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Chromatin remodelling during development
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New methods for the genome-wide analysis of chromatin are providing insight into its roles in development and their underlying mechanisms. Current studies indicate that chromatin is dynamic, with its structure and its histone modifications undergoing global changes during transitions in development and in response to extracellular cues. In addition to DNA methylation and histone modification, ATP-dependent enzymes that remodel chromatin are important controllers of chromatin structure and assembly, and are major contributors to the dynamic nature of chromatin. Evidence is emerging that these chromatin-remodelling enzymes have instructive and programmatic roles during development. Particularly intriguing are the findings that specialized assemblies of ATP-dependent remodellers are essential for establishing and maintaining pluripotent and multipotent states in cells.
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“However, it has been well established that chromatin remodelings also comprise ATP-dependent enzymes [83].”
From Revisiting Epigenetics Fundamentals and Its Biomedical Implications (2024) · cites this paper as [83]
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1 retracted
Yoshimura, K., Kitagawa, H., Fujiki, R., Tanabe, M., Takezawa, S., Takada, I., Yamaoka, I., Yonezawa, M., Kondo, T., Furutani, Y., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901184106 · Cited by 56
RetractedCapturing Chromosome Conformation
Dekker, J., Rippe, K., Dekker, M., & Kleckner, N. (2002) · Science · doi:10.1126/science.1067799 · Cited by 3,652
DNA methylation landscapes: Provocative insights from epigenomics
Suzuki, M. M., & Bird, A. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2341 · Cited by 3,039
Chromatin Structure: A Repeating Unit of Histones and DNA
Kornberg, R. D. (1974) · Science · doi:10.1126/science.184.4139.868 · Cited by 2,662
Stem Cells, the Molecular Circuitry of Pluripotency and Nuclear Reprogramming
Jaenisch, R., & Young, R. A. (2008) · Cell · doi:10.1016/j.cell.2008.01.015 · Cited by 1,465
ATP-Driven Exchange of Histone H2AZ Variant Catalyzed by SWR1 Chromatin Remodeling Complex
Mizuguchi, G., Shen, X., Landry, J., Wu, W.-H., Sen, S., & Wu, C. (2003) · Science · doi:10.1126/science.1090701 · Cited by 1,312
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
Vissers, L. E. L. M., van Ravenswaaij‐Arts, C. M. A., Admiraal, R. J. C., Hurst, J. A., Vries, B. B. A. D., Janssen, I. M., van der Vliet, W. A., Huys, E., de Jong, P. J., Hamel, B. C. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1407 · Cited by 1,281
Hyperdynamic Plasticity of Chromatin Proteins in Pluripotent Embryonic Stem Cells
Meshorer, E., Yellajoshyula, D., George, E. M., Scambler, P. J., Brown, D. T., & Misteli, T. (2006) · Developmental Cell · doi:10.1016/j.devcel.2005.10.017 · Cited by 1,008
Stimulation of GAL4 Derivative Binding to Nucleosomal DNA by the Yeast SWI/SNF Complex
Côté, J., Quinn, J., Workman, J. L., & Peterson, C. L. (1994) · Science · doi:10.1126/science.8016655 · Cited by 861
A Brg1 Null Mutation in the Mouse Reveals Functional Differences among Mammalian SWI/SNF Complexes
Bultman, S. J., Gebuhr, T., Yee, D., LaMantia, C., Nicholson, J., Gilliam, A. C., Randazzo, F. M., METZGER, D., Chambon, P., Crabtree, G. R., et al. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00127-1 · Cited by 824
Flagged first, then by citations
Research works printed but not linked: 1
- Feng, Q. & Zhang, Y. The MeCP1 complex represses transcription through preferential binding, remodeling, and deacetylating methylated nucleosomes. Genes Dev. 15, 827–832 (2001).
