The DOI matches its Crossref record; 100 of the 100 references it cites were found in a registry or an index.
Beyond IκBs: alternative regulation of NF‐KB activity
Abstract
The transcription factor nuclear factor-kappa B (NF-kappaB) is a crucial regulator of many physiological and patho-physiological processes, including control of the adaptive and innate immune responses, inflammation, proliferation, tumorigenesis, and apoptosis. Thus, the tight regulation of NF-kappaB activity within a cell is extremely important. The central mechanism of NF-kappaB regulation is the signal-induced proteolytic degradation of a family of cytoplasmic inhibitors of NF-kappaB, the IkappaBs. However, with the discovery of an IkappaB-independent noncanonical or "alternative" pathway of NF-kappaB activation, the importance of other regulatory mechanisms responsible for the fine-tuning of NF-kappaB became clear. Post-translational modification, especially phosphorylation, of the Rel proteins, of which dimeric NF-kappaB is composed, are such alternative regulatory mechanisms. The best analyzed example is RelA phosphorylation, which takes place at specific amino acids resulting in distinct functional changes of this gene regulatory protein. The interaction of NF-kappaB with other proteins such as glucocorticoid receptors is very important for the regulation of NF-kappaB activity. Recently, exciting new concepts of IkappaB-independent NF-kappaB control like dimer exchange and nucleolar sequestration of RelA have been described, indicating that many aspects of NF-kappaB control are waiting to be discovered.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Although NF-κB nuclear translocation is the best-known mechanism for its activation [12], several lines of evidence indicate that posttranslational modifications in p65 subunit, such as phosphorylation and acetylation, impact its activity by altering DNA binding, interaction with inhibitor of κB α (IκBα) in the nucleus, and association with chromatin structure modifiers such as histone acetyltrans”
From Edible blue-green algae reduce the production of pro-inflammatory cytokines by inhibiting NF-κB pathway in macrophages and splenocytes (2013) · cites this paper as [33]
Citations
Cites
Phosphorylation meets ubiquitination: the control of NF-κB activity
Karin, M., & Ben-Neriah, Y. (2000) · Annual Review of Immunology · doi:10.1146/annurev.immunol.18.1.621 · Cited by 4,766
Taganov, K. D., Boldin, M. P., Chang, K.-J., & Baltimore, D. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605298103 · Cited by 4,317
Hayden, M. S., & Ghosh, S. (2004) · Genes & Development · doi:10.1101/gad.1228704 · Cited by 3,842
Haine, M. M.-L., & Meeùs, N. (1986) · Cited by 3,464
Modulation of NF‐κB‐dependent transcription and cell survival by the SIRT1 deacetylase
Yeung, F., Hoberg, J. E., Ramsey, C. S., Keller, M. D., Jones, D. R., Frye, R. A., & Mayo, M. W. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600244 · Cited by 2,750
Introduction to NF-κB: players, pathways, perspectives
Gilmore, T. D. (2006) · Oncogene · doi:10.1038/sj.onc.1209954 · Cited by 2,293
De-ubiquitination and ubiquitin ligase domains of A20 downregulate NF-κB signalling
Wertz, I. E., O’Rourke, K. M., Zhou, H., Eby, M. T., Aravind, L., Seshagiri, S., Wu, P., Wiesmann, C., Baker, R. T., Boone, D. L., et al. (2004) · Nature · doi:10.1038/nature02794 · Cited by 1,889
