The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
about
Biotechnology. A prudent path forward for genomic engineering and germline gene modificationEmerging Technologies to Create Inducible and Genetically Defined Porcine Cancer ModelsGenome Editing and Its Applications in Model OrganismsAn inducible CRISPR-ON system for controllable gene activation in human pluripotent stem cells.UAP56 is a conserved crucial component of a divergent mRNA export pathway in Toxoplasma gondiiRS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiencyAn easy and efficient inducible CRISPR/Cas9 platform with improved specificity for multiple gene targetingModeling Alzheimer's disease with human induced pluripotent stem (iPS) cells.Genome Editing of Lineage Determinants in Human Pluripotent Stem Cells Reveals Mechanisms of Pancreatic Development and Diabetes.In vivo blunt-end cloning through CRISPR/Cas9-facilitated non-homologous end-joiningPrecision genome editing in the CRISPR era.Editing genetics, stem cells are prophetic, what's the best way to model cells of diabetics?The emerging molecular biology toolbox for the study of long noncoding RNA biology.A CRISPR/Cas-Mediated Selection-free Knockin Strategy in Human Embryonic Stem Cells.Genome Editing and Directed Differentiation of hPSCs for Interrogating Lineage Determinants in Human Pancreatic Development.Nanoporous Immunoprotective Device for Stem-Cell-Derived β-Cell Replacement Therapy.CRISPR/Cas9-Mediated Mutagenesis of Human Pluripotent Stem Cells in Defined Xeno-Free E8 Medium.CRISPR/Cas-Mediated Knockin in Human Pluripotent Stem Cells.TET proteins safeguard bivalent promoters from de novo methylation in human embryonic stem cells.Site-specific randomization of the endogenous genome by a regulatable CRISPR-Cas9 piggyBac system in human cells.Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9.Hspb7 is a cardioprotective chaperone facilitating sarcomeric proteostasis.The p53 Family Coordinates Wnt and Nodal Inputs in Mesendodermal Differentiation of Embryonic Stem Cells.Deoxyribonucleic Acid Damage and Repair: Capitalizing on Our Understanding of the Mechanisms of Maintaining Genomic Integrity for Therapeutic Purposes.
P2860
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P2860
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
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
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
@ast
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
@en
type
label
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
@ast
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
@en
prefLabel
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
@ast
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
@en
P2860
P1476
The iCRISPR platform for rapid genome editing in human pluripotent stem cells.
@en
P2093
Zengrong Zhu
P2860
P304
P356
10.1016/B978-0-12-801185-0.00011-8
P407
P577
2014-01-01T00:00:00Z