Lista de obras - Henrik Lilljebjörn - Dominio Público Uruguay

A glioma classification scheme based on coexpression modules of EGFR and PDGFRA.

artículo científico publicado en 2014

A novelSERPINE1-FOSBfusion gene results in transcriptional up-regulation ofFOSBin pseudomyogenic haemangioendothelioma

article

Activation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney

artículo científico publicado en 2014

Arrayed molecular barcoding identifies TNFSF13 as a positive regulator of acute myeloid leukemia-initiating cells

artículo científico publicado en 2019

BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias

artículo científico publicado en 2008

CD36 defines primitive chronic myeloid leukemia cells less responsive to imatinib but vulnerable to antibody-based therapeutic targeting.

artículo científico publicado en 2017

Clonal competition within complex evolutionary hierarchies shapes AML over time

artículo científico publicado en 2020

Clonal conversion of B lymphoid leukemia reveals cross-lineage transfer of malignant states.

artículo científico publicado en 2016

Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within

artículo científico publicado en 2007

Distinct global binding patterns of the Wilms tumor gene 1 (WT1) -KTS and +KTS isoforms in leukemic cells

artículo científico publicado en 2016

Ebf1 heterozygosity results in increased DNA damage in pro-B cells and their synergistic transformation by Pax5 haploinsufficiency

artículo científico publicado en 2015

FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns

artículo científico publicado en 2008

FLT3N676K drives acute myeloid leukemia in a xenograft model of KMT2A-MLLT3 leukemogenesis

scientific article published on 05 April 2019

Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome

artículo científico publicado en 2007

Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma

artículo científico publicado en 2014

GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.

artículo científico publicado en 2014

Genetic analysis of dasatinib-treated chronic myeloid leukemia rapidly developing into acute myeloid leukemia with monosomy 7 in Philadelphia-negative cells

artículo científico publicado en 2010

Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2010

Genomic profiling and directed ex vivo drug analysis of an unclassifiable myelodysplastic/myeloproliferative neoplasm progressing into acute myeloid leukemia

artículo científico publicado en 2016

IL1RAP antibodies block IL-1-induced expansion of candidate CML stem cells and mediate cell killing in xenograft models.

artículo científico publicado en 2016

Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

artículo científico publicado en 2016

Integrative analysis of gene expression and copy number alterations using canonical correlation analysis

artículo científico publicado en 2010

Isolated myelosarcoma is characterized by recurrent NFE2 mutations and concurrent preleukemic clones in the bone marrow.

artículo científico publicado en 2017

MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia.

artículo científico publicado en 2006

Modeling chronic myeloid leukemia in immunodeficient mice reveals expansion of aberrant mast cells and accumulation of pre-B cells.

artículo científico publicado en 2014

Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia.

artículo científico publicado en 2018

Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations

scientific article published on 17 November 2011

New oncogenic subtypes in pediatric B-cell precursor acute lymphoblastic leukemia

artículo científico publicado en 2017

PAX5 is part of a functional transcription factor network targeted in lymphoid leukemia

artículo científico publicado en 2019

Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2019

RNA-seq identifies clinically relevant fusion genes in leukemia including a novel MEF2D/CSF1R fusion responsive to imatinib

artículo científico publicado en 2014

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.

artículo científico publicado en 2010

The DNA methylome of pediatric acute lymphoblastic leukemia

artículo científico publicado en 2009

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2015

Transcriptional landscape of B cell precursor acute lymphoblastic leukemia based on an international study of 1,223 cases. ⬇️

artículo científico publicado en 2018

Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia

artículo científico publicado en 2018

Whole-exome sequencing of pediatric acute lymphoblastic leukemia.

artículo científico publicado en 2011

Lista de obras de Henrik Lilljebjörn

A glioma classification scheme based on coexpression modules of EGFR and PDGFRA.

A novelSERPINE1-FOSBfusion gene results in transcriptional up-regulation ofFOSBin pseudomyogenic haemangioendothelioma

Activation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney

Arrayed molecular barcoding identifies TNFSF13 as a positive regulator of acute myeloid leukemia-initiating cells

BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias

CD36 defines primitive chronic myeloid leukemia cells less responsive to imatinib but vulnerable to antibody-based therapeutic targeting.

Clonal competition within complex evolutionary hierarchies shapes AML over time

Clonal conversion of B lymphoid leukemia reveals cross-lineage transfer of malignant states.

Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within

Distinct global binding patterns of the Wilms tumor gene 1 (WT1) -KTS and +KTS isoforms in leukemic cells

Ebf1 heterozygosity results in increased DNA damage in pro-B cells and their synergistic transformation by Pax5 haploinsufficiency

FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns

FLT3N676K drives acute myeloid leukemia in a xenograft model of KMT2A-MLLT3 leukemogenesis

Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome

Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma

GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.

Genetic analysis of dasatinib-treated chronic myeloid leukemia rapidly developing into acute myeloid leukemia with monosomy 7 in Philadelphia-negative cells

Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

Genomic profiling and directed ex vivo drug analysis of an unclassifiable myelodysplastic/myeloproliferative neoplasm progressing into acute myeloid leukemia

IL1RAP antibodies block IL-1-induced expansion of candidate CML stem cells and mediate cell killing in xenograft models.

Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

Integrative analysis of gene expression and copy number alterations using canonical correlation analysis

Isolated myelosarcoma is characterized by recurrent NFE2 mutations and concurrent preleukemic clones in the bone marrow.

MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia.

Modeling chronic myeloid leukemia in immunodeficient mice reveals expansion of aberrant mast cells and accumulation of pre-B cells.

Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia.

Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations

New oncogenic subtypes in pediatric B-cell precursor acute lymphoblastic leukemia

PAX5 is part of a functional transcription factor network targeted in lymphoid leukemia

Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

RNA-seq identifies clinically relevant fusion genes in leukemia including a novel MEF2D/CSF1R fusion responsive to imatinib

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.

The DNA methylome of pediatric acute lymphoblastic leukemia

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

Transcriptional landscape of B cell precursor acute lymphoblastic leukemia based on an international study of 1,223 cases. ⬇️

Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia

Whole-exome sequencing of pediatric acute lymphoblastic leukemia.