253 related articles for article (PubMed ID: 23237192)
1. Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.
Wei Q; Xu D; Chen Z; Li H; Lu Y; Liu C; Bu X; Xing G; Cao X
Int J Audiol; 2013 Feb; 52(2):98-103. PubMed ID: 23237192
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations.
Ding Y; Xia BH; Liu Q; Li MY; Huang SX; Zhuo GC
Gene; 2016 Oct; 591(1):148-152. PubMed ID: 27397648
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
Lu J; Qian Y; Li Z; Yang A; Zhu Y; Li R; Yang L; Tang X; Chen B; Ding Y; Li Y; You J; Zheng J; Tao Z; Zhao F; Wang J; Sun D; Zhao J; Meng Y; Guan MX
Mitochondrion; 2010 Jan; 10(1):69-81. PubMed ID: 19818876
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
Wang X; Lu J; Zhu Y; Yang A; Yang L; Li R; Chen B; Qian Y; Tang X; Wang J; Zhang X; Guan MX
Pharmacogenet Genomics; 2008 Dec; 18(12):1059-70. PubMed ID: 18820594
[TBL] [Abstract][Full Text] [Related]
9. A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.
Bai Y; Wang Z; Dai W; Li Q; Chen G; Cong N; Guan M; Li H
BMC Med Genet; 2010 Sep; 11():129. PubMed ID: 20822538
[TBL] [Abstract][Full Text] [Related]
10. 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
Biochem Biophys Res Commun; 2005 Oct; 336(3):967-73. PubMed ID: 16168391
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.
Zhu Y; Qian Y; Tang X; Wang J; Yang L; Liao Z; Li R; Ji J; Li Z; Chen J; Choo DI; Lu J; Guan MX
Biochem Biophys Res Commun; 2006 Apr; 342(3):843-50. PubMed ID: 16500624
[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. 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]
15. Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.
Rodríguez-Ballesteros M; Olarte M; Aguirre LA; Galán F; Galán R; Vallejo LA; Navas C; Villamar M; Moreno-Pelayo MA; Moreno F; del Castillo I
J Med Genet; 2006 Nov; 43(11):e54. PubMed ID: 17085680
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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]
18. 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
Biochem Biophys Res Commun; 2006 Sep; 348(1):200-5. PubMed ID: 16875663
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
