Dynamic regulation of transcriptional states by chromatin and transcription factors

Stochastic Gene Expression in a Single Cell

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Network motifs: theory and experimental approaches

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A decade of exploring the cancer epigenome—biological and translational implications

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The accessible chromatin landscape of the human genome

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The biology of chromatin remodeling complexes.

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Stochasticity in gene expression: from theories to phenotypes

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Transcription factors: from enhancer binding to developmental control

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Stability and flexibility of epigenetic gene regulation in mammalian development

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Stochastic mRNA Synthesis in Mammalian Cells

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Intrinsic and extrinsic contributions to stochasticity in gene expression

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Sentinels of chromatin: chromodomain helicase DNA-binding proteins in development and diseasePreprint

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Nascent RNA sequencing reveals mechanisms of gene regulation in the human malaria parasite Plasmodium falciparum

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Visualizing the Architectures and Interactions of Nuclear Receptors

Khorasanizadeh, S., & Rastinejad, F. (2016) · Endocrinology · doi:10.1210/en.2016-1559 · Cited by 65

Dynamic assembly and activation of estrogen receptor α enhancers through coregulator switchingPreprint

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Quantitation of Glucocorticoid Receptor DNA-Binding Dynamics by Single-Molecule Microscopy and FRAP

Groeneweg, F. L., van Royen, M. E., Fenz, S. F., Keizer, V. I. P., Geverts, B., Prins, J., de Kloet, E. R., Houtsmuller, A. B., Schmidt, T. S., & Schaaf, M. J. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090532 · Cited by 63

Gene-Specific Actions of Transcriptional Coregulators Facilitate Physiological Plasticity: Evidence for a Physiological Coregulator Code

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Cytokinin modulates context-dependent chromatin accessibility through the type-B response regulators

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KIT mutations and expression: current knowledge and new insights for overcoming IM resistance in GIST

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Epigenetic gene regulation by histone demethylases: emerging role in oncogenesis and inflammation

Kang, M., Mehrazarin, S., Park, N., & Wang, C. (2016) · Oral Diseases · doi:10.1111/odi.12569 · Cited by 63

Nuclear factor one transcription factors as epigenetic regulators in cancer

Fane, M. E., Harris, L., Smith, A. G., & Piper, M. (2017) · International Journal of Cancer · doi:10.1002/ijc.30603 · Cited by 63

Regulation of neuronal connectivity in the mammalian brain by chromatin remodeling

Goodman, J. V., & Bonni, A. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.04.010 · Cited by 64

Depletion of the chromatin remodeler CHD4 sensitizes AML blasts to genotoxic agents and reduces tumor formation

Sperlazza, J. R., Rahmani, M., Beckta, J. M., Aust, M. M., Hawkins, E., Wang, S. Z., Zhu, S. Z., Podder, S., Dumur, C. I., Archer, K. J., et al. (2015) · Blood · doi:10.1182/blood-2015-03-631606 · Cited by 59

Introduction to Transcription Factor Structure and Function

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FOXA1 forms biomolecular condensates that unpack condensed chromatin to function as a pioneer factor

Ji, D., Shao, C., Yu, J., Hou, Y., Gao, X., Wu, Y., Wang, L., & Chen, P. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.11.020 · Cited by 58

The impact of chromatin remodelling on cellulase expression in Trichoderma reesei

Mello-de-Sousa, T. M., Rassinger, A., Pucher, M. E., Castro, L. D. S., Persinoti, G. F., Silva‐Rocha, R., Poças-Fonseca, M. J., Mach, R. L., Silva, R. N., & Mach-Aigner, A. R. (2015) · BMC Genomics · doi:10.1186/s12864-015-1807-7 · Cited by 57

The embryo as a laboratory: quantifying transcription in Drosophila

Gregor, T., García, H. G., & Little, S. C. (2014) · Trends in Genetics · doi:10.1016/j.tig.2014.06.002 · Cited by 60

The Crosstalk between Acetylation and Phosphorylation: Emerging New Roles for HDAC Inhibitors in the Heart

