Evidence map›Paper›PMID 22575750›Full record

ArticlePrion

The ZIP-prion connection.

Sepehr Ehsani, Mohadeseh Mehrabian, Cosmin L Pocanschi, Gerold Schmitt-Ulms

Open access · bronzeAbstract read
In one paragraph

Article in Prion. 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
0.3field-weighted citation impact, top 43% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Prions and prion diseases: Insights from the eye.Experimental eye research · 2020
    Review
  5. Article
  6. Article
  7. Physiological Functions of the Cellular Prion Protein.Frontiers in molecular biosciences · 2017
    Review
  8. Review
  9. Article
  10. 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

4 authors at 2 institutions in 2 countries.

Sepehr EhsaniTanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, ON Canada.
Mohadeseh Mehrabian
Cosmin L Pocanschi
Gerold Schmitt-Ulms
German Center for Neurodegenerative Diseases · DEUniversity of Toronto · CA

Funding

Medical Research Council MC_G1000734Wellcome Trust 089703
6 · The paper itself

Abstract

The evolutionary origins of vertebrate prion genes had remained elusive until recently when multiple lines of evidence converged to the proposition that members of the prion gene family represent an ancient branch of a larger family of ZIP metal ion transporters. (1) A follow-up investigation which explored the mechanism of evolution in more detail led to the surprising conclusion that the emergence of the prion founder gene likely involved the reverse transcription of a spliced transcript of a LIV-1 ZIP predecessor gene. (2) The objective of this perspective is to discuss the possible significance of this reunion of ZIP and prion gene subfamilies for understanding the biology of the prion protein in health and disease. While a recent review article broadly introduced this area of research, (3) the emphasis here is to comment on some of the more pertinent concepts, experimental paradigms, ongoing developments and challenges.

Indexed as

AnimalsCation Transport ProteinsEvolution, MolecularHumansModels, MolecularPrionsZincCation Transport ProteinsPrionsZinc

Identifiers

PMID22575750
PMCPMC3609057
OpenAlexW2005380845

What OpenQuestion holds

Textmetadata
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.