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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

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

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

Dysregulated paired related homeobox 1 impacts on hepatocellular carcinoma phenotypes

2021 . Piorońska, Weronika | Nwosu, Zeribe Chike | Han, Mei | Büttner, Michael | Ebert, Matthias Philip | Dooley, Steven | Meyer, Christoph

Converting fibroblastic fates leads to wound healing without scar

2021 . Jiang, Dongsheng | Rinkevich, Yuval

Genome sequencing in families with congenital limb malformations

Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update

2021 . Schätzl, Teresa | Kaiser, Lars | Deigner, Hans-Peter

Microbiota changes associated with ADNP deficiencies: rapid indicators for NAP (CP201) treatment of the ADNP syndrome and beyond

2020 . Kapitansky, Oxana | Giladi, Eliezer | Jaljuli, Iman | Bereswill, Stefan | Heimesaat, Markus M. | Gozes, Illana

Cohesin controls intestinal stem cell identity by maintaining association of Escargot with target promoters

2020 . Khaminets, Aliaksandr | Ronnen-Oron, Tal | Baldauf, Maik | Meier, Elke | Jasper, Heinrich