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Telomere length in poor-risk chronic lymphocytic leukemia: associations with disease characteristics and outcome.
Leuk Lymphoma. 2018 Jul;59(7):1614-1623. doi: 10.1080/10428194.2017.1390236. Epub 2017 Oct 24.
Leuk Lymphoma. 2018.
PMID: 29063805
Clinical Trial.
Genomic alterations in high-risk chronic lymphocytic leukemia frequently affect cell cycle key regulators and NOTCH1-regulated transcription.
Edelmann J, Holzmann K, Tausch E, Saunderson EA, Jebaraj BMC, Steinbrecher D, Dolnik A, Blätte TJ, Landau DA, Saub J, Estenfelder S, Ibach S, Cymbalista F, Leblond V, Delmer A, Bahlo J, Robrecht S, Fischer K, Goede V, Bullinger L, Wu CJ, Mertens D, Ficz G, Gribben JG, Hallek M, Döhner H, Stilgenbauer S.
Edelmann J, et al. Among authors: steinbrecher d.
Haematologica. 2020 May;105(5):1379-1390. doi: 10.3324/haematol.2019.217307. Epub 2019 Aug 29.
Haematologica. 2020.
PMID: 31467127
Free PMC article.
Clinical Trial.
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Impact of telomere length on the outcome of allogeneic stem cell transplantation for poor-risk chronic lymphocytic leukaemia: results from the GCLLSG CLL3X trial.
Scheffold A, Jebaraj BMC, Jaramillo S, Tausch E, Steinbrecher D, Hahn M, Böttcher S, Ritgen M, Bunjes D, Zeis M, Stadler M, Uharek L, Scheid C, Hegenbart U, Hallek M, Kneba M, Schmitz N, Döhner H, Dreger P, Stilgenbauer S.
Scheffold A, et al. Among authors: steinbrecher d.
Br J Haematol. 2017 Oct;179(2):342-346. doi: 10.1111/bjh.14219. Epub 2016 Jul 8.
Br J Haematol. 2017.
PMID: 27391907
Free article.
No abstract available.
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Rapid detection of ATM/p53 function with p27Kip FACS analysis: a novel diagnostic tool for chronic lympocytic leukemia?
Meyer-Pannwitt V, Steinbrecher D, Stilgenbauer S, Mertens D.
Meyer-Pannwitt V, et al. Among authors: steinbrecher d.
Leuk Lymphoma. 2017 Jan;58(1):6-7. doi: 10.1080/10428194.2016.1213837. Epub 2016 Aug 22.
Leuk Lymphoma. 2017.
PMID: 27545008
No abstract available.
Item in Clipboard
Targeted therapy in CLL: changing the treatment paradigm.
Schneider C, Steinbrecher D, Stilgenbauer S.
Schneider C, et al. Among authors: steinbrecher d.
Oncotarget. 2019 Jun 18;10(40):4002-4003. doi: 10.18632/oncotarget.26964. eCollection 2019 Jun 18.
Oncotarget. 2019.
PMID: 31258844
Free PMC article.
No abstract available.
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IGLV3-21*01 is an inherited risk factor for CLL through the acquisition of a single-point mutation enabling autonomous BCR signaling.
Maity PC, Bilal M, Koning MT, Young M, van Bergen CAM, Renna V, Nicolò A, Datta M, Gentner-Göbel E, Barendse RS, Somers SF, de Groen RAL, Vermaat JSP, Steinbrecher D, Schneider C, Tausch E, Bittolo T, Bomben R, Mazzarello AN, Del Poeta G, Kroes WGM, van Wezel JT, Imkeller K, Busse CE, Degano M, Bakchoul T, Schulz AR, Mei H, Ghia P, Kotta K, Stamatopoulos K, Wardemann H, Zucchetto A, Chiorazzi N, Gattei V, Stilgenbauer S, Veelken H, Jumaa H.
Maity PC, et al. Among authors: steinbrecher d.
Proc Natl Acad Sci U S A. 2020 Feb 25;117(8):4320-4327. doi: 10.1073/pnas.1913810117. Epub 2020 Feb 11.
Proc Natl Acad Sci U S A. 2020.
PMID: 32047037
Free PMC article.
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