Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCs.
about
Phenotypic correction of Fanconi anemia cells in the murine bone marrow after carrier cell mediated delivery of lentiviral vector.Emerging cellular and gene therapies for congenital anemias.Hematopoietic cell transplantation in Fanconi anemia: current evidence, challenges and recommendations.Stem Cell Therapy for Fanconi Anemia.
P2860
Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCs.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Lentiviral-Mediated Gene Thera ...... us Turnover of Corrected HSCs.
@en
type
label
Lentiviral-Mediated Gene Thera ...... us Turnover of Corrected HSCs.
@en
prefLabel
Lentiviral-Mediated Gene Thera ...... us Turnover of Corrected HSCs.
@en
P2093
P50
P1433
P1476
Lentiviral-Mediated Gene Thera ...... ous Turnover of Corrected HSCs
@en
P2093
Ali Nowrouzi
Christof von Kalle
M Luz Lozano
Manfred Schmidt
Sabine Charrier
P304
P356
10.2174/1566523215666150929110903
P407
P577
2015-01-01T00:00:00Z