BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

410 related articles for article (PubMed ID: 19705751)

  • 1. [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]  

  • 2. [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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. [Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].
    Li W; Han D; Yuan H; Wang Y; Cao J; Yang W; Jiang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb; 19(1):64-7. PubMed ID: 11836692
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. 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]  

  • 11. [Sequence analysis of mtDNA 12S rRNA, tRNA(Leu(UUR)),tRNA(Ser(UCN))and 16S rRNA gene of 12 nonsyndromic inherited deafness pedigrees].
    Li W; Han D; Yuan H; Wang Y; Cao J; Yang W; Jiang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):415-20. PubMed ID: 11774206
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. [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]  

  • 17. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
    Kupka S; Tóth T; Wróbel M; Zeissler U; Szyfter W; Szyfter K; Niedzielska G; Bal J; Zenner HP; Sziklai I; Blin N; Pfister M
    Hum Mutat; 2002 Mar; 19(3):308-9. PubMed ID: 11857751
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family.
    Malik S; Sudoyo H; Sasmono T; Winata S; Arhya IN; Pramoonjago P; Sudana W; Marzuki S
    J Hum Genet; 2003; 48(3):119-24. PubMed ID: 12624722
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides.
    Gürtler N; Schmuziger N; Kim Y; Mhatre AN; Jungi M; Lalwani AK
    Laryngoscope; 2005 Apr; 115(4):640-4. PubMed ID: 15805873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.