7 Einträge gefunden

1. Subclones with the t(9;22)/BCR-ABL1 rearrangement occur in AML and seem to cooperate with distinct genetic alterations.

   1. Bacher, Ulrike
   2. Haferlach, Torsten
   3. Alpermann, Tamara
   4. Zenger, Melanie
   5. Hochhaus, Andreas
   6. Beelen, Dietrich W
   7. Uppenkamp, Michael

   2011 - Forschungsinformationssystem des UKE
2. Several lymphoma-specific genetic events in parallel can be found in mature B-cell neoplasms.

   1. Bacher, Ulrike
   2. Haferlach, Torsten
   3. Alpermann, Tamara
   4. Kern, Wolfgang
   5. Schnittger, Susanne
   6. Haferlach, Claudia

   2011 - Forschungsinformationssystem des UKE
3. 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.

   1. Schnittger, Susanne
   2. Bacher, Ulrike
   3. Eder, Christiane
   4. Lohse, Peter
   5. Haferlach, Claudia
   6. Kern, Wolfgang
   7. Haferlach, Torsten

   2011 - Forschungsinformationssystem des UKE
4. 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.

   1. Bacher, Ulrike
   2. Haferlach, Claudia
   3. Alpermann, Tamara
   4. Kern, Wolfgang
   5. Schnittger, Susanne
   6. Haferlach, Torsten

   2011 - Forschungsinformationssystem des UKE - frei zugänglich
5. 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.

   1. Haferlach, Claudia
   2. Bacher, Ulrike
   3. Kohlmann, Alexander
   4. Schindela, Sonja
   5. Alpermann, Tamara
   6. Kern, Wolfgang
   7. Schnittger, Susanne

   2011 - Forschungsinformationssystem des UKE - frei zugänglich
6. Acute monoblastic/monocytic leukemia and chronic myelomonocytic leukemia share common immunophenotypic features but differ in the extent of aberrantly expressed antigens and amount of granulocytic cells.

   1. Kern, Wolfgang
   2. Bacher, Ulrike
   3. Haferlach, Claudia
   4. Schnittger, Susanne
   5. Haferlach, Torsten

   2011 - Forschungsinformationssystem des UKE
7. Clinical impact of FLT3 mutation load in acute promyelocytic leukemia with t(15;17)/PML-RARA.

   1. Schnittger, Susanne
   2. Bacher, Ulrike
   3. Haferlach, Claudia
   4. Kern, Wolfgang
   5. Alpermann, Tamara
   6. Haferlach, Torsten

   2011 - Forschungsinformationssystem des UKE - frei zugänglich