Similar articles for PMID: 18261986

Year	Number of Results
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1985	1
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1

A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.

Chaig MR, Zernotti ME, Soria NW, Romero OF, Romero MF, Gerez NM. Chaig MR, et al. Biochem Biophys Res Commun. 2008 Apr 11;368(3):631-6. doi: 10.1016/j.bbrc.2008.01.143. Epub 2008 Feb 7. Biochem Biophys Res Commun. 2008. PMID: 18261986

2

Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.

Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X. Xing G, et al. Biochem Biophys Res Commun. 2006 Aug 11;346(4):1131-5. doi: 10.1016/j.bbrc.2006.05.208. Epub 2006 Jun 12. Biochem Biophys Res Commun. 2006. PMID: 16782057

3

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.

Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX. Dai P, et al. Biochem Biophys Res Commun. 2006 Feb 3;340(1):194-9. doi: 10.1016/j.bbrc.2005.11.156. Biochem Biophys Res Commun. 2006. PMID: 16375862 Clinical Trial.

4

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.

Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX. Wang Q, et al. Biochem Biophys Res Commun. 2006 Feb 10;340(2):583-8. doi: 10.1016/j.bbrc.2005.12.045. Epub 2005 Dec 19. Biochem Biophys Res Commun. 2006. PMID: 16380089

5

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.

Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX. Dai P, et al. Biochem Biophys Res Commun. 2006 Sep 15;348(1):200-5. doi: 10.1016/j.bbrc.2006.07.031. Epub 2006 Jul 17. Biochem Biophys Res Commun. 2006. PMID: 16875663

6

Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family.

Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X. Xing G, et al. Biochem Biophys Res Commun. 2006 Jun 16;344(4):1253-7. doi: 10.1016/j.bbrc.2006.04.033. Epub 2006 May 2. Biochem Biophys Res Commun. 2006. PMID: 16650816

7

Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.

Wu CC, Chiu YH, Chen PJ, Hsu CJ. Wu CC, et al. Ear Hear. 2007 Jun;28(3):332-42. doi: 10.1097/AUD.0b013e318047941e. Ear Hear. 2007. PMID: 17485982

8

Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides.

Gürtler N, Schmuziger N, Kim Y, Mhatre AN, Jungi M, Lalwani AK. Gürtler N, et al. Laryngoscope. 2005 Apr;115(4):640-4. doi: 10.1097/01.mlg.0000161355.28073.f5. Laryngoscope. 2005. PMID: 15805873

9

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.

Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX. Zhao L, et al. Biochem Biophys Res Commun. 2005 Oct 28;336(3):967-73. doi: 10.1016/j.bbrc.2005.08.199. Biochem Biophys Res Commun. 2005. PMID: 16168391

10

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.

Bindu LH, Reddy PP. Bindu LH, et al. Int J Audiol. 2008 Nov;47(11):702-7. doi: 10.1080/14992020802215862. Int J Audiol. 2008. PMID: 19031229 Review.

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