In Vivo Excision of HIV-1 Provirus by saCas9 and Multiplex Single-Guide RNAs in Animal Models.
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Recent Advances in CRISPR-Cas9 Genome Editing Technology for Biological and Biomedical Investigations.CRISPR Editing Technology in Biological and Biomedical Investigation.Type II CRISPR/Cas9 approach in the oncological therapy.Interplay between Autophagy, Exosomes and HIV-1 Associated Neurological Disorders: New Insights for Diagnosis and Therapeutic Applications.Combinatorial CRISPR-Cas9 and RNA Interference Attack on HIV-1 DNA and RNA Can Lead to Cross-Resistance.Excision of Latent HIV-1 from Infected Cells In Vivo: An Important Step Forward.A directed evolution approach to select for novel Adeno-associated virus capsids on an HIV-1 producer T cell line.Designing broad-spectrum anti-HIV-1 gRNAs to target patient-derived variants.Genome modification of CXCR4 by Staphylococcus aureus Cas9 renders cells resistance to HIV-1 infection.The fourth annual BRDS on genome editing and silencing for precision medicines.Targeting TRIM5α in HIV Cure Strategies for the CRISPR-Cas9 Era.CRISPR-Cas Targeting of Host Genes as an Antiviral Strategy.In vivo genome editing in animals using AAV-CRISPR system: applications to translational research of human disease.Synthetic AAV/CRISPR vectors for blocking HIV-1 expression in persistently infected astrocytes.Therapeutic Genome Editing With CRISPR/Cas9 in a Humanized Mouse Model Ameliorates α1-antitrypsin Deficiency Phenotype.In vivo genome editing thrives with diversified CRISPR technologies.CRISPR/Cas9 and Genome Editing for Viral Disease-Is Resistance Futile?Comparison of the editing patterns and editing efficiencies of TALEN and CRISPR-Cas9 when targeting the human CCR5 gene.Tackling HIV Persistence: Pharmacological versus CRISPR-Based Shock Strategies.CRISPR Gene Editing in the Kidney.EcoHIV infection of mice establishes latent viral reservoirs in T cells and active viral reservoirs in macrophages that are sufficient for induction of neurocognitive impairment.Follicular Dendritic Cells of Lymph Nodes as Human Immunodeficiency Virus/Simian Immunodeficiency Virus Reservoirs and Insights on Cervical Lymph Node.Removal of HIV DNA by CRISPR from Patient Blood Engrafts in Humanized Mice.Viral diversity is an obligate consideration in CRISPR/Cas9 designs for targeting the HIV reservoir.Adult neurogenic deficits in HIV-1 Tg26 transgenic miceCRISPR/Cas9 System: A Bacterial Tailor for Genomic EngineeringCSGID Solves Structures and Identifies Phenotypes for Five Enzymes in Toxoplasma gondiiPairwise library screen systematically interrogates Staphylococcus aureus Cas9 specificity in human cellsIn Vivo Genome Editing as a Therapeutic ApproachComprehensive off-target analysis of dCas9-SAM-mediated HIV reactivation via long noncoding RNA and mRNA profiling
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P2860
In Vivo Excision of HIV-1 Provirus by saCas9 and Multiplex Single-Guide RNAs in Animal Models.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
In Vivo Excision of HIV-1 Prov ...... e-Guide RNAs in Animal Models.
@en
type
label
In Vivo Excision of HIV-1 Prov ...... e-Guide RNAs in Animal Models.
@en
altLabel
In Vivo Excision of HIV-1 Prov ...... le-Guide RNAs in Animal Models
@en
prefLabel
In Vivo Excision of HIV-1 Prov ...... e-Guide RNAs in Animal Models.
@en
P2093
P2860
P921
P1433
P1476
In Vivo Excision of HIV-1 Prov ...... e-Guide RNAs in Animal Models.
@en
P2093
Chaoran Yin
Huaqing Zhao
Kamel Khalili
Raj Putatunda
Ting Zhang
Weidong Xiao
Won-Bin Young
P2860
P304
P356
10.1016/J.YMTHE.2017.03.012
P407
P577
2017-03-30T00:00:00Z