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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
(295)
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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Translation
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Thesis
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Unpublished / Preprint
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Mimicking titration experiments with MD simulations: A protocol for the investigation of pH-dependent effects on proteins (2016)
Socher E, Sticht H
Journal article, Original article
Selection and Characterization of Tau Binding ᴅ-Enantiomeric Peptides with Potential for Therapy of Alzheimer Disease (2016)
Dammers C, Yolcu D, Kukuk L, Willbold D, Pickhardt M, Mandelkow E, Horn A, et al.
Journal article
Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma (2016)
Mauri L, Uebe S, Sticht H, Vossmerbaeumer U, Weisschuh N, Manfredini E, Maselli E, et al.
Journal article
The Prolyl Isomerase Pin1 Promotes the Herpesvirus-Induced Phosphorylation-Dependent Disassembly of the Nuclear Lamina Required for Nucleocytoplasmic Egress (2016)
Milbradt J, Hutterer C, Bahsi H, Wagner S, Sonntag E, Horn A, Kaufer BB, et al.
Journal article
Analysis of amino acid residues in the predicted transmembrane pore influencing transport kinetics of the hepatic drug transporter organic anion transporting polypeptide 1B1 (OATP1B1) (2016)
Gruetz M, Sticht H, Gläser H, Fromm M, König J
Journal article
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly (2016)
Breuss MW, Sultan T, James KN, Rosti RO, Scott E, Musaev D, Furia B, et al.
Journal article, Erratum
Modulation of Recombinant Human ?1 Glycine Receptors by Mono- and Disaccharides: A Kinetic Study (2016)
Breitinger U, Sticht H, Breitinger HG
Journal article
Investigation of the dynamics of the viral immediate-early protein 1 in different conformations and oligomerization states (2016)
Stump J, Sticht H
Journal article
N(8)-acetylspermidine as a potential plasma biomarker for Snyder-Robinson syndrome identified by clinical metabolomics (2016)
Abela L, Simmons L, Steindl K, Schmitt B, Mastrangelo M, Joset P, Papuc M, et al.
Journal article
SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss (2016)
Buchert R, Nesbitt AI, Tawamie H, Krantz ID, Medne L, Helbig I, Matalon DR, et al.
Journal article
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