Novel splice variants of human IKKε negatively regulate IKKε-induced IRF3 and NF-kB activation by Koop, Anja, Lepenies, Inga, Braum, Oliver, Davarnia, Parvin, Scherer, Gudrun, Fickenscher, Helmut, Kabelitz, Dieter, Adam-Klages, Sabine

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Interaction with XIAP prevents full caspase-3/-7 activation in proliferating human T lymphocytes by Paulsen, Maren, Ussat, Sandra, Jakob, Marten, Scherer, Gudrun, Lepenies, Inga, Schütze, Stefan, Kabelitz, Dieter, Adam-Klages, Sabine

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Sensitization to Death Receptor Cytotoxicity by Inhibition of Fas-associated Death Domain Protein (FADD)/Caspase Signaling by Lüschen, Silke, Ussat, Sandra, Scherer, Gudrun, Kabelitz, Dieter, Adam-Klages, Sabine

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Novel splice variants of human IKK[epsi] negatively regulate IKK[epsi]-induced IRF3 and NF-kB activation by Koop, Anja, Lepenies, Inga, Braum, Oliver, Davarnia, Parvin, Scherer, Gudrun, Fickenscher, Helmut, Kabelitz, Dieter, Adam-Klages, Sabine

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Inhibition of p38 mitogen-activated protein kinase reduces TNF-induced activation of NF-κB, elicits caspase activity, and enhances cytotoxicity by Lüschen, Silke, Scherer, Gudrun, Ussat, Sandra, Ungefroren, Hendrik, Adam-Klages, Sabine

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The Fas-associated death domain protein/caspase-8/c-FLIP signaling pathway is involved in TNF-induced activation of ERK by Lüschen, Silke, Falk, Markus, Scherer, Gudrun, Ussat, Sandra, Paulsen, Maren, Adam-Klages, Sabine

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Impaired neutral sphingomyelinase activation and cutaneous barrier repair in FAN-deficient mice by Kreder, Dirk, Krut, Oleg, Adam-Klages, Sabine, Wiegmann, Katja, Scherer, Gudrun, Plitz, Tom, Jensen, Jens-Michael, Proksch, Ehrhardt, Steinmann, Jörg, Pfeffer, Klaus, Krönke, Martin

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Inhibition of p38 mitogen-activated protein kinase reduces TNF-induced activation of NF-kappaB, elicits caspase activity, and enhances cytotoxicity by Lüschen, Silke, Scherer, Gudrun, Ussat, Sandra, Ungefroren, Hendrik, Adam-Klages, Sabine

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Caspase 7-induced cleavage of kinectin in apoptotic cells by Machleidt, Thomas, Geller, Patricia, Schwandner, Ralf, Scherer, Gudrun, Krönke, Martin

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Upregulation of p21WAF1/Cip1 precedes tumor necrosis factor-induced necrosis-like cell death by Ussat, Sandra, Werner, Ulf-Eike, Kruse, Marie-Luise, Lüschen, Silke, Scherer, Gudrun, Kabelitz, Dieter, Adam-Klages, Sabine

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Upregulation of p21 WAF1/Cip1 precedes tumor necrosis factor-induced necrosis-like cell death by Ussat, Sandra, Werner, Ulf-Eike, Kruse, Marie-Luise, Lüschen, Silke, Scherer, Gudrun, Kabelitz, Dieter, Adam-Klages, Sabine

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Upregulation of p21(WAF1/Cip1) precedes tumor necrosis factor-induced necrosis-like cell death by Ussat, Sandra, Werner, Ulf-Eike, Kruse, Marie-Luise, Lüschen, Silke, Scherer, Gudrun, Kabelitz, Dieter, Adam-Klages, Sabine

