Evidence map›Paper›PMID 31900205›Full record

ArticleBMC research notes2020

Two-hybrid screening of FAM13A protein partners in lung epithelial cells.

Manon Ruffin, Kristin E Thompson, Harriet Corvol, Loic Guillot

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Long isoforms of the COPD risk gene FAM13A orchestrate human lung epithelial development.American journal of respiratory cell and molecular biology · 2026
    Article
  2. Article
  3. Article
  4. Review
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 at 1 institution in 1 country.

Manon RuffinSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, Paris, France.
Kristin E ThompsonSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, Paris, France.
Harriet CorvolSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, Paris, France.
Loic GuillotSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, Paris, France. loic.guillot@inserm.fr.ORCID http://orcid.org/0000-0001-6853-7945
Inserm · FR

Funding

Association Vaincre la Mucoviscidose (FR) RF20150501336
6 · The paper itself

Abstract

objectivesFamily with sequence similarity 13 member A (FAM13A) genetic variants have been associated with several chronic respiratory diseases including chronic obstructive pulmonary disease (COPD), cystic fibrosis (CF), idiopathic pulmonary fibrosis (IPF) and lung cancer. The FAM13A protein includes a RhoGTPase activating protein (RhoGAP) domain known to participate in various cellular mechanisms including cell proliferation. While intensive genomic studies have been performed to reveal its involvement in lung diseases, the biological role of FAM13A protein is still not completely elucidated.

resultsWe therefore performed a two-hybrid screening to identify protein partners of FAM13A using a human lung cancer cDNA library. We identified several protein partners with a high confidence score. Researchers in the field of chronic lung diseases may benefit from this two-hybrid screening data which may reveal new research pathways to decipher.

Indexed as

Two-Hybrid System TechniquesA549 CellsCarrier ProteinsCell Line, TumorEpithelial CellsGene LibraryGTPase-Activating ProteinsHumansLungLung NeoplasmsProtein BindingCarrier ProteinsFAM13A protein, humanGTPase-Activating ProteinsChronic lung diseasesFAM13ALung epitheliumTwo-hybrid screening

Identifiers

PMID31900205
PMCPMC6942259
OpenAlexW2997324032

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.