Silke Appenzeller - Dissemin

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Papers authored by Silke Appenzeller

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2019 Jenny Wegert, Lisa Zauter, Silke Appenzeller

ORCID

, Christoph Otto, Sabrina Bausenwein, Christian Vokuhl, Karen Ernestus, Rhoikos Furtwängler

ORCID

, Norbert Graf, Manfred Gessler

ORCID

High-risk blastemal Wilms tumor can be modeled by 3D spheroid cultures in vitro

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2018 Silke Appenzeller

ORCID

, Anja Gesierich, Alexander Thiem, Anita Hufnagel, Christina Jessen, Hermann Kneitz, Martina Regensburger, Cornelia Schmidt, Vanessa Zirkenbach, Thorsten Bischler

ORCID

, Bastian Schilling, Claudia Siedel, Maria‐Elisabeth Goebeler, Roland Houben, David Schrama and 8 other authors

The identification of patient‐specific mutations reveals dual pathway activation in most patients with melanoma and activated receptor tyrosine kinases in BRAF/NRAS wild‐type melanomas

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Silke Appenzeller

ORCID

Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication.

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Juliane Lippert, Silke Appenzeller

ORCID

, Raimunde Liang, Silviu Sbiera, Stefan Kircher, Indrajit Nanda, Barbara Altieri, Andrea Gehrig, Isabel Weigand, Sonja Steinhauer, Renzo J. M. Riemens, Riemens Rjm, Clemens R. Müller, Andreas Rosenwald, Matthias Kroiss and 5 other authors

Targeted molecular analysis in adrenocortical carcinomas: a strategy towards improved personalized prognostication

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Verena Surrey, Caren Zöller, Alicia Andrea Lork, Mehri Moradi, Stefanie Balk, Benjamin Dombert, Lena Saal-Bauernschubert, Michael Briese, Silke Appenzeller

ORCID

, Utz Fischer, Sibylle Jablonka

Impaired Local Translation of β-actin mRNA in Ighmbp2-Deficient Motoneurons: Implications for Spinal Muscular Atrophy with respiratory Distress (SMARD1)

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Katja Maurus, Silke Appenzeller

ORCID

, Sabine Roth, Jochen Kuper, Simone Rost, Svenja Meierjohann, Panagiota Arampatzi

ORCID

, Matthias Goebeler, Andreas Rosenwald, Eva Geissinger, Marion Wobser

Panel Sequencing Shows Recurrent Genetic FAS Alterations in Primary Cutaneous Marginal Zone Lymphoma

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Alexander Thiem, Patrick Schummer, Simon Ueberschaar, Andreas Kerstan, Hermann Kneitz, David Schrama, Silke Appenzeller

ORCID

, Svenja Meierjohann, Bastian Schilling, Matthias Goebeler, Anja Gesierich

Early onset of diffuse melanosis cutis under pembrolizumab therapy illustrates the limitations of anti-PD-1 checkpoint inhibitors:

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Julia Böck, Silke Appenzeller

ORCID

, Larissa Haertle, Tamara Schneider, Andrea Gehrig, Jörg Schröder, Simone Rost, Beat Wolf, Claus R. Bartram, Christian Sutter, Thomas Haaf

ORCID

Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation‐negative early‐onset and high‐risk breast cancer patients

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Michael Briese, Lena Saal-Bauernschubert, Changhe Ji, Mehri Moradi, Hanaa Ghanawi, Michael Uhl, Silke Appenzeller

ORCID

, Rolf Backofen, Michael Sendtner

hnRNP R and its main interactor, the noncoding RNA 7SK, coregulate the axonal transcriptome of motoneurons

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2017 M. Wobser, K. Maurus, S. Roth, S. Appenzeller

ORCID

, G. Weyandt, M. Goebeler, A. Rosenwald, E. Geissinger

Myeloid differentiation primary response 88 mutations in a distinct type of cutaneous marginal-zone lymphoma with a nonclass-switched immunoglobulin M immunophenotype

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2016 Antoine-Emmanuel Saliba