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SHANK1 Deletions in Males with Autism Spectrum Disorder by Sato, Daisuke, Lionel, Anath C., Leblond, Claire S., Prasad, Aparna, Pinto, Dalila, Walker, Susan, O'Connor, Irene, Russell, Carolyn, Drmic, Irene E., Hamdan, Fadi F., Michaud, Jacques L., Endris, Volker, Roeth, Ralph, Delorme, Richard, Huguet, Guillaume, Leboyer, Marion, Rastam, Maria, Gillberg, Christopher, Lathrop, Mark, Stavropoulos, Dimitri J., Anagnostou, Evdokia, Weksberg, Rosanna, Fombonne, Eric, Zwaigenbaum, Lonnie, Fernandez, Bridget A., Roberts, Wendy, Rappold, Gudrun A., Marshall, Christian R., Bourgeron, Thomas, Szatmari, Peter, Scherer, Stephen W.

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Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments by Leblond, Claire S, Nava, Caroline, Polge, Anne, Gauthier, Julie, Huguet, Guillaume, Lumbroso, Serge, Giuliano, Fabienne, Stordeur, Coline, Depienne, Christel, Mouzat, Kevin, Pinto, Dalila, Howe, Jennifer, Lemière, Nathalie, Durand, Christelle M, Guibert, Jessica, Ey, Elodie, Toro, Roberto, Peyre, Hugo, Mathieu, Alexandre, Amsellem, Frédérique, Rastam, Maria, Gillberg, I Carina, Rappold, Gudrun A, Holt, Richard, Monaco, Anthony P, Maestrini, Elena, Galan, Pilar, Heron, Delphine, Jacquette, Aurélia, Afenjar, Alexandra, Rastetter, Agnès, Brice, Alexis, Devillard, Françoise, Assouline, Brigitte, Laffargue, Fanny, Lespinasse, James, Chiesa, Jean, Rivier, François, Bonneau, Dominique, Regnault, Beatrice, Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Sanlaville, Damien, Schluth-Bolard, Caroline, Edery, Patrick, Perrin, Laurence, Tabet, Anne Claude, Schmeisser, Michael J, Boeckers, Tobias M, Coleman, Mary, Sato, Daisuke, Szatmari, Peter, Scherer, Stephen W, Rouleau, Guy A, Betancur, Catalina, Leboyer, Marion, Gillberg, Christopher, Delorme, Richard, Bourgeron, Thomas

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Analysis of shared heritability in common disorders of the brain by Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer, Patsopoulos, Nikolaos A, Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H, Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Letenneur, Luc, Hannequin, Didier, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Duron, Emmanuelle, Vardarajan, Badri N, Reitz, Christiane, Goate, Alison M, Huentelman, Matthew J, Kamboh, M Ilyas, Larson, Eric B, Rogaeva, Ekaterina, St George-Hyslop, Peter, Hakonarson, Hakon, Kukull, Walter A, Farrer, Lindsay A, Barnes, Lisa L, Beach, Thomas G, Demirci, F Yesim, Head, Elizabeth, Hulette, Christine M, Jicha, Gregory A, Kauwe, John S K, Kaye, Jeffrey A, Leverenz, James B, Levey, Allan I, Lieberman, Andrew P, Pankratz, Vernon S, Poon, Wayne W, Quinn, Joseph F, Saykin, Andrew J, Schneider, Lon S, Smith, Amanda G, Sonnen, Joshua A, Stern, Robert A, Van Deerlin, Vivianna M, Van Eldik, Linda J, Harold, Denise, Russo, Giancarlo, Rubinsztein, David C, Bayer, Anthony, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C, Hampel, Harald, Owen, Michael J, Mead, Simon, Passmore, Peter, Morgan, Kevin, Nöthen, Markus M, Rossor, Martin, Lupton, Michelle K, Hoffmann, Per, Kornhuber, Johannes, Lawlor, Brian, McQuillin, Andrew, Al-Chalabi, Ammar, Bis, Joshua C, Ruiz, Agustin, Boada, Mercè, Seshadri, Sudha, Beiser, Alexa, Rice, Kenneth, van der Lee, Sven J, De Jager, Philip L, Geschwind, Daniel H, Riemenschneider, Matthias, Riedel-Heller, Steffi, Rotter, Jerome I, Ransmayr, Gerhard, Hyman, Bradley T, Cruchaga, Carlos, Alegret, Montserrat, Winsvold, Bendik, Palta, Priit, Farh, Kai-How, Cuenca-Leon, Ester, Furlotte, Nicholas, Kurth, Tobias

