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Human iPS cells have a great potential to be cell sources for regenerative medicine because of the promise of infinite self-renewal and the capability to differentiate into multiple cell types. This book focuses on another great potential of human iPS cells, which is the establishment of human disease models using patient-specific iPS cells. Human iPS cells can be easily obtained from a patient’s somatic cells and provide the entire information on the patient’s genome. Accordingly, we can generate disease models for inheritable diseases in cell culture dishes using iPS cells. This is a quite…mehr
Human iPS cells have a great potential to be cell sources for regenerative medicine because of the promise of infinite self-renewal and the capability to differentiate into multiple cell types. This book focuses on another great potential of human iPS cells, which is the establishment of human disease models using patient-specific iPS cells. Human iPS cells can be easily obtained from a patient’s somatic cells and provide the entire information on the patient’s genome. Accordingly, we can generate disease models for inheritable diseases in cell culture dishes using iPS cells. This is a quite new technique but holds tremendous potential for our increased understanding of pathogenesis, and will then be the basis for novel drug development industries. All the authors are leading researchers in this field and they have reported many kinds of patient-derived iPS cells. In this book, they introduce the aspects that could be recapitulated in terms of disease modelling as well as further innovative findings such as novel pathogenetic insights and novel therapies.
Dr. Keiichi Fukuda obtained PhD degree in Division of Medicine, Keio University Graduate School, Japan in 1987. He started his carrier as an assistant Professor at Keio University, and promoted to full Professor in 2005. He is one of the top scientists in Japan and renowned as he had established a new therapy using regenerated cardiomyocytes obtained from stem cells.
Inhaltsangabe
Chapter 1 Recent Improvements and Emerging Issues in iPSC Generation for the Modeling of Disease.- Chapter 2 Cardiomyopathy.- Chapter 3 Modelling Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy with Patient-specific iPSCs.- Chapter 4 Cardiac Arrhythmia Modelling Using iPS Cells.- Chapter 5 iPSC Disease Modeling of Laminopathies.- Chapter 6 Hematological Disorders.- Chapter 7 Inherited Metabolic Disorders of the Liver.
Chapter1 Recent Improvements and Emerging Issues in iPSC Generation for the Modelingof Disease.- Chapter 2 Cardiomyopathy.- Chapter 3 Modelling ArrhythmogenicRight Ventricular Dysplasia/Cardiomyopathy with Patient-specific iPSCs.-Chapter 4 Cardiac Arrhythmia Modelling Using iPS Cells.- Chapter 5 iPSC DiseaseModeling of Laminopathies.- Chapter 6 Hematological Disorders.- Chapter 7 InheritedMetabolic Disorders of the Liver.
Chapter 1 Recent Improvements and Emerging Issues in iPSC Generation for the Modeling of Disease.- Chapter 2 Cardiomyopathy.- Chapter 3 Modelling Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy with Patient-specific iPSCs.- Chapter 4 Cardiac Arrhythmia Modelling Using iPS Cells.- Chapter 5 iPSC Disease Modeling of Laminopathies.- Chapter 6 Hematological Disorders.- Chapter 7 Inherited Metabolic Disorders of the Liver.
Chapter1 Recent Improvements and Emerging Issues in iPSC Generation for the Modelingof Disease.- Chapter 2 Cardiomyopathy.- Chapter 3 Modelling ArrhythmogenicRight Ventricular Dysplasia/Cardiomyopathy with Patient-specific iPSCs.-Chapter 4 Cardiac Arrhythmia Modelling Using iPS Cells.- Chapter 5 iPSC DiseaseModeling of Laminopathies.- Chapter 6 Hematological Disorders.- Chapter 7 InheritedMetabolic Disorders of the Liver.
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