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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)
Types of publications
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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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Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures (2019)
Zweier M, Begemann A, Mcwalter K, Cho MT, Abela L, Banka S, Behring B, et al.
Journal article
A Metadynamics-Based Protocol for the Determination of GPCR-Ligand Binding Modes (2019)
Söldner C, Horn A, Sticht H
Journal article, Original article
A Multiple Piccolino-RIBEYE Interaction Supports Plate-Shaped Synaptic Ribbons in Retinal Neurons (2019)
Müller T, Gierke K, Joachimsthaler A, Sticht H, Izsvak Z, Hamra FK, Fejtová A, et al.
Journal article
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot (2019)
Reuter MS, Jobling R, Chaturvedi RR, Manshaei R, Costain G, Heung T, Curtis M, et al.
Journal article
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study (2019)
Papuc SM, Abela L, Steindl K, Begemann A, Simmons TL, Schmitt B, Zweier M, et al.
Journal article
Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes (2019)
Begemann A, Acuna MA, Zweier M, Vincent M, Steindl K, Bachmann-Gagescu R, Hackenberg A, et al.
Journal article
Campylobacter jejuni enters gut epithelial cells and impairs intestinal barrier function through cleavage of occludin by serine protease HtrA (2019)
Harrer A, Buecker R, Böhm M, Zarzecka U, Tegtmeyer N, Sticht H, Schulzke JD, Backert S
Journal article
De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies (2019)
Platzer K, Sticht H, Edwards SL, Allen W, Angione KM, Bonati MT, Brasington C, et al.
Journal article
Alkali ion influence on structure and stability of fibrillar amyloid-beta oligomers (2019)
Huraskin D, Horn A
Journal article
Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia (2019)
Iqbal Z, Tawamie H, Ba W, Reis A, Halak BA, Sticht H, Uebe S, et al.
Journal article
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