Simon Hippenmeyer
Affiliations: | IST Austria, Klosterneuburg, Niederösterreich, Austria |
Area:
Neural DevelopmentGoogle:
"Simon Hippenmeyer"Mean distance: 14.36 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Silvia Arber | grad student | Biozentrum, University of Basel | |
| Liqun Luo | post-doc | Stanford |
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Publications
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| Miranda OA, Cheung G, Hippenmeyer S. (2024) Morphological Analysis of Neurons and Glia Using Mosaic Analysis with Double Markers. Methods in Molecular Biology (Clifton, N.J.). 2831: 283-299 |
| Hansen AH, Hippenmeyer S. (2024) Time-lapse imaging of cortical projection neuron migration in mice using mosaic analysis with double markers. Star Protocols. 5: 102795 |
| Cheung G, Pauler FM, Koppensteiner P, et al. (2023) Multipotent progenitors instruct ontogeny of the superior colliculus. Neuron. 112: 230-246.e11 |
| Ladle DR, Hippenmeyer S. (2023) Loss of ETV1/ER81 in motor neurons leads to reduced monosynaptic inputs from proprioceptive sensory neurons. Journal of Neurophysiology |
| Hansen AH, Pauler FM, Riedl M, et al. (2022) Tissue-Wide Effects Override Cell-Intrinsic Gene Function in Radial Neuron Migration. Oxford Open Neuroscience. 1: kvac009 |
| Amberg N, Pauler FM, Streicher C, et al. (2022) Tissue-wide genetic and cellular landscape shapes the execution of sequential PRC2 functions in neural stem cell lineage progression. Science Advances. 8: eabq1263 |
| Anderson DJ, Pauler FM, McKenna A, et al. (2022) Simultaneous brain cell type and lineage determined by scRNA-seq reveals stereotyped cortical development. Cell Systems |
| Contreras X, Amberg N, Davaatseren A, et al. (2021) A genome-wide library of MADM mice for single-cell genetic mosaic analysis. Cell Reports. 35: 109274 |
| Pauler FM, Hudson QJ, Laukoter S, et al. (2021) Inducible Uniparental Chromosome Disomy to Probe Genomic Imprinting at Single-cell Level in Brain and Beyond. Neurochemistry International. 104986 |
| Laukoter S, Amberg N, Pauler FM, et al. (2020) Generation and isolation of single cells from mouse brain with mosaic analysis with double markers-induced uniparental chromosome disomy. Star Protocols. 1: 100215 |