List of works - Sabrina Tosi

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome

scientific article published on 01 June 2002

Human chromosome 7: DNA sequence and biology

scientific article

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

scientific article

t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia

scientific article

The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia case

scientific article published in June 2001

Delineation of multiple deleted regions in 7q in myeloid disorders

scientific article published on 01 August 1999

Microgranular variant of acute promyelocytic leukemia in children

scientific article published on 01 September 1992

The radial arrangement of the human chromosome 7 in the lymphocyte cell nucleus is associated with chromosomal band gene density

article

The 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.

scientific article

Identification of new partner chromosomes involved in fusions with the ETV6 (TEL) gene in hematologic malignancies

scientific article published in March 1998

Familial partial monosomy 7 and myelodysplasia

scientific article published on 01 January 2001

Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia

scientific article

Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wld(s)) mouse

scientific article (publication date: 6 February 2002)

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.

scientific article

Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias

scientific article published on 12 February 2009

HLXB9 gene expression, and nuclear location during in vitro neuronal differentiation in the SK-N-BE neuroblastoma cell line

scientific article

Folate deficiency as predisposing factor for childhood leukaemia: a review of the literature.

scientific article

Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization

scientific article published on March 1999

Establishment and characterization of a new granulocyte-macrophage colony-stimulating factor-dependent and interleukin-3-dependent human acute myeloid leukemia cell line (GF-D8).

scientific article published on March 1993

Double target in situ hybridization applied to the study of numerical aberrations in childhood acute lymphoblastic leukemia

scientific article published on 01 April 1994

Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH.

scientific article published on September 1997

Paediatric acute myeloid leukaemia with the t(7;12)(q36;p13) rearrangement: a review of the biological and clinical management aspects

scientific article

Reciprocal translocation t(12;13)(p13;q14) in acute nonlymphoblastic leukemia: Report and cytogenetic analysis of two cases

scientific article published on 01 October 1994

First-trimester human trophoblast is class II major histocompatibility complex mRNA+/antigen−

scientific article published on 01 April 1994

Detection of the breakpoint cluster region-ABL fusion in chronic myeloid leukemia with variant Philadelphia chromosome translocations by in situ hybridization

scientific article published on 01 July 1996

Genomic properties of chromosomal bands are linked to evolutionary rearrangements and new centromere formation in primates

scientific article published on 17 July 2017

Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH)

scientific article published on 01 April 1996

Physical mapping of the human T-cell receptor beta gene complex, using yeast artificial chromosomes

scientific article published on January 1995

The RS4;11 cell line as a model for leukaemia with t(4;11)(q21;q23): Revised characterisation of cytogenetic features

scientific article published on 07 August 2019

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

scientific article

Nuclear Repositioning of the Non-Translocated HLXB9 Allele in the Leukaemia Cell Line GDM-1 Harbouring a t(6;7)(q23;q36).

scientific article published on 29 September 2017

Deletions of Chromosome 7q Affect Nuclear Organization and HLXB9Gene Expression in Hematological Disorders

scientific article published on 25 April 2019

List of works by Sabrina Tosi

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome

Human chromosome 7: DNA sequence and biology

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

t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia

The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia case

Delineation of multiple deleted regions in 7q in myeloid disorders

Microgranular variant of acute promyelocytic leukemia in children

The radial arrangement of the human chromosome 7 in the lymphocyte cell nucleus is associated with chromosomal band gene density

The 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.

Identification of new partner chromosomes involved in fusions with the ETV6 (TEL) gene in hematologic malignancies

Familial partial monosomy 7 and myelodysplasia

Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia

Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wld(s)) mouse

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.

Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias

HLXB9 gene expression, and nuclear location during in vitro neuronal differentiation in the SK-N-BE neuroblastoma cell line

Folate deficiency as predisposing factor for childhood leukaemia: a review of the literature.

Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization

Establishment and characterization of a new granulocyte-macrophage colony-stimulating factor-dependent and interleukin-3-dependent human acute myeloid leukemia cell line (GF-D8).

Double target in situ hybridization applied to the study of numerical aberrations in childhood acute lymphoblastic leukemia

Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH.

Paediatric acute myeloid leukaemia with the t(7;12)(q36;p13) rearrangement: a review of the biological and clinical management aspects

Reciprocal translocation t(12;13)(p13;q14) in acute nonlymphoblastic leukemia: Report and cytogenetic analysis of two cases

First-trimester human trophoblast is class II major histocompatibility complex mRNA+/antigen−

Detection of the breakpoint cluster region-ABL fusion in chronic myeloid leukemia with variant Philadelphia chromosome translocations by in situ hybridization

Genomic properties of chromosomal bands are linked to evolutionary rearrangements and new centromere formation in primates

Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH)

Physical mapping of the human T-cell receptor beta gene complex, using yeast artificial chromosomes

The RS4;11 cell line as a model for leukaemia with t(4;11)(q21;q23): Revised characterisation of cytogenetic features

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

Nuclear Repositioning of the Non-Translocated HLXB9 Allele in the Leukaemia Cell Line GDM-1 Harbouring a t(6;7)(q23;q36).

Deletions of Chromosome 7q Affect Nuclear Organization and HLXB9Gene Expression in Hematological Disorders