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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2006 1
2009 1
2010 8
2011 6
2012 1
2013 1
2020 0
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16 results
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Page 1
Hereditary hearing loss: from human mutation to mechanism.
Lenz DR, Avraham KB. Lenz DR, et al. Hear Res. 2011 Nov;281(1-2):3-10. doi: 10.1016/j.heares.2011.05.021. Epub 2011 Jun 6. Hear Res. 2011. PMID: 21664957 Review.
Hearing impairment: a panoply of genes and functions.
Dror AA, Avraham KB. Dror AA, et al. Neuron. 2010 Oct 21;68(2):293-308. doi: 10.1016/j.neuron.2010.10.011. Neuron. 2010. PMID: 20955936 Free article. Review.
Hearing loss: a common disorder caused by many rare alleles.
Raviv D, Dror AA, Avraham KB. Raviv D, et al. Ann N Y Acad Sci. 2010 Dec;1214:168-79. doi: 10.1111/j.1749-6632.2010.05868.x. Ann N Y Acad Sci. 2010. PMID: 21175685 Free PMC article. Review.
Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity.
Clough RL, Sud R, Davis-Silberman N, Hertzano R, Avraham KB, Holley M, Dawson SJ. Clough RL, et al. Biochem Biophys Res Commun. 2004 Nov 5;324(1):372-81. doi: 10.1016/j.bbrc.2004.09.074. Biochem Biophys Res Commun. 2004. PMID: 15465029
Connexin-associated deafness and speech perception outcome of cochlear implantation.
Taitelbaum-Swead R, Brownstein Z, Muchnik C, Kishon-Rabin L, Kronenberg J, Megirov L, Frydman M, Hildesheimer M, Avraham KB. Taitelbaum-Swead R, et al. Arch Otolaryngol Head Neck Surg. 2006 May;132(5):495-500. doi: 10.1001/archotol.132.5.495. Arch Otolaryngol Head Neck Surg. 2006. PMID: 16702564
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.
Pierce SB, Chisholm KM, Lynch ED, Lee MK, Walsh T, Opitz JM, Li W, Klevit RE, King MC. Pierce SB, et al. Proc Natl Acad Sci U S A. 2011 Apr 19;108(16):6543-8. doi: 10.1073/pnas.1103471108. Epub 2011 Apr 4. Proc Natl Acad Sci U S A. 2011. PMID: 21464306 Free PMC article.
A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA.
Walsh VL, Raviv D, Dror AA, Shahin H, Walsh T, Kanaan MN, Avraham KB, King MC. Walsh VL, et al. Mamm Genome. 2011 Apr;22(3-4):170-7. doi: 10.1007/s00335-010-9310-6. Epub 2010 Dec 17. Mamm Genome. 2011. PMID: 21165622
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
Shahin H, Walsh T, Rayyan AA, Lee MK, Higgins J, Dickel D, Lewis K, Thompson J, Baker C, Nord AS, Stray S, Gurwitz D, Avraham KB, King MC, Kanaan M. Shahin H, et al. Eur J Hum Genet. 2010 Apr;18(4):407-13. doi: 10.1038/ejhg.2009.190. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888295 Free PMC article.
Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.
Pierce SB, Walsh T, Chisholm KM, Lee MK, Thornton AM, Fiumara A, Opitz JM, Levy-Lahad E, Klevit RE, King MC. Pierce SB, et al. Am J Hum Genet. 2010 Aug 13;87(2):282-8. doi: 10.1016/j.ajhg.2010.07.007. Epub 2010 Jul 30. Am J Hum Genet. 2010. PMID: 20673864 Free PMC article.
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families.
Brownstein Z, Friedman LM, Shahin H, Oron-Karni V, Kol N, Abu Rayyan A, Parzefall T, Lev D, Shalev S, Frydman M, Davidov B, Shohat M, Rahile M, Lieberman S, Levy-Lahad E, Lee MK, Shomron N, King MC, Walsh T, Kanaan M, Avraham KB. Brownstein Z, et al. Genome Biol. 2011 Sep 14;12(9):R89. doi: 10.1186/gb-2011-12-9-r89. Genome Biol. 2011. PMID: 21917145 Free PMC article.
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