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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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New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics (2020)
Begemann A, Sticht H, Begtrup A, Vitobello A, Faivre L, Banka S, Alhaddad B, et al.
Journal article
Fine-Tuning of Neuronal Ion Channels-Mapping of Residues Involved in Glucose Sensitivity of Recombinant Human Glycine Receptors (2020)
Hussein RA, Ahmed M, Sticht H, Breitinger HG, Breitinger U
Journal article
A proline-rich motif in the large intracellular loop of the glycine receptor α1 subunit interacts with the Pleckstrin homology domain of collybistin (2020)
Breitinger U, Weinländer K, Pechmann Y, Langlhofer G, Enz R, Becker CM, Sticht H, et al.
Journal article
Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine (2020)
Durmus H, Sticht H, Ceylaner S, Hashemolhosseini S, Deymeer F
Journal article
Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders (2020)
Abdelfattah F, Kariminejad A, Kahlert AK, Morrison PJ, Gumus E, Mathews KD, Darbro BW, et al.
Journal article
Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis (2020)
Frey S, Sticht H, Wilsmann-Theis D, Gerschütz A, Wolf K, Löhr S, Haskamp S, et al.
Journal article
T4SS-dependent TLR5 activation by Helicobacter pylori infection (2019)
Suneesh Kumar P, Tegtmeyer N, Arnold IC, Lind J, Neddermann M, Falkeis-Veits C, Chattopadhyay S, et al.
Journal article
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum (2019)
Konrad E, Nardini N, Caliebe A, Nagel I, Young D, Horvath G, Santoro SL, et al.
Journal article
De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures (2019)
Horn S, Au M, Basel-Salmon L, Bayrak-Toydemir P, Chapin A, Cohen L, Elting MW, et al.
Journal article
Solution structure of the autophagy-related protein LC3C reveals a polyproline II motif on a mobile tether with phosphorylation site (2019)
Krichel C, Möckel C, Schillinger O, Huesgen PF, Sticht H, Strodel B, Weiergräber OH, et al.
Journal article
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