
- 320 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
Recent Advances in iPSC Disease Modeling
About this book
Recent Advances in iPSC Disease Modeling, Volume One addresses how induced pluripotent stem cells can be used to model various diseases. This new volume teaches readers about current advances in the field, describing the use of induced pluripotent stem cells to model several diseases in vitro, and thus enabling us to study the cellular and molecular mechanisms involved in different pathologies. Further insights into these mechanisms will have important implications for our understanding of disease appearance, development and progression. The volume is written for researchers and scientists in stem cell therapy, cell biology, regenerative medicine and organ transplantation specialists.In recent years, remarkable progress has been made in the obtention of induced pluripotent stem cells and their differentiation into several cell types, tissues and organs using state-of-art techniques. Hence, these advantages have facilitated the identification of key targets and further defining on the molecular basis of several disorders.- 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
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Table of contents
- Cover image
- Title page
- Table of Contents
- Copyright
- Dedication
- About the Editor
- Preface
- Chapter 1. iPSCs for modeling lysosomal storage diseases
- Chapter 2. Sickle cell anemia: HBB haplotypes; clinical heterogeneity; iPSC modeling
- Chapter 3. iPSCs for modeling mtDNA diseases
- Chapter 4. iPSCs for modeling Diamond–Blackfan anemia
- Chapter 5. Modeling severe congenital neutropenia in induced pluripotent stem cells
- Chapter 6. iPSCs for modeling Duchenne muscular dystrophy
- Chapter 7. Induced pluripotent stem cell modeling of genetic small vessel disease
- Chapter 8. The contribution of human pluripotent stem cells to the study of myotonic dystrophy type 1
- Chapter 9. Induced pluripotent stem cells for the modeling of Bernard-Soulier syndrome
- Chapter 10. iPSCs for modeling familial hypercholesterolemia type II A
- Chapter 11. Induced pluripotent stem cells for modeling elastin-associated vasculopathy
- Chapter 12. iPSCs for modeling of sarcomeric cardiomyopathies
- Chapter 13. Werner syndrome induced pluripotent stem cells, a study of pathologic aging
- Index