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 *

99 related articles for article (PubMed ID: 24021014)

  • 1. The role of mitochondrial tRNAPhe C628T variant in deafness expression.
    Zhu Q; Zhou Y; Jin X; Lin X
    Mitochondrial DNA; 2015 Feb; 26(1):2-6. PubMed ID: 24021014
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variant at position 10,055 in mitochondrial tRNA(Gly) gene has a negative association with aplastic anemia.
    Jiang Z; Wu X; Zhu Y
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Sep; 27(5):3086-8. PubMed ID: 25629498
    [TBL] [Abstract][Full Text] [Related]  

  • 3. No association between mitochondrial tRNA(Val) T1658C mutation and chronic progressive external ophthalmoplegia (CPEO).
    Zhou L; Wang H; Wei J; Wang Y; Wang Y
    Mitochondrial DNA; 2014 Oct; 25(5):385-6. PubMed ID: 23815321
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome.
    Ling J; Roy H; Qin D; Rubio MA; Alfonzo JD; Fredrick K; Ibba M
    Proc Natl Acad Sci U S A; 2007 Sep; 104(39):15299-304. PubMed ID: 17878308
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A unique tRNA gene family and a novel, highly expressed ORF in the mitochondrial genome of the silver-lip pearl oyster, Pinctada maxima (Bivalvia: Pteriidae).
    Wu X; Li X; Li L; Yu Z
    Gene; 2012 Nov; 510(1):22-31. PubMed ID: 22960401
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNA
    Chen X; Nie Z; Wang F; Wang J; Liu XW; Zheng J; Guo YF; Guan MX
    Mitochondrion; 2017 Jul; 35():111-118. PubMed ID: 28579530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ts mutations in mitochondrial tRNA genes: characterization and effects of two point mutations in the mitochondrial gene for tRNAphe in Saccharomyces cerevisiae.
    Francisci S; Bohn C; Frontali L; Bolotin-Fukuhara M
    Curr Genet; 1998 Feb; 33(2):110-6. PubMed ID: 9506898
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The role of mitochondrial DNA mutations in hearing loss.
    Ding Y; Leng J; Fan F; Xia B; Xu P
    Biochem Genet; 2013 Aug; 51(7-8):588-602. PubMed ID: 23605717
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial tRNA mutations associated with deafness.
    Zheng J; Ji Y; Guan MX
    Mitochondrion; 2012 May; 12(3):406-13. PubMed ID: 22538251
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A comprehensive collection of annotations to interpret sequence variation in human mitochondrial transfer RNAs.
    Diroma MA; Lubisco P; Attimonelli M
    BMC Bioinformatics; 2016 Nov; 17(Suppl 12):338. PubMed ID: 28185569
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Elements of thermodynamics in RNA evolution.
    Kierzek E; Biała E; Kierzek R
    Acta Biochim Pol; 2001; 48(2):485-93. PubMed ID: 11732618
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial tRNAArg T10454C variant may not influence the clinical expression of deafness associated 12S rRNA A1555G mutation.
    Luo Z
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016; 27(2):1137-40. PubMed ID: 24983150
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evolution of a mitochondrial tRNA PHE gene in A. thaliana: import of cytosolic tRNA PHE into mitochondria.
    Chen HC; Viry-Moussaïd M; Dietrich A; Wintz H
    Biochem Biophys Res Commun; 1997 Aug; 237(2):432-7. PubMed ID: 9268729
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel variant m.641A>T in the mitochondrial MT-TF gene is associated with epileptic encephalopathy in adolescent.
    Itkis Y; Krylova T; Pechatnikova NL; De Grassi A; Tabakov VY; Pierri CL; Aleshin V; Boyko A; Bunik VI; Zakharova EY
    Mitochondrion; 2019 Jul; 47():10-17. PubMed ID: 31009750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mutations of mitochondrial tRNA
    Fan W; Tang X; Zheng B; Guan M; Xue L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):128-132. PubMed ID: 28186612
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.
    Tabebi M; Mkaouar-Rebai E; Mnif M; Kallabi F; Ben Mahmoud A; Ben Saad W; Charfi N; Keskes-Ammar L; Kamoun H; Abid M; Fakhfakh F
    Biochem Biophys Res Commun; 2015 Apr; 459(3):353-60. PubMed ID: 25701779
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.
    Yan X; Wang X; Wang Z; Sun S; Chen G; He Y; Mo JQ; Li R; Jiang P; Lin Q; Sun M; Li W; Bai Y; Zhang J; Zhu Y; Lu J; Yan Q; Li H; Guan MX
    J Med Genet; 2011 Oct; 48(10):682-90. PubMed ID: 21931169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial transfer RNA mutations and hypertension.
    Yin SL; Lan C; Pei H; Zhu ZQ
    Genet Mol Res; 2015 Dec; 14(4):17692-8. PubMed ID: 26782414
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heterologous inferential analysis (HIA) as a method to understand the role of mitochondrial rRNA mutations in pathogenesis.
    Elson JL; Smith PM; Vila-Sanjurjo A
    Methods Mol Biol; 2015; 1264():369-83. PubMed ID: 25631029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: a case study.
    Dowlati MA; Derakhshandeh-Peykar P; Houshmand M; Farhadi M; Shojaei A; Bazzaz JT
    Mitochondrial DNA; 2013 Apr; 24(2):132-6. PubMed ID: 22979943
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.