Chromatin remodelling during development

Capturing 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

Neuroblastoma Epigenetic Landscape: Drugging Opportunities

Veschi, V., Durinck, K., Thiele, C. J., & Speleman, F. (2024) · Pediatric oncology · doi:10.1007/978-3-031-51292-6_5 · Cited by 2

The Autism-Related Protein CHD8 Cooperates with C/EBPβ to Regulate Adipogenesis

Kita, Y., Katayama, Y., Shiraishi, T., Oka, T., Sato, T., Suyama, M., Ohkawa, Y., Miyata, K., Oike, Y., Shirane, M., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.050 · Cited by 2

Induced Pluripotent Stem Cells

Mobley, A. S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-811014-0.00004-4 · Cited by 4

Membrane Computing Aggregation (MCA): An Upgraded Framework for Transition P-Systems

Arteta, A., López, L. F. D. M., Blas, N. G., & Zhao, Y. (2019) · Lecture notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering · doi:10.1007/978-3-030-24202-2_15 · Cited by 2

Basics of epigenetics: It is more than simple changes in sequence that govern gene expression

Sharma, S., & Aazmi, O. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814259-2.00001-7 · Cited by 2

Subunit redundancy within the NuRD complex ensures fidelity of ES cell lineage commitmentPreprint

Burgold, T., Barber, M., Kloet, S. L., Cramard, J., Gharbi, S., Floyd, R., Kinoshita, M., Ralser, M., Vermeulen, M., Reynolds, N., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/362988 · Cited by 2

Investigation of DNA Damage and Genomic Organization in the Cellular Response to Platinum Chemotherapy

Abdulwahed, A. (2020) · FIU - Digital Commons (Florida International University) · doi:10.25148/etd.fidc009544 · Cited by 1

Detection and characterization of replication origins defined by DNA polymerase epsilonPreprint

Jaksik, R., Wheeler, D. A., & Kimmel, M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.27.453931 · Cited by 2

Epigenetics of autoimmune diseases

Farhadi, E., & Mahmoudi, M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814259-2.00009-1 · Cited by 1

Striatal neuronal models of Huntington's disease via direct conversion: Modeling age-dependent disease phenotypes

Oh, Y. M., Lee, S. W., & Yoo, A. S. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95672-7.00012-1 · Cited by 1

The epigenetic system, evo-devo, and the Extended Evolutionary Synthesis

Müller, G. B. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-19051-3.00002-4 · Cited by 1

Overview of cancer: Mechanisms of carcinogenesis

Saran, U., & Thakur, C. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13209-4.00008-8 · Cited by 1

EpiMapper: A new tool for analyzing high-throughput sequencing from CUT&Tag

Dragland, J. S., Liu, G., Nilsen, H. L., Böttcher, Y., & Wang, J. (2025) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2025.109692 · Cited by 1

Bibliometric analysis of ferroptosis: a comprehensive evaluation of its contribution to lung cancer

Yao, F., Guo, F., Sun, C., Wang, E., Wang, H., & Li, N. (2025) · Frontiers in Genetics · doi:10.3389/fgene.2024.1449491 · Cited by 1

Assessing In Silico Tools for Accurate Pathogenicity Prediction in CHD Nucleosome Remodelers

Rabouhi, N., Guindon, S., Coleman, E. A., van Heesbeen, H. J., Greenwood, C. M. T., Lu, T., & Campeau, P. M. (2025) · Journal of Molecular Biology · doi:10.1016/j.jmb.2025.169413 · Cited by 1

FET fusion oncoproteins enrich SWI/SNF complex subtypes and interaction partners

Lindén, M., Andersson, L., Albatrok, H., Canfjorden, V., Jonasson, E., Grönqvist, K., Sjövall, D., Jaako, P., Crescitelli, R., Fagman, H., et al. (2025) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00792-w · Cited by 1

The Knockdown of ACTL6A Enhances the Radiosensitivity of Esophageal Squamous Cell Carcinoma by Modulating the Wnt/β‐Catenin Signaling Pathway

Zhou, S., Sun, T., Liu, L., Guo, D., Zhang, X., Shen, W., Gao, S., & Zhu, S. (2025) · The FASEB Journal · doi:10.1096/fj.202501681r · Cited by 1

Clinical Insights From a Case of Sifrim‐Hitz‐Weiss Syndrome With a CHD4 Variant: Expanding the Phenotypic Spectrum and Its Response to Growth Hormone Therapy

