Combined polymerase chain reaction methods to detect c-myc/IgH rearrangement in childhood Burkitt's lymphoma for minimal residual disease analysis
Jochen Harbott , Wilhelm Wössmann , Kerstin Busch , Alfred Reiter
Haematologica 89 ( 7) 818 -825
30
2004
Improved effector function of leukemia-specific T-lymphocyte clones trained with AML-derived dendritic cells.
Bernd Hubner , Helga Schmetzer , Roland Reibke , Anja Liepert
Cancer Genomics & Proteomics 5 ( 5) 275 -286
6
2008
NQO1 C609T polymorphism in distinct entities of pediatric hematologic neoplasms
Jochen Harbott , Rolf Marschalek , Sabine Strehl , Gunnar Cario
Haematologica 89 ( 12) 1492 -1497
35
2004
RNA interference: new mechanisms for targeted treatment?
Christine Damm-Welk , Willi Woessmann , Arndt Borkhardt , Uta Fuchs
Reviews in Clinical and Experimental Hematology 7 ( 3) 270
17
2003
Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome. Commentary
Charles G. Mullighan , Gilad Wainreb , Smadar Avigad , Chen Shochat
The Lancet 372 ( 9648)
2008
HEMATOPOIETIC STEM CELL TRANSPLANTATION RESCUES THE VASCULAR, HAEMATOLOGICAL AND IMMUNOLOGICAL PHENOTYPE IN ADENOSINE DEAMINASE 2 DEFICIENCY
Stephan Ehl , Michael Hershfield , Robert A Krance , Joris van Montfrans
Journal of Clinical Immunology 37 ( 2) 247 -248
1
2017
Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II
Zahra Aryan , Nima Rezaei , Samaneh Zoghi , Aziz Eghbali
Acta medica Iranica 56 ( 8) 494 -497
2018
A novel mtDNA large-scale mutation clinically exclusively presenting with refractory anemia: is there a chance to predict disease progression?
Arndt Borkhardt , Vera Binder , Hans-Juergen Laws , Laura Steenpass
Journal of Pediatric Hematology Oncology 34 ( 4) 283 -292
7
2012
The Landscape of Circular RNAs in Drug Resistant TCF3-Rearranged Childhood Leukemia
Sebastian Ginzel , Daniel Picard , Michael Gombert , Ute Fischer
Blood 130 1432 -1432
2017
Development of Novel Proteasome-HDAC6 Hybrid Inhibitors for Resistant ALL Phenotype
Finn Hansen , Arndt Borkhardt , Sanil Bhatia , Julia Hauer
Blood 130 2070 -2070
2017
AML SCT-BFM 2007: Results of the Prospective Hematopoietic Stem Cell Transplantation (HCT) Trial of the Berlin-Frankfurt-Münster (BFM) Study Group for Children with Very High Risk Acute Myeloid Leukemia
Dirk Reinhardt , Martin G. Sauer , Christina Peters , Arndt Borkhardt
Blood 130 599 -599
1
2017
Osteonecrosis after Allogeneic HSCT in Children with High-Risk or Relapsed ALL Treated in the ALL-SCT 2003 Trial
Evgenia Glogova , Arend von Stackelberg , Johanna Schrum , Brigitte Strahm
Blood 130 2004 -2004
2017
Response to Front-Line Imatinib Treatment in Children and Adolescents with CML - Data from a Large Pediatric Cohort
Andreas H Groll , Guenter Henze , Martin Schrappe , Christoph Klein
Blood 130 898 -898
2017
Oxa Analogues of Nexturastat A Demonstrate Improved HDAC6 Selectivity and Superior Antileukaemia Activity
Matthias U. Kassack , Alexandra Hamacher , Finn K. Hansen , Thomas Kurz
ChemMedChem
2021
HLA-E expression constitutes a novel determinant for ALL disease monitoring following hematopoietic stem cell transplantation.
Leonid Karawajew , Stefanie Groeneveld-Krentz , Sarah B. Reusing , Roland Meisel
Bone Marrow Transplantation 1 -5
2021
Haematological characteristics and spontaneous haematological recovery in Pearson syndrome.
Holger Cario , Stephan Lobitz , Daniela Karall , Sarah C Grünert
British Journal of Haematology
2021
Deep Transfer Learning Approach for Automatic Recognition of Drug Toxicity and Inhibition of SARS-CoV-2.
Julia Werner , Raphael M Kronberg , Pawel Stachura , Philipp N Ostermann
Viruses 13 ( 4) 610
2021
Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer.
Christoph Bartenhagen , Andishe Attarbaschi , Udo Kontny , Ute Fischer
European Journal of Human Genetics 1 -11
25
2021
Circular RNA profiling distinguishes medulloblastoma groups and shows aberrant RMST overexpression in WNT medulloblastoma
Guido Reifenberger , Guido Reifenberger , Daniel Picard , Christelle Dufour
Acta Neuropathologica 141 ( 6) 975 -978
2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation.
Elsa Wiame , Ramona Salvarinova , Miriam Elbracht , Daniela Choukair
Journal of Clinical Investigation 143078
1
2021