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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
2005 | 1 |
2011 | 1 |
2012 | 1 |
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2015 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (cited) for id: 614591
7 results
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Page 1
Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment.
J Med Genet. 2018 Aug;55(8):555-560. doi: 10.1136/jmedgenet-2018-105349. Epub 2018 Apr 27.
J Med Genet. 2018.
PMID: 29703829
Free PMC article.
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.
Wang H, Wang X, He C, Li H, Qing J, Grati M, Hu Z, Li J, Hu Y, Xia K, Mei L, Wang X, Yu J, Chen H, Jiang L, Liu Y, Men M, Zhang H, Guan L, Xiao J, Zhang J, Liu X, Feng Y.
Wang H, et al.
J Hum Genet. 2015 Mar;60(3):119-126. doi: 10.1038/jhg.2014.114. Epub 2015 Jan 15.
J Hum Genet. 2015.
PMID: 25589040
Free PMC article.
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Loss of the tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions.
Cheatham MA, Goodyear RJ, Homma K, Legan PK, Korchagina J, Naskar S, Siegel JH, Dallos P, Zheng J, Richardson GP.
Cheatham MA, et al.
J Neurosci. 2014 Jul 30;34(31):10325-38. doi: 10.1523/JNEUROSCI.1256-14.2014.
J Neurosci. 2014.
PMID: 25080593
Free PMC article.
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Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.
Kammerer R, Rüttiger L, Riesenberg R, Schäuble C, Krupar R, Kamp A, Sunami K, Eisenried A, Hennenberg M, Grunert F, Bress A, Battaglia S, Schrewe H, Knipper M, Schneider MR, Zimmermann W.
Kammerer R, et al.
J Biol Chem. 2012 Jun 22;287(26):21584-98. doi: 10.1074/jbc.M111.320481. Epub 2012 Apr 27.
J Biol Chem. 2012.
PMID: 22544735
Free PMC article.
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Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).
Zheng J, Miller KK, Yang T, Hildebrand MS, Shearer AE, DeLuca AP, Scheetz TE, Drummond J, Scherer SE, Legan PK, Goodyear RJ, Richardson GP, Cheatham MA, Smith RJ, Dallos P.
Zheng J, et al.
Proc Natl Acad Sci U S A. 2011 Mar 8;108(10):4218-23. doi: 10.1073/pnas.1005842108. Epub 2011 Feb 22.
Proc Natl Acad Sci U S A. 2011.
PMID: 21368133
Free PMC article.
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Identification of a novel group of evolutionarily conserved members within the rapidly diverging murine Cea family.
Zebhauser R, Kammerer R, Eisenried A, McLellan A, Moore T, Zimmermann W.
Zebhauser R, et al.
Genomics. 2005 Nov;86(5):566-80. doi: 10.1016/j.ygeno.2005.07.008. Epub 2005 Sep 1.
Genomics. 2005.
PMID: 16139472
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Linkage of a gene for dominant non-syndromic deafness to chromosome 19.
Chen AH, Ni L, Fukushima K, Marietta J, O'Neill M, Coucke P, Willems P, Smith RJ.
Chen AH, et al.
Hum Mol Genet. 1995 Jun;4(6):1073-6. doi: 10.1093/hmg/4.6.1073.
Hum Mol Genet. 1995.
PMID: 7655461
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