Cited by
Sorted by citations
Items 401–500 of 1,000
Du, H., Wang, Z., Guo, R., Yang, L., Liu, G., Zhang, Z., Xu, Z., Tian, Y., Yang, Z., Li, X., et al. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab437 · Cited by 40
Epigenetic landscape and miRNA involvement during neural crest development
Strobl‐Mazzulla, P. H., Marini, M., & Buzzi, A. L. (2012) · Developmental Dynamics · doi:10.1002/dvdy.23868 · Cited by 39
Brahma is required for cell cycle arrest and late muscle gene expression during skeletal myogenesis
Albini, S., Toto, P. C., Dall’Agnese, A., Malecová, B., Cenciarelli, C., Felsani, A., Caruso, M., Bultman, S. J., & Puri, P. (2015) · EMBO Reports · doi:10.15252/embr.201540159 · Cited by 39
McBride, M. J., & Kadoch, C. (2018) · The Journal of Pathology · doi:10.1002/path.5042 · Cited by 41
Chromatin remodelling and epigenetic state regulation by non-coding RNAs in the diseased heart
Majo, F. D., & Calore, M. (2018) · Non-coding RNA Research · doi:10.1016/j.ncrna.2018.02.003 · Cited by 40
Advancing biology-based therapeutic approaches for atypical teratoid rhabdoid tumors
Hoffman, L. M., Richardson, E. A., Ho, B., Margol, A., Reddy, A. T., Lafay‐Cousin, L., Chi, S. N., Slavc, I., Judkins, A. R., Hasselblatt, M., et al. (2020) · Neuro-Oncology · doi:10.1093/neuonc/noaa046 · Cited by 39
Nuclear lactate dehydrogenase modulates histone modification in human hepatocytes
Castonguay, Z., Auger, C., Thomas, S. C., Chahma, M., & Appanna, V. D. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.10.071 · Cited by 39
Cui, H., Schlesinger, J., Schoenhals, S., Tönjes, M., Dunkel, I., Meierhofer, D., Cano, E., Schulz, K., Berger, M. F., Haack, T., et al. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1244 · Cited by 39
Epigenetics in cardiac development, function, and disease
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
Jégu, T., Domenichini, S., Blein, T., Ariel, F., Christ, A., Kim, S.-K., Crespi, M. D., Boutet‐Mercey, S., Mouille, G., Bourge, M., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138276 · Cited by 38
Liu, M., Chen, L., Ma, N., Chow, R. K. K., Li, Y., Song, Y., Chan, T. H. M., Fang, S., Yang, X., Xi, S., et al. (2016) · Hepatology · doi:10.1002/hep.28437 · Cited by 38
Rapid tissue regeneration induced by intracellular ATP delivery—A preliminary mechanistic study
Sarojini, H., Billeter, A. T., Eichenberger, S. C., Druen, D., Barnett, R. E., Gardner, S. A., Galbraith, N. J., Polk, H. C., & Chien, S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174899 · Cited by 38
Semba, Y., Harada, A., Maehara, K., Oki, S., Meno, C., Ueda, J., Yamagata, K., Suzuki, A., Onimaru, M., Nogami, J., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx475 · Cited by 38
Hernández‐García, J., Diego‐Martin, B., Kuo, P. H., Jami‐Alahmadi, Y., Vashisht, A. A., Wohlschlegel, J. A., Jacobsen, S. E., Blázquez, M. A., & Gallego‐Bartolomé, J. (2022) · Communications Biology · doi:10.1038/s42003-022-03490-x · Cited by 38
Lü, H., Cui, J. Y., Gunewardena, S., Yoo, B., Zhong, X., & Klaassen, C. D. (2012) · Epigenetics · doi:10.4161/epi.21113 · Cited by 38
Wurster, A. L., Precht, P., Becker, K. G., Wood, W. H., Zhang, Y., Wang, Z., & Pazin, M. J. (2012) · BMC Immunology · doi:10.1186/1471-2172-13-9 · Cited by 38
Genomic Approaches to Deconstruct Pluripotency
Loh, Y., Yang, L., Yang, J. C., Li, H., Collins, J. J., & Daley, G. Q. (2011) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082410-101506 · Cited by 37
