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Publications by Robin Raymer
Liver-Directed Lentiviral Gene Therapy in a Dog Model of Hemophilia B
Science Translational Medicine
Medicine
Circumventing Furin Enhances Factor VIII Biological Activity and Ameliorates Bleeding Phenotypes in Hemophilia Models
JCI insight
Medicine
Related publications
Immune Modulatory Cell Therapy for Hemophilia B Based on CD20-Targeted Lentiviral Gene Transfer to Primary B Cells
Molecular Therapy - Methods and Clinical Development
Molecular Medicine
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Molecular Biology
447. Lentiviral Gene Therapy in a Preclinical Model of Omenn Syndrome
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
Designer Nuclease-Mediated Gene Correction via Homology-Directed Repair in an in Vitro Model of Canine Hemophilia B
Journal of Gene Medicine
Molecular Medicine
Drug Discovery
Genetics
Molecular Biology
Gene Therapy for Hemophilia
Frontiers in Bioscience - Landmark
Immunology
Molecular Biology
Biochemistry
Microbiology
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Generation of an Optimized Lentiviral Vector Encoding a High-Expression Factor VIII Transgene for Gene Therapy of Hemophilia A
Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Hemophilia B Acquired Through Liver Transplantation
Liver Transplantation
Hepatology
Transplantation
Surgery
28. Intravenous Administration of Lentiviral Vectors Expressing Hyperactive Factor IX Converts Severe Into Mild Hemophilia B in a Canine Model
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
Lentiviral Gene Replacement Therapy of Retinas in a Mouse Model for Usher Syndrome Type 1B
Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Platelet-Targeted Gene Therapy for Hemophilia
Molecular Therapy - Methods and Clinical Development
Molecular Medicine
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Molecular Biology
