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Regulation of Transcription by a Protein Methyltransferase

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Coactivator and corepressor complexes in nuclear receptor function

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Histone Deacetylase Activity Is Required for Full Transcriptional Repression by mSin3A

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A human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor.

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Chromatin remodelling by the glucocorticoid receptor requires the BRG1 complex

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Roles of SWI1, SWI2, and SWI3 Proteins for Transcriptional Enhancement by Steroid Receptors

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CORTICOSTEROIDS | Glucocorticoid Receptors

Adcock, I. M., Hayashi, R., Ito, K., & Caramori, G. (2006) · Elsevier eBooks · doi:10.1016/b0-12-370879-6/00100-9 · Cited by 1

G&DvignettesPreprint

Zaret, K. S. (2023) · Genes & Development · doi:10.1101/gad.350444.123 · Cited by 1

An investigation into the role of acetylation and ligand-dependent nuclear localisation in glucocorticoid receptor transcriptional regulation

Hadley, K. (2010) · Open University of Cape Town (University of Cape Town) · Cited by 1

Kinetic proofreading as a mechanism for transcriptional specificity in living human cellsPreprint

Kim, J. M., Ball, D. A., Johnson, T. A., DInzeo, C., Cho, H. J., Ozbun, L. L., Karpova, T., Pegoraro, G., & Larson, D. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.17.711757 · Cited by 1

Overexpression of a Transcription Factor to Maximize Glycoprotein Production in an Inducible Expression System

Murthy, M. V. R., Lipscomb, M. L., & Kompala, D. S. (2001) · Springer eBooks · doi:10.1007/978-94-010-0369-8_13

The Recruitment And Dynamics Of Transcription Factors At The Hsp70 Loci In Living Cells

Zobeck, K. L. (2011) · eCommons (Cornell University)

Modulation of allergic airway inflammation by glucocorticoids

Karabinskaya, A. (2014) · doi:10.53846/goediss-4399

A functional analysis of the epigenetic regulator CTCF

Kitchen, N. S. (2010) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)

Quantifying ER Function Using High-Throughput Imaging in Breast and Other Cancer Cells

Sharp, Z. D. (2008) · doi:10.21236/ada502583

Structure/Function Studies of the Androgen Receptor DNA-Binding Region

Rastinejad, F. (2001) · doi:10.21236/ada398061

An Estrogen Receptor-Selective Coactivator: A Potential Regulator of Tamoxifen Effectiveness in Breast Cancer Treatment and Prevention

Rajendran, R. R. (2000) · doi:10.21236/ada395524

Regulation of beta-Casein Gene Expression by Octamer Transcription Factors and Utilization of beta-Casein Gene Promoter to Produce Recombinant Human Proinsulin in the Transgenic Milk

Qian, X. (2014) · ScholarWorks -A service of University of Vermont Libraries (University of Vermont)

Imaging Cellular Metabolism

Bubulya, A., & Paula, A. (2012) · InTech eBooks · doi:10.5772/22469

Regulation of Estrogen Receptor alpha Ubiquitination and Proteasome-mediated Receptor Degradation

Berry, N. B. (2008) · IUScholarWorks (Indiana University)

Proceedings of the 30th Annual Biochemical Engineering Symposium

Kompala, D. S. (2000) · Iowa State University Digital Repository (Iowa State University)

Fluorescence Correlation Spectroscopy: A Tool for Measuring Dynamic and Equilibrium Properties of Molecules in Cells

Elson, E. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.20094-1

VDR and RXR Subcellular Trafficking

Bársony, J. (2010) · Humana Press eBooks · doi:10.1007/978-1-60327-303-9_6

Studies of glucocorticoid receptor interacting proteins

Widén, C. (2005) · Figshare

Glucocorticoid control of gene transcription in neural tissue

Morsink, M. C. (2007) · Leiden Repository (Leiden University)

Nuclear Receptors and Multiple Endocrine Neoplasia type 1 (MEN1)

Dreijerink, K. M. A. (2003) · Utrecht University Repository (Utrecht University)

JAK/STAT Signaling: A Tale of Jeeps and Trains

Costa‐Pereira, A. P., Strobl, B., Lillemeier, B. F., Is’harc, H., & Kerr, I. M. (2003) · Springer eBooks · doi:10.1007/978-94-017-3000-6_24

