Evidence map›Paper›PMID 37657945›Full record

ReviewFEBS letters2023

Nuclear pore complex and nucleocytoplasmic transport disruption in neurodegeneration.

América Chandía Cristi, Sampath Rapuri, Alyssa N Coyne

Open access · bronzeAbstract readReview
In one paragraph

Review in FEBS letters, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Molecular Crowing in Nuclear Pore.Sub-cellular biochemistry · 2025
    Review
  11. Review
  12. Review
  13. Postexercise downregulation ofTranslational cancer research · 2024
    Article
  14. Review
  15. 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

3 authors at 1 institution in 1 country.

América Chandía CristiDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sampath RapuriDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-4747-5623
Alyssa N CoyneDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-3658-5325
Johns Hopkins University · US

Funding

Mechanisms of impaired ESCRT-III nuclear surveillance in ALS/FTDR01NS132836 · NINDS · JOHNS HOPKINS UNIVERSITY · PI Alyssa Coyne · 2023 to 2026
$2.3M
Mechanisms of nuclear pore complex homeostasis and injury in ALS/FTD and related neurodegenerative diseasesR00NS123242 · NINDS · JOHNS HOPKINS UNIVERSITY · PI COYNE, ALYSSA · 2022 to 2024
$747k
NINDS NIH HHS R00 NS123242NINDS NIH HHS R01 NS132836
6 · The paper itself

Abstract

Nuclear pore complexes (NPCs) play a critical role in maintaining the equilibrium between the nucleus and cytoplasm, enabling bidirectional transport across the nuclear envelope, and are essential for proper nuclear organization and gene regulation. Perturbations in the regulatory mechanisms governing NPCs and nuclear envelope homeostasis have been implicated in the pathogenesis of several neurodegenerative diseases. The ESCRT-III pathway emerges as a critical player in the surveillance and preservation of well-assembled, functional NPCs, as well as nuclear envelope sealing. Recent studies have provided insights into the involvement of nuclear ESCRT-III in the selective reduction of specific nucleoporins associated with neurodegenerative pathologies. Thus, maintaining quality control of the nuclear envelope and NPCs represents a pivotal element in the pathological cascade leading to neurodegenerative diseases. This review describes the constituents of the nuclear-cytoplasmic transport machinery, encompassing the nuclear envelope, NPC, and ESCRT proteins, and how their structural and functional alterations contribute to the development of neurodegenerative diseases.

Indexed as

Neurodegenerative DiseasesNuclear PoreActive Transport, Cell NucleusEndosomal Sorting Complexes Required for TransportHumansNuclear EnvelopeNuclear Pore Complex ProteinsEndosomal Sorting Complexes Required for TransportNuclear Pore Complex ProteinsALSESCRTFTDneurodegenerationnuclear pore complexnucleocytoplasmic transportnucleoporins

Identifiers

PMID37657945
PMCPMC10612469
OpenAlexW4386360205

What OpenQuestion holds

Textmetadata
LicenceTDM
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.