Lista de obras - Angelo Lonoce - Dominio Público Uruguay

A rare but recurrent t(8;13)(q24;q14) translocation in B-cell chronic lymphocytic leukaemia causingMYCup-regulation and concomitant loss ofPVT1,miR-15/16andDLEU7

Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation

artículo científico publicado en 2008

CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia.

artículo científico publicado en 2010

Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.

artículo científico publicado en 2009

Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells

artículo científico publicado en 2017

Extramedullary molecular evidence of the 5′KIAA1509/3′PDGFRB fusion gene in chronic eosinophilic leukemia

article

Familial adenomatous polyposis: identification of a new frameshift mutation of the APC gene in an Italian family

artículo científico publicado en 1992

Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure

artículo científico publicado en 2010

Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer

artículo científico publicado en 2014

Identification and molecular characterization of recurrent genomic deletions on 7p12 in the IKZF1 gene in a large cohort of BCR-ABL1-positive acute lymphoblastic leukemia patients: on behalf of Gruppo Italiano Malattie Ematologiche dell'Adulto Acute

artículo científico publicado en 2009

Linkage studies in Italian families with familial adenomatous polyposis.

artículo científico publicado en 1993

MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences.

artículo científico publicado en 2018

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

article

Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia

artículo científico publicado en 2002

RALE051: a novel established cell line of sporadic Burkitt lymphoma

artículo científico publicado en 2017

Two alternatively spliced 5′BCR/3′JAK2 fusion transcripts in a myeloproliferative neoplasm with a three-way t(9;18;22)(p23;p11.3;q11.2) translocation

artículo científico publicado en 2011

Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma

artículo científico publicado en 2007

t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.

artículo científico publicado en 2015

t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene

article

Lista de obras de Angelo Lonoce

A rare but recurrent t(8;13)(q24;q14) translocation in B-cell chronic lymphocytic leukaemia causingMYCup-regulation and concomitant loss ofPVT1,miR-15/16andDLEU7

Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation

CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia.

Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.

Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells

Extramedullary molecular evidence of the 5′KIAA1509/3′PDGFRB fusion gene in chronic eosinophilic leukemia

Familial adenomatous polyposis: identification of a new frameshift mutation of the APC gene in an Italian family

Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure

Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer

Identification and molecular characterization of recurrent genomic deletions on 7p12 in the IKZF1 gene in a large cohort of BCR-ABL1-positive acute lymphoblastic leukemia patients: on behalf of Gruppo Italiano Malattie Ematologiche dell'Adulto Acute

Linkage studies in Italian families with familial adenomatous polyposis.

MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences.

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia

RALE051: a novel established cell line of sporadic Burkitt lymphoma

Two alternatively spliced 5′BCR/3′JAK2 fusion transcripts in a myeloproliferative neoplasm with a three-way t(9;18;22)(p23;p11.3;q11.2) translocation

Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma

t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.

t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene