نتایج جستجو برای: antithrombins

تعداد نتایج: 1775  

Journal: :Haematologica 2011
Tienan Zhu Qiulan Ding Xia Bai Xiaoyan Wang Florentia Kaguelidou Corinne Alberti Xuqian Wei Baolai Hua Renchi Yang Xuefeng Wang Zhaoyue Wang Changgeng Ruan Nicole Schlegel Yongqiang Zhao

BACKGROUND Inherited deficiency of antithrombin, protein C and protein S, three important, naturally occurring coagulation inhibitors, might play a major role in the occurrence of venous thromboembolism in Chinese. The establishment of age- and gender-related normal ranges of these inhibitors is crucial for an accurate diagnosis of these deficiencies. DESIGN AND METHODS We designed a prospect...

Journal: :Journal of thrombosis and haemostasis : JTH 2007
S Butenas K G Mann

1 Fritsch P, Cvirn G, Cimenti C, Baier K, Gallistl S, Koestenberger M, Roschitz B, Leschnik B, Muntean W. Thrombin generation in factor VIII-depleted neonatal plasma: nearly normal because of physiologically low antithrombin and tissue factor pathway inhibitor. J Thromb Haemost 2006; 4: 1071–7. 2 Hemker HC, Al Dieri R, De Smedt E, Beguin S. Thrombin generation, a function test of the haemostati...

Journal: :The Biochemical journal 1954
J W LYTTLETON

Astrup, T. & Darling, S. (1942). Acta physiol. 8cand. 4, 293. Bodansky, 0. (1937). J. biol. Chem. 120, 555. Collingwood, B. J. & MacMahon, M. T. (1912). J. Physiol. 45, 119. Collingwood, B. J. & MacMahon, M. T. (1913). J. Physiol. 47, 44. Gerendas, M. (1948). Hung. acta physiol. 1, 7. Herbert, F. K. (1940). Biochem. J. 34, 1554. Howell, W. H. (1916). Harvey Led. xii, 1. Kekwick, R. A., Lyttleto...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Trevor P Baglin Robin W Carrell Frank C Church Charles T Esmon James A Huntington

The serine proteases sequentially activated to form a fibrin clot are inhibited primarily by members of the serpin family, which use a unique beta-sheet expansion mechanism to trap and destroy their targets. Since the discovery that serpins were a family of serine protease inhibitors there has been controversy as to the role of conformational change in their mechanism. It now is clear that prot...

Journal: :European journal of medicinal chemistry 2009
Arjun Raghuraman Aiye Liang Chandravel Krishnasamy Trish Lauck Gunnar T Gunnarsson Umesh R Desai

Antithrombin, a plasma glycoprotein serpin, requires conformational activation by heparin to induce an anticoagulant effect, which is mediated through accelerated factor Xa inhibition. Heparin, a highly charged polymer and an allosteric activator of the serpin, is associated with major adverse effects. To design better, but radically different activators of antithrombin from heparin, we utilize...

Journal: :The Journal of biological chemistry 2000
J A Huntington A McCoy K J Belzar X Y Pei P G Gettins R W Carrell

Antithrombin is unique among the serpins in that it circulates in a native conformation that is kinetically inactive toward its target proteinase, factor Xa. Activation occurs upon binding of a specific pentasaccharide sequence found in heparin that results in a rearrangement of the reactive center loop removing constraints on the active center P1 residue. We determined the crystal structure of...

Journal: :Journal of biomedical materials research 1995
C J van Delden G H Engbers J Feijen

The interaction between antithrombin III (ATIII) and albumin-heparin conjugates covalently coupled onto carboxylated polystyrene beads either in buffer containing albumin or in plasma was studied using 14C-labeled ATIII. Binding isotherms of ATIII were modeled using a summation of two Langmuir equations. These equations describe the binding of ATIII to two different sets of binding sites, one w...

Journal: :Blood 1982
J M Teitel K A Bauer H K Lau R D Rosenberg

We have evaluated the efficacy of utilizing radioimmunoassays (RIAs) for prothrombin activation fragments (F2/F1 + 2) and for thrombin--antithrombin complex (TAT) in purified systems and in whole blood. During venipuncture, appropriate anticoagulants were employed in order to prevent the generation of thrombin and factor Xa. The RIAs were shown to be specific for F2/F1 + 2 as well as TAT and di...

Journal: :Pathophysiology of haemostasis and thrombosis 2003
U Lange G Nowak E Bucha

A new sensitive and precise method for quantitative determination of direct thrombin inhibitors is described, the ecarin chromogenic assay (ECA). Ecarin is used as the specific prothrombin-activating principle. The cleavage of a chromogenic substrate by meizothrombin is inhibited in a concentration-dependent fashion by direct thrombin inhibitors. For the ECA, the linear measuring range is about...

Journal: :Pathophysiology of haemostasis and thrombosis 2003
Tomas Velan Wayne L Chandler

The in vivo concentration of active thrombin and the second-order rate constant for the inhibition of thrombin by antithrombin (k(inh)) were estimated in patients undergoing cardiopulmonary bypass (CPB) based on measured levels of hemostatic markers in combination with a computer model of the patient's hemostatic and vascular systems. At baseline k(inh) = 0.6 +/- 0.1 microM(-1) s(-1) leaving 27...

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