Evidence map›Paper›PMID 27699209›Full record

ArticleeNeuro

Loss of

Yumi Ueki, Grisela Ramirez, Ernesto Salcedo, Maureen E Stabio, Frances Lefcort

Open access · goldAbstract read
In one paragraph

Article in eNeuro. 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
1.5field-weighted citation impact, top 19% 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, 33 citations in OpenAlex.

  1. Article
  2. ELP1 gene augmentation restores visual function in a mouse model of familial dysautonomia.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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  5. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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  11. Elongator regulates the melanocortin satiety pathway.Biochemical and biophysical research communications · 2022
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  12. Article
  13. Article
  14. Article
  15. Article
  16. Bone biomechanical properties and tissue-scale bone quality in a genetic mouse model of familial dysautonomia.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2021
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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.

Yumi UekiDepartment of Cell Biology and Neuroscience, Montana State University , Bozeman, MT 59717.
Grisela RamirezDepartment of Cell and Developmental Biology, University of Colorado School of Medicine , Aurora, CO 80045.
Ernesto SalcedoDepartment of Cell and Developmental Biology, University of Colorado School of Medicine , Aurora, CO 80045.ORCID 0000-0002-1142-8980
Maureen E StabioDepartment of Cell and Developmental Biology, University of Colorado School of Medicine , Aurora, CO 80045.ORCID 0000-0002-2159-5301
Frances LefcortDepartment of Cell Biology and Neuroscience, Montana State University , Bozeman, MT 59717.ORCID 0000-0002-2064-8678
University of Colorado Denver · USMontana State University · US

Funding

WHY DO MUTATIONS IN IKBKAP CAUSE FAMILIAL DYSAUTONOMIA?R01NS086796 · NINDS · MONTANA STATE UNIVERSITY - BOZEMAN · PI LEFCORT, FRANCES · 2014 to 2018
$1.6M
In vivo regeneration of mammalian retinas by Ascl1F32EY023498 · NEI · UNIVERSITY OF WASHINGTON · PI UEKI, YUMI · 2014 to 2015
$117k
NEI NIH HHS F32 EY023498NINDS NIH HHS R01 NS086796
6 · The paper itself

Abstract

Familial dysautonomia (FD) is an autosomal recessive congenital neuropathy that is caused by a mutation in the gene for inhibitor of kappa B kinase complex-associated protein (

Indexed as

AnimalsCarrier ProteinsDisease Models, AnimalDisease ProgressionDysautonomia, FamilialFemaleGene Knockout TechniquesIntracellular Signaling Peptides and ProteinsMaleMelanopsinMice, KnockoutNeurogliaOptic NerveOptic NeuritisPhotoreceptor Cells, VertebrateRetinal DegenerationCarrier ProteinsIkbkap protein, mouseIntracellular Signaling Peptides and ProteinsMelanopsinRod Opsinsfamilial dysautonomiaIKAP/Elp1Ikbkapretinal degenerationretinal ganglion cell

Identifiers

PMID27699209
PMCPMC5037323
OpenAlexW2521795737

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.