Lista de obras - Jude Fitzgibbon - Dominio Público Uruguay

A multi-gene signature predicts outcome in patients with pancreatic ductal adenocarcinoma

artículo científico publicado en 2014

A novel K509I mutation of KIT identified in familial mastocytosis-in vitro and in vivo responsiveness to imatinib therapy

artículo científico publicado en 2005

AZD1152 rapidly and negatively affects the growth and survival of human acute myeloid leukemia cells in vitro and in vivo

artículo científico publicado en 2009

Advances in the molecular diagnosis of diffuse large B-cell lymphoma in the era of precision medicine

artículo científico publicado en 2016

BLUEPRINT to decode the epigenetic signature written in blood.

artículo científico publicado en 2012

Chemosensitization of B-cell lymphomas by methylseleninic acid involves nuclear factor-kappaB inhibition and the rapid generation of other selenium species

artículo científico publicado en 2007

Chromosomal localization of three mouse diacylglycerol kinase (DAGK) genes: genes sharing sequence homology to the Drosophila retinal degeneration A (rdgA) gene ⬇️

artículo científico publicado el 10 de abril de 1995

Clinical relevance of MDM2 SNP 309 and TP53 Arg72Pro in follicular lymphoma

artículo científico publicado en 2008

Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies

artículo científico publicado en 2016

Development of a quantitative real-time polymerase chain reaction method for monitoring CEBPA mutations in normal karyotype acute myeloid leukaemia.

artículo científico publicado en 2006

Disease evolution and outcomes in familial AML with germline CEBPA mutations

artículo científico publicado en 2015

Drug ranking using machine learning systematically predicts the efficacy of anti-cancer drugs

artículo científico publicado en 2021

EZH2 mutations are frequent and represent an early event in follicular lymphoma

artículo científico publicado en 2013

Epigenetic dysregulation in follicular lymphoma

artículo científico

Erratum: Corrigendum: Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma

scholarly article published in Nature Genetics

Familial CEBPA-mutated acute myeloid leukemia

artículo científico publicado en 2017

Familial myelodysplasia and acute myeloid leukaemia--a review

artículo científico publicado en 2008

Follicular lymphoma: State-of-the-art ICML workshop in Lugano 2015.

artículo científico publicado en 2017

Follicular lymphomas with and without translocation t(14;18) differ in gene expression profiles and genetic alterations

artículo científico publicado en 2009

Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma

artículo científico publicado en 2016

Functional analysis of a breast cancer-associated FGFR2 single nucleotide polymorphism using zinc finger mediated genome editing

artículo científico publicado en 2013

GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations

artículo científico publicado en 2013

Genome-wide copy-number analyses reveal genomic abnormalities involved in transformation of follicular lymphoma

artículo científico publicado en 2013

Genomic analysis reveals epigenetic ‘addiction’ underpinning follicular lymphoma and its transformation – a rationale for targeted epigenetic therapies

artículo científico publicado en 2013

Genomic profiling for clinical decision making in lymphoid neoplasms

High Throughput Sequencing Analysis of the Immunoglobulin Heavy Chain Gene from Flow-Sorted B Cell Sub-Populations Define the Dynamics of Follicular Lymphoma Clonal Evolution

artículo científico publicado en 2015

Inherited DDX41 mutations: 11 genes and counting.

artículo científico publicado en 2016

Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma

artículo científico publicado en 2013

MicroRNA profiles of t(14;18)-negative follicular lymphoma support a late germinal center B-cell phenotype

artículo científico publicado en 2011

Molecular signatures in the diagnosis and management of follicular lymphoma

artículo científico publicado en 2010

Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party

artículo científico publicado en 2008

Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2.

artículo científico publicado en 2003

Mutations of the PU.1 Ets domain are specifically associated with murine radiation-induced, but not human therapy-related, acute myeloid leukaemia

artículo científico publicado en 2005

Myeloblative therapy with autologous haematopoietic stem cell support as consolidation of first remission in acute myeloid leukaemia - very long follow-up

artículo científico publicado en 2014

Presentation serum selenium predicts for overall survival, dose delivery, and first treatment response in aggressive non-Hodgkin's lymphoma

artículo científico publicado en 2003

Reduced Expression of Histone Methyltransferases KMT2C and KMT2D Correlates with Improved Outcome in Pancreatic Ductal Adenocarcinoma

artículo científico publicado en 2016

Regions of acquired uniparental disomy at diagnosis of follicular lymphoma are associated with both overall survival and risk of transformation

artículo científico publicado en 2009

SNP rs6457327 in the HLA region on chromosome 6p is predictive of the transformation of follicular lymphoma ⬇️

artículo científico publicado en 2011

TNFRSF14 aberrations in follicular lymphoma increase clinically significant allogeneic T-cell responses

artículo científico publicado en 2016

The clinical relevance of Wilms Tumour 1 (WT1) gene mutations in acute leukaemia

scientific article published on March 2010

The co-receptor BTLA negatively regulates human Vγ9Vδ2 T-cell proliferation: a potential way of immune escape for lymphoma cells.

