Signaling to Chromatin through Histone Modifications

Crystal structure of the nucleosome core particle at 2.8 Å resolution

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DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139

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Regulation of chromatin structure by site-specific histone H3 methyltransferases

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Chromatin Structure: A Repeating Unit of Histones and DNA

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Signaling—2000 and Beyond

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IAP family proteins---suppressors of apoptosisPreprint

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Megabase Chromatin Domains Involved in DNA Double-Strand Breaks in Vivo

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CREB: A Stimulus-Induced Transcription Factor Activated by A Diverse Array of Extracellular Signals

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Phosphorylated CREB binds specifically to the nuclear protein CBP

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Mitosis-specific phosphorylation of histone H3 initiates primarily within pericentromeric heterochromatin during G2 and spreads in an ordered fashion coincident with mitotic chromosome condensation

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Thermodynamic Studies of the Core Histones: Stability of the Octamer Subunits Is Not Altered by Removal of Their Terminal Domains

Karantza, V., Freire, E., & Moudrianakis, E. N. (2001) · Biochemistry · doi:10.1021/bi0110140 · Cited by 21

Nuclear dynamics: where genes are and how they got there.

Swedlow, J. R., & Lamond, A. I. (2001) · Genome biology · doi:10.1186/gb-2001-2-3-reviews0002 · Cited by 21

A Nonenzymatic Modification of the Amino-terminal Domain of Histone H3 by Bile Acid Acyl Adenylate

Mano, N., Kasuga, K., Kobayashi, N., & Goto, J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m409205200 · Cited by 21

Increases in intracellular calcium dephosphorylate histone H3 at serine 10 in human hepatoma cells: Potential role of protein phosphatase 2A–protein kinase CβII complex

Huang, W., Batra, S., Atkins, B. A., Mishra, V., & Mehta, K. D. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20372 · Cited by 21

Control of IL-2Ralpha gene expression: structural changes within the proximal enhancer/core promoter during T-cell development

Yeh, J.-H. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.9.1944 · Cited by 21

An increasingly complex code

Spotswood, H. T., & Turner, B. M. (2002) · Journal of Clinical Investigation · doi:10.1172/jci200216547 · Cited by 22

Banding patterns in Drosophila melanogaster polytene chromosomes correlate with DNA‐binding protein occupancy

Zhimulev, I. F., Belyaeva, E. S., Vatolina, T. Y., & Demakov, S. A. (2012) · BioEssays · doi:10.1002/bies.201100142 · Cited by 20

The Emerging Role of Chromatin Remodeling Factors in Female Pubertal Development

Aylwin, C. F., Vigh‐Conrad, K. A., & Lomniczi, A. (2019) · Neuroendocrinology · doi:10.1159/000497745 · Cited by 20

Epigenetic Reprogramming in Host-Parasite Coevolution: TheToxoplasmaParadigm

Hakimi, M. (2022) · Annual Review of Microbiology · doi:10.1146/annurev-micro-041320-011520 · Cited by 21

Methylation-mediated control of aurora kinase B and Haspin with epigenetically modified histone H3 N-terminal peptides

Han, A., Lee, K. H., Hyun, S., Lee, N. J., Lee, S. J., Hwang, H., & Yu, J. (2011) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2011.02.011 · Cited by 20

Acute Alcohol Exposure Induces Apoptosis and Increases Histone H3K9/18 Acetylation in the Mid-Gestation Mouse Lung

Wang, X., Gomutputra, P., Wolgemuth, D. J., & Baxi, L. (2010) · Reproductive Sciences · doi:10.1177/1933719109356984 · Cited by 20

Alterations of Histone Modifications in Cancer

Hosseini, A., & Minucci, S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812215-0.00006-6 · Cited by 22

Histone Modification Patterns During Gene Activation

Lo, W., Henry, K. W., Schwartz, M. F., & Berger, S. L. (2003) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(03)77007-4 · Cited by 20

Inhibiting estrogen responses in breast cancer cells using a fusion protein encoding estrogen receptor-α and the transcriptional repressor PLZF

Buluwela, L., Pike, J., Mazhar, D., Kamalati, T., Hart, S., Al-Jehani, R. M., Yahaya, H., Patel, N. R., Sarwarl, N., Heathcote, D. A., et al. (2005) · Gene Therapy · doi:10.1038/sj.gt.3302421 · Cited by 20

Acetylation of Histone H3 and Adrenergic-Regulated Gene Transcription in Rat Pinealocytes

