inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations. Hum Mol Genet 2017; 26(9): 1716-1731 Kröger N, Panagiota V, Badbaran A, Zabelina T, Triviai I, Araujo Cruz MM, Shahswar [...] encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease. Nat Genet 2017; 49(7): 1025-1034 Lüdemann W, Banan R , Hartmann C , Bertalanffy H, Di Rocco C: Pediatric in
A, Hagedorn M, Ebersold J, Kreipe HH, Krüger A, Schambach A, Schlegelberger B, Göhring G. Cancer Genet. 2016 Jun;209(6):258-66. doi: 10.1016/j.cancergen.2016.04.004. Preclinical validation: LV/IL-12 t [...] Maeder ML, Riedel H, Fisch P, Cantz T, Rudolph C, Mussolino C, Joung JK, Schambach A, Cathomen T. PLoS Genet. 2015 May 22;11(5):e1005239. doi: 10.1371/journal.pgen.1005239. eCollection 2015 May. Hyperactivation
improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy. Hum Mol Genet. 2019 Apr 15;28(8):1260-1273. Fledrich R, Akkermann D, Schütza V, Abdelaal TA, Hermes D, Schäffner [...] ameliorates neurophysiology and hypomyelination in a Charcot-Marie-Tooth type 1B mouse model. Hum Mol Genet. 2019 Mar 15;28(6):992-1006. Stapel B, Gorinski N, Gmahl N, Rhein M, Preuss V, Hilfiker-Kleiner D
141- Embryologie QS 604- Endokrinologie WK Forensik W 601- Gastroenterologie WI Geburtshilfe WQ Genetik QU 450- Geriatrie WT Geschichte der Medizin WZ Gesetzgebung K Gesundheitswesen WA Gynäkologie WP
Ethische, psychologische und soziale Implikationen in der Bereitstellung von Risikoinformationen durch genetische und andere relevante Technologien“ gefördert durch den Riksbankens Jubileumsfonds for the Humanities
(2015). Context-Dependent Functional Divergence of the Notch Ligands DLL1 and DLL4 In Vivo. PLoS Genet 11, e1005328. 48. Ramalingam, N., Franke, C., Jaschinski, E., Winterhoff, M., Lu, Y., Bruhmann, S [...] type-specific role of septins in microtubule destabilization for the completion of cytokinesis. PLoS Genet 10: e1004558. 79. Muller, J., Rana, N.A., Serth, K., Kakuda, S., Haltiwanger, R.S. and Gossler, A [...] spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilin. Hum Mol Genet 20, 4865-4878. 163. Nothmann, D., Leinenweber, A., Torres-Salazar, D., Kovermann, P., Hotzy, J., Gameiro
ting protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT). Hum Genet 2016; 135(1): 69-87 Krüger M, Zinne N, Shin H, Zhang R, Biancosino C, Kropivnitskaja I, Länger F [...] factors inducing chromosomal instability in myelodysplastic syndrome: Pitfalls and successes. Cancer Genet 2016; 209(6): 258-266 Schlenk RF, Stegelmann F, Reiter A, Jost E, Gattermann N, Hebart H, Waller C
multisomatoform disorder in a group of German multisomatoform disorder patients and healthy controls. Genet Test Mol Biomarkers. 2010 Jun;14(3):293-7. Jörgens G , Bange FC, Mühlradt PF, Pabst R, Maus UA, Tschernig [...] CCR7 in patients with systemic lupus erythematosus, Sjogren's syndrome and systemic sclerosis. BMC Genet. 2007;8:33. Tischer S, Kaireit T , Figueiredo C, Hiller O, Maecker-Kolhoff B, Geyeregger R, Immenschuh [...] modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation. Eur J Hum Genet. 2011 Dec;19(12):1281-8. Amrute-Nayak, M.*, Lambeck, K.* , Radocaj, A., Huhnt, H., Scholz, T., Hahn
Birgit/Stoff, Heiko/Rehmann-Sutter, Christoph, “The Past and Future of ‘Sex Genes’”, in: Medizinische Genetik 35.3. (2023), S. 153-161. Bock von Wülfingen, Bettina, et al. "Hochschulpolitischer Aktivismus in
Laenger F, Jonigk D, Luisetti M: Clinical utility gene card for: α-1-antitrypsin deficiency. Eur J Hum Genet 2011; 19(5): doi:10.1038/ejhg.2010.246 Jonigk D, Golpon H, Bockmeyer CL, Maegel L, Hoeper MM, Gottlieb