Evidence map›Paper›PMID 26247888›Full record

ReviewJournal of neuroscience methods2015

α-Synuclein and nonhuman primate models of Parkinson's disease.

Scott C Vermilyea, Marina E Emborg

Abstract readReview
In one paragraph

Review in Journal of neuroscience methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Parkinson's Disease: Exploring Different Animal Model Systems.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Acute Exposure to the Food-Borne PathogenJournal of inflammation research · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Non-human primate models of PD to test novel therapies.Journal of neural transmission (Vienna, Austria : 1996) · 2018
    Review
  20. α-Synuclein nonhuman primate models of Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2018
    Review
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

2 authors.

Scott C VermilyeaNeuroscience Training Program, University of Wisconsin, Madison, United States; Wisconsin National Primate Research Center, University of Wisconsin, Madison, United States. Electronic address: svermilyea@primate.wisc.edu.
Marina E EmborgNeuroscience Training Program, University of Wisconsin, Madison, United States; Wisconsin National Primate Research Center, University of Wisconsin, Madison, United States; Department of Medical Physics, University of Wisconsin, Madison, 1220 Capitol Court, Madison, WI 53715, United States. Electronic address: emborg@primate.wisc.edu.

Funding

WNPRC Supplemental Request for Nonhuman Primate Enclosures to Equip HIV/AIDS-Related Research FacilitiesP51OD011106 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI Dorota A. Grejner-Brzezinska · 2012 to 2026
$150.7M
Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
NEUROSCIENCE TRAINING PROGRAMT32GM007507 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HALLORAN, MARY C · 1985 to 2017
$9.3M
EXTRAMURAL RES FACIL CONST: REPRODUCTIVE, GROWTH &DVMT, MENOPAUSEC06RR020141 · NCRR · UNIVERSITY OF WISCONSIN MADISON · PI CADWALLADER, MARTIN · 2004 to 2004
$3.6M
Transgenic marmosets for translational stem cell researchR24OD019803 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI EMBORG, MARINA, GOLOS, THADDEUS G · 2015 to 2018
$2.7M
EXTRAMURAL REGIONAL FACILITIES CONSTRUCTIONC06RR015459 · NCRR · UNIVERSITY OF WISCONSIN MADISON · PI CADWALLADER, MARTIN · 2000 to 2000
$1.9M
NCATS NIH HHS UL1 TR000427NCATS NIH HHS UL1TR000427NCRR NIH HHS C06 RR015459NCRR NIH HHS C06 RR020141NCRR NIH HHS RR020141-01NCRR NIH HHS RR15459-01NIGMS NIH HHS T32 GM007507NIH HHS P51 OD011106NIH HHS P51OD011106NIH HHS P51OD011106-53S2NIH HHS R24 OD019803
6 · The paper itself

Abstract

Accumulation of α-synuclein (α-syn) leading to the formation of insoluble intracellular aggregates named Lewy bodies is proposed to have a significant role in Parkinson's disease (PD) pathology. Nonhuman primate (NHP) models of PD have proven essential for understanding the neurobiological basis of the disease and for the preclinical evaluation of first-in-class and invasive therapies. In addition to neurotoxin, aging and intracerebral gene transfer models, a new generation of models using inoculations of α-syn formulations, as well as transgenic methods is emerging. Understanding of their advantages and limitations will be essential when choosing a platform to evaluate α-syn-related pathology and interpreting the test results of new treatments targeting α-syn aggregation. In this review we aim to provide insight on this issue by critically analyzing the differences in endogenous α-syn, as well as α-syn pathology in PD and PD NHP models.

Indexed as

alpha-SynucleinAnimalsBrainHumansParkinsonian DisordersPrimatesalpha-SynucleinAlpha synucleinAnimal modelsLewy bodyLewy neuriteNonhuman primatesParkinson's disease

Identifiers

PMID26247888
PMCPMC4604057

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.