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NTIS 바로가기The FASEB journal : official publication of the Federation of American Societies for Experimental Biology, v.34 no.3, 2020년, pp.4369 - 4383
Kang, Kidong (Department of Pharmacology and Department of Medical Science, College of Medicine Chungnam National University Daejeon Republic of Korea) , Quan, Khong Trong (College of Pharmacy Chungnam National University Daejeon Republic of Korea) , Byun, Hee Sun (Department of Pharmacology and Department of Medical Science, College of Medicine Chungnam National University Daejeon Republic of Korea) , Lee, So‐Ra (Department of Pharmacology and Department of Medical Science, College of Medicine Chungnam National University Daejeon Republic of Korea) , Piao, Xuezhe (Department of Pharmacology and Department of Medical Science, College of Medicine Chungnam National University Daejeon Republic of Korea) , Ju, Eunjin (Department of Pharmacology and Department of Medical Science, College of Medicine Chungnam National University Daejeon Republic of Korea) , Park, Kyeong Ah (Department of Pharmacology and Department of Medical Science, College of Medicine Chungnam National University Daejeon Republic of Korea) , Sohn, Kyung‐Cheol (Department of Pharmacology and Department of Medical Science, College of Medicine Chungna) , Shen, Han‐Ming , Na, MinKyun , Hur, Gang Min
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Walczak, Henning. TNF and ubiquitin at the crossroads of gene activation, cell death, inflammation, and cancer. Immunological reviews, vol.244, no.1, 9-28.
Balkwill, Frances. Tumour necrosis factor and cancer. Nature reviews. Cancer, vol.9, no.5, 361-371.
Micheau, Olivier, Tschopp, Jürg. Induction of TNF Receptor I-Mediated Apoptosis via Two Sequential Signaling Complexes. Cell, vol.114, no.2, 181-190.
Brenner, Dirk, Blaser, Heiko, Mak, Tak W.. Regulation of tumour necrosis factor signalling: live or let die. Nature reviews. Immunology, vol.15, no.6, 362-374.
Silke, J.. The regulation of TNF signalling: what a tangled web we weave. Current opinion in immunology, vol.23, no.5, 620-626.
Ea, Chee-Kwee, Deng, Li, Xia, Zong-Ping, Pineda, Gabriel, Chen, Zhijian J.. Activation of IKK by TNFα Requires Site-Specific Ubiquitination of RIP1 and Polyubiquitin Binding by NEMO. Molecular cell, vol.22, no.2, 245-257.
Gerlach, Bj철rn, Cordier, Stefanie M., Schmukle, Anna C., Emmerich, Christoph H., Rieser, Eva, Haas, Tobias L., Webb, Andrew I., Rickard, James A., Anderton, Holly, Wong, Wendy W.-L., Nachbur, Ueli, Gangoda, Lahiru, Warnken, Uwe, Purcell, Anthony W., Silke, John, Walczak, Henning. Linear ubiquitination prevents inflammation and regulates immune signalling. Nature, vol.471, no.7340, 591-596.
Fritsch, J., Zingler, P., Sarchen, V., Heck, A.L., Schutze, S.. Role of ubiquitination and proteolysis in the regulation of pro- and anti-apoptotic TNF-R1 signaling. Biochimica et biophysica acta, Molecular cell research, vol.1864, no.11, 2138-2146.
Fritsch, Jürgen, Stephan, Mario, Tchikov, Vladimir, Winoto-Morbach, Supandi, Gubkina, Svetlana, Kabelitz, Dieter, Schütze, Stefan. Cell Fate Decisions Regulated by K63 Ubiquitination of Tumor Necrosis Factor Receptor 1. Molecular and cellular biology, vol.34, no.17, 3214-3228.
Wertz, I.E.. TNFR1-activated NF-κB signal transduction: regulation by the ubiquitin/proteasome system. Current opinion in chemical biology, vol.23, 71-77.
Shi, Jian-Hong, Sun, Shao-Cong. Tumor Necrosis Factor Receptor-Associated Factor Regulation of Nuclear Factor κB and Mitogen-Activated Protein Kinase Pathways. Frontiers in immunology, vol.9, 1849-.
Jordens, Ingrid, Marsman, Marije, Kuijl, Coen, Neefjes, Jacques. Rab Proteins, Connecting Transport and Vesicle Fusion. Traffic, vol.6, no.12, 1070-1077.
RIPK1 and RIPK3: critical regulators of inflammation and cell death. Trends in cell biology, vol.25, no.6, 347-353.
Liu, X, Shi, F, Li, Y, Yu, X, Peng, S, Li, W, Luo, X, Cao, Y. Post-translational modifications as key regulators of TNF-induced necroptosis. Cell death & disease, vol.7, no.7, e2293-.
