BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

62 related articles for article (PubMed ID: 20662562)

  • 1. Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of China.
    Guo YF; Liu XW; Xu BC; Zhu YM; Wang YL; Zhao FF; Wang DY; Zhao YL; Ji YB; Wang QJ
    Genet Test Mol Biomarkers; 2010 Aug; 14(4):527-31. PubMed ID: 20662562
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.
    Duan SH; Zhu YM; Wang YL; Guo YF
    Acta Otolaryngol; 2015 Jun; 135(6):586-91. PubMed ID: 25761933
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Audio profiles in mitochondrial deafness m.1555A>G and m.3243A>G show distinct differences.
    Iwanicka-Pronicka K; Pollak A; Skórka A; Lechowicz U; Korniszewski L; Westfal P; Skarżyński H; Płoski R
    Med Sci Monit; 2015 Mar; 21():694-700. PubMed ID: 25744662
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC; Chiu YH; Chen PJ; Hsu CJ
    Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China.
    Zhang M; Han Y; Zhang F; Bai X; Wang H
    Acta Otolaryngol; 2019 Jul; 139(7):612-617. PubMed ID: 31107121
    [No Abstract]   [Full Text] [Related]  

  • 6. A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions.
    Mezghani N; Mnif M; Mkaouar-Rebai E; Kallel N; Charfi N; Abid M; Fakhfakh F
    Biochem Biophys Res Commun; 2013 Feb; 431(4):670-4. PubMed ID: 23357420
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid screening for the mitochondrial DNA C1494T mutation in a deaf population in China using real-time quantitative PCR.
    Li Q; Yuan YY; Huang DL; Han DY; Dai P
    Acta Otolaryngol; 2012 Aug; 132(8):814-8. PubMed ID: 22497215
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Genetic epidemiologic study of mitochondrial DNA 7445A-->G mutation among non-syndromic deafness in Chinese population].
    Liu YH; Ke XM; Qi Y; Xu HB; Gu ZP; Liu XC; Liu JF
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 14(4):177-8. PubMed ID: 12541497
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Mitochondrial DNA A1555G mutation analysis in 802 nonsyndromic hearing impairment patients].
    Liu XW; Guo YF; Han DY; Zhao YL; Lan L; Zhao C; Wang QJ
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Oct; 42(10):739-42. PubMed ID: 18229583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated?
    Al-Malky G; Suri R; Sirimanna T; Dawson SJ
    Int J Pediatr Otorhinolaryngol; 2014 Jun; 78(6):969-73. PubMed ID: 24703164
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
    Liu X; Dai P; Huang DL; Yuan HJ; Li WM; Cao JY; Yu F; Zhang RN; Lin HY; Zhu XH; He Y; Yu YJ; Yao K
    Zhonghua Yi Xue Za Zhi; 2006 May; 86(19):1318-22. PubMed ID: 16796900
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China].
    Zhu Q; Liu X; Han D; Kang D; Zhang X; Jin Z; Li M; Dai P
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 May; 21(10):460-2. PubMed ID: 17650818
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Nonsyndromic deafness and mitochondrial DNA mutation].
    Liu YH; Ke XM; Gu ZP
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2000 Jan; 14(1):9-11. PubMed ID: 12541433
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss.
    Uehara DT; Rincon D; Abreu-Silva RS; Auricchio MT; Tabith A; Kok F; Mingroni-Netto RC
    Genet Test Mol Biomarkers; 2010 Oct; 14(5):611-6. PubMed ID: 20722495
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants.
    Göpel W; Berkowski S; Preuss M; Ziegler A; Küster H; Felderhoff-Müser U; Gortner L; Mögel M; Härtel C; Herting E;
    BMC Pediatr; 2014 Aug; 14():210. PubMed ID: 25155176
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial tRNAGln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness.
    Ding Y; Teng Y; Guo Q; Leng J
    Genes (Basel); 2022 Oct; 13(10):. PubMed ID: 36292680
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
    Kato T; Nishigaki Y; Noguchi Y; Ueno H; Hosoya H; Ito T; Kimura Y; Kitamura K; Tanaka M
    J Hum Genet; 2010 Mar; 55(3):147-54. PubMed ID: 20111055
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Aminoglycoside ototoxicity associated with mitochondrial DNA mutation].
    Ke X; Qi Y; Gu Z; Zhang Z; Zhang W; Jiang S; Liu J
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 1999 May; 13(5):195-7. PubMed ID: 12563999
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hearing in 44-45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study.
    Rahman S; Ecob R; Costello H; Sweeney MG; Duncan AJ; Pearce K; Strachan D; Forge A; Davis A; Bitner-Glindzicz M
    BMJ Open; 2012; 2(1):e000411. PubMed ID: 22223843
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Aminoglycoside-induced deafness during treatment of acute leukaemia.
    Bitner-Glindzicz M; Osei-Lah V; Colvin I; Sirimanna T; Lucas D; Mac Ardle B; Webb D; Shankar A; Kingston J; Jenkins L; Rahman S
    Arch Dis Child; 2010 Feb; 95(2):153-5. PubMed ID: 20172897
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.