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Therapeutical interference with the epigenetic landscape of germ cell tumors: a comparative drug study and new mechanistical insights

2022 . Müller, Melanie R. | Burmeister, Aaron | Skowron, Margaretha A. | Stephan, Alexa | Bremmer, Felix | Wakileh, Gamal A. | Petzsch, Patrick | Köhrer, Karl | Albers, Peter | Nettersheim, Daniel

Epigenetic adaptations of the masticatory mucosa to periodontal inflammation

Estimands in epigenome-wide association studies

2021 . Kruppa, Jochen | Sieg, Miriam | Richter, Gesa | Pohrt, Anne

Integrative study of EZH2 mutational status, copy number, protein expression and H3K27 trimethylation in AML/MDS patients

2021 . Stomper, Julia | Meier, Ruth | Ma, Tobias | Pfeifer, Dietmar | Ihorst, Gabriele | Blagitko-Dorfs, Nadja | Greve, Gabriele | Zimmer, Dennis | Platzbecker, Uwe | Hagemeijer, Anne | Schmitt-Graeff, Ingrid | Lübbert, Michael

Characteristics of epigenetic aging across gestational and perinatal tissues

Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation

2021 . Czamara, Darina | Dieckmann, Linda | Röh, Simone | Kraemer, Sarah | Rancourt, Rebecca C. | Sammallahti, Sara | Kajantie, Eero | Laivuori, Hannele | Eriksson, Johan G. | Räikkönen, Katri | Henrich, Wolfgang | Plagemann, Andreas | Binder, Elisabeth B. | Braun, Thorsten | Entringer, Sonja

CAMK2N1/RUNX3 methylation is an independent prognostic biomarker for progression-free and overall survival of platinum-sensitive epithelial ovarian cancer patients

2021 . Heinze, Karolin | Rengsberger, Matthias | Gajda, Mieczyslaw | Jansen, Lars | Osmers, Linea | Oliveira-Ferrer, Leticia | Schmalfeldt, Barbara | Dürst, Matthias | Häfner, Norman | Runnebaum, Ingo B.

Genome-wide DNA methylation profiling is able to identify prefibrotic PMF cases at risk for progression to myelofibrosis

2021 . Lehmann, Ulrich | Stark, Helge | Bartels, Stephan | Schlue, Jerome | Büsche, Guntram | Kreipe, Hans

Tracing TET1 expression in prostate cancer: discovery of malignant cells with a distinct oncogenic signature

2021 . Schagdarsurengin, U. | Luo, C. | Slanina, H. | Sheridan, D. | Füssel, S. | Böğürcü-Seidel, N. | Gattenloehner, S. | Baretton, G. B. | Hofbauer, L. C. | Wagenlehner, F. | Dansranjav, Temuujin

Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains

2021 . Eggermann, Thomas | Begemann, Matthias | Pfeiffer, Lutz

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