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Reversing DNA Methylation: Mechanisms, Genomics, and Biological Functions
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Methylation of cytosines in the mammalian genome represents a key epigenetic modification and is dynamically regulated during development. Compelling evidence now suggests that dynamic regulation of DNA methylation is mainly achieved through a cyclic enzymatic cascade comprised of cytosine methylation, iterative oxidation of methyl group by TET dioxygenases, and restoration of unmodified cytosines by either replication-dependent dilution or DNA glycosylase-initiated base excision repair. In this review, we discuss the mechanism and function of DNA demethylation in mammalian genomes, focusing particularly on how developmental modulation of the cytosine-modifying pathway is coupled to active reversal of DNA methylation in diverse biological processes.
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“Although sequencing-based approaches have only found 5hmC in CG dinucleotides in mESC and brain cortical tissue (24), 5hmCH accounted for 38% of 5mCH+5hmCH in cerebellar granule cells, suggesting that 5mCH is also targeted for TET mediated methylation turnover (40).”
From Dynamic DNA methylation: In the right place at the right time (2018) · cites this paper as [24]
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Cites
DNA methylation patterns and epigenetic memory
Bird, A. (2002) · Genes & Development · doi:10.1101/gad.947102 · Cited by 7,124
Jaenisch, R., & Bird, A. (2003) · Nature Genetics · doi:10.1038/ng1089 · Cited by 6,325
Okano, M., Bell, D. W., Haber, D. A., & Li, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81656-6 · Cited by 6,143
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
Tahiliani, M., Koh, K. P., Shen, Y., Pastor, W. A., Bandukwala, H., Brudno, Y., Agarwal, S., Iyer, L. M., Liu, D. R., Aravind, L., et al. (2009) · Science · doi:10.1126/science.1170116 · Cited by 5,836
A bivalent chromatin structure marks key developmental genes in embryonic stem cells
Bernstein, B. E., Mikkelsen, T. S., Xie, X., Kamal, M., Huebert, D. J., Cuff, J., Fry, B., Meissner, A., Wernig, M., Plath, K., et al. (2006) · Cell · doi:10.1016/j.cell.2006.02.041 · Cited by 5,361
Human DNA methylomes at base resolution show widespread epigenomic differences
Lister, R., Pelizzola, M., Dowen, R. H., Hawkins, R. D., Hon, G., Tonti-Filippini, J., Nery, J. R., Lee, L., Ye, Z., Ngo, Q.-M., et al. (2009) · Nature · doi:10.1038/nature08514 · Cited by 4,673
Cancer-associated IDH1 mutations produce 2-hydroxyglutarate
Dang, L., White, D. W., Gross, S., Bennett, B. D., Bittinger, M. A., Driggers, E. M., Fantin, V. R., Jang, H. G., Jin, S., Keenan, M. C., et al. (2009) · Nature · doi:10.1038/nature08617 · Cited by 4,154
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells
Mikkelsen, T. S., Ku, M., Jaffe, D. B., Issac, B., Lieberman, E., Giannoukos, G., Alvarez, P., Brockman, W., Kim, T.-K., Koche, R. P., et al. (2007) · Nature · doi:10.1038/nature06008 · Cited by 4,129
Establishing, maintaining and modifying DNA methylation patterns in plants and animals
Law, J. A., & Jacobsen, S. E. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2719 · Cited by 3,925
Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine
Ito, S., Shen, L., Dai, Q., Wu, S. C., Collins, L. B., Swenberg, J. A., He, C., & Zhang, Y. (2011) · Science · doi:10.1126/science.1210597 · Cited by 3,451
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Structure and Function of TET Enzymes
Yin, X., & Xu, Y. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-43624-1_12 · Cited by 48
Jiang, D., Sun, M., You, L., Lü, K., Gao, L., Hu, C., Wu, S., Chang, G., Tao, H., & Zhang, D. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.03.021 · Cited by 46
Inoue, A., Shen, L., Matoba, S., & Zhang, Y. (2015) · Cell Reports · doi:10.1016/j.celrep.2014.12.049 · Cited by 48
