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AAV Vector Production for Gene TherapyPosted by: National Institutes of Health (NIH)
Posted date: 2019-Mar-01
A major limitation for the advancement of the field of gene therapy is the ability to produce large quantities of high quality vectors. Recent work has identified that many particles are defective and can interfere with production of competent gene transfer vectors. A fully funded two year Post-doctoral positions are available to study the role of the AAV Rep proteins in the production of recombinant vectors for gene therapy. Techniques to be used include state of the art GMP AAV vector production processes, protein engineering, and bioinformatics.Qualifications:
Applicants with experience in parvovirus biology, helicase proteins, or recombinant baculovirus are encouraged to apply.To Apply:
Please send cover letter, curriculum vitae, bibliography, and a brief description of your interest in the field of AAV biology to: John A. Chiorini, Molecular Physiology and Therapeutics Branch, NIDCR,
Building 10 Room 1N113, 10 Center Dr MSC 1190, Bethesda MD 20892-1190, USA
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