(Q36486848)

14 August 2017

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title

Genetic risk factors for deep vein thrombosis among Japanese: importance of protein S K196E mutation (English)

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14 August 2017

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3

Yoshihiro Kokubo

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14 August 2017

Toshiyuki Miyata

1

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14 August 2017

Rina Kimura

series ordinal

2

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14 August 2017

Toshiyuki Sakata

series ordinal

4

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14 August 2017

publication date

1 April 2006

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International Journal of Hematology

14 August 2017

published in

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14 August 2017

volume

83

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14 August 2017

issue

3

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14 August 2017

page(s)

217-223

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Potential of free-form TFPI and PAI-1 to be useful markers of early atherosclerosis in a Japanese general population (the Suita Study): association with the intimal-medial thickness of carotid arteries

14 August 2017

cites work

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A phenotypically neutral dimorphism of protein S: the substitution of Lys155 by Glu in the second EGF domain predicted by an A to G base exchange in the gene

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World distribution of factor V Leiden

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Isolated familial plasminogen deficiency may not be a risk factor for thrombosis

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Population-based distribution of plasminogen activity and estimated prevalence and relevance to thrombotic diseases of plasminogen deficiency in the Japanese: the Suita Study

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Protein S Tokushima: an abnormal protein S found in a Japanese family with thrombosis

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

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The prothrombin gene G20210A mutation is not found among Japanese patients with deep vein thrombosis and healthy individuals

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Abnormal plasminogen. A hereditary molecular abnormality found in a patient with recurrent thrombosis

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Molecular mechanism of the dysfunction of protein S(Tokushima) (Lys155-->Glu) for the regulation of the blood coagulation system

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Plasminogen Tochigi: inactive plasmin resulting from replacement of alanine-600 by threonine in the active site

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Protein S Tokushima: abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S

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Hypertension susceptibility genes on chromosome 2p24-p25 in a general Japanese population.

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Absence of Pro475Ser polymorphism in ADAMTS-13 in Caucasians

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Protein C and antithrombin deficiency are important risk factors for deep vein thrombosis in Japanese

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12 December 2020

The frequency of P475S polymorphism in von Willebrand factor-cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders

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The 46C-->T polymorphism in the factor XII gene (F12) and the risk of venous thrombosis

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12 December 2020

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Absence of thrombosis in subjects with heterozygous protein C deficiency

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12 December 2020

Common mutation of plasminogen detected in three Asian populations by an amplification refractory mutation system and rapid automated capillary electrophoresis

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12 December 2020

Characterization of dysfunctional protein S-Tokushima (K155-->E) in relation to the molecular interactions required for the regulation of blood coagulation

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12 December 2020

Arterial and venous thrombosis is not associated with the 4G/5G polymorphism in the promoter of the plasminogen activator inhibitor gene in a large cohort of US men.

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12 December 2020

Protein S-K196E mutation as a genetic risk factor for deep vein thrombosis in Japanese patients

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12 December 2020

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

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Genotype frequency of plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism in healthy Japanese males and its relation to PAI-1 levels

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12 December 2020

Is plasminogen deficiency a thrombotic risk factor? A study on 23 thrombophilic patients and their family members.

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12 December 2020

Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C

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12 December 2020

Frequency of natural coagulation inhibitor (antithrombin III, protein C and protein S) deficiencies in Japanese patients with spontaneous deep vein thrombosis

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12 December 2020

Association of genetic polymorphisms of sodium-calcium exchanger 1 gene, NCX1, with hypertension in a Japanese general population

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12 December 2020

Protein S and protein C gene mutations in Japanese deep vein thrombosis patients

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12 December 2020

Regulation of blood coagulation by the protein C anticoagulant pathway: novel insights into structure-function relationships and molecular recognition

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12 December 2020

Prevalence of protein S deficiency in the Japanese general population: the Suita Study

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12 December 2020

A study of Protein S antigen levels in 3788 healthy volunteers: influence of age, sex and hormone use, and estimate for prevalence of deficiency state

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12 December 2020

Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction

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12 December 2020

A single genetic origin for a common Caucasian risk factor for venous thrombosis

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12 December 2020

DNA restriction fragments associated with alpha 1-antitrypsin indicate a single origin for deficiency allele PI Z.

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12 December 2020

Identifiers

DOI

10.1532/IJH97.A20514

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Dimensions Publication ID

14 August 2017

1036382059

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