Fu, W., Yu, Y., Shu, J., Yu, Z., Zhong, Y., Zhu, T., Zhang, Z., Liang, Z., Cui, Y., Chen, C., et al. (2023) · The Plant Cell · doi:10.1093/plcell/koad111 · Cited by 37
Harmacek, L. D., Watkins‐Chow, D. E., Chen, J., Jones, K. L., Pavan, W. J., Salbaum, J. M., & Niswander, L. A. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22142 · Cited by 37
Chromatin Remodeling in Development and Disease: Focus on CHD7
Martin, D. M. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001010 · Cited by 37
Epigenetics of Neural Repair Following Spinal Cord Injury
York, E. M., Petit, A., & Roskams, A. J. (2013) · Neurotherapeutics · doi:10.1007/s13311-013-0228-z · Cited by 37
Epigenetic and lncRNA regulation of cardiac pathophysiology
Chang, C., & Han, P. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.03.005 · Cited by 36
Chromatin regulation and dynamics in stem cells
Klein, D. C., & Hainer, S. J. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.11.002 · Cited by 41
Frontiers in Bladder Cancer Genomic Research
Li, Y., Sun, L., Guo, X., Mo, N., Zhang, J., & Li, C. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.670729 · Cited by 36
Epigenetics and Early Development
Gopinathan, G., & Diekwisch, T. G. H. (2022) · Journal of Developmental Biology · doi:10.3390/jdb10020026 · Cited by 35
The role of HDAC2 in chromatin remodelling and response to chemotherapy in ovarian cancer
Huang, R., Langdon, S. P., Tse, M., Mullen, P., Um, I. H., Faratian, D., & Harrison, D. J. (2015) · Oncotarget · doi:10.18632/oncotarget.6618 · Cited by 36
Structural Insights into BAF47 and BAF155 Complex Formation
Yan, L., Xie, S., Du, Y., & Qian, C. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.04.008 · Cited by 36
Boogerd, C. J. J., Perini, I., Kyriakopoulou, E., Han, S. J., La, P., van der Swaan, B., Berkhout, J. B., Versteeg, D., Monshouwer‐Kloots, J., & van Rooij, E. (2023) · Nature Communications · doi:10.1038/s41467-023-40203-2 · Cited by 39
CECR2 Is Involved in Spermatogenesis and Forms a Complex with SNF2H in the Testis
Thompson, P. J., Norton, K. A., Niri, F., Dawe, C. E., & McDermid, H. E. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.11.041 · Cited by 36
Pike, J. W., Meyer, M. B., John, H. C. S., & Benkusky, N. A. (2015) · Bone · doi:10.1016/j.bone.2015.03.012 · Cited by 35
Mechanisms of pluripotency maintenance in mouse embryonic stem cells
Chen, C.-Y., Cheng, Y., Yen, C. Y. T., & Hsieh, P. C. H. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2438-0 · Cited by 39
Medie, F. M., Sharma‐Kuinkel, B. K., Ruffin, F., Chan, L. C., Rossetti, M. M., Chang, Y., Park, L. P., Bayer, A. S., Filler, S. G., Ahn, R. S., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1909849116 · Cited by 34
Oncogene-dependent function of BRG1 in hepatocarcinogenesis
Wang, P., Song, X., Cao, D., Cui, K., Wang, J., Utpatel, K., Shang, R., Wang, H., Che, L., Evert, M., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2289-3 · Cited by 35
Zhao, J., Li, L., & Yang, T. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29783 · Cited by 35
Gao, X., Zhang, Y., He, Z., & Fu, X. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-811562-6.00004-9 · Cited by 35
Transcriptional activators and activation mechanisms
Ma, J. (2011) · Protein & Cell · doi:10.1007/s13238-011-1101-7 · Cited by 40
Diverse Functions of Lipids and Lipid Metabolism in Development
Yao, Y., Ding, L., & Huang, X. (2019) · Small Methods · doi:10.1002/smtd.201900564 · Cited by 37
Nazim, M., Lin, C.-H., Feng, A., Xiao, W., Yeom, K., Li, M., Daly, A. E., Tan, X., Vu, H., Ernst, J., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.04.001 · Cited by 36
