Lista de obras - James Taylor - Dominio Público Uruguay

A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia

artículo científico publicado en 2014

A network model to predict the risk of death in sickle cell disease

artículo científico publicado en 2007

Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia

artículo científico publicado en 2014

Ancestry of African Americans with sickle cell disease

artículo científico publicado en 2011

Association between chronic disseminated candidiasis in adult acute leukemia and common IL4 promoter haplotypes

artículo científico publicado en 2003

Association between plasma and urinary orosomucoid and chronic kidney disease in adults with sickle cell disease

scientific article published on 05 May 2020

Case series: biliary leak after transjugular liver biopsy

artículo científico publicado en 2013

Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia

artículo científico publicado en 2017

Cerebrovascular disease associated with sickle cell pulmonary hypertension

artículo científico publicado en 2006

Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain

artículo científico publicado en 2008

Common polymorphisms in critical genes of innate immunity do not contribute to the risk for chronic disseminated candidiasis in adult leukemia patients

artículo científico publicado en 2005

Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2.

artículo científico publicado en 2004

Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United Kingdom

artículo científico publicado en 2011

Endogenous nitric oxide synthase inhibitors in sickle cell disease: abnormal levels and correlations with pulmonary hypertension, desaturation, haemolysis, organ dysfunction and death

artículo científico publicado en 2008

Fetal haemoglobin response to hydroxycarbamide treatment and sar1a promoter polymorphisms in sickle cell anaemia

artículo científico publicado en 2008

Frequency of Hospitalizations for Pain and Association With Altered Brain Network Connectivity in Sickle Cell Disease

artículo científico publicado en 2015

Functional profiling of uncommon VCAM1 promoter polymorphisms prevalent in African American populations

artículo científico publicado en 2007

Genetic determinants of haemolysis in sickle cell anaemia

artículo científico publicado en 2013

Genomic and functional analysis of the sodium-dependent vitamin C transporter SLC23A1-SVCT1.

artículo científico publicado en 2007

Harnessing genomics to identify environmental determinants of heritable disease

artículo científico publicado en 2012

Hematologic, biochemical, and cardiopulmonary effects of L-arginine supplementation or phosphodiesterase 5 inhibition in patients with sickle cell disease who are on hydroxyurea therapy

artículo científico publicado en 2008

Heme-bound iron activates placenta growth factor in erythroid cells via erythroid Krüppel-like factor

artículo científico publicado en 2014

Hemodynamic predictors of mortality in adults with sickle cell disease

artículo científico publicado en 2013

Hydroxyurea-Increased Fetal Hemoglobin Is Associated with Less Organ Damage and Longer Survival in Adults with Sickle Cell Anemia

artículo científico publicado en 2015

Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models

artículo científico publicado en 2009

Identification of novel microRNA signatures linked to acquired aplastic anemia

artículo científico publicado en 2015

Introduction to next-generation nucleic acid sequencing in cardiovascular disease research

artículo científico publicado en 2013

Iron, inflammation, and early death in adults with sickle cell disease

artículo científico publicado en 2014

Laboratory and echocardiography markers in sickle cell patients with leg ulcers ⬇️

artículo científico publicado en 2011

Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease

artículo científico publicado en 2005

Lipid levels in sickle-cell disease associated with haemolytic severity, vascular dysfunction and pulmonary hypertension

artículo científico publicado en 2010

Liver injury is associated with mortality in sickle cell disease

artículo científico publicado en 2015

Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia

artículo científico publicado en 2011

Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans

artículo científico publicado en 2012

Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease

artículo científico publicado en 2008

Oscillatory haematopoiesis in adults with sickle cell disease treated with hydroxycarbamide

artículo científico publicado en 2014

Patterns of low-affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease

artículo científico publicado en 2002

Pleiotropic effects of intravascular haemolysis on vascular homeostasis

artículo científico publicado en 2009

Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models

artículo científico publicado en 2014

Prostacyclin-analog therapy in sickle cell pulmonary hypertension.

artículo científico publicado en 2017

Reconstruction of Thermographic Signals to Map Perforator Vessels in Humans

artículo científico publicado en 2012

Reduced sensitivity of the ferroportin Q248H mutant to physiological concentrations of hepcidin

artículo científico publicado en 2012

Relative systemic hypertension in patients with sickle cell disease is associated with risk of pulmonary hypertension and renal insufficiency

artículo científico publicado en 2008

Restriction of HIV-1 infection in sickle cell trait

artículo científico publicado en 2021

Risk factors for death in 632 patients with sickle cell disease in the United States and United Kingdom

artículo científico publicado en 2014

Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection

scientific article published on 01 September 2004

Sequencing PCR-amplified DNA in lipoprotein and cardiovascular disease research

artículo científico publicado en 2013

Severe painful vaso-occlusive crises and mortality in a contemporary adult sickle cell anemia cohort study

