Living-Will
发表于 2025-3-30 11:35:21
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Recess
发表于 2025-3-30 12:52:53
Adenovirus-Mediated Gene Delivery to Dendritic Cells to mount a specific cellular and humoral response. Recognition of this crucial function makes the development of technologies for DC-based immuno-therapies a priority for the treatment of a wide variety of diseases. The most immediate impact of this emerging technology will be in the treatment of c
清澈
发表于 2025-3-30 18:36:35
Overview of Adeno-Associated Viral Vectorsticularly useful for applications where sustained gene expression is required. Prolonged in vivo expression following A AV treatment has been seen in the liver (.,.), brain (.,.), skeletal muscle (.,.), lung (.,.), and hematopoietic stem cells (.,.) of animal models. Therapeutic benefit from A AV tr
GAVEL
发表于 2025-3-31 00:11:23
AAV Vector Delivery to Cells in Cultureuman diseases. AAV’s inability to self-propagate, ability to be maintained as an episome in the transduced cell, and relatively innocuous effects on the immune system make it the vector of choice for prolonged in vivo gene expression. AAV type 2 is the most commonly used serotype for gene delivery.
熔岩
发表于 2025-3-31 04:15:58
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