U, Kreipe H. Combination of myeloproliferative neoplasm driver gene activation with mutations of splice factor or epigenetic modifier genes increases risk of rapid blastic progression. Eur J Haematol. 2021 [...] Wolf S, Preller M, Aretz S, Wiese B, Hartmann C , Weber RG. Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin. Acta [...] Klöppel G. Mesenchymal/non-epithelial mimickers of neuroendocrine neoplasms with a focus on fusion gene-associated and SWI/SNF-deficient tumors. Virchows Arch. 2021 Aug 5. doi: 10.1007/s00428-021-03156-9
Hülskötter K, Schreiner T, Wohlsein P, Schmitz J , Bräsen JH , Distl O. Genes (Basel) . 2023 Nov 25;14(12):2126. doi: 10.3390/genes14122126. Valuing vicinity: Memory attention framework for context-based [...] 1164/rccm.202212-2314LE. Online ahead of print. PMID: 36731065 No abstract available. Fibrosis-Related Gene Profiling in Liver Biopsies of PiZZ α1-Antitrypsin Children with Different Clinical Courses Kamp JC [...] Mastrocola R, Kar A, Khan B, Gand L, Nayak A, Hartmann C , Kunz WS, Samii A, Bertalanffy H, Retta SF. Genes Dis. 2023 Apr 3;11(1):67-71. doi: 10.1016/j.gendis.2023.02.045. eCollection 2024 Jan. A Novel Alu
Interferon-lambda and interleukin 22 act synergistically for the induction of interferon-stimulated genes and control of rotavirus infection. Nat Immunol 2015; 16: 698-707. Horst SA, Itzek A, Klos A, Beineke [...] M, Bleich A, Johnsen JM, Vallance BA, Baines JF, Grassl GA. Expression of the blood-group-related gene B4galnt2 alters susceptibility to Salmonella infection PLoS Pathog 2015; 11: e1005008. Rücker N, Billig
Down-regulation of the fetal stem cell factor SOX17 by H33342: a mechanism responsible for differential gene expression in breast cancer side population cells. J Biol Chem. 2010; 285(9):6412-8 4. Poehnert D [...] Wicke DC, Meyer J, Buesche G , Heckl D, Kreipe H , Li Z, Welte KH, Ballmaier M, Baum C, Modlich U: Gene therapy of MPL deficiency: challenging balance between leukemia and pancytopenia. Mol Ther. 2010;
eine erbliche Motoneuronerkrankung, hervorgerufen durch Mutationen im SMN (survival of motoneuron) Gen. Durch Verlust motorischer Nervenzellen im Rückenmark kommt es zu einer fortschreitenden Abnahme der
from a patient's symptoms down to the specific molecular mechanisms involved. Mutations in the actin genes ACTB and ACTG1 can result in developmental disorders and organ malformations collectively referred
chronisch entzündlichen ebenso wie angeborene Krankheiten betreffen und darüber hinau s. Zell- und Gen-basierte Therapien, die von der Transplantation von klassischen blutbildenden oder mesenchymalen S
Tsiavaliaris, G., Hensel, N., Viero, G., Ponimaskin, E., & Claus, P. ( 2024 ). The spinal muscular atrophy gene product regulates actin dynamics. FASEB Journal , https://doi.org/10.1096/fj.202300183R Diensthuber
Gadzicki D, v Neuhoff N, Steinemann D, Just M, Büsche G, Kreipe H, Wilkens L, Schlegelberger B: BCR-ABL gene amplification and overexpression in a patient with chronic myeloid leukemia treated with imatinib [...] Serinsöz E, Bock O, Kirsch T, Haller H, Lehmann U, Kreipe H, Mengel M: Compartment-specific quantitative gene expression analysis after laser microdissection from archival renal allograft biopsies. Clin Nephrol
März 2022 bis voraussichtlich Dezember 2025 Links zu Ergebnissen des Vorläuferprojektes (GEENGOV): Gene and Genome Editing 2022 , Science & Engineering Ethics 2022 Klausurwoche „Tierversuchsethik als Z