Habibian, J. S., & Ferguson, B. S. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms20010102 · Cited by 60

Skeletal muscle methylome and transcriptome integration reveals profound sex differences related to muscle function and substrate metabolism

Landen, S., Jacques, M., Hiam, D., Alvarez‐Romero, J., Harvey, N. R., Haupt, L. M., Griffiths, L. R., Ashton, K. J., Lamon, S., Voisin, S. A. C., et al. (2021) · Clinical Epigenetics · doi:10.1186/s13148-021-01188-1 · Cited by 60

Cofactor squelching: Artifact or fact?

Schmidt, S. F., Larsen, B. D., Loft, A., & Mandrup, S. (2016) · BioEssays · doi:10.1002/bies.201600034 · Cited by 56

Single molecule tracking of Ace1p in Saccharomyces cerevisiae defines a characteristic residence time for non-specific interactions of transcription factors with chromatin

Ball, D. A., Mehta, G., Salomon‐Kent, R., Mazza, D., Morisaki, T., Mueller, F., McNally, J. G., & Karpova, T. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw744 · Cited by 56

Proteomic analysis of proteome and histone post-translational modifications in heat shock protein 90 inhibition-mediated bladder cancer therapeutics

Li, Q. Q., Hao, J.-J., Zhang, Z., Krane, L. S., Hammerich, K. H., Sanford, T. H., Trepel, J. B., Neckers, L., & Agarwal, P. K. (2017) · Scientific Reports · doi:10.1038/s41598-017-00143-6 · Cited by 60

Three-dimensional genome organization in immune cell fate and function

Cuartero, S., Stik, G., & Stadhouders, R. (2022) · Nature reviews. Immunology · doi:10.1038/s41577-022-00774-5 · Cited by 56

Systematic Evaluation of Site-Specific Recombinant Gene Expression for Programmable Mammalian Cell Engineering

Pristovšek, N., Nallapareddy, S., Grav, L. M., Hefzi, H., Lewis, N. E., Rugbjerg, P., Hansen, H. G., Lee, G. M., Andersen, M. R., & Kildegaard, H. F. (2019) · ACS Synthetic Biology · doi:10.1021/acssynbio.8b00453 · Cited by 56

A high-resolution map of transcriptional repression

Liang, Z., Brown, K. E., Carroll, T., Taylor, B., Vidal, I. F., Hendrich, B., Rueda, D., Fisher, A. G., & Merkenschlager, M. (2017) · eLife · doi:10.7554/elife.22767 · Cited by 54

DNA residence time is a regulatory factor of transcription repression

Clauß, K., Popp, A. P., Schulze, L., Hettich, J., Reisser, M., Escoter-Torres, L., Uhlenhaut, N. H., & Gebhardt, J. C. M. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx728 · Cited by 54

Vision from next generation sequencing: Multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease

Yang, H., Ratnapriya, R., Cogliati, T., Kim, J.-W., & Swaroop, A. (2015) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2015.01.005 · Cited by 52

Dose Response and Prediction Characteristics of a Methylation Sensitive Digital PCR Assay for Cigarette Consumption in Adults

Philibert, R. A., Dogan, M. V., Noel, A., Miller, S., Krukow, B., Papworth, E., Cowley, J., Long, J. D., Beach, S. R. H., & Black, D. W. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00137 · Cited by 52

Targeting the epigenome: Screening bioactive compounds that regulate histone deacetylase activity

Godoy, L., Lucas, J. E., Bender, A., Romanick, S., & Ferguson, B. S. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201600744 · Cited by 50

Genome-wide prediction of DNase I hypersensitivity using gene expression

Zhou, W., Sherwood, B., Ji, Z., Xue, Y., Du, F., Bai, J., Ying, M., & Ji, H. (2017) · Nature Communications · doi:10.1038/s41467-017-01188-x · Cited by 52

Long-term association of a transcription factor with its chromatin binding site can stabilize gene expression and cell fate commitment

