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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 1 |
2014 | 2 |
2015 | 2 |
2024 | 0 |
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4 results
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Page 1
Expression and replication studies to identify new candidate genes involved in normal hearing function.
PLoS One. 2014 Jan 14;9(1):e85352. doi: 10.1371/journal.pone.0085352. eCollection 2014.
PLoS One. 2014.
PMID: 24454846
Free PMC article.
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss.
Girotto G, Abdulhadi K, Buniello A, Vozzi D, Licastro D, d'Eustacchio A, Vuckovic D, Alkowari MK, Steel KP, Badii R, Gasparini P.
Girotto G, et al.
PLoS One. 2013 Dec 2;8(12):e80323. doi: 10.1371/journal.pone.0080323. eCollection 2013.
PLoS One. 2013.
PMID: 24312468
Free PMC article.
Clinical Trial.
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A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
Nyegaard M, Rendtorff ND, Nielsen MS, Corydon TJ, Demontis D, Starnawska A, Hedemand A, Buniello A, Niola F, Overgaard MT, Leal SM, Ahmad W, Wikman FP, Petersen KB, Crüger DG, Oostrik J, Kremer H, Tommerup N, Frödin M, Steel KP, Tranebjærg L, Børglum AD.
Nyegaard M, et al.
PLoS Genet. 2015 Jul 21;11(7):e1005386. doi: 10.1371/journal.pgen.1005386. eCollection 2015 Jul.
PLoS Genet. 2015.
PMID: 26197441
Free PMC article.
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ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells.
Morozko EL, Nishio A, Ingham NJ, Chandra R, Fitzgerald T, Martelletti E, Borck G, Wilson E, Riordan GP, Wangemann P, Forge A, Steel KP, Liddle RA, Friedman TB, Belyantseva IA.
Morozko EL, et al.
Hum Mol Genet. 2015 Feb 1;24(3):609-24. doi: 10.1093/hmg/ddu474. Epub 2014 Sep 12.
Hum Mol Genet. 2015.
PMID: 25217574
Free PMC article.
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