Lista de obras -

A heparin-bonded vascular graft generates no systemic effect on markers of hemostasis activation or detectable heparin-induced thrombocytopenia-associated antibodies in humans

artículo científico publicado en 2008

A nonsynonymous SNP in the ITGB3 gene disrupts the conserved membrane-proximal cytoplasmic salt bridge in the alphaIIbbeta3 integrin and cosegregates dominantly with abnormal proplatelet formation and macrothrombocytopenia

artículo científico publicado en 2007

A novel nanobody that detects the gain-of-function phenotype of von Willebrand factor in ADAMTS13 deficiency and von Willebrand disease type 2B.

artículo científico publicado en 2005

A single high-affinity binding site for von Willebrand factor in collagen III, identified using synthetic triple-helical peptides

artículo científico publicado en 2006

ADAMTS13 deficiency with elevated levels of ultra-large and active von Willebrand factor in P. falciparum and P. vivax malaria.

artículo científico publicado en 2009

Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia

artículo científico publicado en 2013

Activated factor V is a cofactor for the activation of factor XI by thrombin in plasma.

artículo científico publicado en 2010

Antiphospholipid antibodies promote leukocyte-endothelial cell adhesion and thrombosis in mice by antagonizing eNOS via β2GPI and apoER2.

artículo científico publicado en 2010

Antiphospholipid syndrome: clinical and immunologic manifestations and patterns of disease expression in a cohort of 1,000 patients

artículo científico publicado en 2002

Beta2-glycoprotein I can exist in 2 conformations: implications for our understanding of the antiphospholipid syndrome.

artículo científico publicado en 2010

Cell-collagen interactions: the use of peptide Toolkits to investigate collagen-receptor interactions.

artículo científico publicado en 2008

Challenges of molecular nutrition research 6: the nutritional phenotype database to store, share and evaluate nutritional systems biology studies

artículo científico publicado en 2010

Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients

artículo científico publicado en 2008

Dimers of beta 2-glycoprotein I increase platelet deposition to collagen via interaction with phospholipids and the apolipoprotein E receptor 2'

artículo científico publicado en 2003

Endocannabinoids control platelet activation and limit aggregate formation under flow

artículo científico publicado en 2014

Functional platelet defects in children with severe chronic ITP as tested with 2 novel assays applicable for low platelet counts

artículo científico publicado en 2014

Higher and lower active circulating VWF levels: different facets of von Willebrand disease

artículo científico publicado en 2015

Imbalance of angiopoietin-1 and angiopoetin-2 in severe dengue and relationship with thrombocytopenia, endothelial activation, and vascular stability

artículo científico publicado en 2012

Indications for a protective function of beta2-glycoprotein I in thrombotic thrombocytopenic purpura

artículo científico publicado en 2012

Interference with the host haemostatic system by schistosomes

artículo científico publicado en 2013

Keeping von Willebrand Factor under Control: Alternatives for ADAMTS13.

artículo científico publicado en 2015

Misfolded proteins activate factor XII in humans, leading to kallikrein formation without initiating coagulation

artículo científico publicado en 2008

Molecular Imaging of Activated von Willebrand Factor to Detect High-Risk Atherosclerotic Phenotype ⬇️

artículo científico publicado el 1 de septiembre de 2010

Mutation and ADAMTS13-dependent modulation of disease severity in a mouse model for von Willebrand disease type 2B.

artículo científico publicado en 2010

Plasmin cleavage of von Willebrand factor as an emergency bypass for ADAMTS13 deficiency in thrombotic microangiopathy

artículo científico publicado en 2014

Prolonged fluid shear stress induces a distinct set of endothelial cell genes, most specifically lung Krüppel-like factor (KLF2)

artículo científico publicado en 2002

Severe dengue is associated with consumption of von Willebrand factor and its cleaving enzyme ADAMTS-13

artículo científico publicado en 2012

Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain

artículo científico publicado en 2002

Synergism between platelet collagen receptors defined using receptor-specific collagen-mimetic peptide substrata in flowing blood

artículo científico publicado en 2010

Synergistic effects of hypofibrinolysis and genetic and acquired risk factors on the risk of a first venous thrombosis

artículo científico publicado en 2008

The effect of recombinant IgG antibodies against the leucine-33 form of the platelet beta3 integrin (HPA-1a) on platelet function

artículo científico publicado en 2004

The embryonic genes Dkk3, Hoxd8, Hoxd9 and Tbx1 identify muscle types in a diet-independent and fiber-type unrelated way.

artículo científico publicado en 2010

The functions of the A1A2A3 domains in von Willebrand factor include multimerin 1 binding

artículo científico publicado en 2016

The low-frequency allele of the platelet collagen signaling receptor glycoprotein VI is associated with reduced functional responses and expression

artículo científico publicado en 2003

The presence of active von Willebrand factor under various pathological conditions

artículo científico publicado en 2007

The rate of hemolysis in sickle cell disease correlates with the quantity of active von Willebrand factor in the plasma.