Phosphorylation of NF-κB and IκB proteins: implications in cancer and inflammation
Viatour, P., Merville, M., Bours, V., & Chariot, A. (2004) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2004.11.009 · Cited by 1,516
Failure to Regulate TNF-Induced NF-κB and Cell Death Responses in A20-Deficient Mice
Lee, E. G., Boone, D. L., Chai, S., Libby, S. L., Chien, M., Lodolce, J. P., & Ma, A. (2000) · Science · doi:10.1126/science.289.5488.2350 · Cited by 1,409
Requirement for glycogen synthase kinase-3β in cell survival and NF-κB activation
Hoeflich, K. P., Luo, J., Rubie, E. A., Tsao, M., Jin, O., & Woodgett, J. R. (2000) · Nature · doi:10.1038/35017574 · Cited by 1,401
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 267
Wiklund, M., Steinert, S., Junell, A., Hultmark, D., & Stöven, S. (2009) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2008.12.002 · Cited by 49
Nuclear Factor κB Signaling and Its Related Non-coding RNAs in Cancer Therapy
Liu, X., Shao, Y., Zhou, J., Qian, G., & Ma, Z. (2019) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2019.11.007 · Cited by 46
Inhibition of monosodium urate crystal-induced inflammation by scopoletin and underlying mechanisms
Yao, X., Ding, Z., Xia, Y., Wei, Z., Luo, Y., Feleder, C., & Dai, Y. (2012) · International Immunopharmacology · doi:10.1016/j.intimp.2012.07.024 · Cited by 45
Tian, R., Li, Y., & Gao, M. (2015) · Bioscience Reports · doi:10.1042/bsr20150002 · Cited by 45
RetractedKavandi, L., Lee, L. R., Bokhari, A. A., Pirog, J. E., Jiang, Y., Ahmad, K. A., & Syed, V. (2013) · Molecular Carcinogenesis · doi:10.1002/mc.22107 · Cited by 44
Budak, Y., & Huysal, K. (2011) · PubMed · Cited by 44
Ho, T., Chen, S., Shih, S., Wu, J.-Y., Han, W.-H., Cheng, H.-C., Yang, S.-L., & Tsao, Y. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.091085 · Cited by 45
Sokolova, O. V., Borgmann, M., Rieke, C., Schweitzer, K., Rothkötter, H., & Naumann, M. (2013) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2013.07.008 · Cited by 46
Zafar, A., Wu, F., Hardy, K., Li, J., Tu, W. J., McCuaig, R., Harris, J. L., Khanna, K. K., Attema, J. L., Gregory, P. A., et al. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01693-13 · Cited by 43
MicroRNA-142–3p relieves neuropathic pain by targeting high mobility group box 1
Zhang, Y., Mou, J., Cao, L., Zhen, S., Huang, H., & Bao, H. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3222 · Cited by 43
Dai, Y., Chen, S., Wang, L., Pei, X., Funk, V. L., Kramer, L. B., Dent, P., & Grant, S. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.284216 · Cited by 42
Strzeszewska, A., Alster, O., Mosieniak, G., Ciolko, A., & Sikora, E. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0069-5 · Cited by 42
Transactivation of gene expression by NF-κB is dependent on thioredoxin reductase activity
Heilman, J. M., Burke, T. J., McClain, C. J., & Watson, W. H. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.06.028 · Cited by 41
Moore, A. Z., Hernandez, D. G., Tanaka, T., Pilling, L. C., Nalls, M. A., Bandinelli, S., Singleton, A., & Ferrucci, L. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv118 · Cited by 38
Jia, J., Zhang, P., Zhang, C., Jiang, G., Zheng, W., Song, S., & Ai, C. (2021) · Food & Function · doi:10.1039/d1fo02431k · Cited by 37
Kai, M., Yasuda, S., Imai, S.-I., Toyota, M., Kanoh, H., & Sakane, F. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.09.017 · Cited by 37
