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Peroxisomes

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Cover of 'Peroxisomes'

Table of Contents

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    Book Overview
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    Chapter 1 Isolation of Peroxisomes from Rat Liver and Cultured Hepatoma Cells by Density Gradient Centrifugation
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    Chapter 2 Isolation of Peroxisomes from Mouse Brain Using a Continuous Nycodenz Gradient: A Comparison to the Isolation of Liver and Kidney Peroxisomes
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    Chapter 3 Determining the Topology of Peroxisomal Proteins Using Protease Protection Assays
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    Chapter 4 Isolation of Native Soluble and Membrane-Bound Protein Complexes from Yeast Saccharomyces cerevisiae.
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    Chapter 5 Method for Measurement of Peroxisomal Very Long-Chain Fatty Acid Beta-Oxidation and De Novo C26:0 Synthesis Activity in Living Cells Using Stable-Isotope Labeled Docosanoic Acid
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    Chapter 6 Analysis of Plasmalogen Synthesis in Cultured Cells
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    Chapter 7 Transfection of Primary Human Skin Fibroblasts for Peroxisomal Studies
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    Chapter 8 siRNA-mediated Silencing of Peroxisomal Genes in Mammalian Cells
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    Chapter 9 Dual Reporter Systems for the Analysis of Translational Readthrough in Mammals
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    Chapter 10 Cytochemical Detection of Peroxisomes in Light and Electron Microscopy with 3,3′-diaminobenzidine
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    Chapter 11 Cryo-Immuno Electron Microscopy of Peroxisomal Marker Proteins
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    Chapter 12 Detection and Immunolabeling of Peroxisomal Proteins
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    Chapter 13 Labeling of Peroxisomes for Live Cell Imaging in the Filamentous Fungus Ustilago maydis.
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    Chapter 14 Quantitative Monitoring of Subcellular Redox Dynamics in Living Mammalian Cells Using RoGFP2-Based Probes
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    Chapter 15 KillerRed as a Tool to Study the Cellular Responses to Peroxisome-Derived Oxidative Stress
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    Chapter 16 Determination of Peroxisomal pH in Living Mammalian Cells Using pHRed
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    Chapter 17 In Cellulo Approaches to Study Peroxisomal Protein Import - Yeast Immunofluorescence Microscopy.
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    Chapter 18 Blue Native PAGE: Applications to Study Peroxisome Biogenesis
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    Chapter 19 In Vitro PMP Import Analysis Using Cell-Free Synthesized PMP and Isolated Peroxisomes
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    Chapter 20 Peroxisomal Membrane and Matrix Protein Import Using a Semi-Intact Mammalian Cell System
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    Chapter 21 The Use of Glycosylation Tags as Reporters for Protein Entry into the Endoplasmic Reticulum in Yeast and Mammalian Cells.
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    Chapter 22 Detection of Ubiquitinated Peroxisomal Proteins in Yeast.
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    Chapter 23 Assessing Pexophagy in Mammalian Cells.
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    Chapter 24 Experimental Systems to Study Yeast Pexophagy.
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    Chapter 25 Flow Cytometric Analysis of the Expression Pattern of Peroxisomal Proteins, Abcd1, Abcd2, and Abcd3 in BV-2 Murine Microglial Cells
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    Chapter 26 Study of Peroxisomal Protein Phosphorylation by Functional Proteomics.
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    Chapter 27 Analysis of Peroxisomal β-Oxidation During Storage Oil Mobilization in Arabidopsis thaliana Seedlings
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    Chapter 28 Peroxisome Mini-Libraries: Systematic Approaches to Study Peroxisomes Made Easy.
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    Chapter 29 Generation of Peroxisome-Deficient Somatic Animal Cell Mutants
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    Chapter 30 Clinical and Laboratory Diagnosis of Peroxisomal Disorders.
Attention for Chapter 20: Peroxisomal Membrane and Matrix Protein Import Using a Semi-Intact Mammalian Cell System
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Chapter title
Peroxisomal Membrane and Matrix Protein Import Using a Semi-Intact Mammalian Cell System
Chapter number 20
Book title
Peroxisomes
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6937-1_20
Pubmed ID
Book ISBNs
978-1-4939-6935-7, 978-1-4939-6937-1
Authors

Okumoto, Kanji, Honsho, Masanori, Liu, Yuqiong, Fujiki, Yukio, Kanji Okumoto, Masanori Honsho, Yuqiong Liu, Yukio Fujiki

Editors

Michael Schrader

Abstract

Peroxisomes are essential intracellular organelles that catalyze a number of essential metabolic pathways including β-oxidation of very long chain fatty acids, synthesis of plasmalogen, bile acids, and generation and degradation of hydrogen peroxide. These peroxisomal functions are accomplished by strictly and spatiotemporally regulated compartmentalization of the enzymes catalyzing these reactions. Defects in peroxisomal protein import result in inherited peroxisome biogenesis disorders in humans. Peroxisomal matrix and membrane proteins are synthesized on free ribosomes and transported to peroxisomes in a manner dependent on their specific targeting signals and their receptors. Peroxisomal protein import can be analyzed using a semi-intact assay system, in which targeting efficiency is readily monitored by immunofluorescence microscopy. Furthermore, cytosolic factors required for peroxisomal protein import can be manipulated, suggesting that the semi-intact system is a useful and convenient system to uncover the molecular mechanisms of peroxisomal protein import.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 20%
Student > Bachelor 1 20%
Student > Postgraduate 1 20%
Student > Master 1 20%
Unknown 1 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 60%
Chemistry 1 20%
Unknown 1 20%
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 15 April 2017.
All research outputs
#15,453,139
of 22,963,381 outputs
Outputs from Methods in molecular biology
#5,373
of 13,137 outputs
Outputs of similar age
#257,159
of 421,054 outputs
Outputs of similar age from Methods in molecular biology
#466
of 1,074 outputs
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So far Altmetric has tracked 13,137 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 44th percentile – i.e., 44% of its peers scored the same or lower than it.
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