BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

407 related articles for article (PubMed ID: 16826519)

  • 21. 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]  

  • 22. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
    Tang X; Yang L; Zhu Y; Liao Z; Wang J; Qian Y; Tao Z; Hu L; Wu G; Lan J; Wang X; Ji J; Wu J; Ji Y; Feng J; Chen J; Li Z; Zhang X; Lu J; Guan MX
    Gene; 2007 May; 393(1-2):11-9. PubMed ID: 17341440
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients.
    Chen C; Guan MX
    Hum Mol Genet; 2022 Sep; 31(18):3068-3082. PubMed ID: 35467742
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation.
    Li X; Li R; Lin X; Guan MX
    J Biol Chem; 2002 Jul; 277(30):27256-64. PubMed ID: 12011058
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 7(8):e42463. PubMed ID: 22879993
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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; 30(6):728-34. PubMed ID: 18550495
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function.
    Zhang Q; Zhang L; Chen D; He X; Yao S; Zhang Z; Chen Y; Guan MX
    Nucleic Acids Res; 2018 Nov; 46(20):10930-10945. PubMed ID: 30137487
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.
    Liao Z; Zhao J; Zhu Y; Yang L; Yang A; Sun D; Zhao Z; Wang X; Tao Z; Tang X; Wang J; Guan M; Chen J; Li Z; Lu J; Guan MX
    Biochem Biophys Res Commun; 2007 Oct; 362(3):670-6. PubMed ID: 17723226
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation.
    Bykhovskaya Y; Mengesha E; Wang D; Yang H; Estivill X; Shohat M; Fischel-Ghodsian N
    Mol Genet Metab; 2004 May; 82(1):27-32. PubMed ID: 15110318
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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]  

  • 32. 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]  

  • 33. [Mitochondrial tRNAThr G15927A mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation.].
    Tang XW; Li ZY; Lu JX; Zhu Y; Li RH; Wang JD; Guan MX
    Yi Chuan; 2008 Oct; 30(10):1287-94. PubMed ID: 18930888
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Nuclear modifier MTO2 modulates the aminoglycoside-sensitivity of mitochondrial 15S rRNA C1477G mutation in Saccharomyces cerevisiae.
    He X; Zhu X; Wang X; Wang W; Dai Y; Yan Q
    PLoS One; 2013; 8(12):e81490. PubMed ID: 24339937
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 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. 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]  

  • 38. 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]  

  • 39. [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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 21.