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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Targeted Deep Sequencing of Mycosis Fungoides Reveals Intracellular Signaling Pathways Associated with Aggressiveness and Large Cell Transformation by Marion Wobser, Sabine Roth, Silke Appenzeller, Roland Houben, David Schrama, Matthias Goebeler, Eva Geissinger, Andreas Rosenwald, Katja Maurus

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Panel Sequencing of Primary Cutaneous B-Cell Lymphoma by Marion Wobser, Patrick Schummer, Silke Appenzeller, Hermann Kneitz, Sabine Roth, 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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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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Exon-4 Mutations in KRAS Affect MEK/ERK and PI3K/AKT Signaling in Human Multiple Myeloma Cell Lines by Susann Weißbach, Sofia Catalina Heredia-Guerrero, Stefanie Barnsteiner, Lukas Großhans, Jochen Bodem, Hanna Starz, Christian Langer, Silke Appenzeller, Stefan Knop, Torsten Steinbrunn, Simone Rost, Hermann Einsele, Ralf Christian Bargou, Andreas Rosenwald, Thorsten Stühmer, Ellen Leich

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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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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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