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Titlebook: Gene Therapy for HIV; From Inception to a Gerhard Bauer,Joseph S. Anderson Book 2014 Gerhard Bauer and Joseph S. Anderson 2014 Anti-HIV ge

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樓主: Stenosis
11#
發(fā)表于 2025-3-23 11:11:37 | 只看該作者
Stem Cells for HIV Gene Therapy,stem cells that were gene modified with anti-HIV genes. A pluripotent, anti-HIV gene-modified cell clone could be used to generate enough hematopoietic stem cells to engraft the recipient. The generation of a patient’s own gene-modified stem cells is possible by the use of autologous, induced pluripotent stem cells.
12#
發(fā)表于 2025-3-23 17:25:34 | 只看該作者
Is a Cure for HIV Possible?,e can be expected. In the future, stem cells may also be generated from pluripotent stem cells, particularly induced pluripotent stem cells, promising large numbers of tested, HIV-resistant autologous stem cells for patients with HIV.
13#
發(fā)表于 2025-3-23 19:58:41 | 只看該作者
Bulk-Edge Dualities in Topological Matter,hematopoietic origin, derived from hematopoietic stem cells. Anti-HIV genes inserted into hematopoietic stem cells will be passed onto all progeny, including all the target cells for HIV. Newly arising cells will therefore be protected from the detrimental effects of HIV.
14#
發(fā)表于 2025-3-24 02:12:53 | 只看該作者
https://doi.org/10.1007/978-1-4615-6261-0Both vector and cellular products need to be manufacturing in a GMP facility designed for this purpose, and stringent release criteria need to be applied before they can be administered into patients in clinical trials.
15#
發(fā)表于 2025-3-24 04:52:32 | 只看該作者
16#
發(fā)表于 2025-3-24 08:43:55 | 只看該作者
17#
發(fā)表于 2025-3-24 10:58:48 | 只看該作者
Manufacturing of a GMP Grade Product for HIV Gene Therapy,Both vector and cellular products need to be manufacturing in a GMP facility designed for this purpose, and stringent release criteria need to be applied before they can be administered into patients in clinical trials.
18#
發(fā)表于 2025-3-24 16:37:00 | 只看該作者
Clinical Applications of HIV Gene Therapy,ovide continued benefits. Stem cell gene therapy offers to be a onetime treatment, but currently only low transduction efficiencies can be achieved. Future clinical trials of stem cell gene therapy need to be designed to overcome this problem.
19#
發(fā)表于 2025-3-24 19:58:13 | 只看該作者
978-1-4939-0433-4Gerhard Bauer and Joseph S. Anderson 2014
20#
發(fā)表于 2025-3-25 01:08:15 | 只看該作者
Gene Therapy for HIV978-1-4939-0434-1Series ISSN 2211-9353 Series E-ISSN 2211-9361
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