The difficulty to model Huntington’s disease in vitro using striatal medium spiny neurons differentiated from human induced pluripotent stem cells by Le Cann, Kim, Foerster, Alec, Rösseler, Corinna, Erickson, Andelain, Hautvast, Petra, Giesselmann, Sebastian, Pensold, Daniel, Kurth, Ingo, Rothermel, Markus, Mattis, Virginia B., Zimmer-Bensch, Geraldine, von Hörsten, Stephan, Denecke, Bernd, Clarner, Tim, Meents, Jannis, Lampert, Angelika

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The role of Nav1.7 in human nociceptors: insights from human induced pluripotent stem cell-derived sensory neurons of erythromelalgia patients by Meents, Jannis E, Bressan, Elisangela, Sontag, Stephanie, Foerster, Alec, Hautvast, Petra, Rösseler, Corinna, Hampl, Martin, Schüler, Herdit, Goetzke, Roman, Le, Thi Kim Chi, Kleggetveit, Inge Petter, Le Cann, Kim, Kerth, Clara, Rush, Anthony M, Rogers, Marc, Kohl, Zacharias, Schmelz, Martin, Wagner, Wolfgang, Jørum, Ellen, Namer, Barbara, Winner, Beate, Zenke, Martin, Lampert, Angelika

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Beyond mobile phone displays: Flat panel display technology for biomedical applications by Mameli, Alfredo, Akkerman, Hylke B., González-Lana, Sandra, Castro-Abril, Héctor, Le Cann, Kim, Lampert, Angelika, Gelinck, Gerwin H., Kronemeijer, Auke Jisk, van Breemen, Albert J.J.M.

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A novel human pain insensitivity disorder caused by a point mutation in ZFHX2 by Habib, Abdella M, Matsuyama, Ayako, Okorokov, Andrei L, Santana-Varela, Sonia, Bras, Jose T, Aloisi, Anna Maria, Emery, Edward C, Bogdanov, Yury D, Follenfant, Maryne, Gossage, Sam J, Gras, Mathilde, Humphrey, Jack, Kolesnikov, Anna, Le Cann, Kim, Li, Shengnan, Minett, Michael S, Pereira, Vanessa, Ponsolles, Clara, Sikandar, Shafaq, Torres, Jesus M, Yamaoka, Kenji, Zhao, Jing, Komine, Yuriko, Yamamori, Tetsuo, Maniatis, Nikolas, Panov, Konstantin I, Houlden, Henry, Ramirez, Juan D, Bennett, David L H, Marsili, Letizia, Bachiocco, Valeria, Wood, John N, Cox, James J

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Assessing the impact of pain-linked Nav1.7 variants: An example of two variants with no biophysical effect by Le Cann, Kim, Meents, Jannis E., Sudha Bhagavath Eswaran, Vishal, Dohrn, Maike F., Bott, Raya, Maier, Andrea, Bialer, Martin, Hautvast, Petra, Erickson, Andelain, Rolke, Roman, Rothermel, Markus, Körner, Jannis, Kurth, Ingo, Lampert, Angelika

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Genetic variation in the HSD17B1 gene and risk of prostate cancer by Kraft, Peter, Hayes, Richard B., Pharoah, Paul D., Chanock, Stephen, Albanes, Demetrius, Kolonel, Laurence N., Altshuler, David, Andriole, Gerald, Berg, Christina, Boeing, Heiner, Burtt, Noel, Bueno-de-Mesquita, Bas, Calle, Eugenia, Cann, Howard, Canzian, Federico, Chen, Yen-Ching, Crawford, David E., Dunning, Alison, Feigelson, Heather S., Freedman, Matthew L., Gaziano, John M., Giovannucci, Edward, Gonzales, Carlos Alberto, Hallmans, Goran, Henderson, Brian E., Hirschhorn, Joel, Hunter, David, Kaaks, Rudolf, Key, Timothy, Le Marchand, Loic, Ma, Jing, Overvad, Kim, Palli, Domenico, Pike, Malcolm C, Riboli, Elio, Rodriguez, Carmen, Setiawan, Wendy V, Stampfer, Meir, Stram, Daniel O., Thomas, Gilles, Thun, Michael, Travis, Ruth, Trichopoulou, Antonia, Virtamo, Jorma, Wacholder, Sholom

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