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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 11

Zeitschriftenartikel

Bao, Xuanwen; Wang, Jing; Zhou, Guangming; Aszodi, Attila; Schoenitzer, Veronika; Scherthan, Harry; Atkinson, Michael J. und Rosemann, Michael (2020): Extended in vitro culture of primary human mesenchymal stem cells downregulates Brca1-related genes and impairs DNA double-strand break recognition. In: FEBS Open Bio, Bd. 10, Nr. 7: S. 1238-1250

Beinke, Christina; Scherthan, Harry; Port, Matthias; Popp, Tanja; Hermann, Cornelius und Eder, Stefan (2020): Triterpenoid CDDO-Me induces ROS generation and up-regulates cellular levels of antioxidative enzymes without induction of DSBs in human peripheral blood mononuclear cells. In: Radiation and Environmental Biophysics, Bd. 59, Nr. 3: S. 461-472

Jensen, Lars R.; Garrett, Lillian; Hoelter, Sabine M.; Rathkolb, Birgit; Racz, Ildiko; Adler, Thure; Prehn, Cornelia; Hans, Wolfgang; Rozman, Jan; Becker, Lore; Aguilar-Pimentel, Juan Antonio; Puk, Oliver; Moreth, Kristin; Dopatka, Monika; Walther, Diego J.; Bohlen und Halbach, Viola von; Rath, Matthias; Delatycki, Martin; Bert, Bettina; Fink, Heidrun; Bluemlein, Katharina; Ralser, Markus; Dijck, Anke van; Kooy, Frank; Stark, Zornitza; Müller, Sabine; Scherthan, Harry; Gecz, Jozef; Wurst, Wolfgang; Wolf, Eckhard; Zimmer, Andreas; Klingenspor, Martin; Graw, Jochen; Klopstock, Thomas; Busch, Dirk; Adamski, Jerzy; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Bohlen und Halbach, Oliver von; Ropers, Hans-Hilger und Kuss, Andreas W. (2019): A mouse model for intellectual disability caused by mutations in the X-linked 2 '-O-methyltransferase Ftsj1 gene. In: Biochimica et Biophysica Acta-Molecular Basis of Disease, Bd. 1865, Nr. 9: S. 2083-2093

Styllou, Panorea; Styllou, Marianthi; Nickel, Reinhard; Högg, Christof; Reichl, Franz Xaver und Scherthan, Harry (2017): NAC ameliorates dental composite-induced DNA double-strand breaks and chromatin condensation. In: Dental Materials Journal, Bd. 36, Nr. 5: S. 638-646

Wittmann, Anke; Grimm, Marcus O. W.; Scherthan, Harry; Horsch, Marion; Beckers, Johannes; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Ford, Steven J.; Burton, Neal C.; Razansky, Daniel; Trümbach, Dietrich; Aichler, Michaela; Walch, Axel Karl; Calzada-Wack, Julia; Neff, Frauke; Wurst, Wolfgang; Hartmann, Tobias und Floss, Thomas (2016): Sphingomyelin Synthase 1 Is Essential for Male Fertility in Mice.
In: PLOS ONE 11(10), e0164298 [PDF, 5MB]

Caldwell, Randolph B.; Braselmann, Herbert; Schötz, Ulrike; Heuer, Steffen; Scherthan, Harry und Zitzelsberger, Horst (2016): Positive Cofactor 4 (PC4) is critical for DNA repair pathway re-routing in DT40 cells. In: Scientific Reports, Bd. 6, 28890 [PDF, 1MB]

Scherthan, Harry; Cremer, Thomas; Arnason, U.; Weier, Heinz-Ulrich; Lima-de-Faria, A. und Fönicke, L. (1994): Comparative chromosome painting discloses homologous Segments in distantly related mammals. In: Nature Genetics, Bd. 6: S. 342-347 [PDF, 1MB]

Scherthan, Harry und Cremer, Thomas (1994): Nonisotopic in situ hybridization in paraffin-embedded tissue sections. In: Methods in Molecular Genetics, Bd. 5: S. 223-238 [PDF, 1MB]

Joos, Stefan; Scherthan, Harry; Speicher, Michael R.; Schlegel, Jürgen; Cremer, Thomas und Lichter, Peter (1993): Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe. In: Human Genetics, Bd. 90, Nr. 6: S. 584-589 [PDF, 2MB]

Cremer, Thomas; Kurz, A.; Zirbel, R. M.; Dietzel, S.; Rinke, B.; Schröck, Evelin; Speicher, Michael R.; Mathieu, U. R.; Jauch, Anna; Emmerich, Patricia; Scherthan, Harry; Ried, Thomas; Cremer, Christoph und Lichter, Peter (1993): The role of chromosome territories in the funtional compartmentalization of the cell nucleus. In: Cold Spring Harbor Symposia on Quantitative Biology, Bd. 58: S. 777-792 [PDF, 3MB]

Buchbeitrag

Cremer, Thomas; Lichter, Peter; Popp, Susanne; Schröck, Evelin; Jauch, Anna; Manoir, Stanislas du; Joos, Stefan; Lengauer, Christoph; Scherthan, Harry; Ried, Thomas und Speicher, Michael R. (1993): Detection of genetic imbalances in tumor genomes by fluorescence in situ hybridization with tumor genomic DNA and subregional DNA probes. In: Obe, Günter und Natarajan, Adayapalam T. (Hrsg.): Chromosomal alterations. Berlin u.a.: Springer. S. 42-49 [PDF, 1MB]

Diese Liste wurde am Sat Dec 21 19:09:14 2024 CET erstellt.