Glucocorticoid receptor function; interactions, mutants and ligand responses

Hedman, E. (2008) · Figshare

CDP/Cutl1 controls differentiation-specific MMTV and cellular gene expression in the mammary gland

Maitra, U. (2006) · Texas ScholarWorks (Texas Digital Library)

CHROMATIN STRUCTURE AND HISTONE MODIFICATIONS IN GENE REGULATION

Åstrand, C. (2006) · Figshare

Protein Dynamics in Mammalian Genome Maintenance

Zotter, A. (2008) · RePub (Erasmus University Rotterdam)

Transcription factot effects on chromatin organisation and gene regulation

Holmqvist, P.-H. (2005)

Modulation of folate receptor-α by glucocorticoid receptor and progesterone receptor.

Tran, T. (2005) · Europe PMC (PubMed Central)

Cushing's syndrome results from lengthy and inappropriate exposure to excessive glucocorticoids. Untreated, it has signifi cant morbidity and mortality. The syndrome remains a challenge to diagnose and manage. Here, we review the current understanding of pathogenesis, clinical features, diagnostic, and diff erential diagnostic approaches. We provide diagnostic algorithms and recommendations for management.

Newell-Price, J. D. C., BERTAGNA, X. Y., Grossman, A. B., & Nieman, L. K. (2006)

Modulation of GR transcriptional signalling by HIV-1 Vpr: insights into regulation by progestins

Grantham, N. J. (2012) · Open University of Cape Town (University of Cape Town)

Differential regulation of glucocorticoid and progesterone receptor subcellular localization by tetratricopeptide repeat domain proteins

Banerjee, A. T. (2007) · OhioLink ETD Center (Ohio Library and Information Network)

Effects of glucocorticoids in macrophages

Jubb, A. W. (2015) · ERA

Cell-cycle-dependent trafficking in the endocytic pathway

Bergeland, T. (2008) · NORA - Norwegian Open Research Archives

Heart rate variability and rhythmic influences in human endotoxemia

Scheff, J. D. (2013) · doi:10.7282/t3571922

Thermodynamic and kinetic analyses of androgen and glucocorticoid receptor-promoter interactions suggest phylogenetic partitioning of energetics and the presence of functionally distinct DNA-bound state

Angelis, D., & Wray, R. (2015)

Glucocorticoid receptor: translocation from the cytoplasm to the nuclei, chromatin and intranuclear chaperone cycles

Merkulov, V. M., Klimova, N. V., & Merkulova, T. I. (2015) · Vavilov Journal of Genetics and Breeding · doi:10.18699/vj15.032

DYNAMIK UND LOKALISATION DES DOSISKOMPENSATIONSKOMPLEXES IN DROSOPHILA MELANOGASTER

Becker, P. B. (2005)

Nuclear Protein Import

Jans, D. A., & Forwood, J. K. (2007) · Springer eBooks · doi:10.1007/0-387-27747-1_9

Clone Novel E2F Target Promoters Use of Chromatin Immunoprecipitation To

Zhang, M. Q., Farnham, P., Weinmann, A. S., Bartley, S. M., & Zhang, T. (2014)

Dynamic Regulation of Chromatin Modification and Transcription by GR and the Steroid Receptors

George, C. L., & Conway-Campbell, B. L. (2016) · Epigenetics and human health · doi:10.1007/978-3-319-24493-8_2

Stochastic Effects in Signaling Pathways in Cells: Interaction between Visualization and Modeling

Kimmel, M. (2009) · Advances in intelligent and soft computing · doi:10.1007/978-3-642-00563-3_2

Рецептор глюкокортикоидов: переход из цитоплазмы в клеточное ядро, хроматиновый и внутриядерный шапероновый циклы

Merkulov, V. M., Klimova, N. V., & Merkulova, T. I. (2015)

CHAPTER 2B – The Normal Human Ovary Part II: How Steroid Hormones Work

Kase, N. (2003) · Elsevier eBooks · doi:10.1016/b978-012053642-9/50007-7

Quantitative analysis of the dynamic properties of chromatin associated proteins by uorescence recovery after photobleaching experiments

