152 related articles for article (PubMed ID: 18636170)
1. Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss.
Bae JW; Lee KY; Choi SY; Lee SH; Park HJ; Kim UK
Int J Mol Med; 2008 Aug; 22(2):175-80. PubMed ID: 18636170
[TBL] [Abstract][Full Text] [Related]
2. Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes.
Rydzanicz M; Wróbel M; Cywińska K; Froehlich D; Gawecki W; Szyfter W; Szyfter K
Genet Test Mol Biomarkers; 2009 Apr; 13(2):167-72. PubMed ID: 19371214
[TBL] [Abstract][Full Text] [Related]
3. Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
Shen Z; Zheng J; Chen B; Peng G; Zhang T; Gong S; Zhu Y; Zhang C; Li R; Yang L; Zhou J; Cai T; Jin L; Lu J; Guan MX
J Transl Med; 2011 Jan; 9():4. PubMed ID: 21205314
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people.
Zhu Y; Zhao J; Feng B; Su Y; Kang D; Yuan H; Zhai S; Dai P
Acta Otolaryngol; 2015 Jan; 135(1):26-34. PubMed ID: 25376778
[TBL] [Abstract][Full Text] [Related]
5. The role of mitochondrial DNA mutations in hearing loss.
Ding Y; Leng J; Fan F; Xia B; Xu P
Biochem Genet; 2013 Aug; 51(7-8):588-602. PubMed ID: 23605717
[TBL] [Abstract][Full Text] [Related]
6. Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
Yuan H; Chen J; Liu X; Cheng J; Wang X; Yang L; Yang S; Cao J; Kang D; Dai P; Zhai S; Han D; Young WY; Guan MX
Biochem Biophys Res Commun; 2007 Oct; 362(1):94-100. PubMed ID: 17698030
[TBL] [Abstract][Full Text] [Related]
7. Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.
Wei Q; Wang S; Yao J; Lu Y; Chen Z; Xing G; Cao X
J Transl Med; 2013 Jul; 11():163. PubMed ID: 23826813
[TBL] [Abstract][Full Text] [Related]
8. [Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees].
Peng GH; Zheng BJ; Fang F; Wu Y; Liang LZ; Zheng J; Nan BY; Yu X; Tang XW; Zhu Y; Lu JX; Chen BB; Guan MX
Yi Chuan; 2013 Jan; 35(1):62-72. PubMed ID: 23357266
[TBL] [Abstract][Full Text] [Related]
9. [Mutation analysis of mitochondrial 12S rRNA gene G709A in a maternally inherited pedigree with non-syndromic deafness].
Wei Q; Lu Y; Zhang Y; Chen Z; Xing G; Cao X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):610-4. PubMed ID: 19953480
[TBL] [Abstract][Full Text] [Related]
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
Biochem Biophys Res Commun; 2006 Feb; 340(4):1251-8. PubMed ID: 16406239
[TBL] [Abstract][Full Text] [Related]
11. [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
Genetika; 2009 Jul; 45(7):982-91. PubMed ID: 19705751
[TBL] [Abstract][Full Text] [Related]
12. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.
Li Z; Li R; Chen J; Liao Z; Zhu Y; Qian Y; Xiong S; Heman-Ackah S; Wu J; Choo DI; Guan MX
Hum Genet; 2005 Jun; 117(1):9-15. PubMed ID: 15841390
[TBL] [Abstract][Full Text] [Related]
13. [Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].
Zheng BJ; Peng GH; Chen BB; Fang F; Zheng J; Wu Y; Liang LZ; Nan BY; Tang XW; Zhu Y; Lu JX; Guan MX
Yi Chuan; 2012 Jun; 34(6):695-704. PubMed ID: 22698740
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.
Chen T; Liu Q; Jiang L; Liu C; Ou Q
Genet Test Mol Biomarkers; 2013 Feb; 17(2):122-30. PubMed ID: 23256547
[TBL] [Abstract][Full Text] [Related]
15. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
Tang X; Yang L; Zhu Y; Liao Z; Wang J; Qian Y; Tao Z; Hu L; Wu G; Lan J; Wang X; Ji J; Wu J; Ji Y; Feng J; Chen J; Li Z; Zhang X; Lu J; Guan MX
Gene; 2007 May; 393(1-2):11-9. PubMed ID: 17341440
[TBL] [Abstract][Full Text] [Related]
16. Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
Yuan H; Qian Y; Xu Y; Cao J; Bai L; Shen W; Ji F; Zhang X; Kang D; Mo JQ; Greinwald JH; Han D; Zhai S; Young WY; Guan MX
Am J Med Genet A; 2005 Oct; 138A(2):133-40. PubMed ID: 16152638
[TBL] [Abstract][Full Text] [Related]
17. Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.
Bae JW; Kim DB; Choi JY; Park HJ; Lee JD; Hur DG; Bae SH; Jung DJ; Lee SH; Kim UK; Lee KY
PLoS One; 2012; 7(8):e42463. PubMed ID: 22879993
[TBL] [Abstract][Full Text] [Related]
18. Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.
Young WY; Zhao L; Qian Y; Li R; Chen J; Yuan H; Dai P; Zhai S; Han D; Guan MX
Am J Med Genet A; 2006 Oct; 140(20):2188-97. PubMed ID: 16955413
[TBL] [Abstract][Full Text] [Related]
19. [Mitochondrial 12S rRNA gene A827G in two pedigrees with nonsyndromic deafness].
Chen ZB; Cao X; Xing GQ; Tian HQ; Zhou AD; Wei QU; Bu XK
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):415-8. PubMed ID: 16883529
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.
Lu J; Li Z; Zhu Y; Yang A; Li R; Zheng J; Cai Q; Peng G; Zheng W; Tang X; Chen B; Chen J; Liao Z; Yang L; Li Y; You J; Ding Y; Yu H; Wang J; Sun D; Zhao J; Xue L; Wang J; Guan MX
Mitochondrion; 2010 Jun; 10(4):380-90. PubMed ID: 20100600
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]