Evidence map›Paper›PMID 33322555›Full record

ArticleCells2020

Establishment and Characterization of a Sclerosing Spindle Cell Rhabdomyosarcoma Cell Line with a Complex Genomic Profile.

Sabine Schleicher, Stefan Grote, Elke Malenke, Kenneth Chun-Ho Chan, Martin Schaller, Birgit Fehrenbacher, Rosa Riester, Torsten Kluba, Leonie Frauenfeld, Hans Boesmueller and 6 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Functional impact and targetability ofCold Spring Harbor molecular case studies · 2022
    Article
  2. Article
  3. Article
  4. 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

16 authors at 7 institutions in 1 country.

Sabine SchleicherDepartment of Hematology and Oncology, Eberhard Karls University Tuebingen, Children's Hospital, 72076 Tuebingen, Germany.ORCID 0000-0002-1847-2984
Stefan GroteDepartment of Hematology and Oncology, Eberhard Karls University Tuebingen, Children's Hospital, 72076 Tuebingen, Germany.ORCID 0000-0001-8713-6709
Elke MalenkeDepartment of Hematology and Oncology, Eberhard Karls University Tuebingen, Children's Hospital, 72076 Tuebingen, Germany.
Kenneth Chun-Ho ChanDepartment of Hematology and Oncology, Eberhard Karls University Tuebingen, Children's Hospital, 72076 Tuebingen, Germany.
Martin SchallerDepartment of Dermatology, Eberhard Karls University Tuebingen, 72076 Tuebingen, Germany.
Birgit FehrenbacherDepartment of Dermatology, Eberhard Karls University Tuebingen, 72076 Tuebingen, Germany.ORCID 0000-0003-3022-7567
Rosa RiesterDepartment of Orthopaedic Surgery, Eberhard Karls University Tuebingen, 72072 Tuebingen, Germany.
Torsten KlubaDepartment for Orthopaedic Surgery, Hospital Dresden-Friedrichstadt, 01067 Dresden, Germany.
Leonie FrauenfeldInstitute of Pathology and Neuropathology, University Hospital Tuebingen, 72076 Tuebingen, Germany.
Hans BoesmuellerInstitute of Pathology and Neuropathology, University Hospital Tuebingen, 72076 Tuebingen, Germany.
Gudrun GöhringDepartment of Human Genetics, Hannover Medical School, 30625 Hannover, Germany.
Brigitte SchlegelbergerDepartment of Human Genetics, Hannover Medical School, 30625 Hannover, Germany.
Rupert HandgretingerDepartment of Hematology and Oncology, Eberhard Karls University Tuebingen, Children's Hospital, 72076 Tuebingen, Germany.
Hans-Georg KoppRobert Bosch Cancer Center/RBCT Stuttgart, 70376 Stuttgart, Germany.
Frank TraubDepartment of Orthopedics and Traumatology, University Medical Centre Mainz, Johannes Gutenberg-University Mainz, 55131 Mainz, Germany.ORCID 0000-0002-6400-3257
Karen A BoehmeDepartment of Orthopaedic Surgery, Eberhard Karls University Tuebingen, 72072 Tuebingen, Germany.
University Children's Hospital Tübingen · DEUniversity of Tübingen · DEMedizinische Hochschule Hannover · DEJohannes Gutenberg University Mainz · DEKrankenhaus Dresden-Friedrichstadt · DERobert Bosch Hospital · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sclerosing spindle cell rhabdomyosarcoma (SSRMS) is a rare rhabdomyosarcomas (RMS) subtype. Especially cases bearing a myogenic differentiation 1 (

Indexed as

GenomicsAdipogenesisAnimalsBiomarkersCell DifferentiationCell Line AuthenticationComparative Genomic HybridizationFemaleHumansKaryotypingMiceMice, Inbred NODMice, SCIDMyoD ProteinRhabdomyosarcomaSignal TransductionBiomarkersMyoD1 myogenic differentiation proteinMyoD ProteinTumor Suppressor Protein p53cell line establishmentdifferentiationgeneticsMYOD1p53rhabdomyosarcomasclerosingspindle cellstem cellWNT

Identifiers

PMID33322555
PMCPMC7763666
OpenAlexW3113252742

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.