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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
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Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta (2012)
Tagariello A, Breuer C, Birkner Y, Schmidt S, Koch AM, Cesnjevar R, Rueffer A, et al.
Journal article
Specific residues of a conserved domain in the N terminus of the human cytomegalovirus pUL50 protein determine its intranuclear interaction with pUL53 (2012)
Milbradt J, Auerochs S, Sevvana M, Muller Y, Sticht H, Marschall M
Journal article
Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I (2011)
Rotthier A, Penno A, Rautenstrauss B, Auer-Grumbach M, Stettner GM, Asselbergh B, Van Hoof K, et al.
Journal article
A comparative study of HIV-1 and HTLV-I protease structure and dynamics reveals a conserved residue interaction network (2011)
Ruecker P, Horn A, Meiselbach H, Sticht H
Journal article
Rational design of ?-sheet ligands against A?42-induced toxicity (2011)
Hochdoerffer K, Maerz-Berberich J, Nage-Steger L, Epple M, Meyer-Zaika W, Horn A, Sticht H, et al.
Journal article
Phenotypic variability in a large Czech family with a Dynamin 2-associated Charcot-Marie-Tooth neuropathy (2011)
Haberlova J, Mazanec R, Ridzon P, Barankova L, Nuernberg G, Nuernberg P, Sticht H, et al.
Journal article
Structural characterization of intracellular C-terminal domains of group III metabotropic glutamate receptors. (2011)
Seebahn A, Dinkel H, Mohrlüder J, Hartmann R, Vogel N, Becker CM, Sticht H, Enz R
Journal article
Sumo E3 ligases are expressed in the retina and regulate sumoylation of the metabotropic glutamate receptor 8b. (2011)
Duetting E, Schroeder-Kress N, Sticht H, Enz R
Journal article
Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6) (2011)
Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, Sticht H, et al.
Journal article
Effect of the SH3-SH2 domain linker sequence on the structure of Hck kinase (2011)
Meiselbach H, Sticht H
Journal article
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