Emerging roles of the corepressors NCoR1 and SMRT in homeostasis

mTOR Signaling in Growth Control and Disease

Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509

Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres

Lin, J., Wu, H., Tarr, P. T., Zhang, C.-Y., Wu, Z., Boss, O., Michael, L. F., Puigserver, P., Isotani, E., Olson, E. N., et al. (2002) · Nature · doi:10.1038/nature00904 · Cited by 2,546

Suppression of Reactive Oxygen Species and Neurodegeneration by the PGC-1 Transcriptional Coactivators

St-Pierre, J., Drori, S., Uldry, M., Silvaggi, J. M., Rhee, J., Jäger, S., Handschin, C., Zheng, K., Lin, J., Yang, W., et al. (2006) · Cell · doi:10.1016/j.cell.2006.09.024 · Cited by 2,233

The coregulator exchange in transcriptional functions of nuclear receptors

Glass, C. K., & Rosenfeld, M. G. (2000) · Genes & Development · doi:10.1101/gad.14.2.121 · Cited by 2,233

Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor

Hörlein, A., Näär, A. M., Heinzel, T., Torchia, J., Gloss, B. R., Kurokawa, R., Ryan, A. K., Kamei, Y., Söderström, M., Glass, C. K., et al. (1995) · Nature · doi:10.1038/377397a0 · Cited by 2,072

Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-γ

Picard, F., Kurtev, M. V., Chung, N., Topark‐Ngarm, A., Senawong, T., de Oliveira, R. M., Leid, M. E., McBurney, M. W., & Guarente, L. (2004) · Nature · doi:10.1038/nature02583 · Cited by 1,943

A transcriptional co-repressor that interacts with nuclear hormone receptors

Chen, J. D., & Evans, R. M. (1995) · Nature · doi:10.1038/377454a0 · Cited by 1,794

A SUMOylation-dependent pathway mediates transrepression of inflammatory response genes by PPAR-γ

Pascual, G., Fong, A. L., Ogawa, S., Gamliel, A., Li, A. C., Perissi, V., Rose, D. W., Willson, T. M., Rosenfeld, M. G., & Glass, C. K. (2005) · Nature · doi:10.1038/nature03988 · Cited by 1,287

Nuclear Receptor Repression Mediated by a Complex Containing SMRT, mSin3A, and Histone Deacetylase

Nagy, L., Kao, H.-Y., Chakravarti, D., Lin, R. J., Hassig, C. A., Ayer, D. E., Schreiber, S. L., & Evans, R. M. (1997) · Cell · doi:10.1016/s0092-8674(00)80218-4 · Cited by 1,230

A complex containing N-CoR, mSln3 and histone deacetylase mediates transcriptional repression

Heinzel, T., Lavinsky, R. M., Mullen, T.-M., Söderström, M., Laherty, C. D., Torchia, J., Yang, W., Brard, G., Ngo, S. D., Davie, J., et al. (1997) · Nature · doi:10.1038/387043a0 · Cited by 1,210

TET3 epigenetically controls feeding and stress response behaviors via AGRP neurons

Xie, D., Stutz, B., Li, F., Chen, F., Lv, H., Šestan-Peša, M., Catarino, J. D. S., Gu, J., Zhao, H., Stoddard, C. E., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci162365 · Cited by 27

The Optimal Corepressor Function of Nuclear Receptor Corepressor (NCoR) for Peroxisome Proliferator-activated Receptor γ Requires G Protein Pathway Suppressor 2

Guo, C. H., Li, Y., Gow, C., Wong, M., Zha, J., Yan, C., Liu, H., Wang, Y., Burris, T. P., & Zhang, J. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.598797 · Cited by 27

The endocannabinoid anandamide has an anti-inflammatory effect on CCL2 expression in vascular smooth muscle cells

Pflüger‐Müller, B., Oo, J. A., Heering, J., Warwick, T., Proschak, E., Günther, S., Looso, M., Rezende, F., Fork, C., Geißlinger, G., et al. (2020) · Basic Research in Cardiology · doi:10.1007/s00395-020-0793-3 · Cited by 26

Post-Translational Modifications of Histones in Vertebrate Neurogenesis

Mitrousis, N., Tropepe, V., & Hermanson, O. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00483 · Cited by 26

