Evidence map›Paper›PMID 29371244›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2018

Cell Type-Specific Contributions of the Angiotensin II Type 1a Receptor to Aorta Homeostasis and Aneurysmal Disease-Brief Report.

Josephine Galatioto, Cristina I Caescu, Jens Hansen, Jason R Cook, Irving Miramontes, Ravi Iyengar, Francesco Ramirez

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.4field-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

43 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Mechanics and mechanobiology of arterial development.Biomechanics and modeling in mechanobiology · 2026
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  16. Protective Role of Endothelial Fibulin-4 in Valvulo-Arterial Integrity.Journal of the American Heart Association · 2023
    Article
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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

7 authors at 1 institution in 1 country.

Josephine GalatiotoFrom the Department of Pharmacological Sciences and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York.
Cristina I CaescuFrom the Department of Pharmacological Sciences and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York.
Jens HansenFrom the Department of Pharmacological Sciences and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York.
Jason R CookFrom the Department of Pharmacological Sciences and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York.
Irving MiramontesFrom the Department of Pharmacological Sciences and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York.
Ravi IyengarFrom the Department of Pharmacological Sciences and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York.
Francesco RamirezFrom the Department of Pharmacological Sciences and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York. francesco.ramirez@mssm.edu.
Icahn School of Medicine at Mount Sinai · US

Funding

Hormones: Molecular Mechanism of Action and FunctionsT32DK007328 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KOUSTENI, STAVROULA · 1986 to 2025
$7.8M
Mouse Models for Systems Therapeutics Degenerative DiseasesR01AR069307 · NIAMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI IYENGAR, SRINIVAS RAVI V, RAMIREZ, FRANCESCO B · 2017 to 2021
$2.6M
Transforming Genomics with 5 PB Big Omics Data Engine Cray CS300-AC SupercomputerS10OD018522 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2014 to 2014
$1.9M
Characterization of a novel pathway of aortic aneurysm formation.R01HL126173 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI RAMIREZ, FRANCESCO B · 2015 to 2018
$1.7M
NHLBI NIH HHS R01 HL126173NIAMS NIH HHS R01 AR069307NIDDK NIH HHS T32 DK007328NIH HHS S10 OD018522
6 · The paper itself

Abstract

objectiveTwo were the aims of this study: first, to translate whole-genome expression profiles into computational predictions of functional associations between signaling pathways that regulate aorta homeostasis and the activity of angiotensin II type 1a receptor (At1ar) in either vascular endothelial or smooth muscle cells; and second, to characterize the impact of endothelial cell- or smooth muscle cell-specific At1ar disruption on the development of thoracic aortic aneurysm in fibrillin-1 hypomorphic (

conclusionsPhysiological At1ar signaling in the intimal and medial layers is associated with distinct regulatory processes of aorta homeostasis and function; improper At1ar activity in the vascular endothelium is a significant determinant of thoracic aortic aneurysm development in Marfan syndrome mice.

Indexed as

AdipokinesAnimalsAorta, ThoracicAortic Aneurysm, ThoracicComputational BiologyDilatation, PathologicDisease Models, AnimalEndothelial CellsFibrillin-1Gene Expression ProfilingGene Expression RegulationHomeostasisMaleMarfan SyndromeMice, 129 StrainMice, Inbred C57BLAdipokinesAgtr1a protein, mouseFbn1 protein, mouseFibrillin-1Receptor, Angiotensin, Type 1aneurysmendothelial cellsfibrillin-1homeostasisMarfan syndrome

Identifiers

PMID29371244
PMCPMC5823778
OpenAlexW2784688519

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.