Kowalski K, Makul M, Ernstberger P , Radocaj A, Beck J, Becker E, Tripathi S, Keyser B, Mühlfeld C, Wissel K, Pich A, van der Velden J, Dos Remedios CG, Perrot A, Francino A, Navarro-López F, Brenner B, Kraft [...] associated with variants of BRD7, a component of p53 and BRCA1 pathways. Fam Cancer. 2012 Dec;11(4):601-6. Poffers M, Bühne N , Herzog C, Thorenz A, Chen R, Güler F, Hage A, Leffler A, Echtermeyer F. Sodium Channel [...] R, Beckmann J, Schürmann P, Hanel P, Jentschke M, Böhmer G, Strauß HG, Hirchenhain C, Schmidmayr M, Müller F, Fasching P, Luyten A, Häfner N, Dürst M, Runnebaum IB, Hillemanns P, Dörk T, Ramachandran D

6. Möbus S, Yang D, Yuan Q, Lüdtke TH, Balakrishnan A, Sgodda M, Rani B, Kispert A, Vogel A, Manns MP, Ott M, Cantz T, Sharma AD . MicroRNA-199a-5p inhibition enhances liver repopulation ability of human [...] 100626. Dai Z, Song G, Balakrishnan A, Yang T, Yuan Q, Möbus S, Weiss AC, Bentler M, Zhu J, Jiang XM, Shen X, Bantel H, Jaeckel E, Kispert A, Vogel A, Saborowski A, Büning H, Manns MP, Cantz T, Ott M and [...] Jul;73(1):6-8. Krooss SA, Dai Z, Schmidt F, Rovai A, Fakhiri J, Dhingra A, Yuan Q, Yang T, Balakrishnan A, Steinbruck L, Srivaratharajan S, Manns MP, Schambach A, Grimm D, Bohne J, Sharma AD , Buning H, Ott

then receive a therapy recommendation and, if necessary, a prescription. If required, we will arrange for nutritional counselling including keeping a food diary. If there is a suspicion of a familial lipid [...] lipid metabolism disorder, we will recommend a genetic examination, which can then be carried out by a referral from your GP during a consultation with a human geneticist. If your lipid metabolism disorder [...] specialist practices. Contact and office hours Appointments Mon, Wed and Fri: 8:00 a.m. to 2:00 p.m. Tue and Thu: 8:00 a.m. to 12:00 p.m. Telephone +49 511 532-3161 Fax +49 511 532-6268 Location Building K2, Level

https://orcid.org/0000-0002-7280-5663 ): Oelschlegel AM, Bhattacharjee R, Wenk P, Harit K, Rothkötter HJ, Koch SP, Boehm-Sturm P, Matuschewski K, Budinger E, Schlüter D, Goldschmidt J, Nishanth G ( 2024) Beyond [...] s E, Bhuria V, Baldauf CK, Korthals M, Handschuh J, Müller P, Li J, Harit K, Nishanth G , Frey S, Böttcher M, Fischer KD, Dudeck J, Dudeck A, Lipka DB, Schraven B, Green AR, Müller AJ, Mougiakakos D, Fischer [...] ligase TRAF2. Cell Death Dis. 14(7):480. doi: 10.1038/s41419-023-06014-5. Stutz A, Nishanth G , Zenclussen AC, Schumacher A(2022) Partial otubain 1 deficiency compromises fetal well-being in allogeneic

Bruder, G. Hansen, A.-M. Dittrich. PLoS One. 2012;7(9):e45916. A new mechanism for inhalational priming: IL-4 bypasses innate immune signals . A.- M. Dittrich, H.-C. Chen, L. Xu, P. Ranney, S. Connolly [...] fibrosis lung disease . M. Hagner, M. Albrecht, M.Guerra, P.Braubach, O. Halle, Z. Zhou-Suckow, S. Butz, D. Jonigk, G.Hansen, C. Schultz, A.-M. Dittrich, M. A Mall. Eur Respir J2020. Preventive Inhalation of [...] Bovermann, L. Liboschik, A. Steinmetz, D. Tennhardt, F. Dörfler, J. Röhmel, K. Unorji-Frank, C. Rückes-Nilges, B. von Stoutz, L. Naehrlich, M. V. Kopp, A.-M. Dittrich, O. Sommerburg, M. A. Mall. ERJ Open Res