NCoR1 restrains thymic negative selection by repressing Bim expression to spare thymocytes undergoing positive selection

Wang, J., He, N., Zhang, N., Quan, D., Zhang, S., Zhang, C., Yu, R. T., Atkins, A. R., Zhu, R., Yang, C., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00931-8 · Cited by 26

Humanized UGT1 Mice, Regulation of UGT1A1, and the Role of the Intestinal Tract in Neonatal Hyperbilirubinemia and Breast Milk-Induced Jaundice

Chen, S., & Tukey, R. H. (2018) · Drug Metabolism and Disposition · doi:10.1124/dmd.118.083212 · Cited by 25

Regulation of PXR Function by Coactivator and Corepressor Proteins: Ligand Binding Is Just the Beginning

Rigalli, J. P., Theile, D., Nilles, J., & Weiß, J. (2021) · Cells · doi:10.3390/cells10113137 · Cited by 24

Intestinal NCoR1, a regulator of epithelial cell maturation, controls neonatal hyperbilirubinemia

Chen, S., Lü, W., Yueh, M., Rettenmeier, E., Liu, M., Paszek, M., Auwerx, J. H., Yu, R. T., Evans, R. M., Wang, K., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1700232114 · Cited by 23

Macrophage NCOR1 Deficiency Ameliorates Myocardial Infarction and Neointimal Hyperplasia in Mice

Du, L., Sun, J., Zhang, W., Wang, Y., Zhu, H., Liu, T., Gao, M., Zheng, C., Zhang, Y., Liu, Y., et al. (2020) · Journal of the American Heart Association · doi:10.1161/jaha.120.015862 · Cited by 23

The Role of BTB-Zinc Finger Transcription Factors During T Cell Development and in the Regulation of T Cell-mediated Immunity

Ellmeier, W., & Taniuchi, I. (2014) · Current topics in microbiology and immunology · doi:10.1007/82_2014_374 · Cited by 24

Suppressor mutations in Mecp2 -null mice implicate the DNA damage response in Rett syndrome pathologyPreprint

Enikanolaiye, A., Ruston, J., Zeng, R., Taylor, C., Schrock, M., Buchovecky, C. M., Shendure, J., Acar, E. F., & Justice, M. J. (2020) · Genome Research · doi:10.1101/gr.258400.119 · Cited by 25

Role of the Nuclear Receptor Corepressor 1 (NCOR1) in Atherosclerosis and Associated Immunometabolic Diseases

Geiger, M. A., Guillaumon, A. T., Paneni, F., Matter, C. M., & Stein, S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.569358 · Cited by 24

Dermal wound transcriptomic responses to Infection with Pseudomonas aeruginosa versus Klebsiella pneumoniae in a rabbit ear wound model

Leung, K. P., D’Arpa, P., Seth, A. K., Geringer, M. R., Jett, M., Xu, W., Hong, S. J., Galiano, R. D., Chen, T., & Mustoe, T. A. (2014) · BMC Clinical Pathology · doi:10.1186/1472-6890-14-20 · Cited by 23

Gene Signature Associated with Upregulation of the Wnt/β-Catenin Signaling Pathway Predicts Tumor Response to Transarterial Embolization

Ziv, E., Yarmohammadi, H., Boas, F. E., Petre, E. N., Brown, K. T., Solomon, S. B., Solit, D. B., Reidy‐Lagunes, D. L., & Erinjeri, J. P. (2017) · Journal of Vascular and Interventional Radiology · doi:10.1016/j.jvir.2016.11.004 · Cited by 23

The nuclear DEK interactome supports multi‐functionality

Smith, E. A., Krumpelbeck, E. F., Jegga, A. G., Prell, M., Matrka, M. C., Kappes, F., Greis, K. D., Ali, A. M., Meetei, A. R., & Wells, S. I. (2017) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.25411 · Cited by 23

NCoR1: Putting the Brakes on the Dendritic Cell Immune Tolerance

Ahad, A., Stevanin, M., Smita, S., Mishra, G. P., Gupta, D., Waszak, S. M., Sarkar, U. A., Basak, S., Gupta, B., Acha‐Orbea, H., et al. (2019) · iScience · doi:10.1016/j.isci.2019.08.024 · Cited by 22

Hormones

Norman, A. W., & Henry, H. L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-08-091906-5.00001-x · Cited by 23

TBX2 controls a proproliferative gene expression program in melanomaPreprint

Lu, S., Louphrasitthiphol, P., Goradia, N., Lambert, J., Schmidt, J., Chauhan, J. S., Rughani, M. G., Larue, L., Wilmanns, M., & Goding, C. R. (2021) · Genes & Development · doi:10.1101/gad.348746.121 · Cited by 21

Lipid droplet deposition in the regenerating liver: A promoter, inhibitor, or bystander?

