149 related articles for article (PubMed ID: 15670746)
1. Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.
Li R; Ishikawa K; Deng JH; Heman-Ackah S; Tamagawa Y; Yang L; Bai Y; Ichimura K; Guan MX
Biochem Biophys Res Commun; 2005 Mar; 328(1):32-7. PubMed ID: 15670746
[TBL] [Abstract][Full Text] [Related]
2. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
Tang X; Li R; Zheng J; Cai Q; Zhang T; Gong S; Zheng W; He X; Zhu Y; Xue L; Yang A; Yang L; Lu J; Guan MX
Mol Genet Metab; 2010 May; 100(1):57-64. PubMed ID: 20153673
[TBL] [Abstract][Full Text] [Related]
3. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
Yamasoba T; Tsukuda K; Suzuki M
Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
[TBL] [Abstract][Full Text] [Related]
4. Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness.
Li X; Fischel-Ghodsian N; Schwartz F; Yan Q; Friedman RA; Guan MX
Nucleic Acids Res; 2004; 32(3):867-77. PubMed ID: 14960712
[TBL] [Abstract][Full Text] [Related]
5. [Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].
Zhang T; Chen BB; Zheng J; Gong SS; Zhang CQ; Lv JX; Guan MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):367-73. PubMed ID: 21811972
[TBL] [Abstract][Full Text] [Related]
6. [Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].
Gong SS; Chen BB; Peng GH; Zheng J; Zhang T; Zheng BJ; Fang F; Zhang CQ; Lv JX; Guan MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):382-7. PubMed ID: 22875491
[TBL] [Abstract][Full Text] [Related]
7. [Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family].
Wu Y; Liang LZ; Xiao HL; Yang YL; Yu X; Zheng J; Fang F; Zheng BJ; Tang XW; Jin LJ; Guan MX
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Dec; 48(12):978-84. PubMed ID: 24506995
[TBL] [Abstract][Full Text] [Related]
8. Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
Chen J; Yang L; Yang A; Zhu Y; Zhao J; Sun D; Tao Z; Tang X; Wang J; Wang X; Tsushima A; Lan J; Li W; Wu F; Yuan Q; Ji J; Feng J; Wu C; Liao Z; Li Z; Greinwald JH; Lu J; Guan MX
Gene; 2007 Oct; 401(1-2):4-11. PubMed ID: 17698299
[TBL] [Abstract][Full Text] [Related]
9. [Mutations analysis in a pedigree with maternally inherited sensorineural hearing loss].
Xu C; Zhang H; Zhang Y; Zhao S; Geng X; Shan Y; Shan X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):125-8. PubMed ID: 15793769
[TBL] [Abstract][Full Text] [Related]
10. 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
Biochem Biophys Res Commun; 2006 Jun; 344(4):1253-7. PubMed ID: 16650816
[TBL] [Abstract][Full Text] [Related]
11. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
Young WY; Zhao L; Qian Y; Wang Q; Li N; Greinwald JH; Guan MX
Biochem Biophys Res Commun; 2005 Mar; 328(4):1244-51. PubMed ID: 15708009
[TBL] [Abstract][Full Text] [Related]
12. Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation.
Abe S; Kelley PM; Kimberling WJ; Usami SI
Am J Med Genet; 2001 Nov; 103(4):334-8. PubMed ID: 11746015
[TBL] [Abstract][Full Text] [Related]
13. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
Chen B; Sun D; Yang L; Zhang C; Yang A; Zhu Y; Zhao J; Chen Y; Guan M; Wang X; Li R; Tang X; Wang J; Tao Z; Lu J; Guan MX
Am J Med Genet A; 2008 May; 146A(10):1248-58. PubMed ID: 18386806
[TBL] [Abstract][Full Text] [Related]
14. Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation.
Qu J; Li R; Tong Y; Hu Y; Zhou X; Qian Y; Lu F; Guan MX
Biochem Biophys Res Commun; 2005 Mar; 328(4):1139-45. PubMed ID: 15707996
[TBL] [Abstract][Full Text] [Related]
15. The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.
Han D; Dai P; Zhu Q; Liu X; Huang D; Yuan Y; Yuan H; Wang X; Qian Y; Young WY; Guan MX
Biochem Biophys Res Commun; 2007 Jun; 357(2):554-60. PubMed ID: 17434445
[TBL] [Abstract][Full Text] [Related]
16. 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
Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982
[TBL] [Abstract][Full Text] [Related]
17. Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.
Zhu Y; Li Q; Chen Z; Kun Y; Liu L; Liu X; Yuan H; Zhai S; Han D; Dai P
Mitochondrion; 2009 Nov; 9(6):418-28. PubMed ID: 19682603
[TBL] [Abstract][Full Text] [Related]
18. Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation.
Ishikawa K; Tamagawa Y; Takahashi K; Kimura H; Kusakari J; Hara A; Ichimura K
Laryngoscope; 2002 Aug; 112(8 Pt 1):1494-9. PubMed ID: 12172268
[TBL] [Abstract][Full Text] [Related]
19. 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
Biochem Biophys Res Commun; 2006 Feb; 340(2):583-8. PubMed ID: 16380089
[TBL] [Abstract][Full Text] [Related]
20. Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing loss.
Chai Y; Sun L; Pang X; Wang X; Chen D; Chen Y; Wu H; Yang T
Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):614-7. PubMed ID: 24507663
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
