Prof. Dr. Heinrich Sticht

Professur für Bioinformatik

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 AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability (2017) Brechet A, Buchert R, Schwenk J, Boudkkazi S, Zolles G, Siquier-Pernet K, Schaber I, et al. Journal article Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly (2017) Tawamie H, Martianov I, Wohlfahrt N, Buchert R, Mengus G, Uebe S, Janiri L, et al. Journal article