Self-citationKowluru, R. A., & Shan, Y. (2017) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-017-3594-0 · Cited by 49
Zeng, H., Qi, C., Liu, T., Xiao, H., Cheng, Q.-Y., Jiang, H.-P., Yuan, B., & Feng, Y. (2017) · Analytical Chemistry · doi:10.1021/acs.analchem.7b00052 · Cited by 46
Melatonin impedes Tet1‐dependent mGluR5 promoter demethylation to relieve pain
Hsieh, M., Ho, Y., Lai, C., Chou, D., Wang, H., Chen, G., Lin, T., & Peng, H. (2017) · Journal of Pineal Research · doi:10.1111/jpi.12436 · Cited by 44
Zhang, X., Chen, X., Weirauch, M. T., Zhang, X., Burleson, J., Brandt, E. B., & Ji, H. (2018) · Current Zoology · doi:10.1093/eep/dvy020 · Cited by 47
Liu, S., Cheng, K., Zhang, H., Kong, R., Wang, S., Mao, C., & Liu, S. (2020) · Advanced Science · doi:10.1002/advs.201903035 · Cited by 46
Ludovici, G. M., de Souza, S. O., Chierici, A., Cascone, M. G., d’Errico, F., & Malizia, A. (2020) · Journal of Environmental Radioactivity · doi:10.1016/j.jenvrad.2020.106375 · Cited by 49
Metabolite regulation of epigenetics in cancer
Wang, P., Chen, L., Xiong, Y., & Ye, D. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114815 · Cited by 50
Gackowski, D., Zarakowska, E., Starczak, M., Modrzejewska, M., & Oliński, R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144859 · Cited by 44
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Festuccia, N., González, I., & Navarro, P. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.12.009 · Cited by 42
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Jimenez‐Pacheco, A., Franco, J. M., Lopez, S., Gómez‐Zumaquero, J. M., Leal‐Lasarte, M., Caballero-Hernández, D. E., Cejudo‐Guillén, M., & Pozo, D. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-53889-1_14 · Cited by 46
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Wiehe, R. S., Gole, B., Châtre, L., Walther, P., Calzia, E., Ricchetti, M., & Wiesmüller, L. (2018) · Oncotarget · doi:10.18632/oncotarget.24822 · Cited by 47
Wang, J., Li, M., Yang, J., Wang, Y.-Q., Wu, X., Huang, J. Y., Ying, Y., & Long, Y. (2020) · ACS Central Science · doi:10.1021/acscentsci.9b01129 · Cited by 45
The proto CpG island methylator phenotype of sessile serrated adenomas/polyps
Parker, H. R., Orjuela, S., Oliveira, A. M., Cereatti, F., Sauter, M. M., Heinrich, H. S., Tanzi, G., Weber, A., Komminoth, P., Vavricka, S. R., et al. (2018) · Epigenetics · doi:10.1080/15592294.2018.1543504 · Cited by 44
Ambrosone, C. B., & Higgins, M. J. (2020) · Cancer Research · doi:10.1158/0008-5472.can-20-0077 · Cited by 44
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Lee, J. J., Granter, S. R., Laga, A. C., Saavedra, A. P., Zhan, Q., Guo, W., Xu, S., Murphy, G. F., & Lian, C. G. (2014) · Modern Pathology · doi:10.1038/modpathol.2014.99 · Cited by 44
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Post-meiotic DNA double-strand breaks occur in Tetrahymena, and require Topoisomerase II and Spo11
Akematsu, T., Fukuda, Y., Garg, J., Fillingham, J., Pearlman, R. E., & Loidl, J. (2017) · eLife · doi:10.7554/elife.26176 · Cited by 44
Roles of vitamins in stem cells
Godoy-Parejo, C., Deng, C., Zhang, Y., Liu, W., & Chen, G. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03352-6 · Cited by 45
Self-citationMaternal factors regulating preimplantation development in mice
Wu, D., & Dean, J. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.10.006 · Cited by 44
Cyclic AMP Affects Oocyte Maturation and Embryo Development in Prepubertal and Adult Cattle
Bernal-Ulloa, S. M., Heinzmann, J., Herrmann, D., Hadeler, K., Aldag, P., Winkler, S., Dorit, P., Baulain, U., Lucas‐Hahn, A., & Niemann, H. (2016) · PLoS ONE · doi:10.1371/journal.pone.0150264 · Cited by 43
O-GlcNAcylation and chromatin remodeling in mammals: an up-to-date overview
Leturcq, M., Lefebvre, T., & Vercoutter‐Edouart, A. (2017) · Biochemical Society Transactions · doi:10.1042/bst20160388 · Cited by 43
Brain iron loading impairs DNA methylation and alters GABAergic function in mice