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50 Years of quantum chromodynamics: Introduction and Review by Gross, Franz, Klempt, Eberhard, Brodsky, Stanley J., Buras, Andrzej J., Burkert, Volker D., Heinrich, Gudrun, Jakobs, Karl, Meyer, Curtis A., Orginos, Kostas, Strickland, Michael, Stachel, Johanna, Zanderighi, Giulia, Brambilla, Nora, Braun-Munzinger, Peter, Britzger, Daniel, Capstick, Simon, Cohen, Tom, Crede, Volker, Constantinou, Martha, Davies, Christine, Del Debbio, Luigi, Denig, Achim, DeTar, Carleton, Deur, Alexandre, Dokshitzer, Yuri, Dosch, Hans Günter, Dudek, Jozef, Dunford, Monica, Epelbaum, Evgeny, Escobedo, Miguel A., Fritzsch, Harald, Fukushima, Kenji, Gambino, Paolo, Gillberg, Dag, Gottlieb, Steven, Grafstrom, Per, Grazzini, Massimiliano, Grube, Boris, Guskov, Alexey, Iijima, Toru, Ji, Xiangdong, Karsch, Frithjof, Kluth, Stefan, Kogut, John B., Krauss, Frank, Kumano, Shunzo, Leinweber, Derek, Leutwyler, Heinrich, Li, Hai-Bo, Li, Yang, Malaescu, Bogdan, Mariotti, Chiara, Maris, Pieter, Marzani, Simone, Melnitchouk, Wally, Messchendorp, Johan, Meyer, Harvey, Mitchell, Ryan Edward, Mondal, Chandan, Nerling, Frank, Neubert, Sebastian, Pappagallo, Marco, Pastore, Saori, Peláez, José R., Puckett, Andrew, Qiu, Jianwei, Rabbertz, Klaus, Ramos, Alberto, Rossi, Patrizia, Rustamov, Anar, Schäfer, Andreas, Scherer, Stefan, Schindler, Matthias, Schramm, Steven, Shifman, Mikhail, Shuryak, Edward, Sjöstrand, Torbjörn, Sterman, George, Stewart, Iain W., Stroth, Joachim, Swanson, Eric, de Téramond, Guy F., Thoma, Ulrike, Vairo, Antonio, van Dyk, Danny, Vary, James, Virto, Javier, Vos, Marcel, Weiss, Christian, Wobisch, Markus, Wu, Sau Lan, Young, Christopher, Yuan, Feng, Zhao, Xingbo, Zhou, Xiaorong

