Evidence map›Paper›PMID 37333770›Full record

ArticleHGG advances2023

Deoxyhypusine synthase mutations alter the post-translational modification of eukaryotic initiation factor 5A resulting in impaired human and mouse neural homeostasis.

Leah R Padgett, Mollie R Shinkle, Spencer Rosario, Tracy Murray Stewart, Jackson R Foley, Robert A Casero, Myung Hee Park, Wendy K Chung, Teresa L Mastracci

Open access · goldAbstract read
In one paragraph

Article in HGG advances, 2023. 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
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

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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 at 6 institutions in 1 country.

Leah R PadgettIndiana Biosciences Research Institute, Indianapolis, IN 46202, USA.
Mollie R ShinkleDepartment of Biology, Indiana University Purdue University Indianapolis, Indianapolis, IN 46202, USA.
Spencer RosarioDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14203, USA.
Tracy Murray StewartSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Jackson R FoleySidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Robert A CaseroSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Myung Hee ParkNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892-4340, USA.
Wendy K ChungDepartments of Pediatrics and Medicine, Columbia University, New York, NY 10032, USA.
Teresa L MastracciDepartment of Biology, Indiana University Purdue University Indianapolis, Indianapolis, IN 46202, USA.
Johns Hopkins University · USUniversity of Indianapolis · USColumbia University · USIndiana Biosciences Research Institute · USNational Institutes of Health · USRoswell Park Comprehensive Cancer Center · US

Funding

Exocrine-Endocrine Crosstalk and Determinants of Beta Cell GrowthR01DK121987 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI MASTRACCI, TERESA LOUISE · 2020 to 2024
$2.0M
NIDDK NIH HHS R01 DK121987
6 · The paper itself

Abstract

DHPS deficiency is a rare genetic disease caused by biallelic hypomorphic variants in the

Indexed as

Oxidoreductases Acting on CH-NH Group DonorsPeptide Initiation FactorsRare DiseasesAnimalsEukaryotic Translation Initiation Factor 5AHomeostasisHumansInfant, NewbornMiceMutationProtein Processing, Post-Translationaldeoxyhypusine synthaseEukaryotic Translation Initiation Factor 5AOxidoreductases Acting on CH-NH Group DonorsPeptide Initiation FactorsDHPSDHPS deficiencyeIF5AhypusinationhypusinemRNA translationneurodevelopmentrare disease

Identifiers

PMID37333770
PMCPMC10275725
OpenAlexW4377103002

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.