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Professur für Bioinformatik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die nicht zum Universitätsklinikum Erlangen gehören
Institut für Biochemie
Overview
Publications
(290)
Research Grants
(4)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Authored book
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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
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