Evidence map›Paper›PMID 31861214›Full record

ReviewInternational journal of molecular sciences2019

S1P/S1P Receptor Signaling in Neuromuscolar Disorders.

Elisabetta Meacci, Mercedes Garcia-Gil

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Potential Vitamin E Signaling Mediators in Skeletal Muscle.Antioxidants (Basel, Switzerland) · 2024
    Review
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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

2 authors at 2 institutions in 1 country.

Elisabetta MeacciClinical Biochemistry and Clinical Molecular Biology Unit, Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Viale Pieraccini 6, 50139 Florence, Italy.ORCID 0000-0002-5820-7800
Mercedes Garcia-GilDepartment of Biology, Unit of Physiology, University of Pisa, via S. Zeno 31, 56127 Pisa, Italy.ORCID 0000-0002-1344-2786
University of Florence · ITUniversity of Pisa · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca 2017university of Pisa 2018
6 · The paper itself

Abstract

The bioactive sphingolipid metabolite, sphingosine 1-phosphate (S1P), and the signaling pathways triggered by its binding to specific G protein-coupled receptors play a critical regulatory role in many pathophysiological processes, including skeletal muscle and nervous system degeneration. The signaling transduced by S1P binding appears to be much more complex than previously thought, with important implications for clinical applications and for personalized medicine. In particular, the understanding of S1P/S1P receptor signaling functions in specific compartmentalized locations of the cell is worthy of being better investigated, because in various circumstances it might be crucial for the development or/and the progression of neuromuscular diseases, such as Charcot-Marie-Tooth disease, myasthenia gravis, and Duchenne muscular dystrophy.

Indexed as

Signal TransductionAnimalsCharcot-Marie-Tooth DiseaseHumansLysophospholipidsMuscle, SkeletalMuscular Dystrophy, DuchenneMyasthenia GravisNeuromuscular DiseasesSphingosineSphingosine-1-Phosphate ReceptorsLysophospholipidsSphingosinesphingosine 1-phosphateSphingosine-1-Phosphate ReceptorsceramideCharcot-Marie-Tooth diseaseduchenne muscular dystrophymyasthenia gravisnervous systemneuromuscular diseaseskeletal musclesphingolipidssphingosine 1-phosphate receptors

Identifiers

PMID31861214
PMCPMC6941007
OpenAlexW2995300252

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.