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Nuclear G-Protein Coupled Receptors

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Cover of 'Nuclear G-Protein Coupled Receptors'

Table of Contents

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    Book Overview
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    Chapter 1 Studies of Intracellular Angiotensin II
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    Chapter 2 Single-Cell Microinjection Coupled to Confocal Microscopy to Characterize Nuclear Membrane Receptors in Freshly Isolated Cardiomyocytes
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    Chapter 3 Design and Application of Light-Activated Probes for Cellular Signaling
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    Chapter 4 Using Caged Ligands to Study Intracrine Endothelin Signaling in Intact Cardiac Myocytes
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    Chapter 5 Quantification of Catecholamine Uptake in Adult Cardiac Myocytes
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    Chapter 6 Characterization of the Interaction Between the Prostaglandin D 2 DP1 Receptor and the Intracellular l -Prostaglandin D Synthase
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    Chapter 7 Isolation and Study of Cardiac Nuclei from Canine Myocardium and Adult Ventricular Myocytes
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    Chapter 8 High Resolution Imaging and Function of Nuclear G Protein-Coupled Receptors (GPCRs).
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    Chapter 9 Biochemical fractionation of membrane receptors in the nucleus.
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    Chapter 10 Functional g protein-coupled receptors on nuclei from brain and primary cultured neurons.
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    Chapter 11 Automated Microscopy of Cardiac Myocyte Hypertrophy: A Case Study on the Role of Intracellular α-Adrenergic Receptors
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    Chapter 12 Measuring Intranuclear and Nuclear Envelope [Ca 2+ ] vs. Cytosolic [Ca 2+ ]
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    Chapter 13 Assessing GPCR and G Protein Signaling to the Nucleus in Live Cells Using Fluorescent Biosensors.
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    Chapter 14 Tandem Affinity Purification to Identify Cytosolic and Nuclear Gβγ-Interacting Proteins
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    Chapter 15 Examining the Effects of Nuclear GPCRs on Gene Expression Using Isolated Nuclei
  17. Altmetric Badge
    Chapter 16 Trafficking and Function of GPCRs in the Endosomal Compartment
Attention for Chapter 9: Biochemical fractionation of membrane receptors in the nucleus.
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Chapter title
Biochemical fractionation of membrane receptors in the nucleus.
Chapter number 9
Book title
Nuclear G-Protein Coupled Receptors
Published in
Methods in molecular biology, September 2014
DOI 10.1007/978-1-4939-1755-6_9
Pubmed ID
Book ISBNs
978-1-4939-1754-9, 978-1-4939-1755-6
Authors

Ying-Nai Wang, Longfei Huo, Jennifer L Hsu, Mien-Chie Hung, Wang YN, Huo L, Hsu JL, Hung MC, Wang, Ying-Nai, Huo, Longfei, Hsu, Jennifer L., Hung, Mien-Chie, Jennifer L. Hsu

Abstract

Fractionation of cytoplasmic and nuclear proteins is a well-recognized biochemical technique to detect the intracellular distribution and expression level of proteins of interest. In the last decade, accumulating evidence shows that various types of cell surface receptors, such as receptor tyrosine kinases (RTKs), peptide hormone receptors, and cytokine receptors, are detected in the nuclei. Therefore, subcellular fractionation, including nonnuclear/nuclear extraction and the subsequent subnuclear fractionation without detectable cross-contamination during the process, is critical for studying membrane receptors that transit from the cell surface to the nucleus. Here, we utilize the epidermal growth factor receptor (EGFR) tyrosine kinase as an example of a comprehensive biochemical protocol for isolating membrane receptors in the nuclei of cancer cells.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 17%
Professor > Associate Professor 1 17%
Student > Bachelor 1 17%
Researcher 1 17%
Unknown 2 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 2 33%
Biochemistry, Genetics and Molecular Biology 1 17%
Chemistry 1 17%
Unknown 2 33%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 12 October 2014.
All research outputs
#20,239,689
of 22,766,595 outputs
Outputs from Methods in molecular biology
#9,865
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Outputs of similar age
#209,363
of 250,567 outputs
Outputs of similar age from Methods in molecular biology
#82
of 116 outputs
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