Hyperspectral LED models for optical simulations by Rotscholl, Ingo, Katona, Markus, Trampert, Klaus, Krüger, Udo, Schmidt, Franz, Neumann, Cornelius

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High-Intensity Discharge Lamps With High Color Rendering Indices Based on Molecular Radiation of Indium Iodide by Kaiser, Christoph, Katona, Markus, Ogun, Celal Mohangn, Kling, Rainer, Heering, Wolfgang

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β-Hydroxybutyrate suppresses colorectal cancer by Dmitrieva-Posocco, Oxana, Wong, Andrea C., Lundgren, Patrick, Golos, Aleksandra M., Descamps, Hélène C., Dohnalová, Lenka, Cramer, Zvi, Tian, Yuhua, Yueh, Brian, Eskiocak, Onur, Egervari, Gabor, Lan, Yemin, Liu, Jinping, Fan, Jiaxin, Kim, Jihee, Madhu, Bhoomi, Schneider, Kai Markus, Khoziainova, Svetlana, Andreeva, Natalia, Wang, Qiaohong, Li, Ning, Furth, Emma E., Bailis, Will, Kelsen, Judith R., Hamilton, Kathryn E., Kaestner, Klaus H., Berger, Shelley L., Epstein, Jonathan A., Jain, Rajan, Li, Mingyao, Beyaz, Semir, Lengner, Christopher J., Katona, Bryson W., Grivennikov, Sergei I., Thaiss, Christoph A., Levy, Maayan

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Pathomechanisms of ALS8: altered autophagy and defective RNA binding protein (RBP) homeostasis due to the VAPB P56S mutation by Tripathi, Priyanka, Guo, Haihong, Dreser, Alice, Yamoah, Alfred, Sechi, Antonio, Jesse, Christopher Marvin, Katona, Istvan, Doukas, Panagiotis, Nikolin, Stefan, Ernst, Sabrina, Aronica, Eleonora, Glaß, Hannes, Hermann, Andreas, Steinbusch, Harry, Feller, Alfred C., Bergmann, Markus, Jaarsma, Dick, Weis, Joachim, Goswami, Anand

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Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G 4 C 2 ) n expression in C9orf72 ALS/FTD by Czuppa, Mareike, Dhingra, Ashutosh, Zhou, Qihui, Schludi, Carina, König, Laura, Scharf, Elisabeth, Farny, Daniel, Dalmia, Anupriya, Täger, Joachim, Castillo-Lizardo, Melissa, Katona, Eszter, Mori, Kohji, Aumer, Tina, Schelter, Florian, Müller, Markus, Carell, Thomas, Kalliokoski, Tuomo, Messinger, Josef, Rizzu, Patrizia, Heutink, Peter, Edbauer, Dieter

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Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies by Dohrn, Maike F., Glöckle, Nicola, Mulahasanovic, Lejla, Heller, Corina, Mohr, Julia, Bauer, Christine, Riesch, Erik, Becker, Andrea, Battke, Florian, Hörtnagel, Konstanze, Hornemann, Thorsten, Suriyanarayanan, Saranya, Blankenburg, Markus, Schulz, Jörg B., Claeys, Kristl G., Gess, Burkhard, Katona, Istvan, Ferbert, Andreas, Vittore, Debora, Grimm, Alexander, Wolking, Stefan, Schöls, Ludger, Lerche, Holger, Korenke, G. Christoph, Fischer, Dirk, Schrank, Bertold, Kotzaeridou, Urania, Kurlemann, Gerhard, Dräger, Bianca, Schirmacher, Anja, Young, Peter, Schlotter‐Weigel, Beate, Biskup, Saskia

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