Lista de obras - Martin Figeac - Dominio Público Uruguay

1q12 chromosome translocations form aberrant heterochromatic foci associated with changes in nuclear architecture and gene expression in B cell lymphoma

artículo científico publicado en 2010

Accurate Classification of Germinal Center B-Cell-Like/Activated B-Cell-Like Diffuse Large B-Cell Lymphoma Using a Simple and Rapid Reverse Transcriptase-Multiplex Ligation-Dependent Probe Amplification Assay: A CALYM Study

Activating mutations in genes related to TCR signaling in angioimmunoblastic and other follicular helper T-cell-derived lymphomas.

artículo científico publicado en 2016

Applicability and Efficiency of NGS in Routine Diagnosis: In-Depth Performance Analysis of a Complete Workflow for CFTR Mutation Analysis

artículo científico publicado en 2016

Application of the cghRA framework to the genomic characterization of Diffuse Large B-Cell Lymphoma.

artículo científico publicado en 2017

Authors' Reply

scientific article published on 01 March 2018

Autocrine induction of invasive and metastatic phenotypes by the MIF-CXCR4 axis in drug-resistant human colon cancer cells

artículo científico publicado en 2010

BAP1 Is Altered by Copy Number Loss, Mutation, and/or Loss of Protein Expression in More Than 70% of Malignant Peritoneal Mesotheliomas

artículo científico publicado en 2016

BCL2 expression but not MYC and BCL2 coexpression predicts survival in elderly patients with diffuse large B-cell lymphoma independently of cell of origin in the phase 3 LNH03-6B trial.

artículo científico publicado en 2017

Beneficial Effect of a Selective Adenosine A Receptor Antagonist in the APPswe/PS1dE9 Mouse Model of Alzheimer's Disease

article

Beneficial effects of exercise in a transgenic mouse model of Alzheimer's disease-like Tau pathology.

artículo científico publicado en 2011

Biological and Clinical Relevance of Associated Genomic Alterations in MYD88 L265P and non-L265P-Mutated Diffuse Large B-Cell Lymphoma: Analysis of 361 Cases.

artículo científico publicado en 2016

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

artículo científico publicado en 2016

Corrigendum: Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease Patients

artículo científico publicado en 2016

Determination of Molecular Subtypes of Diffuse Large B-Cell Lymphoma Using a Reverse Transcriptase Multiplex Ligation-Dependent Probe Amplification Classifier: A CALYM Study.

artículo científico publicado en 2017

DiNAMO: highly sensitive DNA motif discovery in high-throughput sequencing data.

artículo científico publicado en 2018

Dominance hierarchy arising from the evolution of a complex small RNA regulatory network.

artículo científico publicado en 2014

Evolution of the human cold/menthol receptor, TRPM8

scientific article published on 10 April 2019

Fast multiclonal clusterization of V(D)J recombinations from high-throughput sequencing

artículo científico publicado en 2014

Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.

artículo científico publicado en 2014

Functional Analysis of Somatic Mutations Affecting Receptor Tyrosine Kinase Family in Metastatic Colorectal Cancer

scientific article published on 29 March 2019

Galectin-3 is a non-classic RNA binding protein that stabilizes the mucin MUC4 mRNA in the cytoplasm of cancer cells.

artículo científico publicado en 2017

Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia

artículo científico publicado en 2015

Genomic characterization of Imatinib resistance in CD34+ cell populations from chronic myeloid leukaemia patients

artículo científico publicado en 2010

Genomic copy number alterations in 33 malignant peritoneal mesothelioma analyzed by comparative genomic hybridization array.

artículo científico publicado en 2016

Heterocyclic Diamidine DNA Ligands as HOXA9 Transcription Factor Inhibitors: Design, Molecular Evaluation, and Cellular Consequences in a HOXA9-Dependant Leukemia Cell Model

artículo científico publicado en 2019

High-throughput sequencing in acute lymphoblastic leukemia: Follow-up of minimal residual disease and emergence of new clones.

artículo científico publicado en 2016

IDH1/2 but not DNMT3A mutations are suitable targets for minimal residual disease monitoring in acute myeloid leukemia patients: a study by the Acute Leukemia French Association

artículo científico publicado en 2015

Immunoglobulin heavy chain/light chain pair measurement is associated with survival in diffuse large B-cell lymphoma.

artículo científico publicado en 2013

Impact of the Timing of Antibiotic Administration on Digestive Colonization with Carbapenemase-Producing Enterobacteriaceae in a Murine Model

scientific article published on 24 May 2019

Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis.

artículo científico publicado en 2015

Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease

artículo científico publicado en 2013

MPAgenomics: an R package for multi-patient analysis of genomic markers.

artículo científico publicado en 2014

Melanoma dormancy in a mouse model is linked to GILZ/FOXO3A-dependent quiescence of disseminated stem-like cells.

