Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.
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Site-Specific Genome Engineering in Human Pluripotent Stem CellsApplications of CRISPR/Cas9 for Gene Editing in Hereditary Movement DisordersGenetic Correction of SOD1 Mutant iPSCs Reveals ERK and JNK Activated AP1 as a Driver of Neurodegeneration in Amyotrophic Lateral Sclerosis.Stem cell models of Alzheimer's disease: progress and challenges.Pluripotent stem cells: the last 10 years.Engineering Hematopoietic Stem Cells: Lessons from Development.Efficient CRISPR/Cas9-Mediated Versatile, Predictable, and Donor-Free Gene Knockout in Human Pluripotent Stem CellsAlzheimer disease research in the 21st century: past and current failures, new perspectives and funding prioritiesThe translational potential of human induced pluripotent stem cells for clinical neurology : The translational potential of hiPSCs in neurology.Systematic gene tagging using CRISPR/Cas9 in human stem cells to illuminate cell organization.Adeno-Associated Virus Vectors and Stem Cells: Friends or Foes?Linking adult hippocampal neurogenesis with human physiology and disease.Comprehensive Protocols for CRISPR/Cas9-based Gene Editing in Human Pluripotent Stem CellsRoad to the future of systems biotechnology: CRISPR-Cas-mediated metabolic engineering for recombinant protein production.CRISPR: express delivery to any DNA address.Generation of improved human cerebral organoids from single copy DYRK1A knockout induced pluripotent stem cells in trisomy 21: hypothetical solutions for neurodevelopmental models and therapeutic alternatives in down syndrome.Induced Pluripotent Stem Cells in Huntington's Disease Research: Progress and Opportunity.Perspectives and Challenges of Pluripotent Stem Cells in Cardiac Arrhythmia Research.Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis.3D brain Organoids derived from pluripotent stem cells: promising experimental models for brain development and neurodegenerative disorders.New tools for experimental diabetes research: Cellular reprogramming and genome editing.Rapid and efficient CRISPR/Cas9 gene inactivation in human neurons during human pluripotent stem cell differentiation and direct reprogramming.A Scaled Framework for CRISPR Editing of Human Pluripotent Stem Cells to Study Psychiatric Disease.Modeling and correction of structural variations in patient-derived iPSCs using CRISPR/Cas9.Generation and Characterization of Functional Human Hypothalamic Neurons.iPS cells in the study of PD molecular pathogenesis.Stem Cell Technology for (Epi)genetic Brain Disorders.Small molecules promote CRISPR-Cpf1-mediated genome editing in human pluripotent stem cells.
P2860
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P2860
Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.
@en
type
label
Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.
@en
prefLabel
Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.
@en
P2093
P2860
P1433
P1476
Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.
@en
P2093
Chad A Cowan
Curtis R Warren
William T Hendriks
P2860
P356
10.1016/J.STEM.2015.12.002
P407
P577
2016-01-01T00:00:00Z