Evidence map›Paper›PMID 39076976›Full record

ArticleFrontiers in immunology2024

Immune dysregulation due to bi-allelic mutation of the actin remodeling protein DIAPH1.

Sagar Bhattad, Somashekara H Ramakrishna, Ratan Kumar, Joseph M Choi, Janet G Markle

Abstract readCase Reports
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

5 authors.

Sagar BhattadDivision of Pediatric Immunology and Rheumatology, Department of Pediatrics, Aster CMI Hospital, Bengaluru, India.
Somashekara H RamakrishnaDepartment of Pediatric Hepatology, Gleneagles Health City, Chennai, India.
Ratan KumarDepartment of Pediatrics, Tata Main Hospital, Jamshedpur, India.
Joseph M ChoiDivision of Molecular Pathogenesis, Department of Pathology Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, United States.
Janet G MarkleDivision of Molecular Pathogenesis, Department of Pathology Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, United States.

Funding

From genetic variants to mechanisms: understanding drivers of inflammationR35GM155339 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Janet G Markle · 2024 to 2026
$1.3M
NIGMS NIH HHS R35 GM155339
6 · The paper itself

Abstract

Children with severe inflammatory diseases are challenging to diagnose and treat, and the etiology of disease often remains unexplained. Here we present DIAPH1 deficiency as an unexpected genetic finding in a child with fatal inflammatory bowel disease who also displayed complex neurological and developmental phenotypes. Bi-allelic mutations of

Indexed as

ForminsMutationAdaptor Proteins, Signal TransducingAllelesFemaleHumansInflammatory Bowel DiseasesPhenotypeAdaptor Proteins, Signal TransducingDIAPH1 protein, humanForminsenteropathyinborn errors of immunityinflammatory bowel diseasemedical geneticspediatrics

Identifiers

PMID39076976
PMCPMC11284534

What OpenQuestion holds

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LicenceCC BY
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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.