Methyl-CpG-Binding Domain Proteins: Readers of the Epigenome

The cBio Cancer Genomics Portal: An Open Platform for Exploring Multidimensional Cancer Genomics Data

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Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal

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

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Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

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CpG Islands in vertebrate genomes

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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Linking DNA methylation and histone modification: patterns and paradigms

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Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases

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Identification and Characterization of a Family of Mammalian Methyl-CpG Binding Proteins

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The role of cytosine modification symmetry in mammalian epigenome regulation

Cakil, Z. V., Engelhard, L., & Summerer, D. (2025) · Chemical Science · doi:10.1039/d5sc09022a · Cited by 1

Embracing change: Chemical modifications of nucleic acid bases as epigenetic marks

Nain, N., Khan, S., Phogat, P., Bansal, A., & Kukreti, S. (2025) · Next research. · doi:10.1016/j.nexres.2025.101292 · Cited by 1

Luteolin Modulates DNA Methylation and Histone Acetylation To Restore Nrf2 and Alleviate Hyperglycemia-Induced Oxidative Stress in Vitro

Divyajanani, S., Harithpriya, K., & Ramkumar, K. M. (2026) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-026-02014-2 · Cited by 1

The Dual Role of DNA Hypermethylation and Hypomethylation in Colorectal and Gastric Tumorigenesis: Mechanisms and Non-Invasive Biomarker

Long, B., Yan, X., Wang, Z., & Zhang, Z. (2026) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl46159 · Cited by 1

Glutamate-induced nuclear translocation of PYK2 in hippocampal neurons, interaction with MBD2, and role in cell death in a model of epilepsy

Giralt, A., Mendes, T., Montalban, E., Cifuentes-Díaz, C., Galán-Ganga, M., Chouchana, M., de Pins, B., Longueville, S., Carrel, D., & Girault, J. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08628-x · Cited by 1

Epigenetic signatures and risk determinants in bladder cancer: Implications for diagnostic and therapeutic interventions

Pradhan, B., Mishra, P., Dash, P., Niharika, Baral, T., Mishra, J., Chakraborty, S., Nandi, P., & Patra, S. K. (2026) · Urologic Oncology Seminars and Original Investigations · doi:10.1016/j.urolonc.2026.04.294 · Cited by 1

Epigenetics and One-Carbon Metabolism in Cancer: Mechanisms and Therapeutic Implications

Serpa, J., & Costa, J. R. (2026) · Advances in experimental medicine and biology · doi:10.1007/978-3-032-12166-0_9 · Cited by 1

Fundamental Mechanisms of Orofacial Clefts

Garland, M. A., Reynolds, K., Zhang, S., Sun, B. H., Frates, R. D., & Zhou, C. J. (2021) · Springer eBooks · doi:10.1007/978-3-030-46024-2_8 · Cited by 1

Quality assessment of enzymatic methyl-seq library constructed using crude cell lysate

Tanaka, Y., Mizuguchi, R., Koseki, N., Suzuki, H., & Suzuki, T. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.149488 · Cited by 1

Comparison of hypoxia- and hyperoxia-induced alteration of epigene expression pattern in lungs of Pleurodeles waltl and Mus musculus

Hasan, M. M., Sekiya, R., Zhang, X., Yassouf, M. Y., & Li, T. (2024) · PLoS ONE · doi:10.1371/journal.pone.0299661 · Cited by 1

Application of Machine Learning in Cancer Epigenetics: A Deeper Look into the Epigenome

Gomes, M. T., Kaushik, A., Chirayil, A. S., Garg, K., Sharma, G., & Jain, P. (2025) · Advances in Science, Technology & Innovation/Advances in science, technology & innovation · doi:10.1007/978-3-031-80973-6_14 · Cited by 1

Loss of MBD2 is associated with tumor growth in small intestinal neuroendocrine tumors

Barazeghi, E., Backman, S., Hellman, P., Norlén, O., & Stalberg, P. L. H. (2025) · Endocrine Connections · doi:10.1530/ec-25-0169 · Cited by 1

