Evidence map›Paper›PMID 32098873›Full record

ArticleThe Journal of biological chemistry2020

Site-specific 5-hydroxytryptophan incorporation into apolipoprotein A-I impairs cholesterol efflux activity and high-density lipoprotein biogenesis.

Maryam Zamanian-Daryoush, Valentin Gogonea, Anthony J DiDonato, Jennifer A Buffa, Ibrahim Choucair, Bruce S Levison, Randall A Hughes, Andrew D Ellington, Ying Huang, Xinmin S Li and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 18 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

12 authors at 5 institutions in 1 country.

Maryam Zamanian-DaryoushDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Valentin GogoneaDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Anthony J DiDonatoDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Jennifer A BuffaDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Ibrahim ChoucairDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Bruce S LevisonDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.ORCID 0000-0002-1816-368X
Randall A HughesUnited States Army Research Laboratory South, University of Texas, Austin, Texas 78712.
Andrew D EllingtonCenter for Systems and Synthetic Biology, University of Texas, Austin, Texas 78712.
Ying HuangDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Xinmin S LiDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Joseph A DiDonatoDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Stanley L HazenDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195 hazens@ccf.org.ORCID 0000-0001-7124-6639
Cleveland Clinic · USCleveland State University · USCleveland Clinic Lerner College of Medicine · USDEVCOM Army Research Laboratory · USThe University of Texas at Austin · US

Funding

Project 3: Microbiota generated aryl sulfates and secondary bile acids in cardiometabolic diseaseP01HL147823 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI MICHAEL ANDREW FISCHBACH · 2019 to 2026
$17.0M
Gut Flora Metabolism of Dietary Phosphatidylcholine and CVDR01HL103866 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI HAZEN, STANLEY L · 2010 to 2023
$10.8M
HDL Structure, Function and DysfunctionR01HL128300 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI HAZEN, STANLEY L · 2016 to 2019
$3.1M
AB/SCIEX QTrap 6500 Mass Spectrometer Metabolic profiling systemS10OD016346 · OD · CLEVELAND CLINIC LERNER COM-CWRU · PI DIDONATO, JOSEPH · 2014 to 2014
$600k
NHLBI NIH HHS P01 HL147823NHLBI NIH HHS R01 HL103866NHLBI NIH HHS R01 HL128300NIH HHS S10 OD016346
6 · The paper itself

Abstract

Apolipoprotein A-I (apoA-I) is the major protein constituent of high-density lipoprotein (HDL) and a target of myeloperoxidase-dependent oxidation in the artery wall. In atherosclerotic lesions, apoA-I exhibits marked oxidative modifications at multiple sites, including Trp

Indexed as

5-HydroxytryptophanAnimalsApolipoprotein A-IAryldialkylphosphataseATP Binding Cassette Transporter 1Biological TransportCholesterolHumansLipoproteins, HDLMiceMice, KnockoutOxidation-ReductionProtein BindingTyrosine5-HydroxytryptophanABCA1 protein, humanAPOA1 protein, humanApolipoprotein A-IAryldialkylphosphataseATP Binding Cassette Transporter 1CholesterolLipoproteins, HDLPON1 protein, humanTyrosineapolipoproteinapolipoprotein A-I dysfunctionatherosclerosiscardiovascular diseasecholesterolcoronary artery diseasegenetic code expansionhigh-density lipoprotein (HDL)non-canonical amino acidsorthogonal translationposttranslational modificationrecombinant protein expressionsynthetic biologytryptophan

Identifiers

PMID32098873
PMCPMC7152772
OpenAlexW3008848398

What OpenQuestion holds

Textmetadata
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.