Found: 12
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Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency.
- Published in:
- Human Genetics, 2010, v. 127, n. 1, p. 45, doi. 10.1007/s00439-009-0742-6
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- Publication type:
- Article
Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene.
- Published in:
- British Journal of Haematology, 2000, v. 110, n. 3, p. 731, doi. 10.1046/j.1365-2141.2000.02245.x
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- Publication type:
- Article
Erratum: Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
- Published in:
- Human Mutation, 2006, v. 27, n. 11, p. 1160, doi. 10.1002/humu.9468
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- Publication type:
- Article
Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
- Published in:
- Human Mutation, 2006, v. 27, n. 6, p. 600, doi. 10.1002/humu.9425
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- Publication type:
- Article
Interleukin 8 is differently expressed and modulated by PAR-1 activation in early and late endothelial progenitor cells.
- Published in:
- Journal of Cellular & Molecular Medicine, 2009, v. 13, n. 8b, p. 2534, doi. 10.1111/j.1582-4934.2008.00429.x
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- Publication type:
- Article
No influence of the VAMP8 rs1010 single nucleotide polymorphism on platelet functions in vitro.
- Published in:
- 2009
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- Publication type:
- Letter
Thrombin bound to a fibrin clot confers angiogenic and haemostatic properties on endothelial progenitor cells.
- Published in:
- Journal of Cellular & Molecular Medicine, 2008, v. 12, n. 3, p. 975, doi. 10.1111/j.1582-4934.2008.00161.x
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- Publication type:
- Article
Increased VEGFR2 expression during human late endothelial progenitor cells expansion enhances in vitroangiogenesis with up-regulation of integrin α<sub>6</sub>.
- Published in:
- Journal of Cellular & Molecular Medicine, 2007, v. 11, n. 5, p. 1149, doi. 10.1111/j.1582-4934.2007.00090.x
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- Publication type:
- Article
Thrombomodulin gene polymorphisms in brain infarction and mortality after stroke.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 4, p. 514, doi. 10.1007/s00415-008-0725-x
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- Publication type:
- Article
Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutation.
- Published in:
- British Journal of Haematology, 1999, v. 106, n. 4, p. 889, doi. 10.1046/j.1365-2141.1999.01661.x
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- Publication type:
- Article
Lack of sequence variations in the C4b-BP β-chain in patients with type III protein S deficiency bearing the Ser 460 to Pro mutation: description of two new intragenic isomorphisms in the C4b-BP β-chain gene (C4BPB).
- Published in:
- British Journal of Haematology, 1998, v. 101, n. 1, p. 10, doi. 10.1046/j.1365-2141.1998.00646.x
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- Publication type:
- Article
Interdonor variability of platelet response to thrombin receptor activation: influence of Pl<sup>A2</sup> polymorphism.
- Published in:
- British Journal of Haematology, 1997, v. 99, n. 4, p. 801, doi. 10.1046/j.1365-2141.1997.4973300.x
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- Publication type:
- Article