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Peroxisome Proliferator-Activated Receptors (PPARs)

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Cover of 'Peroxisome Proliferator-Activated Receptors (PPARs)'

Table of Contents

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    Book Overview
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    Chapter 1 PPARs: History and Advances
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    Chapter 2 PPAR-Alpha Cloning, Expression, and Characterization
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    Chapter 3 PPARGC1A and PPARG Genotyping: Beginner’s Guide to Genotyping with Unlabeled Probes
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    Chapter 4 Generation of an Inducible, Cardiomyocyte-Specific Transgenic Mouse Model with PPAR β/δ Overexpression
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    Chapter 5 Specific Knockdown of PPARδ Gene in Colon Cancer Cells by Lentivirus-Mediated RNA Interfering
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    Chapter 6 Dominant-Negative and Knockdown Approaches to Studying PPAR Activity
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    Chapter 7 Producing PPARgamma2 Knockdown in Mouse Liver
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    Chapter 8 Adipose Tissue-Specific PPARγ Gene Targeting
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    Chapter 9 Site-Directed Mutagenesis to Study the Role of Specific Amino Acids in the Ligand Binding Domain of PPARs
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    Chapter 10 PPAR SUMOylation: Some Useful Experimental Tips
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    Chapter 11 Analyzing Phosphorylation-Dependent Regulation of Subcellular Localization and Transcriptional Activity of Transcriptional Coactivator NT-PGC-1α
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    Chapter 12 In Vivo Studies of PPAR-Chromatin Interactions: Chromatin Immunoprecipitation for Single-Locus and Genomewide Analyses
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    Chapter 13 FISH Analysis Using PPAR γ -Specific Probes for Detection of PAX8 - PPAR γ Translocation in Follicular Thyroid Neoplasms
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    Chapter 14 Immunohistochemical Techniques to Identify and Localize Proteins of Interest in Paraffin Embedded Tissue Sections
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    Chapter 15 Determination of PPAR Expression by Western Blot
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    Chapter 16 Fluorescence Resonance Energy Transfer Techniques to Study Ligand-Mediated Interactions of PPARs with Coregulators
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    Chapter 17 Estimation of the PPARα Agonism of Fibrates by a Combined MM-Docking Approach
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    Chapter 18 Combined Biophysical and Cell-Based Approaches for the Assessment of Ligand Binding to PPARγ
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    Chapter 19 Exploring PPAR Modulation in Experimental Mice
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    Chapter 20 Induction of Adipogenic Differentiation in Three-Dimensional Culture Model on a Novel Microfabricated Scaffold
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    Chapter 21 Analyzing PPARα/Ligand Interactions by Chemical Cross-Linking and High-Resolution Mass Spectrometry
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    Chapter 22 Synthesis, Mass Spectrometric Characterization, and Analysis of the PPARδ Agonist GW1516 and Its Major Human Metabolites: Targets in Sports Drug Testing.
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    Chapter 23 LC-MS-Based Method for the Qualitative and Quantitative Analysis of the Novel PPARγ Agonist KR-62980
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    Chapter 24 Behavioral Paradigms to Evaluate PPAR Modulation in Animal Models of Brain Injury.
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    Chapter 25 In Vivo Studies of PPAR-Chromatin Interactions: Chromatin Immunoprecipitation for Single-Locus and Genomewide Analyses
Attention for Chapter 22: Synthesis, Mass Spectrometric Characterization, and Analysis of the PPARδ Agonist GW1516 and Its Major Human Metabolites: Targets in Sports Drug Testing.
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  • Good Attention Score compared to outputs of the same age (67th percentile)
  • Good Attention Score compared to outputs of the same age and source (76th percentile)

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Chapter title
Synthesis, Mass Spectrometric Characterization, and Analysis of the PPARδ Agonist GW1516 and Its Major Human Metabolites: Targets in Sports Drug Testing.
Chapter number 22
Book title
Peroxisome Proliferator-Activated Receptors (PPARs)
Published in
Methods in molecular biology, October 2012
DOI 10.1007/978-1-62703-155-4_22
Pubmed ID
Book ISBNs
978-1-62703-154-7, 978-1-62703-155-4
Authors

Thevis M, Möller I, Beuck S, Schänzer W, Mario Thevis, Ines Möller, Simon Beuck, Wilhelm Schänzer

Abstract

The elucidation of metabolic pathways and the detection of emerging therapeutics potentially enhancing athletic performance are of paramount importance to doping control authorities to protect the integrity of elite sports. A new drug candidate belonging to the family of the peroxisome proliferator-activated receptor-delta agonists termed GW1516 (also referred to as GW501516) has been prohibited by the World Anti-Doping Agency in 2009 due to its potential to artificially increase endurance. Consequently, sports drug testing laboratories need to establish detection methods enabling the identification of the intact substance and/or its metabolite(s) that unambiguously prove the presence or absence of the target substances in doping control specimens. Simulating human metabolic reactions using liver microsomal preparations, minute amounts of possible urinary metabolites were obtained that were characterized by mass spectrometry-based methods. Subsequently, the most abundant metabolic products were chemically synthesized and as well characterized by mass spectrometry and nuclear magnetic resonance spectroscopy. Finally, GW1516 and two oxidized metabolites were implemented in a routine doping control analytical assay based on liquid chromatography-(tandem) mass spectrometry (LC-MS/MS), which was tested for its -fitness-for-purpose using spiked urine samples.

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X Demographics

The data shown below were collected from the profiles of 4 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

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 %
Student > Ph. D. Student 5 25%
Student > Master 3 15%
Student > Doctoral Student 1 5%
Unspecified 1 5%
Student > Bachelor 1 5%
Other 1 5%
Unknown 8 40%
Readers by discipline Count As %
Sports and Recreations 5 25%
Neuroscience 2 10%
Agricultural and Biological Sciences 2 10%
Chemical Engineering 1 5%
Medicine and Dentistry 1 5%
Other 1 5%
Unknown 8 40%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 4. 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 04 April 2013.
All research outputs
#7,419,409
of 22,703,044 outputs
Outputs from Methods in molecular biology
#2,297
of 13,076 outputs
Outputs of similar age
#58,886
of 183,312 outputs
Outputs of similar age from Methods in molecular biology
#13
of 55 outputs
Altmetric has tracked 22,703,044 research outputs across all sources so far. This one has received more attention than most of these and is in the 67th percentile.
So far Altmetric has tracked 13,076 research outputs from this source. They receive a mean Attention Score of 3.3. This one has done well, scoring higher than 82% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 183,312 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 67% of its contemporaries.
We're also able to compare this research output to 55 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 76% of its contemporaries.