Ho, A., Price, D. M., Dukewich, W. G., Steinberg, N., Arnason, T., & Chik, C. L. (2007) · Endocrinology · doi:10.1210/en.2007-0578 · Cited by 20

A fluorescence resonance energy transfer-based probe to monitor nucleosome structure

Lovullo, D., Daniel, D. C., Yodh, J. G., Lohr, D., & Woodbury, N. W. (2005) · Analytical Biochemistry · doi:10.1016/j.ab.2005.03.022 · Cited by 20

A major role for the TATA box in recruitment of chromatin modifying complexes to a globin gene promoter

Gui, C.-Y., & Dean, A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1236499100 · Cited by 20

Chromatin Structure and Transcriptional Regulation of the β-Globin Locus

Fu, X., Liu, D., & Liang, C. (2002) · Experimental Cell Research · doi:10.1006/excr.2002.5555 · Cited by 20

The ARF tumor suppressor targets PPM1G/PP2Cγ to counteract NF-κB transcription tuning cell survival and the inflammatory response

Hyder, U., McCann, J. L., Wang, J., Fung, V., Bayo, J., & D’Orso, I. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2004470117 · Cited by 19

Epigenetic-Mediated Regulation of Gene Expression for Biological Control and Cancer: Cell and Tissue Structure, Function, and Phenotype

Fritz, A. J., Dika, M. E., Toor, R. H., Rodriguez, P. D., Foley, S. J., Ullah, R., Nie, D., Banerjee, B., Lohese, D., Tracy, K. M., et al. (2022) · Results and problems in cell differentiation · doi:10.1007/978-3-031-06573-6_12 · Cited by 23

Targeting the epigenome with advanced delivery strategies for epigenetic modulators

Guha, S., Jagadeesan, Y., Pandey, M. M., Mittal, A., & Chitkara, D. (2024) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10710 · Cited by 22

Histone Modifications: Implications in Renal Cell Carcinoma

Ramakrishnan, S., Ellis, L., & Пили, Р. (2013) · Epigenomics · doi:10.2217/epi.13.40 · Cited by 19

Altered expression and chromatin structure of the hippocampal IGF1r gene is associated with impaired hippocampal function in the adult IUGR male rat

Caprau, D., Schober, M. E., Bass, K. E., O'Grady, S., Ke, X., Block, B., Callaway, C. W., Hale, M. A., Yu, X., McKnight, R. A., et al. (2012) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174411000791 · Cited by 19

Collective mass spectrometry approaches reveal broad and combinatorial modification of high mobility group protein A1a

Young, N. L., Plazas-Mayorca, M. D., DiMaggio, P. A., Flaniken, I. Z., Beltran, A., Mishra, N., LeRoy, G., Floudas, C. A., & Garcia, B. A. (2010) · Journal of the American Society for Mass Spectrometry · doi:10.1016/j.jasms.2010.01.020 · Cited by 19

The role of histone variability in chromatin stability and folding

Ausió, J., & Abbott, D. W. (2004) · New comprehensive biochemistry · doi:10.1016/s0167-7306(03)39010-6 · Cited by 19

Altered acetylation in polyglutamine disease: an opportunity for therapeutic intervention?

Taylor, J. P., & Fischbeck, K. H. (2002) · Trends in Molecular Medicine · doi:10.1016/s1471-4914(02)02332-8 · Cited by 19

Association of histone modification with the development of schizophrenia

Chen, Y.-Z., Zhu, X.-M., Lv, P., Hou, X.-K., Pan, Y., Li, A., Du, Z., Xuan, J.-F., Guo, X., Xing, J.-X., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116747 · Cited by 18

Interference of viral effector proteins with chromatin, transcription, and the epigenome

Marazzi, I., & García‐Sastre, A. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.06.009 · Cited by 18

Elucidating the temporal dynamics of chromatin-associated protein release upon DNA digestion by quantitative proteomic approach

Dutta, B., Adav, S. S., Koh, C.-G., Lim, S. K., Meshorer, E., & Sze, S. K. (2012) · Journal of Proteomics · doi:10.1016/j.jprot.2012.06.030 · Cited by 18

Retroviral Vectors Induce Epigenetic Chromatin Modifications and IL-10 Production in Transduced B Cells via Activation of Toll-like Receptor 2

