All Stories

  1. Gene therapy for haemophilia B
  2. Human Congenital Diseases with Mixed Modes of Inheritance Have a Shortage of Recessive Disease. A Demographic Scenario?
  3. Normal Haemostasis
  4. Postgraduate Haematology
  5. Menorrhagia in Adolescents with Inherited Bleeding Disorders
  6. Anticoagulation after liver transplantation: a retrospective audit and case–control study
  7. Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiency
  8. Genetic and Laboratory Diagnosis
  9. Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing
  10. Hemophilia and Other Bleeding Disorders: Genetics
  11. Live birth following the first mutation specific pre-implantation genetic diagnosis for haemophilia A
  12. Ways to bypass a blocked tenase complex
  13. Characterisation of blood coagulation factor XIT475I
  14. Postgraduate Haematology
  15. Normal Haemostasis
  16. Molecular Basis of Hemophilia A
  17. Inhibitors to Factor VIII—Molecular Basis
  18. Pharmacodynamic resistance to warfarin associated with a Val66Met substitution in vitamin K epoxide reductase complex subunit 1
  19. Complete Inhibition of Acute Humoral Rejection Using Regulated Expression of Membrane-tethered Anticoagulants on Xenograft Endothelium
  20. Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
  21. Environmental and genetic factors influencing inhibitor development
  22. Factor VIII – novel insights into form and function
  23. RNA as drug and antidote
  24. Use of a non‐depleting anti‐CD4 antibody to modulate the immune response to coagulation factors VIII and IX
  25. The Hemophilias — From Royal Genes to Gene Therapy
  26. Stable recombinant expression and characterization of the two haemophilic factor VIII variants C329S (CRM−) and G1948D (CRMr)
  27. Contact activation in shock caused by invasive group A Streptococcus pyogenes
  28. EXPRESSION OF NOVEL ANTICOAGULANT FUSION PROTEINS INHIBITS FACTOR XA- AND THROMBIN-INDUCED ACTIVATION OF PORCINE VASCULAR ENDOTHELIAL CELLS.
  29. Factor VII deficiency and the FVII mutation database
  30. Postgraduate Haematology
  31. INHIBITION OF TISSUE FACTOR-DEPENDENT AND -INDEPENDENT COAGULATION BY CELL SURFACE EXPRESSION OF NOVEL ANTICOAGULANT FUSION PROTEINS
  32. Factor VIII gene analysis in Japanese CRM‐positive and CRM‐reduced haemophilia A patients by single‐strand conformation polymorphism
  33. Thrombophilia: an expanding group of genetic defects that predispose to thrombosis
  34. Factor VIIa and the extracellular domains of human tissue factor form a compact complex: A study by X‐ray and neutron solution scattering
  35. Thrombogenic mechanisms investigated with coagulation activation markers after infusion of factor IX concentrates in patients with haemophilia B
  36. Book Review Molecular Genetics of Haemostasis and Its Inherited Disorders (Oxford Monograph on Medical Genetics. No. 25.) By Edward G.D. Tuddenham and David N. Cooper. 585 pp. New York, Oxford University Press, 1994. $145. 0-19-261661-7
  37. Molecular etiology of factor VIII deficiency in hemophilia A
  38. Efficient gene transfer into human umbilical vein endothelial cells allows functional analysis of the human tissue factor gene promoter
  39. Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene
  40. Relationship between hemostatic abnormalities and neuroendocrine activity in heart failure
  41. Synthesis and characterization of wild-type and variant .gamma.-carboxyglutamic acid-containing domains of factor VII
  42. Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII
  43. Inactivation of factor VIII by factor IXa
  44. Cardiovascular disease: hyperlipidaemia and coagulation
  45. Application of PCR to the Detection and Analysis of Point Mutations in the Human Factor VIII Gene
  46. Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months
  47. Production of factor VIII deficient plasma by immunodepletion using three monoclonal antibodies
  48. Identification of six functional clotting factor VIII:C epitopes by analysis of cross-reactive public idiotypes in murine monoclonal VIII:C inhibitors
  49. A monoclonal antibody based immunoradiometric assay for von willebrand factor: Survey of a large patient group
  50. A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A
  51. Distribution of factor VIII mRNA and antigen in human liver and other tissues
  52. Purification of human factor VIII:C and its characterization by Western blotting using monoclonal antibodies
  53. Detection and sequence of mutations in the factor VIII gene of haemophiliacs  
  54. Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene
  55. An immunoradiometric assay for human factor VIII/von Willebrand factor (VIII:vWF) using a monoclonal antibody that defines a functional epitope
  56. Von Willebrand factor multimer patterns in von Willebrand's disease
  57. Synthesis and Release of Factor VIII by Cultured Human Endothelial Cells
  58. Immunologic studies of factor VIII coagulant activity (VIII:C) 1. Assays based on a haemophilic and an acquired antibody to VIII:C
  59. Professor Sen and Hare's Rule
  60. Professor Jowett
  61. Monograph of the Echinodermata of the British tertiaries. By Professor Edward Forbes.