H, Jankowski J, Lebherz C, Boor P, Marx N and Lehrke M. 2,8-Dihydroxyadenine-induced nephropathy causes hexosylceramide accumulation with increased mTOR signaling, reduced levels of protective SirT3 expression [...] H, Jankowski J, Lebherz C, Boor P, Marx N and Lehrke M. 2,8-Dihydroxyadenine-induced nephropathy causes hexosylceramide accumulation with increased mTOR signaling, reduced levels of protective SirT3 expression [...] Schmidt R, Boxem M and Leube RE. Intermediate filament network perturbation in the C. elegans intestine causes systemic dysfunctions. Elife . 2023;12. Bhargava S, Jankowski J, Merckelbach E, Roth CE, Craveiro
Das Institut für Pharmakologie und Toxikologie der Uniklinik RWTH Aachen erforscht, wie Arzneimittel wirken.
2020 Publikationen Lipprandt M ., Liedtke W., Langanke M., Klausen A., Baumgarten N., Röhrig R. : Causes of adverse events in home mechanical ventilation: a nursing perspective. BMC Nurs 21, 264 (2022) [...] Inform. 2023 May 18;302:626-630. doi: 10.3233/SHTI230224 Coldewey B , Diruf A, Röhrig R, Lipprandt M . Causes of use errors in ventilation devices - Systematic review. Appl Ergon. 2022 Jan;98:103544. doi: 10
Schmidt R, Boxem M and Leube RE. Intermediate filament network perturbation in the C. elegans intestine causes systemic dysfunctions. Elife . 2023;12. 2020 Wu Z, Jankowski V and Jankowski J. Irreversible pos [...] M, Jankowski J, Flockerzi V, Nusing R, Uhlig S and Kuebler WM. Stimulation of the EP(3) receptor causes lung oedema by activation of TRPC6 in pulmonary endothelial cells. Eur Respir J . 2022;60. Jiang [...] Schaefer M, Jankowski J, Flockerzi V, Nusing R, Uhlig S and Kuebler WM. Stimulation of the EP3 receptor causes lung edema by activation of TRPC6 in pulmonary endothelial cells. Eur Respir J . 2022. Jankowski
Wang LL, Antonin W, Jachimowicz RD, von Felbert V, Distelmaier F (2023). Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence. Genetics in Medicine: 100836 [...] P, Khokha MK, Hildebrandt F (2018). Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome . The Journal of Clinical Investigations. pii: 98688. doi: 10.1172/JCI98688. Holzer [...] 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. Antonin W and Neumann H (2016)
to say and makes your knees tremble. In this workshop, we will take some time to find out what may cause these uncomfortable feelings and will together collect some useful hints and background in order to
MRI, CT and PET images using analysis software. (Willuweit; 5 d). Genetics and gene therapy Genetic causes of retinal degenerative diseases, general principles of gene therapy, specifically the ocular gene
MC, Waters CS, Chen E, Chu LP, Novina CD, Lindsley RC, Carr SA, Ebert BL. Rps14 haploinsufficiency causes a block in erythroid differentiation mediated by S100A8/S100A9. Nature Medicine 2016 Mar;22(3):288-97 [...] Buonamici S, Smith PG, Mullally A, Wu CJ, Fleming MD and Ebert BL. Physiologic expression of Sfb1 K700E causes impaired erythropoiesis, aberrant splicing, and sensitivity to a spliceosome inhibitor. Cancer Cell
Das Institut für Neuropathologie der Uniklinik RWTH Aachen diagnostiziert und erforscht Krankheiten des Nervensystems und der Skelettmuskulatur am erkrankten Gewebe. Es untersucht das bei neurochirurgischen Operationen entnommene Material, vor allem Hirntumoren, außerdem Nerven-, Muskel- und Hautbiopsien, Liquor cerebrospinalis (Nervenwasser) und Autopsiegewebe, sowie Tier- und Zellkulturmodelle neurologischer Krankheiten.
In their work published today in Cell Stem Cell ( http://www.cell.com/action/showMethods?pii=S1934-5909(17)30079-6 ), they demonstrate that Gli1 marks a subset of bone marrow stromal cells that turn i