artículo científico publicado en 2011

The role of the small intestine in the development of dietary fat-induced obesity and insulin resistance in C57BL/6J mice

artículo científico publicado en 2008

Thrombocytopenia and release of activated von Willebrand Factor during early Plasmodium falciparum malaria

artículo científico publicado en 2007

Thrombocytopenia in early malaria is associated with GP1b shedding in absence of systemic platelet activation and consumptive coagulopathy

artículo científico publicado en 2010

beta2-Glycoprotein I inhibits von Willebrand factor dependent platelet adhesion and aggregation

artículo científico publicado en 2007

Lista de obras de

A heparin-bonded vascular graft generates no systemic effect on markers of hemostasis activation or detectable heparin-induced thrombocytopenia-associated antibodies in humans

A nonsynonymous SNP in the ITGB3 gene disrupts the conserved membrane-proximal cytoplasmic salt bridge in the alphaIIbbeta3 integrin and cosegregates dominantly with abnormal proplatelet formation and macrothrombocytopenia

A novel nanobody that detects the gain-of-function phenotype of von Willebrand factor in ADAMTS13 deficiency and von Willebrand disease type 2B.

A single high-affinity binding site for von Willebrand factor in collagen III, identified using synthetic triple-helical peptides

ADAMTS13 deficiency with elevated levels of ultra-large and active von Willebrand factor in P. falciparum and P. vivax malaria.

Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia

Activated factor V is a cofactor for the activation of factor XI by thrombin in plasma.

Antiphospholipid antibodies promote leukocyte-endothelial cell adhesion and thrombosis in mice by antagonizing eNOS via β2GPI and apoER2.

Antiphospholipid syndrome: clinical and immunologic manifestations and patterns of disease expression in a cohort of 1,000 patients

Beta2-glycoprotein I can exist in 2 conformations: implications for our understanding of the antiphospholipid syndrome.

Cell-collagen interactions: the use of peptide Toolkits to investigate collagen-receptor interactions.

Challenges of molecular nutrition research 6: the nutritional phenotype database to store, share and evaluate nutritional systems biology studies

Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients

Dimers of beta 2-glycoprotein I increase platelet deposition to collagen via interaction with phospholipids and the apolipoprotein E receptor 2'

Endocannabinoids control platelet activation and limit aggregate formation under flow

Functional platelet defects in children with severe chronic ITP as tested with 2 novel assays applicable for low platelet counts

Higher and lower active circulating VWF levels: different facets of von Willebrand disease

Imbalance of angiopoietin-1 and angiopoetin-2 in severe dengue and relationship with thrombocytopenia, endothelial activation, and vascular stability

Indications for a protective function of beta2-glycoprotein I in thrombotic thrombocytopenic purpura

Interference with the host haemostatic system by schistosomes

Keeping von Willebrand Factor under Control: Alternatives for ADAMTS13.

Misfolded proteins activate factor XII in humans, leading to kallikrein formation without initiating coagulation

Molecular Imaging of Activated von Willebrand Factor to Detect High-Risk Atherosclerotic Phenotype ⬇️

Mutation and ADAMTS13-dependent modulation of disease severity in a mouse model for von Willebrand disease type 2B.

Plasmin cleavage of von Willebrand factor as an emergency bypass for ADAMTS13 deficiency in thrombotic microangiopathy

Prolonged fluid shear stress induces a distinct set of endothelial cell genes, most specifically lung Krüppel-like factor (KLF2)

Severe dengue is associated with consumption of von Willebrand factor and its cleaving enzyme ADAMTS-13

Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain

Synergism between platelet collagen receptors defined using receptor-specific collagen-mimetic peptide substrata in flowing blood

Synergistic effects of hypofibrinolysis and genetic and acquired risk factors on the risk of a first venous thrombosis

The effect of recombinant IgG antibodies against the leucine-33 form of the platelet beta3 integrin (HPA-1a) on platelet function

The embryonic genes Dkk3, Hoxd8, Hoxd9 and Tbx1 identify muscle types in a diet-independent and fiber-type unrelated way.

The functions of the A1A2A3 domains in von Willebrand factor include multimerin 1 binding

The low-frequency allele of the platelet collagen signaling receptor glycoprotein VI is associated with reduced functional responses and expression

The presence of active von Willebrand factor under various pathological conditions

The rate of hemolysis in sickle cell disease correlates with the quantity of active von Willebrand factor in the plasma.

The role of the small intestine in the development of dietary fat-induced obesity and insulin resistance in C57BL/6J mice

Thrombocytopenia and release of activated von Willebrand Factor during early Plasmodium falciparum malaria

Thrombocytopenia in early malaria is associated with GP1b shedding in absence of systemic platelet activation and consumptive coagulopathy

beta2-Glycoprotein I inhibits von Willebrand factor dependent platelet adhesion and aggregation