DC03402/DC/NIDCD NIH HHS/United States[Grants and Funding] - Search Results

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Subject: DC03402/DC/NIDCD NIH HHS/United States[Grants and - PubMed

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Results by year

Year	Number of Results
1998	2
1999	2
2000	2
2001	2
2002	3
2003	2
2004	2
2005	4
2006	3
2007	3
2008	2
2010	1
2011	1
2012	1
2014	1
2024	0

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Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.

Robertson NG, O'Malley JT, Ong CA, Giersch AB, Shen J, Stankovic KM, Morton CC. Robertson NG, et al. J Assoc Res Otolaryngol. 2014 Dec;15(6):961-74. doi: 10.1007/s10162-014-0481-9. Epub 2014 Jul 22. J Assoc Res Otolaryngol. 2014. PMID: 25049087 Free PMC article.

A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domain.

Cho HJ, Park HJ, Trexler M, Venselaar H, Lee KY, Robertson NG, Baek JI, Kang BS, Morton CC, Vriend G, Patthy L, Kim UK. Cho HJ, et al. J Mol Med (Berl). 2012 Nov;90(11):1321-1331. doi: 10.1007/s00109-012-0911-2. Epub 2012 May 19. J Mol Med (Berl). 2012. PMID: 22610276 Free PMC article.

Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder.

Jones SM, Robertson NG, Given S, Giersch AB, Liberman MC, Morton CC. Jones SM, et al. Hear Res. 2011 Feb;272(1-2):42-8. doi: 10.1016/j.heares.2010.11.002. Epub 2010 Nov 10. Hear Res. 2011. PMID: 21073934 Free PMC article.

A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.

Robertson NG, Jones SM, Sivakumaran TA, Giersch AB, Jurado SA, Call LM, Miller CE, Maison SF, Liberman MC, Morton CC. Robertson NG, et al. Hum Mol Genet. 2008 Nov 1;17(21):3426-34. doi: 10.1093/hmg/ddn236. Epub 2008 Aug 12. Hum Mol Genet. 2008. PMID: 18697796 Free PMC article.

Expression studies of osteoglycin/mimecan (OGN) in the cochlea and auditory phenotype of Ogn-deficient mice.

Williamson RE, Darrow KN, Giersch AB, Resendes BL, Huang M, Conrad GW, Chen ZY, Liberman MC, Morton CC, Tasheva ES. Williamson RE, et al. Hear Res. 2008 Mar;237(1-2):57-65. doi: 10.1016/j.heares.2007.12.006. Epub 2007 Dec 28. Hear Res. 2008. PMID: 18243607 Free PMC article.

Ion channel gene expression in the inner ear.

Gabashvili IS, Sokolowski BH, Morton CC, Giersch AB. Gabashvili IS, et al. J Assoc Res Otolaryngol. 2007 Sep;8(3):305-28. doi: 10.1007/s10162-007-0082-y. Epub 2007 Jun 1. J Assoc Res Otolaryngol. 2007. PMID: 17541769 Free PMC article.

Methylthioadenosine phosphorylase (MTAP) in hearing: gene disruption by chromosomal rearrangement in a hearing impaired individual and model organism analysis.

Williamson RE, Darrow KN, Michaud S, Jacobs JS, Jones MC, Eberl DF, Maas RL, Liberman MC, Morton CC. Williamson RE, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1630-9. doi: 10.1002/ajmg.a.31724. Am J Med Genet A. 2007. PMID: 17534888

Characterization of an abundant COL9A1 transcript in the cochlea with a novel 3' UTR: Expression studies and detection of miRNA target sequence.

Sivakumaran TA, Resendes BL, Robertson NG, Giersch AB, Morton CC. Sivakumaran TA, et al. J Assoc Res Otolaryngol. 2006 Jun;7(2):160-72. doi: 10.1007/s10162-006-0032-0. Epub 2006 Apr 19. J Assoc Res Otolaryngol. 2006. PMID: 16718610 Free PMC article.

Newborn hearing screening--a silent revolution.

Morton CC, Nance WE. Morton CC, et al. N Engl J Med. 2006 May 18;354(20):2151-64. doi: 10.1056/NEJMra050700. N Engl J Med. 2006. PMID: 16707752 Review. No abstract available.

Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.

Robertson NG, Cremers CW, Huygen PL, Ikezono T, Krastins B, Kremer H, Kuo SF, Liberman MC, Merchant SN, Miller CE, Nadol JB Jr, Sarracino DA, Verhagen WI, Morton CC. Robertson NG, et al. Hum Mol Genet. 2006 Apr 1;15(7):1071-85. doi: 10.1093/hmg/ddl022. Epub 2006 Feb 15. Hum Mol Genet. 2006. PMID: 16481359

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