Chun, J., & Prince, A. S. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0209072 · Cited by 37
Schmitz, I. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-8289-5_4 · Cited by 34
Ikeguchi, S., Izumi, Y., Kitamura, N., Kishino, S., Ogawa, J., Akaike, A., & Kume, T. (2018) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2018.06.015 · Cited by 38
Liao, Y., Gui, Y., Li, Q., An, J., & Wang, D. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.188998 · Cited by 35
Chen, D., Niu, M. Y., Jiao, X., Zhang, K., Liang, J., & Zhang, D. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms13011186 · Cited by 35
RetractedGlycogen synthase kinase-3β is a crucial mediator of signal-induced RelB degradation
Neumann, M., Klar, S., Wilisch-Neumann, A., Hollenbach, E., Kavuri, S. M., Leverkus, M., Kandolf, R., Brunner-Weinzierl, M. C., & Klingel, K. (2011) · Oncogene · doi:10.1038/onc.2010.580 · Cited by 34
Microbial-induced immunomodulation by targeting the NF-κB system
Neish, A. S., & Naumann, M. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.08.004 · Cited by 33
Li, X., Su, J., Cui, X., Li, Y., Barochia, A. V., & Eichacker, P. Q. (2009) · Expert Opinion on Investigational Drugs · doi:10.1517/13543780903018880 · Cited by 35
Doyle, T., Chen, Z., Muscoli, C., Obeid, L., & Salvemini, D. (2011) · The FASEB Journal · doi:10.1096/fj.10-178095 · Cited by 37
Allison, R. L., Welby, E., Khayrullina, G., Burnett, B. G., & Ebert, A. D. (2022) · Glia · doi:10.1002/glia.24153 · Cited by 30
Megid, T. B. C., Farooq, A. R., Wang, X., & Elimova, E. C. (2023) · Cancers · doi:10.3390/cancers15205075 · Cited by 34
Choi, J., Song, Y.-S., Lee, H. J., Kim, G., & Hong, J. W. (2017) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-017-1850-9 · Cited by 31
Oxidative, multistep activation of the noncanonical NF‐κB pathway via disulfide Bcl‐3/p50 complex
Cristofanon, S., Morceau, F., Scovassi, A. I., Dicato, M. A., Ghibelli, L., & Diederich, M. F. (2008) · The FASEB Journal · doi:10.1096/fj.07-104109 · Cited by 31
Flagellin-stimulated Cl− secretion and innate immune responses in airway epithelia: role for p38
Illek, B., Fu, Z., Schwarzer, C., Banzon, T. M., Jalickee, S., Miller, S. S., & Machen, T. E. (2008) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.90292.2008 · Cited by 31
Dihydroartemisinin suppresses pancreatic cancer cells via a microRNA-mRNA regulatory network
Li, Y., Wang, Y., Kong, R., Xue, D., Pan, S., Chen, H., & Sun, B. (2016) · Oncotarget · doi:10.18632/oncotarget.11517 · Cited by 30
Renoprotective effect of ramulus mori polysaccharides on renal injury in STZ-diabetic mice
Guo, C., Liang, T., He, Q., Wei, P., Zheng, N., & Xu, L. (2013) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2013.09.022 · Cited by 30
Zaragozá, R., García–Trevijano, E. R., Lluch, A. M., Ribas, G., & Vinã, J. R. (2015) · IUBMB Life · doi:10.1002/iub.1365 · Cited by 29
Control of NF-κB activation by the COP9 signalosome
Schweitzer, K., & Naumann, M. (2010) · Biochemical Society Transactions · doi:10.1042/bst0380156 · Cited by 29
FGD3 binds with HSF4 to suppress p65 expression and inhibit pancreatic cancer progression
Guo, F., Cheng, X. C., Jing, B., Wu, H., & Jin, X. (2022) · Oncogene · doi:10.1038/s41388-021-02140-6 · Cited by 28
NF-κB: a mediator that promotes or inhibits angiogenesis in human diseases?
