Yüklüyor......
Phenotypic correction of Fanconi anemia cells in the murine bone marrow after carrier cell mediated delivery of lentiviral vector
Fanconi anemia (FA) is an autosomal-recessive disorder associated with hematopoietic failure and it is a candidate for hematopoietic stem cell (HSC)-directed gene therapy. However, the characteristically reduced HSC numbers found in FA patients, their ineffective mobilization from the marrow, and re...
Kaydedildi:
| Yayımlandı: | Stem Cell Res Ther |
|---|---|
| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2016
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5116221/ https://ncbi.nlm.nih.gov/pubmed/27865213 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13287-016-0431-z |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|