Lista de obras - Fred G Pluthero - Dominio Público Uruguay

A Hypoxia-Inducible HIF1-GAL3ST1-Sulfatide Axis Enhances ccRCC Immune Evasion via Increased Tumor Cell-Platelet Binding

artículo científico publicado en 2019

Abnormal fibrinolysis recognized by thromboelastography in a case of severe bleeding with normal coagulation and platelet function, leads to detection of a novel SERPINF2 variant causing severe alpha-2-antiplasmin deficiency

scientific article published on 08 July 2019

Abnormal megakaryocyte development and platelet function in Nbeal2(-/-) mice

artículo científico publicado en 2013

Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy

artículo científico publicado en 2013

Abnormalities in villin gene expression and canalicular microvillus structure in progressive cholestatic liver disease of childhood

artículo científico

Balancing the yin and yang of SINE.

artículo científico publicado en 2017

Complement Activation Induces Neutrophil Adhesion and Neutrophil-Platelet Aggregate Formation on Vascular Endothelial Cells

artículo científico publicado en 2016

Decreased in vitro thrombin generation and clot stability in human FXII-null blood and plasma

artículo científico publicado en 2010

Decreased numbers of dense granules in fetal and neonatal platelets

artículo científico publicado en 2016

Diannexin, an annexin A5 homodimer, binds phosphatidylserine with high affinity and is a potent inhibitor of platelet-mediated events during thrombus formation.

artículo científico publicado en 2012

Discrepant platelet and plasma von Willebrand factor in von Willebrand disease patients with p.Pro2808Leufs*24.

artículo científico publicado en 2017

Dynamin 2-dependent endocytosis is required for normal megakaryocyte development in mice

artículo científico publicado en 2014

Eculizumab and Refractory Membranoproliferative Glomerulonephritis

artículo científico publicado en 2012

Eculizumab therapy in children with severe hematopoietic stem cell transplantation-associated thrombotic microangiopathy.

artículo científico publicado en 2013

Effect of moderate intensity exercise on haemostatic capacity in adults with haemophilia A and B: pilot study.

artículo científico publicado en 2017

FlnA binding to PACSIN2 F-BAR domain regulates membrane tubulation in megakaryocytes and platelets

artículo científico publicado en 2015

Genetic differences in malathion avoidance and resistance in Drosophila melanogaster.

artículo científico publicado en 1981

Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.

artículo científico publicado en 2015

Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryocyte and platelet function defects

scientific article published on 10 December 2020

Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

artículo científico publicado en 2013

Impact of aerobic exercise on haemostatic indices in paediatric patients with haemophilia

artículo científico publicado en 2016

Intracellular Trafficking, Localization, and Mobilization of Platelet-Borne Thiol Isomerases.

artículo científico publicado en 2016

Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.

artículo científico publicado en 2017

Megakaryocyte and platelet abnormalities in a patient with a W33C mutation in the conserved SH3-like domain of myosin heavy chain IIA.

artículo científico publicado en 2009

Monitoring and modeling treatment of atypical hemolytic uremic syndrome

artículo científico publicado en 2012

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome

artículo científico publicado en 2011

NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes

artículo científico publicado en 2018

NETosing Neutrophils Activate Complement Both on Their Own NETs and Bacteria via Alternative and Non-alternative Pathways

artículo científico publicado en 2016

Non-genomic activities of retinoic acid receptor alpha control actin cytoskeletal events in human platelets.

artículo científico publicado en 2016

Platelet production: new players in the field

artículo científico publicado en 2016

Platelet-associated complement factor H in healthy persons and patients with atypical HUS.

artículo científico publicado en 2009

Purification of an inhibitor of erythroid progenitor cell cycling and antagonist to interleukin 3 from mouse marrow cell supernatants and its identification as cytosolic superoxide dismutase

artículo científico publicado en 1990

Rapid purification of high-activity Taq DNA polymerase

artículo científico publicado en 1993

Relative antibacterial functions of complement and NETs: NETs trap and complement effectively kills bacteria.

artículo científico publicado en 2018

Some aspects of maze behavior in Drosophila melanogaster ⬇️

artículo científico publicado el 1 de junio de 1979

Successful treatment of DEAP-HUS with eculizumab

artículo científico publicado en 2013

Superoxide Dismutase Specifically Inhibits Erythroid Cell DNA Synthesis and Proliferation ⬇️

artículo científico publicado el 1 de enero de 1991

The Birth and Death of Platelets in Health and Disease.

