Laura Krumm

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Professur für Molekulare Neurologie Professur für Stammzell-Modelle seltener neuraler Erkrankungen

Publications

(8)

Rescue of mitochondrial and neurite pathology in SPG7 hereditary spastic paraplegia patient-derived cortical neurons (2026) Neubauer D, Kaißer C, Krumm L, Börstler T, Metzner KL, Al Hamad T, Böttcher M, et al. Journal article RNA splicing modulator for Huntington's disease treatment induces peripheral neuropathy (2025) Krach F, Börstler T, Neubert S, Krumm L, Regensburger M, Winkler J, Winner B Journal article Plasma Neurofilaments: Potential Biomarkers of SPG11-Related Hereditary Spastic Paraplegia (2024) Krumm L, Winkler J, Winner B, Regensburger M Journal article Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients. (2024) Krumm L, Pozner T, Zagha N, Coras R, Arnold P, Tsaktanis T, Scherpelz K, et al. Journal article Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia. (2022) Winner B, Marterstock D, Kopp C, Dörfler A, Regensburger M, Krumm L, Schmidt M, et al. Journal article Efficient and Easy Conversion of Human iPSCs into Functional Induced Microglia-like Cells (2022) Lanfer J, Winner B, Kaindl J, Krumm L, Acera MG, Neurath M, Regensburger M, Krach F Journal article, Review article Genetically Single Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in (2021) Krumm L, Pozner T, Kaindl J, Regensburger M, Günther C, Turan S, Asadollahi R, et al. Journal article Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in (2021) Winner B, Krumm L, Pozner T, Kaindl J, Regensburger M, Günther C, Turan S, et al. Journal article, Original article