Pellegrini D, Nasr A, Kutys B, Guo L, Cornelissen A , et al. Pathological Evidence for SARS-CoV-2 as a Cause of Myocarditis: JACC Review Topic of the Week. J Am Coll Cardiol. 2021 Jan 26; 77(3):314-325. doi: [...] Sakamoto A, Kawai K, Gianatti A, Nasr A, Kutys R, Guo L, Cornelissen A , et al. Microthrombi as a Major Cause of Cardiac Injury in COVID-19: A Pathologic Study. Circulation. 2021 Mar 9; 143(10):1031-1042. doi:
Die Epileptologie in Aachen beschäftigt sich mit der Untersuchung von genetischen Epilepsien mit dem Ziel der Entwicklung neuer Therapiestrategien.
emerging evidence suggests that microcalcification may contribute to plaque rupture the leading cause of myocardial infarction. Our major area of research is the identification of differential mechanisms
Lifton RP, Antonin W, Hildebrandt F (2016). Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome . Nature Genetics, 48 (4): 457-465. Weberruss M and Antonin W
P, Hansen NL, Bieling HB, Brümmendorf TH, Kuhl CK. Target lesion selection: an important factor causing variability of response classification in the Response Evaluation Criteria for Solid Tumors 1.1.
van Loo KM , van Bakel NN, Ellenbroek BA, Cools AR, Martens GJ (2006) Reduced Aph-1b expression causes tissue- and substrate-specific changes in gamma-secretase activity in rats with a complex phenotype
in Kooperation mit Kooperationspartnern im bundesweiten BMBF-geförderten Verbundprojekt "Diseases caused by imprinting defects" bearbeitet. Weiterhin leitet die Arbeitsgruppe das COST-geförderte (BM1208)
Riester M, Groß M, Maurer J, Diederichs S. A pan-cancer analysis reveals nonstop extension mutations causing SMAD4 tumour suppressor degradation . Nat Cell Biol. 2020 Aug;22(8):999-1010. doi: 10.1038/s4155 [...] Riester M, Groß M, Maurer J , Diederichs S. A pan-cancer analysis reveals nonstop extension mutations causing SMAD4 tumour suppressor degradation. Nat Cell Biol . 2020;22(8):999-1010. doi:10.1038/s41556-020-0551-7
Lifton RP, Antonin W, Hildebrandt F (2016). Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome . Nature Genetics, 48 (4): 457-465. Contact: Prof. Dr. Wolfram [...] for a medical thesis. Fetal akinesia deformation sequence (FADS) is a lethal neuromuscular disorder caused by defective proteins of the neuromuscular junction. Affected fetuses present with an inability to [...] Vermeersch M, Supply L, Martins N, Pirenne L, et al. 2018. Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence. PLoS Genet 14:e1007845. Jühlen R and Fahrenkrog B. 2018
Med . 2024;210:406-415. 5. Zhang X and van der Vorst EPC. High-Density Lipoprotein Modifications: Causes and Functional Consequences in Type 2 Diabetes Mellitus. Cells . 2024;13. 6. Wang Y, Li G, Chen B [...] Nazir S and van der Vorst EPC. High-Density Lipoprotein Modifications: A Pathological Consequence or Cause of Disease Progression? Biomedicines . 2020;8. Kiouptsi K, Pontarollo G, Todorov H, Braun J, Jackel