Jiang, Y., Zhang, J., Shi, C., Li, X., Jiang, Y., & Mao, R. (2023) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2023.20 · Cited by 28
Huang, L., Verstrepen, L., Heyninck, K., Wullaert, A., Revets, H., BAETSELIER, P. D., & Beyaert, R. (2008) · Oncogene · doi:10.1038/onc.2008.208 · Cited by 27
Xi, Y., Zhang, X., Luo, Q.-X., Gan, H.-N., Liu, Y.-S., Shao, S., & Mao, X. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1187638 · Cited by 26
Lacaze, P. A., Raza, S., Sing, G. K., Page, D. L., Forster, T., Storm, P., Craigon, M., Awad, T. A., Ghazal, P., & Freeman, T. C. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-372 · Cited by 26
Halasz, H., Malekos, E., Covarrubias, S., Yitiz, S., Montano, C., Sudek, L. A., Katzman, S. J., Liu, S. J., Horlbeck, M. A., Namvar, L., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2322524121 · Cited by 25
Inflammation-related miRNAs in obesity, CVD, and NAFLD
Aghaei, S. M., & Hosseini, S. M. (2024) · Cytokine · doi:10.1016/j.cyto.2024.156724 · Cited by 26
Vessichelli, M., Mariggiò, S., Varone, A., Zizza, P., Santo, A. D., Amore, C., Dell’Elba, G., Cutignano, A., Fontana, A., Cacciapuoti, C., et al. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.773861 · Cited by 27
Huang, Z., Hsu, E., Li, H., Rosner, A. L., Rupert, R. L., & Song, X. (2010) · Journal of Pain · doi:10.1016/j.jpain.2010.06.008 · Cited by 25
Lanucara, F., Lam, C. W., Mann, J., Monie, T. P., Colombo, S. A. P., Holman, S. W., Boyd, J., Dange, M. C., Mann, D. A., White, M., et al. (2016) · Open Biology · doi:10.1098/rsob.160055 · Cited by 26
Zheng, J.-P., Zhang, Y., Edvinsson, L. I., Hjalt, T. Å. H., & Xu, C. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.04.006 · Cited by 24
Homocysteine regulates endothelin type B receptors in vascular smooth muscle cells.
Chen, Y., Zhang, H.-M., Liu, E.-Q., Xu, C.-B., & Zhang, Y.-P. (2016) · Vascular pharmacology · doi:10.1016/j.vph.2016.08.011 · Cited by 23
Minutoli, L., Antonuccio, P., Polito, F., Bitto, A., Squadrito, F., Stefano, V. D., Nicòtina, P. A., Fazzari, C., Maisano, D., Romeo, C., et al. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2008.12.028 · Cited by 23
New determinates of disease progression and outcome in metastatic ovarian carcinoma.
Davidson, B., Reich, R., Trope, C. G., Wang, T., & Shih, I. (2010) · PubMed · doi:10.14670/hh-25.1591 · Cited by 22
Lim, M. C. C., Maubach, G., Birkl-Toeglhofer, A. M., Haybaeck, J., Vieth, M. W., & Naumann, M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04139-y · Cited by 21
DC-SCRIPT Regulates IL-10 Production in Human Dendritic Cells by Modulating NF-κBp65 Activation
Søndergaard, J. N., Poghosyan, S., Hontelez, S., Louche, P., Looman, M. W. G., Ansems, M., & Adema, G. J. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402924 · Cited by 21
Melarangi, T., Zhuang, J., Lin, K., Rockliffe, N., Bosanquet, A. G., Oates, M., Slupsky, J. R., & Pettitt, A. R. (2012) · Cell Death and Disease · doi:10.1038/cddis.2012.102 · Cited by 21
Deubiquitinylase USP47 Promotes RelA Phosphorylation and Survival in Gastric Cancer Cells
Naghavi, L., Schwalbe, M., Ghanem, A., & Naumann, M. (2018) · Biomedicines · doi:10.3390/biomedicines6020062 · Cited by 21