artículo científico publicado en 2016

MicroRNAs in lymphoma, from diagnosis to targeted therapy

artículo científico publicado en 2013

Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA

artículo científico publicado en 2014

Molecular prognostic factors in acute myeloid leukemia receiving first-line therapy with azacitidine

artículo científico publicado en 2015

Multi-loci diagnosis of acute lymphoblastic leukaemia with high-throughput sequencing and bioinformatics analysis

artículo científico publicado en 2016

Mutation mismatch repair gene deletions in diffuse large B-cell lymphoma

artículo científico publicado en 2012

Nail-Patella Syndrome: clinical and molecular data in 55 families raising the hypothesis of a genetic heterogeneity.

artículo científico publicado en 2015

Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia

artículo científico publicado en 2013

Next-Generation Sequencing in Diffuse Large B-Cell Lymphoma Highlights Molecular Divergence and Therapeutic Opportunities: a LYSA Study.

artículo científico publicado en 2016

Next-generation sequencing of FLT3 internal tandem duplications for minimal residual disease monitoring in acute myeloid leukemia

artículo científico publicado en 2015

Optimization of Routine Testing for MET Exon 14 Splice Site Mutations in NSCLC Patients

scientific article published on 07 September 2018

Peroxisome proliferator-activated receptor gamma (PPARγ) regulates lactase expression and activity in the gut.

artículo científico publicado en 2017

Persistence of Coxsackievirus B4 in pancreatic ductal-like cells results in cellular and viral changes.

artículo científico publicado en 2017

Persistent coxsackievirus B4 infection induces microRNA dysregulation in human pancreatic cells.

artículo científico publicado en 2017

Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease Patients

artículo científico publicado en 2016

Quantification of JAK2V617F mutation by next-generation sequencing technology.

artículo científico publicado en 2013

RNA-binding disturbances as a continuum from spinocerebellar ataxia type 2 to Parkinson disease

artículo científico publicado en 2016

Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1/S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

article

Recurrent mutations of the exportin 1 gene (XPO1) and their impact on selective inhibitor of nuclear export compounds sensitivity in primary mediastinal B-cell lymphoma

artículo científico publicado en 2016

Repression of the RHOH gene by JunD.

artículo científico publicado en 2011

SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.

artículo científico publicado en 2011

Sub-clonal analysis of the murine C1498 acute myeloid leukaemia cell line reveals genomic and immunogenic diversity.

artículo científico publicado en 2017

TRPC3 shapes the ER-mitochondria Ca<sup>2+</sup> transfer characterizing tumour-promoting senescence

artículo científico publicado en 2022

The costimulatory molecule CD70 is regulated by distinct molecular mechanisms and is associated with overall survival in diffuse large B-cell lymphoma.

artículo científico publicado en 2013

The lncRNA 'UCA1' modulates the response to chemotherapy of ovarian cancer through direct binding to miR-27a-5p and control of UBE2N levels

artículo científico publicado en 2021

The stem cell-associated gene expression signature allows risk stratification in pediatric acute myeloid leukemia

scientific article published on 08 August 2018

Vaginal Mucosal Homeostatic Response May Determine Pregnancy Outcome in Women With Bacterial Vaginosis: A Pilot Study

artículo científico publicado en 2016

Waved aCGH: to smooth or not to smooth.

artículo científico publicado en 2010

s-SHIP Promoter Expression Identifies Mouse Mammary Cancer Stem Cells

scientific article published on 13 June 2019

Lista de obras de Martin Figeac

1q12 chromosome translocations form aberrant heterochromatic foci associated with changes in nuclear architecture and gene expression in B cell lymphoma

Accurate Classification of Germinal Center B-Cell-Like/Activated B-Cell-Like Diffuse Large B-Cell Lymphoma Using a Simple and Rapid Reverse Transcriptase-Multiplex Ligation-Dependent Probe Amplification Assay: A CALYM Study

Activating mutations in genes related to TCR signaling in angioimmunoblastic and other follicular helper T-cell-derived lymphomas.

Applicability and Efficiency of NGS in Routine Diagnosis: In-Depth Performance Analysis of a Complete Workflow for CFTR Mutation Analysis

Application of the cghRA framework to the genomic characterization of Diffuse Large B-Cell Lymphoma.

Authors' Reply

Autocrine induction of invasive and metastatic phenotypes by the MIF-CXCR4 axis in drug-resistant human colon cancer cells

BAP1 Is Altered by Copy Number Loss, Mutation, and/or Loss of Protein Expression in More Than 70% of Malignant Peritoneal Mesotheliomas

BCL2 expression but not MYC and BCL2 coexpression predicts survival in elderly patients with diffuse large B-cell lymphoma independently of cell of origin in the phase 3 LNH03-6B trial.

Beneficial Effect of a Selective Adenosine A Receptor Antagonist in the APPswe/PS1dE9 Mouse Model of Alzheimer's Disease

Beneficial effects of exercise in a transgenic mouse model of Alzheimer's disease-like Tau pathology.

