Patient-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization

Author:   Andras Nagy ,  Kursad Turksen
Publisher:   Humana Press Inc.
Edition:   1st ed. 2016
Volume:   1353
ISBN:  

9781493930333


Pages:   368
Publication Date:   08 November 2015
Format:   Hardback
Availability:   Manufactured on demand   Availability explained
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Patient-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization


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Overview

This volume captures the rapid developments in the field of induced pluripotent stem (iPS) cells, which have provided novel opportunities and approaches both for better understanding a number of human diseases and for developing new platforms for drug development and screening for such diseases. Specifically, representative protocols on various disease models have been collected from labs around the world. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Patient-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization is an ideal reference for scientists working on furthering iPS research.

Full Product Details

Author:   Andras Nagy ,  Kursad Turksen
Publisher:   Humana Press Inc.
Imprint:   Humana Press Inc.
Edition:   1st ed. 2016
Volume:   1353
Dimensions:   Width: 17.80cm , Height: 2.60cm , Length: 25.40cm
Weight:   9.499kg
ISBN:  

9781493930333


ISBN 10:   1493930338
Pages:   368
Publication Date:   08 November 2015
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of Contents

Generation of Patient-Specific Induced Pluripotent Stem Cell from Peripheral Blood Mononuclear Cells by Sendai Reprogramming Vectors.- A Doxycycline-Inducible System for Genetic Correction of iPSC Disease Models.- Generation and Characterization Of Patient-Specific Induced Pluripotent Stem Cell For Disease Modeling.- Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells.- Generation and Characterization of Induced Pluripotent Stem Cells from Patients with mtDNA Mutations.- Skin Biopsy and Patient-Specific Stem Cell Lines.- Directed Myogenic Differentiation of Human Induced Pluripotent Stem Cells.- Using Human Induced Pluripotent Stem Cells to Model Skeletal Diseases.- Modeling Cardiovascular Diseases with Patient-Specific Human Pluripotent Stem Cell-Derived Cardiomyocytes.- Calcium Imaging in Pluripotent Stem Cell-Derived Cardiac Myocytes.- Patient-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization of Cardiac Cells.- Differentiation of Human Pluripotent Stem Cells to Cardiomyocytes Under Defined Conditions.- Generation of Cardiomyocytes from Pluripotent Stem Cells.- Generation and Characterization of Patient-Specific iPSC-Model for Cardiovascular Disease.- Transgene-Free Disease-Specific iPSC Generation from Fibroblasts and Peripheral Blood Mononuclear Cells.- Generation and Neuronal Differentiation of Patient-Specific Induced Pluripotent Stem Cells Derived from Niemann-Pick Type C1 Fibroblasts.- Multisystemic Disease Modeling of Liver-Derived Protein Folding Disorders Using Induced Pluripotent Stem Cells (iPSCs).- In Vitro Modeling of Alcohol-Induced Liver Injury Using Human Induced Pluripotent Stem Cells.- Generation of Human Induced Pluripotent Stem Cells Using RNA-Based Sendai Virus System and Pluripotency Validation of the Resulting Cell Population.- Modeling Axonal Phenotypes with Human Pluripotent Stem Cells.- Mitochondrial Disease-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization.- Patient-Specific Induced Pluripotent Stem Cell Models: Characterization of iPS Cell-Derived Cardiomyocytes.- Generation of Integration-Free Patient Specific iPS Cells Using Episomal Plasmids Under Feeder Free Conditions.

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