about
Barriers to HIV Cure.CRISPR/Cas9 in allergic and immunologic diseases.Propagating Humanized BLT Mice for the Study of Human Immunology and Immunotherapy.Novel AIDS therapies based on gene editing.Gene Therapy in Tyrosinemia: Potential and Pitfalls.Engineering HIV-Resistant, Anti-HIV Chimeric Antigen Receptor T Cells.Clinical Applications of Genome Editing to HIV Cure.In trans paired nicking triggers seamless genome editing without double-stranded DNA cutting.Interferons and beyond: Induction of antiretroviral restriction factors.CRISPR-Cas Targeting of Host Genes as an Antiviral Strategy.Modeling Anti-HIV-1 HSPC-Based Gene Therapy in Humanized Mice Previously Infected with HIV-1.Inducing CCR5Δ32/Δ32 Homozygotes in the Human Jurkat CD4+ Cell Line and Primary CD4+ Cells by CRISPR-Cas9 Genome-Editing Technology.
P2860
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P2860
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
The clinical applications of genome editing in HIV.
@en
type
label
The clinical applications of genome editing in HIV.
@en
prefLabel
The clinical applications of genome editing in HIV.
@en
P2860
P1433
P1476
The clinical applications of genome editing in HIV
@en
P2093
Paula M Cannon
P2860
P304
P356
10.1182/BLOOD-2016-01-678144
P407
P50
P577
2016-04-06T00:00:00Z