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Experimental Hematology|October 5, 2010
A copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: an analysis in 1135 patients with AML and 187 healthy controlsSusanne Schnittger, Ulrike Bacher, Christiane Eder, et al.Leukemia Research|January 17, 2015
AML with gain of chromosome 8 as the sole chromosomal abnormality (+8sole) is associated with a specific molecular mutation pattern including ASXL1 mutations in 46.8% of the patientsTamara Alpermann, Claudia Haferlach, Christiane Eder, et al.Particle and Fibre Toxicology|October 20, 2009
Ultrafine carbon particles down-regulate CYP1B1 expression in human monocytesChristiane Eder, Marion Frankenberger, Franz Stanzel, et al.Annals of Hematology|September 10, 2015
Evaluation of IDH1G105 polymorphism as prognostic marker in intermediate-risk AMLAnnette Fasan, Claudia Haferlach, Christiane Eder, et al.Plos One|February 6, 2013
Frequency and prognostic impact of CEBPA proximal, distal and core promoter methylation in normal karyotype AML: a study on 623 casesAnnette Fasan, Tamara Alpermann, Claudia Haferlach, et al.Haematologica|April 19, 2012
Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflowSusanne Schnittger, Ulrike Bacher, Christiane Eder, et al.The Journal of Molecular Diagnostics : JMD|March 1, 2011
Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technologyVera Grossmann, Susanne Schnittger, Sonja Schindela, et al.Molecular Medicine (Cambridge, Mass.)|February 18, 2011
Chemokine expression by small sputum macrophages in COPDMarion Frankenberger, Christiane Eder, Thomas P J Hofer, et al.Cytometry. Part a : the Journal of the International Society for Analytical Cytology|July 28, 2010
Standardized single-platform assay for human monocyte subpopulations: Lower CD14+CD16++ monocytes in femalesIrene Heimbeck, Thomas P J Hofer, Christiane Eder, et al.British Journal of Haematology|March 26, 2013
CEBPA double-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosisVera Grossmann, Claudia Haferlach, Niroshan Nadarajah, et al.Pageof 2