Ye, Q., Trivedi, M. S., Zhang, Y., Böhlke, M., Alsulimani, H. H., Chang, J., Maher, T. J., Deth, R. C., & Kim, J. (2018) · The FASEB Journal · doi:10.1096/fj.201801116rr · Cited by 43
Self-citationPensold, D., Reichard, J., van Loo, K. M. J., Ciganok-Hückels, N., Hahn, A., Bayer, C., Liebmann, L., Groß, J., Tittelmeier, J., Lingner, T., et al. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa009 · Cited by 45
García-Fernández, P., García‐Souto, D., Almansa, E., Morán, P., & Gestal, C. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00292 · Cited by 44
Mechanisms of DNA Methylation and Demethylation During Mammalian Development
Veland, N., & Chen, T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805388-1.00002-x · Cited by 43
Liang, W., Li, J., Sun, L., Liu, Y., Lan, Z., & Qian, W. (2021) · New Phytologist · doi:10.1111/nph.17804 · Cited by 44
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Jiang, Y., Domínguez, P. M., & Melnick, A. M. (2016) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000249 · Cited by 42
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Role of ten‐eleven translocation proteins and 5‐hydroxymethylcytosine in hepatocellular carcinoma
Wang, P., Yan, Y., Yu, W., & Zhang, H. (2019) · Cell Proliferation · doi:10.1111/cpr.12626 · Cited by 41
Single-cell bisulfite-free 5mC and 5hmC sequencing with high sensitivity and scalability
Cao, Y., Bai, Y., Yuan, T., Song, L., Fan, Y., Ren, L., Song, W., Peng, J., An, R., Gu, Q., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2310367120 · Cited by 45
DNA methylation dynamics at imprinted genes during bovine pre-implantation embryo development
O’Doherty, A., Magee, D. A., O’Shea, L. C., Forde, N., Beltman, M. E., Mamo, S., & Fair, T. (2015) · BMC Developmental Biology · doi:10.1186/s12861-015-0060-2 · Cited by 41
Rathi, P., Maurer, S., & Summerer, D. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0078 · Cited by 41
Li, J., Liang, W., Li, Y., & Qian, W. (2018) · The Plant Cell · doi:10.1105/tpc.18.00287 · Cited by 40
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Steinacher, R., Barekati, Z., Botev, P., Kuśnierczyk, A., Slupphaug, G., & Schär, P. (2018) · The EMBO Journal · doi:10.15252/embj.201899242 · Cited by 41
Burleson, J., Siniard, D. J., Yadagiri, V. K., Chen, X., Weirauch, M. T., Ruff, B. P., Brandt, E. B., Hershey, G. K. K., & Ji, H. (2019) · Scientific Reports · doi:10.1038/s41598-019-43767-6 · Cited by 43
Jovčevska, I. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00798 · Cited by 41
Nguyen, H., Sokpor, G., Pham, L., Rosenbusch, J., Stoykova, A., Staiger, J. F., & Tuoc, T. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1160984 · Cited by 41
Zhang, H., Yuan, Q., Pan, Z., Ling, X., Tan, Q., Wu, M., Zheng, D., Xie, P., Xie, D., & Liu, L. (2019) · Toxicology Letters · doi:10.1016/j.toxlet.2019.12.028 · Cited by 40
Role of Rare Earth Elements in Plants
Öztürk, M., Metin, M., Altay, V., Prasad, M. N. V., Gul, A., Bhat, R. A., Dervash, M. A., Hasanuzzaman, M., Nahar, K., Ünal, D., et al. (2023) · Plant Molecular Biology Reporter · doi:10.1007/s11105-023-01369-7 · Cited by 42
Hong, T., Li, J., Guo, L., Cavalier, M., Wang, T., Dou, Y., de-la-Fuente, A. L. C., Fang, S., Guzman, A. G., Wohlan, K., et al. (2023) · Nature Aging · doi:10.1038/s43587-023-00505-y · Cited by 45
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Koijam, A. S., Singh, K. D., Singh, N. B., Haobam, R., & Rajashekar, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115951 · Cited by 45
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Misawa, K., Imai, A., Mochizuki, D., Mima, M., Endo, S., Misawa, Y., Kanazawa, T., & Mineta, H. (2018) · Oncotarget · doi:10.18632/oncotarget.25333 · Cited by 40
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Cheung, P., Khatri, P., Utz, P. J., & Kuo, A. J. (2019) · Nature Reviews Rheumatology · doi:10.1038/s41584-019-0220-z · Cited by 39
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Saitou, M. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.01.008 · Cited by 42
