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In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiency

Journal of thrombosis and haemostasis, 2024-02, Vol.22 (2), p.410-422

2024

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Low plasma levels of tissue factor pathway inhibitor in patients with congenital factor V deficiency

Blood, 2008-11, Vol.112 (9), p.3615-3623

2008

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A novel factor V compound heterozygous mutation associated with thrombosis (Y1961C; FV-Kanazawa, together with 1982_1983del)

Journal of thrombosis and haemostasis, 2024-10, Vol.22 (10), p.2810-2822

2024

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Clinical and laboratory diagnosis of autoimmune factor V inhibitors: A single institutional experience

Thrombosis research, 2018-11, Vol.171, p.14-21

2018

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Parahemophilia: new insights into factor v deficiency

Seminars in thrombosis and hemostasis, 2013-09, Vol.39 (6), p.607-612

2013

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Generation of an anticoagulant aptamer that targets factor V/Va and disrupts the FVa-membrane interaction in normal and COVID-19 patient samples

Cell chemical biology, 2022-02, Vol.29 (2), p.215-225.e5

2022

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Factor V and thrombotic disease: description of a janus-faced protein

Arteriosclerosis, thrombosis, and vascular biology, 2002-04, Vol.22 (4), p.530-538

2002

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Desmopressin acetate as a haemostatic elevator in individuals with combined deficiency of factors V and VIII: a clinical trial

Journal of thrombosis and haemostasis, 2016-02, Vol.14 (2), p.336-339

2016

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Prevalence of rare F5 variants in general population from Bosnia and Herzegovina

Molecular biology reports, 2021-06, Vol.48 (6), p.5181-5186

2021

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Acquired factor V deficiency in a patient with a urinary tract infection presenting with haematuria followed by multiple haemorrhages with an extremely low level of factor V inhibitor: a case report and review of the literature

Blood coagulation & fibrinolysis, 2017-06, Vol.28 (4), p.334-341

2017

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Regulation of factor V by the anticoagulant protease activated protein C: Influence of the B-domain and TFPIα

The Journal of biological chemistry, 2022-11, Vol.298 (11), p.102558-102558, Article 102558

2022

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High Mutational Heterogeneity, and New Mutations in the Human Coagulation Factor V Gene. Future Perspectives for Factor V Deficiency Using Recombinant and Advanced Therapies

International journal of molecular sciences, 2021-09, Vol.22 (18), p.9705

2021

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The Magic of Proteases: From a Procoagulant and Anticoagulant Factor V to an Equitable Treatment of Its Inherited Deficiency

International journal of molecular sciences, 2023-03, Vol.24 (7), p.6243

2023

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High incidence of intracranial bleeding in factor V‐deficient patients with homozygous F5 splicing mutations

British journal of haematology, 2017-10, Vol.179 (1), p.163-166

2017

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Profiling the mutational landscape of coagulation factor V deficiency

Haematologica (Roma), 2020-04, Vol.105 (4), p.e180-e185

2020

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Acquired factor V inhibitor: a nation‐wide study of 38 patients

British journal of haematology, 2021-03, Vol.192 (5), p.892-899

2021

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A Comprehensive Overview of Coagulation Factor V and Congenital Factor V Deficiency

Seminars in thrombosis and hemostasis, 2019-07, Vol.45 (5), p.523-543

2019

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The TFPIα C-terminal tail is essential for TFPIα-FV-short-protein S complex formation and synergistic enhancement of TFPIα

Journal of thrombosis and haemostasis, 2023-12, Vol.21 (12), p.3568-3580

2023

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Acquired factor V inhibitor after exposure to topical human thrombin related to an otorhinolaryngological procedure

Journal of thrombosis and haemostasis, 2015-10, Vol.13 (10), p.1787-1789

2015

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Persistent hiccups in a patient with mild congenital factor V deficiency and COVID‐19; clinical and laboratory finding of a rare bleeding disorder

International journal of laboratory hematology, 2021-04, Vol.43 (2), p.e87-e88

2021

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Severe thrombophilia in a factor V‐deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)

Journal of thrombosis and haemostasis, 2021-05, Vol.19 (5), p.1186-1199

2021

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NUCLEOCYTOPLASMIC shuttling of ETHYLENE RESPONSE FACTOR 5 mediated by nitric oxide suppresses ethylene biosynthesis in apple fruit

The New phytologist, 2022-06, Vol.234 (5), p.1714-1734

2022

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Platelets and platelet-derived factor Va confer hemostatic competence in complete factor V deficiency

Blood, 2015-06, Vol.125 (23), p.3647-3650

2015

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Transfusion management of factor V deficiency: three case reports and review of the literature

Transfusion (Philadelphia, Pa.), 2016-07, Vol.56 (7), p.1745-1749

2016

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Discoidin Domains as Emerging Therapeutic Targets

Trends in pharmacological sciences (Regular ed.), 2016-08, Vol.37 (8), p.641-659

2016

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In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiency

Low plasma levels of tissue factor pathway inhibitor in patients with congenital factor V deficiency

A novel factor V compound heterozygous mutation associated with thrombosis (Y1961C; FV-Kanazawa, together with 1982_1983del)

Clinical and laboratory diagnosis of autoimmune factor V inhibitors: A single institutional experience

Parahemophilia: new insights into factor v deficiency

Generation of an anticoagulant aptamer that targets factor V/Va and disrupts the FVa-membrane interaction in normal and COVID-19 patient samples

Factor V and thrombotic disease: description of a janus-faced protein

Desmopressin acetate as a haemostatic elevator in individuals with combined deficiency of factors V and VIII: a clinical trial

Prevalence of rare F5 variants in general population from Bosnia and Herzegovina

Acquired factor V deficiency in a patient with a urinary tract infection presenting with haematuria followed by multiple haemorrhages with an extremely low level of factor V inhibitor: a case report and review of the literature

Regulation of factor V by the anticoagulant protease activated protein C: Influence of the B-domain and TFPIα

High Mutational Heterogeneity, and New Mutations in the Human Coagulation Factor V Gene. Future Perspectives for Factor V Deficiency Using Recombinant and Advanced Therapies

The Magic of Proteases: From a Procoagulant and Anticoagulant Factor V to an Equitable Treatment of Its Inherited Deficiency

High incidence of intracranial bleeding in factor V‐deficient patients with homozygous F5 splicing mutations

Profiling the mutational landscape of coagulation factor V deficiency

Acquired factor V inhibitor: a nation‐wide study of 38 patients

A Comprehensive Overview of Coagulation Factor V and Congenital Factor V Deficiency

The TFPIα C-terminal tail is essential for TFPIα-FV-short-protein S complex formation and synergistic enhancement of TFPIα

Acquired factor V inhibitor after exposure to topical human thrombin related to an otorhinolaryngological procedure

Persistent hiccups in a patient with mild congenital factor V deficiency and COVID‐19; clinical and laboratory finding of a rare bleeding disorder

Severe thrombophilia in a factor V‐deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)

NUCLEOCYTOPLASMIC shuttling of ETHYLENE RESPONSE FACTOR 5 mediated by nitric oxide suppresses ethylene biosynthesis in apple fruit

Platelets and platelet-derived factor Va confer hemostatic competence in complete factor V deficiency

Transfusion management of factor V deficiency: three case reports and review of the literature

Discoidin Domains as Emerging Therapeutic Targets

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