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Antibody Mediated Rejection Associated With Complement Factor H–Related Protein 3/1 Deficiency Successfully Treated With Eculizumab

American journal of transplantation, 2012-09, Vol.12 (9), p.2546-2553

2012

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Insights into abnormal hemostasis in the Quebec platelet disorder from analyses of clot lysis

Journal of thrombosis and haemostasis, 2006-05, Vol.4 (5), p.1086-1094

2006

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Discrepant platelet and plasma von Willebrand factor in von Willebrand disease patients with p.Pro2808Leufs24

Journal of thrombosis and haemostasis, 2017-07, Vol.15 (7), p.1403-1411

2017

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

Journal of thrombosis and haemostasis, 2016-05, Vol.14 (5), p.1082-1094

2016

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Clinical probability score and D‐dimer estimation lack utility in the diagnosis of childhood pulmonary embolism

Journal of thrombosis and haemostasis, 2009-10, Vol.7 (10), p.1633-1638

2009

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Unfractionated heparin dosing in young infants: clinical outcomes in a cohort monitored with anti‐factor Xa levels

Journal of thrombosis and haemostasis, 2012-03, Vol.10 (3), p.368-374

2012

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

Journal of thrombosis and haemostasis, 2012-06, Vol.10 (6), p.1109-1119

2012

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Combined variants in factor VIII and prostaglandin synthase‐1 amplify hemorrhage severity across three generations of descendants

Journal of thrombosis and haemostasis, 2016-11, Vol.14 (11), p.2230-2240

2016

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

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.e162-e165

2017

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Intracranial haemorrhage in von Willebrand disease: a report on six cases

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.602-606

2013

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

Blood, 2015-02, Vol.125 (6), p.1014-1024

2015

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The value of proteomics for the diagnosis of a platelet-related bleeding disorder

Platelets (Edinburgh), 2008-01, Vol.19 (5), p.342-351

2008

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2015 proceedings of the National Heart, Lung, and Blood Institute's State of the Science in Transfusion Medicine symposium

Transfusion (Philadelphia, Pa.), 2015-09, Vol.55 (9), p.2282-2290

2015

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Intracranial haemorrhage in von W illebrand disease: a report on six cases

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.602-606

2013

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Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator

Blood, 2001-07, Vol.98 (2), p.257-265

2001

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Substrate- and Inhibitor-induced Conformational Changes in the Yeast V-ATPase Provide Evidence for Communication between the Catalytic and Proton-translocating Sectors

The Journal of biological chemistry, 1999-09, Vol.274 (37), p.26057-26064

1999

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H3 Cys-110 is in close proximity to the C-terminal regions of H2B and H4 in a nucleosome core with an altered internal arrangement of histones

Biochemistry (Easton), 1990-06, Vol.29 (24), p.5821-5829

1990

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Testicular plasmacytoma following chemical orchiectomy: potential role of hypogonadism in myeloma proliferation

Leukemia & lymphoma, 1998-01, Vol.28 (3-4), p.437-442

1998

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

Nature genetics, 2011-08, Vol.43 (8), p.738-740

2011

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

Nature communications, 2017-04, Vol.8 (1), p.14816-14816, Article 14816

2017

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Anucleate platelets generate progeny

Blood, 2010-05, Vol.115 (18), p.3801-3809

2010

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Abnormal megakaryocyte development and platelet function in Nbeal2−/− mice

Blood, 2013-11, Vol.122 (19), p.3349-3358

2013

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

Arteriosclerosis, thrombosis, and vascular biology, 2016-06, Vol.36 (6), p.1164-1173

2016

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

Arteriosclerosis, thrombosis, and vascular biology, 2018-10, Vol.38 (10), p.2435-2447

2018

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Antibody Mediated Rejection Associated With Complement Factor H–Related Protein 3/1 Deficiency Successfully Treated With Eculizumab

Insights into abnormal hemostasis in the Quebec platelet disorder from analyses of clot lysis

Discrepant platelet and plasma von Willebrand factor in von Willebrand disease patients with p.Pro2808Leufs24

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

Clinical probability score and D‐dimer estimation lack utility in the diagnosis of childhood pulmonary embolism

Unfractionated heparin dosing in young infants: clinical outcomes in a cohort monitored with anti‐factor Xa levels

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

Combined variants in factor VIII and prostaglandin synthase‐1 amplify hemorrhage severity across three generations of descendants

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

Intracranial haemorrhage in von Willebrand disease: a report on six cases

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

The value of proteomics for the diagnosis of a platelet-related bleeding disorder

2015 proceedings of the National Heart, Lung, and Blood Institute's State of the Science in Transfusion Medicine symposium

Intracranial haemorrhage in von W illebrand disease: a report on six cases

Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator

Substrate- and Inhibitor-induced Conformational Changes in the Yeast V-ATPase Provide Evidence for Communication between the Catalytic and Proton-translocating Sectors

H3 Cys-110 is in close proximity to the C-terminal regions of H2B and H4 in a nucleosome core with an altered internal arrangement of histones

Testicular plasmacytoma following chemical orchiectomy: potential role of hypogonadism in myeloma proliferation

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

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

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

Anucleate platelets generate progeny

Abnormal megakaryocyte development and platelet function in Nbeal2−/− mice

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

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

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