Evidence map›Paper›PMID 21479110›Full record

ArticlePLoS currents2011

Circadian Abnormalities in Motor Activity in a BAC Transgenic Mouse Model of Huntington's Disease.

Stephen Oakeshott, Fuat Balci, Igor Filippov, Carol Murphy, Russell Port, David Connor, Ahmad Paintdakhi, Joseph Lesauter, Liliana Menalled, Sylvie Ramboz and 4 more

Open access · greenAbstract read
In one paragraph

Article in PLoS currents, 2011. 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
1.9field-weighted citation impact, top 16% 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, 44 citations in OpenAlex.

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  15. High-throughput analysis of behavior for drug discovery.European journal of pharmacology · 2015
    Review
  16. Review
  17. Article
  18. How to fix a broken clock.Trends in pharmacological sciences · 2013
    Article
  19. Article
  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

14 authors at 4 institutions in 1 country.

Stephen OakeshottPsychoGenics, Inc.; Princeton University; Barnard College; CHDI Foundation; Barnard College and Columbia University and PsychoGenics/Columbia Univ.
Fuat Balci
Igor Filippov
Carol Murphy
Russell Port
David Connor
Ahmad Paintdakhi
Joseph Lesauter
Liliana Menalled
Sylvie Ramboz
Seung Kwak
David Howland
Rae Silver
Dani Brunner
Barnard College · USCHDI Foundation · USPrinceton University · USTarget (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Huntington's disease (HD) is a progressive neurodegenerative disease marked by psychiatric and motor problems. Recently, these findings have been extended to deficits in sleep and circadian function that can be observed in HD patients and in HD mouse models, with abnormal sleep patterns correlating with symptom severity in patients. Here, we studied the behavior of the BAC HD mouse model using an 24/7 automated system; the results indicate significant lengthening of the circadian period in the mutant mice. These results reinforce previous findings in HD models and symptomatic HD patients, indicating that circadian dysfunction is a core feature of HD.

Identifiers

PMID21479110
PMCPMC3072044
OpenAlexW2054021269

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.