288 related articles for article (PubMed ID: 21047563)
1. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.
Guan MX
Mitochondrion; 2011 Mar; 11(2):237-45. PubMed ID: 21047563
[TBL] [Abstract][Full Text] [Related]
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
Biochem Biophys Res Commun; 2006 Aug; 346(4):1131-5. PubMed ID: 16782057
[TBL] [Abstract][Full Text] [Related]
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
Biochem Biophys Res Commun; 2006 Feb; 340(1):194-9. PubMed ID: 16375862
[TBL] [Abstract][Full Text] [Related]
4. Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides.
Gürtler N; Schmuziger N; Kim Y; Mhatre AN; Jungi M; Lalwani AK
Laryngoscope; 2005 Apr; 115(4):640-4. PubMed ID: 15805873
[TBL] [Abstract][Full Text] [Related]
5. [Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].
YANG AF; ZHENG J; LV JX; GUAN MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):165-71. PubMed ID: 21462128
[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. 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]
8. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
Bindu LH; Reddy PP
Int J Audiol; 2008 Nov; 47(11):702-7. PubMed ID: 19031229
[TBL] [Abstract][Full Text] [Related]
9. 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]
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
Biochem Biophys Res Commun; 2008 Apr; 368(3):631-6. PubMed ID: 18261986
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.
Jin L; Yang A; Zhu Y; Zhao J; Wang X; Yang L; Sun D; Tao Z; Tsushima A; Wu G; Xu L; Chen C; Yi B; Cai J; Tang X; Wang J; Li D; Yuan Q; Liao Z; Chen J; Li Z; Lu J; Guan MX
Biochem Biophys Res Commun; 2007 Sep; 361(1):133-9. PubMed ID: 17659260
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Discrimination of A1555G and C1494T point mutations in the mitochondrial 12S rRNA gene by on/off switch.
Guo ZF; Guo WS; Xiao L; Gao GQ; Lan F; Lu XG; Li K; Liao DF
Appl Biochem Biotechnol; 2012 Jan; 166(1):234-42. PubMed ID: 22068689
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Mitochondrial rRNA and tRNA and hearing function.
Xing G; Chen Z; Cao X
Cell Res; 2007 Mar; 17(3):227-39. PubMed ID: 17199108
[TBL] [Abstract][Full Text] [Related]
19. Genetic mutations and aminoglycoside-induced ototoxicity in neonates.
Johnson RF; Cohen AP; Guo Y; Schibler K; Greinwald JH
Otolaryngol Head Neck Surg; 2010 May; 142(5):704-7. PubMed ID: 20416460
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