Ahangarani, R. R., Janssens, W., Carlier, V. A., VanderElst, L., VandenDriessche, T., Chuah, M., Jacquemin, M. G., & Saint‐Remy, J. (2010) · Molecular Therapy · doi:10.1038/mt.2010.275 · Cited by 18

Biochemical Analysis of Transcriptional Repression byDrosophila Histone Deacetylase 1

Huang, X., & Kadonaga, J. T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.c100034200 · Cited by 18

Chromosome Remodeling Related to Hepatitis B Virus Replication in HepG2 Cells

Gong, Q., Chen, S., Guo, J., Sun, H., Zheng, G., Liu, Q., Ren, H., & He, S. (2011) · DNA and Cell Biology · doi:10.1089/dna.2010.1172 · Cited by 18

Activating transcription factor 3, an early cellular adaptive responder in ischemia/reperfusion-induced injury

Cheng, C., & Lin, H. (2018) · Tzu Chi Medical Journal · doi:10.4103/tcmj.tcmj_37_18 · Cited by 19

Native Mass Spectrometry of Protein and DNA Complexes Prepared in Nonvolatile Buffers

Saikusa, K., Kato, D., Nagadoi, A., Kurumizaka, H., & Akashi, S. (2020) · Journal of the American Society for Mass Spectrometry · doi:10.1021/jasms.9b00145 · Cited by 18

Signaling‐to‐chromatin pathways in the immune system

de Paz, A. M., & Josefowicz, S. Z. (2021) · Immunological Reviews · doi:10.1111/imr.12955 · Cited by 18

An Assessment on Ethanol-Blended Gasoline/Diesel Fuels on Cancer Risk and Mortality

Mueller, S., Dennison, G., & Liu, S. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18136930 · Cited by 18

Stage-Specific Expression of Two Neighboring Crlz1 and IgJ Genes during B Cell Development Is Regulated by Their Chromatin Accessibility and Histone Acetylation

Lim, J.-H., Cho, S.-J., Park, S.-K., Kim, J., Cho, D., Lee, W. J., & Kang, C.-J. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.8.5420 · Cited by 18

Regulation of Mammalian Oocyte Maturation

Viveiros, M. M., & Fuente, R. D. L. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813209-8.00011-x · Cited by 18

OVEREXPRESSION OF CYCLIN D1 IS ASSOCIATED WITH THE DECONDENSATION OF CHROMATIN DURING DEN‐INDUCED SEQUENTIAL HEPATOCARCINOGENESIS

Sundarrajan, M., Gupta, S., & Rao, K. V. K. (2002) · Cell Biology International · doi:10.1006/cbir.2002.0923 · Cited by 18

Cellular and molecular effects of nonreciprocal chromosome translocations in Saccharomyces cerevisiae

Nikitin, D. V., Tosato, V., Zavec, A. B., & Bruschi, C. V. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800464105 · Cited by 18

Randomly inserted and targeted Hox/ reporter fusions transcriptionally silenced in Polycomb mutants

de Graaff, W., Tomotsune, D., Oosterveen, T., Takihara, Y., Koseki, H., & Deschamps, J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2237046100 · Cited by 18

KLHL4, a novel p53 target gene, inhibits cell proliferation by activating p21

Choi, S., Cho, S.-Y., Song, J.-Y., & Hur, M. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.07.100 · Cited by 17

Role of epigenetics in cellular reprogramming; from iPSCs to disease modeling and cell therapy

Li, Y., & Darabi, R. (2022) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30164 · Cited by 16

Rosiglitazone promotes cardiac hypertrophy and alters chromatin remodeling in isolated cardiomyocytes

Pharaon, L. F., El-Orabi, N. F., Kunhi, M., Al‐Yacoub, N., Awad, S. M., & Poizat, C. I. (2017) · Toxicology Letters · doi:10.1016/j.toxlet.2017.08.011 · Cited by 16

Comparative Proteomic Analysis Identifies Age-Dependent Increases in the Abundance of Specific Proteins after Deletion of the Small Heat Shock Proteins αA- and αB-Crystallin

Andley, U. P., Malone, J. P., Hamilton, P. D., Ravi, N., & Townsend, R. R. (2013) · Biochemistry · doi:10.1021/bi400180d · Cited by 16

Discovery of a potent and selective inhibitor of histone lysine demethylase KDM4D

Fang, Z. Y., Liu, Y., Zhang, R., Chen, Q., Wang, T., Yang, W. M., Fan, Y. L., Yu, C., Xiang, R., & Yang, S. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.113662 · Cited by 16

