Lista de obras - Sabrina Tosi - Dominio Público Uruguay

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.

artículo científico publicado en 2005

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

artículo científico

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

scientific article published on 01 April 1996

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

artículo científico publicado en 2019

Delineation of multiple deleted regions in 7q in myeloid disorders

scientific article published on 01 August 1999

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

artículo científico publicado en 1996

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

artículo científico publicado en 1994

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

artículo científico publicado en 2009

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

artículo científico publicado en 1993

Familial partial monosomy 7 and myelodysplasia

scientific article published on 01 January 2001

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

artículo científico publicado en 1994

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

artículo científico publicado en 2017

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

artículo científico publicado en 2011

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

artículo científico

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

artículo científico publicado en 2014

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

artículo científico publicado en 2003

Human chromosome 7: DNA sequence and biology

artículo científico publicado en 2003

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

artículo científico publicado en 2002

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

artículo científico publicado en 1998

Microgranular variant of acute promyelocytic leukemia in children

artículo científico publicado en 1992

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

artículo científico publicado en 2009

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

artículo científico publicado en 2002

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 1995

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

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

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

artículo científico publicado en 2001

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.

artículo científico publicado en 1999

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

artículo científico

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

artículo científico publicado en 2000

Lista de obras de Sabrina Tosi

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.

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

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

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

Delineation of multiple deleted regions in 7q in myeloid disorders

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

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

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

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

Familial partial monosomy 7 and myelodysplasia

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

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

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

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

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

Human chromosome 7: DNA sequence and biology

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

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

Microgranular variant of acute promyelocytic leukemia in children

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

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

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

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

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

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

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

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

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.

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

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