Evidence map›Paper›PMID 26330608›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Expanding the prion disease repertoire.

Surachai Supattapone

Abstract readComment
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Surachai SupattaponeDepartments of Biochemistry and Medicine, Geisel School of Medicine at Dartmouth, Hanover, NH 03755 supattapone@dartmouth.edu.

Funding

Origin and Mechanism of Promiscuous Prion StrainsR01NS046478 · NINDS · DARTMOUTH COLLEGE · PI SUPATTAPONE, SURACHAI · 2004 to 2017
$5.0M
NINDS NIH HHS R01 NS046478
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

alpha-SynucleinAnimalsFemaleHumansMaleMultiple System AtrophyParkinsonian DisordersPrionsalpha-SynucleinPrions

Identifiers

PMID26330608
PMCPMC4586830

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.