Delivery of Genome Editing Reagents to Hematopoietic Stem/Progenitor Cells.
about
Integrase-Deficient Lentiviral Vector as an All-in-One Platform for Highly Efficient CRISPR/Cas9-Mediated Gene EditingCRISPR/Cas9-Mediated Correction of the Sickle Mutation in Human CD34+ cells.Enhancement of mouse hematopoietic stem/progenitor cell function via transient gene delivery using integration-deficient lentiviral vectors.A Protocol for the Production of Integrase-deficient Lentiviral Vectors for CRISPR/Cas9-mediated Gene Knockout in Dividing Cells.
P2860
Delivery of Genome Editing Reagents to Hematopoietic Stem/Progenitor Cells.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Delivery of Genome Editing Reagents to Hematopoietic Stem/Progenitor Cells.
@en
type
label
Delivery of Genome Editing Reagents to Hematopoietic Stem/Progenitor Cells.
@en
prefLabel
Delivery of Genome Editing Reagents to Hematopoietic Stem/Progenitor Cells.
@en
P2093
P2860
P1476
Delivery of Genome Editing Reagents to Hematopoietic Stem/Progenitor Cells.
@en
P2093
Donald B Kohn
Gregory J Cost
Matthew Mendel
Megan D Hoban
Michael Holmes
Zulema Romero
P2860
P304
P356
10.1002/9780470151808.SC05B04S36
P577
2016-02-03T00:00:00Z