Evidence map›Paper›PMID 22440327›Full record

ReviewBiochimica et biophysica acta2012

Ferroportin-mediated iron transport: expression and regulation.

Diane M Ward, Jerry Kaplan

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 197 papers.

0numbers the graph read from it
0cells of the map it votes in
197citing papers in PubMed
9.6field-weighted citation impact, top 1% 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

197 citing papers in PubMed, 367 citations in OpenAlex.

  1. Trial
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  4. mBio · 2026
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  11. PCBP2 Regulates p16Aging cell · 2025
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137 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Diane M WardDepartment of Pathology, School of Medicine, University of Utah, Salt Lake City, Utah 84132, USA.
Jerry Kaplan
University of Utah · US

Funding

Mechanism and Regulation of Iron Export by FerroportinR01DK070947 · NIDDK · UNIVERSITY OF UTAH · PI KAPLAN, JERRY · 2005 to 2014
$3.7M
NIDDK NIH HHS DK070947NIDDK NIH HHS R01 DK070947
6 · The paper itself

Abstract

The distinguishing feature between iron homeostasis in single versus multicellular organisms is the need for multicellular organisms to transfer iron from sites of absorption to sites of utilization and storage. Ferroportin is the only known iron exporter and ferroportin plays an essential role in the export of iron from cells to blood. Ferroportin can be regulated at many different levels including transcriptionally, post-transcriptionally, through mRNA stability and post-translationally, through protein turnover. Additionally, ferroportin may be regulated in both cell-dependent and cell-autonomous fashions. Regulation of ferroportin is critical for iron homeostasis as alterations in ferroportin may result in either iron deficiency or iron overload. This article is part of a Special Issue entitled: Cell Biology of Metals.

Indexed as

Gene ExpressionAnimalsAntimicrobial Cationic PeptidesCations, DivalentCation Transport ProteinsCeruloplasminFerroportinHepcidinsHomeostasisHumansIon TransportIronProtein Processing, Post-TranslationalProtein Structure, TertiaryRNA StabilityTranscriptional ActivationAntimicrobial Cationic PeptidesCations, DivalentCation Transport ProteinsCeruloplasminFerroportinHepcidinsIron

Identifiers

PMID22440327
PMCPMC3718258
OpenAlexW1972051185

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.