Hu, Y., Wang, R., Liu, J., Wang, Y., & Dong, J. (2023) · Hepatology Communications · doi:10.1097/hc9.0000000000000267 · Cited by 22

Epigenetic Regulation of Circadian Clocks and Its Involvement in Drug Addiction

Saad, L., Zwiller, J., Kalsbeek, A., & Anglard, P. (2021) · Genes · doi:10.3390/genes12081263 · Cited by 24

Evidence that HDAC7 acts as an epigenetic “reader” of AR acetylation through NCoR-HDAC3 dissociation

Zhang, Y., Andrade, R. E., Hanna, A. A., & Pflum, M. K. H. (2022) · Cell chemical biology · doi:10.1016/j.chembiol.2022.05.008 · Cited by 22

Prolactin regulatory element-binding (PREB) protein regulates hepatic glucose homeostasis

Park, J.-M., Kim, M., Kim, T. H., Min, D., Yang, G. E., & Ahn, Y. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.03.024 · Cited by 22

Whole Exome Sequencing of Ulcerative Colitis–associated Colorectal Cancer Based on Novel Somatic Mutations Identified in Chinese Patients

Yan, P., Wang, Y., Meng, X., Yang, H. B., Liu, Z., Qian, J., Zhou, W., & Li, J. (2019) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izz020 · Cited by 22

NCoR1 Protects Mice From Dextran Sodium Sulfate–Induced Colitis by Guarding Colonic Crypt Cells From Luminal Insult

Mennillo, E., Yang, X., Paszek, M., Auwerx, J. H., Benner, C. W., & Chen, S. (2020) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2020.01.014 · Cited by 22

NCOR1 maintains the homeostasis of vascular smooth muscle cells and protects against aortic aneurysm

Du, L., Sun, J., Zhang, W., Liu, Y., Liu, Y., Lin, W.-Z., Liu, T., Zhu, H., Wang, Y., Shao, S., et al. (2022) · Cell Death and Differentiation · doi:10.1038/s41418-022-01065-1 · Cited by 21

Roles of transducin-like enhancer of split (TLE) family proteins in tumorigenesis and immune regulation

Yu, G., Chen, Y., Hu, Y., Zhou, Y., Ding, X., & Zhou, X. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1010639 · Cited by 25

Branched-chain amino acid ratios modulate lipid metabolism in adipose tissues of growing pigs

Duan, Y., Li, F., Guo, Q., Wang, W., Zhang, L., Wen, C., & Yin, Y. (2017) · Journal of Functional Foods · doi:10.1016/j.jff.2017.12.004 · Cited by 21

The nuclear receptor corepressor NCoR1 regulates hematopoiesis and leukemogenesis in vivo

Wan, X., Liu, L., Zhou, P., Hui, X., He, Q., Yu, F., Zhang, W., Ding, X., Yuan, X., Zhang, N., et al. (2019) · Blood Advances · doi:10.1182/bloodadvances.2018022756 · Cited by 21

Phenotypic variation reveals sites of evolutionary constraint in the androgenic signaling pathway

Schuppe, E. R., & Fuxjager, M. J. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.06.002 · Cited by 21

Epigenetic Reprogramming in Host-Parasite Coevolution: TheToxoplasmaParadigm

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

Chaperone-mediated autophagy dysregulation during aging impairs hepatic fatty acid oxidation via accumulation of NCoR1

Choi, Y., Yun, S. H., Yu, J., Mun, Y., Lee, W., Park, C. J., Han, B. W., & Lee, B. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101784 · Cited by 20

PPARβ/δ recruits NCOR and regulates transcription reinitiation of ANGPTL4

Legrand, N., Bretscher, C., Zielke, S., Wilke, B., Daude, M., Fritz, B., Diederich, W. E., & Adhikary, T. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz685 · Cited by 21

