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SERPINC1 wt Allele

Known as: THPH7, ATIII, MGC22579 
Human SERPINC1 wild-type allele is located in the vicinity of 1q25.1 and is approximately 14 kb in length. This allele, which encodes antithrombin… Expand
National Institutes of Health

Papers overview

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2009
2009
Intestinal ischemia/reperfusion causes severe injury and alters motility. N-methyl-D-aspartate (NMDA) receptor antagonists have… Expand
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2006
2006
Protein C, protein S, and antithrombin III were measured in 35 patients with acute leukemia (13 with AML and 22 with ALL). Low… Expand
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2000
2000
Nephrotic syndrome is a hypercoagulable state with variable prevalence of clinical thrombosis. The role of platelet aggregation… Expand
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1999
1999
  • Meral Kanbak
  • Canadian journal of anaesthesia = Journal…
  • 1999
  • Corpus ID: 24438996
PurposeTo report three patients who developed heparin resistance during cardiac surgery which was successfully managed with 1000… Expand
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1999
1999
The role of hereditary antithrombotic protein defects in juvenile deep vein thrombosis (DVT) was evaluated. Fifty six young… Expand
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1997
1997
AIM The activation pattern of the clotting and fibrinolytic systems in 63 preterm infants (GA 31, 6 +/- 2.3 weeks) was studied… Expand
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1995
1995
The inhibition of thrombin generation (TG) was studied in plasma from human volunteers after single subcutaneous administrations… Expand
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1992
1992
Haemostatic measurements were undertaken in 46 camels (Camelus dromedarius) and the results were compared to human reference… Expand
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1991
1991
The plasma levels of several haemostatic and fibrinolytic parameters were measured before and after delivery in 61 hypertensive… Expand
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1990
1990
An hereditary abnormal antithrombin III (ATIII Geneva) with defective heparin cofactor activity was characterized by DNA single… Expand
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