Lista de obras - Olivier Bluteau - Dominio Público Uruguay

A landscape of germline mutations in a cohort of inherited bone marrow failure patients

artículo científico publicado en 2017

An incomplete trafficking defect to the cell-surface leads to paradoxical thrombocytosis for human and murine MPL P106L.

artículo científico publicado en 2016

Beta-catenin mutations in hepatocellular carcinoma correlate with a low rate of loss of heterozygosity.

artículo científico publicado en 1999

Bi-allelic inactivation of TCF1 in hepatic adenomas

artículo científico publicado en 2002

Biallelic inactivation of REV7 is associated with Fanconi anemia

artículo científico publicado en 2016

Biallelic inactivation of REV7 is associated with Fanconi anemia

artículo científico publicado en 2017

Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models

artículo científico publicado en 2012

Clinical and molecular analysis of combined hepatocellular-cholangiocarcinomas.

artículo científico publicado en 2004

Critical role of the HDAC6-cortactin axis in human megakaryocyte maturation leading to a proplatelet-formation defect.

artículo científico publicado en 2017

Developmental changes in human megakaryopoiesis.

artículo científico publicado en 2013

Differential association of calreticulin type 1 and type 2 mutations with myelofibrosis and essential thrombocytemia: relevance for disease evolution

scientific article published on 12 September 2014

Frequent mutations of hepatocyte nuclear factor 1 in colorectal cancer with microsatellite instability.

artículo científico publicado en 2003

Hepatocyte nuclear factor 1alpha and beta control terminal differentiation and cell fate commitment in the gut epithelium

artículo científico publicado en 2010

Ikaros inhibits megakaryopoiesis through functional interaction with GATA-1 and NOTCH signaling

artículo científico publicado en 2013

PCR-based genotyping can generate artifacts in LOH analyses

artículo científico publicado en 1999

Presence of atypical thrombopoietin receptor (MPL) mutations in triple-negative essential thrombocythemia patients

artículo científico publicado en 2015

Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.

artículo científico publicado en 2012

RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization

artículo científico publicado en 2012

Specific association between alcohol intake, high grade of differentiation and 4q34-q35 deletions in hepatocellular carcinomas identified by high resolution allelotyping

artículo científico publicado en 2002

The cell division control protein 42-Src family kinase-neural Wiskott-Aldrich syndrome protein pathway regulates human proplatelet formation.

artículo científico publicado en 2016

Thrombocytopenia induced by the histone deacetylase inhibitor abexinostat involves p53-dependent and -independent mechanisms.

artículo científico publicado en 2013

Thrombospondin-1 is not the major activator of TGF-β1 in thrombopoietin-induced myelofibrosis

artículo científico publicado en 2010

[Genetic alterations in hepatocellular carcinomas: associations with clinical parameters]

artículo científico publicado en 2001

[Semi-automated quantitative method for detecting the loss of heterozygosity at the long arm of chromosome 4 in hepatocellular carcinoma]

artículo científico publicado en 1999

[The activation of p53 in tumors: a promising strategy against cancer]

scientific article published on 01 June 2007

p19 INK4d controls hematopoietic stem cells in a cell-autonomous manner during genotoxic stress and through the microenvironment during aging

artículo científico publicado en 2014

Lista de obras de Olivier Bluteau

A landscape of germline mutations in a cohort of inherited bone marrow failure patients

An incomplete trafficking defect to the cell-surface leads to paradoxical thrombocytosis for human and murine MPL P106L.

Beta-catenin mutations in hepatocellular carcinoma correlate with a low rate of loss of heterozygosity.

Bi-allelic inactivation of TCF1 in hepatic adenomas

Biallelic inactivation of REV7 is associated with Fanconi anemia

Biallelic inactivation of REV7 is associated with Fanconi anemia

Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models

Clinical and molecular analysis of combined hepatocellular-cholangiocarcinomas.

Critical role of the HDAC6-cortactin axis in human megakaryocyte maturation leading to a proplatelet-formation defect.

Developmental changes in human megakaryopoiesis.

Differential association of calreticulin type 1 and type 2 mutations with myelofibrosis and essential thrombocytemia: relevance for disease evolution

Frequent mutations of hepatocyte nuclear factor 1 in colorectal cancer with microsatellite instability.

Hepatocyte nuclear factor 1alpha and beta control terminal differentiation and cell fate commitment in the gut epithelium

Ikaros inhibits megakaryopoiesis through functional interaction with GATA-1 and NOTCH signaling

PCR-based genotyping can generate artifacts in LOH analyses

Presence of atypical thrombopoietin receptor (MPL) mutations in triple-negative essential thrombocythemia patients

Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.

RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization

Specific association between alcohol intake, high grade of differentiation and 4q34-q35 deletions in hepatocellular carcinomas identified by high resolution allelotyping

The cell division control protein 42-Src family kinase-neural Wiskott-Aldrich syndrome protein pathway regulates human proplatelet formation.

Thrombocytopenia induced by the histone deacetylase inhibitor abexinostat involves p53-dependent and -independent mechanisms.

Thrombospondin-1 is not the major activator of TGF-β1 in thrombopoietin-induced myelofibrosis

[Genetic alterations in hepatocellular carcinomas: associations with clinical parameters]

[Semi-automated quantitative method for detecting the loss of heterozygosity at the long arm of chromosome 4 in hepatocellular carcinoma]

[The activation of p53 in tumors: a promising strategy against cancer]

p19 INK4d controls hematopoietic stem cells in a cell-autonomous manner during genotoxic stress and through the microenvironment during aging