Lista de obras - Alba Navarro - Dominio Público Uruguay

A B-cell epigenetic signature defines three biologic subgroups of chronic lymphocytic leukemia with clinical impact.

artículo científico publicado en 2014

A gene signature that distinguishes conventional and leukemic nonnodal mantle cell lymphoma helps predict outcome

article

A new genetic abnormality leading to TP53 gene deletion in chronic lymphocytic leukaemia

article

CCND2 rearrangements are the most frequent genetic events in cyclin D1(-) mantle cell lymphoma

artículo científico publicado en 2012

Chronic lymphocytic leukemia in the elderly: clinico-biological features, outcomes, and proposal of a prognostic model

artículo científico publicado en 2014

Clinical impact of MYD88 mutations in chronic lymphocytic leukemia

artículo científico publicado en 2016

Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia.

artículo científico publicado en 2016

Clonal evolution in chronic lymphocytic leukemia: analysis of correlations with IGHV mutational status, NOTCH1 mutations and clinical significance

artículo científico publicado en 2013

Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads

artículo científico publicado en 2014

Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell Lineage.

artículo científico publicado en 2016

Detection of chromothripsis-like patterns with a custom array platform for chronic lymphocytic leukemia.

artículo científico publicado en 2015

Different distribution of NOTCH1 mutations in chronic lymphocytic leukemia with isolated trisomy 12 or associated with other chromosomal alterations.

artículo científico publicado en 2012

Different spectra of recurrent gene mutations in subsets of chronic lymphocytic leukemia harboring stereotyped B-cell receptors

artículo científico publicado en 2016

EML4-ALK rearrangement in non-small cell lung cancer and non-tumor lung tissues

artículo científico publicado en 2009

Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia.

artículo científico publicado en 2012

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

artículo científico publicado en 2011

Genome-wide methylation analyses identify a subset of mantle cell lymphoma with a high number of methylated CpGs and aggressive clinicopathological features.

artículo científico publicado en 2013

Genomic and Gene Expression Profiling Defines Indolent Forms of Mantle Cell Lymphoma

article

Genomic complexity and IGHV mutational status are key predictors of outcome of chronic lymphocytic leukemia patients with TP53 disruption

artículo científico publicado en 2014

Identification of methylated genes associated with aggressive clinicopathological features in mantle cell lymphoma

artículo científico publicado en 2011

Increased tumor cell proliferation in mantle cell lymphoma is associated with elevated insulin-like growth factor 2 mRNA-binding protein 3 expression

artículo científico publicado en 2012

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma.

artículo científico publicado en 2013

MicroRNA expression, chromosomal alterations, and immunoglobulin variable heavy chain hypermutations in Mantle cell lymphomas.

artículo científico publicado en 2009

Molecular pathogenesis of mantle cell lymphoma: new perspectives and challenges with clinical implications

artículo científico publicado en 2011

Molecular subsets of mantle cell lymphoma defined by the IGHV mutational status and SOX11 expression have distinct biologic and clinical features

artículo científico publicado en 2012

Mutations in CHD2 cause defective association with active chromatin in chronic lymphocytic leukemia

artículo científico publicado en 2015

Mutations of MAP2K1 are frequent in pediatric-type follicular lymphoma and result in ERK pathway activation

artículo científico publicado en 2017

NOTCH1 mutations in chronic lymphocytic leukemia with trisomy 12

NOTCH1, TP53, and MAP2K1 Mutations in Splenic Diffuse Red Pulp Small B-cell Lymphoma Are Associated With Progressive Disease

artículo científico publicado en 2015

Non-coding recurrent mutations in chronic lymphocytic leukaemia

artículo científico publicado en 2015

Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease

artículo científico publicado en 2012

Pathogenic role of B-cell receptor signaling and canonical NF-κB activation in mantle cell lymphoma

artículo científico publicado en 2016

Patients with relapsed/refractory chronic lymphocytic leukaemia may benefit from inclusion in clinical trials irrespective of the therapy received: a case-control retrospective analsysis.

artículo científico publicado en 2015

Plasma cell and terminal B-cell differentiation in mantle cell lymphoma mainly occur in the SOX11-negative subtype

Recurrent mutations of NOTCH genes in follicular lymphoma identify a distinctive subset of tumours.

artículo científico publicado en 2014

Recurrent mutations refine prognosis in chronic lymphocytic leukemia.

