Evidence map›Paper›PMID 36446400›Full record

ArticleLymphology2022

Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a

X Geng, L Chen, R S Srinivasan, R J Kylat, M H Witte, R J Erickson

Open access · hybridAbstract read
PubMed Full text at PMC
In one paragraph

Article in Lymphology, 2022. 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
0.1field-weighted citation impact, top 51% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

6 authors at 2 institutions in 1 country.

X GengCardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
L ChenCardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
R S SrinivasanCardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
R J KylatDepartment of Pediatrics, University of Arizona-Tucson, Tucson, AZ, USA.
M H WitteDepartment of Surgery, University of Arizona-Tucson, Tucson, AZ, USA.
R J EricksonDepartment of Pediatrics, University of Arizona-Tucson, Tucson, AZ, USA.
Oklahoma Medical Research Foundation · USUniversity of Arizona · US

Funding

Defining the Mechanisms of Lymphatic Vascular Growth and FunctionR01HL131652 · NHLBI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI SRINIVASAN, RAJANARAYANAN S · 2016 to 2025
$3.9M
NHLBI NIH HHS R01 HL131652
6 · The paper itself

Abstract

We have studied the lymphatic phenotypes of 2 mutations, known to cause abnormalities of lymphatics in humans, in mice. The

Indexed as

Lymphatic DiseasesLymphatic VesselsSOS1 ProteinAnimalsConnexinsHeterozygoteHomozygoteHumansLymphedemaMiceMutationPhenotypeconnexin 47ConnexinsSOS1 ProteinSOS1 protein, humanembryonic/adult phenotypeslymphatic micemutationsNoonan syndromeprimary Lymphedema

Identifiers

PMID36446400
PMCPMC10583265
OpenAlexW4310566232

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.