Institut für Biochemie

De novo missense variants in RHOBTB2 cause a developmental and epileptic encephalopathy in humans, and altered levels cause neurological defects in Drosophila (2019) Straub J, Konrad E, Grüner J, Toutain A, Bok LA, Cho MT, Crawford HP, et al. Conference contribution Identification of novel candidate genes for idiopathic short stature using whole exome sequencing (2019) Thiel C, Hauer N, Vogl C, Ahmadian R, Dhandapany PS, Popp B, Buettner C, et al. Conference contribution The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and high-resolution copy number study (2019) Papuc S, Abela L, Steindl K, Begemann A, Simmons T, Schmitt B, Zweier M, et al. Conference contribution The functional consequences of SCN2A mutations determine the phenotype (2019) Begemann A, Acuna M, Zweier M, Sticht H, Steindl K, Besnard M, Hackenberg A, et al. Conference contribution SPARCL1 is an angiocrine inhibitor of tumorigenesis in colorectal carcinoma (2019) Tenkerian C, Regensburger D, Langer V, Klingler A, Borau A, Sticht H, Ramming A, et al. Conference contribution Transcriptional control in myelinating glia: from extrinsic signals to intrinsic factors and networks (2019) Wegner M Conference contribution Phototherapy-induced elevation of serum level of melanoma inhibitory activity (2019) Datz E, Zeman F, Koller M, Szeimies RM, Berneburg M, Landthaler M, Boßerhoff AK, Karrer S Journal article Deficient IL-6/Stat3 Signaling, High TLR7, and Type I Interferons in Early Human Alcoholic Liver Disease: A Triad for Liver Damage and Fibrosis (2019) Starkel P, Schnabl B, Leclercq S, Komuta M, Bataller R, Argemi J, Palma E, et al. Journal article Endogenous Expression of the Human CD83 Attenuates EAE Symptoms in Humanized Transgenic Mice and Increases the Activity of Regulatory T Cells (2019) Zinser E, Naumann R, Wild A, Michalski J, Deinzer A, Stich L, Kuhnt C, et al. Journal article Th17 Lymphocytes Induce Neuronal Cell Death in a Human iPSC-Based Model of Parkinson's Disease (2019) Sommer A, Marxreiter F, Krach F, Fadler T, Grosch J, Maroni M, Gräf D, et al. Journal article, Erratum