Evidence map›Paper›PMID 38765012›Full record

ArticleFrontiers in immunology2024

KMT2D regulates activation, localization, and integrin expression by T-cells.

Sarah J Potter, Li Zhang, Michael Kotliar, Yuehong Wu, Caitlin Schafer, Kurtis Stefan, Leandros Boukas, Dima Qu'd, Olaf Bodamer, Brittany N Simpson and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. KMT2C and KMT2D amplify GRHL2-driven enhancer activation.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

13 authors.

Sarah J Potter *Division of Allergy & Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Li Zhang *McKusick-Nathans Department of Genetics, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Michael KotliarDivision of Allergy & Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Yuehong WuDivision of Allergy & Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Caitlin SchaferDivision of Allergy & Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Kurtis StefanDivision of Allergy & Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Leandros BoukasMcKusick-Nathans Department of Genetics, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Dima Qu'dDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Olaf BodamerDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA, United States.
Brittany N SimpsonDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Artem BarskiDivision of Allergy & Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Andrew W Lindsley *Division of Allergy & Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Hans T Bjornsson *McKusick-Nathans Department of Genetics, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI LEE ARMISTEAD DENSON · 2007 to 2026
$24.4M
Tissue Repository CoreP30AR070549 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI Leah Claire Kottyan · 2016 to 2026
$7.7M
Epigenetic mechanisms of disrupted neurodevelopment in Menke-Hennekam syndromeR03NS133727 · NINDS · CINCINNATI CHILDRENS HOSP MED CTR · PI BARSKI, ARTEM, POTTER, SARAH J · 2023 to 2023
$161k
NIAMS NIH HHS P30 AR070549NIDDK NIH HHS P30 DK078392NINDS NIH HHS R03 NS133727
6 · The paper itself

Abstract

Individuals with Kabuki syndrome present with immunodeficiency; however, how pathogenic variants in the gene encoding the histone-modifying enzyme lysine methyltransferase 2D (KMT2D) lead to immune alterations remain poorly understood. Following up on our prior report of KMT2D-altered integrin expression in B-cells, we performed targeted analyses of KMT2D's influence on integrin expression in T-cells throughout development (thymocytes through peripheral T-cells) in murine cells with constitutive- and conditional-targeted

Indexed as

Gene Expression RegulationHistone-Lysine N-MethyltransferaseIntegrinsMyeloid-Lymphoid Leukemia ProteinT-LymphocytesAbnormalities, MultipleAnimalsDNA-Binding ProteinsFaceHematologic DiseasesHumansLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutNeoplasm ProteinsDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseIntegrinsKmt2d protein, mouseMyeloid-Lymphoid Leukemia ProteinNeoplasm Proteinsintegrin switchingItgalItgb7Kabuki syndrome (KS)KS1-associated immune deficiency (KSAID)recent thymic emigrant (RTE)thymocyte

Identifiers

PMID38765012
PMCPMC11099208

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.