Evidence map›Paper›PMID 29114221›Full record

ArticleFrontiers in pharmacology2017

Phenotypic Screen Identifies a Small Molecule Modulating ERK2 and Promoting Stem Cell Proliferation.

Chang Yin, Temesgen Fufa, Gayathri Chandrasekar, Madhu Aeluri, Verina Zaky, Shaimaa Abdelhady, Antonio B Rodríguez, Johan Jakobsson, Farzaneh Shahin Varnoosfaderani, Jayashri Mahalingam and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2017. 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
0.1field-weighted citation impact, top 48% 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, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Secretome-Based Screening in Target Discovery.SLAS discovery : advancing life sciences R & D · 2020
    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

17 authors at 5 institutions in 4 countries.

Chang YinDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Temesgen FufaDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Gayathri ChandrasekarDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Madhu AeluriDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Verina ZakyDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Shaimaa AbdelhadyDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Antonio B RodríguezDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Johan JakobssonDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Farzaneh Shahin VarnoosfaderaniDepartment of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden.
Jayashri MahalingamThe Pirbright Institute, Woking, United Kingdom.
Jianping LiuDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Olle LarssonDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Outi HovattaDivision of Obstetrics and Gynecology, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Frank GaunitzKlinik und Poliklinik für Neurochirurgie, Universitätsklinikum Leipzig, Leipzig, Germany.
Anita GöndörDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Michael AndängDr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad, India.
Satish S KitambiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEInstitute of Life Sciences · INThe Pirbright Institute · GBUniversity Hospital Leipzig · DEUniversity of Hyderabad · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells display a fundamentally different mechanism of proliferation control when compared to somatic cells. Uncovering these mechanisms would maximize the impact in drug discovery with a higher translational applicability. The unbiased approach used in phenotype-based drug discovery (PDD) programs can offer a unique opportunity to identify such novel biological phenomenon. Here, we describe an integrated phenotypic screening approach, employing a combination of

Indexed as

mousePDDphenotypesmall moleculesstem cellszebrafish

Identifiers

PMID29114221
PMCPMC5660848
OpenAlexW2766267736

What OpenQuestion holds

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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.