Evidence map›Paper›PMID 24735419›Full record

ReviewAnnals of the New York Academy of Sciences2014

Translational research investigations on ATP7A: an important human copper ATPase.

Stephen G Kaler

Open access · greenAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. FOXC1-ATP7A Axis Activates PI3K/AKT Signaling to Suppress Cuproptosis and Drive Fibroblast Pathogenesis in Rheumatoid Arthritis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Copper metabolism as a unique vulnerability in cancer.Biochimica et biophysica acta. Molecular cell research · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Bioavailable Trace Metals in Neurological Diseases.Current treatment options in neurology · 2016
    Review
  12. Review
  13. Endogenous concentrations of biologically relevant metals in rat brain and cochlea determined by inductively coupled plasma mass spectrometry.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2015
    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

1 author at 1 institution in 1 country.

Stephen G KalerSection on Translational Neuroscience, Molecular Medicine Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
Eunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Inherited Disorders of Copper TransportZIAHD008768 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KALER, STEPHEN · 2009 to 2019
$5.5M
Mechanisms of Motor Neuron DiseaseZIAHD008892 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KALER, STEPHEN · 2009 to 2019
$2.2M
Intramural NIH HHS ZIA HD008768
6 · The paper itself

Abstract

In more than 40 years since copper deficiency was delineated in pediatric subjects with Menkes disease, remarkable advances in our understanding of the clinical, biochemical, and molecular aspects of the human copper transporter ATP7A have emerged. Mutations in the gene encoding this multitasking molecule are now implicated in at least two other distinctive phenotypes: occipital horn syndrome and ATP7A-related isolated distal motor neuropathy. Several other novel inherited disorders of copper metabolism have been identified in the past several years, aided by advances in human gene mapping and automated DNA sequencing. In this paper, I review the history and evolution of our understanding of disorders caused by impaired ATP7A function, and outline future challenges.

Indexed as

Adenosine TriphosphatasesCation Transport ProteinsCopperCopper-Transporting ATPasesCutis LaxaEhlers-Danlos SyndromeGene Transfer TechniquesHumansMenkes Kinky Hair SyndromeMetal Metabolism, Inborn ErrorsAdenosine TriphosphatasesATP7A protein, humanCation Transport ProteinsCopperCopper-Transporting ATPasesATP7Ahuman copper metabolismMenkes diseaseoccipital horn syndromeviral gene therapy

Identifiers

PMID24735419
PMCPMC4095951
OpenAlexW2161313420

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.