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 *

173 related articles for article (PubMed ID: 8285309)

  • 1. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.
    Fischel-Ghodsian N; Prezant TR; Bu X; Oztas S
    Am J Otolaryngol; 1993; 14(6):399-403. PubMed ID: 8285309
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications.
    Casano RA; Johnson DF; Bykhovskaya Y; Torricelli F; Bigozzi M; Fischel-Ghodsian N
    Am J Otolaryngol; 1999; 20(3):151-6. PubMed ID: 10326749
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.
    Scrimshaw BJ; Faed JM; Tate WP; Yun K
    J Hum Genet; 1999; 44(6):388-90. PubMed ID: 10570910
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.
    Pandya A; Xia X; Radnaabazar J; Batsuuri J; Dangaansuren B; Fischel-Ghodsian N; Nance WE
    J Med Genet; 1997 Feb; 34(2):169-72. PubMed ID: 9039999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness.
    Bacino C; Prezant TR; Bu X; Fournier P; Fischel-Ghodsian N
    Pharmacogenetics; 1995 Jun; 5(3):165-72. PubMed ID: 7550368
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.
    Prezant TR; Agapian JV; Bohlman MC; Bu X; Oztas S; Qiu WQ; Arnos KS; Cortopassi GA; Jaber L; Rotter JI
    Nat Genet; 1993 Jul; 4(3):289-94. PubMed ID: 7689389
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Aminoglycoside ototoxicity associated with mitochondrial DNA mutation].
    Ke X; Qi Y; Gu Z; Zhang Z; Zhang W; Jiang S; Liu J
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 1999 May; 13(5):195-7. PubMed ID: 12563999
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.
    Fischel-Ghodsian N; Prezant TR; Chaltraw WE; Wendt KA; Nelson RA; Arnos KS; Falk RE
    Am J Otolaryngol; 1997; 18(3):173-8. PubMed ID: 9164619
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Aminoglycoside-induced hearing loss in a patient with the 961 mutation in mitochondrial DNA.
    Yoshida M; Shintani T; Hirao M; Himi T; Yamaguchi A; Kikuchi K
    ORL J Otorhinolaryngol Relat Spec; 2002; 64(3):219-22. PubMed ID: 12037390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic factors in aminoglycoside toxicity.
    Fischel-Ghodsian N
    Ann N Y Acad Sci; 1999 Nov; 884():99-109. PubMed ID: 10842587
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial mutation associated with nonsyndromic deafness.
    Fischel-Ghodsian N; Prezant TR; Fournier P; Stewart IA; Maw M
    Am J Otolaryngol; 1995; 16(6):403-8. PubMed ID: 8572257
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The relation between mitochondrial DNA mutation and aminogly- coside antibiotics-induced deafness].
    Zhang L; Lu M; Huang Y; Zhou X; Qiu D; Wang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):138-40. PubMed ID: 10359860
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Screening for the 1555G mutation in mitochondrial DNA in pedigrees with aminoglycoside antibiotic induced deafness].
    Yuan H; Jiang S; Yang W
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1998 Apr; 33(2):67-70. PubMed ID: 11498854
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.
    Yamasoba T; Goto Yi; Oka Y; Nishino I; Tsukuda K; Nonaka I
    Neuromuscul Disord; 2002 Jun; 12(5):506-12. PubMed ID: 12031626
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness].
    Yuan H; Jiang S; Yang W; Guo W; Cao J; Dai P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):141-4. PubMed ID: 10359861
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12s rRNA gene: evidence of heteroplasmy.
    el-Schahawi M; López de Munain A; Sarrazin AM; Shanske AL; Basirico M; Shanske S; DiMauro S
    Neurology; 1997 Feb; 48(2):453-6. PubMed ID: 9040738
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.