ORCID

, Lei Li

ORCID

, Alexander J. Westermann, Silke Appenzeller

ORCID

, Daphne Ac C. Stapels, Leon N. Schulte, Sophie Helaine, Jörg Vogel

ORCID

Single-cell RNA-seq ties macrophage polarization to growth rate of intracellular Salmonella

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Cristina Ronchi, Ronchi Cl, Dalmazi Guido Di, S. Faillot, Silviu Sbiera, Guillaume Assie

ORCID

, Isabel Weigand, Detlef Bartsch, Davide Calebiro, Franco Mantero, T. Schwarzmayr, Beatrice Rubin, Massimo Mannelli, Jens Waldmann, Silke Appenzeller

ORCID

and 9 other authors

Genetic landscape of sporadic unilateral adrenocortical adenomas without PRKACA p.Leu206Arg mutation

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2015 Cristina L. Ronchi, Erika Peverelli, Sabine Herterich, Isabel Weigand, Giovanna Mantovani, Thomas Schwarzmayr, Silviu Sbiera, Bruno Allolio, Jürgen Honegger, Silke Appenzeller

ORCID

, Andrea G. Lania, Martin Reincke, Davide Calebiro, Anna Spada, Michael Buchfelder and 3 other authors

Landscape of somatic mutations in sporadic GH-secreting pituitary adenomas

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Karl Martin Klein, Manuela Pendziwiat, Rony Cohen, Silke Appenzeller

ORCID

, Carolien G. F. de Kovel

ORCID

, Felix Rosenow, Bobby P. C. Koeleman, Gregor Kuhlenbäumer, Liron Sheintuch, Ronel Veksler, Alon Friedman, Zaid Afawi, Ingo Helbig

Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia

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Michael Briese, Lena Saal, Silke Appenzeller

ORCID

, Mehri Moradi, Apoorva Baluapuri

ORCID

, Michael Sendtner

Whole transcriptome profiling reveals the RNA content of motor axons

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Silke Appenzeller

ORCID

, Christian Gilissen, Jos Rijntjes, Bastiaan B. J. Tops, Annemiek Kastner-Van Raaij, Konnie M. Hebeda, Loes Nissen, Bas E. Dutilh

ORCID

, J. Han J. M. van Krieken

ORCID

, Patricia J. T. A. Groenen

Immunoglobulin rearrangement analysis from multiple lesions in the same patient using next-generation sequencing

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2014 S. Von Spiczak, Silke Appenzeller

ORCID

, Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande Caglayan, Dana Craiu

ORCID

, Peter De Jonghe, Christel Depienne, Petia Dimova, Tania Djémié, Padhraig Gormley, Renzo Guerrini, Angela Robbiano, Ingo Helbig and 113 other authors

De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies

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May Bungeroth, Silke Appenzeller

ORCID

, Annika Regulin, Wolfgang Völker, Inken Lorenzen, Joachim Grötzinger, Manuela Pendziwiat, Gregor Kuhlenbäumer

Differential aggregation properties of alpha-synuclein isoforms

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2013 Hadassa Goldberg-Stern, Sharon Aharoni, Zaid Afawi, Odeya Bennett, Silke Appenzeller

ORCID

, Manuela Pendziwiat, Dipl Biochem, Gregor Kuhlenbäumer, Lina Basel-Vanagaite, Avinoam Shuper, Amos D. Korczyn, Ingo Helbig

Broad Phenotypic Heterogeneity due to a Novel SCN1A Mutation in a Family With Genetic Epilepsy With Febrile Seizures Plus

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Arvid Suls, Jaehn Ja, Johanna A. Jaehn, Angela Kecskés, Yvonne G. Weber, Sarah Weckhuysen, Craiu Dc, Dana C. Craiu

ORCID

, Aleksandra Siekierska, Tania Djémié, Tatiana Afrikanova, Padhraig Gormley, Sarah von Spiczak, Gerhard Kluger, Catrinel M. Iliescu and 64 other authors

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

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