Evidence map›Paper›PMID 41756958›Full record

ArticlebioRxiv : the preprint server for biology2026

Modeling Somatic Second-Hit Mutations in Novel Mouse Models of Hereditary Hemorrhagic Telangiectasia.

Adella P Bartoletti, Shreya Bavishi, K C Rajan, Stryder M Meadows

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Adella P BartolettiCell and Molecular Biology Department, Tulane University, New Orleans, Louisiana, United States of America.ORCID 0009-0004-7547-7898
Shreya BavishiCell and Molecular Biology Department, Tulane University, New Orleans, Louisiana, United States of America.ORCID 0000-0003-3161-8973
K C RajanCell and Molecular Biology Department, Tulane University, New Orleans, Louisiana, United States of America.ORCID 0000-0003-1121-3661
Stryder M MeadowsCell and Molecular Biology Department, Tulane University, New Orleans, Louisiana, United States of America.ORCID 0000-0003-0968-7155

Funding

Angiopoietin-2 Signaling Targeted Therapeutics for Arteriovenous MalformationsR01HL163196 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI MARAMBAUD, PHILIPPE, MEADOWS, STRYDER MEDOAH · 2022 to 2025
$2.7M
Molecular mechanisms underlying Arteriovenous Malformations associated with HHTR01HL139713 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI MEADOWS, STRYDER MEDOAH · 2018 to 2022
$1.8M
EVALUATING THE IMPACT OF LOSS OF HETEROZYGOSITY ON LOCALIZED AVM FORMATION IN HHTF31HL174077 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI BARTOLETTI, ADELLA PATIENCE · 2024 to 2025
$99k
NHLBI NIH HHS F31 HL174077NHLBI NIH HHS R01 HL139713NHLBI NIH HHS R01 HL163196
6 · The paper itself

Abstract

Hereditary Hemorrhagic Telangiectasia (HHT) is a genetic vascular disorder characterized by distinct vascular malformations, including deep organ arteriovenous malformations (AVMs) and mucocutaneous telangiectasias. People with HHT inherit monoallelic pathogenic variants in members of the TGFβ signaling cascade (

Indexed as

Arteriovenous Malformation (AVM)EngHereditary Hemorrhagic Telangiectasia (HHT)Loss of Heterozygosity (LOH)Smad4Somatic

Identifiers

PMID41756958
PMCPMC12933570

What OpenQuestion holds

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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.