Feige, M. H., Sokolova, O. V., Pickenhahn, A., Maubach, G., & Naumann, M. (2018) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2018.05.003 · Cited by 21
Spinelli, S. L., Xi, X., McMillan, D. H., Woeller, C. F., Richardson, M. E., Cavet, M. E., Zhang, J.-Z., Feldon, S. E., & Phipps, R. P. (2014) · Experimental Eye Research · doi:10.1016/j.exer.2014.07.013 · Cited by 20
Avery-Cooper, G., Doerr, M. D., Gilbert, R. W. D., Youssef, M., Richard, A. F., Huether, P., & Viloria‐Petit, A. (2014) · Cancer Cell International · doi:10.1186/1475-2867-14-19 · Cited by 20
Intersection of the p63 and NF‐κB pathways in epithelial homeostasis and disease
King, K. E., George, A. L., Sakakibara, N., Mahmood, K., Moses, M. A., & Weinberg, W. C. (2019) · Molecular Carcinogenesis · doi:10.1002/mc.23081 · Cited by 20
Ubiquitin D Promotes Progression of Oral Squamous Cell Carcinoma via NF-Kappa B Signaling
Song, A., Wang, Y., Jiang, F., Yan, E., Zhou, J., Ye, J., Zhang, H., Ding, X., Li, G., Wu, Y., et al. (2021) · Molecules and Cells · doi:10.14348/molcells.2021.2229 · Cited by 20
Dunnione ameliorates cisplatin ototoxicity through modulation of NAD + metabolism
Kim, H., Pandit, A., Oh, G., Shen, A., Lee, S., Khadka, D., Lee, S., Shim, H., Yang, S., Cho, E. Y., et al. (2015) · Hearing Research · doi:10.1016/j.heares.2015.08.017 · Cited by 20
NAD+ Metabolism in Age-Related Hearing Loss
Kim, H. (2014) · Aging and Disease · doi:10.14336/ad.2014.0500150 · Cited by 20
Involvement of kinase PKC-zeta in the p62/p62P392L-driven activation of NF-κB in human osteoclasts
Chamoux, E., McManus, S., Laberge, G., Bisson, M., & Roux, S. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2012.12.008 · Cited by 22
Phogat, A., Singh, J., Kumar, V. J., & Malik, V. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-28279-1 · Cited by 19
Chou, W., Guh, J., Tsai, J., Hwang, C., Chiou, S.-J., & Chuang, L. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22137 · Cited by 19
Matsuda, A., Tanaka, A., Muto, S., Ohmori, K., Furusaka, T., Jung, K., Karasawa, K., Okamoto, N., Oida, K., Itai, A., et al. (2010) · Research in Veterinary Science · doi:10.1016/j.rvsc.2010.03.017 · Cited by 19
Bajova, H., Nelson, T. E., & Gruol, D. L. (2008) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2008.01.003 · Cited by 19
He, Z., Zhao, J., Zhang, J., Jung, J. U., & Feng, P. (2013) · Journal of Virology · doi:10.1128/jvi.01716-13 · Cited by 19
Quantification of CD95-induced apoptosis and NF-κB activation at the single cell level
Schmidt, J. H., Pietkiewicz, S., Naumann, M., & Lavrik, I. N. (2015) · Journal of Immunological Methods · doi:10.1016/j.jim.2015.04.026 · Cited by 21
He, H., Cui, Z., & Tang, Y.-X. (2021) · Human Cell · doi:10.1007/s13577-021-00603-2 · Cited by 18
Cell survival and apoptosis‐related molecules in cancer cells in effusions: A comprehensive review
Kleinberg, L., & Davidson, B. (2009) · Diagnostic Cytopathology · doi:10.1002/dc.21095 · Cited by 18
Liu, J., Sun, R. W., Leung, C., Lok, C., & Che, C. (2011) · Chemical Communications · doi:10.1039/c1cc15317j · Cited by 19
dos Santos, N. R., Ghezzo, M. N., da Silva, R. C., & Fernandes, M. T. (2010) · Cancers · doi:10.3390/cancers2041838 · Cited by 18