Mller, F. (2008)

Proteomics of Sub-cellular Protein Distribution in Oestrogen and Tamoxifen Stimulated MCF-7 Breast Cancer Cells

Alkhanjaf, A. A. M. (2016) · UCL Discovery (University College London)

The Discovery of Potent and Selective Nonsteroidal Glucocorticoid Receptor Modulators AZD5423 and AZD7594, for the Inhaled Treatment of Respiratory Diseases

Sjö, P., Hansson, T. G., & Edman, K. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-409547-2.12466-7

Characterization of Boundary Element-Associated Factors BEAF-32A and BEAF-32B and Identification of Novel Interaction Partners in Drosophila Melanogaster

Avva, S. V. S. P. (2016) · Louisiana State University · doi:10.31390/gradschool_dissertations.617

Epigenetics and Chromatin Remodeling

Kinyamu, H. K., Mackey, L. C., Crusselle‐Davis, V. J., & Archer, T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.65388-6

Towards X-ray crystallographic characterization of nucleosome interactions with linker histones, FOXA proteins and high mobility group N factors

Ravi, S. (2018) · doi:10.32657/10356/74380

Cell Nucleus Biogenesis, Structure and Function

Jackson, D. A. (2006) · Encyclopedia of Molecular Cell Biology and Molecular Medicine · doi:10.1002/3527600906.mcb.200300097

Energy Cost and Mean Dwell Times for the Activity of Promoter with Complex Structure

Li, Q., Din, A., & Zhou, T. (2018) · Journal of Systems Science and Complexity · doi:10.1007/s11424-018-7180-2

Associação da expressão circadiana do cortisol de enfermeiros segundo trabalho em turnos, estresse ocupacional e fadiga

de Assis, D. C. (2018) · doi:10.11606/t.22.2018.tde-04072018-144422

Progesterone Resistance and Adult Stem Cells’ Genomic and Epigenetic Changes in the Puzzle of Endometriosis

Russu, M. C. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.84203

The Nucleus

Urnov, F. D., & Wolffe, A. P. (2002) · Elsevier eBooks · doi:10.1016/b978-012174597-4.50005-3

Injected cells provide a valuable complement to cell-free systems for analysis of gene expression

Gurdon, J. B., Javed, K., Wen, M.-H., & Triana, H. B. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.112296

Transcription regulation dynamics

de Jonge, W. J. (2020) · doi:10.33540/73

The Cell Nucleus and Its Compartments

Mierke, C. T. (2020) · Biological and medical physics, biomedical engineering · doi:10.1007/978-3-030-58532-7_10

Investigating phase separation mechanisms for transcriptional control

Boehning, M. (2020) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8312

Sequence and Effects of Glucocorticoid Receptor Nuclear Retention: An Aid to Understanding Nuclear Retention in Other Proteins?

Carrigan, A. (2011) · Library and Archives Canada (Government of Canada) · doi:10.20381/ruor-4388

Nuclear Mechanisms of Glucocorticoid Action

Hager, G. L., Stavreva, D. A., & Voss, T. C. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00040-1

Faculty Opinions recommendation of Synergy among nuclear receptor coactivators: selective requirement for protein methyltransferase and acetyltransferase activities.

Workman, J. L. (2002) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1006307.78955

Faculty Opinions recommendation of From silencing to gene expression: real-time analysis in single cells.

Sweedler, J. V. (2004) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1018099.207671

Steroid Hormones

Simons, S. S. (2008) · Wiley Encyclopedia of Chemical Biology · doi:10.1002/9780470048672.wecb563

Glucocorticoid Receptors

Oakley, R. H., Lewis‐Tuffin, L. J., Malchoff, C. D., Malchoff, D. M., & Cidlowski, J. A. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-5583-9.00098-8

Faculty Opinions recommendation of Glucocorticoid receptor binding to chromatin is selectively controlled by the coregulator Hic-5 and chromatin remodeling enzymes.

Lightman, S. L., & Stubbs, F. E. (2017) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727484269.793538924

Faculty Opinions recommendation of Large-scale chromatin decondensation and recondensation regulated by transcription from a natural promoter.

