Professur für Humangenetik

Schwabachanlage 10
91054 Erlangen

Publikationen (Download BibTeX)

Zundler, S., Becker, E., Spocinska, M., Slawik, M., Parga-Vidal, L., Stark, R.,... Neurath, M. (2019). Hobit- and Blimp-1-driven CD4(+) tissue-resident memory T cells control chronic intestinal inflammation. Nature Immunology, 20(3), 288-+.
Jitschin, R., Böttcher, M., Saul, D., Lukassen, S., Bruns, H., Loschinski, R.,... Mougiakakos, D. (2019). Inflammation-induced glycolytic switch controls suppressivity of mesenchymal stem cells via STAT1 glycosylation. Leukemia.
Lukassen, S., Bosch, E., Ekici, A.B., & Winterpacht, A. (2018). Characterization of germ cell differentiation in the male mouse through single-cell RNA sequencing. Scientific Reports, 8(1).
Reichel, A., Stilp, A.-C., Scherer, M., Reuter, N., Lukassen, S., Kasmapour, B.,... Stamminger, T. (2018). Chromatin-Remodeling Factor SPOC1 Acts as a Cellular Restriction Factor against Human Cytomegalovirus by Repressing the Major Immediate Early Promoter. Journal of Virology, 92(14).
Lukassen, S., Bosch, E., Ekici, A.B., & Winterpacht, A. (2018). Single-cell RNA sequencing of adult mouse testes. Scientific Data, 5.
Namer, B., Schmidt, D., Eberhardt, E., Maroni, M., Dorfmeister, E., Kleggetveit, I.P.,... Lampert, A. (2018). Pain relief in a neuropathy patient by lacosamide: Proof of principle of clinical translation from patient-specific iPS cell-derived nociceptors. EBioMedicine.
Klinger, P., Lukassen, S., Ferrazzi, F., Ekici, A.B., Hotfiel, T., Swoboda, B.,... Gelse, K. (2017). PEDF Is Associated with the Termination of Chondrocyte Phenotype and Catabolism of Cartilage Tissue. BioMed Research International, 2017, 7183516.
Dimova, V., Loetsch, J., Hühne, K., Winterpacht, A., Heesen, M., Parthum, A.,... Lautenbacher, S. (2015). Association of genetic and psychological factors with persistent pain after cosmetic thoracic surgery. Journal of Pain Research, 8, 829-44.
Rohde, D., Schmitt, H., Winterpacht, A., & Münster, T. (2014). Duchenne muscular dystrophy and malignant hyperthermia: a genetic study of the ryanodine receptor in 47 patients. European Journal of Anaesthesiology, 31(6), 341-2.
Eberhardt, M., Nakajima, J., Klinger, A., Neacsu, C., Hühne, K., o' Reilly, A.,... Lampert, A. (2014). Inherited pain: sodium channel Nav1.7 A1632T mutation causes erythromelalgia due to a shift of fast inactivation. Journal of Biological Chemistry, 289(4), 1971-80.
Neacsu, C.D., Ko, Y.-P., Tagariello, A., Karlsen, K.R., Neiss, W.F., Paulsson, M., & Wagener, R. (2014). Matrilin-1 is essential for zebrafish development by facilitating collagen II secretion. Journal of Biological Chemistry, 289(3), 1505-18.
Tagariello, A., Breuer, C., Birkner, Y., Schmidt, S., Koch, A.M., Cesnjevar, R.,... Toka, O. (2012). Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta. Current Molecular Medicine, 12(2), 199-205.

Zuletzt aktualisiert 2019-24-04 um 10:29