Literature DB >> 27609877

Lentiviral vectors, two decades later.

Luigi Naldini1, Didier Trono2, Inder M Verma3.   

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Year:  2016        PMID: 27609877     DOI: 10.1126/science.aah6192

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


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  42 in total

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Review 3.  New frontiers in the therapy of primary immunodeficiency: From gene addition to gene editing.

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4.  Aberrant Clonal Hematopoiesis following Lentiviral Vector Transduction of HSPCs in a Rhesus Macaque.

Authors:  Diego A Espinoza; Xing Fan; Di Yang; Stefan F Cordes; Lauren L Truitt; Katherine R Calvo; Idalia M Yabe; Selami Demirci; Kristin J Hope; So Gun Hong; Allen Krouse; Mark Metzger; Aylin Bonifacino; Rong Lu; Naoya Uchida; John F Tisdale; Xiaolin Wu; Suk See DeRavin; Harry L Malech; Robert E Donahue; Chuanfeng Wu; Cynthia E Dunbar
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Review 5.  Evolving Gene Therapy in Primary Immunodeficiency.

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6.  [A method for efficient transduction of miR-483-5p in the kidney of mice].

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7.  Lentiviral delivery of co-packaged Cas9 mRNA and a Vegfa-targeting guide RNA prevents wet age-related macular degeneration in mice.

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Review 8.  Nanotherapy for Duchenne muscular dystrophy.

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9.  Enhancing therapeutic efficacy of in vivo platelet-targeted gene therapy in hemophilia A mice.

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Journal:  Blood Adv       Date:  2020-11-24

10.  Versatile targeting system for lentiviral vectors involving biotinylated targeting molecules.

Authors:  Kathy Situ; Bernadette Anne Chua; Song Yi Bae; Aaron Samuel Meyer; Kouki Morizono
Journal:  Virology       Date:  2018-10-02       Impact factor: 3.616

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