Evidence map›Paper›PMID 34179020›Full record

ArticleFrontiers in cell and developmental biology2021

Endothelial Aryl Hydrocarbon Receptor Nuclear Translocator Mediates the Angiogenic Response to Peripheral Ischemia in Mice With Type 2 Diabetes Mellitus.

Tu Nguyen, Mei Zheng, Maura Knapp, Nikola Sladojevic, Qin Zhang, Lizhuo Ai, Devin Harrison, Anna Chen, Albert Sitikov, Le Shen and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
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

15 authors at 3 institutions in 1 country.

Tu NguyenBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Mei ZhengBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Maura KnappBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Nikola SladojevicBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Qin ZhangBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Lizhuo AiBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Devin HarrisonSection of Pulmonary and Critical Care, Department of Medicine, University of Chicago, Chicago, IL, United States.
Anna ChenBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Albert SitikovBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Le ShenSection of General Surgery, Department of Surgery, University of Chicago, Chicago, IL, United States.
Frank J GonzalezLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States.
Qiong ZhaoDivision of Cardiology, Department of Medicine, Inova Heart and Vascular Institute, Annandale, VA, United States.
Yun FangSection of Pulmonary and Critical Care, Department of Medicine, University of Chicago, Chicago, IL, United States.
James J K LiaoBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
Rongxue WuBiological Sciences Division - Cardiology, Department of Medicine, University of Chicago, Chicago, IL, United States.
University of Chicago · USAlaska Heart and Vascular Institute · USCenter for Cancer Research · US

Funding

Pilot and Feasibility ProgramP30DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI RONALD N COHEN · 2013 to 2026
$20.9M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
MULTIDISCIPLINARY CARDIAC SCIENCEST32HL007381 · NHLBI · UNIVERSITY OF CHICAGO · PI JEANNE M DECARA, Yoav Gilad · 1985 to 2026
$12.5M
ARNT: A novel regulator of cardiac vascular endothelial barrier function in heart failureR01HL140114 · NHLBI · UNIVERSITY OF CHICAGO · PI WU, RONGXUE · 2019 to 2023
$2.1M
Role of p67phox in myocardial hypertrophyR01HL083218 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI XIAO, LEI · 2008 to 2013
$2.0M
Mechanisms Underlying Vascular AgingR01HL136962 · NHLBI · UNIVERSITY OF CHICAGO · PI LIAO, JAMES KUANG-JAN · 2018 to 2021
$1.8M
NCATS NIH HHS UL1 TR000430NHLBI NIH HHS R01 HL083218NHLBI NIH HHS R01 HL136962NHLBI NIH HHS R01 HL140114NHLBI NIH HHS T32 HL007381NIDDK NIH HHS P30 DK020595
6 · The paper itself

Abstract

Hypoxia-inducible factors (HIFs) are the master regulators of angiogenesis, a process that is impaired in patients with diabetes mellitus (DM). The transcription factor aryl hydrocarbon receptor nuclear translocator (ARNT, also known as HIF1β) has been implicated in the development and progression of diabetes. Angiogenesis is driven primarily by endothelial cells (ECs), but both global and EC-specific loss of ARNT-cause are associated with embryonic lethality. Thus, we conducted experiments in a line of mice carrying an inducible, EC-specific ARNT-knockout mutation (

Indexed as

ARNTcell deathdiabetic animalendothelial angiogenesishindlimb ischemia

Identifiers

PMID34179020
PMCPMC8222825
OpenAlexW3169964746

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.