Zhang, Yingying, Su, Sheng Sean, Zhao, Shubo, Yang, Zhentao, Zhong, Chuan-Qi, Chen, Xin, Cai, Qixu, Yang, Zhang-Hua, Huang, Deli, Wu, Rui, Han, Jiahuai. RIP1 autophosphorylation is promoted by mitochondrial ROS and is essential for RIP3 recruitment into necrosome. Nature communications, vol.8, 14329-.
Ting, Adrian T., Bertrand, Mathieu J.M.. More to Life than NF-κB in TNFR1 Signaling. Trends in immunology, vol.37, no.8, 535-545.
Annibaldi, Alessandro, Meier, Pascal. Checkpoints in TNF-Induced Cell Death: Implications in Inflammation and Cancer. Trends in molecular medicine, vol.24, no.1, 49-65.
Dondelinger, Y., Jouan-Lanhouet, S., Divert, T., Theatre, E., Bertin, J., Gough, Peter J., Giansanti, P., Heck, Albert J.R., Dejardin, E., Vandenabeele, P., Bertrand, Mathieu J.M.. NF-κB-Independent Role of IKKα/IKKβ in Preventing RIPK1 Kinase-Dependent Apoptotic and Necroptotic Cell Death during TNF Signaling. Molecular cell, vol.60, no.1, 63-76.
Totzke, Juliane, Gurbani, Deepak, Raphemot, Rene, Hughes, Philip F., Bodoor, Khaldon, Carlson, David A., Loiselle, David R., Bera, Asim K., Eibschutz, Liesl S., Perkins, Marisha M., Eubanks, Amber L., Campbell, Phillip L., Fox, David A., Westover, Kenneth D., Haystead, Timothy A.J., Derbyshire, Emily R.. Takinib, a Selective TAK1 Inhibitor, Broadens the Therapeutic Efficacy of TNF-α Inhibition for Cancer and Autoimmune Disease. Cell chemical biology, vol.24, no.8, 1029-1039.e7.
Geng, Jiefei, Ito, Yasushi, Shi, Linyu, Amin, Palak, Chu, Jiachen, Ouchida, Amanda Tomie, Mookhtiar, Adnan Kasim, Zhao, Heng, Xu, Daichao, Shan, Bing, Najafov, Ayaz, Gao, Guangping, Akira, Shizuo, Yuan, Junying. Regulation of RIPK1 activation by TAK1-mediated phosphorylation dictates apoptosis and necroptosis. Nature communications, vol.8, no.1, 359-.
Dondelinger, Yves, Delanghe, Tom, Priem, Dario, Wynosky-Dolfi, Meghan A., Sorobetea, Daniel, Rojas-Rivera, Diego, Giansanti, Piero, Roelandt, Ria, Gropengiesser, Julia, Ruckdeschel, Klaus, Savvides, Savvas N., Heck, Albert J. R., Vandenabeele, Peter, Brodsky, Igor E., Bertrand, Mathieu J. M.. Serine 25 phosphorylation inhibits RIPK1 kinase-dependent cell death in models of infection and inflammation. Nature communications, vol.10, no.1, 1729-.
Dondelinger, Yves, Delanghe, Tom, Rojas-Rivera, Diego, Priem, Dario, Delvaeye, Tinneke, Bruggeman, Inge, Van Herreweghe, Franky, Vandenabeele, Peter, Bertrand, Mathieu J. M.. MK2 phosphorylation of RIPK1 regulates TNF-mediated cell death. Nature cell biology, vol.19, no.10, 1237-1247.
Menon, Manoj B., Gropengießer, Julia, Fischer, Jessica, Novikova, Lena, Deuretzbacher, Anne, Lafera, Juri, Schimmeck, Hanna, Czymmeck, Nicole, Ronkina, Natalia, Kotlyarov, Alexey, Aepfelbacher, Martin, Gaestel, Matthias, Ruckdeschel, Klaus. p38MAPK/MK2-dependent phosphorylation controls cytotoxic RIPK1 signalling in inflammation and infection. Nature cell biology, vol.19, no.10, 1248-1259.
Menon, Manoj B., Gaestel, Matthias. MK2–TNF–Signaling Comes Full Circle. Trends in biochemical sciences, vol.43, no.3, 170-179.
Gill, Balraj Singh, Kumar, Sanjeev, Navgeet,. Triterpenes in cancer: significance and their influence. Molecular biology reports, vol.43, no.9, 881-896.
Salvador, Jorge A.R., Leal, Ana S., Valdeira, Ana S., Gonçalves, Bruno M.F., Alho, Daniela P.S., Figueiredo, Sandra A.C., Silvestre, Samuel M., Mendes, Vanessa I.S.. Oleanane-, ursane-, and quinone methide friedelane-type triterpenoid derivatives: Recent advances in cancer treatment. European journal of medicinal chemistry, vol.142, 95-130.
