These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 22030963)

  • 1. mtDNA mutations, hearing loss and aminoglycoside treatment in Mexicans.
    Meza G; Torres-Ruíz NM; Tirado-Gutiérrez C; Aguilera P
    Braz J Otorhinolaryngol; 2011; 77(5):573-6. PubMed ID: 22030963
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics.
    Postal M; Palodeto B; Sartorato EL; Oliveira CA
    Braz J Otorhinolaryngol; 2009; 75(6):884-7. PubMed ID: 20209292
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. [Molecular genetic analysis of mitochondrial DNA C1494T mutation in non-syndromic hearing loss of Chinese population].
    Tian G; Liu YH; Ma YN; Li YJ; Zhang Y; Niu SL; Xu YE; Pei P; Wang ST; Bu DF; Du BR; Zhou X; Ke XM; Qi Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):464-6. PubMed ID: 17680545
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss.
    Rydzanicz M; Wróbel M; Pollak A; Gawecki W; Brauze D; Kostrzewska-Poczekaj M; Wojsyk-Banaszak I; Lechowicz U; Mueller-Malesińska M; Ołdak M; Płoski R; Skarzyński H; Szyfter K
    Biochem Biophys Res Commun; 2010 Apr; 395(1):116-21. PubMed ID: 20353758
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial COI/tRNASer(UCN) G7444A mutation may be associated with aminoglycoside-induced and non-syndromic hearing impairment.
    Liu Q; Liu P; Ding Y; Dong XJ; Wang ZX; Qian YE; Wang Q; Yang GC
    Mol Med Rep; 2015 Dec; 12(6):8176-8. PubMed ID: 26497601
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [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]  

  • 15. [Mutational screening of the mitochondrial 12S rRNA gene in Polish patients with aminoglycoside-induced hearing loss].
    Rydzanicz M
    Otolaryngol Pol; 2011; 65(4):297-9. PubMed ID: 22000150
    [No Abstract]   [Full Text] [Related]  

  • 16. [Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].
    Yang AF; Zhu Y; Lu JX; Yang L; Zhao JY; Sun DM
    Yi Chuan; 2008 Jun; 30(6):728-34. PubMed ID: 18550495
    [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. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated?
    Al-Malky G; Suri R; Sirimanna T; Dawson SJ
    Int J Pediatr Otorhinolaryngol; 2014 Jun; 78(6):969-73. PubMed ID: 24703164
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial mutations associated with aminoglycoside ototoxicity and hearing loss susceptibility identified by meta-analysis.
    Jing W; Zongjie H; Denggang F; Na H; Bin Z; Aifen Z; Xijiang H; Cong Y; Yunping D; Ring HZ; Ring BZ
    J Med Genet; 2015 Feb; 52(2):95-103. PubMed ID: 25515069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss.
    Tang X; Zheng J; Ying Z; Cai Z; Gao Y; He Z; Yu H; Yao J; Yang Y; Wang H; Chen Y; Guan MX
    Mitochondrion; 2015 Jul; 23():17-24. PubMed ID: 25968158
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.