Lista de obras - S Lavorgna - Dominio Público Uruguay

A Leukemia-Associated CD34/CD123/CD25/CD99+ Immunophenotype Identifies FLT3-Mutated Clones in Acute Myeloid Leukemia.

artículo científico publicado en 2015

A monoclonal antibody against mutated nucleophosmin 1 for the molecular diagnosis of acute myeloid leukemias

artículo científico publicado en 2010

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups

artículo científico

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups.

artículo científico publicado en 2013

An allele-specific rt-PCR assay to detect type A mutation of the nucleophosmin-1 gene in acute myeloid leukemia.

artículo científico publicado en 2008

Analysis of mutational status, SNP rs16754, and expression levels of Wilms tumor 1 (WT1) gene in acute promyelocytic leukemia.

artículo científico publicado en 2012

Comparative genomic analysis of PML and RARA breakpoints in paired diagnosis/relapse samples of patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy.

artículo científico publicado en 2017

Comparative molecular analysis of therapy-related and de novo acute promyelocytic leukemia.

artículo científico publicado en 2011

Cytogenetic and molecular diagnostic characterization combined to postconsolidation minimal residual disease assessment by flow cytometry improves risk stratification in adult acute myeloid leukemia

artículo científico publicado en 2010

Detection of the nucleophosmin gene mutations in acute myelogenous leukemia through RT-PCR and polyacrylamide gel electrophoresis

scientific article published on 01 January 2009

Diagnostic refinement of chronic myeloproliferative disorders and thrombocytoses of unknown origin by multiple RT-PCR and capillary electrophoresis of BCR-ABL rearrangements and JAK2 (V617F) mutation

scientific article published on 07 February 2007

GIMEMA AML1310 trial of risk-adapted, MRD-directed therapy for young adults with newly diagnosed acute myeloid leukemia

artículo científico publicado en 2019

Identification of emerging FLT3 ITD-positive clones during clinical remission and kinetics of disease relapse in acute myeloid leukaemia with mutated nucleophosmin.

artículo científico publicado en 2013

Longitudinal detection of DNMT3AR882H transcripts in patients with acute myeloid leukemia.

artículo científico publicado en 2018

MRD in AML: The Role of New Techniques

scientific article published on 23 July 2019

Mutational landscape of patients with acute promyelocytic leukemia at diagnosis and relapse

scientific article published on 23 July 2019

NPM1 gene deletions in myelodysplastic syndromes with 5q- and complex karyotype ⬇️

artículo científico publicado el 10 de marzo de 2011

PML-RARA-associated cooperating mutations belong to a transcriptional network that is deregulated in myeloid leukemias.

artículo científico

PML-RARα kinetics and impact of FLT3-ITD mutations in newly diagnosed acute promyelocytic leukaemia treated with ATRA and ATO or ATRA and chemotherapy.

artículo científico publicado en 2016

Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia.

artículo científico publicado en 2005

The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemia

artículo científico publicado en 2017

The genotype nucleophosmin mutated and FLT3-ITD negative is characterized by high bax/bcl-2 ratio and favourable outcome in acute myeloid leukaemia.

artículo científico publicado en 2010

The hidden genomic landscape of acute myeloid leukemia: subclonal structure revealed by undetected mutations

artículo científico publicado en 2014

The poly(ADP-ribose) polymerase inhibitor olaparib induces up-regulation of death receptors in primary acute myeloid leukemia blasts by NF-κB activation

scientific article published on 08 March 2018

Two Novel Methods for Rapid Detection and Quantification of DNMT3A R882 Mutations in Acute Myeloid Leukemia

artículo científico publicado en 2014

miRNA let-7c promotes granulocytic differentiation in acute myeloid leukemia.

artículo científico publicado en 2012

Lista de obras de S Lavorgna

A Leukemia-Associated CD34/CD123/CD25/CD99+ Immunophenotype Identifies FLT3-Mutated Clones in Acute Myeloid Leukemia.

A monoclonal antibody against mutated nucleophosmin 1 for the molecular diagnosis of acute myeloid leukemias

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups.

An allele-specific rt-PCR assay to detect type A mutation of the nucleophosmin-1 gene in acute myeloid leukemia.

Analysis of mutational status, SNP rs16754, and expression levels of Wilms tumor 1 (WT1) gene in acute promyelocytic leukemia.

Comparative genomic analysis of PML and RARA breakpoints in paired diagnosis/relapse samples of patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy.

Comparative molecular analysis of therapy-related and de novo acute promyelocytic leukemia.

Cytogenetic and molecular diagnostic characterization combined to postconsolidation minimal residual disease assessment by flow cytometry improves risk stratification in adult acute myeloid leukemia

Detection of the nucleophosmin gene mutations in acute myelogenous leukemia through RT-PCR and polyacrylamide gel electrophoresis

Diagnostic refinement of chronic myeloproliferative disorders and thrombocytoses of unknown origin by multiple RT-PCR and capillary electrophoresis of BCR-ABL rearrangements and JAK2 (V617F) mutation

GIMEMA AML1310 trial of risk-adapted, MRD-directed therapy for young adults with newly diagnosed acute myeloid leukemia

Identification of emerging FLT3 ITD-positive clones during clinical remission and kinetics of disease relapse in acute myeloid leukaemia with mutated nucleophosmin.

Longitudinal detection of DNMT3AR882H transcripts in patients with acute myeloid leukemia.

MRD in AML: The Role of New Techniques

Mutational landscape of patients with acute promyelocytic leukemia at diagnosis and relapse

NPM1 gene deletions in myelodysplastic syndromes with 5q- and complex karyotype ⬇️

PML-RARA-associated cooperating mutations belong to a transcriptional network that is deregulated in myeloid leukemias.

PML-RARα kinetics and impact of FLT3-ITD mutations in newly diagnosed acute promyelocytic leukaemia treated with ATRA and ATO or ATRA and chemotherapy.

Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia.

The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemia

The genotype nucleophosmin mutated and FLT3-ITD negative is characterized by high bax/bcl-2 ratio and favourable outcome in acute myeloid leukaemia.

The hidden genomic landscape of acute myeloid leukemia: subclonal structure revealed by undetected mutations

The poly(ADP-ribose) polymerase inhibitor olaparib induces up-regulation of death receptors in primary acute myeloid leukemia blasts by NF-κB activation

Two Novel Methods for Rapid Detection and Quantification of DNMT3A R882 Mutations in Acute Myeloid Leukemia

miRNA let-7c promotes granulocytic differentiation in acute myeloid leukemia.