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 *

163 related articles for article (PubMed ID: 30592262)

  • 21. [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; 29(4):382-7. PubMed ID: 22875491
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 19(2):136-146. PubMed ID: 30854964
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. [Analysis of mtDNA 12SrRNA A1555G mutations of Uigur patients with nonsyndromic hereditary hearing loss in Xinjiang].
    Jiang H; Li Y; Sheng G; Yang L; Li H; Li H; Luo Y; Wang C
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 May; 24(10):439-41, 446. PubMed ID: 20669656
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Mutation analysis of mitochondrial 12S rRNA gene G709A in a maternally inherited pedigree with non-syndromic deafness].
    Wei Q; Lu Y; Zhang Y; Chen Z; Xing G; Cao X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):610-4. PubMed ID: 19953480
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 40(5):. PubMed ID: 32400865
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees].
    Peng GH; Zheng BJ; Fang F; Wu Y; Liang LZ; Zheng J; Nan BY; Yu X; Tang XW; Zhu Y; Lu JX; Chen BB; Guan MX
    Yi Chuan; 2013 Jan; 35(1):62-72. PubMed ID: 23357266
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. [Mitochondrial tRNA(Thr)T15943C mutation may be a new position that affects the phenotypic expression of deafness associated 12s rRNA A1555G mutation].
    Xiao H; He Z; Gao Y; Yang Y; Zheng J; Cai Z; Zheng B; Tang X; Guan M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):163-8. PubMed ID: 25863077
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [GJB2 235delC single allelic mutation modulates the phenotype associated with the mitochondrial A1555G mutation].
    Li Q; Fang RP; Zhou HG; Dai P; Tian L; Lin D; Huang Q; Song JM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):194-7. PubMed ID: 20376804
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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; 22(2):125-8. PubMed ID: 15793769
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment.
    Ballana E; Morales E; Rabionet R; Montserrat B; Ventayol M; Bravo O; Gasparini P; Estivill X
    Biochem Biophys Res Commun; 2006 Mar; 341(4):950-7. PubMed ID: 16458854
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitochondrial tRNAIle A4317G mutation may be associated with hearing impairment in a Han Chinese family.
    Cui Y; He DJ
    Mol Med Rep; 2018 Dec; 18(6):5159-5165. PubMed ID: 30272361
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hearing loss due to the mitochondrial A1555G mutation in Italian families.
    Casano RA; Bykhovskaya Y; Johnson DF; Hamon M; Torricelli F; Bigozzi M; Fischel-Ghodsian N
    Am J Med Genet; 1998 Oct; 79(5):388-91. PubMed ID: 9779807
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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; 15():26. PubMed ID: 24533451
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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; 328(4):1244-51. PubMed ID: 15708009
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.
    Malik SG; Pieter N; Sudoyo H; Kadir A; Marzuki S
    J Hum Genet; 2003; 48(9):480-483. PubMed ID: 12955586
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees.
    Chen H; Zheng J; Xue L; Meng Y; Wang Y; Zheng B; Fang F; Shi S; Qiu Q; Jiang P; Lu Z; Mo JQ; Lu J; Guan MX
    Eur J Hum Genet; 2012 Jun; 20(6):607-12. PubMed ID: 22317974
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.