Anna Schick
Ludwig Maximilian University of Munich
4 Papers
34 Citations
Anna Schick is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Agrin & Synaptogenesis. The author has an hindex of 3, co-authored 4 publications. Previous affiliations of Anna Schick include Stockholm University.
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Papers
A nuclear ubiquitin-proteasome pathway targets the inner nuclear membrane protein Asi2 for degradation
TL;DR: A molecular pathway that affects the stability of integral proteins of the inner nuclear membrane is revealed and Asi2, an integral INM protein in Saccharomyces cerevisiae, is subject to protein quality control in the nucleus.
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Neuronal LRP4 regulates synapse formation in the developing CNS
Andromachi Karakatsani,Andromachi Karakatsani,Nicolás Marichal,Severino Urban,Georgios Kalamakis,Alexander Ghanem,Anna Schick,Yina Zhang,Karl-Klaus Conzelmann,Markus A. Rüegg,Benedikt Berninger,Carmen Ruiz de Almodovar,Susan Gascon,Susan Gascon,Stephan Kröger +14 more
TL;DR: Overexpression and knockdown of LRP4 in mouse cortical and hippocampal neurons both in vitro and in vivo reveals a key role for LRP3 in dendrite and synapse formation during development, demonstrating an essential and novel role of neuronal L RP4 in dendedritic development and synaptogenesis in the CNS.
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The role of agrin, Lrp4 and MuSK during dendritic arborization and synaptogenesis in cultured embryonic CNS neurons.
Gerry Handara,Florian J.A. Hetsch,René Jüttner,Anna Schick,Corinna Haupt,Fritz G. Rathjen,Stephan Kröger +6 more
TL;DR: Results establish selective roles for agrin, Lrp4 and MuSK during dendritogenesis and synaptogenesis in cultured CNS neurons.
25
Direct cloning of isogenic murine DNA in yeast and relevance of isogenicity for targeting in embryonic stem cells.
Claes Andréasson,Anna Schick,Susanne Pfeiffer,Mihail Sarov,Francis Stewart,Wolfgang Wurst,Joel A. Schick +6 more
TL;DR: A novel method for the direct cloning of genomic DNA into a targeting vector, pRTVIR, using oligonucleotide-directed homologous recombination in yeast is described, demonstrating the applicability of the method by constructing functional targeting vectors for mammalian genes Uhrf1 and Gfap.