209 related articles for article (PubMed ID: 30523288)
1. The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.
Igumnova V; Veidemane L; Vīksna A; Capligina V; Zole E; Ranka R
J Hum Genet; 2019 Mar; 64(3):199-206. PubMed ID: 30523288
[TBL] [Abstract][Full Text] [Related]
2. The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.
Ealy M; Lynch KA; Meyer NC; Smith RJ
Laryngoscope; 2011 Jun; 121(6):1184-6. PubMed ID: 21495045
[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. 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. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
Qu J; Wang J; Xu S
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1936-40. PubMed ID: 26911053
[TBL] [Abstract][Full Text] [Related]
6. Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype.
McDermott JH; Wolf J; Hoshitsuki K; Huddart R; Caudle KE; Whirl-Carrillo M; Steyger PS; Smith RJH; Cody N; Rodriguez-Antona C; Klein TE; Newman WG
Clin Pharmacol Ther; 2022 Feb; 111(2):366-372. PubMed ID: 34032273
[TBL] [Abstract][Full Text] [Related]
7. Genetic susceptibility to aminoglycoside ototoxicity.
Nguyen T; Jeyakumar A
Int J Pediatr Otorhinolaryngol; 2019 May; 120():15-19. PubMed ID: 30743189
[TBL] [Abstract][Full Text] [Related]
8. Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment.
de Moraes VC; Alexandrino F; Andrade PB; Câmara MF; Sartorato EL
Biochem Biophys Res Commun; 2009 Apr; 381(2):210-3. PubMed ID: 19338775
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Novel mutations affecting the secondary structure of MT-RNR1 gene: a causal relationship with profound nonsyndromic hearing impairment.
Padma G; Ramchander PV; Nandur VU; Kumar KR; Padma T
Genet Test Mol Biomarkers; 2012 Sep; 16(9):1092-7. PubMed ID: 22852811
[TBL] [Abstract][Full Text] [Related]
11. Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.
Guaran V; Astolfi L; Castiglione A; Simoni E; Olivetto E; Galasso M; Trevisi P; Busi M; Volinia S; Martini A
Int J Mol Med; 2013 Oct; 32(4):785-94. PubMed ID: 23969527
[TBL] [Abstract][Full Text] [Related]
12. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss.
Uehara DT; Rincon D; Abreu-Silva RS; Auricchio MT; Tabith A; Kok F; Mingroni-Netto RC
Genet Test Mol Biomarkers; 2010 Oct; 14(5):611-6. PubMed ID: 20722495
[TBL] [Abstract][Full Text] [Related]
13. The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients.
Rydzanicz M; Cywińska K; Wróbel M; Pollak A; Gawęcki W; Wojsyk-Banaszak I; Lechowicz U; Mueller-Malesińska M; Ołdak M; Płoski R; Skarżyński H; Szyfter K; Szyfter W
Mol Genet Metab; 2011; 104(1-2):153-9. PubMed ID: 21621438
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Increased risk of hearing loss associated with MT-RNR1 gene mutations: a real-world investigation among Han Taiwanese Population.
Chen HK; Hsieh YW; Hsu HY; Liu TY; Zhang YT; Lin CD; Tsai FJ
BMC Med Genomics; 2024 Jun; 17(1):155. PubMed ID: 38840095
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. [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]
19. 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]
20. Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides.
Human H; Hagen CM; de Jong G; Harris T; Lombard D; Christiansen M; Bardien S
Biochem Biophys Res Commun; 2010 Mar; 393(4):751-6. PubMed ID: 20171168
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
