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Organ Regeneration

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Cover of 'Organ Regeneration'

Table of Contents

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    Book Overview
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    Chapter 1 Generation of Various Telencephalic Regions from Human Embryonic Stem Cells in Three-Dimensional Culture
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    Chapter 2 Generation of a Three-Dimensional Retinal Tissue from Self-Organizing Human ESC Culture
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    Chapter 3 3D Culture for Self-Formation of the Cerebellum from Human Pluripotent Stem Cells Through Induction of the Isthmic Organizer
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    Chapter 4 Reconstitution of a Patterned Neural Tube from Single Mouse Embryonic Stem Cells
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    Chapter 5 Functional Pituitary Tissue Formation
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    Chapter 6 Directed Differentiation of Mouse Embryonic Stem Cells Into Inner Ear Sensory Epithelia in 3D Culture
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    Chapter 7 Generation of Functional Thyroid Tissue Using 3D-Based Culture of Embryonic Stem Cells
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    Chapter 8 Functional Tooth Regeneration
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    Chapter 9 Functional Hair Follicle Regeneration by the Rearrangement of Stem Cells
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    Chapter 10 Functional Salivary Gland Regeneration
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    Chapter 11 Generation of a Bioengineered Lacrimal Gland by Using the Organ Germ Method
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    Chapter 12 Generation of Gastrointestinal Organoids from Human Pluripotent Stem Cells
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    Chapter 13 Generation of a Three-Dimensional Kidney Structure from Pluripotent Stem Cells
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    Chapter 14 Making a Kidney Organoid Using the Directed Differentiation of Human Pluripotent Stem Cells
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    Chapter 15 Liver Regeneration Using Cultured Liver Bud
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    Chapter 16 Formation of Stomach Tissue by Organoid Culture Using Mouse Embryonic Stem Cells
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    Chapter 17 In Vivo Model of Small Intestine
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    Chapter 18 Erratum to: In Vivo Model of Small Intestine
Attention for Chapter 8: Functional Tooth Regeneration
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Chapter title
Functional Tooth Regeneration
Chapter number 8
Book title
Organ Regeneration
Published in
Methods in molecular biology, March 2017
DOI 10.1007/978-1-4939-6949-4_8
Pubmed ID
Book ISBNs
978-1-4939-6947-0, 978-1-4939-6949-4
Authors

Masamitsu Oshima, Miho Ogawa, Takashi Tsuji

Editors

Takashi Tsuji

Abstract

Three-dimensional organogenesis in vivo is principally regulated by the spatiotemporal developmental process that relies on the cellular behavior such as cell growth, migration, differentiation, and cell-to-cell interaction. Organ development and morphogenesis have been elucidated to be regulated by the proper transient expression of various signaling molecules including cytokines, extracellular matrix, and adhesion molecules based on the epithelial and mesenchymal interactions. Current bioengineering technology for regenerating three-dimensional organ has progressed to the replication of organogenesis, thereby enabling the development of fully functional bioengineered organs using bioengineered organ germs that are generated from immature stem cells via tissue engineering technology in vitro.To achieve precise replication of organogenesis, we have developed a novel three-dimensional cell manipulation method designated the organ germ method, and enabled the generation of a structurally correct and fully functional bioengineered tooth in vivo. This method is also expected to be utilized for analyzing gene and protein functions during organogenesis. Here, we describe protocols for the tooth germ reconstitution by using the organ germ method and for the functional analysis of tooth development in vitro and in vivo.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 15%
Student > Bachelor 2 10%
Researcher 2 10%
Student > Master 2 10%
Lecturer 1 5%
Other 0 0%
Unknown 10 50%
Readers by discipline Count As %
Medicine and Dentistry 7 35%
Agricultural and Biological Sciences 2 10%
Design 1 5%
Unknown 10 50%