155 results on '"Gandrille, Sophie"'
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2. Induced forms of α2-macroglobulin neutralize heparin and direct oral anticoagulant effects
3. Modified ROTEM for the detection of rivaroxaban and apixaban anticoagulant activity in whole blood: A diagnostic test study
4. Elevated soluble endothelial cell protein C receptor (sEPCR) levels in women with preeclampsia: A marker of endothelial activation/damage?
5. Antithrombotic potential of a single-domain antibody enhancing the activated protein C-cofactor activity of protein S
6. Membrane binding and anticoagulant properties of protein S natural variants
7. Alternative mRNA is favored by the A3 haplotype of the EPCR gene PROCR and generates a novel soluble form of EPCR in plasma
8. Comparison of Endothelial Biomarkers According to Reversibility of Pulmonary Hypertension Secondary to Congenital Heart Disease
9. Assessment of the Interplay between Blood and Skin Vascular Abnormalities in Adult Purpura Fulminans
10. Endothelial colony-forming cells from patients with paroxysmal nocturnal haemoglobinuria are not PIGA mutated
11. Role of oculocerebrorenal syndrome of Lowe (OCRL) protein in megakaryocyte maturation, platelet production and functions: a study in patients with Lowe syndrome
12. No influence of the VAMP8 rs1010 single nucleotide polymorphism on platelet functions in vitro
13. The γ-carboxyglutamic acid domain of anticoagulant protein S is involved in activated protein C cofactor activity, independently of phospholipid binding
14. A Comparative Study of the Protein C Pathway in Septic and Nonseptic Patients with Organ Failure
15. A haplotype of the EPCR gene is associated with increased plasma levels of sEPCR and is a candidate risk factor for thrombosis
16. Functional properties of the sex-hormone-binding globulin (SHBG)-like domain of the anticoagulant protein S
17. Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutation
18. Lack of sequence variations in the C4b-BP beta-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 beta-chain gene (C4BPB)
19. Molecular basis for protein S hereditary deficiency: Genetic defects observed in 118 patients with type I and type IIa deficiencies
20. Unexplained thrombosis and factor V Leiden mutation
21. Expression and Characterization of Recombinant Protein S with the Ser 460 Pro Mutation
22. Genotype–Phenotype Relationships in a Large French Cohort of Subjects with Inherited Protein C Deficiency.
23. FXa-α2-Macroglobulin Complex Neutralizes Direct Oral Anticoagulants Targeting FXa In Vitro and In Vivo
24. FXa-α2-Macroglobulin Complex Neutralizes Direct Oral Anticoagulants Targeting FXa In Vitro and In Vivo.
25. Low-Molecular-Weight Fucoidan Induces Endothelial Cell Migration via the PI3K/AKT Pathway and Modulates the Transcription of Genes Involved in Angiogenesis
26. Low-Molecular-Weight Fucoidan Induces Endothelial Cell Migration via the PI3K/AKT Pathway and Modulates the Transcription of Genes Involved in Angiogenesis
27. Three-Dimensional Environment Sustains Hematopoietic Stem Cell Differentiation into Platelet-Producing Megakaryocytes
28. Activated protein C: from structure/function relationship to the design of recombinant proteins with targeted activities
29. Endothelial Progenitor Cells in Paroxysmal Nocturnal Hemoglobinuria
30. No Influence of the VAMP8 Rs1010 Single Nucleotide Polymorphism on Platelet FunctionsIn Vitro
31. Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement
32. Mutations des protéines de la coagulation et thromboses
33. Identification of functional polymorphisms of the thromboxane A2 receptor gene in healthy volunteers
34. Adenosine Diphosphate–Induced Platelet Aggregation Is Associated WithP2Y 12Gene Sequence Variations in Healthy Subjects
35. Cleaved Protein S (PS), Total PS, Free PS, and Activated Protein C Cofactor Activity as Risk Factors for Venous Thromboembolism
36. Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the γ-carboxyglutamic acid-rich domain
37. Three-dimensional model of the SHBG-like region of anticoagulant protein S: New structure-function insights
38. Characterization of Cleaved Plasma Protein S with a Monoclonal Antibody-based Assay
39. Complex Association of Protein C Gene Promoter Polymorphism With Circulating Protein C Levels and Thrombotic Risk
40. Mutations in Promoter Region of Thrombomodulin and Venous Thromboembolic Disease
41. The Factor V Gene A4070G Mutation and the Risk of Venous Thrombosis
42. 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)
43. Protein S Deficiency
44. Molecular Basis For Protein C Hereditary Deficiency
45. Five Novel Mutations of the Protein S Active Gene (PROS 1) in 8 Norman Families
46. Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor V
47. Role of FCγRIIA Gene Polymorphism in Human Platelet Activation by Monoclonal Antibodies
48. Influence of Six Mutations of the Protein C Gene on the Gla Domain Conformation and Calcium Affinity
49. Arg-129 plays a specific role in the confirmation of antithrombin and in the enhancement of factor Xa inhibition by the pentasaccharode sequence of heparin
50. Massive Thrombosis of Venous Cerebral Sinuses in a 2-Year-Old Boy with a Combined Inherited Deficiency of Antithrombin III and Protein C
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