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Factor XI in haemostasis and thrombosis: past, present and future

Thrombosis and haemostasis, 2007-07, Vol.98 (1), p.84-89

Seligsohn, Uri

2007

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The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies

PLoS medicine, 2010-06, Vol.7 (6), p.e1000292-e1000292

2010

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Recombinant activated factor VII and tranexamic acid are haemostatically effective during major surgery in factor XI-deficient patients with inhibitor antibodies

Thrombosis and haemostasis, 2009-09, Vol.102 (3), p.487-492

2009

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Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex

Nature genetics, 2003-06, Vol.34 (2), p.220-225

2003

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Variable effects of alpha v suppression on VEGFR-2 expression in endothelial cells of different vascular beds

Thrombosis and haemostasis, 2009-11, Vol.102 (5), p.975-982

2009

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Genotype-phenotype correlation in combined deficiency of factor V and factor VIII

Blood, 2008-06, Vol.111 (12), p.5592-5600

2008

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Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome

The Journal of biological chemistry, 2001-10, Vol.276 (40), p.36923-36930

2001

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Disulfide bond disruption by a β3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active αIIbβ3

Thrombosis and haemostasis, 2007-12, Vol.98 (12), p.1257-1265

2007

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Mutations in the ER–Golgi Intermediate Compartment Protein ERGIC-53 Cause Combined Deficiency of Coagulation Factors V and VIII

Cell, 1998-04, Vol.93 (1), p.61-70

1998

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Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Blood, 2002-04, Vol.99 (7), p.2448-2454

2002

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Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians

Haematologica (Roma), 2008-05, Vol.93 (5), p.715-721

2008

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Genetic Susceptibility to Venous Thrombosis

The New England journal of medicine, 2001-04, Vol.344 (16), p.1222-1231

2001

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A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Blood, 1998-08, Vol.92 (4), p.1119-1124

1998

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A single genetic origin for a common Caucasian risk factor for venous thrombosis

Blood, 1997-01, Vol.89 (2), p.397-402

1997

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Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency

Journal of thrombosis and haemostasis, 2014-07, Vol.12 (7), p.1121-1130

2014

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The role of factor XI in thrombin generation induced by low concentrations of tissue factor

Thrombosis and haemostasis, 2001-06, Vol.85 (6), p.1060-1065

2001

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Plasma levels of microparticles at 24 weeks of gestation do not predict subsequent pregnancy complications

Fertility and sterility, 2009-08, Vol.92 (2), p.682-687

2009

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Reduced incidence of ischemic stroke in patients with severe factor XI deficiency

Blood, 2008-04, Vol.111 (8), p.4113-4117

2008

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Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis

Thrombosis and haemostasis, 2011-02, Vol.105 (2), p.269-273

2011

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ADAMTS-13 regulates platelet adhesion under flow. A new method for differentiation between inherited and acquired thrombotic thrombocytopenic purpura

Thrombosis and haemostasis, 2006-08, Vol.96 (2), p.160-166

2006

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Characterization of seven novel mutations causing factor XI deficiency

Haematologica (Roma), 2007-10, Vol.92 (10), p.1375-1380

2007

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Platelet glycoprotein IIb/IIIa receptors and Glanzmann's thrombasthenia

Arteriosclerosis, thrombosis, and vascular biology, 2000-03, Vol.20 (3), p.607-610

2000

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Low Concentrations of Recombinant Factor VIIa May Improve the Impaired Thrombin Generation of Glanzmann Thrombasthenia Patients

Thrombosis and haemostasis, 2019-01, Vol.119 (1), p.117-127

2019

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Persistent neonatal thrombocytopenia can be caused by IgA antiplatelet antibodies in breast milk of immune thrombocytopenic mothers

Blood, 2015-07, Vol.126 (5), p.661-664

2015

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Platelets from Calreticulin mutated essential thrombocythemia patients are less reactive than JAK2 V617F mutated platelets

American journal of hematology, 2020-04, Vol.95 (4), p.379-386

2020

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Factor XI in haemostasis and thrombosis: past, present and future

The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies

Recombinant activated factor VII and tranexamic acid are haemostatically effective during major surgery in factor XI-deficient patients with inhibitor antibodies

Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex

Variable effects of alpha v suppression on VEGFR-2 expression in endothelial cells of different vascular beds

Genotype-phenotype correlation in combined deficiency of factor V and factor VIII

Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome

Disulfide bond disruption by a β3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active αIIbβ3

Mutations in the ER–Golgi Intermediate Compartment Protein ERGIC-53 Cause Combined Deficiency of Coagulation Factors V and VIII

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians

Genetic Susceptibility to Venous Thrombosis

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

A single genetic origin for a common Caucasian risk factor for venous thrombosis

Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency

The role of factor XI in thrombin generation induced by low concentrations of tissue factor

Plasma levels of microparticles at 24 weeks of gestation do not predict subsequent pregnancy complications

Reduced incidence of ischemic stroke in patients with severe factor XI deficiency

Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis

ADAMTS-13 regulates platelet adhesion under flow. A new method for differentiation between inherited and acquired thrombotic thrombocytopenic purpura

Characterization of seven novel mutations causing factor XI deficiency

Platelet glycoprotein IIb/IIIa receptors and Glanzmann's thrombasthenia

Low Concentrations of Recombinant Factor VIIa May Improve the Impaired Thrombin Generation of Glanzmann Thrombasthenia Patients

Persistent neonatal thrombocytopenia can be caused by IgA antiplatelet antibodies in breast milk of immune thrombocytopenic mothers

Platelets from Calreticulin mutated essential thrombocythemia patients are less reactive than JAK2 V617F mutated platelets

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