H
Herbert Hildebrandt
Researcher at Hannover Medical School
Publications - 69
Citations - 3644
Herbert Hildebrandt is an academic researcher from Hannover Medical School. The author has contributed to research in topics: Polysialic acid & Neural cell adhesion molecule. The author has an hindex of 32, co-authored 64 publications receiving 3255 citations. Previous affiliations of Herbert Hildebrandt include Hochschule Hannover & Johns Hopkins University.
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Journal ArticleDOI
Sialic Acids in the Brain: Gangliosides and Polysialic Acid in Nervous System Development, Stability, Disease, and Regeneration
Ronald L. Schnaar,Rita Gerardy-Schahn,Rita Gerardy-Schahn,Herbert Hildebrandt,Herbert Hildebrandt +4 more
TL;DR: In the brain, two families of sialoglycans are of particular interest: gangliosides and polysialic acid as discussed by the authors, which regulate cell-cell interactions, modulate the activities of their glycoprotein and glycolipid scaffolds as well as other cell surface molecules.
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Genetic Ablation of Polysialic Acid Causes Severe Neurodevelopmental Defects Rescued by Deletion of the Neural Cell Adhesion Molecule
Birgit Weinhold,Ralph Seidenfaden,Iris Röckle,Iris Röckle,Martina Mühlenhoff,Frank Schertzinger,Sidonie Conzelmann,Jamey D. Marth,Rita Gerardy-Schahn,Herbert Hildebrandt +9 more
TL;DR: It is revealed that the essential role of polySia resides in the control and coordination of NCAM interactions during mouse brain development, and this first demonstration in vivo that a highly specific glycan structure is more important than the glycoconjugate as a whole provides a novel view on the relevance of protein glycosylation for the complex process of building the vertebrate brain.
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Polysialic acid directs tumor cell growth by controlling heterophilic neural cell adhesion molecule interactions.
TL;DR: It is established that PSA controls tumor cell growth and differentiation by interfering with NCAM signaling at cell-cell contacts, providing a mechanism for how PSA may promote the genesis and progression of highly aggressive PSA-NCAM-positive tumors.
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Synaptic cell adhesion molecule SynCAM 1 is a target for polysialylation in postnatal mouse brain
Sebastian P. Galuska,Manuela Rollenhagen,Moritz Kaup,Katinka Eggers,Imke Oltmann-Norden,Miriam Schiff,Maike Hartmann,Birgit Weinhold,Herbert Hildebrandt,Rudolf Geyer,Martina Mühlenhoff,Hildegard Geyer +11 more
TL;DR: It is suggested that polySia may act as a dynamic modulator of SynCAM 1 functions during integration of NG2 cells into neural networks during integration in vertebrate brain development and synaptic plasticity.
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Dissecting polysialic acid and NCAM functions in brain development.
TL;DR: This review focuses on a phenotype comparison between the newly established mouse strains which combine polySia‐deficiency with normal NCAM expression and the well‐characterized NCAM negative mouse model, and revealed thatpolySia plays a vital role as a specific control element of NCAM‐mediated interactions.