Evidence map›Paper›PMID 30046585›Full record

ArticleInternational journal of genomics2018

Cerebellar lncRNA Expression Profile Analysis of SCA3/MJD Mice.

Zhe Long, Tianjiao Li, Zhao Chen, Yun Peng, Chunrong Wang, Xiaocan Hou, Hongyu Yuan, Puzhi Wang, Yue Xie, Lang He and 6 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of genomics, 2018. 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
0.3field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

16 authors at 2 institutions in 3 countries.

Zhe LongDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Tianjiao LiDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Zhao ChenDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Yun PengDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Chunrong WangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Xiaocan HouDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Hongyu YuanDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Puzhi WangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Yue XieDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Lang HeDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Xin ZhouDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Huirong PengDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Rong QiuSchool of Information Science and Engineering, Central South University, Changsha, Hunan 410083, China.
Kun XiaLaboratory of Medical Genetics, Central South University, Changsha, Hunan 410078, China.
Beisha TangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.ORCID 0000-0003-2120-1576
Hong JiangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.ORCID 0000-0003-2812-4120
Central South University · CNThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinocerebellar ataxia type 3 (SCA3) or Machado-Joseph disease (MJD) is the most common autosomal dominant spinocerebellar ataxia in China with highly clinical heterogeneity, such as progressive cerebellar ataxia, dysarthria, pyramidal signs, external ophthalmoplegia, dysphagia, and distal muscle atrophy. It is caused by the abnormal expansion of CAG repeats in a coding region of

Identifiers

PMID30046585
PMCPMC6036799
OpenAlexW2810623869

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.