15 results on '"Morishita, E."'
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2. Role of plasminogen activator inhibitor-1 (PAI-1) in DIC
3. Prothrombin Fragment 1 + 2 Measures Treatment Effect in Patients with Antiphospholipid Syndrome
4. Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles.
5. Functional analysis of two abnormal antithrombin proteins with different intracellular kinetics.
6. Protein S deficiency caused by cryptic splicing due to the novel intron variant c.346+5G>C in PROS1.
7. Potential of continuous tPA infusion for multiple-organ failure from lipopolysaccharide-induced disseminated intravascular coagulation in rats.
8. Molecular genetic analysis of inherited protein C deficiency caused by the novel large deletion across two exons of PROC.
9. Gene analysis of six cases of congenital protein S deficiency and functional analysis of protein S mutations (A139V, C449F, R451Q, C475F, A525V and D599TfsTer13).
10. Late onset thrombosis in two Japanese patients with compound heterozygote protein S deficiency.
11. Antithrombin deficiency in three Japanese families: one novel and two reported point mutations in the antithrombin gene.
12. Carbon monoxide (CO)-releasing molecule-derived CO regulates tissue factor and plasminogen activator inhibitor type 1 in human endothelial cells.
13. Expression of annexin II in human atherosclerotic abdominal aortic aneurysms.
14. Changes in molecular markers of hemostatic and fibrinolytic activation under various sampling conditions using vacuum tube samples from healthy volunteers.
15. Prothrombin Himi; an abnormal prothrombin characterized by a defective thrombin activity.
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