Evidence map›Paper›PMID 28986436›Full record

ArticleJournal of lipid research2017

Normal human adipose tissue functions and differentiation in patients with biallelic

Michele Pelosi, Eric Testet, Soazig Le Lay, Isabelle Dugail, Xiaoyun Tang, Guillaume Mabilleau, Yamina Hamel, Marine Madrange, Thomas Blanc, Thierry Odent and 4 more

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

Article in Journal of lipid research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Effects ofGut microbes · 2026
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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

14 authors at 8 institutions in 3 countries.

Michele PelosiCentre de Référence des Maladies Héréditaires du Métabolisme, Institut Imagine des Maladies Génétiques, Laboratoire de génétique des maladies autoinflammatoires monogéniques, INSERM UMR1163, Université Paris Descartes et Hôpital Necker-Enfants malades (Assistance publique - Hôpitaux de Paris), Paris, France pdelonlay@neuf.fr michi_pelo@libero.it.
Eric TestetLaboratoire de Biogenèse Membranaire-UMR 5200, CNRS, Université de Bordeaux, Villenave d'Ornon, France.
Soazig Le LayINSERM, UMR1063, Université d'Angers, UBL, Angers, France.
Isabelle DugailINSERM, U1166, Equipe 6, Université Pierre et Marie Curie, Paris, France.
Xiaoyun TangDepartment of Biochemistry, Signal Transduction Research Group, University of Alberta, Edmonton, Alberta, Canada.
Guillaume MabilleauSCIAM, Université d'Angers, Angers, France.
Yamina HamelCentre de Référence des Maladies Héréditaires du Métabolisme, Institut Imagine des Maladies Génétiques, Laboratoire de génétique des maladies autoinflammatoires monogéniques, INSERM UMR1163, Université Paris Descartes et Hôpital Necker-Enfants malades (Assistance publique - Hôpitaux de Paris), Paris, France.
Marine MadrangeCentre de Référence des Maladies Héréditaires du Métabolisme, Institut Imagine des Maladies Génétiques, Laboratoire de génétique des maladies autoinflammatoires monogéniques, INSERM UMR1163, Université Paris Descartes et Hôpital Necker-Enfants malades (Assistance publique - Hôpitaux de Paris), Paris, France.
Thomas BlancDepartment of Pediatric Surgery and Urology, Hôpital Necker-Enfants malades-Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
Thierry OdentDepartment of Pediatric Orthopedics, Hôpital Necker-Enfants malades-Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
Todd P W McMullenDepartment of Surgery, University of Alberta, Edmonton, Alberta, Canada.
Marco AlfòDipartimento di Scienze Statistiche, Sapienza Università di Roma, Rome, Italy.
David N BrindleyDepartment of Biochemistry, Signal Transduction Research Group, University of Alberta, Edmonton, Alberta, Canada.
Pascale de LonlayCentre de Référence des Maladies Héréditaires du Métabolisme, Institut Imagine des Maladies Génétiques, Laboratoire de génétique des maladies autoinflammatoires monogéniques, INSERM UMR1163, Université Paris Descartes et Hôpital Necker-Enfants malades (Assistance publique - Hôpitaux de Paris), Paris, France pdelonlay@neuf.fr michi_pelo@libero.it.
Institut des Maladies Génétiques Imagine · FRUniversity of Alberta · CAAssistance Publique – Hôpitaux de Paris · FRBiomatériaux et Bioingénierie · FRLaboratoire de Biogenèse Membranaire · FRLaboratoire Stress Oxydant et Pathologies Métaboliques · FRSapienza University of Rome · ITUnité de recherche sur les maladies cardiovasculaires et métaboliques · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipin-1 is a Mg

Indexed as

MutationAdipocytesAdipose Tissue, WhiteAdolescentAllelesBody Fat DistributionBody WeightCase-Control StudiesCell DifferentiationChildChild, PreschoolFemaleGene Expression RegulationHumansMaleMiddle AgedLPIN1 protein, humanPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPhosphatidate PhosphatasePPAR gammaPPARGC1A protein, humanSREBF1 protein, humanSterol Regulatory Element Binding Protein 1adipocytesadipogenic differentiationgene expressionhuman fat lipid analysishuman lipidsinborn errors of metabolismlipodystrophiesphosphatases/lipid

Identifiers

PMID28986436
PMCPMC5711497
OpenAlexW2761354111

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.