Multifaceted Transcriptional Network of Estrogen-Related Receptor Alpha in Health and Disease

Cerutti, C., Shi, J., & Vanacker, J.-M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054265 · Cited by 20

DNA hypermethylation of CD3+ T cells from cord blood of infants exposed to intrauterine growth restriction

Williams, L., Seki, Y., Delahaye, F., Cheng, A., Fuloria, M., Einstein, F. H., & Charron, M. J. (2016) · Diabetologia · doi:10.1007/s00125-016-3983-7 · Cited by 20

Nuclear corepressors NCOR1/NCOR2 regulate B cell development, maintain genomic integrity and prevent transformation

Lee, R. D., Knutson, T. P., Munro, S. A., Miller, J. T., Heltemes-Harris, L. M., Mullighan, C. G., Jepsen, K., & Farrar, M. A. (2022) · Nature Immunology · doi:10.1038/s41590-022-01343-7 · Cited by 20

Forkhead box O1 mediates defects in palmitate-induced insulin granule exocytosis by downregulation of calcium/calmodulin-dependent serine protein kinase expression in INS-1 cells

Wang, Y., Lin, H., Hao, N., Zhu, Z., Wang, D., Li, Y., Chen, H., Zhu, Y., & Han, X. (2015) · Diabetologia · doi:10.1007/s00125-015-3561-4 · Cited by 18

Identification of the global miR-130a targetome reveals a role for TBL1XR1 in hematopoietic stem cell self-renewal and t(8;21) AML

Krivdova, G., Voisin, V., Schoof, E. M., Marhon, S. A., Murison, A., McLeod, J. L., Gabra, M., Zeng, A. G. X., Aigner, S., Yee, B. A., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110481 · Cited by 17

Sequence-based prediction of transcription upregulation by auxin in plants

Пономаренко, П. М., & Ponomarenko, M. P. (2015) · Journal of Bioinformatics and Computational Biology · doi:10.1142/s0219720015400090 · Cited by 17

NCOR1 Orchestrates Transcriptional Landscapes and Effector Functions of CD4+ T Cells

Hainberger, D., Stolz, V., Zhu, C., Schuster, M. K., Müller, L., Hamminger, P., Rîca, R., Waltenberger, D., Alteneder, M., Krausgruber, T., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00579 · Cited by 17

Touch and go: nuclear proteolysis in the regulation of metabolic genes and cancer

Maneix, L., & Catic, A. (2016) · FEBS Letters · doi:10.1002/1873-3468.12087 · Cited by 17

Regulation of corepressor alternative mRNA splicing by hormonal and metabolic signaling

Snyder, C. A., Goodson, M. L., Schroeder, A. C., & Privalsky, M. L. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.06.036 · Cited by 17

Classical pathways of gene regulation by retinoids

Pohl, E., & Tomlinson, C. W. E. (2020) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2020.03.008 · Cited by 16

Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer Patients

Ronowicz, A., Janaszak‐Jasiecka, A., Skokowski, J., Madanecki, P., Bartoszewski, R., Bałut, M., Seroczyńska, B., Kochan, K., Bogdan, A., Butkus, M., et al. (2015) · Human Mutation · doi:10.1002/humu.22845 · Cited by 17

The corepressor NCOR1 regulates the survival of single-positive thymocytes

Müller, L., Hainberger, D., Stolz, V., Hamminger, P., Hassan, H., Preglej, T., Boucheron, N., Sakaguchi, S., Wiegers, G. J., Villunger, A., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15918-0 · Cited by 15

Ontogenetic expression of thyroid hormone signaling genes: An in vitro and in vivo species comparison

Walter, K. M., Dach, K., Hayakawa, K. A., Giersiefer, S., Heuer, H., Lein, P. J., & Fritsche, E. (2019) · PLoS ONE · doi:10.1371/journal.pone.0221230 · Cited by 15

Lgr5 + cell fate regulation by coordination of metabolic nuclear receptors during liver repair

Qin, D., Liu, S., Lu, Y., Yan, Y. L., Zhang, J., Cao, S., Chen, M., Chen, N., Huang, W., Wang, L., et al. (2022) · Theranostics · doi:10.7150/thno.74194 · Cited by 14

