Učitavanje...
Enhancing therapeutic efficacy of in vivo platelet-targeted gene therapy in hemophilia A mice
Our previous studies demonstrated that intraosseous (IO) infusion of lentiviral vectors (LVs) carrying a modified B domain–deleted factor VIII (FVIII) transgene driven by a megakaryocyte-specific promoter (GP1Bα promoter; G-F8/N6-LV) successfully transduced hematopoietic stem cells (HSCs) to produce...
Spremljeno u:
| Izdano u: | Blood Adv |
|---|---|
| Glavni autori: | , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
American Society of Hematology
2020
|
| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7686911/ https://ncbi.nlm.nih.gov/pubmed/33216891 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2020002479 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|