artículo científico publicado en 2018

The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis

artículo científico publicado en 2012

The cell motility modulator Slit2 is a potent inhibitor of platelet function

artículo científico publicado en 2012

Thromboelastography and thrombin generation assessments for pediatric severe hemophilia A patients are highly variable and not predictive of clinical phenotypes

artículo científico publicado en 2022

Von Willebrand factor regulates complement on endothelial cells.

artículo científico publicado en 2016

α-granule biogenesis: from disease to discovery

artículo científico publicado en 2017

Lista de obras de Fred G Pluthero

A Hypoxia-Inducible HIF1-GAL3ST1-Sulfatide Axis Enhances ccRCC Immune Evasion via Increased Tumor Cell-Platelet Binding

Abnormal fibrinolysis recognized by thromboelastography in a case of severe bleeding with normal coagulation and platelet function, leads to detection of a novel SERPINF2 variant causing severe alpha-2-antiplasmin deficiency

Abnormal megakaryocyte development and platelet function in Nbeal2(-/-) mice

Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy

Abnormalities in villin gene expression and canalicular microvillus structure in progressive cholestatic liver disease of childhood

Balancing the yin and yang of SINE.

Complement Activation Induces Neutrophil Adhesion and Neutrophil-Platelet Aggregate Formation on Vascular Endothelial Cells

Decreased in vitro thrombin generation and clot stability in human FXII-null blood and plasma

Decreased numbers of dense granules in fetal and neonatal platelets

Diannexin, an annexin A5 homodimer, binds phosphatidylserine with high affinity and is a potent inhibitor of platelet-mediated events during thrombus formation.

Discrepant platelet and plasma von Willebrand factor in von Willebrand disease patients with p.Pro2808Leufs*24.

Dynamin 2-dependent endocytosis is required for normal megakaryocyte development in mice

Eculizumab and Refractory Membranoproliferative Glomerulonephritis

Eculizumab therapy in children with severe hematopoietic stem cell transplantation-associated thrombotic microangiopathy.

Effect of moderate intensity exercise on haemostatic capacity in adults with haemophilia A and B: pilot study.

FlnA binding to PACSIN2 F-BAR domain regulates membrane tubulation in megakaryocytes and platelets

Genetic differences in malathion avoidance and resistance in Drosophila melanogaster.

Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.

Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryocyte and platelet function defects

Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

Impact of aerobic exercise on haemostatic indices in paediatric patients with haemophilia

Intracellular Trafficking, Localization, and Mobilization of Platelet-Borne Thiol Isomerases.

Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.

Megakaryocyte and platelet abnormalities in a patient with a W33C mutation in the conserved SH3-like domain of myosin heavy chain IIA.

Monitoring and modeling treatment of atypical hemolytic uremic syndrome

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome

NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes

NETosing Neutrophils Activate Complement Both on Their Own NETs and Bacteria via Alternative and Non-alternative Pathways

Non-genomic activities of retinoic acid receptor alpha control actin cytoskeletal events in human platelets.

Platelet production: new players in the field

Platelet-associated complement factor H in healthy persons and patients with atypical HUS.

Purification of an inhibitor of erythroid progenitor cell cycling and antagonist to interleukin 3 from mouse marrow cell supernatants and its identification as cytosolic superoxide dismutase

Rapid purification of high-activity Taq DNA polymerase

Relative antibacterial functions of complement and NETs: NETs trap and complement effectively kills bacteria.

Some aspects of maze behavior in Drosophila melanogaster ⬇️

Successful treatment of DEAP-HUS with eculizumab

Superoxide Dismutase Specifically Inhibits Erythroid Cell DNA Synthesis and Proliferation ⬇️

The Birth and Death of Platelets in Health and Disease.

The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis

The cell motility modulator Slit2 is a potent inhibitor of platelet function

Thromboelastography and thrombin generation assessments for pediatric severe hemophilia A patients are highly variable and not predictive of clinical phenotypes

Von Willebrand factor regulates complement on endothelial cells.

α-granule biogenesis: from disease to discovery