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Platelet dysfunction associated with the novel Trp29Cys thromboxane A2 receptor variant

Journal of thrombosis and haemostasis, 2013-03, Vol.11 (3), p.547-554

2013

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Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency

Human genetics, 2009-09, Vol.126 (3), p.449-456

2009

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Late onset thrombosis in a case of severe protein S deficiency due to compound heterozygosity for PROS1 mutations

Journal of thrombosis and haemostasis, 2008-07, Vol.6 (7), p.1235-1237

2008

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Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency

Human genetics, 2010-01, Vol.127 (1), p.121-121

2010

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The protein S thrombin‐sensitive region modulates phospholipid binding and the γ‐carboxyglutamic acid‐rich (Gla) domain conformation in a non‐specific manner

Journal of thrombosis and haemostasis, 2006-03, Vol.4 (3), p.704-706

2006

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Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects

Circulation (New York, N.Y.), 2003-08, Vol.108 (8), p.989-995

2003

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Incidence of Activated Protein C Resistance Caused by the ARG 506 GLN Mutation in Factor V in 113 Unrelated Symptomatic Protein C-Deficient Patients

Blood, 1995-07, Vol.86 (1), p.219-224

1995

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PB0997 Utility of Thrombin Generation Assay for Inherited Thrombophilia Screening

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101795, Article 101795

2023

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PB0994 Intronic Exploration of PROC in Patients with Unexplained Protein C Deficiencies

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101796, Article 101796

2023

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A rapid screening method for the factor V Arg506-->Gln mutation

Blood coagulation & fibrinolysis, 1995-05, Vol.6 (3), p.245-248

1995

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Endothelial cell protein C receptor and the risk of venous thrombosis

Haematologica (Roma), 2008-06, Vol.93 (6), p.812-816

Gandrille, Sophie

2008

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Molecular bases of type II protein S deficiency: the I203‐D204 deletion in the EGF4 domain alters GLA domain function

Journal of thrombosis and haemostasis, 2006-01, Vol.4 (1), p.186-191

2006

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Protein C and protein S deficiencies

Seminars in hematology, 1997-07, Vol.34 (3), p.205-216

1997

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Assessment of the Interplay between Blood and Skin Vascular Abnormalities in Adult Purpura Fulminans

American journal of respiratory and critical care medicine, 2013-09, Vol.188 (6), p.684-692

2013

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A review of mutations causing deficiencies of antithrombin, protein C and protein S

Thrombosis and haemostasis, 1995-07, Vol.74 (1), p.81-89

1995

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PB1439 Diversity of Hereditary Protein C Deficiency in North France: A Genotype-Phenotype Correlation

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101778, Article 101778

2023

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A haplotype of the EPCR gene is associated with increased plasma levels of sEPCR and is a candidate risk factor for thrombosis

Blood, 2004-02, Vol.103 (4), p.1311-1318

2004

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Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain

Biochemical journal, 2001-12, Vol.360 (Pt 2), p.499-506

2001

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Thrombin-mediated cleavage of membrane endoglin: Implications in endothelial dysfunction

HAEMOPHILIA, 2024, Vol.30, p.166

2024

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Identification of 15 Different Candidate Causal Point Mutations and Three Polymorphisms in 19 Patients With Protein S Deficiency Using a Scanning Method for the Analysis of the Protein S Active Gene

Blood, 1995-01, Vol.85 (1), p.130-138

1995

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Diagnostic du déficit en protéine S

Immuno-analyse & biologie spécialisée, 2007-12, Vol.22 (6), p.366-372

2007

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A Mutation of the Active Protein S Gene Leading to an EGF1-Lacking Protein in a Family With Qualitative (Type II) Deficiency

Blood, 1998-06, Vol.91 (12), p.4608-4615

1998

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The Ser 460 to Pro Substitution of the Protein S α (PROS1) Gene Is a Frequent Mutation Associated With Free Protein S (type IIa) Deficiency

Blood, 1995-11, Vol.86 (9), p.3436-3443

1995

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Characterization of cleaved plasma protein S with a monoclonal antibody-based assay

Thrombosis and haemostasis, 2000-10, Vol.84 (4), p.604-610

2000

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Role of Fc gamma RIIA gene polymorphism in human platelet activation by monoclonal antibodies

Thrombosis and haemostasis, 1995-12, Vol.74 (6), p.1557-1563

1995

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Platelet dysfunction associated with the novel Trp29Cys thromboxane A2 receptor variant

Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency

Late onset thrombosis in a case of severe protein S deficiency due to compound heterozygosity for PROS1 mutations

Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency

The protein S thrombin‐sensitive region modulates phospholipid binding and the γ‐carboxyglutamic acid‐rich (Gla) domain conformation in a non‐specific manner

Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects

Incidence of Activated Protein C Resistance Caused by the ARG 506 GLN Mutation in Factor V in 113 Unrelated Symptomatic Protein C-Deficient Patients

PB0997 Utility of Thrombin Generation Assay for Inherited Thrombophilia Screening

PB0994 Intronic Exploration of PROC in Patients with Unexplained Protein C Deficiencies

A rapid screening method for the factor V Arg506-->Gln mutation

Endothelial cell protein C receptor and the risk of venous thrombosis

Molecular bases of type II protein S deficiency: the I203‐D204 deletion in the EGF4 domain alters GLA domain function

Protein C and protein S deficiencies

Assessment of the Interplay between Blood and Skin Vascular Abnormalities in Adult Purpura Fulminans

A review of mutations causing deficiencies of antithrombin, protein C and protein S

PB1439 Diversity of Hereditary Protein C Deficiency in North France: A Genotype-Phenotype Correlation

A haplotype of the EPCR gene is associated with increased plasma levels of sEPCR and is a candidate risk factor for thrombosis

Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain

Thrombin-mediated cleavage of membrane endoglin: Implications in endothelial dysfunction

Identification of 15 Different Candidate Causal Point Mutations and Three Polymorphisms in 19 Patients With Protein S Deficiency Using a Scanning Method for the Analysis of the Protein S Active Gene

Diagnostic du déficit en protéine S

A Mutation of the Active Protein S Gene Leading to an EGF1-Lacking Protein in a Family With Qualitative (Type II) Deficiency

The Ser 460 to Pro Substitution of the Protein S α (PROS1) Gene Is a Frequent Mutation Associated With Free Protein S (type IIa) Deficiency

Characterization of cleaved plasma protein S with a monoclonal antibody-based assay

Role of Fc gamma RIIA gene polymorphism in human platelet activation by monoclonal antibodies

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