Tea, J. S., Chihara, T., & Luo, L. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1643-10.2010 · Cited by 34
Maher, R. L., Prasad, A., Rizvanova, O., Wallace, S. S., & Pederson, D. S. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.08.010 · Cited by 34
BRG1 overexpression in smooth muscle cells promotes the development of thoracic aortic dissection
Yuan, Y., Wang, C., Xu, J., Tao, J., Xu, Z., & Huang, S. (2014) · BMC Cardiovascular Disorders · doi:10.1186/1471-2261-14-144 · Cited by 34
Metabolism, longevity and epigenetics
Cosentino, C., & Mostoslavsky, R. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1295-3 · Cited by 35
Functional Interactions between NURF and Ctcf Regulate Gene Expression
Qiu, Z., Song, C., Malakouti, N., Murray, D. T., Hariz, A., Zimmerman, M., Gygax, D. M., Alhazmi, A., & Landry, J. W. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00553-14 · Cited by 33
McNicholas, M., Cola, A. D., Bashardanesh, Z., Foss, A., Lloyd, C. B., Hébert, S., Faury, D., Andrade, A. F., Jabado, N., Kleinman, C. L., et al. (2023) · Cancer Discovery · doi:10.1158/2159-8290.cd-23-0004 · Cited by 32
Gene regulatory systems that control gene expression in the Ciona embryo
Satou, Y., & Imai, K. S. (2015) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.91.33 · Cited by 34
Wiley, M. M., Muthukumar, V., Griffin, T. M., & Griffin, C. T. (2015) · Journal of the American Heart Association · doi:10.1161/jaha.115.001972 · Cited by 31
Toto, P. C., Puri, P., & Albini, S. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2273-3 · Cited by 33
The integration of epigenetics and genetics in nutrition research for CVD risk factors
Ma, Y., & Ordovás, J. M. (2016) · Proceedings of The Nutrition Society · doi:10.1017/s0029665116000823 · Cited by 34
Cancer-Associated Gain-of-Function Mutations Activate a SWI/SNF-Family Regulatory Hub
Clapier, C. R., Verma, N., Parnell, T. J., & Cairns, B. R. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.09.024 · Cited by 33
Molecular characteristics of pediatric high-grade gliomas
Chamdine, O., & Gajjar, A. J. (2014) · CNS Oncology · doi:10.2217/cns.14.43 · Cited by 36
Padilla‐Benavides, T., Nasipak, B. T., & Imbalzano, A. N. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25031 · Cited by 32
Loughran, S. J., Comoglio, F., Hamey, F., Giustacchini, A., Errami, Y., Earp, E., Göttgens, B., Jacobsen, S. E. W., Mead, A. J., Hendrich, B., et al. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20161827 · Cited by 33
Li, Y., Hu, Y., Zhu, Z., Zhao, K., Liu, G., Wang, L., Qu, Y., Zhao, J., & Qin, Y. (2019) · Biotechnology for Biofuels · doi:10.1186/s13068-019-1539-z · Cited by 32
Ye, Y., Chen, X. X., & Zhang, W. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.626383 · Cited by 32
Enhanced chromatin accessibility contributes to X chromosome dosage compensation in mammals
Talón, I., Janiszewski, A., Theeuwes, B., Lefevre, T., Song, J., Bervoets, G., Vanheer, L., Geest, N. D., Poovathingal, S. K., Allsop, R., et al. (2021) · Genome biology · doi:10.1186/s13059-021-02518-5 · Cited by 29
Pan, H., Yang, Y., Xu, H., Jin, A., Huang, X., Gao, X., Sun, S., Liu, Y., Liu, J., Lu, T., et al. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1174579 · Cited by 31
NUCKS: a potential biomarker in cancer and metabolic disease
Qiu, B., Han, W., & Tergaonkar, V. (2015) · Clinical Science · doi:10.1042/cs20140656 · Cited by 34
