Evidence map›Paper›PMID 31675530›Full record

ArticlePlacenta2019

Klf14 is an imprinted transcription factor that regulates placental growth.

Erik Koppes, Ben Shaffer, Elena Sadovsky, Katherine Himes, Yaacov Barak, Yoel Sadovsky, J Richard Chaillet

Open access · greenAbstract read
In one paragraph

Article in Placenta, 2019. 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
0.9field-weighted citation impact, top 21% 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, 18 citations in OpenAlex.

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  11. Transcription Factor KLF14 and Metabolic Syndrome.Frontiers in cardiovascular medicine · 2020
    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

7 authors at 1 institution in 1 country.

Erik KoppesMagee-Womens Research Institute, Program in Integrative Molecular Biology, University of Pittsburgh School of Medicine, USA.
Ben ShafferMagee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, USA.
Elena SadovskyMagee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, USA.
Katherine HimesMagee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, USA.
Yaacov BarakMagee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, USA.
Yoel SadovskyMagee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, USA.
J Richard ChailletMagee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, USA. Electronic address: chaillet@pitt.edu.
University of Pittsburgh · US

Funding

Transcriptional and developmental regulation of placental fuel storage and metabP01HD069316 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI BARAK, YAACOV · 2012 to 2016
$5.0M
Extracellular vesicles and their ncRNA cargo as markers of trophoblast injuryR01HD086325 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SADOVSKY, YOEL · 2015 to 2019
$3.6M
NICHD NIH HHS P01 HD069316NICHD NIH HHS R01 HD086325
6 · The paper itself

Abstract

introductionImprinted genes are preferentially expressed from one parentally inherited allele, and many are crucial to the regulation of placental function and fetal growth. Murine Krüppel-like factor 14 (Klf14) is a maternally expressed imprinted transcription factor that is a component of the Mest imprinted gene cluster on mouse chromosome 6. We sought to determine if loss of Klf14 expression alters the course of normal mouse extraembryonic development. We also used high-throughput RNA sequencing (RNAseq) to identify a set of differentially expressed genes (DEGs) in placentas with loss of Klf14.

methodsWe generated a Klf14 knockout (Klf14

resultsWe found that 17.5dpc placentas inheriting a maternal null allele (Klf14

conclusionThese results suggest that loss of the maternal Klf14 locus in the mouse placenta acts results in changes in gene expression patterns that modulate placental growth.

Indexed as

PlacentationAnimalsCalcium-Binding ProteinsExtracellular Matrix ProteinsFemaleGene Regulatory NetworksGenomic ImprintingGrowth Differentiation Factor 10Kruppel-Like Transcription FactorsMice, KnockoutPregnancyRecombinant ProteinsCalcium-Binding ProteinsExtracellular Matrix ProteinsFbln5 protein, mouseGdf10 protein, mouseGrowth Differentiation Factor 10Klf14 protein, mouseKruppel-Like Transcription FactorsNell1 protein, mouseRecombinant ProteinsImprintingKLF14Mouse modelRNAseqTranscription

Identifiers

PMID31675530
PMCPMC7774094
OpenAlexW2976528342

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.