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- Kern, Wolfgang
- Bacher, Ulrike 37
- Schnittger, Susanne 37
- Haferlach, Claudia 35
- Haferlach, Torsten 35
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38 Einträge gefunden
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TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining allele.
- Bacher, Ulrike
- Weissmann, Sandra
- Kohlmann, Alexander
- Schindela, Sonja
- Alpermann, Tamara
- Schnittger, Susanne
- Kern, Wolfgang
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Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases.
- Schnittger, Susanne
- Bacher, Ulrike
- Alpermann, Tamara
- Reiter, Andreas
- Ulke, Madlen
- Dicker, Frank
- Eder, Christiane
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Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflow.
- Schnittger, Susanne
- Bacher, Ulrike
- Eder, Christiane
- Dicker, Frank
- Alpermann, Tamara
- Grossmann, Vera
- Kohlmann, Alexander
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Multilineage dysplasia does not influence prognosis in CEBPA-mutated AML, supporting the WHO proposal to classify these patients as a unique entity.
- Bacher, Ulrike
- Schnittger, Susanne
- Macijewski, Katja
- Grossmann, Vera
- Kohlmann, Alexander
- Alpermann, Tamara
- Kowarsch, Andreas
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CDKN1B, encoding the cyclin-dependent kinase inhibitor 1B (p27), is located in the minimally deleted region of 12p abnormalities in myeloid malignancies and its low expression is a favorable prognostic marker in acute myeloid leukemia.
- Haferlach, Claudia
- Bacher, Ulrike
- Kohlmann, Alexander
- Schindela, Sonja
- Alpermann, Tamara
- Kern, Wolfgang
- Schnittger, Susanne
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Clinical impact of FLT3 mutation load in acute promyelocytic leukemia with t(15;17)/PML-RARA.
- Schnittger, Susanne
- Bacher, Ulrike
- Haferlach, Claudia
- Kern, Wolfgang
- Alpermann, Tamara
- Haferlach, Torsten
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Comparison of genetic and clinical aspects in patients with acute myeloid leukemia and myelodysplastic syndromes all with more than 50% of bone marrow erythropoietic cells.
- Bacher, Ulrike
- Haferlach, Claudia
- Alpermann, Tamara
- Kern, Wolfgang
- Schnittger, Susanne
- Haferlach, Torsten
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Several lymphoma-specific genetic events in parallel can be found in mature B-cell neoplasms.
- Bacher, Ulrike
- Haferlach, Torsten
- Alpermann, Tamara
- Kern, Wolfgang
- Schnittger, Susanne
- Haferlach, Claudia
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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 controls.
- Schnittger, Susanne
- Bacher, Ulrike
- Eder, Christiane
- Lohse, Peter
- Haferlach, Claudia
- Kern, Wolfgang
- Haferlach, Torsten
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Comparison of cytogenetic clonal evolution patterns following allogeneic hematopoietic transplantation versus conventional treatment in patients at relapse of AML.
- Bacher, Ulrike
- Haferlach, Torsten
- Alpermann, Tamara
- Zenger, Melanie
- Kröger, Nicolaus
- Beelen, Dietrich W
- Kern, Wolfgang
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The role of multiparameter flow cytometry for disease monitoring in AML.
2010 - Forschungsinformationssystem des UKE -
Multilineage dysplasia (MLD) in acute myeloid leukemia (AML) correlates with MDS-related cytogenetic abnormalities and a prior history of MDS or MDS/MPN but has no independent prognostic relevance: a comparison of 408 cases classified as "AML not otherwise specified" (AML-NOS) or "AML with myelodysplasia-related changes" (AML-MRC).
- Miesner, Miriam
- Haferlach, Claudia
- Bacher, Ulrike
- Weiss, Tamara
- Macijewski, Katja
- Kohlmann, Alexander
- Klein, Hans-Ulrich