BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 20153673)

  • 1. 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; 100(1):57-64. PubMed ID: 20153673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNA
    Fan W; Zheng J; Kong W; Cui L; Aishanjiang M; Yi Q; Wang M; Cang X; Tang X; Chen Y; Mo JQ; Sondheimer N; Ge W; Guan MX
    J Biol Chem; 2019 Dec; 294(50):19292-19305. PubMed ID: 31685661
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss.
    Tang X; Zheng J; Ying Z; Cai Z; Gao Y; He Z; Yu H; Yao J; Yang Y; Wang H; Chen Y; Guan MX
    Mitochondrion; 2015 Jul; 23():17-24. PubMed ID: 25968158
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 344(4):1253-7. PubMed ID: 16650816
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 146A(10):1248-58. PubMed ID: 18386806
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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; 48(12):978-84. PubMed ID: 24506995
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
    Wang X; Lu J; Zhu Y; Yang A; Yang L; Li R; Chen B; Qian Y; Tang X; Wang J; Zhang X; Guan MX
    Pharmacogenet Genomics; 2008 Dec; 18(12):1059-70. PubMed ID: 18820594
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 32(3):867-77. PubMed ID: 14960712
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
    Yuan H; Chen J; Liu X; Cheng J; Wang X; Yang L; Yang S; Cao J; Kang D; Dai P; Zhai S; Han D; Young WY; Guan MX
    Biochem Biophys Res Commun; 2007 Oct; 362(1):94-100. PubMed ID: 17698030
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel m.4268T>C mutation in the mitochondrial tRNA
    Zhao LJ; Zhang ZL; Fu Y
    World J Clin Cases; 2022 Jan; 10(1):205-216. PubMed ID: 35071519
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hearing loss and epilepsy may be associated with the novel mitochondrial tRNASer(UCN) 7472delC mutation in a Chinese family].
    Zhao JY; Tang XW; Lan JS; Lv JX; Yang L; Li ZY; Zhu Y; Sun DM; Yang AF; Wang JD; Xu J; Guan MX
    Yi Chuan; 2008 Dec; 30(12):1557-62. PubMed ID: 19073569
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 328(1):32-7. PubMed ID: 15670746
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.
    Chen J; Yuan H; Lu J; Liu X; Wang G; Zhu Y; Cheng J; Wang X; Han B; Yang L; Yang S; Yang A; Sun Q; Kang D; Zhang X; Dai P; Zhai S; Han D; Young WY; Guan MX
    Mitochondrion; 2008 Sep; 8(4):285-92. PubMed ID: 18639500
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family.
    Li R; Liu Y; Li Z; Yang L; Wang S; Guan MX
    Hypertension; 2009 Aug; 54(2):329-37. PubMed ID: 19546379
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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; 28(4):367-73. PubMed ID: 21811972
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Low penetrance of hearing loss in two Chinese families carrying the mitochondrial tRNASer(UCN) mutations.
    Peng W; Zhong Y; Zhao X; Yuan J
    Mol Med Rep; 2020 Jul; 22(1):77-86. PubMed ID: 32377700
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 401(1-2):4-11. PubMed ID: 17698299
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial COI/tRNA
    Ding Y; Xia BH; Teng YS; Zhuo GC; Leng JH
    Int J Clin Exp Pathol; 2017; 10(9):9496-9502. PubMed ID: 31966824
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 12.