Identification of Mytilus edulis genetic regulators during early development
Bassim, S., Tanguy, A., Génard, B., Moraga, D., & Tremblay, R. (2014) · Gene · doi:10.1016/j.gene.2014.08.042 · Cited by 32
The role of ARID1B, a BAF chromatin remodeling complex subunit, in neural development and behavior
Moffat, J. J., Jung, E., Ka, M., Smith, A. L., Jeon, B. T., Santen, G. W. E., & Kim, W.-Y. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.08.021 · Cited by 31
Imran, M., Shafiq, S., Naeem, M. K., Widemann, É., Munir, M. Z., Jensen, K. B., & Wang, R. R. ‐. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21010321 · Cited by 31
A Chromodomain-Helicase-DNA-Binding Factor Functions in Chromatin Modification and Gene Regulation
Lu, Y., Tan, F., Zhao, Y. J., Zhou, S., Chen, X., Hu, Y., & Zhou, D. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00453 · Cited by 31
Abou-Taleb, H., Yamaguchi, K. D., Matsumura, N., Murakami, R., Nakai, H., Higasa, K., Amano, Y., Abiko, K., Yoshioka, Y., Hamanishi, J., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.10181 · Cited by 32
Chen, L., Zhou, A. S., & West, A. E. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00067.2017 · Cited by 35
Versatile Roles of the Chromatin Remodeler CHD7 during Brain Development and Disease
Feng, W., Shao, C., & Liu, H. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00309 · Cited by 31
Epigenetic regulation of motivated behaviors by histone deacetylase inhibitors
Elvir, L., Duclot, F., Wang, Z., & Kabbaj, M. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.09.030 · Cited by 33
Cho, S., Lee, C.-H., Gi, E., Yim, Y., Koh, H., Kang, K., & Paek, N. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00364 · Cited by 32
Acute depletion of BRG1 reveals its primary function as an activator of transcription
Ren, G., Ku, W. L., Ge, G.-Z., Hoffman, J. A., Kang, J. Y., Tang, Q.-S., Cui, K.-R., He, Y., Guan, Y., Gao, B., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-48911-z · Cited by 32
ATAC-pipe: general analysis of genome-wide chromatin accessibility
Zuo, Z.-Q., Jin, Y., Zhang, W., Lu, Y., Li, B., & Qu, K. (2018) · Briefings in Bioinformatics · doi:10.1093/bib/bby056 · Cited by 30
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Hong, S. H., Son, K. H., Ha, S. Y., Wee, T. I., Choi, S. K., Won, J. E., Han, H. D., Ro, Y., Park, Y., Eun, J. W., et al. (2020) · Cancer Research · doi:10.1158/0008-5472.can-20-0568 · Cited by 30
The BAF chromatin remodeling complexes: structure, function, and synthetic lethalities
Varga, J., Kube, M., Luck, K., & Schick, S. (2021) · Biochemical Society Transactions · doi:10.1042/bst20190960 · Cited by 31
Nuclear Phosphoinositides as Key Determinants of Nuclear Functions
Vidalle, M. C., Sheth, B., Fazio, A., Marvi, M. V., Leto, S., Koufi, F., Neri, I., Casalin, I., Ramazzotti, G., Follo, M. Y., et al. (2023) · Biomolecules · doi:10.3390/biom13071049 · Cited by 29
自閉症関連タンパク質CHD8はC/EBPβと協調して脂肪分化を制御する
Kita, Y. (2018) · Institutional Repositories DataBase (IRDB) · Cited by 30
Epigenetic regulation of open chromatin in pluripotent stem cells
Kobayashi, H., & Kikyo, N. (2014) · Translational research · doi:10.1016/j.trsl.2014.03.004 · Cited by 29
Analysis of Human Nuclear Protein Complexes by Quantitative Mass Spectrometry Profiling
Connelly, K. E., Hedrick, V., Sobreira, T. J. P., Dykhuizen, E. C., & Aryal, U. K. (2018) · PROTEOMICS · doi:10.1002/pmic.201700427 · Cited by 28
Subhash, S., Mishra, K., Akhade, V. S., Kanduri, M., Mondal, T., & Kanduri, C. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky635 · Cited by 32
