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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

144 related items for PubMed ID: 15670746

  • 1. Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.
    Li R, Ishikawa K, Deng JH, Heman-Ackah S, Tamagawa Y, Yang L, Bai Y, Ichimura K, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 04; 328(1):32-7. PubMed ID: 15670746
    [Abstract] [Full Text] [Related]

  • 2. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
    Tang X, Li R, Zheng J, Cai Q, Zhang T, Gong S, Zheng W, He X, Zhu Y, Xue L, Yang A, Yang L, Lu J, Guan MX.
    Mol Genet Metab; 2010 May 04; 100(1):57-64. PubMed ID: 20153673
    [Abstract] [Full Text] [Related]

  • 3. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec 04; (559):13-8. PubMed ID: 18340555
    [Abstract] [Full Text] [Related]

  • 4. 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 Dec 04; 32(3):867-77. PubMed ID: 14960712
    [Abstract] [Full Text] [Related]

  • 5. [Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].
    Zhang T, Chen BB, Zheng J, Gong SS, Zhang CQ, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 04; 28(4):367-73. PubMed ID: 21811972
    [Abstract] [Full Text] [Related]

  • 6. [Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].
    Gong SS, Chen BB, Peng GH, Zheng J, Zhang T, Zheng BJ, Fang F, Zhang CQ, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug 04; 29(4):382-7. PubMed ID: 22875491
    [Abstract] [Full Text] [Related]

  • 7. [Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family].
    Wu Y, Liang LZ, Xiao HL, Yang YL, Yu X, Zheng J, Fang F, Zheng BJ, Tang XW, Jin LJ, Guan MX.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Dec 04; 48(12):978-84. PubMed ID: 24506995
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 401(1-2):4-11. PubMed ID: 17698299
    [Abstract] [Full Text] [Related]

  • 9. [Mutations analysis in a pedigree with maternally inherited sensorineural hearing loss].
    Xu C, Zhang H, Zhang Y, Zhao S, Geng X, Shan Y, Shan X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 15; 22(2):125-8. PubMed ID: 15793769
    [Abstract] [Full Text] [Related]

  • 10. Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family.
    Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X.
    Biochem Biophys Res Commun; 2006 Jun 16; 344(4):1253-7. PubMed ID: 16650816
    [Abstract] [Full Text] [Related]

  • 11. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
    Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1244-51. PubMed ID: 15708009
    [Abstract] [Full Text] [Related]

  • 12. Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation.
    Abe S, Kelley PM, Kimberling WJ, Usami SI.
    Am J Med Genet; 2001 Nov 01; 103(4):334-8. PubMed ID: 11746015
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
    Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, Zhao J, Chen Y, Guan M, Wang X, Li R, Tang X, Wang J, Tao Z, Lu J, Guan MX.
    Am J Med Genet A; 2008 May 15; 146A(10):1248-58. PubMed ID: 18386806
    [Abstract] [Full Text] [Related]

  • 14. Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation.
    Qu J, Li R, Tong Y, Hu Y, Zhou X, Qian Y, Lu F, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1139-45. PubMed ID: 15707996
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 357(2):554-60. PubMed ID: 17434445
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 28(3):332-42. PubMed ID: 17485982
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 9(6):418-28. PubMed ID: 19682603
    [Abstract] [Full Text] [Related]

  • 18. Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation.
    Ishikawa K, Tamagawa Y, Takahashi K, Kimura H, Kusakari J, Hara A, Ichimura K.
    Laryngoscope; 2002 Aug 01; 112(8 Pt 1):1494-9. PubMed ID: 12172268
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing loss.
    Chai Y, Sun L, Pang X, Wang X, Chen D, Chen Y, Wu H, Yang T.
    Int J Pediatr Otorhinolaryngol; 2014 Apr 10; 78(4):614-7. PubMed ID: 24507663
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.