artículo científico publicado en 2015

SOX11 regulates PAX5 expression and blocks terminal B-cell differentiation in aggressive mantle cell lymphoma

artículo científico publicado en 2013

Sorafenib inhibits cell migration and stroma-mediated bortezomib resistance by interfering B-cell receptor signaling and protein translation in mantle cell lymphoma

artículo científico publicado en 2012

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis.

artículo científico publicado en 2013

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis.

artículo científico publicado en 2015

The prognostic impact of minimal residual disease in patients with chronic lymphocytic leukemia requiring first-line therapy

artículo científico publicado en 2014

Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling.

artículo científico publicado en 2008

microRNA expression profiles identify subtypes of mantle cell lymphoma with different clinicobiological characteristics

artículo científico publicado en 2013

Lista de obras de Alba Navarro

A B-cell epigenetic signature defines three biologic subgroups of chronic lymphocytic leukemia with clinical impact.

A gene signature that distinguishes conventional and leukemic nonnodal mantle cell lymphoma helps predict outcome

A new genetic abnormality leading to TP53 gene deletion in chronic lymphocytic leukaemia

CCND2 rearrangements are the most frequent genetic events in cyclin D1(-) mantle cell lymphoma

Chronic lymphocytic leukemia in the elderly: clinico-biological features, outcomes, and proposal of a prognostic model

Clinical impact of MYD88 mutations in chronic lymphocytic leukemia

Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia.

Clonal evolution in chronic lymphocytic leukemia: analysis of correlations with IGHV mutational status, NOTCH1 mutations and clinical significance

Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads

Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell Lineage.

Detection of chromothripsis-like patterns with a custom array platform for chronic lymphocytic leukemia.

Different distribution of NOTCH1 mutations in chronic lymphocytic leukemia with isolated trisomy 12 or associated with other chromosomal alterations.

Different spectra of recurrent gene mutations in subsets of chronic lymphocytic leukemia harboring stereotyped B-cell receptors

EML4-ALK rearrangement in non-small cell lung cancer and non-tumor lung tissues

Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia.

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

Genome-wide methylation analyses identify a subset of mantle cell lymphoma with a high number of methylated CpGs and aggressive clinicopathological features.

Genomic and Gene Expression Profiling Defines Indolent Forms of Mantle Cell Lymphoma

Genomic complexity and IGHV mutational status are key predictors of outcome of chronic lymphocytic leukemia patients with TP53 disruption

Identification of methylated genes associated with aggressive clinicopathological features in mantle cell lymphoma

Increased tumor cell proliferation in mantle cell lymphoma is associated with elevated insulin-like growth factor 2 mRNA-binding protein 3 expression

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma.

MicroRNA expression, chromosomal alterations, and immunoglobulin variable heavy chain hypermutations in Mantle cell lymphomas.

Molecular pathogenesis of mantle cell lymphoma: new perspectives and challenges with clinical implications

Molecular subsets of mantle cell lymphoma defined by the IGHV mutational status and SOX11 expression have distinct biologic and clinical features

Mutations in CHD2 cause defective association with active chromatin in chronic lymphocytic leukemia

Mutations of MAP2K1 are frequent in pediatric-type follicular lymphoma and result in ERK pathway activation

NOTCH1 mutations in chronic lymphocytic leukemia with trisomy 12

NOTCH1, TP53, and MAP2K1 Mutations in Splenic Diffuse Red Pulp Small B-cell Lymphoma Are Associated With Progressive Disease

Non-coding recurrent mutations in chronic lymphocytic leukaemia

Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease

Pathogenic role of B-cell receptor signaling and canonical NF-κB activation in mantle cell lymphoma

Patients with relapsed/refractory chronic lymphocytic leukaemia may benefit from inclusion in clinical trials irrespective of the therapy received: a case-control retrospective analsysis.

Plasma cell and terminal B-cell differentiation in mantle cell lymphoma mainly occur in the SOX11-negative subtype

Recurrent mutations of NOTCH genes in follicular lymphoma identify a distinctive subset of tumours.

Recurrent mutations refine prognosis in chronic lymphocytic leukemia.

SOX11 regulates PAX5 expression and blocks terminal B-cell differentiation in aggressive mantle cell lymphoma

Sorafenib inhibits cell migration and stroma-mediated bortezomib resistance by interfering B-cell receptor signaling and protein translation in mantle cell lymphoma

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis.

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis.

The prognostic impact of minimal residual disease in patients with chronic lymphocytic leukemia requiring first-line therapy

Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling.

microRNA expression profiles identify subtypes of mantle cell lymphoma with different clinicobiological characteristics