
Recent Advances in iPSC Disease Modeling
Description
Key Features
- Provides an overview on the fast-moving field of induced pluripotent stem cell technology, regenerative medicine and therapeutics
- Covers the following diseases: severe congenital neutropenia, sickle cell and Diamond-Blackfan anemias, muscular dystrophies, Bernard-Soulier syndrome, familial hypercholesterolemia type II A, Werner syndrome, lysosomal storage diseases, and more
- Contains descriptions of cutting-edge research on the development of disease-specific human pluripotent stem cells
Readership
Researchers and scientists in stem cell therapy, cell biology, regenerative medicine, and organ transplantation. Graduate and undergraduate students in the above fields
Table of Contents
1. iPSCs for Modeling Lysosomal Storage Diseases
2. Sickle Cell Anemia: HBB Haplotypes; Clinical Heterogeneity; iPSC Modelling
3. iPSCs for Modeling mtDNA Diseases
4. iPSCs for Modeling Diamond Blackfan Anemia
5. Modeling Severe Congenital Neutropenia in Induced Pluripotent Stem Cells
6. iPSCs for Modeling Duchenne Muscular Dystrophy
7. Induced Pluripotent Stem Cell Modelling of Genetic Small Vessel Disease
8. The Contribution of Human Pluripotent Stem Cells to the Study of Myotonic Dystrophy Type 1
9. Induced Pluripotent Stem Cells (iPSCs) for Modeling of Bernard-Soulier Syndrome
10. iPSCs for Modelling Familial Hypercholesterolemia Type II A
11. iPSCs for Modeling Elastin-Associated Vasculopathy
12. iPSCs for Modeling of Sarcomeric Cardiomyopathies
13. Werner Syndrome iPS Cell, A Study of Pathologic Aging
Product details
- No. of pages: 320
- Language: English
- Copyright: © Academic Press 2020
- Published: July 16, 2020
- Imprint: Academic Press
- Paperback ISBN: 9780128222270
- eBook ISBN: 9780128232699
About the Editor
ALEXANDER BIRBRAIR
Affiliations and Expertise
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