HM-DyadCap – capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA

Engelhard, L., Schiller, D., Zambrano-Mila, M. S., Keliuotyte, K., Buchmuller, B. C., Tiwari, S., Imig, J., Simeone, A., Schröter, C. J., Becker, S. M., et al. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag389 · Cited by 1

Interplay Between Maternal Micronutrients, DNA Methylation, and Brain Development

Rathod, R. S., & Joshi, S. (2019) · Springer eBooks · doi:10.1007/978-3-319-55530-0_59 · Cited by 1

Recognition of Oxidized 5‐Methylcytosine Derivatives in DNA by Natural and Engineered Protein Scaffolds

Muñoz‐López, Á., & Summerer, D. (2017) · The Chemical Record · doi:10.1002/tcr.201700088 · Cited by 2

Design and Application of DNA Modification-Specific Transcription-Activator-Like Effectors

Buchmuller, B. C., Muñoz‐López, Á., Gieß, M., & Summerer, D. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0876-0_29 · Cited by 1

Methylation of the HCBP6 promoter is associated with primary biliary cholangitis pathogenesis

Gao, L., Zhang, Y., Gao, X., Xu, L., & Duan, X. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.03.080 · Cited by 1

MIF-Modulated Spinal Proteins Associated with Persistent Bladder Pain: A Proteomics Study

Ye, S., Agalave, N. M., Ma, F., Mahmood, D. F. D., Al-Grety, A., Khoonsari, P. E., Leng, L., Svensson, C. I., Bucala, R., Kultima, K., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084484 · Cited by 1

Effects of 5-aza-2'-deoxycytidine on DNA Methylation within Female Mouse Reproductive TissuesPreprint

Colwell, M., Flack, N., Medida, R. L., Drown, C., Faulk, C. D., & Mauro, L. J. (2022) · Research Square · doi:10.21203/rs.3.rs-1547192/v3 · Cited by 1

Yes1-mediated Cul9 phosphorylation promotes the metabolic reprogramming in gastric cancerPreprint

Wu, Y., Zhang, H., Zhang, S., Wang, M., Wang, H., Huang, H., Hong, X., Zhang, Z., & Li, Y. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.18.562906 · Cited by 1

MBD2/3 lost its methyl-CpG binding ability in multiple families of HolometabolaPreprint

Israel, E., Länger, Z. M., Heckenhauer, J., Kurtz, J., & Prohaska, S. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.22.650097 · Cited by 1

Coping with extremes: How Epigenetic and Molecular Adaptations Enable Earthworms to Thrive in Volcanic SoilsPreprint

Rimington, O., Novo, M., Hodson, M. E., Camarinho, R., Viveiros, F., Silva, C., Arruda, H., Rodrigues, A., Bruford, M. W., Short, S., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.24.666578 · Cited by 1

mIDEA: An Interpretable Structure–Sequence Model for Methylation-Dependent Protein–DNA Binding SensitivityPreprint

Zhang, Y., Li, R., Zhong, J., & Lin, X. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.14.688575 · Cited by 1

Multiple redundant mechanisms account for the majority of gene silencing downstream of DNA methylationPreprint

Wang, S., Wu, Z., Li, Z., Movilli, A., He, L., Zhou, Y., Lin, E. K., Chuang, R., Thiri, W. W., Convery, S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.08.704674 · Cited by 1

Epigenetic alterations in sporadic and familial cancers

Joensuu, E. I. (2015) · Työväentutkimus Vuosikirja

Epigenética en el asma. Lo esencial

Tordera, M. P. (2016)

Das Tumorepigenom – von der Genregulation über die Tumorklassifikation zum Therapietarget

Ammerpohl, O., Deckert, M., & Montesinos‐Rongen, M. (2016) · Medizinische Genetik · doi:10.1007/s11825-016-0115-1

Régulations épigénétiques et plasticité cérébrale : vers de nouvelles thérapies dans les maladies neurodégénératives ?

