Evidence map›Paper›PMID 36250069›Full record

ReviewFrontiers in medicine2022

An update on preclinical models of hereditary haemorrhagic telangiectasia: Insights into disease mechanisms.

Helen M Arthur, Beth L Roman

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Gene-Specific Endothelial Programs Drive AVM Pathogenesis inArteriosclerosis, thrombosis, and vascular biology · 2026
    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

2 authors at 2 institutions in 2 countries.

Helen M ArthurBiosciences Institute, Centre for Life, University of Newcastle, Newcastle, United Kingdom.
Beth L RomanDepartment of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
Centre for Life · GBUniversity of Pittsburgh · US

Funding

Interaction between blood flow and ALK1 signaling in AVM developmentR01HL136566 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROMAN, BETH L · 2017 to 2020
$1.7M
BMP10 IN CARDIOVASCULAR DEVELOPMENT AND HEREDITARY HEMORRHAGIC TELANGIECTASIAR01HL133009 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROMAN, BETH L · 2016 to 2019
$1.6M
NHLBI NIH HHS R01 HL133009NHLBI NIH HHS R01 HL136566
6 · The paper itself

Abstract

Endoglin (ENG) is expressed on the surface of endothelial cells (ECs) where it efficiently binds circulating BMP9 and BMP10 ligands to initiate activin A receptor like type 1 (ALK1) protein signalling to protect the vascular architecture. Patients heterozygous for

Indexed as

activin receptor-like kinase 1 (ACVRL1)arteriovenous malformation (AVM)BMP-SMAD signalling pathwaycell polarity and migrationendoglin (CD105)HHT

Identifiers

PMID36250069
PMCPMC9556665
OpenAlexW4298005499

What OpenQuestion 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 OpenQuestion graph.