Gurdon, J. B., Javed, K., Vodnala, M., & Garrett, N. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2000467117 · Cited by 50

Dealing with transcription-blocking DNA damage: Repair mechanisms, RNA polymerase II processing and human disorders

Jia, N., Guo, C., Nakazawa, Y., van den Heuvel, D., Luijsterburg, M. S., & Ogi, T. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103192 · Cited by 50

NFE2L1 and NFE2L3 Complementarily Maintain Basal Proteasome Activity in Cancer Cells through CPEB3-Mediated Translational Repression

Waku, T., Katayama, H., Hiraoka, M., Hatanaka, A., Nakamura, N., Tanaka, Y., Tamura, N., Watanabe, A., & Kobayashi, A. (2020) · Molecular and Cellular Biology · doi:10.1128/mcb.00010-20 · Cited by 42

Cell2fate infers RNA velocity modules to improve cell fate prediction

Aivazidis, A., Memi, F., Kleshchevnikov, V., Er, S., Clarke, B., Stegle, O., & Bayraktar, O. A. (2025) · Nature Methods · doi:10.1038/s41592-025-02608-3 · Cited by 50

Characterization of the chromatin accessibility in an Alzheimer’s disease (AD) mouse model

Wang, Y., Zhang, X., Song, Q., Hou, Y., Liu, J., Sun, Y., & Wang, P. (2020) · Alzheimer s Research & Therapy · doi:10.1186/s13195-020-00598-2 · Cited by 51

Chromatin accessibility dynamics during cell fate reprogramming

Li, D., Shu, X., Zhu, P., & Pei, D. (2021) · EMBO Reports · doi:10.15252/embr.202051644 · Cited by 50

Epigenetic contributions to the developmental origins of adult lung disease

Joss‐Moore, L. A., Lane, R. H., & Albertine, K. H. (2014) · Biochemistry and Cell Biology · doi:10.1139/bcb-2014-0093 · Cited by 47

Gene Regulation by H-NS as a Function of Growth Conditions Depends on Chromosomal Position in Escherichia coli

Brambilla, E., & Sclavi, B. (2015) · G3 Genes Genomes Genetics · doi:10.1534/g3.114.016139 · Cited by 46

Histone Modifications in Major Depressive Disorder and Related Rodent Models

Deussing, J. M., & Jakovcevski, M. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-53889-1_9 · Cited by 46

hnRNPU/TrkB Defines a Chromatin Accessibility Checkpoint for Liver Injury and Nonalcoholic Steatohepatitis Pathogenesis

Xiong, J., Liu, T., Mi, L., Kuang, H., Xiong, X., Chen, Z., Li, S., & Lin, J. D. (2019) · Hepatology · doi:10.1002/hep.30921 · Cited by 46

Expression and chromatin structures of cellulolytic enzyme gene regulated by heterochromatin protein 1

Zhang, X., Qu, Y., & Qin, Y. (2016) · Biotechnology for Biofuels · doi:10.1186/s13068-016-0624-9 · Cited by 45

CHD1 regulates cell fate determination by activation of differentiation-induced genes

Baumgart, S. J., Najafova, Z., Hossan, T., Xie, W., Nagarajan, S., Kari, V., Ditzel, N., Kassem, M. S., & Johnsen, S. A. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx377 · Cited by 45

MOZ and Menin–MLL complexes are complementary regulators of chromatin association and transcriptional output in gastrointestinal stromal tumor

Hemming, M. L., Benson, M. R., Loycano, M. A., Anderson, J. A., Andersen, J. L., Taddei, M. L., Krivtsov, A. V., Aubrey, B. J., Cutler, J. A., Hatton, C., et al. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-21-0646 · Cited by 39

Multifaceted Control of GR Signaling and Its Impact on Hepatic Transcriptional Networks and Metabolism

Præstholm, S. M., Correia, C. M., & Grøntved, L. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.572981 · Cited by 45