Mérienne, K., & Boutillier, A. (2016) · Biologie Aujourd hui · doi:10.1051/jbio/2017002

Epigenetics and major depression disorder

Lepeduš, H., Mikulaj, K., & Gall‐Tros̆elj, K. (2017) · Medicina · doi:10.21860/medflum2017_179753

Designing Epigenome Editing Tools to Understand the Functional Role of DNA Methylation Changes in Cancer

McDonald, J. I. (2017) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k73f4p2b

Crystal structure of the MBD domain of MBD3 in complex with methylated CG DNAPreprint

Liu, K., Lei, M., Gan, B., Cheng, H., Li, Y., & Min, J. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/338061

Cell-type-specific epigenetics of organ-derived neurons and adipocytes

Yu, P. (2017)

CD44 alternative splicing is a sensor of intragenic DNA methylation in tumorsPreprint

Batsché, É., Mauger, O., Kornobis, É., Hopkins, B., Hanmer-Lloyd, C., & Muchardt, C. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/685651

Advances in epigenetic techniques to study development and diseases

Dzobo, K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819414-0.00032-x

m6A RNA methylation and TARDBP, a gene implicated in amyotrophic lateral sclerosis

Quoibion, A. (2017) · doi:10.82308/31337

A Comprehensive In Silico Perspective For Discovery of Novel Inhibitory Candidates Targeting Versatile Transcriptional Repressor MBD2Preprint

Çalışkaner, Z. O. (2021) · Research Square · doi:10.21203/rs.3.rs-578382/v1

Uso de SMPSs en aplicaciones MPI con desbalance de carga

Herrero, V. L. (2011) · RECERCAT (Consorci de Serveis Universitaris de Catalunya)

Epigenetic ecotypes in animals: persistent environmental adaptation in the absence of genetic variationPreprint

Vogt, G. (2022) · doi:10.22541/au.164619271.14974300/v1

Effects of 5-aza-2'-deoxycytidine on DNA Methylation within Female Mouse Reproductive TissuesPreprint

Colwell, M., Wanner, N. M., Medida, R. L., Drown, C., Faulk, C. D., & Mauro, L. J. (2022) · Research Square · doi:10.21203/rs.3.rs-1547192/v1

OBSOLETE: Epigenomics

Ylä-Herttuala, S. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.99575-8

Introducing, OncoTarget

Blagosklonny, M. V., & Gudkov, A. V. (2010) · Oncotarget · doi:10.18632/oncotarget.18947

Epigenetics

Bressler, J. P., Lee, R. S., & Pulczinski, J. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813602-7.00009-0

Introducing, OncoTarget

Blagosklonny, M. V., & Gudkov, A. V. (2010) · Oncotarget · doi:10.18632/oncotarget.18942

Introducing, OncoTarget

Blagosklonny, M. V., & Gudkov, A. V. (2010) · Oncotarget · doi:10.18632/oncotarget.18953

Transcription | Chromatin: Methyl-CpG-Binding Proteins

Lee, J., & Skalnik, D. G. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00213-9

Introducing, OncoTarget

Blagosklonny, M. V., & Gudkov, A. V. (2010) · Oncotarget · doi:10.18632/oncotarget.18940

Introducing, OncoTarget

Blagosklonny, M. V., & Gudkov, A. V. (2010) · Oncotarget · doi:10.18632/oncotarget.18794

Introducing, OncoTarget

Blagosklonny, M. V., & Gudkov, A. V. (2010) · Oncotarget · doi:10.18632/oncotarget.18944

Introducing, OncoTarget

Blagosklonny, M. V., & Gudkov, A. V. (2010) · Oncotarget · doi:10.18632/oncotarget.18938

A clustered regularly interspaced short palindromic repeats knockout method to reveal methyl-CpG binding domain 4 functionPreprint

Ng, A. (2022) · Research Square · doi:10.21203/rs.3.rs-2266782/v1

A clustered regularly interspaced short palindromic repeats knockout method to reveal methyl-CpG binding domain 4 functionPreprint

Ng, A. (2022) · doi:10.31219/osf.io/a8eg7

A clustered regularly interspaced short palindromic repeats knockout method to reveal methyl-CpG binding domain 4 functionPreprint

