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TGF-β Signaling

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Cover of 'TGF-β Signaling'

Table of Contents

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    Book Overview
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    Chapter 1 Regulation of TGF-β Receptors
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    Chapter 2 Determining TGF-β Receptor Levels in the Cell Membrane.
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    Chapter 3 Posttranslational Modifications of TGF-β Receptors.
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    Chapter 4 Production, Isolation, and Structural Analysis of Ligands and Receptors of the TGF-β Superfamily
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    Chapter 5 Phosphorylation of Smads by Intracellular Kinases
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    Chapter 6 Analysis of Smad Phosphatase Activity In Vitro
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    Chapter 7 Three-dimensional Mammary Epithelial Cell Morphogenesis Model for Analysis of TGFß Signaling.
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    Chapter 8 TGF-β Signaling in Stem Cell Regulation.
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    Chapter 9 Analysis of Epithelial-Mesenchymal Transition Induced by Transforming Growth Factor β.
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    Chapter 10 In Vitro Th Differentiation Protocol.
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    Chapter 11 Interrogating TGF-β Function and Regulation in Endothelial Cells.
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    Chapter 12 Isolation and Manipulation of Adipogenic Cells to Assess TGF-β Superfamily Functions.
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    Chapter 13 Imaging TGFβ Signaling in Mouse Models of Cancer Metastasis.
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    Chapter 14 Generation and Characterization of Smad7 Conditional Knockout Mice
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    Chapter 15 Monitoring Smad Activity In Vivo Using the Xenopus Model System.
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    Chapter 16 Animal Cap Assay for TGF-β Signaling.
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    Chapter 17 Detection of Smad Signaling in Zebrafish Embryos.
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    Chapter 18 Role of TGF-β Signaling in Coupling Bone Remodeling
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    Chapter 19 Studying the Functions of TGF-β Signaling in the Ovary.
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    Chapter 20 Quantitative Real-Time PCR Analysis of MicroRNAs and Their Precursors Regulated by TGF-β Signaling.
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    Chapter 21 TGF-β-Regulated MicroRNAs and Their Function in Cancer Biology.
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    Chapter 22 Epigenomic Regulation of Smad1 Signaling During Cellular Senescence Induced by Ras Activation.
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    Chapter 23 The Role of Ubiquitination to Determine Non-Smad Signaling Responses
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    Chapter 24 Genome-Wide RNAi Screening to Dissect the TGF-β Signal Transduction Pathway.
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    Chapter 25 TGF-β Signaling
Attention for Chapter 1: Regulation of TGF-β Receptors
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Chapter title
Regulation of TGF-β Receptors
Chapter number 1
Book title
TGF-β Signaling
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-2966-5_1
Pubmed ID
Book ISBNs
978-1-4939-2965-8, 978-1-4939-2966-5
Authors

Erine H. Budi, Jian Xu, Rik Derynck, Budi, Erine H., Xu, Jian, Derynck, Rik

Abstract

In cells responding to extracellular polypeptide ligands, regulatory mechanisms at the level of cell surface receptors are increasingly seen to define the nature of the ligand-induced signaling responses. Processes that govern the levels of receptors at the plasma membrane, including posttranslational modifications, are crucial to ensure receptor function and specify the downstream signals. Indeed, extracellular posttranslational modifications of the receptors help define stability and ligand binding, while intracellular modifications mediate interactions with signaling mediators and accessory proteins that help define the nature of the signaling response. The use of various molecular biology and biochemistry techniques, based on chemical crosslinking, e.g., biotin or radioactive labeling, immunofluorescence to label membrane receptors and flow cytometry, allows for quantification of changes of cell surface receptor presentation. Here, we discuss recent progress in our understanding of the regulation of TGF-β receptors, i.e., the type I (TβRI) and type II (TβRII) TGF-β receptors, and describe basic methods to identify and quantify TGF-β cell surface receptors.

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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 %
Other 4 20%
Student > Ph. D. Student 3 15%
Student > Master 3 15%
Researcher 1 5%
Unknown 9 45%
Readers by discipline Count As %
Engineering 3 15%
Biochemistry, Genetics and Molecular Biology 3 15%
Agricultural and Biological Sciences 3 15%
Arts and Humanities 1 5%
Mathematics 1 5%
Other 0 0%
Unknown 9 45%