The Hepatitis B Virus Interactome: A Comprehensive Overview

Damme, E. V., Vanhove, J., Severyn, B. S., Verschueren, L., & Pauwels, F. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.724877 · Cited by 44

Global inhibition of transcription causes an increase in histone H2A.Z incorporation within gene bodies

Lashgari, A., Millau, J., Jacques, P., & Gaudreau, L. R. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx879 · Cited by 46

Dynamic switching of transcriptional regulators between two distinct low-mobility chromatin states

Wagh, K., Stavreva, D. A., Jensen, R. A., Paakinaho, V., Fettweis, G., Schiltz, R. L., Wüstner, D., Mandrup, S., Presman, D. M., Upadhyaya, A., et al. (2023) · Science Advances · doi:10.1126/sciadv.ade1122 · Cited by 41

Distinct guard cell–specific remodeling of chromatin accessibility during abscisic acid– and CO 2 -dependent stomatal regulation

Seller, C. A., & Schroeder, J. I. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2310670120 · Cited by 42

Integrated multi-omics approach revealed cellular senescence landscape

Song, Q., Hou, Y., Zhang, Y., Liu, J., Wang, Y., Fu, J., Zhang, C., Cao, M., Cui, Y., Zhang, X., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac885 · Cited by 44

Allosteric conformational ensembles have unlimited capacity for integrating information

Biddle, J. W., Martinez-Corral, R., Wong, F., & Gunawardena, J. (2021) · eLife · doi:10.7554/elife.65498 · Cited by 41

Epigenetic regulation of bone cells

Park‐Min, K. H. (2016) · Connective Tissue Research · doi:10.1080/03008207.2016.1177037 · Cited by 42

Dilution and titration of cell-cycle regulators may control cell size in budding yeast

Heldt, F. S., Lunstone, R., Tyson, J. J., & Novák, B. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006548 · Cited by 41

The Chromatin Remodeler CHD8 Is Required for Activation of Progesterone Receptor-Dependent Enhancers

Ceballos-Chávez, M., Subtil‐Rodríguez, A., Γιαννοπούλου, Ε., Soronellas, D., Vázquez-Chávez, E., Vicent, G. P., Elemento, O., Beato, M., & Reyes, J. C. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005174 · Cited by 43

Functional compensation among HMGN variants modulates the DNase I hypersensitive sites at enhancersPreprint

Deng, T., Zhu, Z., Zhang, S., Postnikov, Y. V., Huang, D., Horsch, M., Furusawa, T., Beckers, J., Rozman, J., Klingenspor, M., et al. (2015) · Genome Research · doi:10.1101/gr.192229.115 · Cited by 42

Real-time single-molecule imaging of transcriptional regulatory networks in living cells

Hwang, D.-W., Maekiniemi, A., Singer, R. H., & Sato, H. (2024) · Nature Reviews Genetics · doi:10.1038/s41576-023-00684-9 · Cited by 44

Landscape of transcriptional deregulation in lung cancer

Zhang, S., Li, M., Ji, H., & Fang, Z. (2018) · BMC Genomics · doi:10.1186/s12864-018-4828-1 · Cited by 40

BRG1 Governs Nanog Transcription in Early Mouse Embryos and Embryonic Stem Cells via Antagonism of Histone H3 Lysine 9/14 Acetylation

Carey, T. S., Cao, Z., Choi, I., Ganguly, A., WILSON, C. A., Paul, S., & Knott, J. G. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00546-15 · Cited by 39

Epigenetics in Kidney Transplantation

Mas, V. R., Le, T. H., & Maluf, D. G. (2015) · Transplantation · doi:10.1097/tp.0000000000000878 · Cited by 39

TFAP2 paralogs facilitate chromatin access for MITF at pigmentation and cell proliferation genes

Kenny, C., Dilshat, R., Seberg, H., Otterloo, E. V., Bonde, G., Helverson, A., Franke, C. M., Steingrı́msson, E., & Cornell, R. A. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010207 · Cited by 40