Zhang, J., Chen, S., DONG, G., Yang, S., Wang, P., Zhou, Q., & Wang, P. (2026) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.70084 · Cited by 1

TGFβ-activated PDHB promotes mitochondrial pyruvate metabolism and contributes to human endoderm differentiation via ATP-dependent BRG1

Meng, L., Lv, J., Yi, Y., Lan, X., Yan, C., Zhu, L., Yang, J., & Jiang, W. (2026) · Nature Communications · doi:10.1038/s41467-026-69510-0 · Cited by 1

DISSECTING THE ROLE OF THE GLUCOCORTICOID RECEPTOR IN EMBRYONIC CORTICAL DEVELOPMENT: INSIGHTS FROM IN UTERO GLUCOCORTICOID EXPOSURE

Tsiarli, M. A. (2014) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1

Epigenetic Reprogramming in Stem Cells

Richard, L., Kizilyer, Y., & Candace, L. (2013) · InTech eBooks · doi:10.5772/56327 · Cited by 1

Epigenetic Therapies for Cancer

Bojang, P., Jr., & Kenneth, S. (2011) · InTech eBooks · doi:10.5772/24818 · Cited by 1

Epigenetic gene regulation and stem cell function

Benyoucef, A., & Brand, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-799958-6.00007-x · Cited by 1

The Recent Progress on SWI/SNF Chromatin Remodeling in Higher Plants

Yuan, T., & Cui, S. (2013) · ACTA AGRONOMICA SINICA · doi:10.3724/sp.j.1206.2013.00205 · Cited by 1

The Design and Development of Polyamine-Based Analogs with Epigenetic Targets

Huang, Y., Marton, L. J., & Woster, P. M. (2011) · Royal Society of Chemistry eBooks · doi:10.1039/9781849733090-00238 · Cited by 1

The SWI/SNF chromatin remodeling complex exerts both negative and positive control over LET-23/EGFR-dependent vulval induction in Caenorhabditis elegans

Flibotte, S., Kim, B. R., de Laar, E. V., Brown, L., & Moghal, N. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.05.009 · Cited by 1

The Human Genome

Meisenberg, G., & Simmons, W. H. (2012) · Elsevier eBooks · doi:10.1016/b978-0-323-07155-0.00007-1 · Cited by 1

Epigenetics in Autism

Ginsberg, M. R., & Natowicz, M. R. (2014) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814602167_0012 · Cited by 1

Chromatin Remodeling in Heart Failure

Han, P., Yang, J., Shang, C., & Chang, C.-P. (2016) · Cardiac and vascular biology · doi:10.1007/978-3-319-41457-7_5 · Cited by 2

Long-Term Complications in Diabetes Mellitus and the Interrelationship of Blood Vessel Formation, Endothelial Progenitor Cells, and gDNA Methylation

Sarras, M. P., & Leontovich, A. A. (2019) · Springer eBooks · doi:10.1007/978-3-319-55530-0_71 · Cited by 1

Molecular Mechanisms of Leaf Morphogenesis

Koyama, T. (2022) · MDPI eBooks · doi:10.3390/books978-3-0365-3162-5 · Cited by 1

Discovery of CECR2 Bromodomain Inhibitors with High Selectivities over BPTF Bromodomain

Lu, H., Zu, S., Duan, Z., Feng, Y., Wang, J., Ma, J., Li, Q., Chen, D., Li, B., Chen, K., et al. (2022) · Chinese Journal of Chemistry · doi:10.1002/cjoc.202200208 · Cited by 2

Epigenetic Mechanisms: DNA Methylation and Histone Protein Modification

Gagnidze, K., & Pfaff, D. W. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3474-4_69 · Cited by 1

Smarca4 deficiency induces Pttg1 oncogene upregulation and hyperproliferation of tubular and interstitial cells during kidney development

Xu, J., Zhou, X., Zhang, T., Zhang, B., & Xu, P. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1233317 · Cited by 1

RNA polymerase II promoter-proximal pausing promotes BAF chromatin binding and remodeling

Chick, B. Y., & Hargreaves, D. C. (2023) · Nature Genetics · doi:10.1038/s41588-023-01628-z · Cited by 1

Epicardial SMARCA4 deletion exacerbates cardiac injury in myocardial infarction and is related to the inhibition of epicardial epithelial-mesenchymal transition

Ma, X., Zhao, J., & Feng, Y. (2024) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2024.05.001 · Cited by 1

