Evidence map›Paper›PMID 41017962›Full record

ArticleHemaSphere2025

Transcriptome profiling of megakaryocytes and platelets: Application to

Koenraad De Wispelaere, Fabienne Ver Donck, Kato Ramaekers, Chantal Thys, Koji Eto, Veerle Labarque, Ernest Turro, Kathleen Freson

Abstract read
In one paragraph

Article in HemaSphere, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Koenraad De WispelaereDepartment of Cardiovascular Sciences Center for Molecular and Vascular Biology KU Leuven Leuven Belgium.ORCID https://orcid.org/0000-0003-1946-3024
Fabienne Ver DonckDepartment of Cardiovascular Sciences Center for Molecular and Vascular Biology KU Leuven Leuven Belgium.
Kato RamaekersDepartment of Cardiovascular Sciences Center for Molecular and Vascular Biology KU Leuven Leuven Belgium.
Chantal ThysDepartment of Cardiovascular Sciences Center for Molecular and Vascular Biology KU Leuven Leuven Belgium.
Koji EtoDepartment of Clinical Application Center for iPS Cell Research and Application Kyoto University Kyoto Japan.
Veerle LabarqueDepartment of Cardiovascular Sciences Center for Molecular and Vascular Biology KU Leuven Leuven Belgium.
Ernest TurroIcahn School of Medicine at Mount Sinai, Mindich Child Health and Development Institute New York New York USA.
Kathleen FresonDepartment of Cardiovascular Sciences Center for Molecular and Vascular Biology KU Leuven Leuven Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platelets are anucleate cells produced in the bone marrow and derived from large progenitor cells called megakaryocytes (MKs). Platelets receive RNA transcripts from their progenitorial MKs during thrombopoiesis. However, the correspondence between platelet and MK transcriptomes is poorly understood, particularly in the context of germline mutations that cause platelet formation defects or thrombocytopenia. We have studied the effects of two such mutations on MK and platelet transcriptomes. We generated immortalized MK cell line (imMKCL)-based models of Bernard-Soulier syndrome and

Identifiers

PMID41017962
PMCPMC12461113

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Registered trials

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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.