A chromosome-scale genome assembly of Dasypyrum villosum provides insights into its application as a broad-spectrum disease resistance resource for wheat improvement

Zhang, X., Wang, H., Sun, H., Li, Y., Feng, Y., Jiao, C., Li, M., Song, X., Wang, T., Wang, Z., et al. (2022) · Molecular Plant · doi:10.1016/j.molp.2022.12.021 · Cited by 39

Extensive epigenomic integration of the glucocorticoid response in primary human monocytes and in vitro derived macrophages

Wang, C., Nanni, L., Novakovic, B., Megchelenbrink, W., Kuznetsova, T., Stunnenberg, H. G., Ceri, S., & Logie, C. (2019) · Scientific Reports · doi:10.1038/s41598-019-39395-9 · Cited by 38

Mechanisms contributing to persistently activated cell phenotypes in pulmonary hypertension

Hu, C., Zhang, H., Laux, A., Pullamsetti, S. S., & Stenmark, K. R. (2018) · The Journal of Physiology · doi:10.1113/jp275857 · Cited by 37

DNAffinity: a machine-learning approach to predict DNA binding affinities of transcription factors

Barissi, S., Sala, A., Wieczór, M., Battistini, F., & Orozco, M. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac708 · Cited by 37

Multi-modality in gene regulatory networks with slow promoter kinetics

Al-Radhawi, M. A., Vecchio, D. D., & Sontag, E. D. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006784 · Cited by 38

H4K12ac is regulated by estrogen receptor-alpha and is associated with BRD4 function and inducible transcription

Nagarajan, S., Benito, E., Fischer, A., & Johnsen, S. A. (2015) · Oncotarget · doi:10.18632/oncotarget.3439 · Cited by 38

Precision control of recombinant gene transcription for CHO cell synthetic biology

Brown, A. J., & James, D. C. (2015) · Biotechnology Advances · doi:10.1016/j.biotechadv.2015.12.012 · Cited by 37

Transcriptional regulation of early T‐cell development in the thymus

Seo, W., & Taniuchi, I. (2016) · European Journal of Immunology · doi:10.1002/eji.201545821 · Cited by 42

Enhancer functions in three dimensions: beyond the flat world perspective

Göndör, A., & OHLSSON, R. I. (2018) · F1000Research · doi:10.12688/f1000research.13842.1 · Cited by 36

Transcriptomics based multi-dimensional characterization and drug screen in esophageal squamous cell carcinoma

Li, Y., Xu, F., Chen, F., Chen, Y., Ge, D., Zhang, S., & Lu, C. (2021) · EBioMedicine · doi:10.1016/j.ebiom.2021.103510 · Cited by 38

RNA polymerase II pausing in development: orchestrating transcription

Abuhashem, A., Garg, V., & Hadjantonakis, A. (2022) · Open Biology · doi:10.1098/rsob.210220 · Cited by 38

Studies on lipoate effects on blood redox state in human immunodeficiency virus infected patients.

Fuchs, J., Schöfer, H., Milbradt, R., Freisleben, H., Buhl, R., Siems, W., & Grune, T. (1993) · PubMed · Cited by 36

The long noncoding RNA Falcor regulates Foxa2 expression to maintain lung epithelial homeostasis and promote regenerationPreprint

Swarr, D. T., Herriges, M. J., Li, S., Morley, M., Fernandes, S., Sridharan, A., Zhou, S., Garcia, B. A., Stewart, K. M., & Morrisey, E. E. (2019) · Genes & Development · doi:10.1101/gad.320523.118 · Cited by 36

Inferring transcriptional bursting kinetics from single-cell snapshot data using a generalized telegraph model

Luo, S., Zhang, Z., Wang, Z., Yang, X., Chen, X., Zhou, T., & Zhang, J. (2023) · Royal Society Open Science · doi:10.1098/rsos.221057 · Cited by 35

Integration of Spatial and Temporal Patterning in the Invertebrate and Vertebrate Nervous System

Chen, Y., & Konstantinides, N. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.854422 · Cited by 35

