Evidence map›Paper›PMID 33158935›Full record

ArticleDisease models & mechanisms2020

Deletion of

Kim Landry-Truchon, Nicolas Houde, Mickaël Lhuillier, Louis Charron, Alice Hadchouel, Christophe Delacourt, William D Foulkes, Louise Galmiche-Rolland, Lucie Jeannotte

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
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

9 authors at 4 institutions in 2 countries.

Kim Landry-TruchonCentre de recherche sur le cancer de l'Université Laval, Centre de recherche du CHU de Québec-Université Laval (Oncology Axis), Québec, Canada G1R 3S3.
Nicolas HoudeCentre de recherche sur le cancer de l'Université Laval, Centre de recherche du CHU de Québec-Université Laval (Oncology Axis), Québec, Canada G1R 3S3.
Mickaël LhuillierInserm U1151, Institut Necker-Enfants Malades, Université de Paris, 75743 Paris, Cedex15, France.
Louis CharronCentre de recherche sur le cancer de l'Université Laval, Centre de recherche du CHU de Québec-Université Laval (Oncology Axis), Québec, Canada G1R 3S3.
Alice HadchouelInserm U1151, Institut Necker-Enfants Malades, Université de Paris, 75743 Paris, Cedex15, France.ORCID 0000-0001-7451-9890
Christophe DelacourtInserm U1151, Institut Necker-Enfants Malades, Université de Paris, 75743 Paris, Cedex15, France.ORCID 0000-0002-0007-7150
William D FoulkesDepartment of Medical Genetics, Lady Davis Institute and Segal Cancer Centre, Jewish General Hospital, Montréal, Canada H3T 1E2.ORCID 0000-0001-7427-4651
Louise Galmiche-RollandAP-HP, Hôpital Necker-Enfants Malades, 75743 Paris, Cedex15, France.ORCID 0000-0001-7081-0437
Lucie JeannotteCentre de recherche sur le cancer de l'Université Laval, Centre de recherche du CHU de Québec-Université Laval (Oncology Axis), Québec, Canada G1R 3S3 lucie.jeannotte@crchudequebec.ulaval.ca.ORCID 0000-0001-5578-420X
Université Laval · CAUniversité Paris-Panthéon-Assas · FRHôpital Necker-Enfants Malades · FRJewish General Hospital · CA

Funding

CIHR FRN169158
6 · The paper itself

Abstract

Pleuropulmonary blastoma (PPB) is a very rare pediatric lung disease. It can progress from abnormal epithelial cysts to an aggressive sarcoma with poor survival. PPB is difficult to diagnose as it can be confounded with other cystic lung disorders, such as congenital pulmonary airway malformation (CPAM). PPB is associated with mutations in

Indexed as

Gene DeletionA549 CellsAnimalsBase SequenceBiomarkersBiopsyCadherinsDisease ProgressionEpithelial CellsEpithelial-Mesenchymal TransitionEpitheliumFibroblast Growth Factor 9Gene Expression RegulationHEK293 CellsHumansLungBiomarkersCadherinsFgfr2 protein, mouseFibroblast Growth Factor 9MicroRNAsProtein IsoformsReceptor, Fibroblast Growth Factor, Type 2YY1 Transcription FactorZEB1 protein, mouseZinc Finger E-box-Binding Homeobox 1Congenital pulmonary airway malformationEMTLung developmentmiR-125a-3pPleuropulmonary blastomaYY1

Identifiers

PMID33158935
PMCPMC7790197
OpenAlexW3095517566

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.