Author
Humboldt-Universität zu BerlinORCID 0000-0003-0790-5040Unclaimed ORCID profile · follow to get notified of new preprints
7 papers
Recent·Most cited
Elisa Pedersen, Sicheng Zhang, Xushuai Dong…·Marta Rosário
This study identifies DTX4 as a regulator of neural progenitor transitions during cortical development, showing its role in maintaining radial glia identity and preventing intermediate progenitor generation.
Ekaterina V. Borisova, Katherine J. Cuthill, Rike Dannenberg…·Mateusz C. Ambrozkiewicz
The paper shows UBE3C regulates cortical neurogenesis and glial fate through m6A methylation, with mutations disrupting this process and offering therapeutic targets.
Avinash V. Dharmadhikari, Maria Alba Abad, Reza Maroofian…·Universitat Autònoma de Barcelona. Departament de Medicina
The paper identifies SPOUT1/CENP-32 as a causative gene for SpADMiSS, linking its dysfunction to mitotic spindle defects and neurodevelopmental disorders.
Ekaterina V. Borisova, Andrew G. Newman, Marta Couce-Iglesias…·Mateusz C. Ambrozkiewicz
The paper shows that Ire1α regulates mRNA translation rates, which control the identity and polarity of upper layer cortical neurons through eIF4A1 and eEF-2.
Paraskevi Bessa, Andrew G. Newman, Kuo Yan…·Victor S. Tarabykin
The paper shows that Sema7A and Sema4D heterodimerization is essential for membrane targeting and neocortical wiring, with a mutation in Sema4D causing epilepsy.
Matthew L. Kraushar, Ferdinand Krupp, Dermot Harnett…·Christian M. T. Spahn
The paper reveals Ebp1's role in neuronal proteostasis by analyzing ribosomal architecture and proteomic changes in the developing mouse neocortex.
Mateusz C. Ambrozkiewicz, Ekaterina V. Borisova, Manuela Schwark…·Hiroshi Kawabe
This study shows that Ube3b regulates dendritic branching and synaptic function by ubiquitinating Ppp3cc, contributing to intellectual disability-like phenotypes in a KOS mouse model.