Evidence map›Paper›PMID 27698679›Full record

ArticleExperimental and therapeutic medicine2016

Huntington's disease: Molecular basis of pathology and status of current therapeutic approaches.

Wen-Juan Huang, Wei-Wei Chen, Xia Zhang

Abstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
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  11. Review
  12. Aptamer Applications in Neuroscience.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Protein Misfolding and ER Stress in Huntington's Disease.Frontiers in molecular biosciences · 2019
    Review
  18. 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

3 authors.

Wen-Juan HuangDepartment of Neurology, Xuzhou Central Hospital, Xuzhou, Jiangsu 221009, P.R. China.
Wei-Wei ChenDepartment of Neurology, Xuzhou Central Hospital, Xuzhou, Jiangsu 221009, P.R. China.
Xia ZhangDepartment of Neurology, Xuzhou Central Hospital, Xuzhou, Jiangsu 221009, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Huntington's disease (HD) is a frequent and incurable hereditary neurodegenerative disorder that impairs motor and cognitive functions. Mutations in huntingtin (HTT) protein, which is essential for neuronal development, lead to the development of HD. An increase in the number of CAG repeats within the

Indexed as

CAG repeatsHuntington's diseaseneurodegenerationpolyglutamine tractproteosomal degradationstriatal medium spiny neurons

Identifiers

PMID27698679
PMCPMC5038571

What OpenQuestion holds

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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.