L2EE: Lightweight Process Coordination & J2EE von Bahlo, Tim

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Two mouse models reveal an actionable PARP1 dependence in aggressive chronic lymphocytic leukemia von Knittel, Gero, Rehkämper, Tim, Korovkina, Darya, Liedgens, Paul, Fritz, Christian, Torgovnick, Alessandro, Al-Baldawi, Yussor, Al-Maarri, Mona, Cun, Yupeng, Fedorchenko, Oleg, Riabinska, Arina, Beleggia, Filippo, Nguyen, Phuong-Hien, Wunderlich, F. Thomas, Ortmann, Monika, Montesinos-Rongen, Manuel, Tausch, Eugen, Stilgenbauer, Stephan, P. Frenzel, Lukas, Herling, Marco, Herling, Carmen, Bahlo, Jasmin, Hallek, Michael, Peifer, Martin, Buettner, Reinhard, Persigehl, Thorsten, Reinhardt, H. Christian

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Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia von Khan, Kamal, Zech, Michael, Morgan, Angela T., Amor, David J., Skorvanek, Matej, Khan, Tahir N., Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Coleman, Matthew, Rigbye, Kristin A., Scheffer, Ingrid E., Bahlo, Melanie, Wagner, Matias, Lam, Daniel D., Berutti, Riccardo, Havránková, Petra, Fečíková, Anna, Strom, Tim M., Han, Vladimir, Dosekova, Petra, Gdovinova, Zuzana, Laccone, Franco, Jameel, Muhammad, Mooney, Marie R., Baig, Shahid M., Jech, Robert, Davis, Erica E., Katsanis, Nicholas, Winkelmann, Juliane

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Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans von Grillet, Nicolas, Schwander, Martin, Hildebrand, Michael S., Sczaniecka, Anna, Kolatkar, Anand, Velasco, Janice, Webster, Jennifer A., Kahrizi, Kimia, Najmabadi, Hossein, Kimberling, William J., Stephan, Dietrich, Bahlo, Melanie, Wiltshire, Tim, Tarantino, Lisa M., Kuhn, Peter, Smith, Richard J.H., Müller, Ulrich

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Multiple sclerosis risk variants regulate gene expression in innate and adaptive immune cells von Gresle, Melissa M, Jordan, Margaret A, Stankovich, Jim, Spelman, Tim, Johnson, Laura J, Laverick, Louise, Hamlett, Alison, Smith, Letitia D, Jokubaitis, Vilija G, Baker, Josephine, Haartsen, Jodi, Taylor, Bruce, Charlesworth, Jac, Bahlo, Melanie, Speed, Terence P, Brown, Matthew A, Field, Judith, Baxter, Alan G, Butzkueven, Helmut

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Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia von Khan, Kamal, Zech, Michael, Morgan, Angela T, Amor, David J, Skorvanek, Matej, Khan, Tahir N, Hildebrand, Michael S, Jackson, Victoria E, Scerri, Thomas S, Coleman, Matthew, Rigbye, Kristin A, Scheffer, Ingrid E, Bahlo, Melanie, Wagner, Matias, Lam, Daniel D, Berutti, Riccardo, Havrankova, Petra, Fecikova, Anna, Strom, Tim M, Han, Vladimir, Dosekova, Petra, Gdovinova, Zuzana, Laccone, Franco, Jameel, Muhammad, Mooney, Marie R, Baig, Shahid M, Jech, Robert, Davis, Erica E, Katsanis, Nicholas, Winkelmann, Juliane

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