chang AN Jackson AL Carleton MO Linsley PS Cleary MA Chau BN 2008 Coordinated regulation of cell cycle transcripts by p53-Inducible microRNAs, miR-192 and miR-215 Cancer research 68 10105 10112 19074876
- Harfe BD McManus MT Mansfield JH Hornstein E Tabin CJ 2005 The RNaseIII enzyme Dicer is required for morphogenesis but not patterning of the vertebrate limb Proc Natl Acad Sci U S A 102 10898 10903 16040801 PMC1182454
- Izzotti A Calin GA Arrigo P Steele VE Croce CM De Flora S 2009 Downregulation of microRNA expression in the lungs of rats exposed to cigarette smoke FASEB J 23 806 812 18952709 PMC2653990
- Kim J Krichevsky A Grad Y Hayes GD Kosik KS Church GM Ruvkun G 2004 Identification of many microRNAs that copurify with polyribosomes in mammalian neurons Proc Natl Acad Sci U S A 101 360 365 14691248 PMC314190
- Kitzmann M Fernandez A 2001 Crosstalk between cell cycle regulators and the myogenic factor MyoD in skeletal myoblasts Cell Mol Life Sci 58 571 579 11361092 PMC11146557
- Kocerha J Faghihi MA Lopez-Toledano MA Huang J Ramsey AJ Caron MG Sales N Willoughby D Elmen J Hansen HF 2009 MicroRNA-219 modulates NMDA receptor-mediated neurobehavioral dysfunction Proc Natl Acad Sci U S A 106 3507 3512 19196972 PMC2651305
- Landgren H Carlsson P 2004 FoxJ3, a novel mammalian forkhead gene expressed in neuroectoderm, neural crest, and myotome Dev Dyn 231 396 401 15366017
- Lang D Powell SK Plummer RS Young KP Ruggeri BA 2007 PAX genes: roles in development, pathophysiology, and cancer Biochem Pharmacol 73 1 14 16904651
- Lappe-Siefke C Goebbels S Gravel M Nicksch E Lee J Braun PE Griffiths IR Nave KA 2003 Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination Nat Genet 33 366 374 12590258
- Lynn FC Skewes-Cox P Kosaka Y McManus MT Harfe BD German MS 2007 MicroRNA expression is required for pancreatic islet cell genesis in the mouse Diabetes 56 2938 2945 17804764
- Matthieu JM Costantino-Ceccarini E Beny M Reigner J 1980 Evidence for the association of 2′,3′-cyclic-nucleotide 3′-phosphodiesterase with myelin-related membranes in peripheral nervous system J Neurochem 35 1345 1350 6255099
- Okado H Ohtaka-Maruyama C Sugitani Y Fukuda Y Ishida R Hirai S Miwa A Takahashi A Aoki K Mochida K 2009 The transcriptional repressor RP58 is crucial for cell-division patterning and neuronal survival in the developing cortex Dev Biol 19409883
- Politis PK Thomaidou D Matsas R 2008 Coordination of cell cycle exit and differentiation of neuronal progenitors Cell Cycle 7 691 697 18239460
- Raff MC Durand B Gao FB 1998 Cell number control and timing in animal development: the oligodendrocyte cell lineage Int J Dev Biol 42 263 267 9654007
- Raff MC Miller RH Noble M 1983 A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium Nature 303 390 396 6304520
- Ruby JG Stark A Johnston WK Kellis M Bartel DP Lai EC 2007 Evolution, biogenesis, expression, and target predictions of a substantially expanded set of Drosophila microRNAs Genome Res 17 1850 1864 17989254 PMC2099593
- Schuller U Heine VM Mao J Kho AT Dillon AK Han YG Huillard E Sun T Ligon AH Qian Y 2008 Acquisition of granule neuron precursor identity is a critical determinant of progenitor cell competence to form Shh-induced medulloblastoma Cancer Cell 14 123 134 18691547 PMC2597270
- Shi L Cheng Z Zhang J Li R Zhao P Fu Z You Y 2008 hsa-mir-181a and hsa-mir-181b function as tumor suppressors in human glioma cells Brain Res 1236 185 193 18710654
- Stolt CC Schlierf A Lommes P Hillgartner S Werner T Kosian T Sock E Kessaris N Richardson WD Lefebvre V Wegner M 2006 SoxD proteins influence multiple stages of oligodendrocyte development and modulate SoxE protein function Dev Cell 11 697 709 17084361
- Takebayashi H Yoshida S Sugimori M Kosako H Kominami R Nakafuku M Nabeshima Y 2000 Dynamic expression of basic helix-loop-helix Olig family members: implication of Olig2 in neuron and oligodendrocyte differentiation and identification of a new member, Olig3 Mech Dev 99 143 148 11091082
- Temple S Raff MC 1985 Differentiation of a bipotential glial progenitor cell in a single cell microculture Nature 313 223 225 3969137
- Temple S Raff MC 1986 Clonal analysis of oligodendrocyte development in culture: evidence for a developmental clock that counts cell divisions Cell 44 773 779 3948247
- Tokumoto YM Tang DG Raff MC 2001 Two molecularly distinct intracellular pathways to oligodendrocyte differentiation: role of a p53 family protein Embo J 20 5261 5268 11566889 PMC125631
