A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

scientific article published on 12 October 2017

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2017NatCo...8..886B
P356DOI10.1038/S41467-017-00595-4
P932PMC publication ID5638796
P698PubMed publication ID29026089

P50authorKaren SteelQ15109532
Allan BradleyQ4730491
Paul FlicekQ28359506
Martin Hrabě de AngelisQ28606776
Ann-Marie MallonQ29840828
Natasha A KarpQ30511243
Colin McKerlieQ37370526
Yann HéraultQ37632594
Damian SmedleyQ44820039
Helen ParkinsonQ47502891
Terrence F MeehanQ54303383
Kent LloydQ56957396
Neil J InghamQ59564661
Michael R BowlQ59582965
Jeremy C. MasonQ59661468
Lauryl M NutterQ63616236
Karen L SvensonQ64363743
S. WellsQ67390418
J.K. WhiteQ67390425
L.R. BowerQ67390428
W. WurstQ67390467
David J AdamsQ87690616
Shigeharu WakanaQ88392157
Monica J JusticeQ88679010
Lydia TeboulQ89168958
Arthur L BeaudetQ89587667
Robert E. BraunQ92436993
John R SeavittQ104607149
Heather CaterQ104607150
Marie-Michelle SimonQ114293521
Ann M FlennikenQ114429503
Hamid MezianeQ114429525
William C SkarnesQ114429575
International Mouse Phenotyping ConsortiumQ114429593
Dave A ClaryQ114429596
P2093author name stringXiang Gao
David B West
Glauco P Tocchini-Valentini
Mark Moore
Steve D M Brown
Stephen A Murray
Osamu Minowa
Sarah Taylor
Mary E Dickinson
Patrick Reilly
Luis Santos
Simon Greenaway
Natalja Kurbatova
Lois Kelsey
Selina Pearson
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Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing lossQ35377676
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Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss.Q36432004
Quiet as a mouse: dissecting the molecular and genetic basis of hearingQ37087936
Molecular characterization of mutant mouse strains generated from the EUCOMM/KOMP-CSD ES cell resourceQ37100323
Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function.Q37219083
ENU mutagenesis, a way forward to understand gene functionQ37307784
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Hearing impairment: a panoply of genes and functionsQ37801082
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A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairmentQ43199676
Using the Auditory Brainstem Response (ABR) to Determine Sensitivity of Hearing in Mutant MiceQ50435456
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue1
P407language of work or nameEnglishQ1860
P921main subjecthearing lossQ16035842
P304page(s)886
P577publication date2017-10-12
P1433published inNature CommunicationsQ573880
P1476titleA large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
P478volume8

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cites work (P2860)
Q90398364Association between Leucocyte Telomere Length and Risk of Hearing Loss in the General Population: A Case-Control Study in Zhejiang Province, China
Q64039625Deficit of mitogen-activated protein kinase phosphatase 1 (DUSP1) accelerates progressive hearing loss
Q90351355GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank
Q90911195Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment
Q57492996Glucose tolerance and insulin sensitivity define adipocyte transcriptional programs in human obesity
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Q62937718MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss
Q64056695Mouse screen reveals multiple new genes underlying mouse and human hearing loss
Q92094940Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes
Q92283778New models for human disease from the International Mouse Phenotyping Consortium
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