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

Year Number of Results
2000 2
2001 6
2002 1
2003 6
2004 5
2005 4
2006 3
2007 4
2008 7
2009 7
2010 5
2011 6
2012 2
2013 7
2014 11
2015 9
2016 3
2017 5
2018 2
2019 5
2020 4
2021 3
2022 5
2023 4
2024 0

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Similar articles for PMID: 20858605

101 results

Results by year

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Page 1
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.
Schütz M, Scimemi P, Majumder P, De Siati RD, Crispino G, Rodriguez L, Bortolozzi M, Santarelli R, Seydel A, Sonntag S, Ingham N, Steel KP, Willecke K, Mammano F. Schütz M, et al. Hum Mol Genet. 2010 Dec 15;19(24):4759-73. doi: 10.1093/hmg/ddq402. Epub 2010 Sep 21. Hum Mol Genet. 2010. PMID: 20858605 Free PMC article.
Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti.
Abbott AC, García IE, Villanelo F, Flores-Muñoz C, Ceriani R, Maripillán J, Novoa-Molina J, Figueroa-Cares C, Pérez-Acle T, Sáez JC, Sánchez HA, Martínez AD. Abbott AC, et al. Front Cell Dev Biol. 2023 Jan 9;10:1071202. doi: 10.3389/fcell.2022.1071202. eCollection 2022. Front Cell Dev Biol. 2023. PMID: 36699003 Free PMC article.
101 results