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Journal Abstract Search

107 related items for PubMed ID: 21838605

  • 21. Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family.
    Ding Y, Li Y, You J, Yang L, Chen B, Lu J, Guan MX.
    J Genet Genomics; 2009 Apr; 36(4):241-50. PubMed ID: 19376484
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. [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 03; 30(6):728-34. PubMed ID: 18550495
    [Abstract] [Full Text] [Related]

  • 24. Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation.
    Zhu Y, Huang S, Kang D, Han M, Wang G, Yuan Y, Su Y, Yuan H, Zhai S, Dai P.
    BMC Genet; 2014 Feb 17; 15():26. PubMed ID: 24533451
    [Abstract] [Full Text] [Related]

  • 25. Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.
    Pan J, Xu P, Tang W, Cui Z, Feng M, Wang C.
    Int J Pediatr Otorhinolaryngol; 2017 Jul 17; 98():39-42. PubMed ID: 28583500
    [Abstract] [Full Text] [Related]

  • 26. [Detection of common deafness-related genes among non-syndromic deafness patients from Shanxi province].
    Zhou Y, Yang H, Hao Z, Ma Y, Zhang Q, Li J, Zhao X, Wang X, Li X, Xia L, Ma S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 17; 32(2):183-6. PubMed ID: 25863082
    [Abstract] [Full Text] [Related]

  • 27. [Genetic epidemiologic study of mitochondrial DNA 7445A-->G mutation among non-syndromic deafness in Chinese population].
    Liu YH, Ke XM, Qi Y, Xu HB, Gu ZP, Liu XC, Liu JF.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2000 Apr 17; 14(4):177-8. PubMed ID: 12541497
    [Abstract] [Full Text] [Related]

  • 28. [Analysis of audiological characteristics and genetic background in patients with nonsyndromic deafness and mitochondrial DNA 1555A>G mutation].
    Zhuo Y, Wu H, Jin H, Liu H, Zhang D, Huang J, Zheng B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct 10; 35(5):625-629. PubMed ID: 30298482
    [Abstract] [Full Text] [Related]

  • 29. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss.
    Uehara DT, Rincon D, Abreu-Silva RS, Auricchio MT, Tabith A, Kok F, Mingroni-Netto RC.
    Genet Test Mol Biomarkers; 2010 Oct 10; 14(5):611-6. PubMed ID: 20722495
    [Abstract] [Full Text] [Related]

  • 30. The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese Pedigree.
    Ding Y, Teng YS, Zhuo GC, Xia BH, Leng JH.
    Curr Mol Med; 2019 Oct 10; 19(2):136-146. PubMed ID: 30854964
    [Abstract] [Full Text] [Related]

  • 31. [Analysis of the deafness gene screening results from newborns in Shijiazhuang].
    Feng J, Li T, Wang L, Li S, Shang H.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Oct 10; 29(19):1676-9. PubMed ID: 26999833
    [Abstract] [Full Text] [Related]

  • 32. 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 10; 78(6):969-73. PubMed ID: 24703164
    [Abstract] [Full Text] [Related]

  • 33. [Nonsyndromic deafness and mitochondrial DNA mutation].
    Liu YH, Ke XM, Gu ZP.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2000 Jan 10; 14(1):9-11. PubMed ID: 12541433
    [Abstract] [Full Text] [Related]

  • 34. A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions.
    Mezghani N, Mnif M, Mkaouar-Rebai E, Kallel N, Charfi N, Abid M, Fakhfakh F.
    Biochem Biophys Res Commun; 2013 Feb 22; 431(4):670-4. PubMed ID: 23357420
    [Abstract] [Full Text] [Related]

  • 35. Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
    Shen Z, Zheng J, Chen B, Peng G, Zhang T, Gong S, Zhu Y, Zhang C, Li R, Yang L, Zhou J, Cai T, Jin L, Lu J, Guan MX.
    J Transl Med; 2011 Jan 04; 9():4. PubMed ID: 21205314
    [Abstract] [Full Text] [Related]

  • 36. Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.
    Bae JW, Kim DB, Choi JY, Park HJ, Lee JD, Hur DG, Bae SH, Jung DJ, Lee SH, Kim UK, Lee KY.
    PLoS One; 2012 Jan 04; 7(8):e42463. PubMed ID: 22879993
    [Abstract] [Full Text] [Related]

  • 37. Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method.
    Ding Y, Lang J, Zhang J, Xu J, Lin X, Lou X, Zheng H, Huai L.
    Biosci Rep; 2020 May 29; 40(5):. PubMed ID: 32400865
    [Abstract] [Full Text] [Related]

  • 38. Candidate locus for a nuclear modifier gene for maternally inherited deafness.
    Bykhovskaya Y, Estivill X, Taylor K, Hang T, Hamon M, Casano RA, Yang H, Rotter JI, Shohat M, Fischel-Ghodsian N.
    Am J Hum Genet; 2000 Jun 29; 66(6):1905-10. PubMed ID: 10788333
    [Abstract] [Full Text] [Related]

  • 39. [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 29; 48(12):978-84. PubMed ID: 24506995
    [Abstract] [Full Text] [Related]

  • 40. 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 Dec 29; 14(6):399-403. PubMed ID: 8285309
    [Abstract] [Full Text] [Related]

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