Prof. Dr. Andreas Winterpacht



Organisation


Professur für Humangenetik


Publications (Download BibTeX)


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). https://dx.doi.org/10.1038/s41598-018-24725-0
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). https://dx.doi.org/10.1128/JVI.00342-18
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. https://dx.doi.org/10.1016/j.ebiom.2018.11.042
Lukassen, S., Bosch, E., Ekici, A.B., & Winterpacht, A. (2018). Single-cell RNA sequencing of adult mouse testes. Scientific Data, 5. https://dx.doi.org/10.1038/sdata.2018.192
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. https://dx.doi.org/10.2147/JPR.S90434
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. https://dx.doi.org/10.1097/EJA.0000000000000053
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. https://dx.doi.org/10.1074/jbc.M113.502211
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. https://dx.doi.org/10.2174/156652412798889027

Last updated on 2016-15-06 at 05:06