Evidence map›Paper›PMID 39774796›Full record

ArticleLeukemia2025

Modeling GATA2 deficiency in mice: the R396Q mutation disrupts normal hematopoiesis.

Trent Hall, Rashid Mehmood, Diana Sá da Bandeira, Anitria Cotton, Jonathon Klein, Shondra M Pruett-Miller, Shai Izraeli, Wilson K Clements, John D Crispino

Abstract read
In one paragraph

Article in Leukemia, 2025. 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
–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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors.

Trent HallDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Rashid MehmoodDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Diana Sá da BandeiraDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Anitria CottonDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Jonathon KleinCenter for Advanced Genome Engineering, St. Jude Children's Research Hospital, Memphis, TN, USA.
Shondra M Pruett-MillerCenter for Advanced Genome Engineering, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID http://orcid.org/0000-0002-3793-585X
Shai IzraeliDepartment of Pediatric Hematology/Oncology, Schneider Children's Medical Center of Israel, Tel Aviv University, Petah Tikva, Israel.ORCID http://orcid.org/0000-0002-6938-2540
Wilson K ClementsDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID http://orcid.org/0000-0003-4365-9553
John D CrispinoDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA. john.crispino@stjude.org.ORCID http://orcid.org/0000-0002-8182-8306

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Shondra Michelle Miller · 1985 to 2026
$166.9M
Identifying the mechanisms of leukemia progressionR35CA253096 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI John D Crispino · 2021 to 2026
$6.1M
Novel hematopoietic stem cell specification signals from the neural crestR01DK113973 · NIDDK · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CLEMENTS, WILSON KENDRICK · 2017 to 2021
$2.0M
NCI NIH HHS P30 CA021765NCI NIH HHS R35 CA253096NIDDK NIH HHS R01 DK113973U.S. Department of Health & Human Services | National Institutes of Health (NIH) P30CA021765U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01DK113973U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35CA253096
6 · The paper itself

Abstract

GATA2 deficiency is an autosomal dominant germline disorder of immune dysfunction and bone marrow failure with a high propensity for leukemic transformation. While sequencing studies have identified several secondary mutations thought to contribute to malignancy, the mechanisms of disease progression have been difficult to identify due to a lack of disease-specific experimental models. Here, we describe a murine model of one of the most common GATA2 mutations associated with leukemic progression in GATA2 deficiency, Gata2

Indexed as

GATA2 DeficiencyGATA2 Transcription FactorHematopoiesisMutationAnimalsDisease Models, AnimalHematopoietic Stem CellsMiceMice, Inbred C57BLGata2 protein, mouseGATA2 Transcription Factor

Identifiers

PMID39774796
PMCPMC11879863

What OpenQuestion holds

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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.