and Endocrinology 2nd year of study (MSE_P_202 Diagnostic methods) In the Diagnostic Methods module, you will learn how to take a medical history and perform a physical examination in small groups. Lecturers [...] techniques, supervise you in your first steps as a doctor and, if possible, examine patients on the wards together with you. 3rd year of study (MSE_P_312 block internship in internal medicine) In the [...] year, please contact Dr. Sabine Bintaro . 4th and 5th year (MSE_P_425 Internal Medicine I and II) In six lectures, our lecturers will give you a case-based orientation on the following topics: Stomach and

Mathias M, Millar CM, Nathwani A, Neerman-Arbez M, Nurden AT, Nurden P, Othman M, Peerlinck K, Perry DJ, Poudel P, Reitsma P, Rondina MT, Smethurst PA, Stevenson W, Szkotak A, Tuna S, van Geet C, Whitehorn [...] 24750412 MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations. Pecci A, Klersy C, Gresele P, Lee KJ, De Rocco D, Bozzi V [...] Epub 2013 Apr 2. PMID: 23463630 A novel G6PC3 gene mutation in a patient with severe congenital neutropenia. Aytekin C, Germeshausen M, Tuygun N, Dogu F, Ikinciogullari A. J Pediatr Hematol Oncol. 2013

for patients in these contexts is that 1. a multitude of diseases can lead to kidney damage, 2. kidney diseases are often characterized by a complex interplay of a multitude of different cell types, and 3 [...] PMID: 28028135; PMCID: PMC5461802. Aue A*, Hinze C* , Walentin K, Ruffert, Yurtdas Y, Werth M, Chen W, Rabien A, Kilic E, Schulzke JD, Schumann M, Schmidt-Ott KM: A grainyhead-like 2/ovo-like 2 pathway regulates [...] of Nephrology , 29:857-868, 2018. Xu K, Rosenstiel P, Paragas N, Hinze C , Gao X, Huai Shen T, Werth M, Forster C, Deng R, Bruck E, Boles RW, Tornato A, Gopal T, Jones M, Konig J, Stauber J, D'Agati V,

Brinkert, S. Hedtfeld, A. Burhop, R. Gastmeier, P. Gad, D. Wedekind, C. Kloth, J. Rothschuh, N. Lachmann, M. Hetzel, A. Chari Jirmo, E. Lopez-Rodriguez, C. Brandenberger, G. Hansen, A. Schambach, M. Ackermann [...] vitro and in vivo genome restoration for cystic fibrosis . S. Guan, A. Munder, S. Hedtfeld, P. Braubach, S. Glage, L. Zhang, S. Lienenklaus, A. Schultze, G. Hasenpusch, W. Garrels, F. Stanke, C. Miskey, S. [...] Ackermann, B. Tümmler, A. Munder. Mol Ther 2020:S1525-0016(20)30660-2. Why? -Successful Pseudomonas aeruginosa clones with a focus on clone. C. Lee, J. Klockgether, S. Fischer, J. Trcek, B. Tümmler, U. Römling

Katzka, C., Rai, A., Wolf, A., Brockmeyer, A., Janning, P., Reubold, T.F. , Eschenburg, S., Manstein, D.J., Hübel, K., Kaiser, M., Waldmann, H. (2009) The Ras pathway modulator melophlin A targets dynamins [...] 696-701. Tossidou I, Teng B, Worthmann K, Muller-Deile J, Jobst-Schwan T, Kardinal C, Schroder P, Bolanos-Palmieri P, Haller H, Willerding J, Drost DM, de Jonge L, Reubold T . F. , Eschenburg S, Johnson RI & [...] cleft: functional characterisation of myosin II with a strut mutation. J. Muscle Res. Cell Motil. 27 , 115-123. Reubold, T.F. , Eschenburg, S., Becker, A., Leonard, M., Schmid, S.L., Vallee, R.B., Kull, F