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Unpublished / Preprint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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Abstract

Journal

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