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Professur für Stammzell-Modelle seltener neuraler Erkrankungen
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Human Genetics
Lehrstuhl für Humangenetik
Overview
Publications
(113)
Research Grants
(15)
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Journal article
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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
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