Prof. Dr. Heinrich Sticht


Professur für Bioinformatik

Mitarbeit in Forschungsprojekten

EFI-MCS: Molekulare Kommunikationssysteme
Prof. Dr.-Ing. Robert Schober
(01.01.2017 - 31.12.2019)

Publikationen (Download BibTeX)

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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).
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.
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.
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.
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.
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.
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.
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.
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.
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.

Zuletzt aktualisiert 2016-04-06 um 05:30