Lista de obras - Matthew J Rose-Zerilli - Dominio Público Uruguay

13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia.

artículo científico publicado en 2010

ADAM33 expression in atherosclerotic lesions and relationship of ADAM33 gene variation with atherosclerosis

article

ATM mutation rather than BIRC3 deletion and/or mutation predicts reduced survival in 11q-deleted chronic lymphocytic leukemia: data from the UK LRF CLL4 trial.

artículo científico publicado en 2014

Alpha-tryptase gene variation is associated with levels of circulating IgE and lung function in asthma

artículo científico publicado en 2014

An optimised tissue disaggregation and data processing pipeline for characterising fibroblast phenotypes using single-cell RNA sequencing

artículo científico publicado en 2019

Antibody Tumor Targeting Is Enhanced by CD27 Agonists through Myeloid Recruitment.

artículo científico publicado en 2017

Association analysis of brain-derived neurotrophic factor gene polymorphisms in asthmatic families

artículo científico publicado en 2009

Authentication and characterisation of a new oesophageal adenocarcinoma cell line: MFD-1.

artículo científico publicado en 2016

Author Correction: Authentication and characterisation of a new oesophageal adenocarcinoma cell line: MFD-1

artículo científico publicado en 2019

CBL-MZ is not a single biological entity: evidence from genomic analysis and prolonged clinical follow-up

artículo científico publicado en 2018

Cancer cachexia is associated with the IL10 -1082 gene promoter polymorphism in patients with gastroesophageal malignancy.

artículo científico publicado en 2009

Clinical significance of DNA methylation in chronic lymphocytic leukemia patients: results from 3 UK clinical trials

scientific article published on 01 August 2019

Copy-number variation genotyping of GSTT1 and GSTM1 gene deletions by real-time PCR.

artículo científico publicado en 2009

Correction: Evaluation of High-Throughput Genomic Assays for the Fc Gamma Receptor Locus.

artículo científico publicado en 2016

Evaluation of High-Throughput Genomic Assays for the Fc Gamma Receptor Locus.

artículo científico publicado en 2015

Evidence of association between interferon regulatory factor 5 gene polymorphisms and asthma

article

Exome sequence read depth methods for identifying copy number changes

artículo científico publicado en 2014

Fcγ receptors: genetic variation, function, and disease.

artículo científico publicado en 2015

Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemia.

artículo científico publicado en 2016

Genomic programming of IRF4-expressing human Langerhans cells

artículo científico publicado en 2020

Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data

artículo científico publicado en 2009

Identification of ATPAF1 as a novel candidate gene for asthma in children

artículo científico publicado en 2011

Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B).

artículo científico publicado en 2017

Longitudinal copy number, whole exome and targeted deep sequencing of 'good risk' IGHV-mutated CLL patients with progressive disease

artículo científico publicado en 2016

Low frequency mutations independently predict poor treatment-free survival in early stage chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis.

artículo científico publicado en 2015

Maternal Nrf2 and gluthathione-S-transferase polymorphisms do not modify associations of prenatal tobacco smoke exposure with asthma and lung function in school-aged children.

artículo científico publicado en 2010

Mortality in adult intensive care patients with severe systemic inflammatory response syndromes is strongly associated with the hypo-immune TNF -238A polymorphism

artículo científico publicado en 2009

Neurophysiological evidence for cognitive and brain functional adaptation in adolescents living at high altitude

article

Non-coding NOTCH1 mutations in chronic lymphocytic leukemia; their clinical impact in the UK CLL4 trial.

scientific article published on 24 October 2016

PLAUR polymorphisms are associated with asthma, PLAUR levels, and lung function decline

artículo científico publicado en 2009

Prenatal and infant acetaminophen exposure, antioxidant gene polymorphisms, and childhood asthma.

artículo científico publicado en 2010

Single-cell analysis based dissection of clonality in myelofibrosis

scientific article published on 07 January 2020

Stem cell-like breast cancer cells with acquired resistance to metformin are sensitive to inhibitors of NADH-dependent CtBP dimerization

scientific article published on 01 July 2019

Subclonal Evolution of Cancer-Related Gene Mutations in p53 Immunopositive Patches in Human Skin.

artículo científico publicado en 2017

Surface IgM expression and function are associated with clinical behavior, genetic abnormalities, and DNA methylation in CLL.

artículo científico publicado en 2016

Telomere length predicts progression and overall survival in chronic lymphocytic leukemia: data from the UK LRF CLL4 trial.

