Evidence map›Paper›PMID 30373376›Full record

ArticleCartilage2021

Julio Granados-Montiel, Monica Cruz-Lemini, Claudia Rangel-Escareño, Gabriela Martinez-Nava, Carlos Landa-Solis, Ricardo Gomez-Garcia, Alberto Lopez-Reyes, Alejandro Espinosa-Gutierrez, Clemente Ibarra

Open access · bronzeAbstract read
In one paragraph

Article in Cartilage, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Serpins in cartilage and osteoarthritis: what do we know?Biochemical Society transactions · 2021
    Review
  8. 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.

Julio Granados-MontielTissue Engineering, Cell Therapy and Regenerative Medicine Research Unit, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City, Mexico.ORCID 0000-0002-0611-6421
Monica Cruz-LeminiFetal Medicine Mexico Foundation and Fetal Surgery Unit, Children and Women's Specialty Hospital of Queretaro, Queretaro, Mexico.ORCID 0000-0002-6807-3578
Claudia Rangel-EscareñoComputational Genomics Lab, Instituto Nacional de Medicina Genómica, Mexico City, México.
Gabriela Martinez-NavaSynovioanalysis Molecular Laboratory, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City, Mexico.
Carlos Landa-SolisTissue Engineering, Cell Therapy and Regenerative Medicine Research Unit, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City, Mexico.
Ricardo Gomez-GarciaTissue Engineering, Cell Therapy and Regenerative Medicine Research Unit, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City, Mexico.
Alberto Lopez-ReyesSynovioanalysis Molecular Laboratory, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City, Mexico.ORCID 0000-0002-2575-2589
Alejandro Espinosa-GutierrezHand Surgery and Microsurgery Department, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City, Mexico.
Clemente IbarraTissue Engineering, Cell Therapy and Regenerative Medicine Research Unit, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City, Mexico.
Instituto Nacional de Rehabilitación · MXFetal Medicine Foundation · GBGuy's Hospital · GBNational Institute of Genomic Medicine · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHuman mesenchymal stem cells (hMSCs) are a promising source for regenerative medicine, especially mesodermal lineages. Clinical applications require an understanding of the mechanisms for transcriptional control to maintain the desired cell type. The aim of this study was to identify novel markers for differentiation of hMSCs into bone or cartilage with the use of Kartogenin, by RNA analysis using microarray technology, and explore the role of RhoA-Rho associated protein kinase (ROCK) inhibition in these.

methodsCommercial human bone marrow derived primary mesenchymal stem cells were purchased from ATCC. Cells were differentiated

resultsWe found a total of 1,757 genes that were either up- or downregulated on differentiation, when compared to P1 hMSC (control) at day 0 of differentiation. Two members of the Serpin superfamily,

conclusions

Indexed as

AnilidesAntigens, DifferentiationBone Morphogenetic Protein 2CartilageCell DifferentiationCell LineageCells, CulturedHumansIntracellular Signaling Peptides and ProteinsMesenchymal Stem CellsNeoplasm ProteinsPhthalic AcidsRNASerpinsUp-RegulationAnilidesAntigens, DifferentiationBMP2 protein, humanBone Morphogenetic Protein 2Intracellular Signaling Peptides and ProteinskartogeninNeoplasm ProteinsPhthalic AcidsRNASERPINA9 protein, humanSERPINB2 protein, humanSerpinschondrocytesmesenchymal stem cellsosteoblastsSERPINA9SERPINB2

Identifiers

PMID30373376
PMCPMC7755963
OpenAlexW2899363946

What OpenQuestion holds

Textmetadata
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.