Evidence map›Paper›PMID 28100642›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2017

Isoform-specific mechanisms of α3β4*-nicotinic acetylcholine receptor modulation by the prototoxin lynx1.

Andrew A George, Abigail Bloy, Julie M Miwa, Jon M Lindstrom, Ronald J Lukas, Paul Whiteaker

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Analogs of α-conotoxin PnIC selectively inhibit α7β2- over α7-only subtype nicotinic acetylcholine receptors via a novel allosteric mechanism.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Concatemers to re-investigate the role of α5 in α4β2 nicotinic receptors.Cellular and molecular life sciences : CMLS · 2021
    Article
  8. Review
  9. Implications of Oligomeric Amyloid-Beta (oAβThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Evolution and Medical Significance of LU Domain-Containing Proteins.International journal of molecular sciences · 2019
    Review
  18. Article
  19. Review
  20. 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

6 authors at 4 institutions in 2 countries.

Andrew A GeorgeDivision of Neurobiology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA; andrew.george@dignityhealth.org.
Abigail BloyDivision of Neurobiology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.
Julie M MiwaDepartment of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania, USA.
Jon M LindstromDepartment of Neuroscience, University of Pennsylvania Medical School, Philadelphia, Pennsylvania, USA.
Ronald J LukasDivision of Neurobiology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.
Paul WhiteakerDivision of Neurobiology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.
Barrow Neurological Institute · USLehigh University · USSt. Joseph's Hospital and Medical Center · USUniversity of Pennsylvania · US

Funding

Variants in CHRNA5/CHRNA3/CHRNB4 and nicotine dependenceR21DA027070 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI CHEN, XIANGNING · 2009 to 2010
$897k
Construction and Expression of Concatemeric alpha6beta2* Nicotinic Acetycholine RR21DA026627 · NIDA · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI WHITEAKER, PAUL · 2009 to 2010
$407k
NIDA NIH HHS R21 DA026627NIDA NIH HHS R21 DA027070
6 · The paper itself

Abstract

This study investigates-for the first time to our knowledge-the existence and mechanisms of functional interactions between the endogenous mammalian prototoxin, lynx1, and α3- and β4-subunit-containing human nicotinic acetylcholine receptors (α3β4*-nAChRs). Concatenated gene constructs were used to express precisely defined α3β4*-nAChR isoforms (α3β4)

Indexed as

Action PotentialsAdaptor Proteins, Signal TransducingAnimalsCell MembraneGPI-Linked ProteinsHumansProtein BindingProtein IsoformsProtein SubunitsProtein TransportReceptors, NicotinicXenopusAdaptor Proteins, Signal TransducingGPI-Linked ProteinsLYNX1 protein, humanProtein IsoformsProtein SubunitsReceptors, Nicotinicconcatenated receptor subunitsGPI-linked proteinsneurotoxinssingle-channel electrophysiologyTEVC

Identifiers

PMID28100642
PMCPMC5349798
OpenAlexW2578147267

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.