Absence of Plekhg5 Results in Myelin Infoldings Corresponding to an Impaired Schwann Cell Autophagy, and a Reduced T-Cell Infiltration Into Peripheral Nerves by Patrick Lüningschrör, Carsten Slotta, Carsten Slotta, Peter Heimann, Michael Briese, Ulrich M. Weikert, Bita Massih, Silke Appenzeller, Silke Appenzeller, Michael Sendtner, Christian Kaltschmidt, Barbara Kaltschmidt, Barbara Kaltschmidt

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Oncogenic Mutations and Gene Fusions in CD30-Positive Lymphoproliferations and Clonally Related Mycosis Fungoides Occurring in the Same Patients by Marion Wobser, Sabine Roth, Silke Appenzeller, Hermann Kneitz, Matthias Goebeler, Eva Geissinger, Andreas Rosenwald, Katja Maurus

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An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during <italic toggle="yes">Salmonella</italic> Infection by Leon N. Schulte, Matthias Schweinlin, Alexander J. Westermann, Harshavardhan Janga, Sara C. Santos, Silke Appenzeller, Heike Walles, Jörg Vogel, Marco Metzger

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Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals. by Larissa Haertle, Anna Maierhofer, Julia Böck, Harald Lehnen, Yvonne Böttcher, Matthias Blüher, Martin Schorsch, Ramya Potabattula, Nady El Hajj, Silke Appenzeller, Thomas Haaf

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Rapid response to selpercatinib in RET fusion positive pancreatic neuroendocrine carcinoma confirmed by smartwatch by Barbara Deschler-Baier, Markus Krebs, Matthias Kroiss, Manik Chatterjee, Daniel Gundel, Christian Kestler, Alexander Kerscher, Volker Kunzmann, Silke Appenzeller, Katja Maurus, Andreas Rosenwald, Ralf Bargou, Elena Gerhard-Hartmann, Vivek Venkataramani

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Case Report: Consecutive Adrenal Cushing’s Syndrome and Cushing’s Disease in a Patient With Somatic CTNNB1, USP8, and NR3C1 Mutations by Mario Detomas, Barbara Altieri, Wiebke Schlötelburg, Wiebke Schlötelburg, Silke Appenzeller, Sven Schlaffer, Roland Coras, Andreas Schirbel, Vanessa Wild, Matthias Kroiss, Matthias Kroiss, Silviu Sbiera, Martin Fassnacht, Timo Deutschbein, Timo Deutschbein

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R-Roscovitine Improves Motoneuron Function in Mouse Models for Spinal Muscular Atrophy by Rocio Tejero, Stefanie Balk, Julio Franco-Espin, Jorge Ojeda, Luisa Hennlein, Hans Drexl, Benjamin Dombert, Jan-Dierk Clausen, Laura Torres-Benito, Lena Saal-Bauernschubert, Robert Blum, Michael Briese, Silke Appenzeller, Lucia Tabares, Sibylle Jablonka

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Intratumor heterogeneity of prognostic DNA-based molecular markers in adrenocortical carcinoma by Anne Jouinot, Juliane Lippert, Martin Fassnacht, Bruno de La Villeon, Amandine Septier, Mario Neou, Karine Perlemoine, Silke Appenzeller, Mathilde Sibony, Sébastien Gaujoux, Bertrand Dousset, Rossella Libe, Lionel Groussin, Cristina L Ronchi, Guillaume Assié, Jérôme Bertherat

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Wilms tumor primary cultures capture phenotypic heterogeneity and facilitate preclinical screening by Lisa Götz, Jenny Wegert, Alireza Paikari, Silke Appenzeller, Sabrina Bausenwein, Christian Vokuhl, Taryn D. Treger, Jarno Drost, Christin Linderkamp, Dominik T. Schneider, Karen Ernestus, Steven W. Warman, Jörg Fuchs, Nils Welter, Norbert Graf, Sam Behjati, Rhoikos Furtwängler, Manfred Gessler

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Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome by Ingo Helbig, Giulia Barcia, Manuela Pendziwiat, Shiva Ganesan, Stefanie H. Mueller, Katherine L. Helbig, Priya Vaidiswaran, Julie Xian, Peter D. Galer, Zaid Afawi, Nicola Specchio, Gerhard Kluger, Gregor Kuhlenbäumer, Silke Appenzeller, Michael Wittig, Uri Kramer, Andreas vanBaalen, Rima Nabbout, FIRES Genetics Study Group

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