Epigenomic Insights Into Model Animals and Their Application in Understanding Livestock Systems in Veterinary Science

Pandey, N., & Yadav, A. K. (2025) · Springer eBooks · doi:10.1007/978-981-97-7395-4_4 · Cited by 1

Overview of the “Epigenetic End Points in Toxicologic Pathology and Relevance to Human Health” Session of the 2014 Society of Toxicologic Pathology Annual Symposium

Hoenerhoff, M. J., & Hartke, J. (2014) · Toxicologic Pathology · doi:10.1177/0192623314553475 · Cited by 1

Transgenerational epigenetic regulation by environmental factors in human diseases

Li, Y. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-799958-6.00009-3 · Cited by 1

Are Epigenetic Features Essential in Advance of Heart Failure Phenotypes?

Berezin, A. Е. (2016) · Journal of Cardiology and Therapy · doi:10.17554/j.issn.2309-6861.2016.03.118 · Cited by 1

Pancreatic plasticity: epigenetic mechanisms and connections to neoplasia

David, C. J. (2019) · Journal of Pancreatology · doi:10.1097/jp9.0000000000000036 · Cited by 1

Understanding immune system development: An epigenetic perspective

Madhok, A., deSouza, A., & Galande, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-817964-2.00003-4 · Cited by 1

Acute Promyelocytic Leukemia

Wiernik, P. H., Gallagher, R. E., & Tallman, M. S. (2017) · Springer eBooks · doi:10.1007/978-3-319-64263-5_21 · Cited by 1

An Encrypted Proposal Method in Membrane Computing Aggregation (MCA)

Arteta, A., Zhao, Y., López, L. F. D. M., & Blas, N. G. (2022) · Mobile Networks and Applications · doi:10.1007/s11036-022-02058-7 · Cited by 1

Epigenetic Regulation in Autism

Peter, C. J., Reichenberg, A., & Akbarian, S. (2015) · Contemporary clinical neuroscience · doi:10.1007/978-1-4939-2190-4_5 · Cited by 1

An Overview of Gene Regulation

Harrison, A., & Shanahan, H. P. (2013) · Springer eBooks · doi:10.1007/978-3-642-41281-3_2 · Cited by 1

Function of the CHD4/Mi-2ß chromatin remodelling ATPase during neural development of Xenopus laevis

Nieberler, M. (2012) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.13954 · Cited by 1

Epigenetic mechanisms of asthma and allergy

Acevedo, N. (2015) · Figshare · Cited by 1

The role of CFP1 in murine embryonic stem cell function and liver regeneration

Mahadevan, J. (2015) · IUScholarWorks (Indiana University) · doi:10.7912/c2/1897 · Cited by 1

Intramolecular dynamics of single molecules in free diffusionPreprint

Limouse, C., Bell, J. C., Fuller, C. J., Straight, A. F., & Mabuchi, H. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/120311 · Cited by 1

Brg1 controls neurosensory cell fate commitment and differentiation in the mammalian inner earPreprint

Xu, J., Li, J., Loh, Y. E., Zhang, T., Jiang, H., Fritzsch, B., Ramakrishnan, A., Shen, L., & Xu, P. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/434159 · Cited by 1

Mechanisms underlying the temporal and selective induction of Ptf1a target genes

Richts, S. (2019) · doi:10.53846/goediss-7262

A guardian of balance: the role of BAF chromatin remodeling complex in astrogliogenesis during mouse forebrain development

Kiszka, K. A. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7790 · Cited by 1

Chromatin dynamics during hematopoiesis reveal discrete regulatory modules instructing differentiationPreprint

Georgolopoulos, G., Psatha, N., Iwata, M., Nishida, A., Som, T., Yiangou, M., Stamatoyannopoulos, J. A., & Vierstra, J. D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.02.022566 · Cited by 1

Cre-mediated deletion of SMARCA5 disrupts pluripotency in mouse embryonic stem cellsPreprint

Cook, D. P., & Vanderhyden, B. C. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.02.022285 · Cited by 1

BAF chromatin remodeling complex subunit diversity promotes temporally distinct gene expression programs in cardiogenesisPreprint

Hota, S. K., Johnson, J. R., Verschueren, E., Thomas, R., Blotnick, A. M., Zhu, Y., Sun, X., Pennacchio, L. A., Krogan, N. J., & Bruneau, B. G. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/166983 · Cited by 1

