Prof. Dr. Heinrich Sticht

Professur für Bioinformatik

The C-terminal coiled-coil domain of Corynebacterium diphtheriae DIP0733 is crucial for interaction with epithelial cells and pathogenicity in invertebrate animal model systems (2018) Weerasekera D, Stengel F, Sticht H, De Mattos Guaraldi AL, Burkovski A, Azevedo Antunes de Oliveira C Journal article, Original article Probing the potential of CnaB-type domains for the design of tag/catcher systems (2017) Pröschel M, Kraner M, Horn A, Schäfer L, Sonnewald U, Sticht H Journal article Structural and functional dissection reveals distinct roles of Ca2+-binding sites in the giant adhesin SiiE of Salmonella enterica (2017) Peters B, Stein J, Klingl S, Sander N, Sandmann A, Taccardi N, Sticht H, et al. Journal article, Original article Structural and functional dissection reveals distinct roles of Ca2+-binding sites in the giant adhesin SiiE of Salmonella enterica (2017) Peters B, Stein J, Klingl S, Sander N, Sandmann A, Taccardi N, Sticht H, et al. Journal article, Original article Dynamic regulatory interaction between cytomegalovirus major tegument protein pp65 and protein kinase pUL97 in intracellular compartments, dense bodies and virions (2017) König P, Buescher N, Steingruber M, Socher E, Sticht H, Tenzer S, Plachter B, Marschall M Journal article Confirmation of mutations inPROSCas a novel cause of vitamin B 6 -dependent epilepsy (2017) Plecko B, Zweier M, Begemann A, Mathis D, Schmitt B, Striano P, Baethmann M, et al. Journal article Role of the N-terminus for the stability of an amyloid-β fibril with three-fold symmetry (2017) Söldner C, Sticht H, Horn A Journal article Protective capacity of neutralizing and non-neutralizing antibodies against glycoprotein B of cytomegalovirus (2017) Bootz A, Karbach A, Spindler J, Kropff B, Reuter N, Sticht H, Winkler T, et al. Journal article Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation (2017) Asadollahi R, Zweier M, Gogoll L, Schiffmann R, Sticht H, Steindl K, Rauch A Journal article Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID (2017) Redler S, Strom TM, Wieland T, Cremer K, Engels H, Distelmaier F, Schaper J, et al. Journal article