Biological and Clinical Relevance of Associated Genomic Alterations in MYD88 L265P and non-L265P-Mutated Diffuse Large B-Cell Lymphoma: Analysis of 361 Cases.

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

Corrigendum: Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease Patients

Determination of Molecular Subtypes of Diffuse Large B-Cell Lymphoma Using a Reverse Transcriptase Multiplex Ligation-Dependent Probe Amplification Classifier: A CALYM Study.

DiNAMO: highly sensitive DNA motif discovery in high-throughput sequencing data.

Dominance hierarchy arising from the evolution of a complex small RNA regulatory network.

Evolution of the human cold/menthol receptor, TRPM8

Fast multiclonal clusterization of V(D)J recombinations from high-throughput sequencing

Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.

Functional Analysis of Somatic Mutations Affecting Receptor Tyrosine Kinase Family in Metastatic Colorectal Cancer

Galectin-3 is a non-classic RNA binding protein that stabilizes the mucin MUC4 mRNA in the cytoplasm of cancer cells.

Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia

Genomic characterization of Imatinib resistance in CD34+ cell populations from chronic myeloid leukaemia patients

Genomic copy number alterations in 33 malignant peritoneal mesothelioma analyzed by comparative genomic hybridization array.

Heterocyclic Diamidine DNA Ligands as HOXA9 Transcription Factor Inhibitors: Design, Molecular Evaluation, and Cellular Consequences in a HOXA9-Dependant Leukemia Cell Model

High-throughput sequencing in acute lymphoblastic leukemia: Follow-up of minimal residual disease and emergence of new clones.

IDH1/2 but not DNMT3A mutations are suitable targets for minimal residual disease monitoring in acute myeloid leukemia patients: a study by the Acute Leukemia French Association

Immunoglobulin heavy chain/light chain pair measurement is associated with survival in diffuse large B-cell lymphoma.

Impact of the Timing of Antibiotic Administration on Digestive Colonization with Carbapenemase-Producing Enterobacteriaceae in a Murine Model

Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis.

Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease

MPAgenomics: an R package for multi-patient analysis of genomic markers.

Melanoma dormancy in a mouse model is linked to GILZ/FOXO3A-dependent quiescence of disseminated stem-like cells.

MicroRNAs in lymphoma, from diagnosis to targeted therapy

Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA

Molecular prognostic factors in acute myeloid leukemia receiving first-line therapy with azacitidine

Multi-loci diagnosis of acute lymphoblastic leukaemia with high-throughput sequencing and bioinformatics analysis

Mutation mismatch repair gene deletions in diffuse large B-cell lymphoma

Nail-Patella Syndrome: clinical and molecular data in 55 families raising the hypothesis of a genetic heterogeneity.

Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia

Next-Generation Sequencing in Diffuse Large B-Cell Lymphoma Highlights Molecular Divergence and Therapeutic Opportunities: a LYSA Study.

Next-generation sequencing of FLT3 internal tandem duplications for minimal residual disease monitoring in acute myeloid leukemia

Optimization of Routine Testing for MET Exon 14 Splice Site Mutations in NSCLC Patients

Peroxisome proliferator-activated receptor gamma (PPARγ) regulates lactase expression and activity in the gut.

Persistence of Coxsackievirus B4 in pancreatic ductal-like cells results in cellular and viral changes.

Persistent coxsackievirus B4 infection induces microRNA dysregulation in human pancreatic cells.

Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease Patients

Quantification of JAK2V617F mutation by next-generation sequencing technology.

RNA-binding disturbances as a continuum from spinocerebellar ataxia type 2 to Parkinson disease

Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1/S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

Recurrent mutations of the exportin 1 gene (XPO1) and their impact on selective inhibitor of nuclear export compounds sensitivity in primary mediastinal B-cell lymphoma

Repression of the RHOH gene by JunD.

SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.

Sub-clonal analysis of the murine C1498 acute myeloid leukaemia cell line reveals genomic and immunogenic diversity.

TRPC3 shapes the ER-mitochondria Ca<sup>2+</sup> transfer characterizing tumour-promoting senescence

The costimulatory molecule CD70 is regulated by distinct molecular mechanisms and is associated with overall survival in diffuse large B-cell lymphoma.

The lncRNA 'UCA1' modulates the response to chemotherapy of ovarian cancer through direct binding to miR-27a-5p and control of UBE2N levels

The stem cell-associated gene expression signature allows risk stratification in pediatric acute myeloid leukemia

Vaginal Mucosal Homeostatic Response May Determine Pregnancy Outcome in Women With Bacterial Vaginosis: A Pilot Study

Waved aCGH: to smooth or not to smooth.

s-SHIP Promoter Expression Identifies Mouse Mammary Cancer Stem Cells