Molecular functions of multi-SUMO-binding protein complexes

Leshem, R. (2019) · Research Explorer (The University of Manchester) · Cited by 1

An RNA binding module of SWI/SNF is required for activation of cell-type specific enhancers and super-enhancers in early developmentPreprint

Saha, D., Animireddy, S., Lee, J., Lin, Y.-C., Feola, K. C., Jain, A. K., Lu, Y., Liu, B., & Bartholomew, B. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.06.506785 · Cited by 1

Organization, genomic targeting and assembly of three distinct SWI/SNF chromatin remodeling complexes in ArabidopsisPreprint

Fu, W., Yu, Y., Shu, J., Yu, Z., Zhu, T., Zhong, Y., Zhang, Z., Liang, Z., Cui, Y., Chen, C., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.24.517835 · Cited by 1

Leveraging the BAF chromatin remodeling complex for targeted transcriptional rewiring in cancerPreprint

Segal, D., Kainacher, L., Muffel, T., Geiger, T. M., Lechner, S., Mavridi, D., Balourdas, D.-I., Nelles, M., Schätz, C., Knapp, S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.30.715217 · Cited by 1

Epigenetic Regulation of Stem Cells

Sacco, A., & Puri, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.30116-x

SWI/SNF chromatin remodeling enzymes as regulators of neural-crest derived cell differentiation

Marathe, H. G. (2013) · OhioLink ETD Center (Ohio Library and Information Network)

Mechanisms of MLL Fusion Protein-Mediated Leukemic Transformation

Monroe, S. (2010) · Deep Blue (University of Michigan)

Mecanismos de resistência à cloroquina em células de glioma humano e o uso de neurônios humanos derivados de células-tronco pluripotentes induzidas como modelo de estudo da síndrome de Cockayne.

Vessoni, A. T. (2015) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2015.tde-06102015-200543

Studies of histone modification systems in schizosaccharomyces pombe

Bonilla, C. (2010) · Figshare

ELUCIDATING REGULATORY NETWORKS PROMOTING B-CELL DEVELOPMENT

Welinder, E. (2012) · Lund University Publications (Lund University)

Function and Regulation of the Tip60-p400 Complex in Embryonic Stem Cells: A Dissertation

Chen, P. B. (2015) · eScholarship@UMassChan · doi:10.13028/m2sw20

The Role of DNA Methylation in Type 1 and 2 Diabetes as Related to Endothelial Cell Dysfunction

Sarras, M. P. (2015) · MOJ Anatomy & Physiology · doi:10.15406/mojap.2015.01.00005

Reasons of carcinogenesis indicate a big-bang inside: A hypothesis for the aberration of DNA methylation

Roy, A., & Chattopadhyay, N. R. (2013) · Medical Hypotheses · doi:10.1016/j.mehy.2013.04.004

Mutacje genów kompleksu BAF jako nowy czynnik etiologiczny izolowanej oraz syndromicznej niepełnosprawności intelektualnej w zespołach Coffina i Siris oraz Nicolaidesa i Baraitsera

Jezela‐Stanek, A., Pelc, M., & Krajewska‐Walasek, M. (2014) · Pediatria Polska · doi:10.1016/j.pepo.2013.12.005

NETWORKS IN EPIGENETICS

Sandhu, K. S. (2010) · Figshare

Molecular analysis of the FET family fusion oncoprotein FUS-DDIT3

Thomsen, C. (2012) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Regulation of Chromatin Remodeling: Linker DNA and Histones

Hwang, W. L. (2015) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)

Fission yeast Mediator complex and its role in transcriptional regulation

Khorosjutina, O. (2011) · Figshare

Transcriptional and Epigenetic Control of T Helper Cell Specification: Molecular Mechanisms Underlying Commitment

Kanno, Y., Vahedi, G., Hirahara, K., & Singleton, K. L. (2012)

Gli2 Accelerates Cardiac Progenitor Gene Expression During Mouse Embryonic Stem Cell Differentiation

Fair, J. (2014) · uO Research (University of Ottawa) · doi:10.20381/ruor-4281

Killing Pre-invasive Breast Cancer by Targeting Autophagy: A New Vision for Chemoprevention

Espina, V. A. (2013) · doi:10.13021/mars/7268

Dual nuclear roles of an essential scavenger decapping enzyme

Shen, V. (2010) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t3df6qzt

Plant Research International, part of Wageningen UR Business Unit Bioscience

van Leeuwen, F., Stam, M., & Erkamp, B. (2011)

