Evidence map›Paper›PMID 38136965›Full record

ReviewGenes2023

NUP85 as a Neurodevelopmental Gene: From Podocyte to Neuron.

Antonella Gambadauro, Giuseppe Donato Mangano, Karol Galletta, Francesca Granata, Antonella Riva, Laura Massella, Isabella Guzzo, Giovanni Farello, Giovanna Scorrano, Ludovica Di Francesco and 9 more

Open access · goldAbstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Genes, 2023. 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
0.6field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Nucleoporin-associated steroid-resistant nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2025
    Review
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

19 authors at 6 institutions in 2 countries.

Antonella GambadauroDepartment of Human Pathology in Adult and Developmental Age "Gaetano Barresi", University of Messina, Via Consolare Valeria 1, 98124 Messina, Italy.ORCID 0000-0002-7421-0903
Giuseppe Donato ManganoDepartment of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, 90127 Palermo, Italy.ORCID 0000-0001-6541-3170
Karol GallettaDepartment of Biomedical, Dental Science and Morphological and Functional Images, Neuroradiology Unit, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Francesca GranataDepartment of Biomedical, Dental Science and Morphological and Functional Images, Neuroradiology Unit, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Antonella RivaUnit of Medical Genetics, IRCSS Giannina Gaslini Institute, Via Gerolamo Gaslini 5, 16147 Genoa, Italy.
Laura MassellaDivision of Nephrology, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00165 Rome, Italy.
Isabella GuzzoDivision of Nephrology, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00165 Rome, Italy.
Giovanni FarelloDepartment of Pediatrics, University of L'Aquila, 67100 L'Aquila, Italy.
Giovanna ScorranoDepartment of Pediatrics, University of L'Aquila, 67100 L'Aquila, Italy.
Ludovica Di FrancescoDepartment of Pediatrics, University of L'Aquila, 67100 L'Aquila, Italy.ORCID 0000-0002-3889-1318
Giulio Di DonatoDepartment of Pediatrics, University of L'Aquila, 67100 L'Aquila, Italy.ORCID 0000-0002-3979-9265
Carolina IanniDepartment of Pediatrics, University of L'Aquila, 67100 L'Aquila, Italy.
Armando Di LudovicoDepartment of Pediatrics, University of L'Aquila, 67100 L'Aquila, Italy.ORCID 0000-0002-2644-1475
Saverio La BellaDepartment of Pediatrics, University of L'Aquila, 67100 L'Aquila, Italy.ORCID 0000-0002-1244-0789
Pasquale StrianoUnit of Medical Genetics, IRCSS Giannina Gaslini Institute, Via Gerolamo Gaslini 5, 16147 Genoa, Italy.ORCID 0000-0002-6065-1476
Stephanie EfthymiouDepartment of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London WC1N 3BG, UK.ORCID 0000-0003-4900-9877
Henry HouldenDepartment of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London WC1N 3BG, UK.
Rosaria NardelloDepartment of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, 90127 Palermo, Italy.
Roberto ChimenzDepartment of Human Pathology in Adult and Developmental Age "Gaetano Barresi", University of Messina, Via Consolare Valeria 1, 98124 Messina, Italy.ORCID 0000-0001-9143-4637
University of L'Aquila · ITUniversity of Messina · ITBambino Gesù Children's Hospital · ITIstituto Giannina Gaslini · ITNational Hospital for Neurology and Neurosurgery · GBUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic gene variants encoding nuclear pore complex (NPC) proteins were previously implicated in the pathogenesis of steroid-resistant nephrotic syndrome (SRNS). The

Indexed as

NeuronsPodocytesChildChild, PreschoolHumansMaleMutationNephrotic SyndromeNuclear Pore Complex ProteinsNuclear Pore Complex ProteinsNUP85 protein, humandevelopmental delayepileptic spasmmicrocephalynephrotic syndrome type 17NUP85steroid-resistant nephrotic syndrome

Identifiers

PMID38136965
PMCPMC10743110
OpenAlexW4389036096

What OpenQuestion 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 OpenQuestion graph.