Belmont, A. S. (2001) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1000830.12858

Structure/Function Studies of the Androgen Receptor DNA-Binding Region

Rastinejad, F. (2002) · doi:10.21236/ada411246

Faculty Opinions recommendation of Single-Molecule Nanoscopy Elucidates RNA Polymerase II Transcription at Single Genes in Live Cells.

Reines, D. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735846974.793578913

Faculty Opinions recommendation of Coactivator cross-talk specifies transcriptional output.

Prywes, R. (2006) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1001649.374753

Faculty Opinions recommendation of Single-molecule imaging correlates decreasing nuclear volume with increasing TF-chromatin associations during zebrafish development.

Goll, M. G. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734564800.793573560

Fluorescence Correlation Spectroscopy: A Tool for Measuring Dynamic and Equilibrium Properties of Molecules in Cells

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Cellular Factors Involved in Transcriptome Dynamics in Early Zebrafish EmbryogenesisPreprint

Rauwerda, H., Pagano, J. F. B., de Leeuw, W. C., Ensink, W. A., van Olst, M. F., Nehrdich, U., Jonker, M. J., Spaink, H. P., & Breit, T. M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.29.510050

TANGO-Light - optogenetic control of transcriptional modulatorsPreprint

Przybyszewska-Podstawka, A., Kałafut, J., Czapiński, J., Ngo, T. H., Czerwonka, A., & Rivero‐Müller, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.31.543150

Nonspecific interactions in transcription regulation and organization of transcriptional condensates

Valyaeva, A. A., & Sheval, E. V. (2024) · Biochemistry (Moscow) · doi:10.31857/s0320972524040087

A Simple Method for Generating Light-induced Clusters of Transcription Factors: Effects on the Nuclear Distribution of OCT4 and on its Interactions With Chromatin

Diaz, M. C., Oses, C., Lareu, A. V., Roberti, S. L., Guberman, A., & Levi, V. (2025) · Journal of Molecular Biology · doi:10.1016/j.jmb.2025.169118

Epigenetics and Chromatin Remodeling

Kinyamu, H. K., Theofilatos, D., Mackey, L. C., & Archer, T. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00260-6

Intrinsically disordered bHLH family member TCF4 drives LLPS in a DNA-dependent mannerPreprint

Sozańska, N., Klepka, B. P., Niedźwiecka-Kornaś, A., Greb‐Markiewicz, B., Ożyhar, A., & Tarczewska, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.18.660356

Functional and cellular analysis of autoimmune regulator (AIRE) protein

Ilmarinen, T. (2007) · Työväentutkimus Vuosikirja

Functional Role of Glycogen synthase Kinase-3β on Glucocorticoid-mediated signaling

Patiño, C. R. (2012) · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)

Roles of the NFI/CTF gene family in transcription and development: update 2025

Gronostajski, R. M. (2025) · Academia Biology · doi:10.20935/acadbiol8079

Biomedical applications of two-foci cross-correlation technique in massively parallel fluorescence correlation spectroscopy

Nikolić, S. N., Oasa, S., Krmpot, A. J., Terenius, L. Y., Belić, M. R., & Vukojević, V. B. (2026) · Dynamics and Fluctuations in Biomedical Photonics · doi:10.1117/12.3090147

QuantiTrack: A unified software to study protein dynamics in living cellsPreprint

Ball, D. A., Wagh, K., Stavreva, D. A., Hoang, L., Schiltz, R. L., Chari, R., Raziuddin, R., Mazza, D., Upadhyaya, A., Hager, G. L., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.19.706877

Mitotic Bookmarking and Chromosomal Coating by Nuclear Receptors: Segregating Myth & Reality

Rizvi, S., & Tyagi, R. K. (2026) · Cell Biology International · doi:10.1002/cbin.70155

Investigating the role of human HAT (histone acetyltransferase) containing complexes, ATAC and SAGA, in living cells

Vosnakis, N. (2014) · theses.fr (ABES) · doi:10.70675/5d9cbef9z606fz45a1za0a6z436a683e624d

Cellular factors controlling human L1 retrotransposition

Galantonu, R. N. (2017) · theses.fr (ABES) · doi:10.70675/f24810a8z4f50z444fz84f0z11863b900b95

