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Publications by V A Geddes
Molecular Basis of Hemophilia B: Identification of the Defect in Factor Ix Vancouver
Related publications
Identification of the Molecular Defect in Factor IX Chapel Hill: Substitution of Histidine for Arginine at Position 145.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Survey of the Anti-Factor IX Immunoglobulin Profiles in Patients With Hemophilia B Using a Fluorescence-Based Immunoassay
Journal of Thrombosis and Haemostasis
Medicine
Hematology
Expression and Characterization of Gly-317 Variants of Factor IX Causing Variable Bleeding in Hemophilia B Patients
Biochemistry
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Three Point Mutations in the Factor IX Genes of Five Hemophilia B Patients. Identification Strategy Using Localization by Altered Epitopes in Their Hemophilic Proteins.
Journal of Clinical Investigation
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Oral Delivery of Bioencapsulated Coagulation Factor IX Prevents Inhibitor Formation and Fatal Anaphylaxis in Hemophilia B Mice
Proceedings of the National Academy of Sciences of the United States of America
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Hemophilia as a Defect of the Tissue Factor Pathway of Blood Coagulation: Effect of Factors VIII and IX on Factor X Activation in a Continuous-Flow Reactor.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Role of the Vector Genome and Underlying Factor IX Mutation in Immune Responses to AAV Gene Therapy for Hemophilia B
Journal of Translational Medicine
Biochemistry
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Genetics
Molecular Biology
Structural and Functional Basis of the Developmental Regulation of Human Coagulation Factor IX Gene: Factor IX Leyden.
Proceedings of the National Academy of Sciences of the United States of America
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Engineered Factor VII, Factor IX, and Factor X Variants for Hemophilia Gene Therapy
Journal of Genetic Syndromes & Gene Therapy
