Evidence map›Paper›PMID 36230742›Full record

ArticleCancers2022

Relevance of Abnormal KCNN1 Expression and Osmotic Hypersensitivity in Ewing Sarcoma.

Sebastian Fuest, Christoph Post, Sebastian T Balbach, Susanne Jabar, Ilka Neumann, Sandra Schimmelpfennig, Sarah Sargin, Elke Nass, Thomas Budde, Sareetha Kailayangiri and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Cancer: A bioelectric disease?Clinical and translational medicine · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. CaInternational journal of molecular sciences · 2023
    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 2 institutions in 1 country.

Sebastian FuestInstitute of Physiology II, University Münster, 48149 Münster, Germany.
Christoph PostInstitute of Physiology II, University Münster, 48149 Münster, Germany.
Sebastian T BalbachDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, 48149 Münster, Germany.ORCID 0000-0003-0212-5758
Susanne JabarPediatrics III, University Hospital Essen, 45147 Essen, Germany.
Ilka NeumannInstitute of Physiology II, University Münster, 48149 Münster, Germany.
Sandra SchimmelpfennigInstitute of Physiology II, University Münster, 48149 Münster, Germany.
Sarah SarginInstitute of Physiology II, University Münster, 48149 Münster, Germany.
Elke NassInstitute of Physiology I, University Münster, 48149 Münster, Germany.
Thomas BuddeInstitute of Physiology I, University Münster, 48149 Münster, Germany.
Sareetha KailayangiriDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, 48149 Münster, Germany.ORCID 0000-0001-7383-7715
Bianca AltvaterDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, 48149 Münster, Germany.ORCID 0000-0003-4936-4879
Andreas RanftPediatrics III, University Hospital Essen, 45147 Essen, Germany.
Wolfgang HartmannDivision of Translational Pathology, Gerhard-Domagk-Institute of Pathology, University Münster, 48149 Münster, Germany.
Uta DirksenPediatrics III, University Hospital Essen, 45147 Essen, Germany.ORCID 0000-0002-5435-7860
Claudia RössigDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, 48149 Münster, Germany.ORCID 0000-0002-8672-5285
Albrecht SchwabInstitute of Physiology II, University Münster, 48149 Münster, Germany.
Zoltán PethőInstitute of Physiology II, University Münster, 48149 Münster, Germany.ORCID 0000-0001-7057-4761
University Hospital Münster · DEEssen University Hospital · DE

Funding

Deutsche Forschungsgemeinschaft GRK 2515/1, ChembionIZKF Münster SEED 013/20Kinderkrebshilfe Münster e.V KKH_BalbachMaria-Möller Stiftung MMS_FF_2020-2MedK Münster MedK_2019-2020_Fuest_Post
6 · The paper itself

Abstract

Ewing sarcoma (EwS) is a rare and highly malignant bone tumor occurring mainly in childhood and adolescence. Physiologically, the bone is a central hub for Ca

Indexed as

Ewing sarcomaGGAA microsatelliteKCa2.1 channelregulatory volume decrease

Identifiers

PMID36230742
PMCPMC9564116
OpenAlexW4303613785

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.