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Richard O. Snyder

Researcher at University of Florida

Publications -  60
Citations -  5725

Richard O. Snyder is an academic researcher from University of Florida. The author has contributed to research in topics: Adeno-associated virus & Viral vector. The author has an hindex of 35, co-authored 59 publications receiving 5437 citations. Previous affiliations of Richard O. Snyder include French Institute of Health and Medical Research & University of Nantes.

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Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors

TL;DR: It is demonstrated that persistent, curative concentrations of functional human factor IX can be achieved using wild-type-free and adenovirus-free rAAV vectors and demonstrates the potential of treating haemophilia B by gene therapy at the natural site of factor IX production.
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Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors.

TL;DR: Reagents and methods for the production and purification of AAV2 inverted terminal repeat-containing vectors pseudotyped with AAV1 or AAV5 capsids are described.
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Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors

TL;DR: Constitutive expression of factor IX was observed, which resulted in the correction of the bleeding disorder over a period of over 17 months in mice, and as a preclinical model for gene therapy, recombinant adeno-associated viral vectors containing the human or canine factor IX cDNAs were infused into the livers of murine and canine models of hemophilia B.
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Midbrain injection of recombinant adeno-associated virus encoding rat glial cell line-derived neurotrophic factor protects nigral neurons in a progressive 6-hydroxydopamine-induced degeneration model of Parkinson’s disease in rats

TL;DR: Data indicate that the use of rAAV, a noncytopathic viral vector, can promote delivery of functional levels of GDNF in a degenerative model of Parkinson's disease.
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Epitope Mapping of Human Anti-Adeno-Associated Virus Type 2 Neutralizing Antibodies: Implications for Gene Therapy and Virus Structure

TL;DR: Recombinant adeno-associated virus type 2 (AAV) is a common vector used in human gene therapy protocols and a subset of six peptides which potentially reconstitute a single neutralizing epitope are identified, which may allow the design of reverse genetic approaches to circumvent the preexisting immunity that can be encountered in some individuals.