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Bejelentkezés
A Tudóstér funkcióinak nagy része bejelentkezés nélkül is elérhető. Bejelentkezésre az alábbi műveletekhez van szükség:
Patsalos, A.,
Halász, L.,
Oleksak, D.,
Wei, X.,
Nagy, G.,
Tzerpos, P.,
Conrad, T.,
Hammers, D. W.,
Sweeney, H. L.,
Nagy, L.:
Spatiotemporal transcriptomic mapping of regenerative inflammation in skeletal muscle reveals a dynamic multilayered tissue architecture.
J. Clin. Invest. 134 (20), 1-20, (cikkazonosító: 173858), 2024.
Patsalos, A.,
Halász, L.,
Medina-Serpas, M. A.,
Berger, W. K.,
Dániel, B.,
Tzerpos, P.,
Kiss, M.,
Nagy, G.,
Fischer, C.,
Simándi, Z.,
Varga, T.,
Nagy, L.:
A growth factor-expressing macrophage subpopulation orchestrates regenerative inflammation via GDF-15.
J. Exp. Med. 219 (1), 1-38, (cikkazonosító: 20210420), 2022.
Göczi, L.,
Csumita, M.,
Horváth, A.,
Nagy, G.,
Póliska, S.,
Pigni, M.,
Thelemann, C.,
Dániel, B.,
Mianesaz, H.,
Varga, T.,
Sen, K.,
Raghav, S. K.,
Schoggins, J. W.,
Nagy, L.,
Acha-Orbea, H.,
Meissner, F.,
Reith, W.,
Széles, L.:
A Multi-Omics Approach Reveals Features That Permit Robust and Widespread Regulation of IFN-Inducible Antiviral Effectors.
J. Immun. 209 (10), 1930-1941, 2022.
Bojcsuk, D.,
Nagy, G.,
Bálint, B. L.:
Alternatively Constructed Estrogen Receptor Alpha-Driven Super-Enhancers Result in Similar Gene Expression in Breast and Endometrial Cell Lines.
Int. J. Mol. Sci. 21, 1-18, (cikkazonosító: 1630), 2020.
Nagy, G.,
Nagy, L.:
Motif grammar: the basis of the language of gene expression.
Computational and Structural Biotechnology Journal. 18, 2026-2032, 2020.
Csumita, M.,
Csermely, A.,
Horváth, A.,
Nagy, G.,
Monori, F.,
Göczi, L.,
Orbea, H. A.,
Reith, W.,
Széles, L.:
Specific enhancer selection by IRF3, IRF5 and IRF9 is determined by ISRE half-sites, 5' and 3' flanking bases, collaborating transcription factors and the chromatin environment in a combinatorial fashion.
Nucleic Acids Res. 48 (2), 589-604, 2020.
Nagy, G.,
Dániel, B.,
Cuaranta-Monroy, I.,
Nagy, L.:
Unraveling the Hierarchy of cis and trans Factors That Determine the DNA Binding by Peroxisome Proliferator-Activated Receptor γ.
Mol. Cell. Biol. 40 (7), 1-20, (cikkazonosító: 00547), 2020.
Patsalos, A.,
Tzerpos, P.,
Halász, L.,
Nagy, G.,
Pap, A.,
Giannakis, N.,
Lyroni, K.,
Koliaraki, V.,
Pintye, É.,
Dezső, B.,
Kollias, G.,
Spilianakis, C. G.,
Nagy, L.:
The BACH1-HMOX1 Regulatory Axis Is Indispensable for Proper Macrophage Subtype Specification and Skeletal Muscle Regeneration.
J. Immunol. 203 (6), 1532-1547, 2019.
Czimmerer, Z.,
Horváth, A.,
Dániel, B.,
Nagy, G.,
Cuaranta-Monroy, I.,
Kiss, M.,
Kolostyák, Z.,
Póliska, S.,
Steiner, L.,
Giannakis, N.,
Varga, T.,
Nagy, L.:
Dynamic transcriptional control of macrophage miRNA signature via inflammation responsive enhancers revealed using a combination of next generation sequencing-based approaches.
