Results 31 to 40 of about 123,279 (307)

OPTIMIZATION OF THE EVALUATION METHOD OF THE PERFORMANCE OF THERAPY USING INDIRECT ACTION ANTICOAGULANTS [PDF]

open access: yesBiotechnologia Acta, 2022
Aim. Treatment by indirect anticoagulants (vitamin K antagonists) requires a personalized approach for controlling the overall level of prothrombin and the accumulation of its decarboxylated forms.
D. S. Korolova   +6 more
doaj   +1 more source

Autocatalysis in prothrombin activation [PDF]

open access: yes, 1962
Two enzymes, thrombin and autoprothrombin C, are derived from purified prothrombin by autocatalytic activation in 25% sodium citrate solution.
Walter H. Seegers   +2 more
core   +1 more source

Controle do tempo de protrombina em sangue capilar e venoso em pacientes com anticoagulação oral: correlação e concordância Comparative study of a portable system for prothrombin monitoring using capillary blood against venous blood measurements in patients using oral anticoagulants: correlation and concordance

open access: yesArquivos Brasileiros de Cardiologia, 2007
FUNDAMENTO: O uso de anticoagulantes orais (ACO) é comum na prática cardiológica, tendo como principais indicações a fibrilação atrial e próteses valvares. Os pacientes em uso de ACO necessitam de controle freqüente do tempo de protrombina (TP).
Tiago Luiz Luz Leiria   +3 more
doaj   +1 more source

Efficacy and safety of sorafenib plus vitamin K treatment for hepatocellular carcinoma: A phase II, randomized study

open access: yesCancer Medicine, 2021
The previous retrospective study suggested that dosing vitamin K may enhance the anticancer action of sorafenib against hepatocellular carcinoma. To confirm it, we performed a phase II, randomized, open‐label study. Patients with hepatocellular carcinoma
Yoshimichi Haruna   +2 more
doaj   +1 more source

Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patients

open access: yesTurkish Journal of Hematology, 2011
OBJECTIVE: Budd-Chiari syndrome is a multifactorial disease in which several prothrombotic disorders may predispose patients to the development of thrombosis at this uncommon location (hepatic veins). The aim of this study was to determine the prevalence
Tawhida Y. Abdel Ghaffar   +7 more
doaj   +3 more sources

Inherited thrombophilia and portal vein thrombosis in cirrhosis: A systematic review and meta‐analysis

open access: yesResearch and Practice in Thrombosis and Haemostasis, 2019
Background Portal vein thrombosis (PVT) is common in cirrhosis. PVT is associated with high morbidity and mortality. Individual reports suggest that PVT occurs more frequently in patients with cirrhosis and inherited thrombophilia.
Steven D. Ma   +5 more
doaj   +1 more source

Association of Factor V Leiden and Prothrombin G20210A Polymorphisms in Women with Recurrent Pregnancy Loss in Isfahan Province, Iran

open access: yesInternational Journal of Preventive Medicine, 2018
Background: Maternal thrombophilia has been identified as a risk factor for recurrent pregnancy loss (RPL). The aim of this study was to investigate the association between prothrombin G20210A and factor V Leiden (FVL) polymorphisms in women with RPL and
Mohammad Taghi Kardi   +3 more
doaj   +1 more source

MASP-1 of the complement system promotes clotting via prothrombin activation. [PDF]

open access: yes, 2015
Mannan-binding lectin-associated serine protease-1 (MASP-1), a protein of the complement lectin pathway, resembles thrombin in terms of structural features and substrate specificity, and it has been shown to activate coagulation factors.
Gál, Péter   +7 more
core   +1 more source

MASP-1 Induced Clotting--The First Model of Prothrombin Activation by MASP-1. [PDF]

open access: yes, 2015
Mannan-binding lectin-associated serine protease-1 (MASP-1), a protein of the complement lectin pathway, resembles thrombin in terms of structural features and substrate specificity.
Gál, Péter   +7 more
core   +1 more source

FXa mediated prothrombin cleavage. [PDF]

open access: yes, 2015
Prothrombin activation by FXa. FXa cleaves prothrombin either at R271 or at R320. Intermediates gain their activity by cleavage at R320 and are then able to perform further cleavages at R155, R284, R383 and R393.
Verena Schroeder (325642)   +3 more
core   +1 more source

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