Institute of Human Genetics

CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome. (2020) Turan S, Winner B, Winner B, Krumbiegel M, Wiesmann da Silva Reis A, Lie DC, Börstler T, et al. Journal article The Status Quo of Rare Diseases Centres for the Development of a Clinical Decision Support System - A Cross-Sectional Study (2020) Schaaf J, Sedlmayr M, Prokosch HU, Ganslandt T, Schade-Brittinger C, von Wagner M, Kadioglu D, et al. Book chapter / Article in edited volumes Analysis of genetically determined gene expression suggest role of inflammatory processes in etiology of exfoliation syndrome (2020) Hirbo J, Pasutto F, Sealock J, Evans P, Pawar P, Tao R, Straub P, et al. Conference contribution Midkine is a tumor cell survival factor that displays metastatic and therapeutic resistance functions in uveal melanoma (2020) Karg M, John L, Refaian N, Büttner C, Rottmar T, Sommer J, Bock B, et al. Conference contribution MiR-29 related deposition of extracellular matrix in Fuchs endothelial corneal dystrophy (2020) Matthaei M, Clahsen T, Büttner C, Ekici AB, Siebelmann S, Heindl LM, Bachmann B, et al. Conference contribution Polyhydroxyphenylvalerate/polycaprolactone nanofibers improve the life-span and mechanoresponse of human IPSC-derived cortical neuronal cells (2020) Cerrone F, Pozner T, Siddiqui A, Ceppi P, Winner B, Rajendiran M, Babu R, et al. Journal article Transcription factor Tcf4 is the preferred heterodimerization partner for Olig2 in oligodendrocytes and required for differentiation (2020) Wedel M, Fröb F, Elsesser O, Wittmann MT, Lie DC, Reis A, Wegner M Journal article Sox11 is an Activity-Regulated Gene with Dentate-Gyrus-Specific Expression Upon General Neural Activation (2020) von Wittgenstein J, Zheng F, Wittmann MT, Balta EA, Ferrazzi F, Schäffner I, Häberle B, et al. Journal article Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups (2020) Assmann G, Köhm M, Schuster V, Behrens F, Mössner R, Magnolo N, Oji V, et al. Journal article Demonstration of brain region-specific neuronal vulnerability in human iPSC-based model of familial Parkinson's disease (2020) Brazdis RM, Alecu JE, Marsch D, Dahms A, Simmnacher K, Lörentz S, Brendler A, et al. Journal article