28. Jahrestagung der Kind-Philipp-Stiftung für pädiatrisch-onkologische Forschung

Abstracts (HTML) List of Authors

Beck, F

PAK2 (p21-activated kinase 2) – A Key Node in FLT3 Dependent Signaling in Acute Lymphoblastic Leukemia

Becker, K

NK1R as a therapeutic target in hepatoblastoma

Bens, S

Incidence and genetic characterization of childhood acute lymphoblastic leukemia with CRLF2 overexpression treated according to the AIEOP-BFM ALL 2009 protocol

Berger, C

What we learned from bench to bedside with the neuroblastoma targeting CD171-specific CAR

Berger, M

NK1R as a therapeutic target in hepatoblastoma

Bertele, D

Identification of compounds protecting donor stem cells from apoptosis and increasing efficacy of hematopoietic stem cell transplantation

Bleckmann, K

Prognostic relevance of the expression of genes associated with the P2RY8-CRLF2 fusion in acute lymphoblastic leukemia in childhood
Incidence and genetic characterization of childhood acute lymphoblastic leukemia with CRLF2 overexpression treated according to the AIEOP-BFM ALL 2009 protocol
Gene expression analysis of NK cell receptors and their ligands in childhood acute lymphoblastic leukemia with involvement of the central nervous system

Bomken, S

Control of Lineage Commitment in Acute Leukaemia

Bornhauser, B

Functional exploration of the leukemic niche of residual disease in the bone marrow

Bourquin, JP

Functional exploration of the leukemic niche of residual disease in the bone marrow

Brandner, JM

MITF controls the interface of nucleotide excision repair and transcription through direct regulation of GTF2H1

Bruckmueller, H

Gene expression analysis of NK cell receptors and their ligands in childhood acute lymphoblastic leukemia with involvement of the central nervous system

Buchmann, S

Prognostic relevance of the expression of genes associated with the P2RY8-CRLF2 fusion in acute lymphoblastic leukemia in childhood

Bulduk, M

A Case of Concordant Twins with Infant ALL and Discordant Clinical Outcome – Part II: highlights on an immunoescape phenotype as a potential mechanism of disease persistence
A Case of Concordant Twins with Infant ALL and Discordant Clinical Outcome – Part I: the genetic basis – identification of DSC2 as a gene with prognostic impact in infant MLL-rearranged ALL