Evidence map›Paper›PMID 29173981›Full record

ArticleMolecular genetics and metabolism2017

Glucocerebrosidase haploinsufficiency in A53T α-synuclein mice impacts disease onset and course.

Nahid Tayebi, Loukia Parisiadou, Bahafta Berhe, Ashley N Gonzalez, Jenny Serra-Vinardell, Raphael J Tamargo, Emerson Maniwang, Zachary Sorrentino, Hideji Fujiwara, Richard J Grey and 10 more

Open access · greenAbstract read
In one paragraph

Article in Molecular genetics and metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-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

26 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  9. Article
  10. International journal of molecular sciences · 2023
    Review
  11. Review
  12. Article
  13. Live cellFrontiers in cellular neuroscience · 2023
    Article
  14. Article
  15. Article
  16. Behavioral Phenotyping in a Murine Model ofInternational journal of molecular sciences · 2021
    Article
  17. The cell biology of Parkinson's disease.The Journal of cell biology · 2021
    Review
  18. Review
  19. Review
  20. 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

20 authors at 5 institutions in 1 country.

Nahid TayebiMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Loukia ParisiadouDepartment of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Bahafta BerheMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Ashley N GonzalezMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Jenny Serra-VinardellMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Raphael J TamargoMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Emerson ManiwangMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Zachary SorrentinoDepartment of Neuroscience, Center for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, FL, USA.
Hideji FujiwaraDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Richard J GreyMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Shahzeb HassanMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Yotam N Blech-HermoniMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA.
Chuyu ChenDepartment of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Ryan McGlincheyLaboratory of Protein Conformation and Dynamics, NHLBI, NIH, Bethesda, MD. USA.
Chrissy Makariou-PikisDepartment of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Mieu BrooksDepartment of Neuroscience, Center for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, FL, USA.
Edward I GinnsLysosomal Disorders Treatment and Research Program, University of Massachusetts Medical School, Worcester, MA, USA.
Daniel S OryDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Benoit I GiassonDepartment of Neuroscience, Center for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, FL, USA.
Ellen SidranskyMedical Genetics Branch, NHGRI, NIH, Bethesda, MD, USA. Electronic address: sidranse@mail.nih.gov.
National Human Genome Research Institute · USNorthwestern University · USUniversity of Florida · USWashington University in St. Louis · USUniversity of Massachusetts Chan Medical School · US

Funding

Genetic and clinical studies of Gaucher disease and other lysosomal disordersZIAHG200336 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI SIDRANSKY, ELLEN · 2009 to 2025
$45.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
LRRK2-mediated molecular and synaptic events in the striatumR01NS097901 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PARISIADOU, LOUKIA · 2016 to 2020
$2.0M
Mechanisms of Aggregated Alpha-Synuclein Induction and ProgressionR01NS089622 · NINDS · UNIVERSITY OF FLORIDA · PI GIASSON, BENOIT I · 2014 to 2018
$1.6M
OXYSTEROL BIOMARKERS FOR NIEMANN-PICK C DISEASER01NS081985 · NINDS · WASHINGTON UNIVERSITY · PI ORY, DANIEL S, SCHAFFER, JEAN E. · 2013 to 2017
$1.3M
Intramural NIH HHS Z99 HG999999NIDDK NIH HHS P30 DK020579NINDS NIH HHS R01 NS081985NINDS NIH HHS R01 NS089622NINDS NIH HHS R01 NS097901
6 · The paper itself

Abstract

Mutations in GBA1 encountered in Gaucher disease are a leading risk factor for Parkinson disease and associated Lewy body disorders. Many GBA1 mutation carriers, especially those with severe or null GBA1 alleles, have earlier and more progressive parkinsonism. To model the effect of partial glucocerebrosidase deficiency on neurological progression in vivo, mice with a human A53T α-synuclein (SNCA

Indexed as

HaploinsufficiencyAge of Onsetalpha-SynucleinAnimalsbeta-GlucosidaseBrainDisease Models, AnimalFemaleGaucher DiseaseGlucosylceramidaseGlucosylceramidesHeterozygoteHumansMaleMiceMice, Knockoutalpha-Synucleinbeta-GlucosidaseGlucosylceramidaseGlucosylceramidesPsychosineSNCA protein, humanSnca protein, mousesphingosyl beta-glucosideAggregatesGaucher diseaseGlucocerebrosidaseMouse modelParkinson diseaseα-synuclein

Identifiers

PMID29173981
PMCPMC6007972
OpenAlexW2768738386

What OpenQuestion holds

Textmetadata
LicenceTDM
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.