Gremlin aggravates periodontitis via activation of the nuclear factor‐kappa B signaling pathway
Guan, X., He, Y., Li, Y., Shi, C., Wei, Z., Zhao, R., Han, Y., Pan, L., Yang, J., & Hou, T. (2022) · Journal of Periodontology · doi:10.1002/jper.21-0474 · Cited by 18
Zaragozá, R., Bosch, A., Garcı́a, C., Sandoval, J., Serna, E., Torres, L., García–Trevijano, E. R., & Vinã, J. R. (2010) · Biochemical Journal · doi:10.1042/bj20091091 · Cited by 18
Ji, L., Zhang, B., & Zhao, G. (2017) · Human Cell · doi:10.1007/s13577-016-0157-3 · Cited by 17
Manifold role of ubiquitin in Helicobacter pylori infection and gastric cancer
Sokolova, O. V., & Naumann, M. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03816-8 · Cited by 17
Eslami, M., Monemi, M., Nazari, M. A., Azami, M. H., Rad, P. S., Oksenych, V., & Naderian, R. (2025) · Pharmaceuticals · doi:10.3390/ph18020197 · Cited by 18
Examination of Novel Immunomodulatory Effects of L-Sulforaphane
Mazarakis, N., Anderson, J., Toh, Z. Q., Higgins, R. A., Do, L. A. H., Luwor, R. B., Snibson, K. J., Karagiannis, T. C., & Licciardi, P. V. (2021) · Nutrients · doi:10.3390/nu13020602 · Cited by 16
Ghanem, A., Schweitzer, K., & Naumann, M. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04587-z · Cited by 16
Shahbazi, S., Zakerali, T., Frycz, B. A., & Kaur, J. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110199 · Cited by 15
Hunting for Serine 276-Phosphorylated p65
Spooren, A., Kolmus, K., Vermeulen, L., Wesemael, K. V., Haegeman, G., & Gerlo, S. (2010) · BioMed Research International · doi:10.1155/2010/275892 · Cited by 15
Anti-Metastatic Effect of Semi-Purified Nuphar Lutea Leaf Extracts
Ozer, J., Fishman, D., Eilam, B., Golan‐Goldhirsh, A., & Gopas, J. (2017) · Journal of Cancer · doi:10.7150/jca.18435 · Cited by 15
Edwards, K. A., Motamedi, V., Osier, N. D., Kim, H., Yun, S., Cho, Y., Lai, C., Dell, K. C., Carr, W. S., Walker, P., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00091 · Cited by 15
Rizzetto, L., Filippo, C. D., Rivero, D., Riccadonna, S., Beltrame, L., & Cavalieri, D. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.07.002 · Cited by 16
Li, S., An, M., Zhao, Y., Zhao, W., Li, P., & Du, B. (2024) · Food Chemistry X · doi:10.1016/j.fochx.2024.101863 · Cited by 14
Wehner, A. B., Milen, A. M., Albin, R. L., & Pierchala, B. A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.02.069 · Cited by 14
Ibaraki, H., Hatakeyama, N., Takeda, A., Arima, N., Seta, Y., & Kanazawa, T. (2022) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2022.103481 · Cited by 14
Kataria, J., Kerr, J., Lourenssen, S. R., & Blennerhassett, M. G. (2022) · Scientific Reports · doi:10.1038/s41598-022-14491-5 · Cited by 14
Li, S., Li, T., Wang, X., Rahmatulla, A., Zhao, Y., Zhang, X., Liu, Y., & Chen, Y. (2025) · Journal of drug targeting · doi:10.1080/1061186x.2025.2514564 · Cited by 13
Molecular Signaling Pathways Involved in Gastric Cancer Chemoresistance
Verma, H. K., Falco, G., & Bhaskar, L. V. (2020) · Diagnostics and therapeutic advances in GI malignancies · doi:10.1007/978-981-15-2017-4_8 · Cited by 13
Shahbazi, S., Kaur, J., Singh, S., Achary, K. G., Wani, S., Jema, S., Akhtar, J., & Sobti, R. C. (2017) · Innate Immunity · doi:10.1177/1753425917740727 · Cited by 13
