Evidence map›Paper›PMID 26209310›Full record

ArticleDatabase : the journal of biological databases and curation2015

SHIELD: an integrative gene expression database for inner ear research.

Jun Shen, Déborah I Scheffer, Kelvin Y Kwan, David P Corey

Open access · goldAbstract readDataset
In one paragraph

Article in Database : the journal of biological databases and curation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 5 pooled it
7.7field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 5 syntheses or guidelines pooled it, 140 citations in OpenAlex.

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  17. LHFPL5 is a key element in force transmission from the tip link to the hair cell mechanotransducer channel.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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31 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 2 countries.

Jun ShenDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School Center for Hereditary Deafness, jshen5@partners.org.
Déborah I SchefferDepartment of Neurobiology.
Kelvin Y KwanDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA and.
David P CoreyHarvard Medical School Center for Hereditary Deafness, Department of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.
Institute of Neurobiology · BGHereditary Disease Foundation · USRutgers, The State University of New Jersey · US

Funding

MOLECULAR MECHANISMS OF AUDITORY TRANSDUCTIONR01DC000304 · NIDCD · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID P COREY, Marcos Sotomayor · 1989 to 2026
$9.3M
MOLECULAR BASIS OF INHERITED DEAFNESSR01DC002281 · NIDCD · MASSACHUSETTS GENERAL HOSPITAL · PI COREY, DAVID P · 1994 to 2018
$4.4M
Clinical Molecular Genetic Diagnosis of Hearing LossR03DC013866 · NIDCD · BRIGHAM AND WOMEN'S HOSPITAL · PI SHEN, JUN · 2014 to 2016
$601k
Howard Hughes Medical InstituteNIDCD NIH HHS R01-DC000304NIDCD NIH HHS R01-DC002281NIDCD NIH HHS R03 DC013866NIDCD NIH HHS R03-DC013866
6 · The paper itself

Abstract

The inner ear is a highly specialized mechanosensitive organ responsible for hearing and balance. Its small size and difficulty in harvesting sufficient tissue has hindered the progress of molecular studies. The protein components of mechanotransduction, the molecular biology of inner ear development and the genetic causes of many hereditary hearing and balance disorders remain largely unknown. Inner-ear gene expression data will help illuminate each of these areas. For over a decade, our laboratories and others have generated extensive sets of gene expression data for different cell types in the inner ear using various sample preparation methods and high-throughput genome-wide approaches. To facilitate the study of genes in the inner ear by efficient presentation of the accumulated data and to foster collaboration among investigators, we have developed the Shared Harvard Inner Ear Laboratory Database (SHIELD), an integrated resource that seeks to compile, organize and analyse the genomic, transcriptomic and proteomic knowledge of the inner ear. Five datasets are currently available. These datasets are combined in a relational database that integrates experimental data and annotations relevant to the inner ear. The SHIELD has a searchable web interface with two data retrieval options: viewing the gene pages online or downloading individual datasets as data tables. Each retrieved gene page shows the gene expression data and detailed gene information with hyperlinks to other online databases with up-to-date annotations. Downloadable data tables, for more convenient offline data analysis, are derived from publications and are current as of the time of publication. The SHIELD has made published and some unpublished data freely available to the public with the hope and expectation of accelerating discovery in the molecular biology of balance, hearing and deafness.

Indexed as

Databases, GeneticEar, InnerGene Expression RegulationGenome-Wide Association StudyGenomicsMechanotransduction, CellularAnimalsHumans

Identifiers

PMID26209310
PMCPMC4513695
OpenAlexW2108798389

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.