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Rallapalli, K. L., & Komor, A. C. (2023) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-052521-013938 · Cited by 44
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Oshima, M., & Iwama, A. (2014) · International Journal of Hematology · doi:10.1007/s12185-014-1647-2 · Cited by 39
Starczak, M., Zarakowska, E., Modrzejewska, M., Dziaman, T., Szpila, A., Linowiecka, K., Guz, J., Szpotan, J., Gawroński, M., Wołowiec, A., et al. (2018) · Journal of Translational Medicine · doi:10.1186/s12967-018-1581-9 · Cited by 38
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Balasubramanian, S., Raghunath, A., & Perumal, E. (2019) · Gene · doi:10.1016/j.gene.2019.144049 · Cited by 42
Xu, L., Chen, Y., Chong, J. P. C., Fin, A., McCoy, L. S., Xu, J., Zhang, C., & Wang, D. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201406220 · Cited by 39
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Nührenberg, T. G., Gilsbach, R., Preißl, S., Schnick, T., & Hein, L. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1887-8 · Cited by 39
Relton, C. L., Hartwig, F. P., & Smith, G. D. (2015) · International Journal of Epidemiology · doi:10.1093/ije/dyv198 · Cited by 39
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Li, B., Hou, L., Zhu, D., Xu, X., An, S., & Wang, X. (2018) · Scientific Reports · doi:10.1038/s41598-018-20831-1 · Cited by 33
Wu, P., Tang, Y., Fang, X., Xie, C., Zeng, J., Wang, W. T., & Zhao, S. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00143 · Cited by 38
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Kubik, G., Batke, S., & Summerer, D. (2015) · Journal of the American Chemical Society · doi:10.1021/ja506022t · Cited by 37
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Gu, Y., Chen, J., Zhang, H., Shen, Z., Liu, H., Lv, S., Yu, X., Zhang, D., Ding, X., & Zhang, X. (2020) · The FASEB Journal · doi:10.1096/fj.201902957rr · Cited by 37
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Supek, F., Lehner, B., Hájková, P., & Warnecke, T. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004585 · Cited by 36
Romagnolo, D. F., Zempleni, J., & Selmin, O. I. (2014) · Advances in Nutrition · doi:10.3945/an.114.005868 · Cited by 36
Wang, J., Zhang, Y., Zhuo, Q., Tseng, Y., Wang, J., Ma, Y., Zhang, J., & Liu, J. (2020) · Nutrition & Metabolism · doi:10.1186/s12986-020-00466-8 · Cited by 36
Self-citationChen, G., & Wang, J. (2019) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.01.005 · Cited by 35
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Xiong, H.-Y., Wyns, A., Campenhout, J. V., Hendrix, J., Bruyne, E. D., Godderis, L., Schabrun, S. M., Nijs, J., & Polli, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158324 · Cited by 39
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Moler, E. R. V., Abakir, A., Eleftheriou, M., Johnson, J. S., Krutovsky, K. V., Lewis, L. C., Ruzov, A. S., Whipple, A. V., & Rajora, O. P. (2018) · Population genomics · doi:10.1007/13836_2018_59 · Cited by 37
Zhang, M.-C., Egan, B., & Wang, J.-X. (2015) · International Journal of Biochemistry and Cell Biology · doi:10.1016/j.biocel.2015.04.019 · Cited by 31
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Sun, F., Abreu‐Rodríguez, I., Ye, S., Gay, S., Distler, O., Neidhart, M., & Karouzakis, E. (2019) · PLoS ONE · doi:10.1371/journal.pone.0218551 · Cited by 34
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Baradaran, P. C., Kozovská, Z., Furdová, A., & Smolková, B. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155314 · Cited by 36
Zhang, X., Gao, S., & Liu, X. (2021) · Stem Cells International · doi:10.1155/2021/6681337 · Cited by 37
Chen, R., Gan, Q., Zhao, S., Zhang, D., Wang, S., Yao, L., Yuan, M., & Cheng, J. (2022) · BMC Cancer · doi:10.1186/s12885-022-09477-5 · Cited by 37
RetractedLi, G., Peng, J., Liu, Y., Li, X., Yang, Q., Li, Y., Tang, Z., Zuo, W., Jiang, Z., & Wei, D. (2014) · Lipids · doi:10.1007/s11745-014-3977-5 · Cited by 35
