Evidence map›Paper›PMID 37047767›Full record

ReviewInternational journal of molecular sciences2023

Ca

Roland Takács, Patrik Kovács, Rana Abdelsattar Ebeid, János Almássy, János Fodor, László Ducza, Richard Barrett-Jolley, Rebecca Lewis, Csaba Matta

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 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
0.9field-weighted citation impact, top 25% 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, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 4 institutions in 2 countries.

Roland TakácsDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.ORCID 0000-0002-1598-3922
Patrik KovácsDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.ORCID 0000-0003-1588-7962
Rana Abdelsattar EbeidDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.ORCID 0000-0001-5412-455X
János AlmássyDepartment of Physiology, Faculty of Medicine, Semmelweis University, H-1428 Budapest, Hungary.ORCID 0000-0002-9620-802X
János FodorDepartment of Physiology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.ORCID 0000-0002-3702-2903
László DuczaDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.ORCID 0000-0002-2753-5748
Richard Barrett-JolleyDepartment of Musculoskeletal Biology, Faculty of Health and Life Sciences, Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool L69 3GA, UK.ORCID 0000-0003-0449-9972
Rebecca LewisDepartment of Comparative Biomedical Sciences, School of Veterinary Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford GU2 7XH, UK.ORCID 0000-0003-1395-3276
Csaba MattaDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.ORCID 0000-0002-9678-7420
University of Debrecen · HUSemmelweis University · HUUniversity of Liverpool · GBUniversity of Surrey · GB

Funding

European Cooperation in Science and Technology Ca211110National Research, Development and Innovation Office FK-134304
6 · The paper itself

Abstract

Musculoskeletal disorders represent one of the main causes of disability worldwide, and their prevalence is predicted to increase in the coming decades. Stem cell therapy may be a promising option for the treatment of some of the musculoskeletal diseases. Although significant progress has been made in musculoskeletal stem cell research, osteoarthritis, the most-common musculoskeletal disorder, still lacks curative treatment. To fine-tune stem-cell-based therapy, it is necessary to focus on the underlying biological mechanisms. Ion channels and the bioelectric signals they generate control the proliferation, differentiation, and migration of musculoskeletal progenitor cells. Calcium- and voltage-activated potassium (K

Indexed as

Large-Conductance Calcium-Activated Potassium ChannelsStem CellsCalciumCalcium, DietaryCalciumCalcium, DietaryLarge-Conductance Calcium-Activated Potassium ChannelsBK channelchannelomechondrogenesision channelmuscle differentiationmusculoskeletal diseasesosteoarthritisosteogenesisprogenitor cell

Identifiers

PMID37047767
PMCPMC10095002
OpenAlexW4362671055

What Socratic 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 Socratic graph.