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High Density Lipoproteins

Overview of attention for book
High Density Lipoproteins
Springer International Publishing

Table of Contents

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    Book Overview
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    Chapter 1 Structure of HDL: Particle Subclasses and Molecular Components.
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    Chapter 2 HDL Biogenesis, Remodeling, and Catabolism.
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    Chapter 3 Regulation of HDL Genes: Transcriptional, Posttranscriptional, and Posttranslational.
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    Chapter 4 Cholesterol efflux and reverse cholesterol transport.
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    Chapter 5 Functionality of HDL: Antioxidation and Detoxifying Effects.
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    Chapter 6 Signal Transduction by HDL: Agonists, Receptors, and Signaling Cascades.
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    Chapter 7 Epidemiology: Disease Associations and Modulators of HDL-Related Biomarkers
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    Chapter 8 High Density Lipoproteins
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    Chapter 9 Mouse Models of Disturbed HDL Metabolism.
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    Chapter 10 Dysfunctional HDL: From Structure-Function-Relationships to Biomarkers.
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    Chapter 11 HDL and Atherothrombotic Vascular Disease.
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    Chapter 12 HDLs, Diabetes, and Metabolic Syndrome.
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    Chapter 13 High-density lipoprotein: structural and functional changes under uremic conditions and the therapeutic consequences.
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    Chapter 14 Impact of Systemic Inflammation and Autoimmune Diseases on apoA-I and HDL Plasma Levels and Functions.
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    Chapter 15 HDL in Infectious Diseases and Sepsis
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    Chapter 16 High-Density Lipoproteins in Stroke
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    Chapter 17 Therapeutic Potential of HDL in Cardioprotection and Tissue Repair.
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    Chapter 18 HDL and Lifestyle Interventions.
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    Chapter 19 Effects of Established Hypolipidemic Drugs on HDL Concentration, Subclass Distribution, and Function.
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    Chapter 20 High Density Lipoproteins
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    Chapter 21 ApoA-I Mimetics.
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    Chapter 22 Antisense Oligonucleotides, microRNAs, and Antibodies.
Attention for Chapter 22: Antisense Oligonucleotides, microRNAs, and Antibodies.
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Chapter title
Antisense Oligonucleotides, microRNAs, and Antibodies.
Chapter number 22
Book title
High Density Lipoproteins
Published in
Handbook of experimental pharmacology, December 2014
DOI 10.1007/978-3-319-09665-0_22
Pubmed ID
Book ISBNs
978-3-31-909664-3, 978-3-31-909665-0
Authors

Alberto Dávalos, Angeliki Chroni, Dávalos, Alberto, Chroni, Angeliki

Editors

Arnold von Eckardstein, Dimitris Kardassis

Abstract

The specificity of Watson-Crick base pairing and the development of several chemical modifications to oligonucleotides have enabled the development of novel drug classes for the treatment of different human diseases. This review focuses on promising results of recent preclinical or clinical studies on targeting HDL metabolism and function by antisense oligonucleotides and miRNA-based therapies. Although many hurdles regarding basic mechanism of action, delivery, specificity, and toxicity need to be overcome, promising results from recent clinical trials and recent approval of these types of therapy to treat dyslipidemia suggest that the treatment of HDL dysfunction will benefit from these unique clinical opportunities. Moreover, an overview of monoclonal antibodies (mAbs) developed for the treatment of dyslipidemia and cardiovascular disease and currently being tested in clinical studies is provided. Initial studies have shown that these compounds are generally safe and well tolerated, but ongoing large clinical studies will assess their long-term safety and efficacy.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 26 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 26 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 31%
Student > Master 4 15%
Student > Ph. D. Student 3 12%
Student > Postgraduate 2 8%
Other 2 8%
Other 3 12%
Unknown 4 15%
Readers by discipline Count As %
Medicine and Dentistry 7 27%
Biochemistry, Genetics and Molecular Biology 4 15%
Agricultural and Biological Sciences 4 15%
Pharmacology, Toxicology and Pharmaceutical Science 4 15%
Social Sciences 1 4%
Other 3 12%
Unknown 3 12%