Transdifferentiation and nuclear reprogramming in hematopoietic development and neoplasia

French, S., Hoyer, K., Shen, R. R., & Teitell, M. (2002) · Immunological Reviews · doi:10.1034/j.1600-065x.2002.18703.x · Cited by 18

Ontogenic expression of hepatic Ahr mRNA is associated with histone H3K4 di-methylation during mouse liver development

Cui, Y., Yeager, R. L., Zhong, X., & Klaassen, C. D. (2009) · Toxicology Letters · doi:10.1016/j.toxlet.2009.05.017 · Cited by 16

When Food Meets Man: the Contribution of Epigenetics to Health

Fabiani, E. D., Mitro, N., Gilardi, F., Galmozzi, A., Caruso, D., & Crestani, M. (2010) · Nutrients · doi:10.3390/nu2050551 · Cited by 15

Activating transcription factor 3 - an endogenous inhibitor of myocardial ischemia-reperfusion injury (Review)

Yang, C., Yang, J., FAN, Z.-X., & Yang, J. M. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4529 · Cited by 16

Efficacy of Beta1 Integrin and EGFR Targeting in Sphere-Forming Human Head and Neck Cancer Cells

Zscheppang, K., Kurth, I., Wachtel, N., Dubrovska, A., Kunz‐Schughart, L. A., & Cordes, N. (2016) · Journal of Cancer · doi:10.7150/jca.14232 · Cited by 16

Aberrant Forms of Histone Acetyltransferases in Human Disease

van Beekum, O., & Kalkhoven, E. (2007) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/1-4020-5466-1_11 · Cited by 16

Deciphering the histone code using mass spectrometry

Ueberheide, B. M., & Mollah, S. (2006) · International Journal of Mass Spectrometry · doi:10.1016/j.ijms.2006.09.001 · Cited by 16

Tumor regression by phenethyl isothiocyanate involves DDB2

Roy, N., Elangovan, I., Kopanja, D., Bagchi, S., & Raychaudhuri, P. (2013) · Cancer Biology & Therapy · doi:10.4161/cbt.22631 · Cited by 16

Interactions between BRCA Proteins and DNA Structure

Scully, R. (2001) · Experimental Cell Research · doi:10.1006/excr.2000.5132 · Cited by 16

GCN5 Dependence of Chromatin Remodeling and Transcriptional Activation by the GAL4 and VP16 Activation Domains in Budding Yeast

Stafford, G. A., & Morse, R. H. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.14.4568-4578.2001 · Cited by 16

Reconstitution of Enhancer Function in Paternal Pronuclei of One-Cell Mouse Embryos

Rastelli, L., Robinson, K. M., Xu, Y., & Majumder, S. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.16.5531-5540.2001 · Cited by 16

Progressive Phosphorylation Modulates the Self-Association of a Variably Modified Histone H3 Peptide

Papamokos, G., Tziatzos, G., Papageorgiou, D. G., Georgatos, S. D., Kaxiras, E., & Politou, A. S. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.698182 · Cited by 15

Discovery of trisubstituted nicotinonitrile derivatives as novel human GCN5 inhibitors through AlphaScreen-based high throughput screening

Tao, H., Wang, J., Lu, W., Zhang, R., Xie, Y., Liu, J. Y.-C., Liu, R., Yue, L., Chen, K., Jiang, H., et al. (2019) · RSC Advances · doi:10.1039/c8ra10074h · Cited by 15

Purification and characterization of a novel histone H2A specific protease (H2Asp) from chicken liver nuclear extract

Panda, P., Chaturvedi, M. M., Panda, A. K., Suar, M., & Purohit, J. S. (2012) · Gene · doi:10.1016/j.gene.2012.09.098 · Cited by 15

Inhibition of histone deacetylases in rats self‐administering cocaine regulates lissencephaly gene‐1 and reelin gene expression, as revealed by microarray technique

Host, L., Anglard, P., Romieu, P., Thibault-Carpentier, C., Dembélé, D., Aunis, D., & Zwiller, J. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06591.x · Cited by 15

Reciprocal actions of ATF5 and Shh in proliferation of cerebellar granule neuron progenitor cells

Lee, H. Y., Angelastro, J. M., Kenney, A. M., Mason, C. A., & Greene, L. A. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20979 · Cited by 15