Quan, Khong Trong, Park, Hyun-Soo, Oh, Joonseok, Park, Hyun Bong, Ferreira, Daneel, Myung, Chang-Seon, Na, MinKyun. Arborinane Triterpenoids from Rubia philippinensis Inhibit Proliferation and Migration of Vascular Smooth Muscle Cells Induced by the Platelet-Derived Growth Factor. Journal of natural products, vol.79, no.10, 2559-2569.
BMC Complement Altern Med Bajpai VK 200 18 2018 10.1186/s12906-018-2253-2 Cytotoxic properties of the anthraquinone derivatives isolated from the roots of Rubia philippinensis
Biophotonics Int Abramoff MD 36 11 2004 Image processing with ImageJ
Li, Chenghai, Yang, Zhengfeng, Zhai, Chunyan, Qiu, Wenwei, Li, Dali, Yi, Zhengfang, Wang, Lei, Tang, Jie, Qian, Min, Luo, Jian, Liu, Mingyao. Maslinic acid potentiates the anti-tumor activity of tumor necrosis factor α by inhibiting NF-κB signaling pathway. Molecular cancer, vol.9, 73-73.
Pratheeshkumar, P., Kuttan, Girija. Oleanolic acid induces Apoptosis by modulating p53, Bax, Bcl-2 and caspase-3 gene expression and regulates the activation of transcription factors and cytokine profile in B16F. Journal of environmental pathology, toxicology, and oncology : official organ of the International Society for Environmental Toxicology and Cancer, vol.30, no.1, 21-31.
Degterev, Alexei, Hitomi, Junichi, Germscheid, Megan, Ch'en, Irene L, Korkina, Olga, Teng, Xin, Abbott, Derek, Cuny, Gregory D, Yuan, Chengye, Wagner, Gerhard, Hedrick, Stephen M, Gerber, Scott A, Lugovskoy, Alexey, Yuan, Junying. Identification of RIP1 kinase as a specific cellular target of necrostatins. Nature chemical biology, vol.4, no.5, 313-321.
Christofferson, Dana E, Li, Ying, Yuan, Junying. Control of Life-or-Death Decisions by RIP1 Kinase. Annual review of physiology, vol.76, 129-150.
Wegner, Kelby W., Saleh, Danish, Degterev, Alexei. Complex Pathologic Roles of RIPK1 and RIPK3: Moving Beyond Necroptosis. Trends in pharmacological sciences, vol.38, no.3, 202-225.
Lin, Yong, Choksi, Swati, Shen, Han-Ming, Yang, Qing-Feng, Hur, Gang Min, Kim, You Sun, Tran, Jamie Hong, Nedospasov, Sergei A., Liu, Zheng-gang. Tumor Necrosis Factor-induced Nonapoptotic Cell Death Requires Receptor-interacting Protein-mediated Cellular Reactive Oxygen Species Accumulation. The Journal of biological chemistry, vol.279, no.11, 10822-10828.
Won, Minho, Byun, Hee Sun, Park, Kyeong Ah, Hur, Gang Min. Post-translational control of NF-κB signaling by ubiquitination. Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea, vol.39, no.8, 1075-1084.
Häcker, Hans, Karin, Michael. Regulation and Function of IKK and IKK-Related Kinases. Science's STKE signal transduction knowledge environment, vol.2006, no.357,
Polley, Smarajit, Huang, De-Bin, Hauenstein, Arthur V., Fusco, Amanda J., Zhong, Xiangyang, Vu, Don, Schröfelbauer, Bärbel, Kim, Youngchang, Hoffmann, Alexander, Verma, Inder M., Ghosh, Gourisankar, Huxford, Tom. A Structural Basis for IκB Kinase 2 Activation Via Oligomerization-Dependent Trans Auto-Phosphorylation. PLoS biology, vol.11, no.6, e1001581-.
Zhang, Jiazhen, Clark, Kristopher, Lawrence, Toby, Peggie, Mark W., Cohen, Philip. An unexpected twist to the activation of IKKβ: TAK1 primes IKKβ for activation by autophosphorylation. The Biochemical journal, vol.461, no.3, 531-537.
Zhang, Duan-Wu, Zheng, Min, Zhao, Jing, Li, Yuan-Yue, Huang, Zhe, Li, Zhu, Han, Jiahuai. Multiple death pathways in TNF-treated fibroblasts: RIP3- and RIP1-dependent and independent routes. Cell research, vol.21, no.2, 368-371.
Yan, J., Xiang, J., Lin, Y., Ma, J., Zhang, J., Zhang, H., Sun, J., Danial, Nika N., Liu, J., Lin, A.. Inactivation of BAD by IKK Inhibits TNFα-Induced Apoptosis Independently of NF-κB Activation. Cell, vol.152, no.1, 304-315.
