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Wnt Signaling

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Cover of 'Wnt Signaling'

Table of Contents

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    Book Overview
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    Chapter 1 Visualizing Wnt Palmitoylation in Single Cells.
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    Chapter 2 Monitoring Wnt Protein Acylation Using an In Vitro Cyclo-Addition Reaction.
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    Chapter 3 Biochemical Methods to Analyze Wnt Protein Secretion.
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    Chapter 4 Methods for Studying Wnt Protein Modifications/Inactivations by Extracellular Enzymes, Tiki and Notum.
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    Chapter 5 Probing Wnt Receptor Turnover: A Critical Regulatory Point of Wnt Pathway.
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    Chapter 6 A Simple Method to Assess Abundance of the β-Catenin Signaling Pool in Cells.
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    Chapter 7 Wnt-Dependent Control of Cell Polarity in Cultured Cells.
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    Chapter 8 The Use of Chick Embryos to Study Wnt Activity Gradients.
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    Chapter 9 Monitoring Wnt Signaling in Zebrafish Using Fluorescent Biosensors.
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    Chapter 10 Wnt Signaling
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    Chapter 11 Wnt Signaling
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    Chapter 12 Delivery of the Porcupine Inhibitor WNT974 in Mice.
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    Chapter 13 Use of Primary Calvarial Osteoblasts to Evaluate the Function of Wnt Signaling in Osteogenesis.
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    Chapter 14 Monitoring Wnt/β-Catenin Signaling in Skin.
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    Chapter 15 The Generation of Organoids for Studying Wnt Signaling.
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    Chapter 16 Methods to Manipulate and Monitor Wnt Signaling in Human Pluripotent Stem Cells.
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    Chapter 17 Wnt Signaling
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    Chapter 18 Erratum to: Delivery of the Porcupine Inhibitor WNT974 in Mice
Attention for Chapter 16: Methods to Manipulate and Monitor Wnt Signaling in Human Pluripotent Stem Cells.
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Chapter title
Methods to Manipulate and Monitor Wnt Signaling in Human Pluripotent Stem Cells.
Chapter number 16
Book title
Wnt Signaling
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-6393-5_16
Pubmed ID
Book ISBNs
978-1-4939-6391-1, 978-1-4939-6393-5
Authors

Ian J. Huggins, David Brafman, Karl Willert

Editors

Quinn Barrett, Lawrence Lum

Abstract

Human pluripotent stem cells (hPSCs) may revolutionize medical practice by providing: (a) a renewable source of cells for tissue replacement therapies, (b) a powerful system to model human diseases in a dish, and (c) a platform for examining efficacy and safety of novel drugs. Furthermore, these cells offer a unique opportunity to study early human development in vitro, in particular, the process by which a seemingly uniform cell population interacts to give rise to the three main embryonic lineages: ectoderm, endoderm. and mesoderm. This process of lineage allocation is regulated by a number of inductive signals that are mediated by growth factors, including FGF, TGFβ, and Wnt. In this book chapter, we introduce a set of tools, methods, and protocols to specifically manipulate the Wnt signaling pathway with the intention of altering the cell fate outcome of hPSCs.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 20%
Researcher 2 20%
Student > Ph. D. Student 1 10%
Unspecified 1 10%
Student > Master 1 10%
Other 0 0%
Unknown 3 30%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 40%
Medicine and Dentistry 2 20%
Psychology 1 10%
Unspecified 1 10%
Unknown 2 20%