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[Report of the molecular pathology working group].
Laßmann S, Haller F, Siebolts U. Laßmann S, et al. Among authors: siebolts u. Pathologe. 2017 Nov;38(Suppl 2):239-241. doi: 10.1007/s00292-017-0345-2. Pathologe. 2017. PMID: 29018876 German. No abstract available.
[Report of the molecular pathology working group].
Haller F, Laßmann S, Siebolts U. Haller F, et al. Among authors: siebolts u. Pathologe. 2018 Dec;39(Suppl 2):339-340. doi: 10.1007/s00292-018-0511-1. Pathologe. 2018. PMID: 30259103 German. No abstract available.
[Report of the working group on molecular pathology].
Haller F, Laßmann S, Siebolts U. Haller F, et al. Among authors: siebolts u. Pathologe. 2019 Dec;40(Suppl 3):393-395. doi: 10.1007/s00292-019-00655-0. Pathologe. 2019. PMID: 31705240 German. No abstract available.
Harmonization and Standardization of Panel-Based Tumor Mutational Burden Measurement: Real-World Results and Recommendations of the Quality in Pathology Study.
Stenzinger A, Endris V, Budczies J, Merkelbach-Bruse S, Kazdal D, Dietmaier W, Pfarr N, Siebolts U, Hummel M, Herold S, Andreas J, Zoche M, Tögel L, Rempel E, Maas J, Merino D, Stewart M, Zaoui K, Schlesner M, Glimm H, Fröhling S, Allen J, Horst D, Baretton G, Wickenhauser C, Tiemann M, Evert M, Moch H, Kirchner T, Büttner R, Schirmacher P, Jung A, Haller F, Weichert W, Dietel M. Stenzinger A, et al. Among authors: siebolts u. J Thorac Oncol. 2020 Jul;15(7):1177-1189. doi: 10.1016/j.jtho.2020.01.023. Epub 2020 Feb 29. J Thorac Oncol. 2020. PMID: 32119917 Free article.
Targeted ultra-deep sequencing reveals recurrent and mutually exclusive mutations of cancer genes in blastic plasmacytoid dendritic cell neoplasm.
Stenzinger A, Endris V, Pfarr N, Andrulis M, Jöhrens K, Klauschen F, Siebolts U, Wolf T, Koch PS, Schulz M, Hartschuh W, Goerdt S, Lennerz JK, Wickenhauser C, Klapper W, Anagnostopoulos I, Weichert W. Stenzinger A, et al. Among authors: siebolts u. Oncotarget. 2014 Aug 15;5(15):6404-13. doi: 10.18632/oncotarget.2223. Oncotarget. 2014. PMID: 25115387 Free PMC article.
Tubular, lactating, and ductal adenomas are devoid of MED12 Exon2 mutations, and ductal adenomas show recurrent mutations in GNAS and the PI3K-AKT pathway.
Volckmar AL, Leichsenring J, Flechtenmacher C, Pfarr N, Siebolts U, Kirchner M, Budczies J, Bockmayr M, Ridinger K, Lorenz K, Herpel E, Noske A, Weichert W, Klauschen F, Schirmacher P, Penzel R, Endris V, Stenzinger A. Volckmar AL, et al. Among authors: siebolts u. Genes Chromosomes Cancer. 2017 Jan;56(1):11-17. doi: 10.1002/gcc.22396. Epub 2016 Aug 9. Genes Chromosomes Cancer. 2017. PMID: 27438523
79 results