Professur für Bioinformatik


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

Structure-based functional analysis of effector protein SifA in living cells reveals motifs important for Salmonella intracellular proliferation (2018) Namakchian M, Kaßler K, Sticht H, Hensel M, Deiwick J Journal article Interaction of Glycolipids with the Macrophage Surface Receptor Mincle - a Systematic Molecular Dynamics Study (2018) Söldner C, Horn A, Sticht H Journal article, Original article Amino-Terminal Processing of Helicobacter pylori Serine Protease HtrA: Role in Oligomerization and Activity Regulation (2018) Albrecht N, Tegtmeyer N, Sticht H, Skorko-Glonek J, Backert S Journal article Binding of histamine to the H1 receptora molecular dynamics study (2018) Söldner C, Horn A, Sticht H Journal article, Original article Conformational Dynamics of Herpesviral NEC Proteins in Different Oligomerization States (2018) Diewald B, Socher E, Söldner C, Sticht H Journal article The polynucleotide kinase 3'-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25 (2018) Leal A, Bogantes-Ledezma S, Ekici AB, Uebe S, Thiel C, Sticht H, Berghoff M, et al. Journal article Analysis of naturally occurring mutations in the human uptake transporter NaCT important for bone and brain development and energy metabolism (2018) Selch S, Chafai A, Sticht H, Birkenfeld AL, Fromm M, König J Journal article Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature (2018) Hauer N, Popp B, Schoeller E, Schuhmann S, Heath KE, Hisado-Oliva A, Klinger P, et al. Journal article De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder (2018) Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, et al. Journal article Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila (2018) Straub J, Konrad E, Grüner J, Toutain A, Bok LA, Cho MT, Crawford HP, et al. Journal article