3D chromatin reprogramming primes human memory T H 2 cells for rapid recall and pathogenic dysfunction

Schoonhoven, A. O.-V., de Bruijn, M. J. W., Stikker, B., Brouwer, R. W. W., Braunstahl, G., van IJcken, W. F. J., Graf, T., Huylebroeck, D., Hendriks, R. W., Stik, G., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.adg3917 · Cited by 35

Chromatin variation associated with liver metabolism is mediated by transposable elements

Du, J., Leung, A., Trac, C., Lee, M., Parks, B. W., Lusis, A. J., Natarajan, R. D., & Schones, D. E. (2016) · Epigenetics & Chromatin · doi:10.1186/s13072-016-0078-0 · Cited by 35

Unravelling the Complexity and Functions of MTA Coregulators in Human Cancer

Li, D., & Kumar, R. (2015) · Advances in cancer research · doi:10.1016/bs.acr.2015.04.005 · Cited by 34

Exactly solvable models of stochastic gene expression

Ham, L., Schnoerr, D., Brackston, R. D., & Stumpf, M. P. H. (2020) · The Journal of Chemical Physics · doi:10.1063/1.5143540 · Cited by 34

Fruiting-Body Development in Ascomycetes

Pöggeler, S., Nowrousian, M., Teichert, I., Beier, A., & Kück, U. (2018) · Springer eBooks · doi:10.1007/978-3-319-71740-1_1 · Cited by 37

A new transcription factor for mitosis: in Schizosaccharomyces pombe , the RFX transcription factor Sak1 works with forkhead factors to regulate mitotic expression

Garg, A., Futcher, B., & Leatherwood, J. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv274 · Cited by 34

Binding of high mobility group A proteins to the mammalian genome occurs as a function of AT-content

Colombo, D., Burger, L., Baubec, T., & Schübeler, D. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1007102 · Cited by 32

Transcription factor–nucleosome dynamics from plasma cfDNA identifies ER-driven states in breast cancer

Rao, S., Han, A., Zukowski, A., Kopin, E. G., Sartorius, C. A., Kabos, P., & Ramachandran, S. (2022) · Science Advances · doi:10.1126/sciadv.abm4358 · Cited by 34

Coexpression Clusters and Allele-Specific Expression in Metabolism-Based Herbicide Resistance

Giacomini, D. A., Patterson, E. L., Küpper, A., Beffa, R., Gaines, T. A., & Tranel, P. J. (2020) · Genome Biology and Evolution · doi:10.1093/gbe/evaa191 · Cited by 31

Dynamic chromatin remodeling in cycling human endometrium at single-cell level

Vrljicak, P., Lucas, E. S., Tryfonos, M., Muter, J., Ott, S., & Brosens, J. J. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113525 · Cited by 30

Ageing and sources of transcriptional heterogeneity

Nikopoulou, C., Parekh, S., & Tessarz, P. (2019) · Biological Chemistry · doi:10.1515/hsz-2018-0449 · Cited by 31

Distinguishing between models of mammalian gene expression: telegraph-like models versus mechanistic models

Braichenko, S., Holehouse, J., & Grima, R. (2021) · Journal of The Royal Society Interface · doi:10.1098/rsif.2021.0510 · Cited by 29

The regulatory genome of the malaria vector Anopheles gambiae : integrating chromatin accessibility and gene expression

Ruiz, J. L., Ranford-Cartwright, L. C., & Gómez‐Díaz, E. (2021) · NAR Genomics and Bioinformatics · doi:10.1093/nargab/lqaa113 · Cited by 33

PRO-IP-seq tracks molecular modifications of engaged Pol II complexes at nucleotide resolution

Vihervaara, A., Versluis, P. P., Himanen, S. V., & Lis, J. T. (2023) · Nature Communications · doi:10.1038/s41467-023-42715-3 · Cited by 29

Leveraging the Mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation

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HNRNPU promotes the progression of hepatocellular carcinoma by enhancing CDK2 transcription

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