Similar articles for PMID: 15286157

Year	Number of Results
1988	1
1989	1
1995	1
1999	1
2000	5
2001	6
2002	5
2003	1
2004	5
2005	4
2006	9
2007	4
2008	6
2009	2
2010	4
2011	3
2012	1
2013	2
2014	2
2015	1
2017	1
2018	1
2019	1
2020	2
2024	0

1

Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss.

Li R, Greinwald JH Jr, Yang L, Choo DI, Wenstrup RJ, Guan MX. Li R, et al. J Med Genet. 2004 Aug;41(8):615-20. doi: 10.1136/jmg.2004.020230. J Med Genet. 2004. PMID: 15286157 Free PMC article. No abstract available.

2

Mutations in the mitochondrial tRNA Ser(UCN) and in the GJB2 (connexin 26) gene are not modifiers of the age at onset or severity of hearing loss in Spanish patients with the 12S rRNA A1555G mutation.

López-Bigas N, Rabionet R, Martinez E, Bravo O, Girons J, Borragan A, Pellicer M, Arbonés ML, Estivill X. López-Bigas N, et al. Am J Hum Genet. 2000 Apr;66(4):1465-7. doi: 10.1086/302870. Am J Hum Genet. 2000. PMID: 10739773 Free PMC article. No abstract available.

3

The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients.

Rydzanicz M, Cywińska K, Wróbel M, Pollak A, Gawęcki W, Wojsyk-Banaszak I, Lechowicz U, Mueller-Malesińska M, Ołdak M, Płoski R, Skarżyński H, Szyfter K, Szyfter W. Rydzanicz M, et al. Mol Genet Metab. 2011 Sep-Oct;104(1-2):153-9. doi: 10.1016/j.ymgme.2011.05.004. Epub 2011 May 13. Mol Genet Metab. 2011. PMID: 21621438

4

[Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia].

Dzhemileva LU, Posukh OL, Tazetdinov AM, Barashkov NA, Zhuravskiĭ SG, Ponidelko SN, Markova TG, Tadinova VN, Fedorova SA, Maksimova NR, Khusnutdinova EK. Dzhemileva LU, et al. Genetika. 2009 Jul;45(7):982-91. Genetika. 2009. PMID: 19705751 Russian.

5

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.

Verhoeven K, Ensink RJ, Tiranti V, Huygen PL, Johnson DF, Schatteman I, Van Laer L, Verstreken M, Van de Heyning P, Fischel-Ghodsian N, Zeviani M, Cremers CW, Willems PJ, Van Camp G. Verhoeven K, et al. Eur J Hum Genet. 1999 Jan;7(1):45-51. doi: 10.1038/sj.ejhg.5200247. Eur J Hum Genet. 1999. PMID: 10094190

6

Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.

Mkaouar-Rebai E, Fendri-Kriaa N, Louhichi N, Tlili A, Triki C, Ghorbel A, Masmoudi S, Fakhfakh F. Mkaouar-Rebai E, et al. Biosci Rep. 2010 Dec;30(6):405-11. doi: 10.1042/BSR20090120. Biosci Rep. 2010. PMID: 20055758

7

[Mutation analysis of 12S rRNA and tRNA-Ser(UCN) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage].

Shu AL, Ji BH, Qin W, Feng GY, Nie YZ, Liu T, He L. Shu AL, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):303-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767669 Chinese.

8

A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment.

Hutchin TP, Parker MJ, Young ID, Davis AC, Pulleyn LJ, Deeble J, Lench NJ, Markham AF, Mueller RF. Hutchin TP, et al. J Med Genet. 2000 Sep;37(9):692-4. doi: 10.1136/jmg.37.9.692. J Med Genet. 2000. PMID: 10978361 Free PMC article.

9

Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.

Labay V, Garrido G, Madeo AC, Nance WE, Friedman TB, Friedman PL, Del Castillo I, Griffith AJ. Labay V, et al. Clin Genet. 2008 Jan;73(1):50-4. doi: 10.1111/j.1399-0004.2007.00925.x. Epub 2007 Nov 17. Clin Genet. 2008. PMID: 18028453

10

Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.

Mkaouar-Rebai E, Tlili A, Masmoudi S, Louhichi N, Charfeddine I, Ben Amor M, Lahmar I, Driss N, Drira M, Ayadi H, Fakhfakh F. Mkaouar-Rebai E, et al. Biochem Biophys Res Commun. 2006 Feb 24;340(4):1251-8. doi: 10.1016/j.bbrc.2005.12.123. Epub 2006 Jan 5. Biochem Biophys Res Commun. 2006. PMID: 16406239 Clinical Trial.

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