Vlantis, Katerina, Wullaert, Andy, Polykratis, Apostolos, Kondylis, Vangelis, Dannappel, Marius, Schwarzer, Robin, Welz, Patrick, Corona, Teresa, Walczak, Henning, Weih, Falk, Klein, Ulf, Kelliher, Michelle, Pasparakis, Manolis. NEMO Prevents RIP Kinase 1-Mediated Epithelial Cell Death and Chronic Intestinal Inflammation by NF-κB-Dependent and -Independent Functions. Immunity, vol.44, no.3, 553-567.
Feoktistova, Maria, Geserick, Peter, Kellert, Beate, Dimitrova, Diana Panayotova, Langlais, Claudia, Hupe, Mike, Cain, Kelvin, MacFarlane, Marion, Häcker, Georg, Leverkus, Martin. cIAPs Block Ripoptosome Formation, a RIP1/Caspase-8 Containing Intracellular Cell Death Complex Differentially Regulated by cFLIP Isoforms. Molecular cell, vol.43, no.3, 449-463.
Yao, Weilong, Yue, Ping, Khuri, Fadlo R., Sun, Shi-Yong. The BET bromodomain inhibitor, JQ1, facilitates c-FLIP degradation and enhances TRAIL-induced apoptosis independent of BRD4 and c-Myc inhibition. Oncotarget, vol.6, no.33, 34669-34679.
Klingbeil, Olaf, Lesche, Ralf, Gelato, Kathy A, Haendler, Bernard, Lejeune, Pascale. Inhibition of BET bromodomain-dependent XIAP and FLIP expression sensitizes KRAS -mutated NSCLC to pro-apoptotic agents. Cell death & disease, vol.7, no.9, e2365-.
Clin Cancer Res Carafa V 2886 24 2018 10.1158/1078-0432.CCR-17-3081 RIP1‐HAT1‐SIRT complex identification and targeting in treatment and prevention of cancer
Chen, Guoqing, Goeddel, David V.. TNF-R1 Signaling: A Beautiful Pathway. Science, vol.296, no.5573, 1634-1635.
Lafont, Elodie, Draber, Peter, Rieser, Eva, Reichert, Matthias, Kupka, Sebastian, de Miguel, Diego, Draberova, Helena, von Mässenhausen, Anne, Bhamra, Amandeep, Henderson, Stephen, Wojdyla, Katarzyna, Chalk, Avigayil, Surinova, Silvia, Linkermann, Andreas, Walczak, Henning. TBK1 and IKKε prevent TNF-induced cell death by RIPK1 phosphorylation. Nature cell biology, vol.20, no.12, 1389-1399.
Dillon, C.P., Balachandran, S.. StIKKing it to a death kinase: IKKs prevent TNF-α-induced cell death by phosphorylating RIPK1. Cytokine, vol.78, 47-50.
Hayden, Matthew S., Ghosh, Sankar. Signaling to NF-κB. Genes & development, vol.18, no.18, 2195-2224.
Hinz, Michael, Scheidereit, Claus. The IκB kinase complex in NF ‐κB regulation and beyond. EMBO reports, vol.15, no.1, 46-61.
Israël, Alain. The IKK Complex, a Central Regulator of NF-kappaB Activation.. Cold Spring Harbor perspectives in biology, vol.2, no.3, a000158-.
Tanaka, Masato, Fuentes, Maria Elena, Yamaguchi, Kyoko, Durnin, Michael H, Dalrymple, Stacie A, Hardy, Kathy L, Goeddel, David V. Embryonic Lethality, Liver Degeneration, and Impaired NF-κB Activation in IKK-β-Deficient Mice. Immunity, vol.10, no.4, 421-429.
Genes Dev Li Q 1729 14 2000 10.1101/gad.14.14.1729 Complete lack of NF‐kappaB activity in IKK1 and IKK2 double‐deficient mice: additional defect in neurulation
Pannicke, Ulrich, Baumann, Bernd, Fuchs, Sebastian, Henneke, Philipp, Rensing-Ehl, Anne, Rizzi, Marta, Janda, Ales, Hese, Katrin, Schlesier, Michael, Holzmann, Karlheinz, Borte, Stephan, Laux, Constanze, Rump, Eva-Maria, Rosenberg, Alan, Zelinski, Teresa, Schrezenmeier, Hubert, Wirth, Thomas, Ehl, Stephan, Schroeder, Marlis L., Schwarz, Klaus. Deficiency of Innate and Acquired Immunity Caused by an IKBKB Mutation. The New England journal of medicine, vol.369, no.26, 2504-2514.
Pediatrics Smart BA S181 134 2014 10.1542/peds.2014-1817EEEE Deficiency of innate and acquired immunity caused by an IKBKB mutation
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