- Truong AB Khavari PA 2007 Control of keratinocyte proliferation and differentiation by p63 Cell Cycle 6 295 299 17264679
- Uhrbom L Hesselager G Ostman A Nister M Westermark B 2000 Dependence of autocrine growth factor stimulation in platelet-derived growth factor-B-induced mouse brain tumor cells Int J Cancer 85 398 406 10652433
- Wang S Sdrulla A Johnson JE Yokota Y Barres BA 2001 A role for the helix-loop-helix protein Id2 in the control of oligodendrocyte development Neuron 29 603 614 11301021
- Watkins TA Emery B Mulinyawe S Barres BA 2008 Distinct stages of myelination regulated by gamma-secretase and astrocytes in a rapidly myelinating CNS coculture system Neuron 60 555 569 19038214 PMC2650711
- Wettenhall JM Smyth GK 2004 limmaGUI: a graphical user interface for linear modeling of microarray data Bioinformatics 20 3705 3706 15297296
- Wienholds E Kloosterman WP Miska E Alvarez-Saavedra E Berezikov E de Bruijn E Horvitz HR Kauppinen S Plasterk RH 2005 MicroRNA expression in zebrafish embryonic development Science 309 310 311 15919954
- Wong TS Liu XB Wong BY Ng RW Yuen AP Wei WI 2008 Mature miR-184 as Potential Oncogenic microRNA of Squamous Cell Carcinoma of Tongue Clin Cancer Res 14 2588 2592 18451220
- Wu L Belasco JG 2008 Let me count the ways: mechanisms of gene regulation by miRNAs and siRNAs Mol Cell 29 1 7 18206964
- Yuan X Chittajallu R Belachew S Anderson S McBain CJ Gallo V 2002 Expression of the green fluorescent protein in the oligodendrocyte lineage: a transgenic mouse for developmental and physiological studies J Neurosci Res 70 529 545 12404507
- Zhou Q Wang S Anderson DJ 2000 Identification of a novel family of oligodendrocyte lineage-specific basic helix-loop-helix transcription factors Neuron 25 331 343 10719889
Cited by
Sorted by citations
Extracellular vesicles round off communication in the nervous system
Budnik, V., Ruiz-Cañada, C., & Wendler, F. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.29 · Cited by 712 · see citing works
Regulation of oligodendrocyte differentiation and myelination
Emery, B. (2010) · Science · doi:10.1126/science.1190927 · Cited by 653 · see citing works
Self-citationNeural tissue engineering options for peripheral nerve regeneration
Gu, X., Ding, F., & Williams, D. F. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.04.064 · Cited by 630 · see citing works
Olig2 Targets Chromatin Remodelers to Enhancers to Initiate Oligodendrocyte Differentiation
Yu, Y., Chen, Y., Kim, B., Wang, H., Zhao, C., He, X., Liu, L., Liu, W., Wu, L. M. N., Mao, M., et al. (2013) · Cell · doi:10.1016/j.cell.2012.12.006 · Cited by 375 · see citing works
Brain injury in premature neonates: A primary cerebral dysmaturation disorder?
Back, S. A., & Miller, S. P. (2014) · Annals of Neurology · doi:10.1002/ana.24132 · Cited by 360 · see citing works
Central nervous system myelin: structure, synthesis and assembly
Aggarwal, S., Yurlova, L., & Simons, M. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.06.004 · Cited by 301 · see citing works
MicroRNAs in resolution of acute inflammation: identification of novel resolvin Dl‐miRNA circuits
Recchiuti, A., Krishnamoorthy, S., Fredman, G., Chiang, N., & Serhan, C. N. (2011) · The FASEB Journal · doi:10.1096/fj.10-169599 · Cited by 292 · see citing works
Transcriptional Convergence of Oligodendrocyte Lineage Progenitors during Development
Marques, S., van Bruggen, D., Vanichkina, D. P., Floriddia, E. M., Munguba, H., Väremo, L., Giacomello, S., Falcão, A. M., Meijer, M., Björklund, Å. K., et al. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.07.005 · Cited by 290 · see citing works
microRNA as Repressors of Stress-Induced Anxiety: The Case of Amygdalar miR-34
Haramati, S., Navon, I., Issler, O., Ezra-Nevo, G., Gil, S., Zwang, R., Hornstein, E., & Chen, A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.1673-11.2011 · Cited by 252 · see citing works
Jovičić, A., Roshan, R., Moisoi, N., Pradervand, S., Moser, R., Pillai, B., & Luthi-Carter, R. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0600-12.2013 · Cited by 251 · see citing works
Glutamatergic model psychoses: prediction error, learning, and inference
Corlett, P. R., Honey, G. D., Krystal, J. H., & Fletcher, P. C. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.163 · Cited by 229 · see citing works
Act1 mediates IL-17-induced EAE pathogenesis selectively in NG2+ glial cells
