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Lehrstuhl für Humangenetik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Human Genetics
Overview
Publications
(514)
Research Grants
(37)
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Journal article
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Differential Effects of Ontamalimab Versus Vedolizumab on Immune Cell Trafficking in Intestinal Inflammation and Inflammatory Bowel Disease (2023)
Schulze L, Becker E, Dedden M, Liu L, Van Passen C, Mohamed Abdou M, Müller T, 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
Ex Vivo Chromosomal Radiosensitivity Testing in Patients with Pathological Germline Variants in Breast Cancer High-Susceptibility Genes BReast CAncer 1 and BReast CAncer 2 (2023)
Zuhair Kassem T, Wunderle M, Kuhlmann L, Rübner M, Hübner H, Hoyer J, Reis A, 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
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder (2023)
Schmid CM, Gregor A, Costain G, Morel CF, Massingham L, Schwab J, Quélin C, et al.
Journal article
ALS is imprinted in the chromatin accessibility of blood cells (2023)
Kühlwein JK, Ruf WP, Kandler K, Witzel S, Lang C, Mulaw MA, Ekici AB, 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
Nanomaterial-based ophthalmic therapies (2023)
Unterweger H, Janko C, Civelek M, Cicha I, Spielvogel H, Tietze R, Friedrich B, Alexiou C
Journal article
Expanding the phenotype of 12q21 deletions: A role of BTG1 in speech development? (2023)
Blum K, Krumbiegel M, Kraus C, Reis A, Hüffmeier U
Journal article
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