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Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors by Mullins, Niamh, Campos, Adrian I., Shabalin, Andrey, Hafferty, Jonathan D., Okazaki, Satoshi, Bohus, Martin, Johnson, Craig, Li, Dong, Magistretti, Pierre J., Van der Auwera, Sandra, Byrne, Enda M., Casas, Miguel, Jonsson, Lina, O’Donovan, Michael C., Pato, Carlos, Ramos-Quiroga, Josep Antoni, Sánchez-Mora, Cristina, Smeland, Olav B., Shannon Weickert, Cynthia, Hauser, Elizabeth R., Andlauer, Till F.M., Colodro-Conde, Lucía, Craddock, Nick, Derks, Eske M., Escott-Price, Valentina, Gordon, Scott D., Wu, Yang, Xi, Hualin S., Esko, Tõnu, Kohane, Isaac S., McGrath, Patrick, McGuffin, Peter, Middeldorp, Christel M., Milaneschi, Yuri, Nauck, Matthias, Nyholt, Dale R., Nöthen, Markus M., Pedersen, Nancy L., Pedersen, Carsten Bøcker, Steinberg, Stacy, Potash, James B., Schaefer, Catherine, Smoller, Jordan W., Völzke, Henry, Drange, Ole Kristian, Ikeda, Masashi, Panagiotaropoulou, Georgia, Sloofman, Laura G., Casas, Miquel, Ferrier, I. Nicol, Guzman-Parra, José, Kogevinas, Manolis, Lee, Phil H., Magnusson, Sigurdur H., Mühleisen, Thomas W., Sirignano, Lea, Adolfsson, Rolf, Alda, Martin, Catts, Stanley, Corvin, Aiden, Craddock, Nicholas, Fullerton, Janice M., Iwata, Nakao, Mayoral, Fermin, Mowry, Bryan, McQuillin, Andrew, Bulik, Cynthia M., Courtet, Philippe, Dina, Christian, Fichter, Manfred M., Föcker, Manuel, Hinney, Anke, Hübel, Christopher, Purves, Kirstin L., Rujescu, Dan, Scherer, Stephen W., Slagboom, P. Eline, Steen, Vidar W., Karhunen, Leila, Kennedy, Martin A., Tsitsika, Artemis, Yao, Shuyang, Schwarze, Cornelia E., Bohus, Martin, Crivelli, Silvia, Muralidhar, Sumitra, Huang, Grant, Moser, Jennifer, Brewer, Jessica V., Connor, Todd, Humphries, Donald E., Hauser, Elizabeth, Whittle, Jeffrey, Hammer, Kimberly, Godschalk, Michael, Sriram, Peruvemba, Liangpunsakul, Suthat, Wallbom, Agnes, Esko, Tõnu, Martin, Nicholas G.

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Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders by Leblond, Claire S, Heinrich, Jutta, Delorme, Richard, Proepper, Christian, Betancur, Catalina, Huguet, Guillaume, Konyukh, Marina, Chaste, Pauline, Ey, Elodie, Rastam, Maria, Anckarsäter, Henrik, Nygren, Gudrun, Gillberg, I Carina, Melke, Jonas, Toro, Roberto, Regnault, Beatrice, Fauchereau, Fabien, Mercati, Oriane, Lemière, Nathalie, Skuse, David, Poot, Martin, Holt, Richard, Monaco, Anthony P, Järvelä, Irma, Kantojärvi, Katri, Vanhala, Raija, Curran, Sarah, Collier, David A, Bolton, Patrick, Chiocchetti, Andreas, Klauck, Sabine M, Poustka, Fritz, Freitag, Christine M, Waltes, Regina, Kopp, Marnie, Duketis, Eftichia, Bacchelli, Elena, Minopoli, Fiorella, Ruta, Liliana, Battaglia, Agatino, Mazzone, Luigi, Maestrini, Elena, Sequeira, Ana F, Oliveira, Barbara, Vicente, Astrid, Oliveira, Guiomar, Pinto, Dalila, Scherer, Stephen W, Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Bonneau, Dominique, Guinchat, Vincent, Devillard, Françoise, Assouline, Brigitte, Mouren, Marie-Christine, Leboyer, Marion, Gillberg, Christopher, Boeckers, Tobias M, Bourgeron, Thomas

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Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution by Parker-Katiraee, Layla, Carson, Andrew R, Yamada, Takahiro, Arnaud, Philippe, Feil, Robert, Abu-Amero, Sayeda N, Moore, Gudrun E, Kaneda, Masahiro, Perry, George H, Stone, Anne C, Lee, Charles, Meguro-Horike, Makiko, Sasaki, Hiroyuki, Kobayashi, Keiko, Nakabayashi, Kazuhiko, Scherer, Stephen W

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Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-sil... by Monk, David, Wagschal, Alexandre, Arnaud, Philippe, Müller, Pari-Sima, Parker-Katiraee, Layla, Bourc'his, Déborah, Scherer, Stephen W, Feil, Robert, Stanier, Philip, Moore, Gudrun E

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