Evidence map›Paper›PMID 28128288›Full record

ArticleScientific reports2017

The spleen microenvironment influences disease transformation in a mouse model of KIT

Natalie Pelusi, Maike Kosanke, Tamara Riedt, Corinna Rösseler, Kristin Seré, Jin Li, Ines Gütgemann, Martin Zenke, Viktor Janzen, Hubert Schorle

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
0.9field-weighted citation impact, top 26% 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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Organ Crosstalk: The Role of Spleen.Phenomics (Cham, Switzerland) · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
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

10 authors at 2 institutions in 1 country.

Natalie PelusiUniversity of Bonn Medical School, Institute of Pathology, Department of Developmental Pathology, 53127 Bonn, Germany.
Maike KosankeInstitute for Biomedical Engineering, Department of Cell Biology, RWTH Aachen University Medical School, Pauwelsstr. 30, 52074 Aachen, Germany.
Tamara RiedtUniversity of Bonn Medical School, Department of Internal Medicine III, Hematology and Oncology, Sigmund-Freud-Str. 25, 53127 Bonn, Germany.
Corinna RösselerInstitute for Biomedical Engineering, Department of Cell Biology, RWTH Aachen University Medical School, Pauwelsstr. 30, 52074 Aachen, Germany.
Kristin SeréInstitute for Biomedical Engineering, Department of Cell Biology, RWTH Aachen University Medical School, Pauwelsstr. 30, 52074 Aachen, Germany.
Jin LiUniversity of Bonn Medical School, Department of Internal Medicine III, Hematology and Oncology, Sigmund-Freud-Str. 25, 53127 Bonn, Germany.
Ines GütgemannUniversity of Bonn Medical School, Institute of Pathology, Department of Developmental Pathology, 53127 Bonn, Germany.
Martin ZenkeInstitute for Biomedical Engineering, Department of Cell Biology, RWTH Aachen University Medical School, Pauwelsstr. 30, 52074 Aachen, Germany.
Viktor JanzenUniversity of Bonn Medical School, Department of Internal Medicine III, Hematology and Oncology, Sigmund-Freud-Str. 25, 53127 Bonn, Germany.
Hubert SchorleUniversity of Bonn Medical School, Institute of Pathology, Department of Developmental Pathology, 53127 Bonn, Germany.
University of Bonn · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activating mutations leading to ligand-independent signaling of the stem cell factor receptor KIT are associated with several hematopoietic malignancies. One of the most common alterations is the D816V mutation. In this study, we characterized mice, which conditionally express the humanized KIT

Indexed as

Tumor MicroenvironmentAnimalsBone Marrow CellsBone Marrow NeoplasmsCell ProliferationCell Transformation, NeoplasticDisease Models, AnimalErythrocytesFibrosisGATA2 Transcription FactorGene Expression Regulation, NeoplasticHematopoiesisHematopoiesis, ExtramedullaryHematopoietic Stem CellsMice, Inbred C57BLPhenotypeGATA2 Transcription FactorProto-Oncogene Proteins c-kit

Identifiers

PMID28128288
PMCPMC5269732
OpenAlexW2582607036

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.