- 136 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
eBook - ePub
CRISPR Genome Surgery in Stem Cells and Disease Tissues
About this book
CRISPR Genome Surgery in Stem Cells and Disease Tissues focuses uniquely on the clinical applications of CRISPR/Cas9 based technology. Topics include the latest advances in gene editing and its translational applications to various diseases, including retinal degenerative disease, recessively inherited diseases, and dominantly inherited diseases, to name a few. The book's target audience includes researchers, students, clinicians and the general public. This space that is not currently served by any existing resource, so this publication fills a gap in current literature.
- Provides a thorough review of CRISPR-Cas9, from discovery to therapy
- Covers the latest advances in gene editing and its translational applications to various diseases
- Written by global leaders in the fields of gene editing and stem cell therapy
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Please note we cannot support devices running on iOS 13 and Android 7 or earlier. Learn more about using the app.
Yes, you can access CRISPR Genome Surgery in Stem Cells and Disease Tissues by Stephen H. Tsang in PDF and/or ePUB format, as well as other popular books in Biological Sciences & Cell Biology. We have over one million books available in our catalogue for you to explore.
Information
Table of contents
- Title of Book
- Cover image
- Title page
- Table of Contents
- Copyright
- List of contributors
- Foreword
- Chapter 1 The history of CRISPR: from discovery to the present
- Chapter 2 CRISPR-Cas orthologs and variants
- Chapter 3 Genome engineering with CRISPR/Cas9, ZFNs, and TALENs
- Chapter 4 Single-guide RNAs: rationale and design
- Chapter 5 CRISPR-mediated dense mutagenesis: a tool for rational targeting of multiprotein complexes and the noncoding genome
- Chapter 6 Targeting Alzheimer’s disease and related dementias with CRISPR and human pluripotent stem cell technologies
- Chapter 7 Gene editing for the cornea
- Chapter 8 Employing nonhomologous end joining and homology-directed repair for treatment of Leber congenital amaurosis and inherited retinal degeneration
- Chapter 9 The ethics of gene editing in human stem cells
- Index