about
A large kindred with X-linked neutropenia with an I294T mutation of the Wiskott-Aldrich syndrome gene.An early thymic precursor phenotype predicts outcome exclusively in HOXA-overexpressing adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia studyDirect interaction of Ikaros and Foxp1 modulates expression of the G protein-coupled receptor G2A in B-lymphocytes and acute lymphoblastic leukemia.Early Response-Based Therapy Stratification Improves Survival in Adult Early Thymic Precursor Acute Lymphoblastic Leukemia: A Group for Research on Adult Acute Lymphoblastic Leukemia Study.Cryptic XPO1-MLLT10 translocation is associated with HOXA locus deregulation in T-ALL.Successful treatment of acute Epstein-Barr virus infection associated with X-linked lymphoproliferative disorder with rituximab.Early thymic precursor-like lymphomatous presentation of the ETV6-NCOA2 translocation.Novel Intergenically Spliced Chimera, NFATC3-PLA2G15, Is Associated with Aggressive T-ALL Biology and Outcome.Use of SAG-M-suspended red cell concentrate in large volume transfusion associated with cardiac surgery in neonates and infants: a retrospective audit.Toward a NOTCH1/FBXW7/RAS/PTEN-based oncogenetic risk classification of adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study.RUNX1-dependent RAG1 deposition instigates human TCR-δ locus rearrangementNAP1L1-MLLT10is a rare recurrent translocation that is associated withHOXAactivation and poor treatment response in T-cell acute lymphoblastic leukaemiaCBFβ-MYH11 interferes with megakaryocyte differentiation via modulating a gene program that includes GATA2 and KLF1Chronic leukemiasDysregulation of the HIF pathway due to VHL mutation causing severe erythrocytosis and pulmonary arterial hypertensionPolymorphism in the PAI-1 (SERPINE1) gene and the risk of osteonecrosis in children with acute lymphoblastic leukemiaAllogeneic stem cell transplantation as immunotherapy for X-linked lymphoproliferative disease-associated cerebral T-cell lymphomaCBFβ-SMMHC regulates ribosomal gene transcription and alters ribosome biogenesisPolycomb repressive complex 2 haploinsufficiency identifies a high-risk subgroup of pediatric acute myeloid leukemiaDNMT3A mutation is associated with increased age and adverse outcome in adult T-cell acute lymphoblastic leukemiaEpigenetics of paediatric acute myeloid leukaemia
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description
researcher ORCID ID = 0000-0001-7636-1599
@en
wetenschapper
@nl
name
Jonathan Bond
@ast
Jonathan Bond
@en
Jonathan Bond
@es
Jonathan Bond
@nl
type
label
Jonathan Bond
@ast
Jonathan Bond
@en
Jonathan Bond
@es
Jonathan Bond
@nl
prefLabel
Jonathan Bond
@ast
Jonathan Bond
@en
Jonathan Bond
@es
Jonathan Bond
@nl
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0000-0001-7636-1599