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Human Embryonic Stem Cell Protocols

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Cover of 'Human Embryonic Stem Cell Protocols'

Table of Contents

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    Book Overview
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    Chapter 54 A Simple Protocol for the Generation of Cardiomyocytes from Human Pluripotent Stem Cells
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    Chapter 55 Use of Multicolor Flow Cytometry for Isolation of Specific Cell Populations Deriving from Differentiated Human Embryonic Stem Cells
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    Chapter 56 Accelerated Three-Dimensional Neuroepithelium Formation from Human Embryonic Stem Cells and Its Use for Quantitative Differentiation to Human Retinal Pigment Epithelium
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    Chapter 57 Efficient Production of Photoreceptor Precursor Cells from Human Embryonic Stem Cells
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    Chapter 58 Human Embryonic Stem Cell Protocols
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    Chapter 59 Dual-SMAD Inhibition/WNT Activation-Based Methods to Induce Neural Crest and Derivatives from Human Pluripotent Stem Cells.
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    Chapter 67 Directed Differentiation of Human Embryonic Stem Cells into Neural Progenitors
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    Chapter 68 Analysis of Intracellular Calcium Signaling in Human Embryonic Stem Cells
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    Chapter 69 Direct Conversion of Pluripotent Human Embryonic Stem Cells Under Defined Culture Conditions into Human Neuronal or Cardiomyocyte Cell Therapy Derivatives
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    Chapter 70 Generation of Epithelial Cell Populations from Human Pluripotent Stem Cells Using a Small-Molecule Inhibitor of Src Family Kinases
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    Chapter 73 Genetic Modification in Human Pluripotent Stem Cells by Homologous Recombination and CRISPR/Cas9 System.
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    Chapter 81 Microgrooved Surface Modulates Neuron Differentiation in Human Embryonic Stem Cells
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    Chapter 82 Efficient Expansion of Dissociated Human Pluripotent Stem Cells Using a Synthetic Substrate
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    Chapter 83 Study of Gap Junctions in Human Embryonic Stem Cells
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    Chapter 85 Derivation of Human Embryonic Stem Cell Lines from Vitrified Human Blastocysts
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    Chapter 86 Erratum to: Microgrooved Surface Modulates Neuron Differentiation in Human Embryonic Stem Cells
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    Chapter 89 Derivation of Chondrogenic Cells from Human Embryonic Stem Cells for Cartilage Tissue Engineering
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    Chapter 109 Characterizing Pluripotent Stem Cells Using the TaqMan® hPSC ScorecardTM Panel
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    Chapter 127 Immunofluorescence Microscopy and mRNA Analysis of Human Embryonic Stem Cells (hESCs) Including Primary Cilia Associated Signaling Pathways
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    Chapter 128 Human Embryonic and Hepatic Stem Cell Differentiation Visualized in Two and Three Dimensions Based on Serial Sections
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    Chapter 130 Differentiation of Human Embryonic Stem Cells on Periodontal Ligament Fibroblasts
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    Chapter 131 Monitoring Stemness in Long-Term hESC Cultures by Real-Time PCR
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    Chapter 132 Derivation of Epithelial Cells from Human Embryonic Stem Cells as an In Vitro Model of Vocal Mucosa.
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    Chapter 149 Derivation of Endothelial Cells and Pericytes from Human Pluripotent Stem Cells
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    Chapter 154 Growth of Human Pluripotent Stem Cells Using Functional Human Extracellular Matrix
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    Chapter 155 Genetic Manipulation of Human Embryonic Stem Cells
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    Chapter 224 Definitive Endoderm Differentiation of Human Embryonic Stem Cells Combined with Selective Elimination of Undifferentiated Cells by Methionine Deprivation
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    Chapter 244 Microarray Approach to Identify the Signaling Network Responsible for Self-Renewal of Human Embryonic Stem Cells.
Attention for Chapter 132: Derivation of Epithelial Cells from Human Embryonic Stem Cells as an In Vitro Model of Vocal Mucosa.
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Chapter title
Derivation of Epithelial Cells from Human Embryonic Stem Cells as an In Vitro Model of Vocal Mucosa.
Chapter number 132
Book title
Human Embryonic Stem Cell Protocols
Published in
Methods in molecular biology, November 2014
DOI 10.1007/7651_2014_132
Pubmed ID
Book ISBNs
978-1-4939-2667-1, 978-1-4939-2668-8
Authors

Vlasta Lungova, Ciara Leydon, Susan Thibeault, Lungova, Vlasta, Leydon, Ciara, Thibeault, Susan

Abstract

Vocal fold epithelial cells are very difficult to study as the vocal fold epithelial cell lines do not exist and they cannot be removed from the healthy larynx without engendering a significant and unacceptable risk to vocal fold function. Here, we describe the procedure to create an engineered vocal fold tissue construct consisting of the scaffold composed of the collagen 1 gel seeded with human fibroblasts and simple epithelial progenitors seeded on the scaffold and cultivated at air-liquid interface for 19-21 days to derive the stratified squamous epithelium. This model of vocal fold mucosa is very similar in morphology, gene expression, and phenotypic characteristics to native vocal fold epithelial cells and the underlying lamina propria and, therefore, offers a promising approach to studying vocal fold biology and biomechanics in health and disease.

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The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 36%
Other 2 18%
Student > Doctoral Student 1 9%
Student > Bachelor 1 9%
Researcher 1 9%
Other 0 0%
Unknown 2 18%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 27%
Biochemistry, Genetics and Molecular Biology 2 18%
Medicine and Dentistry 2 18%
Immunology and Microbiology 1 9%
Materials Science 1 9%
Other 0 0%
Unknown 2 18%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 19 November 2014.
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#20,243,777
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Outputs from Methods in molecular biology
#9,862
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#303,341
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Outputs of similar age from Methods in molecular biology
#657
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