NCoR1 controls Mycobacterium tuberculosis growth in myeloid cells by regulating the AMPK-mTOR-TFEB axis

Biswas, V. K., Sen, K., Ahad, A., Ghosh, A., Verma, S., Pati, R., Prusty, S., Nayak, S. P., Podder, S., Kumar, D., et al. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002231 · Cited by 14

Drivers of cancer metastasis – Arise early and remain present

Dymerska, D., & Marusiak, A. A. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.189060 · Cited by 14

Sperm-borne mRNAs: potential roles in zygote genome activation and epigenetic inheritance

González, B., & González, C. R. (2025) · Open Biology · doi:10.1098/rsob.240321 · Cited by 15

Coregulator-mediated control of skeletal muscle plasticity – A mini-review

Schnyder, S., Kupr, B., & Handschin, C. (2017) · Biochimie · doi:10.1016/j.biochi.2016.12.011 · Cited by 14

The Interface between Cell Signaling Pathways and Pregnane X Receptor

Rogers, R. S., Parker, A., Vainer, P., Elliott, E., Sudbeck, D., Parimi, K., Peddada, V. P., Howe, P. G., D’Ambrosio, N., Ruddy, G., et al. (2021) · Cells · doi:10.3390/cells10113262 · Cited by 14

Ncor1 Deficiency Promotes Osteoclastogenesis and Exacerbates Periodontitis

Ma, X. X., Meng, X.-Q., Wang, Y., Liu, Y., Shi, X., Shao, S., Duan, S., & Lu, H. (2022) · Journal of Dental Research · doi:10.1177/00220345221116927 · Cited by 14

Oxidative phosphorylation and fatty acid oxidation in slow-aging mice

Elmansi, A. M., & Miller, R. A. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.08.018 · Cited by 14

The small molecule PSSM0332 disassociates the CRL4ADCAF8 E3 ligase complex to decrease the ubiquitination of NcoR1 and inhibit the inflammatory response in a mouse sepsis-induced myocardial dysfunction model

Peng, Q., Xu, H., Xiao, M., & Wang, L. (2020) · International Journal of Biological Sciences · doi:10.7150/ijbs.50186 · Cited by 13

Characterization of the Free State Ensemble of the CoRNR Box Motif by Molecular Dynamics Simulations

Cino, E. A., Choy, W., & Karttunen, M. (2016) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.5b11565 · Cited by 13

The transcription cofactor CRTC1 protects from aberrant hepatic lipid accumulation

Kim, H. (2016) · Scientific Reports · doi:10.1038/srep37280 · Cited by 13

A cell type‐specific expression map of NCoR1 and SMRT transcriptional co‐repressors in the mouse brain

Iemolo, A., Montilla‐Perez, P., Lai, I., Meng, Y., Nolan, S. L., Wen, J., Rusu, I., Dulcis, D., & Telese, F. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24886 · Cited by 15

Ncor1 and Ncor2 play essential but distinct roles in zebrafish primitive myelopoiesis

Li, J., Li, K., Dong, X., Liang, D., & Zhao, Q. (2014) · Developmental Dynamics · doi:10.1002/dvdy.24181 · Cited by 13

NCOR1 Sustains Colorectal Cancer Cell Growth and Protects against Cellular Senescence

St‐Jean, S., Castro, A. D., Lecours, M., Jones, C. M., Rivard, N., Rodier, F., Perreault, N., & Boudreau, F. (2021) · Cancers · doi:10.3390/cancers13174414 · Cited by 12

Interaction between poly(A)–binding protein PABPC4 and nuclear receptor corepressor NCoR1 modulates a metabolic stress response

de Oliveira, A. G., Oliveira, L., Cruz, M. V., Guimarães, D. S. P. S. F., de Lima, T. I., Santos-Fávero, B. C., Luchessi, A. D., Pauletti, B. A., Leme, A. F. P., Bajgelman, M. C., et al. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104702 · Cited by 12

Coordinated transcriptional upregulation of oxidative metabolism proteins in long-lived endocrine mutant mice

Elmansi, A. M., & Miller, R. A. (2023) · GeroScience · doi:10.1007/s11357-023-00849-8 · Cited by 13

Stress Molecular Signaling in Interaction With Cognition

Lugenbühl, J. F., Viho, E. M. G., Binder, E. B., & Daskalakis, N. P. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.09.023 · Cited by 12