artículo científico publicado en 2015

The SF3B1 inhibitor spliceostatin A (SSA) elicits apoptosis in chronic lymphocytic leukaemia cells through downregulation of Mcl-1.

artículo científico publicado en 2015

The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial.

artículo científico publicado en 2013

The effects of restricted glycolysis on stem-cell like characteristics of breast cancer cells.

artículo científico publicado en 2018

The relationship between infant lung function and the risk of wheeze in the preschool years.

artículo científico publicado en 2010

The role of histamine degradation gene polymorphisms in moderating the effects of food additives on children's ADHD symptoms

artículo científico publicado en 2010

Whole exome sequencing identifies novel recurrently mutated genes in patients with splenic marginal zone lymphoma

artículo científico publicado en 2013

Lista de obras de Matthew J Rose-Zerilli

13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia.

ADAM33 expression in atherosclerotic lesions and relationship of ADAM33 gene variation with atherosclerosis

ATM mutation rather than BIRC3 deletion and/or mutation predicts reduced survival in 11q-deleted chronic lymphocytic leukemia: data from the UK LRF CLL4 trial.

Alpha-tryptase gene variation is associated with levels of circulating IgE and lung function in asthma

An optimised tissue disaggregation and data processing pipeline for characterising fibroblast phenotypes using single-cell RNA sequencing

Antibody Tumor Targeting Is Enhanced by CD27 Agonists through Myeloid Recruitment.

Association analysis of brain-derived neurotrophic factor gene polymorphisms in asthmatic families

Authentication and characterisation of a new oesophageal adenocarcinoma cell line: MFD-1.

Author Correction: Authentication and characterisation of a new oesophageal adenocarcinoma cell line: MFD-1

CBL-MZ is not a single biological entity: evidence from genomic analysis and prolonged clinical follow-up

Cancer cachexia is associated with the IL10 -1082 gene promoter polymorphism in patients with gastroesophageal malignancy.

Clinical significance of DNA methylation in chronic lymphocytic leukemia patients: results from 3 UK clinical trials

Copy-number variation genotyping of GSTT1 and GSTM1 gene deletions by real-time PCR.

Correction: Evaluation of High-Throughput Genomic Assays for the Fc Gamma Receptor Locus.

Evaluation of High-Throughput Genomic Assays for the Fc Gamma Receptor Locus.

Evidence of association between interferon regulatory factor 5 gene polymorphisms and asthma

Exome sequence read depth methods for identifying copy number changes

Fcγ receptors: genetic variation, function, and disease.

Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemia.

Genomic programming of IRF4-expressing human Langerhans cells

Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data

Identification of ATPAF1 as a novel candidate gene for asthma in children

Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B).

Longitudinal copy number, whole exome and targeted deep sequencing of 'good risk' IGHV-mutated CLL patients with progressive disease

Low frequency mutations independently predict poor treatment-free survival in early stage chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis.

Maternal Nrf2 and gluthathione-S-transferase polymorphisms do not modify associations of prenatal tobacco smoke exposure with asthma and lung function in school-aged children.

Mortality in adult intensive care patients with severe systemic inflammatory response syndromes is strongly associated with the hypo-immune TNF -238A polymorphism

Neurophysiological evidence for cognitive and brain functional adaptation in adolescents living at high altitude

Non-coding NOTCH1 mutations in chronic lymphocytic leukemia; their clinical impact in the UK CLL4 trial.

PLAUR polymorphisms are associated with asthma, PLAUR levels, and lung function decline

Prenatal and infant acetaminophen exposure, antioxidant gene polymorphisms, and childhood asthma.

Single-cell analysis based dissection of clonality in myelofibrosis

Stem cell-like breast cancer cells with acquired resistance to metformin are sensitive to inhibitors of NADH-dependent CtBP dimerization

Subclonal Evolution of Cancer-Related Gene Mutations in p53 Immunopositive Patches in Human Skin.

Surface IgM expression and function are associated with clinical behavior, genetic abnormalities, and DNA methylation in CLL.

Telomere length predicts progression and overall survival in chronic lymphocytic leukemia: data from the UK LRF CLL4 trial.

The SF3B1 inhibitor spliceostatin A (SSA) elicits apoptosis in chronic lymphocytic leukaemia cells through downregulation of Mcl-1.

The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial.

The effects of restricted glycolysis on stem-cell like characteristics of breast cancer cells.

The relationship between infant lung function and the risk of wheeze in the preschool years.

The role of histamine degradation gene polymorphisms in moderating the effects of food additives on children's ADHD symptoms

Whole exome sequencing identifies novel recurrently mutated genes in patients with splenic marginal zone lymphoma