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Comparing ESC and iPSC—based models for human genetic disorders
Tomer Halevy,
Achia Urbach
The Mina and Everard Goodman Faculty of Life Sciences - at Bar-Ilan University
Bar-Ilan University
Research output
:
Contribution to journal
›
Review article
›
peer-review
60
Scopus citations
Overview
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Keyphrases
Embryonic Stem Cells
100%
Human Genetic Disorders
100%
Induced Pluripotent Stem Cells (iPSCs)
100%
Cell-based
66%
Disease Modeling
66%
Somatic Cells
66%
Human Disorders
33%
Molecular Mechanism
33%
Window of Opportunity
33%
Optimal Strategy
33%
Human Embryonic Stem Cells (hESCs)
33%
Genetic Disease
33%
Genome Editing
33%
Blastocyst
33%
Pluripotent Stem Cells
33%
Model Cell
33%
High Similarity
33%
Biochemistry, Genetics and Molecular Biology
Embryonic Stem Cell
100%
Human Genetic Disorder
100%
Induced Pluripotent Stem Cell
75%
Disease Modeling
50%
Somatic Cell
50%
Animal Model
25%
Stem Cell
25%
Genetic Disorder
25%
Genome Editing
25%
Blastocyst
25%
Medicine and Dentistry
Disease
100%
Embryonic Stem Cell
100%
Human Genetic Disorder
100%
Induced Pluripotent Stem Cell
50%
Somatic Cell
33%
Human Embryonic Stem Cell
16%
Blastocyst
16%
Genetic Disorder
16%
Genome Editing
16%
Pluripotent Stem Cell
16%
Neuroscience
Stem Cell
100%
Embryonic Stem Cell
100%
Disease Modeling
50%
Somatic Cell
50%
Blastocyst
25%
Pharmacology, Toxicology and Pharmaceutical Science
Genetic Disorder
100%
Disease
100%