artículo científico publicado en 2013

The presence of TP53 mutation at diagnosis of follicular lymphoma identifies a high-risk group of patients with shortened time to disease progression and poorer overall survival

artículo científico publicado en 2008

The rhodopsin-encoding gene of bony fish lacks introns ⬇️

artículo científico publicado el 27 de octubre de 1995

The routes for transformation of follicular lymphoma

artículo científico publicado en 2016

Transformation of follicular lymphoma to diffuse large B-cell lymphoma may occur by divergent evolution from a common progenitor cell or by direct evolution from the follicular lymphoma clone.

artículo científico publicado en 2009

Transformation of follicular lymphoma to diffuse large B-cell lymphoma proceeds by distinct oncogenic mechanisms

artículo científico publicado en 2007

Transformation of indolent B-cell lymphomas

artículo científico publicado en 2011

Lista de obras de Jude Fitzgibbon

A multi-gene signature predicts outcome in patients with pancreatic ductal adenocarcinoma

A novel K509I mutation of KIT identified in familial mastocytosis-in vitro and in vivo responsiveness to imatinib therapy

AZD1152 rapidly and negatively affects the growth and survival of human acute myeloid leukemia cells in vitro and in vivo

Advances in the molecular diagnosis of diffuse large B-cell lymphoma in the era of precision medicine

BLUEPRINT to decode the epigenetic signature written in blood.

Chemosensitization of B-cell lymphomas by methylseleninic acid involves nuclear factor-kappaB inhibition and the rapid generation of other selenium species

Chromosomal localization of three mouse diacylglycerol kinase (DAGK) genes: genes sharing sequence homology to the Drosophila retinal degeneration A (rdgA) gene ⬇️

Clinical relevance of MDM2 SNP 309 and TP53 Arg72Pro in follicular lymphoma

Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies

Development of a quantitative real-time polymerase chain reaction method for monitoring CEBPA mutations in normal karyotype acute myeloid leukaemia.

Disease evolution and outcomes in familial AML with germline CEBPA mutations

Drug ranking using machine learning systematically predicts the efficacy of anti-cancer drugs

EZH2 mutations are frequent and represent an early event in follicular lymphoma

Epigenetic dysregulation in follicular lymphoma

Erratum: Corrigendum: Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma

Familial CEBPA-mutated acute myeloid leukemia

Familial myelodysplasia and acute myeloid leukaemia--a review

Follicular lymphoma: State-of-the-art ICML workshop in Lugano 2015.

Follicular lymphomas with and without translocation t(14;18) differ in gene expression profiles and genetic alterations

Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma

Functional analysis of a breast cancer-associated FGFR2 single nucleotide polymorphism using zinc finger mediated genome editing

GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations

Genome-wide copy-number analyses reveal genomic abnormalities involved in transformation of follicular lymphoma

Genomic analysis reveals epigenetic ‘addiction’ underpinning follicular lymphoma and its transformation – a rationale for targeted epigenetic therapies

Genomic profiling for clinical decision making in lymphoid neoplasms

High Throughput Sequencing Analysis of the Immunoglobulin Heavy Chain Gene from Flow-Sorted B Cell Sub-Populations Define the Dynamics of Follicular Lymphoma Clonal Evolution

Inherited DDX41 mutations: 11 genes and counting.

Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma

MicroRNA profiles of t(14;18)-negative follicular lymphoma support a late germinal center B-cell phenotype

Molecular signatures in the diagnosis and management of follicular lymphoma

Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party

Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2.

Mutations of the PU.1 Ets domain are specifically associated with murine radiation-induced, but not human therapy-related, acute myeloid leukaemia

Myeloblative therapy with autologous haematopoietic stem cell support as consolidation of first remission in acute myeloid leukaemia - very long follow-up

Presentation serum selenium predicts for overall survival, dose delivery, and first treatment response in aggressive non-Hodgkin's lymphoma

Reduced Expression of Histone Methyltransferases KMT2C and KMT2D Correlates with Improved Outcome in Pancreatic Ductal Adenocarcinoma

Regions of acquired uniparental disomy at diagnosis of follicular lymphoma are associated with both overall survival and risk of transformation

SNP rs6457327 in the HLA region on chromosome 6p is predictive of the transformation of follicular lymphoma ⬇️

TNFRSF14 aberrations in follicular lymphoma increase clinically significant allogeneic T-cell responses

The clinical relevance of Wilms Tumour 1 (WT1) gene mutations in acute leukaemia

The co-receptor BTLA negatively regulates human Vγ9Vδ2 T-cell proliferation: a potential way of immune escape for lymphoma cells.

The presence of TP53 mutation at diagnosis of follicular lymphoma identifies a high-risk group of patients with shortened time to disease progression and poorer overall survival

The rhodopsin-encoding gene of bony fish lacks introns ⬇️

The routes for transformation of follicular lymphoma

Transformation of follicular lymphoma to diffuse large B-cell lymphoma may occur by divergent evolution from a common progenitor cell or by direct evolution from the follicular lymphoma clone.

Transformation of follicular lymphoma to diffuse large B-cell lymphoma proceeds by distinct oncogenic mechanisms

Transformation of indolent B-cell lymphomas