Professur für Stammzell-Modelle seltener neuraler Erkrankungen


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Journal article
Book chapter / Article in edited volumes
Authored book
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Thesis
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Unpublished / Preprint

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Abstract

Journal

A reversible state of hypometabolism in a human cellular model of sporadic Parkinson’s disease (2023) Schmidt S, Stautner C, Vu DT, Heinz A, Regensburger M, Karayel O, Trümbach D, et al. Journal article Impact of Microbiome–Brain Communication on Neuroinflammation and Neurodegeneration (2023) Stolzer I, Scherer E, Süß P, Rothhammer V, Winner B, Neurath M, Günther C Journal article, Review article Human Induced Pluripotent Stem Cell-Derived Pericytes as Scalable and Editable Source to Study Direct Lineage Reprogramming Into Induced Neurons (2023) Menon R, Petrucci L, Lohrer B, Zhang J, Schulze M, Schichor C, Winner B, et al. Journal article Scaffold-Based (Matrigel™) 3D Culture Technique of Glioblastoma Recovers a Patient-like Immunosuppressive Phenotype (2023) Braun FK, Rothhammer-Hampl T, Lorenz J, Pohl S, Menevse AN, Vollmann-Zwerenz A, Bumes E, et al. Journal article Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons (2023) Asadollahi R, Delvendahl , Muff R, Tan G, Rodrieguez DG, Turan S, Russo M, et al. Journal article CRISPR/Cas9-mediated generation of hESC lines with homozygote and heterozygote p.R331W mutation in CTBP1 to model HADDTS syndrome. (2023) Winner B, Akdas EY, Turan S, Guhathakurta D, Ekici AB, Salar S, Lie DC, Fejtová A Journal article CRISPR/Cas9-mediated generation of hESC lines with homozygote and heterozygote p.R331W mutation in CTBP1 to model HADDTS syndrome (2023) Akdas EY, Turan S, Guhathakurta D, Ekici AB, Salar S, Lie DC, Winner B, Fejtová A Journal article Parkinson's disease or multiple system atrophy: potential separation by quantitative susceptibility mapping (2023) Marxreiter F, Lambrecht V, Mennecke A, Hanspach J, Jukic J, Regensburger M, Herrler J, et al. Journal article An alternative splicing modulator decreases mutant HTT and improves the molecular fingerprint in Huntington’s disease patient neurons (2022) Krach F, Stemick J, Börstler T, Weiss A, Lingos I, Reischl S, Meixner H, et al. Journal article Generation of a homozygous and a heterozygous SNCA gene knockout human-induced pluripotent stem cell line by CRISPR/Cas9 mediated allele-specific tuning of SNCA expression (2022) Schneider Y, Turan S, Koller A, Krumbiegel M, Farrell M, Plotz S, Winkler J, Xiang W Journal article