Breast cancer plasticity is restricted by a LATS1-NCOR1 repressive axis

Aylon, Y., Furth, N., Mallel, G., Friedlander, G., Nataraj, N. B., Dong, M., Hassin, O., Zoabi, R., Cohen, B., Drendel, V., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34863-9 · Cited by 14

Opposing action of NCoR1 and PGC-1α in mitochondrial redox homeostasis

de Lima, T. I., Guimarães, D. S. P. S. F., de Oliveira, A. G., Araújo, H. N., Sponton, C. H., de Souza-Pinto, N. C., Saito, Â., Figueira, A. C. M., Palameta, S., Bajgelman, M. C., et al. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.08.006 · Cited by 12

Regulation of Intestinal UDP-Glucuronosyltransferase 1A1 by the Farnesoid X Receptor Agonist Obeticholic Acid Is Controlled by Constitutive Androstane Receptor through Intestinal Maturation

Weber, A. A., Mennillo, E., Yang, X., van der Schoor, L. W. E., Jonker, J. W., Chen, S., & Tukey, R. H. (2020) · Drug Metabolism and Disposition · doi:10.1124/dmd.120.000240 · Cited by 12

Exercise-induced signaling activation by Chrysanthemum zawadskii and its active compound, linarin, ameliorates age-related sarcopenia through Sestrin 1 regulation

Nirmala, F. S., Lee, H., Kim, Y., Hahm, J., Seo, H., Kim, M. J., Jung, C. H., & Ahn, J. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155695 · Cited by 11

De novo missense variants in HDAC3 leading to epigenetic machinery dysfunction are associated with a variable neurodevelopmental disorder

Yoon, J. G., Lim, S.-K., Seo, H., Lee, S., Cho, J., Kim, S. Y., Koh, H. Y., Poduri, A., Ramakumaran, V. S., Vasudevan, P. C., et al. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2024.06.015 · Cited by 11

Identification of the relationship between the variability of the expression of signaling pathway genes in the human brain and the affinity of TATA-binding protein to their promoters

Ponomarenko, M. P., Suslov, V. V., Владимирович, Г. К., Ponomarenko, P. M., Vishnevsky, O. V., & Kolchanov, N. A. (2015) · Russian Journal of Genetics Applied Research · doi:10.1134/s2079059715060088 · Cited by 11

Genetic Alterations in Papillary Thyroid Carcinoma With Hashimoto’s Thyroiditis： ANK3, an Indolent Maintainer of Papillary Thyroid Carcinoma

Zeng, C., Long, J., Deng, C., Xie, L., Ma, H., Guo, Y., Liu, S., & Deng, M. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.894786 · Cited by 11

The Fgf/Erf/NCoR1/2 repressive axis controls trophoblast cell fate

Lackner, A., Müller, M., Gamperl, M., Stoeva, D., Langmann, O., Papúchová, H., Roitinger, E., Dürnberger, G., Imre, R., Mechtler, K., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-38101-8 · Cited by 12

Genetic deletion of hepatic NCOR1 protects from atherosclerosis by promoting alternative bile acid-metabolism and sterol excretion

Geiger, M. A., Oppi, S., Nusser‐Stein, S., Costantino, S., Mohammed, S. A., Gorica, E., Hoogerland, J. A., Matter, C. M., Guillaumon, A. T., Ruschitzka, F. T., et al. (2023) · Cardiovascular Diabetology · doi:10.1186/s12933-023-01865-w · Cited by 11

Tumor suppressive actions of the nuclear receptor corepressor 1

Martínez-Iglesias, O. A., Alonso-Merino, E., & Aranda, A. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.04.027 · Cited by 11

Identification of key genes associated with congenital heart defects in embryos of diabetic mice

Lin, N., Cai, Y., Zhang, L., & Chen, Y. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.8330 · Cited by 11

Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesis

Sakaguchi, Y., Uehara, T., Suzuki, H., Sakamoto, Y., Fujiwara, M., Kosaki, K., & Takenouchi, T. (2018) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.40354 · Cited by 11

NCoR1 fine‐tunes type‐I IFN response in cDC1 dendritic cells by directly regulating Myd88‐IRF7 axis under TLR9

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