about
Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Barth Syndrome: From Mitochondrial Dysfunctions Associated with Aberrant Production of Reactive Oxygen Species to Pluripotent Stem Cell StudiesOral delivery of dsRNA by microbes: Beyond pest controlAn episomal vector-based CRISPR/Cas9 system for highly efficient gene knockout in human pluripotent stem cellsTALEN based HPV-E7 editing triggers necrotic cell death in cervical cancer cellsThe Structural Basis of Asymmetry in DNA Binding and Cleavage as Exhibited by the I-SmaMI LAGLIDADG Meganuclease.The necessity for in vivo functional analysis in human medical genetics.Alzheimer disease research in the 21st century: past and current failures, new perspectives and funding prioritiesMechanotransduction and Metabolism in Cardiomyocyte Microdomains.Genetic manipulation of secondary metabolite biosynthesis for improved production in Streptomyces and other actinomycetes.Modeling Alzheimer's disease with human induced pluripotent stem (iPS) cells.Modeling psychiatric disorders with patient-derived iPSCs.MMEJ-assisted gene knock-in using TALENs and CRISPR-Cas9 with the PITCh systems.CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes.Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studiesA Comprehensive Toolbox for Genome Editing in Cultured Drosophila melanogaster Cells.Efficient CRISPR-Cas9-mediated generation of knockin human pluripotent stem cells lacking undesired mutations at the targeted locus.CRISPR Genome Engineering for Human Pluripotent Stem Cell Research.CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells.Mechanisms of precise genome editing using oligonucleotide donors.Scarless Genome Editing of Human Pluripotent Stem Cells via Transient Puromycin Selection.Using induced pluripotent stem cells to explore genetic and epigenetic variation associated with Alzheimer's disease.One-step genetic correction of hemoglobin E/beta-thalassemia patient-derived iPSCs by the CRISPR/Cas9 system.CRISPR-Cas9-Based Genome Editing of Human Induced Pluripotent Stem Cells.CRISPR/Cas9 System: A Bacterial Tailor for Genomic EngineeringGenome editing of oncogenes with ZFNs and TALENs: caveats in nuclease designExtension of the crRNA enhances Cpf1 gene editing in vitro and in vivoEfficient homology-directed gene editing by CRISPR/Cas9 in human stem and primary cells using tube electroporation
P2860
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P2860
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Genome editing in human stem cells.
@en
Genome editing in human stem cells.
@nl
type
label
Genome editing in human stem cells.
@en
Genome editing in human stem cells.
@nl
prefLabel
Genome editing in human stem cells.
@en
Genome editing in human stem cells.
@nl
P2860
P1476
Genome editing in human stem cells.
@en
P2093
Prashant Mali
Susan M Byrne
P2860
P304
P356
10.1016/B978-0-12-801185-0.00006-4
P407
P577
2014-01-01T00:00:00Z