Evidence map›Paper›PMID 23376683›Full record

ArticleNeurobiology of disease2013

Altered Purkinje cell miRNA expression and SCA1 pathogenesis.

Edgardo Rodriguez-Lebron, Gumei Liu, Megan Keiser, Mark A Behlke, Beverly L Davidson

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of disease, 2013. 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
2.1field-weighted citation impact, top 14% 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, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. RGS2 and female common diseases: a guard of women's health.Journal of translational medicine · 2023
    Review
  5. Article
  6. Modified level of miR-376a is associated with Parkinson's disease.Journal of cellular and molecular medicine · 2020
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. The Emerging Role of microRNAs in Polyglutamine Diseases.Frontiers in molecular neuroscience · 2019
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Unravelling Endogenous MicroRNA System Dysfunction as a New Pathophysiological Mechanism in Machado-Joseph Disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Article
  17. Article
  18. 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

5 authors at 2 institutions in 1 country.

Edgardo Rodriguez-LebronDepartment of Internal Medicine, University of Iowa, Iowa City, IA 52242, USA.
Gumei Liu
Megan Keiser
Mark A Behlke
Beverly L Davidson
University of Iowa · USIntegrated DNA Technologies (United States) · US

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
RNAI for Huntington's DiseaseP01NS050210 · NINDS · UNIVERSITY OF IOWA · PI DAVIDSON, BEVERLY L. · 2005 to 2009
$6.5M
Gene therapy for dominant neurodegenerative diseasesR01HD044093 · NICHD · UNIVERSITY OF IOWA · PI DAVIDSON, BEVERLY L · 2002 to 2006
$1.1M
Splice isoform-specific RNAi as therapy for Spinocerebellar Ataxia type 6R21NS072229 · NINDS · UNIVERSITY OF IOWA · PI RODRIGUEZ, EDGARDO · 2011 to 2012
$415k
NICHD NIH HHS R01 HD044093NIEHS NIH HHS P30 ES005605NINDS NIH HHS NS 072229NINDS NIH HHS NS 44093NINDS NIH HHS NS 50210NINDS NIH HHS P01 NS050210NINDS NIH HHS R21 NS072229
6 · The paper itself

Abstract

Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disorder caused by polyglutamine repeat expansions in Ataxin-1. Recent evidence supports a role for microRNAs (miRNAs) deregulation in SCA1 pathogenesis. However, the extent to which miRNAs may modulate the onset, progression or severity of SCA1 remains largely unknown. In this study, we used a mouse model of SCA1 to determine if miRNAs are misregulated in pre- and post-symptomatic SCA1 cerebellum. We found a significant alteration in the steady-state levels of numerous miRNAs prior to and following phenotypic onset. In addition, we provide evidence that increased miR-150 levels in SCA1 Purkinje neurons may modulate disease pathogenesis by targeting the expression of Rgs8 and Vegfa.

Indexed as

AnimalsAtaxin-1AtaxinsDisease Models, AnimalGene Expression RegulationImmunohistochemistryIn Situ HybridizationMiceMice, TransgenicMicroRNAsNerve Tissue ProteinsNuclear ProteinsPolymerase Chain ReactionPurkinje CellsRGS ProteinsSpinocerebellar AtaxiasAtaxin-1AtaxinsAtxn1 protein, mouseMicroRNAsNerve Tissue ProteinsNuclear ProteinsRGS8 protein, mouseRGS ProteinsVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID23376683
PMCPMC3629010
OpenAlexW2008512986

What OpenQuestion holds

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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.