(Translated by https://www.hiragana.jp/)
author:"Fink, A.-M." - Search Results - DKFZ
DKFZ 6 records found  Search took 0.01 seconds. 
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[DKFZ-2021-01066] Journal Article
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Discovery of candidate DNA methylation cancer driver genes.
Cancer discovery 11(9), 2266-2281 () [10.1158/2159-8290.CD-20-1334]  GO
Epigenetic alterations such as promoter hypermethylation may drive cancer through tumor suppressor genes inactivation. However, we have limited ability to differentiate driver DNA methylation (DNAme) changes from passenger events. [...]
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pmc [DKFZ-2019-02309] Journal Article
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Short telomeres are associated with inferior outcome, genomic complexity, and clonal evolution in chronic lymphocytic leukemia.
Leukemia 33(9), 2183 - 2194 () [10.1038/s41375-019-0446-4]  GO
Telomere length in chronic lymphocytic leukemia (CLL) has been shown to be of prognostic importance, but the analyses have largely been executed on heterogeneous patient cohorts outside of clinical trials. In the present study, we performed a comprehensive analysis of telomere length associations in the well characterized CLL8 trial (n = 620) of the German CLL study group, with validation in a representative cohort of the CLL4 trial (n = 293). [...]
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[DKFZ-2017-04534] Journal Article
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PTK2 expression and immunochemotherapy outcome in chronic lymphocytic leukemia.
Blood 124(3), 420 - 425 () [10.1182/blood-2013-12-538975]  GO
Addition of rituximab (R) to fludarabine and cyclophosphamide (FC) has significantly improved patient outcomes in chronic lymphocytic leukemia (CLL). Whether baseline gene expression can identify patients who will benefit from immunochemotherapy over chemotherapy alone has not been determined. [...]
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[DKFZ-2017-04409] Journal Article
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Gene mutations and treatment outcome in chronic lymphocytic leukemia: results from the CLL8 trial.
Blood 123(21), 3247 - 3254 () [10.1182/blood-2014-01-546150]  GO
Mutations in TP53, NOTCH1, and SF3B1 were analyzed in the CLL8 study evaluating first-line therapy with fludarabine and cyclophosphamide (FC) or FC with rituximab (FCR) among patients with untreated chronic lymphocytic leukemia (CLL). TP53, NOTCH1, and SF3B1 were mutated in 11.5%, 10.0%, and 18.4% of patients, respectively. [...]

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