Assays for pharmacodynamic analysis of histone deacetylase inhibitors

Chung, E. J., Lee, M.-J., Lee, S., & Trepel, J. B. (2006) · Expert Opinion on Drug Metabolism & Toxicology · doi:10.1517/17425255.2.2.213 · Cited by 15

Radiotherapy and radio‐sensitization in H3K27M ‐mutated diffuse midline gliomas

Liu, C., Kuang, S., Wu, L., Cheng, Q., Gong, X., Wu, J., & Zhang, L. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14225 · Cited by 16

Chromatin affinity-precipitation using a small metabolic molecule: its application to analysis of O-acetyl-ADP-ribose

Tung, S., Hong, J., Walz, T., Moazed, D., & Liou, G. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0771-x · Cited by 13

Depletion of pro-oncogenic RUNX2 enhances gemcitabine (GEM) sensitivity of p53-mutated pancreatic cancer Panc-1 cells through the induction of pro-apoptotic TAp63

Ozaki, T., Nakamura, M., Ogata, T., Sang, M., Yoda, H., Hiraoka, K., Sang, M., & Shimozato, O. (2016) · Oncotarget · doi:10.18632/oncotarget.12433 · Cited by 14

Global histone protein surface accessibility in yeast indicates a uniformly loosely packed genome with canonical nucleosomes

Marr, L. T., Ocampo, J., Clark, D. J., & Hayes, J. J. (2021) · Epigenetics & Chromatin · doi:10.1186/s13072-020-00381-5 · Cited by 12

Global profiling of histone modifications in the polyomavirus BK virion minichromosome

Fang, C., Shen, C., Wang, M., Chen, P., Chan, M. W. Y., Hsu, P., & Chang, D. (2015) · Virology · doi:10.1016/j.virol.2015.04.009 · Cited by 14

Epigenetic Activity of Peroxisome Proliferator-Activated Receptor Gamma Agonists Increases the Anticancer Effect of Histone Deacetylase Inhibitors on Multiple Myeloma Cells

Aouali, N., Broukou, A., Bosseler, M., Keunen, O., Schlesser, V., Janji, B., Palissot, V., Stordeur, P., & Berchem, G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0130339 · Cited by 14

SUMO-1 Promotes Ishikawa Cell Proliferation and Apoptosis in Endometrial Cancer by Increasing Sumoylation of Histone H4

Zheng, J., Liu, L., Wang, S., & Huang, X. (2015) · International Journal of Gynecological Cancer · doi:10.1097/igc.0000000000000501 · Cited by 15

PKCβ: Expanding role in hepatic adaptation of cholesterol homeostasis to dietary fat/cholesterol

Mehta, D., & Mehta, K. D. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00373.2016 · Cited by 13

Infant Emotion Development and Temperament

Aktar, E., & Pérez‐Edgar, K. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.026 · Cited by 17

Valproic acid exerts differential effects on CXCR4 expression in leukemic cells

Gül, H., Marquez‐Curtis, L. A., Jahroudi, N., Larratt, L. M., & Janowska‐Wieczorek, A. (2009) · Leukemia Research · doi:10.1016/j.leukres.2009.05.014 · Cited by 14

Nucleosome structural changes induced by binding of non‐histone chromosomal proteins HMGN1 and HMGN2

Shimahara, H., Hirano, T., Ohya, K., Matsuta, S., Seeram, S. S., & Tate, S. (2013) · FEBS Open Bio · doi:10.1016/j.fob.2013.03.002 · Cited by 13

The lamin code

Maraldi, N. M. (2017) · Biosystems · doi:10.1016/j.biosystems.2017.07.006 · Cited by 13

The Role of Epigenetics in Addiction: Clinical Overview and Recent Updates

Beayno, A., Hayek, S. E., Noufi, P. E., Tarabay, Y., & Shamseddeen, W. A. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9554-7_35 · Cited by 13

Identifying modifications on DNA-bound histones with joint deep learning of multiple binding sites in DNA sequence

Li, Y., Quan, L., Zhou, Y., Jiang, Y., Li, K., Wu, T., & Lyu, Q. (2022) · Bioinformatics · doi:10.1093/bioinformatics/btac489 · Cited by 13

DNA damage induces cdk2 protein levels and histone H2B phosphorylation in SH-SY5Y neuroblastoma cells

Yu, X., Caltagarone, J., Smith, M. A., & Bowser, R. P. (2005) · Journal of Alzheimer s Disease · doi:10.3233/jad-2005-8102 · Cited by 13