TET proteins, New Cofactors for Nuclear Receptors

Guan, W. (2017) · theses.fr (ABES) · doi:10.70675/1409d73cz9cabz4b83z80d6z9bb8c8712a7d · Cited by 1

Analysis of transcription factor and histone modification dynamics in the nucleus of single living cells using a novel antibody-based imaging approach

Conic, S. (2018) · theses.fr (ABES) · doi:10.70675/707f76edz3165z4862z987az6066a94046e8

Real time imaging of transcription reveals new features of cellular and viral promoters

Kozulic-Pirher, A. (2018) · theses.fr (ABES) · doi:10.70675/0099e36bz620ez43d7z9b47z2789ed360d73

Implication de l'enzyme Glycogène Synthase Kinase 3 dans la médiation des effets diabétogènes des glucocorticoïdes

Delangre, E. (2021) · theses.fr (ABES) · doi:10.70675/622d48edz59dcz427ez85c9z9da5f8129e84

Exploring the immunomodulating potential of Cocculus hirsutus and Cissampelos pareira in rats through 3β-HSDH/total Ig level/CIC level

Nisha, A., Ahsan, F., Rizvi, A., Goswami, B., Mahmood, T., Bano, S., & Hagras, S. A. A. (2026) · Comparative Clinical Pathology · doi:10.1007/s00580-026-03777-z

Genome-wide chromatin profiling reveals a nonlimiting role for RXR in macrophage-like cells stimulated with multiple nuclear receptor agonists

Mianesaz, H., Göczi, L., Bojcsuk, D., Ghalamkari, S., Fadel, L., Póliska, S., Penyige, A., Nagy, L., Nagy, G., Vámosi, G., et al. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.111486

Intrinsically disordered bHLH family member TCF4 drives phase separation in a DNA-dependent manner

Sozańska, N., Klepka, B. P., Niedzwiecka, A., Greb‐Markiewicz, B., Ożyhar, A., & Tarczewska, A. (2026) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2026.110829

A Transcription Factor-Centric View of Transcription Regulation

He, J., Chi, J., & Feng, S. (2026) · Biology · doi:10.3390/biology15100769

Genome-wide rotational and translational phasing of nucleosomes with human transcription factors

Chen, H., Krebs, J., Lang, O. W., Hu, J., Mellini, D. C., Hyle, J. W., Li, C., Lai, W., & Pugh, B. F. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.06.019

Epigenetic reprogramming of lineage switching in cancer

Boyvatlı, E., Akman, B., Bağırsakçı, E., Atabey, N., & Erkek, S. (2026) · FEBS Letters · doi:10.1002/1873-3468.70433

Lamin A-regulated chromatin organization regulates transcription factor binding

Huang, Y., & Anlaş, A. A. (2026) · Biophysical Journal · doi:10.1016/j.bpj.2026.08.016

Balancing inflammation under stress: glucocorticoid regulation of innate immune pathways

Kenney, K. M., & Burgener, S. S. (2026) · Bioscience Reports · doi:10.1042/bsr20250146

Microscopy Techniques for Investigating Interactions in Microbial Systems

Edwards, A. N. (2011)

Mechanisms of Altered Glucocorticoid Sensitivity

Yang, N. (2013) · Research Explorer (The University of Manchester)

Quantitative Visualization of Sex Steroid Receptor Functions: AR and ERα

Bolt, M. J., Hartig, S. M., Szafran, A. T., Mediwala, S. N., Marcelli, M., & Mancini, M. A. (2011) · Springer eBooks · doi:10.1007/978-1-4614-1764-4_14

Steroid Receptors Hit and Run

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Glucocorticoid receptor dynamics and gene regulation

Biddie, S. C., & Hager, G. L. (2008) · Stress · doi:10.1080/10253890802506409 · Cited by 72

Nuclear Receptor Mobility on Gene Targets

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Subnuclear Trafficking and Gene Targeting by Steroid Receptors

Nagaich, A. K., Rayasam, G. V., Martinez, E. D., BECKER, M., Qiu, Y., Johnson, T. A., Elbi, C., Fletcher, T. M., John, S., & Hager, G. L. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1321.002 · Cited by 48

Nuclear Mechanisms of Glucocorticoid Action

Hager, G. L., Stavreva, D. A., & Voss, T. C. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00040-1