Ng, A. (2022) · doi:10.14293/s2199-1006.1.sor-.pprduyu.v1

Overview of methodology for studying DNA methylation: A review

Uche, N. A., Eboh, S., & Iroanya, G. I. (2022) · Journal of Animal Science and Veterinary Medicine · doi:10.31248/jasvm2022.331

Aberrant DNA methylation of uveal melanoma drivers as an excellent prognostic toolPreprint

Šoltýsová, A., Dvorská, D., Kajabová, V. H., Pecimonova, M., Cepcekova, K., Ficek, A., Demková, L., Buociková, V., Babál, P., Juras, I., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2502537/v1

A Clustered Regularly Interspaced Short Palindromic Repeats Knockout Method to Reveal methyl-CpG Binding Domain 4 Function

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Synonymous alterations of cancer-associated Trp53 CpG mutational hotspots cause fatal developmental jaw malocclusions but no tumors in knock-in mice

Epstein, R. J., Lin, F. P. Y., Brink, R. A., & Blackburn, J. (2023) · PLoS ONE · doi:10.1371/journal.pone.0284327

Investigação do Status Genômico da Metilação na Síndrome Cri Du Chat utilizando Arrays

Almeida, V. T. (2023) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2023.tde-27062023-113621

Epigenetic Alterations in Pancreatic Cancer

Bulbul, C. Z., Bülbül, M. V., & Soner, S. (2023) · Epigenetics and human health · doi:10.1007/978-3-031-42365-9_8

Evolved Readers of 5‐Carboxylcytosine CpG Dyads Reveal a High Versatility of the Methyl‐CpG‐Binding Domain for Recognition of Noncanonical Epigenetic Marks

Kosel, B., Bigler, K., Buchmuller, B. C., Acharyya, S. R., Linser, R., & Summerer, D. (2024) · Angewandte Chemie · doi:10.1002/ange.202318837

Additional file 1 of Genome-wide identification of MBD gene family members in Eleutherococcus senticosus with their expression motifs under drought stress and DNA demethylation

Wang, S., Dong, J., Zhao, X., Song, X., Long, Y., & Xing, Z. (2023) · Figshare · doi:10.6084/m9.figshare.22599727

Analysis of Multiple Years of RNA-Seq Data Using the 3D-RNA-Seq Application Reveals Seasonal Signatures of Differential Gene and Transcript-Level Expression, Alternative-Splicing, and Transcript...

PHILLIPS, D., Guo, W., & Zhang, R. (2021) · doi:10.22186/jyi.40.8.9-22

ABNORMALITAS SELULER DAN MOLEKULER PADA RETT SYNDROME YANG DIPENGARUHI MUTASI GEN MeCP2

Lestari, I. C., & Mustika, S. E. (2025) · Jurnal Kedokteran STM (Sains dan Teknologi Medik) · doi:10.30743/stm.v8i1.763

Effects of MeCP2 on chronic seizures and cognitive function in mice with temporal lobe epilepsy

Chen, Y., Yang, S.-N., Fu, G.-L., Liu, X.-X., Xiao, X., Wu, X., Wu, F., Ma, Y.-B., Ji, S.-F., Zhou, J.-S., et al. (2025) · Epilepsy Research · doi:10.1016/j.eplepsyres.2025.107512

Arsenic in Groundwater and Its Carcinogenicity

Rja, S. (2023) · International journal of high school research · doi:10.36838/v5i7.21

Methyl-CpG-Binding Domain Protein 2 is Involved in Th17 Cell Differentiation by Positively Regulating Leptin Expression

Xia, Y., Zhang, X., & Wu, D. (2025) · Current Molecular Medicine · doi:10.2174/0115665240341834250121080510

Unraveling the interplay of genetic variants and epigenetic signatures in complex traits

Franco‐Gedda, L. P., Heidor, R., & Horst, M. A. (2025) · Advances in genetics · doi:10.1016/bs.adgen.2025.02.004

“The role of long non-coding RNAs in mediating epigenetic changes induced by bisphenol A Exposure: Focus on reproductive and neurodevelopmental outcomes”

