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Updated: Apr 1, 2026

Retroviral CRISPR/Cas9-Mediated Gene Targeting for the Study of Th17 Differentiation in Vitro
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Retroviral CRISPR/Cas9-Mediated Gene Targeting for the Study of Th17 Differentiation in Vitro

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La expresión de un ARN mensajero retroviral subgenómico

D W Stacey

    Cell
    |October 1, 1980
    PubMed
    Resumen

    La inyección de ARNm de la glicoproteína de la envoltura retroviral aviar (env) en las células complementó la deficiencia de env, lo que permitió transformar la producción de virus. Este proceso, que involucra la transcripción inversa del ARNm, es crucial para comprender las relaciones entre retrovirus y huésped.

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