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The Wilms' Tumor (WT1) Gene

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Cover of 'The Wilms' Tumor (WT1) Gene'

Table of Contents

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    Book Overview
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    Chapter 1 WT1 Mutation in Childhood Cancer.
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    Chapter 2 Clinical Aspects of WT1 and the Kidney.
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    Chapter 3 The Role of WT1 in Embryonic Development and Normal Organ Homeostasis.
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    Chapter 4 Tools and Techniques for Wt1-Based Lineage Tracing.
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    Chapter 5 Biological Systems and Methods for Studying WT1 in the Epicardium.
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    Chapter 6 Isolation and Colony Formation of Murine Bone and Bone Marrow Cells.
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    Chapter 7 Isolation and Fluorescence-Activated Cell Sorting of Murine WT1-Expressing Adipocyte Precursor Cells.
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    Chapter 8 The Wilms' Tumor (WT1) Gene
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    Chapter 9 Multiphoton Microscopy for Visualizing Lipids in Tissue.
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    Chapter 10 Function and Regulation of the Wilms' Tumor Suppressor 1 (WT1) Gene in Fish.
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    Chapter 11 Immunofluorescence Staining of Wt1 on Sections of Zebrafish Embryos and Larvae.
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    Chapter 12 Fluorescence-Activated Cell Sorting (FACS) Protocol for Podocyte Isolation in Adult Zebrafish.
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    Chapter 13 In Vitro Transcription to Study WT1 Function.
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    Chapter 14 Measuring Equilibrium Binding Constants for the WT1-DNA Interaction Using a Filter Binding Assay.
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    Chapter 15 The Wilms' Tumor (WT1) Gene
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    Chapter 16 The Wilms' Tumor (WT1) Gene
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    Chapter 17 Methods to Identify and Validate WT1-RNA Interaction.
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    Chapter 18 The Wilms' Tumor (WT1) Gene
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    Chapter 19 The Wilms' Tumor (WT1) Gene
Attention for Chapter 6: Isolation and Colony Formation of Murine Bone and Bone Marrow Cells.
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Chapter title
Isolation and Colony Formation of Murine Bone and Bone Marrow Cells.
Chapter number 6
Book title
The Wilms' Tumor (WT1) Gene
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-4023-3_6
Pubmed ID
Book ISBNs
978-1-4939-4021-9, 978-1-4939-4023-3
Authors

Sophie McHaffie, You-Ying Chau

Editors

Nicholas Hastie

Abstract

Adult homeostasis is dependent on normal Wt1 expression. Loss of Wt1 expression in adult mice causes rapid loss of the mesenchymal tissues, fat and bone, amongst other phenotypes. Bone and bone marrow mesenchymal stromal cells can be studied by cell isolation and expansion. The stemness of these cells can then be characterized by carrying out a colony-forming unit-fibroblast assay and observing clonogenic capabilities.