Evidence map›Paper›PMID 37148985›Full record

ArticleGene expression patterns : GEP2023

hnRNPL expression dynamics in the embryo and placenta.

Vineetha Mathew, Ariel Mei, Hamida Giwa, Agnes Cheong, Ashmita Chander, Aaron Zou, Robert M Blanton, Olga Kashpur, Wei Cui, Donna Slonim and 5 more

Open access · greenAbstract read
In one paragraph

Article in Gene expression patterns : GEP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. 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

15 authors at 3 institutions in 1 country.

Vineetha MathewMother Infant Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Ariel MeiMother Infant Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Hamida GiwaMother Infant Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Agnes CheongDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, 01003, USA.
Ashmita ChanderDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, 01003, USA.
Aaron ZouMolecular Cardiology Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Robert M BlantonMolecular Cardiology Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Olga KashpurMother Infant Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Wei CuiDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, 01003, USA.
Donna SlonimDepartment of Computer Science, Tufts University, 177 College Avenue, Medford, MA, 02155, USA.
Taysir MahmoudMother Infant Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Perrie O'Tierney-GinnMother Infant Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA.
Jesse MagerDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, 01003, USA.
Isabelle DraperMolecular Cardiology Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA. Electronic address: idraper@tuftsmedicalcenter.org.
Mary C WallingfordMother Infant Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA; Molecular Cardiology Research Institute, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA. Electronic address: marycwallingford@gmail.com.
Tufts Medical Center · USUniversity of Massachusetts Amherst · USTufts University · US

Funding

Streamline assessment of early lethal phenotypes in the mouseR01HD083311 · NICHD · UNIVERSITY OF MASSACHUSETTS AMHERST · PI MAGER, JESSE · 2015 to 2024
$6.5M
Investigating Mixed Lineage Kinase 3 as a blood pressure-independent protein kinase G1 effector in heart failureR01HL162919 · NHLBI · TUFTS MEDICAL CENTER · PI Robert Morris Blanton · 2022 to 2026
$3.9M
Placental lipid metabolism impacts fetal adiposity and is programmed by the maternal metabolic milieu in early pregnancyR01HD091054 · NICHD · TUFTS MEDICAL CENTER · PI O'TIERNEY-GINN, PERRIE F · 2017 to 2022
$2.5M
Determination of maternal-fetal phosphate transport mechanisms and the role of sodium-dependent phosphate transporters in extraembryonic tissuesR00HD090198 · NICHD · TUFTS MEDICAL CENTER · PI WALLINGFORD, MARY CATHERINE · 2018 to 2020
$747k
Determination of maternal-fetal phosphate transport mechanisms and the role of sodium-dependent phosphate transporters in extraembryonic tissuesK99HD090198 · NICHD · UNIVERSITY OF WASHINGTON · PI WALLINGFORD, MARY CATHERINE · 2017 to 2017
$108k
NHLBI NIH HHS R01 HL162919NICHD NIH HHS K99 HD090198NICHD NIH HHS R00 HD090198NICHD NIH HHS R01 HD083311NICHD NIH HHS R01 HD091054
6 · The paper itself

Abstract

Heterogeneous nuclear ribonucleoprotein L (hnRNPL) is a conserved RNA binding protein (RBP) that plays an important role in the alternative splicing of gene transcripts, and thus in the generation of specific protein isoforms. Global deficiency in hnRNPL in mice results in preimplantation embryonic lethality at embryonic day (E) 3.5. To begin to understand the contribution of hnRNPL-regulated pathways in the normal development of the embryo and placenta, we determined hnRNPL expression profile and subcellular localization throughout development. Proteome and Western blot analyses were employed to determine hnRNPL abundance between E3.5 and E17.5. Histological analyses supported that the embryo and implantation site display distinct hnRNPL localization patterns. In the fully developed mouse placenta, nuclear hnRNPL was observed broadly in trophoblasts, whereas within the implantation site a discrete subset of cells showed hnRNPL outside the nucleus. In the first-trimester human placenta, hnRNPL was detected in the undifferentiated cytotrophoblasts, suggesting a role for this factor in trophoblast progenitors. Parallel in vitro studies utilizing Htr8 and Jeg3 cell lines confirmed expression of hnRNPL in cellular models of human trophoblasts. These studies [support] coordinated regulation of hnRNPL during the normal developmental program in the mammalian embryo and placenta.

Indexed as

Heterogeneous-Nuclear Ribonucleoprotein LPlacentaAnimalsCell Line, TumorEmbryo, MammalianFemaleHumansMicePregnancyTrophoblastsHeterogeneous-Nuclear Ribonucleoprotein LHeterogeneous nuclear proteinshnRNPLPosttranscriptional regulationPreimplantationSplicing factorsTrophectodermTrophoblasts

Identifiers

PMID37148985
PMCPMC10330435
OpenAlexW4368370423

What Socratic 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 Socratic graph.