Evidence map›Paper›PMID 36429004›Full record

ArticleCells2022

Overexpression of

Yi Li, Veronica Costiniti, Guilherme H Souza Bomfim, Maria Neginskaya, Ga-Yeon Son, Beverly Rothermel, Evgeny Pavlov, Rodrigo S Lacruz

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 2 institutions in 1 country.

Yi LiDepartment of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA.
Veronica CostinitiDepartment of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA.ORCID 0000-0002-8472-7797
Guilherme H Souza BomfimDepartment of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA.ORCID 0000-0001-9454-7266
Maria NeginskayaDepartment of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA.
Ga-Yeon SonDepartment of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA.
Beverly RothermelDepartment of Internal Medicine and Molecular Biology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Evgeny PavlovDepartment of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA.
Rodrigo S LacruzDepartment of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA.
New York University · USSouthwestern Medical Center · US

Funding

Redox and Ca2+ signaling regulation of enamel mineralizationR01DE027679 · NIDCR · NEW YORK UNIVERSITY · PI Rodrigo S. Lacruz · 2018 to 2026
$3.3M
Ca2+ signaling via SOCE in the pathogenesis of Sjögren’s syndromeR01DE027981 · NIDCR · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FESKE, STEFAN, LACRUZ, RODRIGO S. · 2019 to 2023
$2.7M
Molecular mechanisms of the mitochondrial permeability transitionR35GM139615 · NIGMS · NEW YORK UNIVERSITY · PI PAVLOV, EVGENY · 2021 to 2025
$2.3M
Elevated mitochondrial fusion and function in Down syndrome - Revision - 2R01HD101006 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI ROTHERMEL, BEVERLY A · 2019 to 2022
$2.2M
Calcium Control of Enamel DevelopmentR01DE025639 · NIDCR · NEW YORK UNIVERSITY · PI LACRUZ, RODRIGO S. · 2016 to 2020
$2.0M
NICHD NIH HHS R01 HD101006NIDCR NIH HHS DE027679NIDCR NIH HHS DE027981NIDCR NIH HHS R01 DE025639NIDCR NIH HHS R01 DE027679NIDCR NIH HHS R01 DE027981NIGMS NIH HHS R35 GM139615NIGMS NIH HHS R35GM139615
6 · The paper itself

Abstract

The regulator of calcineurin (RCAN1) has been implicated in the pathogenesis of Down syndrome (DS). Individuals with DS show dental abnormalities for unknown reasons, and RCAN1 levels have been found to be elevated in several tissues of DS patients. A previous microarray analysis comparing cells of the two main formative stages of dental enamel, secretory and maturation, showed a significant increase in RCAN1 expression in the latter. Because the function of RCAN1 during enamel formation is unknown, there is no mechanistic evidence linking RCAN1 with the dental anomalies in individuals with DS. We investigated the role of RCAN1 in enamel by overexpressing RCAN1 in the ameloblast cell line LS8 (LS8

Indexed as

Down SyndromeMuscle ProteinsChromosomes, HumanDental EnamelDNA-Binding ProteinsHumansIntracellular Signaling Peptides and ProteinsMitochondriaOxidation-ReductionDNA-Binding ProteinsIntracellular Signaling Peptides and ProteinsMuscle ProteinsRCAN1 protein, humanameloblastsDown syndromemitochondriaredox

Identifiers

PMID36429004
PMCPMC9688881
OpenAlexW4309003885

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.