artículo científico publicado en 2013

Severe pulmonary hypertension in an adolescent with sickle cell disease

artículo científico publicado en 2008

Sickle cell disease and pulmonary hypertension in Africa: a global perspective and review of epidemiology, pathophysiology, and management

artículo científico publicado en 2008

Sleep disturbance, depression and pain in adults with sickle cell disease

artículo científico publicado en 2014

Transcriptome profiling and sequencing of differentiated human hematopoietic stem cells reveal lineage-specific expression and alternative splicing of genes

artículo científico publicado en 2011

Transplant-associated Ochroconis gallopava infections

artículo científico publicado en 2008

Tricuspid Regurgitation Velocity and Other Biomarkers of Mortality in Children, Adolescents and Young Adults with Sickle Cell Disease in the United States: the PUSH Study

scientific article published on 03 April 2020

Using genetic variation to study human disease ⬇️

artículo científico publicado el 1 de noviembre de 2001

Using genetic variation to study immunomodulation

artículo científico publicado en 2002

Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease

artículo científico publicado en 2002

Lista de obras de James Taylor

A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia

A network model to predict the risk of death in sickle cell disease

Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia

Ancestry of African Americans with sickle cell disease

Association between chronic disseminated candidiasis in adult acute leukemia and common IL4 promoter haplotypes

Association between plasma and urinary orosomucoid and chronic kidney disease in adults with sickle cell disease

Case series: biliary leak after transjugular liver biopsy

Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia

Cerebrovascular disease associated with sickle cell pulmonary hypertension

Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain

Common polymorphisms in critical genes of innate immunity do not contribute to the risk for chronic disseminated candidiasis in adult leukemia patients

Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2.

Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United Kingdom

Endogenous nitric oxide synthase inhibitors in sickle cell disease: abnormal levels and correlations with pulmonary hypertension, desaturation, haemolysis, organ dysfunction and death

Fetal haemoglobin response to hydroxycarbamide treatment and sar1a promoter polymorphisms in sickle cell anaemia

Frequency of Hospitalizations for Pain and Association With Altered Brain Network Connectivity in Sickle Cell Disease

Functional profiling of uncommon VCAM1 promoter polymorphisms prevalent in African American populations

Genetic determinants of haemolysis in sickle cell anaemia

Genomic and functional analysis of the sodium-dependent vitamin C transporter SLC23A1-SVCT1.

Harnessing genomics to identify environmental determinants of heritable disease

Hematologic, biochemical, and cardiopulmonary effects of L-arginine supplementation or phosphodiesterase 5 inhibition in patients with sickle cell disease who are on hydroxyurea therapy

Heme-bound iron activates placenta growth factor in erythroid cells via erythroid Krüppel-like factor

Hemodynamic predictors of mortality in adults with sickle cell disease

Hydroxyurea-Increased Fetal Hemoglobin Is Associated with Less Organ Damage and Longer Survival in Adults with Sickle Cell Anemia

Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models

Identification of novel microRNA signatures linked to acquired aplastic anemia

Introduction to next-generation nucleic acid sequencing in cardiovascular disease research

Iron, inflammation, and early death in adults with sickle cell disease

Laboratory and echocardiography markers in sickle cell patients with leg ulcers ⬇️

Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease

Lipid levels in sickle-cell disease associated with haemolytic severity, vascular dysfunction and pulmonary hypertension

Liver injury is associated with mortality in sickle cell disease

Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia

Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans

Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease

Oscillatory haematopoiesis in adults with sickle cell disease treated with hydroxycarbamide

Patterns of low-affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease

Pleiotropic effects of intravascular haemolysis on vascular homeostasis

Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models

Prostacyclin-analog therapy in sickle cell pulmonary hypertension.

Reconstruction of Thermographic Signals to Map Perforator Vessels in Humans

Reduced sensitivity of the ferroportin Q248H mutant to physiological concentrations of hepcidin

Relative systemic hypertension in patients with sickle cell disease is associated with risk of pulmonary hypertension and renal insufficiency

Restriction of HIV-1 infection in sickle cell trait

Risk factors for death in 632 patients with sickle cell disease in the United States and United Kingdom

Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection

Sequencing PCR-amplified DNA in lipoprotein and cardiovascular disease research

Severe painful vaso-occlusive crises and mortality in a contemporary adult sickle cell anemia cohort study

Severe pulmonary hypertension in an adolescent with sickle cell disease

Sickle cell disease and pulmonary hypertension in Africa: a global perspective and review of epidemiology, pathophysiology, and management

Sleep disturbance, depression and pain in adults with sickle cell disease

Transcriptome profiling and sequencing of differentiated human hematopoietic stem cells reveal lineage-specific expression and alternative splicing of genes

Transplant-associated Ochroconis gallopava infections

Tricuspid Regurgitation Velocity and Other Biomarkers of Mortality in Children, Adolescents and Young Adults with Sickle Cell Disease in the United States: the PUSH Study

Using genetic variation to study human disease ⬇️

Using genetic variation to study immunomodulation

Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease