Evidence map›Paper›PMID 25079442›Full record

ReviewInternational journal of molecular sciences2014

Non-synonymous single nucleotide polymorphisms in the P2X receptor genes: association with diseases, impact on receptor functions and potential use as diagnosis biomarkers.

Emily A Caseley, Stephen P Muench, Sebastien Roger, Hong-Ju Mao, Stephen A Baldwin, Lin-Hua Jiang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Early Dry Eye Disease Onset in a NOD.H-2h4 Mouse Model of Sjögren's Syndrome.Investigative ophthalmology & visual science · 2022
    Article
  6. Article
  7. P2XFrontiers in cellular neuroscience · 2021
    Review
  8. Article
  9. Inflammasome genetics and complex diseases: a comprehensive review.European journal of human genetics : EJHG · 2020
    Review
  10. Association of Hypomorphic P2X7 Receptor Genotype With Age.Frontiers in molecular neuroscience · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. P2X receptor channels in chronic pain pathways.British journal of pharmacology · 2018
    Review
  18. Review
  19. Purinergic Signalling: Therapeutic Developments.Frontiers in pharmacology · 2017
    Review
  20. 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

6 authors at 3 institutions in 3 countries.

Emily A CaseleySchool of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK. bs09e2c@leeds.ac.uk.
Stephen P MuenchSchool of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK. s.p.muench@leeds.ac.uk.
Sebastien RogerInserm U1069, University of Tours, Tours 37032, France. sebastien.roger@univ-tours.fr.
Hong-Ju MaoState Key Laboratory of Transducer Technology, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Science, Shanghai 200050, China. hjmao@mail.sim.ac.cn.
Stephen A BaldwinSchool of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK. s.a.baldwin@leeds.ac.uk.
Lin-Hua JiangSchool of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK. l.h.jiang@leeds.ac.uk.
University of Leeds · GBState Key Laboratory of Transducer Technology · CNUniversité de Tours · FR

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council G1000567Wellcome Trust
6 · The paper itself

Abstract

P2X receptors are Ca2+-permeable cationic channels in the cell membranes, where they play an important role in mediating a diversity of physiological and pathophysiological functions of extracellular ATP. Mammalian cells express seven P2X receptor genes. Single nucleotide polymorphisms (SNPs) are widespread in the P2RX genes encoding the human P2X receptors, particularly the human P2X7 receptor. This article will provide an overview of the non-synonymous SNPs (NS-SNPs) that have been associated with or implicated in altering the susceptibility to pathologies or disease conditions, and discuss the consequences of the mutations resulting from such NS-SNPs on the receptor functions. Disease-associated NS-SNPs in the P2RX genes have been valuable in understanding the disease etiology and the receptor function, and are promising as biomarkers to be used for the diagnosis and development of stratified therapeutics.

Indexed as

Polymorphism, Single NucleotideAnimalsBiomarkersHearing LossHumansMacular DegenerationMood DisordersMultiple SclerosisReceptors, Purinergic P2X7SeizuresTuberculosisBiomarkersReceptors, Purinergic P2X7

Identifiers

PMID25079442
PMCPMC4159798
OpenAlexW2059276372

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.