Research Specialist in , for Harvard University Medical School

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PTSI

East Syracuse, New York

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Harvard University Division of Continuing Education

USA - MA - Cambridge

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Harvard University Division of Continuing Education

USA - MA - Cambridge

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

Undergraduate Research and Field Safety Coordinator

University of California Santa Cruz

Santa Cruz, California

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

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Bemidji State University

Bemidji, Minnesota

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

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Harvard University School of Dental Medicine

USA - MA - Boston

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

Research Assistant in Molecular Biology

Harvard University School of Dental Medicine

USA - MA - Boston

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Harvard University School of Dental Medicine

USA - MA - Boston

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

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Rutgers University

New Brunswick, New Jersey

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Harvard University Administration

USA - MA - Cambridge

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

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Harvard University School of Dental Medicine

USA - MA - Boston

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

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Bemidji State University

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Department Administrator, Developmental Biology

Harvard University School of Dental Medicine

USA - MA - Boston

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Harvard University Faculty of Arts and Sciences

USA - MA - Cambridge

Records Specialist

Harvard University Division of Continuing Education

USA - MA - Cambridge

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USA - MA - Cambridge

Research Specialist

We are forming a team in the Harvard Medical School Department of Neurobiology dedicated to repurposing natural mechanisms of gene regulation to engineer precision viral vectors for gene therapy. First-generation gene therapy vectors lack optimal regulatory elements that lead to sub-therapeutic levels of expression and off-target toxicity. Our goal is to employ our in-house single-cell screening platform (PESCA, Hrvatin, et al., 2019), to sift through the mammalian genome and identify regulatory elements capable of driving optimal patterns of viral transgene expression to address a wide range of diseases. We are building a technology platform that fills a critical void in the gene therapy space. Our collective mission is to employ these regulatory elements to create novel

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