Professur für Bioinformatik

Disturbances of Ligand Potency and Enhanced Degradation of the Human Glycine Receptor at Affected Positions G160 and T162 Originally Identified in Patients Suffering from Hyperekplexia (2015) Atak S, Langlhofer G, Schaefer N, Kessler D, Meiselbach H, Delto C, Schindelin H, Villmann C Journal article Crystal structure of the human cytomegalovirus pUL50-pUL53 core nuclear egress complex provides insight into a unique assembly scaffold for virus-host protein interactions (2015) Walzer S, Egerer-Sieber C, Sticht H, Sevvana M, Hohl K, Milbradt J, Muller Y, Marschall M Journal article, Original article CD83 and GRASP55 interact in human dendritic cells (2015) Stein MF, Blume K, Heilingloh C, Kummer M, Biesinger B, Sticht H, Steinkasserer A Journal article Palmoplantar Pustular Psoriasis Is Associated with Missense Variants in CARD14, but Not with Loss-of-Function Mutations in IL36RN in European Patients (2015) Moessner R, Frambach Y, Wilsmann-Theis D, Loehr S, Jacobi A, Weyergraf A, Mueller M, et al. Journal article De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females (2015) Popp B, Stove SI, Endele S, Myklebust LM, Hoyer J, Sticht H, Azzarello-Burri S, et al. Journal article Length of the TM3-4 loop of the glycine receptor modulates receptor desensitization (2015) Langlhofer G, Janzen D, Meiselbach H, Villmann C Journal article Disturbed neuronal ER-Golgi sorting of unassembled glycine receptors suggests altered subcellular processing is a cause of human hyperekplexia (2015) Schaefer N, Kluck C, Price KL, Meiselbach H, Vornberger N, Schwarzinger S, Hartmann S, et al. Journal article The interaction between cyclin B1 and cytomegalovirus protein kinase pUL97 is determined by an active kinase domain (2015) Steingruber M, Socher E, Hutterer C, Webel R, Bergbrede T, Lenac T, Sticht H, Marschall M Journal article, Original article Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma (2015) Pasutto F, Mauri L, Popp B, Sticht H, Ekici AB, Piozzi E, Bonfante A, et al. Journal article A severe congenital myasthenic syndrome with "dropped head" caused by novel MUSK mutations (2015) Giarrana ML, Joset P, Sticht H, Robb S, Steindl K, Rauch A, Klein A Journal article