BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 18325329)

  • 1. New polymorphic mtDNA restriction site in the 12S rRNA gene detected in Tunisian patients with non-syndromic hearing loss.
    Mkaouar-Rebai E; Tlili A; Masmoudi S; Charfeddine I; Fakhfakh F
    Biochem Biophys Res Commun; 2008 May; 369(3):849-52. PubMed ID: 18325329
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia].
    Dzhemileva LU; Posukh OL; Tazetdinov AM; Barashkov NA; Zhuravskiĭ SG; Ponidelko SN; Markova TG; Tadinova VN; Fedorova SA; Maksimova NR; Khusnutdinova EK
    Genetika; 2009 Jul; 45(7):982-91. PubMed ID: 19705751
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.
    Dai P; Yuan Y; Huang D; Qian Y; Liu X; Han D; Yuan H; Wang X; Young WY; Guan MX
    Biochem Biophys Res Commun; 2006 Sep; 348(1):200-5. PubMed ID: 16875663
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.
    Li Z; Li R; Chen J; Liao Z; Zhu Y; Qian Y; Xiong S; Heman-Ackah S; Wu J; Choo DI; Guan MX
    Hum Genet; 2005 Jun; 117(1):9-15. PubMed ID: 15841390
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.
    Xing G; Chen Z; Wei Q; Tian H; Li X; Zhou A; Bu X; Cao X
    Biochem Biophys Res Commun; 2006 Aug; 346(4):1131-5. PubMed ID: 16782057
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH; Reddy PP
    Int J Audiol; 2008 Nov; 47(11):702-7. PubMed ID: 19031229
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.
    Mkaouar-Rebai E; Fendri-Kriaa N; Louhichi N; Tlili A; Triki C; Ghorbel A; Masmoudi S; Fakhfakh F
    Biosci Rep; 2010 Dec; 30(6):405-11. PubMed ID: 20055758
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.
    Wang Q; Li QZ; Han D; Zhao Y; Zhao L; Qian Y; Yuan H; Li R; Zhai S; Young WY; Guan MX
    Biochem Biophys Res Commun; 2006 Feb; 340(2):583-8. PubMed ID: 16380089
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Nonsyndromic inherited hearing impairment caused by mtDNA double mutations of A1555G and 961 insC].
    Cao X; Xing GQ; Wei QJ; Bu XK; Wang DY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):629-32. PubMed ID: 15583999
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.
    Jin L; Yang A; Zhu Y; Zhao J; Wang X; Yang L; Sun D; Tao Z; Tsushima A; Wu G; Xu L; Chen C; Yi B; Cai J; Tang X; Wang J; Li D; Yuan Q; Liao Z; Chen J; Li Z; Lu J; Guan MX
    Biochem Biophys Res Commun; 2007 Sep; 361(1):133-9. PubMed ID: 17659260
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mutation analysis of 12S rRNA and tRNA-Ser(UCN) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage].
    Shu AL; Ji BH; Qin W; Feng GY; Nie YZ; Liu T; He L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):303-5. PubMed ID: 16767669
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.
    Nahili H; Charif M; Boulouiz R; Bounaceur S; Benrahma H; Abidi O; Chafik A; Rouba H; Kandil M; Barakat A
    Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1071-4. PubMed ID: 20637512
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
    Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
    Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].
    YANG AF; ZHENG J; LV JX; GUAN MX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):165-71. PubMed ID: 21462128
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Maternally inherited deafness associated with a T1095C mutation in the mDNA.
    Tessa A; Giannotti A; Tieri L; Vilarinho L; Marotta G; Santorelli FM
    Eur J Hum Genet; 2001 Feb; 9(2):147-9. PubMed ID: 11313749
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.
    Chaig MR; Zernotti ME; Soria NW; Romero OF; Romero MF; Gerez NM
    Biochem Biophys Res Commun; 2008 Apr; 368(3):631-6. PubMed ID: 18261986
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
    Ou QS; Cheng ZJ; Yang B; Jiang L; Chen J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):550-4. PubMed ID: 19806580
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study.
    Gao Z; Yuan YS
    Medicine (Baltimore); 2020 Mar; 99(13):e19373. PubMed ID: 32221064
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.