BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 15722487)

  • 1. Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao H; Young WY; Yan Q; Li R; Cao J; Wang Q; Li X; Peters JL; Han D; Guan MX
    Nucleic Acids Res; 2005; 33(3):1132-9. PubMed ID: 15722487
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.
    Guan MX; Fischel-Ghodsian N; Attardi G
    Hum Mol Genet; 1996 Jul; 5(7):963-71. PubMed ID: 8817331
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.
    Guan MX; Fischel-Ghodsian N; Attardi G
    Hum Mol Genet; 2001 Mar; 10(6):573-80. PubMed ID: 11230176
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.
    Zhao H; Li R; Wang Q; Yan Q; Deng JH; Han D; Bai Y; Young WY; Guan MX
    Am J Hum Genet; 2004 Jan; 74(1):139-52. PubMed ID: 14681830
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. [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]  

  • 11. [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]  

  • 12. A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity.
    Guan MX; Fischel-Ghodsian N; Attardi G
    Hum Mol Genet; 2000 Jul; 9(12):1787-93. PubMed ID: 10915767
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biochemical characterization of the deafness-associated mitochondrial tRNASer(UCN) A7445G mutation in osteosarcoma cell cybrids.
    Li X; Zhang LS; Fischel-Ghodsian N; Guan MX
    Biochem Biophys Res Commun; 2005 Mar; 328(2):491-8. PubMed ID: 15694374
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study.
    Gao Z; Yuan YS
    Medicine (Baltimore); 2020 Mar; 99(13):e19373. PubMed ID: 32221064
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. [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]  

  • 18. [Nuclear gene involves in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation].
    Zhao SY; Zhang HJ; Xu CH; Shan XN
    Fen Zi Xi Bao Sheng Wu Xue Bao; 2006 Feb; 39(1):39-45. PubMed ID: 16944570
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.