Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Annette Sindram"'
Autor:
Thomas Burmeister, Nicola Gökbuget, Stefan Schwartz, Lars Fischer, Daniela Hubert, Annette Sindram, Dieter Hoelzer, Eckhard Thiel
Publikováno v:
Haematologica, Vol 95, Iss 2 (2010)
Background The t(9;22) and t(4;11) chromosomal translocations, which generate the BCR-ABL and MLL-AF4 fusion genes, define high-risk subtypes of acute lymphoblastic leukemia in adults. However, the prognostic impact of other rarer fusion genes is les
Externí odkaz:
https://doaj.org/article/fb2404e92ad24a3a8ec7a7601b21e1e0
Publikováno v:
Leukemia & Lymphoma. 54:145-152
Mutation of the FMS-like tyrosine kinase-3 (FLT3) gene occurs with a frequency of 20-25% in acute myeloid leukemia (AML). Different studies have reported conflicting results, stating the importance of the length, position and number of internal tande
Autor:
Gundula Thiel, Olga Blau, Igor Wolfgang Blau, Thomas Burmeister, Seval Türkmen, Annette Sindram, Stefan Mundlos, Eckhard Thiel, Claudia D. Baldus, Florian Nolte, Wolf-Karsten Hofmann, Mara Molkentin, Ulrich Keilholz, Ouidad Benlasfer, Elke Schümann
Publikováno v:
Blood. 118:5583-5592
Mesenchymal stromal cells (MSCs) are an essential cell type of the hematopoietic microenvironment. Concerns have been raised about the possibility that MSCs undergo malignant transformation. Several studies, including one from our own group, have sho
Autor:
Nicola Gökbuget, Annette Sindram, Stefan Schwartz, Daniela Hubert, Eckhard Thiel, Dieter Hoelzer, Thomas Burmeister, Lars Fischer
Publikováno v:
Haematologica. 95:241-246
Background The t(9;22) and t(4;11) chromosomal translocations, which generate the BCR-ABL and MLL-AF4 fusion genes, define high-risk subtypes of acute lymphoblastic leukemia in adults. However, the prognostic impact of other rarer fusion genes is les
Publikováno v:
Leukemia Research. 25:769-774
In acute lymphoblastic leukemia (ALL) patients, automated fluorescence fragment analysis (ALF) has been reported to improve the monoclonality detection rate of immunoglobulin heavy chain genes (IgH) polymerase chain reaction (PCR) analysis. This stud
Autor:
Annette Sindram, Claudia D. Baldus, Olga Blau, Igor Wolfgang Blau, Bernd Dörken, Antonio Pezzutto, Rimma Berenstein, Asiye Kar, Sophie Schlabitz, Ruhiye Cay, Claudia Seide
Publikováno v:
Blood. 122:2627-2627
Abnormal epigenetic regulation has been implicated in oncogenesis. Mutations in the DNA methyltransferase 3A (DNMT3A) gene were recently demonstrated in acute myeloid leukemia (AML) as a candidate for the initiating of lesions in AML with adverse cli
Publikováno v:
Blood. 118:4868-4868
Abstract 4868 FLT3-ITD occurs with a frequency of 35%–45% in normal karyotype AML and has an adverse impact on prognosis. FLT3-ITD mutations are very variable in length and position of the tandem duplication. We have analyzed 211 AML patients with
Publikováno v:
Blood. 118:4482-4482
Abstract 4482 Allogeneic stem cell transplantation (alloSCT) is a curative treatment option for patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). Relapse after alloSCT is still a major cause for the treatment failure. Mole
Autor:
Eckhard Thiel, Thomas Burmeister, Sandra Heesch, Annette Sindram, Cornelia Schlee, Stefan Schwartz, Claudia D. Baldus, Isabelle Bartram
Publikováno v:
Blood. 116:1692-1692
Abstract 1692 Background: Acute leukemias of ambiguous lineage account for only 3–5% of all cases of acute leukemia and represent a heterogeneous group of rare, poorly characterized leukemia with adverse outcome. The aim of this study was to furthe
Autor:
Olga Blau, Elke Schuemann, Annette Sindram, Verena Nowak, Korinna Kuehne, Igor Wolfgang Blau, Eckhard Thiel, Wolf-Karsten Hofmann, Gundula Thiel, Claudia D. Baldus
Publikováno v:
Blood. 110:985-985
Introduction : The biology of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) is heterogeneous. Ineffective hematopoiesis results from complex interactions between hematopoietic cells (HC) and the hematopoietic microenvironment. Bone