Banabakode, Y., Priscilla, S., Ramkumar, K. M., Ramalingam, S., & Mohideen, S. S. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.152071

Exploring the bistable equilibrium of methylated CpG DNA recognition by the MBD2 protein

Volkenandt, S., Belyaeva, J., Li, T., Elgeti, M., Metzler, R., Imhof, P., Williams, D. C., & Helabad, M. B. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag952

Loss of H3K9 di-methylation perpetuates the type I interferon signature in SLE and is pharmacologically reversible by ribavirinPreprint

Wang, Q., Mitoma, H., Oryoji, D., Semba, Y., Yamauchi, Y., Yokoyama, K., Kawano, S., Ayano, M., Kimoto, Y., Ono, N., et al. (2025) · medRxiv · doi:10.1101/2025.08.04.25332258

Prominent fibroblast growth factor 21 with less abundant tumor-associated macrophages in hepatic mass of the conditional mgmt-deleted mice using LysM-Cre system

Sontidejkul, S., Phuengmaung, P., Saisorn, W., Kaewduangduen, W., Doi, K., Boonmee, A., Benjaskulluecha, S., Palaga, T., & Leelahavanichkul, A. (2025) · Inflammation Research · doi:10.1007/s00011-025-02077-6

Structural insight into the substrate binding of the AMT complex via an inhibitor‐trapped state

Shao, Z., Yoon, S., Lu, J., Athavale, P., Liu, Y., & Song, J. (2025) · Protein Science · doi:10.1002/pro.70265 · Cited by 2

Advances in epigenetic techniques to study development and diseases

Dzobo, K. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-26759-8.00019-9

Epigenetic Biomarkers In Early Alzheimer’s Diagnosis In Aging Populations

Sogi, I. (2025) · American journal of student research. · doi:10.70251/hyjr2348.35764776

Kaiso (ZBTB33) engages with non-canonical binding motifs to regulate DNA damage responses in breast cancer cellsPreprint

Rätze, M. A. K., Tenhagen, M., Vollaers, J., Benner, C. W., Mandoli, A., Singh, A. A., Noordewier, M., Hetzer, M. W., Martens, J. H. A., Stunnenberg, H. G., et al. (2025) · Research Square · doi:10.21203/rs.3.rs-7846387/v1

Convergent Evolution and the Epigenome

Alvarado, S. G., Chang, A., & Tajerian, M. (2025) · Epigenomes · doi:10.3390/epigenomes9040045

Genome-wide demethylation and targeted remethylation during metamorphosis in the jewel wasp Nasonia vitripennis

Thomas, C., & Mallon, E. B. (2025) · Epigenetics & Chromatin · doi:10.1186/s13072-025-00639-w

Additional file 3 of Overexpression of a methyl-CpG-binding protein gene OsMBD707 leads to larger tiller angles and reduced photoperiod sensitivity in rice

Qu, M., Zhang, Z., Liang, T., Niu, P., Wu, M., Chi, W., Chen, Z.-Q., Chen, Z.-J., Zhang, S., & Chen, S. (2021) · Figshare · doi:10.6084/m9.figshare.14059510

Additional file 12 of Overexpression of a methyl-CpG-binding protein gene OsMBD707 leads to larger tiller angles and reduced photoperiod sensitivity in rice

Qu, M., Zhang, Z., Liang, T., Niu, P., Wu, M., Chi, W., Chen, Z., Chen, Z.-J., Zhang, S., & Chen, S. (2021) · Figshare · doi:10.6084/m9.figshare.14059495

Additional file 6 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095524

Additional file 14 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095500

Additional file 10 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095488

Additional file 4 of Overexpression of a methyl-CpG-binding protein gene OsMBD707 leads to larger tiller angles and reduced photoperiod sensitivity in rice

Qu, M., Zhang, Z., Liang, T., Niu, P., Wu, M., Chi, W., Chen, Z., Chen, Z.-J., Zhang, S., & Chen, S. (2021) · Figshare · doi:10.6084/m9.figshare.14059513