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Tsagaratou, A., & Rao, A. (2013) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2013.78.020248 · Cited by 36
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Kaplan, G., Xu, H., Abreu, K., & Feng, J. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.806685 · Cited by 34
Zhong, W., & Sczepanski, J. T. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c03010 · Cited by 33
Wang, Y., Wang, Z.-X., Liu, C., Wang, S., & Huang, B. (2015) · Fungal Biology · doi:10.1016/j.funbio.2015.08.017 · Cited by 35
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O’Doherty, A., & McGettigan, P. (2014) · Reproduction Fertility and Development · doi:10.1071/rd14167 · Cited by 35
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Mahfoudhi, E., Talhaoui, I., Cabagnols, X., Della-Valle, V., Secardin, L., Rameau, P., Bernard, O., Ishchenko, A. A., Abbès, S., Vainchenker, W., et al. (2016) · DNA repair · doi:10.1016/j.dnarep.2016.05.031 · Cited by 38
Li, Z., Heng, J., Yan, J., Guo, X., Tang, L., Chen, M., Peng, L., Wu, Y., Wang, S., Xiao, Z. Q., et al. (2016) · Breast Cancer Research and Treatment · doi:10.1007/s10549-016-4004-8 · Cited by 35
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Gao, T. X., Díaz-Hirashi, Z., & Verdeguer, F. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19124108 · Cited by 34
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Wu, C., Blondin, P., Vigneault, C., Labrecque, R., & Sirard, M. (2019) · Theriogenology · doi:10.1016/j.theriogenology.2019.12.020 · Cited by 34
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Milazzotto, M. P., de Lima, C. B., da Fonseca, A. M., dos Santos, É. C., & Ispada, J. (2020) · Animal Reproduction · doi:10.1590/1984-3143-ar2020-0015 · Cited by 34
Epigenetics: An overview of CpG methylation, chromatin remodeling, and regulatory/noncoding RNAs
Clark, J., & Rager, J. E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819968-8.00001-9 · Cited by 37
DNA N6-Methyladenine (6mA) Modification Regulates Drug Resistance in Triple Negative Breast Cancer
Sheng, X., Wang, J., Guo, Y. F., Zhang, J., & Luo, J. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.616098 · Cited by 35
Coupling of X-Chromosome reactivation with the pluripotent stem cell state
Payer, B., & Lee, J. T. (2014) · RNA Biology · doi:10.4161/rna.29779 · Cited by 34
DNA modifications in the mammalian brain
Shin, J., Ming, G., & Song, H. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0512 · Cited by 34
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Mammalian DNA methylome dynamics: mechanisms, functions and new frontiers
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Metadata
- Authors
- Wu, H., & Zhang, Y.
- Affiliations
- Boston Children's Hospital (US)
- Corresponding author
- Zhang, Yi
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2014-01
- Volume
- 156
- Issue
- 1-2
- Pages
- 45-68
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC3938284
- OpenAlex
- W2036848594
- Cited by
- 1,065
- References
- 219
- Citations by year
- 2026: 36 · 2025: 57 · 2024: 54 · 2023: 66 · 2022: 83 · 2021: 64 · 2020: 96 · 2019: 106 · 2018: 98 · 2017: 110 · 2016: 114 · 2015: 100 · 2014: 80
- FWCI
- 55.31
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute of General Medical Sciences (GM68804, R01GM068804)
- National Institute of Diabetes and Digestive and Kidney Diseases (U01DK089565)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Syndromes and Imprinting
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- DNA demethylation, DNA methylation, TET enzymes, base excision repair, DNA glycosylase, epigenetic regulation, developmental regulation, mammalian genomes
- MeSH terms
- Animals, Humans, Oxidoreductases, N-Demethylating, Promoter Regions, Genetic, Genome, DNA Methylation, 5-Methylcytosine
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