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Journal Abstract Search

500 related items for PubMed ID: 7689389

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3.
    Bykhovskaya Y, Mengesha E, Wang D, Yang H, Estivill X, Shohat M, Fischel-Ghodsian N.
    Mol Genet Metab; 2004 Nov; 83(3):199-206. PubMed ID: 15542390
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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 Nov; 44(6):388-90. PubMed ID: 10570910
    [Abstract] [Full Text] [Related]

  • 5. 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 11; 346(4):1131-5. PubMed ID: 16782057
    [Abstract] [Full Text] [Related]

  • 6. Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness.
    Hamasaki K, Rando RR.
    Biochemistry; 1997 Oct 07; 36(40):12323-8. PubMed ID: 9315872
    [Abstract] [Full Text] [Related]

  • 7. 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 03; 340(1):194-9. PubMed ID: 16375862
    [Abstract] [Full Text] [Related]

  • 8. [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 03; 33(2):67-70. PubMed ID: 11498854
    [Abstract] [Full Text] [Related]

  • 9.
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  • 10. 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 03; 34(2):169-72. PubMed ID: 9039999
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  • 12. [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 03; 16(3):138-40. PubMed ID: 10359860
    [Abstract] [Full Text] [Related]

  • 13. [Sequence analysis of mtDNA 12S rRNA, tRNA(Leu(UUR)),tRNA(Ser(UCN))and 16S rRNA gene of 12 nonsyndromic inherited deafness pedigrees].
    Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec 03; 18(6):415-20. PubMed ID: 11774206
    [Abstract] [Full Text] [Related]

  • 14. [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 03; 13(5):195-7. PubMed ID: 12563999
    [Abstract] [Full Text] [Related]

  • 15. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2005 Oct 28; 336(3):967-73. PubMed ID: 16168391
    [Abstract] [Full Text] [Related]

  • 16. [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 28; 16(3):141-4. PubMed ID: 10359861
    [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 10; 340(2):583-8. PubMed ID: 16380089
    [Abstract] [Full Text] [Related]

  • 18. [Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
    Liu X, Dai P, Huang DL, Yuan HJ, Li WM, Cao JY, Yu F, Zhang RN, Lin HY, Zhu XH, He Y, Yu YJ, Yao K.
    Zhonghua Yi Xue Za Zhi; 2006 May 23; 86(19):1318-22. PubMed ID: 16796900
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial rRNA and tRNA and hearing function.
    Xing G, Chen Z, Cao X.
    Cell Res; 2007 Mar 23; 17(3):227-39. PubMed ID: 17199108
    [Abstract] [Full Text] [Related]

  • 20. Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies.
    Nye JS, Hayes EA, Amendola M, Vaughn D, Charrow J, McLone DG, Speer MC, Nance WE, Pandya A.
    Teratology; 2000 Mar 23; 61(3):165-71. PubMed ID: 10661905
    [Abstract] [Full Text] [Related]

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