Fachrepositorium Lebenswissenschaften

28 Treffer

Seiten

Suche

Publisso-Menue

Seiten

Inhibition of the YAP-MMB interaction and targeting NEK2 as potential therapeutic strategies for YAP-driven cancers

2024 . Jessen, Marco | Gertzmann, Dörthe | Liss, Franziska | Zenk, Franziska | Bähner, Laura | Schöffler, Victoria | Schulte, Clemens | Maric, Hans Michael | Ade, Carsten | von Eyss, Bjoern | Gaubatz, Stefan

Panel-based RNA fusion sequencing improves diagnostics of pediatric acute myeloid leukemia

2023 . Hoffmeister, Lina Marie | Suttorp, Julia | Walter, Christiane | Antoniou, Evangelia | Behrens, Yvonne Lisa | Göhring, Gudrun | Awada, Amani | von Neuhoff, Nils | Reinhardt, Dirk | Schneider, Markus

Immunoproteasome function maintains oncogenic gene expression in KMT2A-complex driven leukemia

HAND2 is a novel obesity-linked adipogenic transcription factor regulated by glucocorticoid signalling

Rapidly fatal SMARCA4-deficient undifferentiated sarcoma originating from hybrid hemosiderotic fibrolipomatous tumor/pleomorphic hyalinizing angiectatic tumor of the foot

2021 . Agaimy, Abbas | Meidenbauer, Norbert | Sukov, William R. | Stoehr, Robert | Vieth, Michael | Roemer, Frank | Grützmann, Robert | Folpe, Andrew L.

Currarino syndrome: a comprehensive genetic review of a rare congenital disorder

2021 . Dworschak, Gabriel | Reutter, Heiko M. | Ludwig, Michael

Diagnostic and Therapeutic Approach in a Metastatic Vaginal Adenocarcinoma: A Case Report

2021 . Egger, Eva Katharina | Ralser, Damian J. | Lindner, Kira | Recker, Florian | Marinova, Milka | Savchenko, Oleksandre | Lau, Jan-Frederic | Mustea, Alexander

Simultaneous Brg1 Knockout and MYCN Overexpression in Cerebellar Granule Neuron Precursors Is Insufficient to Drive Tumor Formation but Temporarily Enhances their Proliferation and Delays their Migration

2021 . Holdhof, Dörthe | On, Ji Hoon | Schoof, Melanie | Göbel, Carolin | Schüller, Ulrich

Exploiting vulnerabilities of SWI/SNF chromatin remodelling complexes for cancer therapy

2021 . Wanior, Marek | Krämer, Andreas | Knapp, Stefan | Joerger, Andreas

Familial cleft tongue caused by a unique translation initiation codon variant in TP63

2021 . Schmidt, Julia | Schreiber, Gudrun | Altmüller, Janine | Thiele, Holger | Nürnberg, Peter | Li, Yun | Kaulfuß, Silke | Funke, Rudolf | Wilken, Bernd | Yigit, Gökhan | Wollnik, Bernd

Seiten