5 results match your criteria: "Leibnitz Institute for Neurobiology[Affiliation]"
Elife
December 2023
Department of Neurology, Otto-von-Guericke University, Magdeburg, Germany.
The visual system has evolved the ability to track features like color and orientation in parallel. This property aligns with the specialization of processing these feature dimensions in the visual cortex. But what if we ask to track changing feature-values within the same feature dimension? Parallel tracking would then have to share the same cortical representation, which would set strong limitations on tracking performance.
View Article and Find Full Text PDFNeurosurgery
July 2017
Department of Neurosurgery International Neuroscience Institute Hannover, Germany.
Sci Data
March 2017
Department of Biomedical Magnetic Resonance, Otto-von-Guericke University, 39120 Magdeburg, Germany.
We present an ultrahigh resolution in vivo human brain magnetic resonance imaging (MRI) dataset. It consists of T-weighted whole brain anatomical data acquired at 7 Tesla with a nominal isotropic resolution of 250 μm of a single young healthy Caucasian subject and was recorded using prospective motion correction. The raw data amounts to approximately 1.
View Article and Find Full Text PDFAdv Exp Med Biol
July 2003
AG Molecular of Plasicity, Department of Neurochemistry/Molecular Biology, Leibnitz Institute for Neurobiology, 39118 Magdeburg, Germany.
Caldendrin is the first member of a novel family of Ca2+-binding proteins (CaBPs). Its unique two-domain structure is composed of a calmodulin-homologous teminus and an unrelated N-terminal part. The latter is thought to mediate the tight association of caldendrin with the subsynaptic cytoskeleton.
View Article and Find Full Text PDFEur J Neurosci
May 1998
Leibnitz Institute for Neurobiology, Magdeburg, Germany.
Brevican is a member of the aggrecan/versican family of proteoglycans. In contrast to the other family members, brevican occurs both as soluble isoforms secreted into the extracellular space and membrane-bound isoforms which are anchored to the cell surface via a glycosylphosphatidylinositol (GPI) moiety. Expression of both variants, which are encoded by two differentially processed transcripts from the same gene, is confined to the nervous system.
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