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 *

206 related articles for article (PubMed ID: 24470521)

  • 1. Mitochondrial tRNA variants in Chinese subjects with coronary heart disease.
    Qin Y; Xue L; Jiang P; Xu M; He Y; Shi S; Huang Y; He J; Mo JQ; Guan MX
    J Am Heart Assoc; 2014 Jan; 3(1):e000437. PubMed ID: 24470521
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Coronary heart disease is associated with a mutation in mitochondrial tRNA.
    Jia Z; Wang X; Qin Y; Xue L; Jiang P; Meng Y; Shi S; Wang Y; Qin Mo J; Guan MX
    Hum Mol Genet; 2013 Oct; 22(20):4064-73. PubMed ID: 23736300
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial tRNA mutations in Chinese hypertensive individuals.
    Liu Y; Li Y; Wang X; Ma Q; Zhu C; Li Z; Yin T; Yang J; Chen Y; Guan M
    Mitochondrion; 2016 May; 28():1-7. PubMed ID: 26923935
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maternally inherited coronary heart disease is associated with a novel mitochondrial tRNA mutation.
    Zhang Z; Liu M; He J; Zhang X; Chen Y; Li H
    BMC Cardiovasc Disord; 2019 Dec; 19(1):293. PubMed ID: 31842766
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.
    Liu Y; Li R; Li Z; Wang XJ; Yang L; Wang S; Guan MX
    Hypertension; 2009 Jun; 53(6):1083-90. PubMed ID: 19398658
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension.
    Xue L; Wang M; Li H; Wang H; Jiang F; Hou L; Geng J; Lin Z; Peng Y; Zhou H; Yu H; Jiang P; Mo JQ; Guan MX
    Mitochondrion; 2016 Sep; 30():208-21. PubMed ID: 27544295
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial tRNA
    Ding Y; Xia BH; Zhang CJ; Zhuo GC
    Gene; 2018 Feb; 642():299-306. PubMed ID: 29155328
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Correlation of mitochondrial tRNA variants with coronary heart disease in a Chinese pedigree].
    Ding Y; Yu J; Gao B; Huang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jul; 40(7):807-814. PubMed ID: 37368381
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.
    Ji Y; Liang M; Zhang J; Zhang M; Zhu J; Meng X; Zhang S; Gao M; Zhao F; Wei QP; Jiang P; Tong Y; Liu X; Qin Mo J; Guan MX
    J Hum Genet; 2014 Mar; 59(3):134-40. PubMed ID: 24430572
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [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]  

  • 15. Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.
    Young WY; Zhao L; Qian Y; Li R; Chen J; Yuan H; Dai P; Zhai S; Han D; Guan MX
    Am J Med Genet A; 2006 Oct; 140(20):2188-97. PubMed ID: 16955413
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNA
    Zhang J; Ji Y; Liu X; Chen J; Wang B; Zhang M; Guan MX
    Mitochondrion; 2018 Sep; 42():84-91. PubMed ID: 29225014
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees.
    Qiu Q; Li R; Jiang P; Xue L; Lu Y; Song Y; Han J; Lu Z; Zhi S; Mo JQ; Guan MX
    Hum Mutat; 2012 Aug; 33(8):1285-93. PubMed ID: 22549939
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.
    Lu Z; Chen H; Meng Y; Wang Y; Xue L; Zhi S; Qiu Q; Yang L; Mo JQ; Guan MX
    Eur J Hum Genet; 2011 Nov; 19(11):1181-6. PubMed ID: 21694735
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.