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- Haferlach, Torsten
- Bacher, Ulrike 49
- Schnittger, Susanne 41
- Haferlach, Claudia 38
- Kern, Wolfgang 35
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50 Einträge gefunden
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Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q)
- Hecht, Anna
- Meyer, Julia A
- Jann, Johann-Christoph
- Sockel, Katja
- Giagounidis, Aristoteles
- Götze, Katharina S
- Letsch, Anne
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Postallogeneic monitoring with molecular markers detected by pretransplant next-generation or Sanger sequencing predicts clinical relapse in patients with myelodysplastic/myeloproliferative neoplasms
- Fu, Yuewen
- Schroeder, Thomas
- Zabelina, Tatiana
- Badbaran, Anita
- Bacher, Ulrike
- Kobbe, Guido
- Ayuketang, Francis Ayuk
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Relapse assessment following allogeneic SCT in patients with MDS and AML
2014 - Forschungsinformationssystem des UKE -
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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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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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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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Ganglioneuroblastoma infiltrating the bone marrow in an adult.
- Bacher, Ulrike
- Christopeit, Maximilian
- Wiedemann, Bettina
- Leuschner, Ivo
- Haferlach, Torsten
- Choschzick, Matthias
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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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Unusual course of myelodysplastic syndrome with presumed familial origin.
- Bacher, Ulrike
- Ocheni, Sunday
- Schafhausen, Philippe
- Oyekunle, Anthony
- Dierlamm, Judith
- Zander, Axel R.
- Bokemeyer, Carsten
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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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Molecular diagnostics, targeted therapy, and the indication for allogeneic stem cell transplantation in acute lymphoblastic leukemia.
- Oyekunle, Anthony
- Haferlach, Torsten
- Kröger, Nicolaus
- Klyuchnikov, Evgeny
- Zander, Axel R.
- Schnittger, Susanne
- Bacher, Ulrike
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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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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