Whsc1 links pluripotency exit with mesendoderm specification
Tian, T. V., Stefano, B. D., Stik, G., Vila-Casadesús, M., Sardina, J. L., Vidal, E., Dasti, A., Segura-Morales, C., de Andrés-Aguayo, L., Gómez, A., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0342-1 · Cited by 29
Epigenetic regulation in antiviral innate immunity
Wang, X., Xia, H., Liu, S., Cao, L., & You, F. (2021) · European Journal of Immunology · doi:10.1002/eji.202048975 · Cited by 29
Mammalian SWI/SNF chromatin remodeler is essential for reductional meiosis in males
Menon, D. U., Kirsanov, O., Geyer, C. B., & Magnuson, T. (2021) · Nature Communications · doi:10.1038/s41467-021-26828-1 · Cited by 32
Takebayashi, S., Lei, I., Ryba, T., Sasaki, T., Dileep, V., Battaglia, D., Gao, X., Fang, P., Fan, Y., Esteban, M. A., et al. (2013) · Epigenetics & Chromatin · doi:10.1186/1756-8935-6-42 · Cited by 29
Jenull, S., Tscherner, M., Gulati, M., Nobile, C. J., Chauhan, N., & Kuchler, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-08239-9 · Cited by 28
Lei, I., Tian, S., Chen, V., Zhao, Y. B., & Wang, Z. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00358 · Cited by 28
Chromatin remodelers in oligodendroglia
Parras, C. M., Marie, C., Zhao, C., & Lu, Q. R. (2020) · Glia · doi:10.1002/glia.23837 · Cited by 28
Tu, Z., Wang, C., Davis, A. K., Hu, M., Zhao, C., Xin, M., Lu, Q. R., & Zheng, Y. (2021) · Blood · doi:10.1182/blood.2020009997 · Cited by 32
HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans
Kim, H., Ding, Y., Zhang, G., Yan, Y., Conte, D., Dong, M., & Mello, C. C. (2021) · eLife · doi:10.7554/elife.63299 · Cited by 27
The Role of Epigenetics in Neurodegenerative Diseases
Lovrei, L., Maver, A., Zadel, M., & Peterli, B. (2013) · InTech eBooks · doi:10.5772/54744 · Cited by 31
Fujita, K., Ogawa, R., Kawawaki, S., & Ito, K. (2014) · Mechanisms of Development · doi:10.1016/j.mod.2014.05.001 · Cited by 28
Tserendulam, B., Schulz, Y., Wolf, S., Rabe, T., Oellerich, T., Urlaub, H., Schaefer, I., & Pauli, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052640 · Cited by 28
SOX2 transcription factor binding and function
Hagey, D. W., Bergsland, M., & Muhr, J. (2022) · Development · doi:10.1242/dev.200547 · Cited by 34
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Metadata
- Authors
- Ho, L., & Crabtree, G. R.
- Affiliations
- Stanford Medicine (US)
- Venue
- Nature
- Published
- 2010-01
- Volume
- 463
- Issue
- 7280
- Pages
- 474-484
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3060774
- OpenAlex
- W1984249881
- Cited by
- 1,114
- References
- 105
- Citations by year
- 2026: 39 · 2025: 42 · 2024: 54 · 2023: 46 · 2022: 57 · 2021: 63 · 2020: 56 · 2019: 64 · 2018: 80 · 2017: 84 · 2016: 78 · 2015: 82 · 2014: 71 · 2013: 78 · 2012: 76
- FWCI
- 8.15
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (R01NS046789)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD055391)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- chromatin remodeling, developmental regulation, histone modifications, DNA methylation, pluripotency, multipotency, chromatin structure, extracellular signalling
- MeSH terms
- Animals, DNA, DNA-Binding Proteins, Drosophila melanogaster, Humans, Nucleic Acid Conformation, Transcription Factors, Body Patterning, Drosophila Proteins, Chromatin Assembly and Disassembly, Genome-Wide Association Study, Mi-2 Nucleosome Remodeling and Deacetylase Complex
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