Biochim. Biophys. Acta. Gene Regul. Mech. 1861 (1), 14-28, 2018.
Czimmerer, Z.,
Nagy, Z. S.,
Nagy, G.,
Horváth, A.,
Silye-Cseh, T.,
Kriston, Á.,
Jonás, D.,
Sauer, S.,
Steiner, L.,
Dániel, B.,
Deleuze, J. F.,
Nagy, L.:
Extensive and functional overlap of the STAT6 and RXR cistromes in the active enhancer repertoire of human CD14+ monocyte derived differentiating macrophages.
Mol. Cell. Endocrinol. 471, 63-74, 2018.
Dániel, B.,
Nagy, G.,
Horváth, A.,
Czimmerer, Z.,
Cuaranta-Monroy, I.,
Póliska, S.,
Hays, T. T.,
Sauer, S.,
Francois-Deleuze, J.,
Nagy, L.:
The IL-4/STAT6/PPAR[gamma] signaling axis is driving the expansion of the RXR heterodimer cistrome, providing complex ligand responsiveness in macrophages.
Nucleic Acids Res. 46 (9), 4425-4439, 2018.
Dániel, B.,
Nagy, G.,
Czimmerer, Z.,
Horváth, A.,
Hammers, D. W.,
Cuaranta-Monroy, I.,
Póliska, S.,
Tzerpos, P.,
Kolostyák, Z.,
Hays, T. T.,
Patsalos, A.,
Houtman, R.,
Sauer, S.,
Francois-Deleuze, J.,
Rastinejad, F.,
Bálint, B. L.,
Sweeney, H. L.,
Nagy, L.:
The Nuclear Receptor PPAR[gamma] Controls Progressive Macrophage Polarization as a Ligand-Insensitive Epigenomic Ratchet of Transcriptional Memory.
Immunity. 49 (4), 615-626, 2018.
Bojcsuk, D.,
Nagy, G.,
Bálint, B. L.:
Inducible super-enhancers are organized based on canonical signal-specific transcription factor binding elements.
Nucleic Acids Res. 45 (7), 3693-3706, 2017.
Varga, T.,
Mounier, R.,
Patsalos, A.,
Gogolák, P.,
Peloquin, M.,
Horváth, A.,
Pap, A.,
Dániel, B.,
Nagy, G.,
Pintye, É.,
Póliska, S.,
Cuvellier, S.,
Ben Larbi, S.,
Sansbury, B. E.,
Spite, M.,
Brown, C. W.,
Chazaud, B.,
Nagy, L.:
Macrophage PPAR[gamma], a Lipid Activated Transcription Factor Controls the Growth Factor GDF3 and Skeletal Muscle Regeneration.
Immunity. 45 (5), 1038-1051, 2016.
Nagy, G.,
Czipa, E.,
Steiner, L.,
Nagy, T.,
Pongor, S.,
Nagy, L.,
Barta, E.:
Motif oriented high-resolution analysis of ChIP-seq data reveals the topological order of CTCF and cohesin proteins on DNA.
BMC Genomics. 17 (637), 1-9, 2016.
Czimmerer, Z.,
Varga, T.,
Kiss, M.,
Vázquez, C. O.,
Doan-Xuan, Q. M.,
Rückerl, D.,
Tattikota, S. G.,
Yan, X.,
Nagy, Z. S.,
Dániel, B.,
Póliska, S.,
Horváth, A.,
Nagy, G.,
Varallyay, É.,
Poy, M. N.,
Allen, J. E.,
Bacsó, Z.,
Abreu-Goodger, C.,
Nagy, L.:
The IL-4/STAT6 signaling axis establishes a conserved microRNA signature in human and mouse macrophages regulating cell survival via miR-342-3p.
Genome Med. 8 (1), 1-22, 2016.
