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1.
Vincendeau, M. et al.: Inhibition of canonical NF-κB signaling by a small molecule targeting NEMO-ubiquitin interaction. Sci. Rep. 6:18934 (2016)
2.
Emerging Risk Factors Collaboration (di Angelantonio, E.* ; Kaptoge, S.* ; Wormser, D.* ; Willeit, P.* ; Butterworth, A.S.* ; Bansal, N.* ; O'Keeffe, L.M.* ; Gao, P.* ; Wood, A.M.* ; Burgess, S.L.* ; Freitag, D.F.* ; Pennells, L.* ; Peters, S.A.* ; Hart, C.L.* ; Håheim, L.L.* ; Gillum, R.F.* ; Nordestgaard, B.G.* ; Psaty, B.M.* ; Yeap, B.B.* ; Knuiman, M.W.* ; Nietert, P.J.* ; Kauhanen, J.* ; Salonen, J.T.* ; Kuller, L.H.* ; Simons, L.A.* ; van der Schouw, Y.T.* ; Barrett-Connor, E.* ; Selmer, R.* ; Crespo, C.J.* ; Rodriguez, B.* ; Verschuren, W.M.* ; Salomaa, V.* ; Svärdsudd, K.* ; van der Harst, P.* ; Björkelund, C.* ; Wilhelmsen, L.* ; Wallace, R.B.* ; Brenner, H.* ; Amouyel, P.* ; Barr, E.L.* ; Iso, H.* ; Onat, A.* ; Trevisan, M.* ; D'Agostino, R.B.* ; Cooper, C.* ; Kavousi, M.* ; Welin, L.* ; Roussel, R.* ; Hu, F.B.* ; Sato, S.* ; Davidson, K.W.* ; Howard, B.V.* ; Leening, M.* ; Rosengren, A.* ; Dörr, M.* ; Deeg, D.J.* ; Kiechl, S.* ; Stehouwer, C.D.* ; Nissinen, A.* ; Giampaoli, S.* ; Donfrancesco, C.* ; Kromhout, D.* ; Price, J.F.* ; Peters, A. ; Meade, T.W.* ; Casiglia, E.* ; Lawlor, D.A.* ; Gallacher, J.* ; Nagel, D.* ; Franco, O.H.* ; Assmann, G.* ; Dagenais, G.R.* ; Jukema, J.W.* ; Sundström, J.* ; Woodward, M.* ; Brunner, E.J.* ; Khaw, K.T.* ; Wareham, N.J.* ; Whitsel, E.A.* ; Njølstad, I.* ; Hedblad, B.* ; Wassertheil-Smoller, S.* ; Engström, G.* ; Rosamond, W.D.* ; Selvin, E.* ; Sattar, N.* ; Thompson, S.G.* ; Danesh, J.*): Association of cardiometabolic multimorbidity with mortality. JAMA 314, 52-60 (2015)
3.
Nagel, D. & Krappmann, D.: Detection of recombinant and cellular MALT1 paracaspase activity. Methods Mol. Biol. 1280, 239-246 (2015)
4.
Nagel, D. et al.: Combinatorial BTK and MALT1 inhibition augments killing of CD79 mutant diffuse large B cell lymphoma. Oncotarget 6, 42232-42242 (2015)
5.
Eitelhuber, A.C. et al.: Activity-based probes for detection of active MALT1 paracaspase in immune cells and lymphomas. Chem. Biol. 22, 129-138 (2014)
6.
Jeltsch, K. et al.: Cleavage of roquin and regnase-1 by the paracaspase MALT1 releases their cooperatively repressed targets to promote TH17 differentiation. Nat. Immunol. 15, 1079-1089 (2014)
7.
Mc Guire, C.* et al.: Pharmacological inhibition of MALT1 protease activity protects mice in a mouse model of multiple sclerosis. J. Neuroinflamm. 11:124 (2014)
8.
Nagel, D. ; Vincendeau, M. ; Eitelhuber, A.C. & Krappmann, D.: Mechanisms and consequences of constitutive NF-κB activation in B-cell lymphoid malignancies. Oncogene 33, 5655-5665 (2014)
9.
Schlauderer, F.* et al.: Structural analysis of phenothiazine derivatives as allosteric inhibitors of the MALT1 paracaspase. Angew. Chem.-Int. Edit. 52, 10384-10387 (2013)
10.
Vincendeau, M. ; Nagel, D. ; Brenke, J.K. ; Brack-Werner, R. & Hadian, K.: Heterogenous nuclear ribonucleoprotein Q increases protein expression from HIV-1 Rev-dependent transcripts. Virol. J. 10:151 (2013)
11.
Vincendeau, M. ; Nagel, D. ; Eitelhuber, A.C. & Krappmann, D.: MALT1 paracaspase: A unique protease involved in B-cell lymphomagenesis. Int. J. Hematol. Oncol. 2, 409-417 (2013)
12.
Nagel, D. et al.: Pharmacologic inhibition of MALT1 protease by phenothiazines as a therapeutic approach for the treatment of aggressive ABC-DLBCL. Cancer Cell 22, 825-837 (2012)
13.
Hadian, K. et al.: NF-κB essential modulator (NEMO) interaction with linear and Lys-63 ubiquitin chains contributes to NF-κB activation. J. Biol. Chem. 286, 26107-26117 (2011)
14.
Kloo, B. et al.: Critical role of PI3K signaling for NF-κB-dependent survival in a subset of activated B-cell-like diffuse large B-cell lymphoma cells. Proc. Natl. Acad. Sci. U.S.A. 108, 272-277 (2011)
15.
Sarwar, N.* et al.: Triglyceride-mediated pathways and coronary disease: Collaborative analysis of 101 studies. Lancet 375, 1634-1639 (2010)
16.
Vincendeau, M. et al.: Control of HIV replication in astrocytes by a family of highly conserved host proteins with a common Rev-interacting domain (Risp). Aids 24, 2433-2442 (2010)
17.
di Angelantonio, E.* et al.: Major lipids, apolipoproteins, and risk of vascular disease. JAMA 302, 1993-2000 (2009)
18.
Erqou, S.* et al.: Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA 302, 412-423 (2009)
19.
Hadian, K. et al.: Identification of a heterogeneous nuclear ribonucleoprotein-recognition region in the HIV Rev protein. J. Biol. Chem. 284, 33384-33391 (2009)