Professur für Bioinformatik

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Fahrstraße 17
91054 Erlangen


Publikationen (Download BibTeX)

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Zweier, M., Begemann, A., Mcwalter, K., Cho, M.T., Abela, L., Banka, S.,... Rauch, A. (2019). Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures. European journal of human genetics, 27(5), 747-759. https://dx.doi.org/10.1038/s41431-018-0331-z
Söldner, C., Horn, A., & Sticht, H. (2019). A Metadynamics-Based Protocol for the Determination of GPCR-Ligand Binding Modes. International Journal of Molecular Sciences, 20(8). https://dx.doi.org/10.3390/ijms20081970
Müller, T., Gierke, K., Joachimsthaler, A., Sticht, H., Izsvak, Z., Hamra, F.K.,... Regus-Leidig, H. (2019). A Multiple Piccolino-RIBEYE Interaction Supports Plate-Shaped Synaptic Ribbons in Retinal Neurons. Journal of Neuroscience, 39(14), 2606-2619. https://dx.doi.org/10.1523/JNEUROSCI.2038-18.2019
Reuter, M.S., Jobling, R., Chaturvedi, R.R., Manshaei, R., Costain, G., Heung, T.,... Bassett, A.S. (2019). Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot. Genetics in Medicine, 21(4), 1001-1007. https://dx.doi.org/10.1038/s41436-018-0260-9
Papuc, S.M., Abela, L., Steindl, K., Begemann, A., Simmons, T.L., Schmitt, B.,... Rauch, A. (2019). The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study. European journal of human genetics, 27(3), 408-421. https://dx.doi.org/10.1038/s41431-018-0299-8
Begemann, A., Acuna, M.A., Zweier, M., Vincent, M., Steindl, K., Bachmann-Gagescu, R.,... Rauch, A. (2019). Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes. Molecular Medicine, 25. https://dx.doi.org/10.1186/s10020-019-0073-6
Harrer, A., Buecker, R., Böhm, M., Zarzecka, U., Tegtmeyer, N., Sticht, H.,... Backert, S. (2019). Campylobacter jejuni enters gut epithelial cells and impairs intestinal barrier function through cleavage of occludin by serine protease HtrA. Gut Pathogens, 11. https://dx.doi.org/10.1186/s13099-019-0283-z
Platzer, K., Sticht, H., Edwards, S.L., Allen, W., Angione, K.M., Bonati, M.T.,... Jamra, R. (2019). De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies. American Journal of Human Genetics, 104(2), 203-212. https://dx.doi.org/10.1016/j.ajhg.2018.12.008
Huraskin, D., & Horn, A. (2019). Alkali ion influence on structure and stability of fibrillar amyloid-beta oligomers. Journal of Molecular Modeling, 25(2). https://dx.doi.org/10.1007/s00894-018-3920-4
Iqbal, Z., Tawamie, H., Ba, W., Reis, A., Halak, B.A., Sticht, H.,... Abou Jamra, R. (2019). Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia. Genetics in Medicine. https://dx.doi.org/10.1038/s41436-018-0415-8
Hauer, N., Popp, B., Taher, L., Vogl, C., Dhandapany, P.S., Büttner, C.,... Thiel, C. (2019). Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature. European journal of human genetics. https://dx.doi.org/10.1038/s41431-019-0362-0
Cantone, M., Küspert, M., Reiprich, S., Lai, X., Eberhardt, M., Göttle, P.,... Vera, J. (2019). A gene regulatory architecture that controls region-independent dynamics of oligodendrocyte differentiation. Glia. https://dx.doi.org/10.1002/glia.23569
Steingruber, M., Keller, L., Socher, E., Ferre, S., Hesse, A.-M., Coute, Y.,... Marschall, M. (2019). Cyclins B1, T1, and H differ in their molecular mode of interaction with cytomegalovirus protein kinase pUL97. Journal of Biological Chemistry, 294(15), 6188-6203. https://dx.doi.org/10.1074/jbc.RA118.007049
Konrad, E., Nardini, N., Caliebe, A., Nagel, I., Young, D., Horvath, G.,... Zweier, C. (2019). CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum. Genetics in Medicine. https://dx.doi.org/10.1038/s41436-019-0585-z
Ilyaskin, A., Kirsch, S., Böckmann, R., Sticht, H., Korbmacher, C., Härteis, S., & Diakov, A. (2018). The degenerin region of the human bile acid-sensitive ion channel (BASIC) is involved in channel inhibition by calcium and activation by bile acids. Pflugers Archiv : European journal of physiology. https://dx.doi.org/10.1007/s00424-018-2142-z
Albrecht, N., Tegtmeyer, N., Sticht, H., Skorko-Glonek, J., & Backert, S. (2018). Amino-Terminal Processing of Helicobacter pylori Serine Protease HtrA: Role in Oligomerization and Activity Regulation. Frontiers in Microbiology, 9. https://dx.doi.org/10.3389/fmicb.2018.00642
Namakchian, M., Kaßler, K., Sticht, H., Hensel, M., & Deiwick, J. (2018). Structure-based functional analysis of effector protein SifA in living cells reveals motifs important for Salmonella intracellular proliferation. International Journal of Medical Microbiology, 308(1), 84-96. https://dx.doi.org/10.1016/j.ijmm.2017.09.004
Söldner, C., Horn, A., & Sticht, H. (2018). Interaction of Glycolipids with the Macrophage Surface Receptor Mincle - a Systematic Molecular Dynamics Study. Scientific Reports, 8. https://dx.doi.org/10.1038/s41598-018-23624-8
Söldner, C., Horn, A., & Sticht, H. (2018). Binding of histamine to the H1 receptora molecular dynamics study. Journal of Molecular Modeling, 24(12). https://dx.doi.org/10.1007/s00894-018-3873-7
Diewald, B., Socher, E., Söldner, C., & Sticht, H. (2018). Conformational Dynamics of Herpesviral NEC Proteins in Different Oligomerization States. International Journal of Molecular Sciences, 19(10). https://dx.doi.org/10.3390/ijms19102908


Zusätzliche Publikationen (Download BibTeX)


Atak, S., Langlhofer, G., Schaefer, N., Kessler, D., Meiselbach, H., Delto, C.,... Villmann, C. (2015). Disturbances of Ligand Potency and Enhanced Degradation of the Human Glycine Receptor at Affected Positions G160 and T162 Originally Identified in Patients Suffering from Hyperekplexia. Frontiers in Molecular Neuroscience, 8, 79. https://dx.doi.org/10.3389/fnmol.2015.00079

Zuletzt aktualisiert 2019-24-04 um 10:29