Transcriptome analysis of Bmp4-induced mesoderm formation in vitro

Shin, E.-H. (2012) · DepositOnce · doi:10.14279/depositonce-3142

Insertional mutagenesis in PLN R9C transgenic mouse: a case report and a review of the literature on cardiac-specific transgenic expressionPreprint

Kraev, A. S. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/075671

Caracterización de nuevos perfiles moleculares en carcinoma de endometrio esporádico

Cieza-Borrella, C. (2013) · Gredos (University of Salamanca) · doi:10.14201/gredos.124099

Epigenetics in Development, Differentiation and Reprogramming

Salts, N., & Meshorer, E. (2016) · Springer eBooks · doi:10.1007/978-3-319-38882-3_18

Regulation of the competence to respond to stem cell self-renewal factors by Earmuff

Paper, B. (2014)

Epigenetics and obesity

Shewchuk, B. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800226-1.00016-2

Epigenetic Regulations in Cardiac Development

Xin, M., & Song, K. (2016) · Cardiac and vascular biology · doi:10.1007/978-3-319-41457-7_3

Cellular processes in the induction of embryonic stem cell differentiation into neural crest cell derivatives

Fielding, S. J. (2026) · e-space (Manchester Metropolitan University) · doi:10.83056/mmu.32438544

Functional Consequences of Embryonic Stem Cell- Specific Alternative Splicing

Nachman, E. N. (2015) · TSpace (University of Toronto)

Ino80 is essential for proximal-distal axis asymmetry in part by regulating Bmp4

Qiu, Z., Elsayed, Z., Peterkin, V., Alkatib, S., Bennett, D. C., & Landry, J. W. (2016)

Whsc1l1 Regulates Estrogen Receptor Activity In Sum44 Breast Cancer Cells

Irish, J. C. (2016) · Human Biology

Gene activity patterns associated with pathological cardiac hypertrophy are mediated by specific chromatin modifying factors

Chang, L. H. C. (2017) · Figshare · doi:10.4225/03/58b60aa3c91d9

Oxytocin and epigenetic mechanisms in mouse models of empathy and autism

Pisansky, M. T. (2016) · University of Minnesota Digital Conservancy (University of Minnesota)

Epigenetic Regulation of Neurogenesis by microRNAs

Liu, Y., Abernathy, D. G., & Yoo, A. S. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804402-5.00007-8

Nucleosome Remodelling and Epigenome Diversification

Becker, P. B. (2012) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-27913-3_1

Identification and characterization of an A-form DNA promoter and its downstream novel Rab-Gdi gene in Xenopus

Nazlamova, L. (2016)

Epigenetic regulators sculpt the plastic brain

Guan, J., Xie, H. B., & Liu, S. (2017) · Frontiers in Biology · doi:10.1007/s11515-017-1465-z

Epigenetic regulation of oncogenes and tumor suppressors in chronic lymphocytic leukemia

Kopparapu, P. K. (2017) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Mesenchymal Differentiation, Epigenetic Dynamics, and Interactions With VDR

Meyer, M. B., Benkusky, N. A., & Pike, J. W. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809965-0.00014-8

Novel interaction partners of the chromatin remodeler CHD7, a protein mutated in CHARGE syndrome

Tserendulam, B. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1453

Genetic Mechanisms Regulating the Spatiotemporal Modulation of Proliferation Rate and Mode in Neural Progenitors and Daughter Cells during Embryonic CNS Development

Salmani, B. Y. (2018) · doi:10.3384/diss.diva-147736 · Cited by 1

ATP-Dependent Chromatin Remodeling

Smith, C. L., & Peterson, C. L. (2004) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(04)65004-6 · Cited by 225

Epigenetic Regulation by ATP-Dependent Chromatin-Remodeling Enzymes

Runge, J. S., Raab, J. R., & Magnuson, T. (2016) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2015.10.009 · Cited by 18

ATP-Dependent Chromatin Remodeling: From Development to Disease

Lezzerini, M., & Riedel, C. G. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803395-1.00004-6 · Cited by 2

ATP-dependent chromatin remodeling during mammalian development

Hota, S. K., & Bruneau, B. G. (2016) · Development · doi:10.1242/dev.128892 · Cited by 253

ATP-dependent Chromatin Remodelling

Choudhary, P., & Varga‐Weisz, P. (2007) · Springer eBooks · doi:10.1007/1-4020-5466-1_2 · Cited by 26