Similar articles for PMID: 11857751

Year	Number of Results
1967	1
1997	1
1998	3
1999	3
2000	3
2002	5
2003	4
2004	5
2005	5
2006	10
2007	5
2008	7
2009	2
2010	2
2011	1
2012	1
2013	1
2014	2
2015	1
2017	1
2018	1
2019	1
2021	2
2024	0

1

Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.

Kupka S, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M. Kupka S, et al. Hum Mutat. 2002 Mar;19(3):308-9. doi: 10.1002/humu.9017. Hum Mutat. 2002. PMID: 11857751

2

Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.

Bravo O, Ballana E, Estivill X. Bravo O, et al. Biochem Biophys Res Commun. 2006 Jun 2;344(2):511-6. doi: 10.1016/j.bbrc.2006.03.143. Epub 2006 Mar 30. Biochem Biophys Res Commun. 2006. PMID: 16631122 Clinical Trial.

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

[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

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

6

Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family.

Malik S, Sudoyo H, Sasmono T, Winata S, Arhya IN, Pramoonjago P, Sudana W, Marzuki S. Malik S, et al. J Hum Genet. 2003;48(3):119-24. doi: 10.1007/s100380300018. J Hum Genet. 2003. PMID: 12624722

7

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

8

[Nonsyndromic inherited hearing impairment caused by mtDNA double mutations of A1555G and 961 insC].

Cao X, Xing GQ, Wei QJ, Bu XK, Wang DY. Cao X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):629-32. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583999 Chinese.

9

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

10

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

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