Fukuzono, S., Kato, T., Fujita, H., Watanabe, N., & Kitagawa, S. (2010) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2010.01.005 · Cited by 13
Ferroptosis-Related Gene Signatures in Epilepsy: Diagnostic and Immune Insights
Li, X., Wu, L., Sun, L., Liu, H., Qiao, X., Mi, N., Shi, Y., Zhang, X., Wang, K., Quan, P., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04385-0 · Cited by 12
Arafa, S. S., Elnoury, H. A., El-Din, S. B., Abdelsattar, S., Sakr, M. A., Ghanem, S. K., Ahmed, O. S., Khalil, D. M., Ghorab, M. A., Salama, R. A. A., et al. (2024) · Environmental Sciences Europe · doi:10.1186/s12302-024-00998-3 · Cited by 12
Eom, T.-K., Kim, I., Kim, H.-J., Choi, Y., & Nam, T. (2021) · Antioxidants · doi:10.3390/antiox10101639 · Cited by 12
Bowick, G. C., Fennewald, S. M., Zhang, L., Yang, X., Aronson, J. F., Shope, R. E., Luxon, B. A., Gorenstein, D. G., & Herzog, N. K. (2009) · Viral Immunology · doi:10.1089/vim.2009.0034 · Cited by 12
NADPH oxidase contributes to conversion of cardiac myocytes to a proinflammatory phenotype in sepsis
Wu, J., Xu, H., Yang, M., Martin, C. M., Kvietys, P. R., & Tao, R. X. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.02.012 · Cited by 12
Qing, Z., Ye, J., & Wu, S. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.03.006 · Cited by 11
Liu, Z., Wilson‐Welder, J. H., Hostetter, J. M., Jergens, A. E., & Wannemuehler, M. J. (2010) · Experimental Biology and Medicine · doi:10.1258/ebm.2009.009269 · Cited by 10
Li, Y., Li, L., Zhang, G., Wang, Y., Chen, H., Kong, R., Pan, S., & Sun, B. (2017) · Investigational New Drugs · doi:10.1007/s10637-017-0508-2 · Cited by 10
Molecular Cross-Talk Between Nuclear Receptors and Nuclear Factor-κB
Beck, I. M. E., Haegeman, G., & Bosscher, K. D. (2010) · Springer eBooks · doi:10.1007/978-90-481-9531-2_10 · Cited by 9
Role of CTCF in EGF-Induced Migration of Immortalized Human Corneal Epithelial Cells
Wang, L., Deng, S. X., & Lu, L. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-8747 · Cited by 9
Metadata
- Authors
- Neumann, M., & Naumann, M.
- Affiliations
- Otto-von-Guericke-Universität Magdeburg (DE)
- ORCID
- Naumann, Michael
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 2007-04-12
- Volume
- 21
- Issue
- 11
- Pages
- 2642-2654
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- OpenAlex
- W1792654735
- Cited by
- 267
- References
- 100
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 11 · 2023: 14 · 2022: 11 · 2021: 14 · 2020: 5 · 2019: 9 · 2018: 8 · 2017: 16 · 2016: 12 · 2015: 11 · 2014: 11 · 2013: 12 · 2012: 12
- FWCI
- 2.24
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The FASEB Journal (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (NE608/3–2, NA292/7–3)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- NF-κB, p65 phosphorylation, Rel proteins, post-translational modification, glucocorticoid receptor, nucleolar sequestration, transcription factor regulation, inflammation, immune response
- MeSH terms
- Animals, DNA-Binding Proteins, Humans, Phosphorylation, Ubiquitins, Signal Transduction, NF-kappa B, I-kappa B Proteins, Transcription Factor RelA
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review