Evidence map›Paper›PMID 24168751›Full record

ReviewJournal of medicinal chemistry2014

Molecules that mimic apolipoprotein A-I: potential agents for treating atherosclerosis.

Luke J Leman, Bruce E Maryanoff, M Reza Ghadiri

Abstract readReview
In one paragraph

Review in Journal of medicinal chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 66 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Luke J LemanDepartment of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute , 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Bruce E Maryanoff
M Reza Ghadiri
Scripps Research Institute · US

Funding

Managing Atherosclerosis by Modulating HDL FunctionR01HL118114 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI GHADIRI, M. REZA · 2013 to 2025
$8.5M
Synthesis and Application of Novel Apolipoprotein MimeticsR21HL104462 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI GHADIRI, M. REZA · 2011 to 2012
$522k
NHLBI NIH HHS R01 HL118114NHLBI NIH HHS R21 HL104462
6 · The paper itself

Abstract

Certain amphipathic α-helical peptides can functionally mimic many of the properties of full-length apolipoproteins, thereby offering an approach to modulate high-density lipoprotein (HDL) for combating atherosclerosis. In this Perspective, we summarize the key findings and advances over the past 25 years in the development of peptides that mimic apolipoproteins, especially apolipoprotein A-I (apoA-I). This assemblage of information provides a reasonably clear picture of the state of the art in the apolipoprotein mimetic field, an appreciation of the potential for such agents in pharmacotherapy, and a sense of the opportunities for optimizing the functional properties of HDL.

Indexed as

Amino Acid SequenceAnimalsAnticholesteremic AgentsApolipoprotein A-IAtherosclerosisBiomimeticsCardiotonic AgentsCholesterol, HDLHumansModels, MolecularMolecular MimicryMolecular Sequence DataPeptide FragmentsProtein ConformationProtein Structure, SecondaryProtein Structure, TertiaryAnticholesteremic AgentsApolipoprotein A-ICardiotonic AgentsCholesterol, HDLPeptide Fragments

Identifiers

PMID24168751
PMCPMC3969399
OpenAlexW2313477780

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.