Evidence map›Paper›PMID 40414313›Full record

ReviewNeurobiology of disease2025

A primer on copper biology in the brain.

Alicia R Lane, Blaine R Roberts, Christoph J Fahrni, Victor Faundez

Abstract readReview
In one paragraph

Review in Neurobiology of disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

4 authors.

Alicia R LaneDepartment of Cell Biology, Emory University, 615 Michael St, Atlanta, GA 30322, USA. Electronic address: alane5@emory.edu.
Blaine R RobertsDepartment of Biochemistry, Emory University, 1510 Clifton Rd, Atlanta, GA 30322, USA; Department of Neurology, Emory University, 12 Executive Park Dr NE, Atlanta, GA 30322, USA. Electronic address: blaine.roberts@emory.edu.
Christoph J FahrniSchool of Chemistry & Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA; Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, USA. Electronic address: christoph.fahrni@chemistry.gatech.edu.
Victor FaundezDepartment of Cell Biology, Emory University, 615 Michael St, Atlanta, GA 30322, USA. Electronic address: vfaunde@emory.edu.

Funding

The Emory Healthy Brain Study: Discovering Predictive Biomarkers for Alzheimer's DiseaseR01AG070937 · NIA · EMORY UNIVERSITY · PI LAH, JAMES J · 2021 to 2025
$35.2M
Neuronal Mechanisms of Copper Transport and ToxicityRF1AG060285 · NIA · EMORY UNIVERSITY · PI FAUNDEZ, VICTOR · 2018 to 2021
$2.4M
Molecular Tools to Illuminate Copper Transport and HomeostasisR35GM136404 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI FAHRNI, CHRISTOPH J · 2020 to 2024
$2.2M
Deciphering the IgG glycosylation code of Alzheimer's DiseaseR01AG085587 · NIA · EMORY UNIVERSITY · PI Blaine Russell Roberts, ERIC JOHN SUNDBERG · 2024 to 2026
$1.6M
Mitochondrial mechanisms and signaling in manganese exposureR01ES034796 · NIEHS · EMORY UNIVERSITY · PI AVANTI GOKHALE, Erica Marlis Werner · 2023 to 2026
$1.4M
Metabolic Mechanisms of Copper-Dependent Neurodegeneration and Excitability in Menkes DiseaseF31NS127419 · NINDS · EMORY UNIVERSITY · PI LANE, ALICIA R · 2022 to 2024
$143k
NIA NIH HHS R01 AG070937NIA NIH HHS R01 AG085587NIA NIH HHS RF1 AG060285NIEHS NIH HHS R01 ES034796NIGMS NIH HHS R35 GM136404NINDS NIH HHS F31 NS127419
6 · The paper itself

Abstract

This primer aims to expose scientists who study the brain to the field of copper biology. We briefly discuss key copper homeostasis mechanisms and proteins and place these functions in the context of the brain and neurodevelopment. A small number of key copper genes are explored as representative examples of the importance of this metal to the brain. We show that these genes are expressed throughout the brain and their defects are linked to a diverse array of neurological phenotypes, which we discuss further in the context of several neurological and neurodegenerative diseases associated with dysregulation of copper. This review aims to expose interested scientists to the fundamental roles for copper in the brain, the primary proteins responsible for maintaining copper homeostasis in the brain, and the classic neurological diseases associated with this metal.

Indexed as

BrainCopperAnimalsHomeostasisHumansCopperCopperCopper biologyMetabolismMitochondriaNeurodegenerative diseaseNeurodevelopment

Identifiers

PMID40414313
PMCPMC12264972

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.