Proteomic changes induced by histone demethylase JMJD3 in TNF alpha-treated human monocytic (THP-1) cells

Das, A., Das, N. D., Jung, K. H., Park, J. H., Lee, H. T., Han, D., Choi, M., Kang, S. C., & Chai, Y. G. (2013) · Molecular Immunology · doi:10.1016/j.molimm.2013.04.013 · Cited by 13

Tissue specific epigenetic differences in CRH gene expression

Abou-Seif, C. (2011) · Frontiers in bioscience · doi:10.2741/3953 · Cited by 13

H3 and H4 Lysine Acetylation Correlates with Developmental and Experimentally Induced Adult Experience-Dependent Plasticity in the Mouse Visual Cortex

Vierci, G., Pannunzio, B., Bornia, N., & Rossi, F. (2016) · Journal of Experimental Neuroscience · doi:10.4137/jen.s39888 · Cited by 13

NS3 Protein from Rice stripe virus affects the expression of endogenous genes in Nicotiana benthamiana

Wu, G., Zheng, G., Hu, Q., Ma, M., Li, M., Sun, X., Yan, F., & Qing, L. (2018) · Virology Journal · doi:10.1186/s12985-018-1014-7 · Cited by 13

Fatty acid‐binding protein 3 regulates differentiation of IgM‐producing plasma cells

Kobayashi, S., Phung, H. T., Tayama, S., Kagawa, Y., Miyazaki, H., Yamamoto, Y., Maruyama, T., Ishii, N., & Owada, Y. (2020) · FEBS Journal · doi:10.1111/febs.15460 · Cited by 13

The TFG-TEC oncoprotein induces transcriptional activation of the humanβ-enolasegene via chromatin modification of the promoter region

Kim, A.-Y., Lim, B., Choi, J.-H., & Kim, J. (2015) · Molecular Carcinogenesis · doi:10.1002/mc.22384 · Cited by 13

A role for protein kinase PKR in the mediation of Epstein–Barr virus latent membrane protein-1-induced IL-6 and IL-10 expression

Lin, S. S., Lee, D. C. W., Law, A. H. Y., Fang, J., Chua, D. T.-T., & Lau, A. S. Y. (2010) · Cytokine · doi:10.1016/j.cyto.2010.01.008 · Cited by 13

A new diaryl urea compound, D181, induces cell cycle arrest in the G1 and M phases by targeting receptor tyrosine kinases and the microtubule skeleton

Zhang, J., Zhou, J., Ren, X., Diao, Y., Li, H., Jiang, H., Ding, K., & Pei, D. (2010) · Investigational New Drugs · doi:10.1007/s10637-010-9577-1 · Cited by 13

Efficient readout of posttranslational codes on the 50-residue tail of histone H3 by high-resolution MS/MS

Siuti, N., & Kelleher, N. L. (2009) · Analytical Biochemistry · doi:10.1016/j.ab.2009.09.022 · Cited by 13

Sperm Nucleoproteins

Oliva, R., & Castillo, J. (2011) · Springer eBooks · doi:10.1007/978-1-4419-6857-9_3 · Cited by 13

Selective Repression of Low-Density Lipoprotein Receptor Expression by SP600125: Coupling of Histone H3-Ser10 Phosphorylation and Sp1 Occupancy

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Analysis of Histone Phosphorylation: Coupling Intracellular Signaling to Chromatin Remodeling

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Alterations in the expression and modification of histonesin the liver after injury

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Cross-Cultural Perspectives on Parent–Infant Interactions

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The Implication of Cancer Progenitor Cells and the Role of Epigenetics in the Development of Novel Therapeutic Strategies for Chronic Myeloid Leukemia

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Mitogen-activated Protein Kinase Signaling Mediates Phosphorylation of Polycomb Ortholog Cbx7

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Effects of Trichostatin A on In vitro Development of Porcine Embryos Derived from Somatic Cell Nuclear Transfer

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The Chromatin Modifier MSK1/2 Suppresses Endocrine Cell Fates during Mouse Pancreatic Development

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Social and Behavioral Epigenetics: Evolving Perspectives on Nature-Nurture Interplay, Plasticity, and Inheritance

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Modifications of histones in parasites as drug targets

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Signal transduction from cell surface to nucleus in development and disease

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Transcriptional Regulation by Extracellular signals: Mechanisms and Specificity

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Signal transduction and gene control

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Histone Phosphorylation

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Signal transduction from the cell surface to the nucleus through the phosphorylation of transcription factors

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