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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 9: Monitoring Wnt Signaling in Zebrafish Using Fluorescent Biosensors.
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Chapter title
Monitoring Wnt Signaling in Zebrafish Using Fluorescent Biosensors.
Chapter number 9
Book title
Wnt Signaling
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-6393-5_9
Pubmed ID
Book ISBNs
978-1-4939-6391-1, 978-1-4939-6393-5
Authors

Nicola Facchinello, Marco Schiavone, Andrea Vettori, Francesco Argenton, Natascia Tiso

Editors

Quinn Barrett, Lawrence Lum

Abstract

In this chapter, we are presenting methods to monitor and quantify in vivo canonical Wnt signaling activities at single-cell resolution in zebrafish. Our technology is based on artificial enhancers, obtained by polymerization of TCF binding elements, cloned upstream to ubiquitous or tissue-specific promoters. The different promoter/enhancer combinations are used to drive fluorescent protein reporter constructs integrated in the zebrafish germline by microinjection of fertilized zebrafish eggs. Fish with a single integration site are selected by Mendelian analysis of fluorescent carriers, and heterozygous offspring are used to monitor and quantify canonical Wnt activities. Open source public domain software such as ImageJ/Fiji is used to calculate the integrated densities in the region of interest and compare the effect of experimental conditions on control and treated animals.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 7 41%
Student > Ph. D. Student 3 18%
Professor 1 6%
Student > Bachelor 1 6%
Student > Postgraduate 1 6%
Other 0 0%
Unknown 4 24%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 24%
Medicine and Dentistry 4 24%
Agricultural and Biological Sciences 2 12%
Neuroscience 1 6%
Unknown 6 35%