Kang, Z., Wang, C., Zepp, J., Wu, L., Sun, K., Zhao, J., Chandrasekharan, U., DiCorleto, P. E., Trapp, B. D., Ransohoff, R. M., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3505 · Cited by 218 · see citing works
Adlakha, Y. K., & Saini, N. (2014) · Molecular Cancer · doi:10.1186/1476-4598-13-33 · Cited by 213 · see citing works
Pathophysiology of glia in perinatal white matter injury
Back, S. A., & Rosenberg, P. A. (2014) · Glia · doi:10.1002/glia.22658 · Cited by 202 · 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
Giera, S., Luo, R., Ying, Y., Ackerman, S. D., Jeong, S.-J., Stoveken, H. M., Folts, C. J., Welsh, C. A., Tall, G. G., Stevens, B., et al. (2018) · eLife · doi:10.7554/elife.33385 · Cited by 145 · see citing works
The emerging role of microRNAs in schizophrenia and autism spectrum disorders
Mellios, N., & Sur, M. (2012) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2012.00039 · Cited by 120 · see citing works
MicroRNA-23a promotes myelination in the central nervous system
Lin, S.-T., Huang, Y., Zhang, L., Heng, M. Y., Ptáček, L. J., & Fu, Y.-H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1317182110 · Cited by 117 · see citing works
Extracellular Vesicles in Brain Tumors and Neurodegenerative Diseases
Ciregia, F., Urbani, A., & Palmisano, G. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00276 · Cited by 110 · see citing works
Swiss, V. A., Nguyen, T., Dugas, J., Ibrahim, A., Barres, B., Androulakis, I. P., & Casaccia, P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018088 · Cited by 112 · see citing works
Self-citationMaki, T., Liang, A. C., Miyamoto, N., Lo, E. H., & Arai, K. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00275 · Cited by 99 · see citing works
Exosomes in neurologic and psychiatric disorders
Tsilioni, I., Panagiotidou, S., & Theoharides, T. C. (2014) · Clinical Therapeutics · doi:10.1016/j.clinthera.2014.05.005 · Cited by 93 · see citing works
Ablation of Dicer from Murine Schwann Cells Increases Their Proliferation while Blocking Myelination
Bremer, J., O'Connor, T., Tiberi, C., Rehrauer, H., Weis, J., & Aguzzi, A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012450 · Cited by 87 · see citing works
Regulation of miRNA 219 and miRNA Clusters 338 and 17-92 in Oligodendrocytes
de Faria Jr., O., Cui, Q.-L., Bin, J. M., Bull, S.-J., Kennedy, T. E., Bar-Or, A., Antel, J. P., Colman, D. R., & Dhaunchak, A. S. (2012) · Frontiers in Genetics · doi:10.3389/fgene.2012.00046 · Cited by 54 · see citing works
MiR-338-3p regulates neuronal maturation and suppresses glioblastoma proliferation.
Howe, J. R., Li, E. S., Streeter, S. E., Rahme, G. J., Chipumuro, E., Russo, G. B., Litzky, J. F., Hills, L. B., Rodgers, K. R., Skelton, P. D., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177661 · Cited by 41 · see citing works
Nazari, B., Soleimani, M., Ebrahimi-Barough, S., Enderami, S. E., Kazemi, M., Negahdari, B., Sadroddiny, E., & Ai, J. (2018) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2018.03.001 · Cited by 24 · see citing works
MicroRNAs change the games in central nervous system pharmacology
Marangon, D., Raffaele, S., Fumagalli, M., & Lecca, D. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.06.019 · Cited by 22 · see citing works
Identification of genome-wide targets of Olig2 in the adult mouse spinal cord using ChIP-Seq
Darr, A. J., Danzi, M. C., Brady, L., Emig-Agius, D., Hackett, A., Golshani, R., Warner, N., Lee, J., Lemmon, V. P., & Tsoulfas, P. (2017) · PLOS ONE · doi:10.1371/journal.pone.0186091 · Cited by 14 · see citing works
Maza, R. M., Barreda-Manso, M. A., Reigada, D., Silván, Á., Muñoz-Galdeano, T., Soto, A., del Águila, Á., & Nieto-Díaz, M. (2022) · Biomedicines · doi:10.3390/biomedicines10071559 · Cited by 12 · see citing works
Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease
Donepudi, K., Eadha, S., Rodarte, D., Sharma, B., & Kumar, S. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103211
- Authors
- Dugas, J. C., Cuellar, T. L., Scholze, A., Ason, B., Ibrahim, A., Emery, B., Zamanian, J. L., Foo, L. C., McManus, M. T., & Barres, B. A.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2010-03
- Volume
- 65
- Issue
- 5
- Pages
- 597-611
- ISSN
- 0896-6273
- PMC
- PMC2843397
- Cited by
- 527
- References
- 5
- Language
- en
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1270 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Funders
- Myelin Repair Foundation
- National Institutes of Health (5R03DA022201)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review