Professur für Biochemie und Molekulare Neurowissenschaften


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

Unlocking the potential of SY-stem cells (2024) Furlanetto F, Frank S, Karow M Journal article Absence of the RING domain in MID1 results in patterning defects in the developing human brain (2024) Frank S, Gabassi E, Käseberg S, Bertin M, Zografidou L, Pfeiffer D, Brennenstuhl H, et al. Journal article Programming of neural progenitors of the adult subependymal zone towards a glutamatergic neuron lineage by neurogenin 2 (2023) Péron S, Miyakoshi LM, Brill MS, Manzano-Franco D, Serrano-López J, Fan W, Marichal N, et al. Journal article Human Induced Pluripotent Stem Cell-Derived Pericytes as Scalable and Editable Source to Study Direct Lineage Reprogramming Into Induced Neurons (2023) Menon R, Petrucci L, Lohrer B, Zhang J, Schulze M, Schichor C, Winner B, et al. Journal article Thymosin β4 Is an Endogenous Iron Chelator and Molecular Switcher of Ferroptosis (2022) Lachowicz JI, Pichiri G, Piludu M, Fais S, Orrù G, Congiu T, Piras M, et al. Journal article Cellular identity through the lens of direct lineage reprogramming (2021) Falk S, Han D, Karow M Journal article, Review article The gut-brain axis in inflammatory bowel disease—current and future perspectives (2021) Günther C, Rothhammer V, Karow M, Neurath M, Winner B Journal article, Review article Astrocytes and neurons share region-specific transcriptional signatures that confer regional identity to neuronal reprogramming (2021) Herrero-Navarro A, Puche-Aroca L, Moreno-Juan V, Sempere-Ferrandez A, Espinosa A, Susin R, Torres-Masjoan L, et al. Journal article Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine (2016) Kurolap A, Armbruster A, Hershkovitz T, Hauf K, Mory A, Paperna T, Hannappel E, et al. Journal article Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxa (2016) Sasaki T, Hanisch FG, Deutzmann R, Sakai LY, Sakuma T, Miyamoto T, Yamamoto T, et al. Journal article
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