Additional file 8 of Toward a base-resolution panorama of the in vivo impact of cytosine methylation on transcription factor binding

Hernandez-Corchado, A., & Najafabadi, H. S. (2022) · Figshare · doi:10.6084/m9.figshare.20267248

Additional file 9 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095533

Additional file 5 of MBD2 regulates the progression and chemoresistance of cholangiocarcinoma through interaction with WDR5

Wang, D., Chen, J., Wu, G., Xiong, F., Liu, W., Wang, Q., Kuai, Y., Huang, W., Qi, Y., Wang, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.27140829

Additional file 1 of MBD2 regulates the progression and chemoresistance of cholangiocarcinoma through interaction with WDR5

Wang, D., Chen, J., Wu, G., Xiong, F., Liu, W., Wang, Q., Kuai, Y., Huang, W., Qi, Y., Wang, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.27140814

Additional file 1 of Overexpression of a methyl-CpG-binding protein gene OsMBD707 leads to larger tiller angles and reduced photoperiod sensitivity in rice

Qu, M., Zhang, Z., Liang, T., Niu, P., Wu, M., Chi, W., Chen, Z., Chen, Z.-J., Zhang, S., & Chen, S. (2021) · Figshare · doi:10.6084/m9.figshare.14059504

Additional file 9 of Overexpression of a methyl-CpG-binding protein gene OsMBD707 leads to larger tiller angles and reduced photoperiod sensitivity in rice

Qu, M., Zhang, Z., Liang, T., Niu, P., Wu, M., Chi, W., Chen, Z., Chen, Z.-J., Zhang, S., & Chen, S. (2021) · Figshare · doi:10.6084/m9.figshare.14059528

Additional file 1 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095509

Additional file 13 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095497

Additional file 4 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095518

Additional file 11 of Overexpression of a methyl-CpG-binding protein gene OsMBD707 leads to larger tiller angles and reduced photoperiod sensitivity in rice

Qu, M., Zhang, Z., Liang, T., Niu, P., Wu, M., Chi, W., Chen, Z., Chen, Z.-J., Zhang, S., & Chen, S. (2021) · Figshare · doi:10.6084/m9.figshare.14059492

Additional file 4 of Thymoquinone upregulates IL17RD in controlling the growth and metastasis of triple negative breast cancer cells in vitro

Khan, M. A., Zheng, M., Fu, J., Tania, M., Li, J., & Fu, J. (2022) · Figshare · doi:10.6084/m9.figshare.20164715

Additional file 5 of Thymoquinone upregulates IL17RD in controlling the growth and metastasis of triple negative breast cancer cells in vitro

Khan, M. A., Zheng, M., Fu, J., Tania, M., Li, J., & Fu, J. (2022) · Figshare · doi:10.6084/m9.figshare.20164718

Additional file 6 of Thymoquinone upregulates IL17RD in controlling the growth and metastasis of triple negative breast cancer cells in vitro

Khan, M. A., Zheng, M., Fu, J., Tania, M., Li, J., & Fu, J. (2022) · Figshare · doi:10.6084/m9.figshare.20164721

Additional file 16 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095506

Additional file 9 of MBD2 regulates the progression and chemoresistance of cholangiocarcinoma through interaction with WDR5

Wang, D., Chen, J., Wu, G., Xiong, F., Liu, W., Wang, Q., Kuai, Y., Huang, W., Qi, Y., Wang, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.27140841

Additional file 1 of Toward a base-resolution panorama of the in vivo impact of cytosine methylation on transcription factor binding

Hernandez-Corchado, A., & Najafabadi, H. S. (2022) · Figshare · doi:10.6084/m9.figshare.20267224

Additional file 5 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095521

Additional file 15 of DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii

Planques, A., Kerner, P., Ferry, L., Grunau, C., Gazave, E., & Vervoort, M. (2021) · Figshare · doi:10.6084/m9.figshare.15095503

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Baubec, T., Ivánek, R., Lienert, F., & Schübeler, D. (2013) · Cell · doi:10.1016/j.cell.2013.03.011 · Cited by 365

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