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Factor X deficiency

Blood Reviews, 2002
Factor X is one of the vitamin K-dependent serine proteases. It plays a crucial role in the coagulation cascade, as the first enzyme in the common pathway of thrombus formation. The gene for factor X maps to the long arm of chromosome 13, approximately 2.8 kb downstream of the factor VII gene.
James, Uprichard, David J, Perry
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Factor X Deficiency

Seminars in Thrombosis and Hemostasis, 2009
Factor X (FX) deficiency is a rare, recessively inherited bleeding disorder representing 10% of all rare bleeding diseases and affecting 1 in every 1,000,000 people. Its clinical presentation places FX deficiency among the most severe of the rare coagulation defects, typically including hemarthroses, hematomas, and umbilical cord, gastrointestinal, and
Marzia, Menegatti, Flora, Peyvandi
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Factor X

Thrombosis and Haemostasis, 1971
SummaryA monospecific antiserum against factor X was prepared in rabbits. The antiserum precipitated factor X in human plasma and serum and monkey serum. The antiserum was used to :1. demonstrate the presence of factor X precursor in blood from patients under anticoagulant therapy,2.
H, Prydz, A, Gladhaug
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Activation of Factor X

Thrombosis and Haemostasis, 1965
Summary1. Methods have been developed for the preparation of factor VII free of prothrombin and factor X, and of factor X with only a very low contamination with factor VII.2. Factors VII and X could be found with one stage methods in purified prothrombin prepared according to Seegers.3. Purified prothrombin was chromatographed on DE AE-cellulose.
K, LECHNER, E, DEUTSCH
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The Factor‐X Defect: Recognition of Abnormal Forms of Factor X

British Journal of Haematology, 1970
Summary. Six patients with the ‘Factor‐X defect’ have been investigated. At least five different forms of the defect were recognized by the use of the following laboratory tests: the kaolin cephalin clotting time as a measure of intrinsic clotting, the factor‐X assay employing either brain extract or Russell's viper venom, and the neutralization of a ...
K W, Denson   +3 more
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Abnormal Factor X (Factor X Friuli) Coagulation Disorder

Acta Haematologica, 2009
A new case with the abnormal factor X (factor X Friuli) coagulation disorder is presented: a 32-year- old female who was born outside Friuli and who complained of a bleeding tendency since childhood. The main laboratory features are prolonged prothrombin time, prolonged partial thromboplastin time, abnormal thromboplastm generation and normal Stypven ...
A, Girolami   +3 more
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One Missense Mutation in the Factor X Gene Causing Factor X Deficiency—Factor X Kanazawa

International Journal of Hematology, 2001
We investigated the molecular basis of factor X deficiency in a Japanese patient whose factor X activity and antigen level were 45% and 50% of normal control values, respectively. All exons and intron/exon junctions of the factor X gene were studied using a strategy combining polymerase chain reaction (PCR) amplification and nonradioactive single ...
E, Morishita   +8 more
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Assessment of Factor VII and Factor X

Thrombosis and Haemostasis, 1966
SummaryA method is described to separate factor VII from factor X in normal serum using electrophoresis in a polyvinyl chloride block. A potent source of factor X is obtained. This may be used in correction studies and for assessment of deficiencies of factor VII in patients.
S, Shaw   +3 more
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Factorization in Z[x]

Proceedings of the 2000 international symposium on Symbolic and algebraic computation, 2000
In this paper we describe ideas used to accelerate the Searching Phase of the Berlekamp--Zassenhaus algorithm, the algorithm most widely used for computing factorizations in $\ZZ[x]$. Our ideas do not alter the theoretical worst-case complexity, but they do have a significant effect in practice: especially in those cases where the cost of the Searching
ABBOTT, JOHN ANTHONY   +2 more
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Biochemistry of factor X

Blood Reviews, 1994
Factor X circulates as a serine protease which is converted to the active form at the point of convergence of the intrinsic and extrinsic coagulation pathways. Subsequently, the enzymatic species, factor Xa, is involved in macromolecular complex formation with its cofactor factor Va, a phospholipid surface and calcium to convert prothrombin into ...
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