Prof. Dr. Heinrich Sticht

Professur für Bioinformatik

A specific A/T polymorphism in Western tyrosine phosphorylation B-motifs regulates Helicobacter pylori CagA epithelial cell interactions (2015) Zhang XS, Tegtmeyer N, Traube L, Jindal S, Perez-Perez G, Sticht H, Backert S, Blaser MJ Journal article Identification of a neutralizing epitope within antigenic domain 5 of glycoprotein B of human cytomegalovirus (2015) Wiegers AK, Sticht H, Winkler T, Britt WJ, Mach M Journal article MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and golgi architecture as a central mechanism in growth regulation (2015) Zahnleiter D, Hauer N, Keßler K, Uebe S, Sugano Y, Neuhauss SCF, Gießl A, et al. Journal article Inhibition of RAS activation due to a homozygous ezrin variant in patients with profound intellectual disability (2015) Riecken LB, Tawamie H, Dornblut C, Buchert R, Ismayel A, Schulz A, Schumacher J, et al. Journal article Characterization of recombinant human cytomegaloviruses encoding IE1 mutants L174P and 1-382 reveals that viral targeting of PML bodies perturbs both intrinsic and innate immune responses (2015) Scherer M, Otto V, Stump J, Klingl S, Müller R, Reuter N, Muller Y, et al. Journal article, Original article Synthetic Peptides as Protein Mimics (2015) Groß A, Hashimoto C, Sticht H, Eichler J 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