about
Paediatric acute myeloid leukaemia with the t(7;12)(q36;p13) rearrangement: a review of the biological and clinical management aspectsThe tyrosine kinase abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): molecular cloning of both reciprocal transcripts.Folate deficiency as predisposing factor for childhood leukaemia: a review of the literature.Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype.HLXB9 gene expression, and nuclear location during in vitro neuronal differentiation in the SK-N-BE neuroblastoma cell line.Mutations of NFKBIA, encoding IkappaB alpha, are a recurrent finding in classical Hodgkin lymphoma but are not a unifying feature of non-EBV-associated cases.Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH.Genomic properties of chromosomal bands are linked to evolutionary rearrangements and new centromere formation in primates.Nuclear Repositioning of the Non-Translocated HLXB9 Allele in the Leukaemia Cell Line GDM-1 Harbouring a t(6;7)(q23;q36).Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias.Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.The radial arrangement of the human chromosome 7 in the lymphocyte cell nucleus is associated with chromosomal band gene densityFirst-trimester human trophoblast is class II major histocompatibility complex mRNA+/antigen−Reciprocal translocation t(12;13)(p13;q14) in acute nonlymphoblastic leukemia: Report and cytogenetic analysis of two casesFamilial partial monosomy 7 and myelodysplasiaNarrowing and genomic annotation of the commonly deleted region of the 5q- syndromeDelineation of multiple deleted regions in 7q in myeloid disordersClassification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH)Detection of the breakpoint cluster region-ABL fusion in chronic myeloid leukemia with variant Philadelphia chromosome translocations by in situ hybridizationDeletions of Chromosome 7q Affect Nuclear Organization and HLXB9Gene Expression in Hematological Disorders
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-0036-0191
@en
name
Sabrina Tosi
@ast
Sabrina Tosi
@en
Sabrina Tosi
@es
Sabrina Tosi
@nl
type
label
Sabrina Tosi
@ast
Sabrina Tosi
@en
Sabrina Tosi
@es
Sabrina Tosi
@nl
prefLabel
Sabrina Tosi
@ast
Sabrina Tosi
@en
Sabrina Tosi
@es
Sabrina Tosi
@nl
P106
P21
P31
P496
0000-0002-0036-0191