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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 2 |
2015 | 5 |
2016 | 1 |
2024 | 0 |
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6 results
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Page 1
Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear.
Nat Commun. 2015 Oct 15;6:8557. doi: 10.1038/ncomms9557.
Nat Commun. 2015.
PMID: 26469390
Free PMC article.
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.
Santos-Cortez RL, Faridi R, Rehman AU, Lee K, Ansar M, Wang X, Morell RJ, Isaacson R, Belyantseva IA, Dai H, Acharya A, Qaiser TA, Muhammad D, Ali RA, Shams S, Hassan MJ, Shahzad S, Raza SI, Bashir ZE, Smith JD, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics; Riazuddin S, Ahmad W, Friedman TB, Leal SM.
Santos-Cortez RL, et al.
Am J Hum Genet. 2016 Feb 4;98(2):331-8. doi: 10.1016/j.ajhg.2015.12.004. Epub 2016 Jan 21.
Am J Hum Genet. 2016.
PMID: 26805784
Free PMC article.
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Challenges and solutions for gene identification in the presence of familial locus heterogeneity.
Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, Ansar M, Jan A, Wang X, Aziz A, Riazuddin S, Smith JD, Wang GT, Ahmed ZM, Gul K, Shearer AE, Smith RJ, Shendure J, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics; Hinnant J, Khan SN, Fisher RA, Ahmad W, Friderici KH, Riazuddin S, Friedman TB, Wilch ES, Leal SM.
Rehman AU, et al.
Eur J Hum Genet. 2015 Sep;23(9):1207-15. doi: 10.1038/ejhg.2014.266. Epub 2014 Dec 10.
Eur J Hum Genet. 2015.
PMID: 25491636
Free PMC article.
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A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
Mujtaba G, Schultz JM, Imtiaz A, Morell RJ, Friedman TB, Naz S.
Mujtaba G, et al.
J Med Genet. 2015 Aug;52(8):548-52. doi: 10.1136/jmedgenet-2015-103023. Epub 2015 May 4.
J Med Genet. 2015.
PMID: 25941349
Free PMC article.
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The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing.
Fang Q, Indzhykulian AA, Mustapha M, Riordan GP, Dolan DF, Friedman TB, Belyantseva IA, Frolenkov GI, Camper SA, Bird JE.
Fang Q, et al.
Elife. 2015 Aug 24;4:e08627. doi: 10.7554/eLife.08627.
Elife. 2015.
PMID: 26302205
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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