BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 15917167)

  • 1. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
    Kobayashi K; Oguchi T; Asamura K; Miyagawa M; Horai S; Abe S; Usami S
    Auris Nasus Larynx; 2005 Jun; 32(2):119-24. PubMed ID: 15917167
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment].
    Morales Angulo C; Gallo-Terán J; Señaris B; Fontalva A; González-Aguado R; Fernández-Luna JL
    Acta Otorrinolaringol Esp; 2011; 62(2):83-6. PubMed ID: 21129708
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
    Verhoeven K; Ensink RJ; Tiranti V; Huygen PL; Johnson DF; Schatteman I; Van Laer L; Verstreken M; Van de Heyning P; Fischel-Ghodsian N; Zeviani M; Cremers CW; Willems PJ; Van Camp G
    Eur J Hum Genet; 1999 Jan; 7(1):45-51. PubMed ID: 10094190
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing loss.
    Scrimshaw BJ; Faed JM; Tate WP; Yun K
    N Z Med J; 1999 Jun; 112(1089):216-7. PubMed ID: 10414625
    [No Abstract]   [Full Text] [Related]  

  • 8. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
    Ulubil SA; Furze AD; Angeli SI
    J Laryngol Otol; 2006 Mar; 120(3):230-2. PubMed ID: 16359140
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
    Nagata H; Kumahara K; Tomemori T; Arimoto Y; Isoyama K; Yoshida K; Konno A
    J Hum Genet; 2001; 46(10):595-9. PubMed ID: 11587074
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mitochondrial DNA mutations and non-syndromic sensorineural hearing loss].
    Kong W; Wang Q; Zheng X; Cheng H
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Oct; 37(5):338-42. PubMed ID: 12772452
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S; Forli F; Passetti S; Rocchi A; Pollina L; Cecchetti D; Mancuso M; Siciliano G
    Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
    Abe S; Usami S; Shinkawa H; Weston MD; Overbeck LD; Hoover DM; Kenyon JB; Horai S; Kimberling WJ
    Eur J Hum Genet; 1998; 6(6):563-9. PubMed ID: 9887373
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.
    Payne M; Yang Z; Katz BJ; Warner JE; Weight CJ; Zhao Y; Pearson ED; Treft RL; Hillman T; Kennedy RJ; Meire FM; Zhang K
    Am J Ophthalmol; 2004 Nov; 138(5):749-55. PubMed ID: 15531309
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
    Matsunaga T; Kumanomido H; Shiroma M; Ohtsuka A; Asamura K; Usami S
    Laryngoscope; 2004 Jun; 114(6):1085-91. PubMed ID: 15179218
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P; Liu X; Han D; Qian Y; Huang D; Yuan H; Li W; Yu F; Zhang R; Lin H; He Y; Yu Y; Sun Q; Qin H; Li R; Zhang X; Kang D; Cao J; Young WY; Guan MX
    Biochem Biophys Res Commun; 2006 Feb; 340(1):194-9. PubMed ID: 16375862
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
    Chapiro E; Feldmann D; Denoyelle F; Sternberg D; Jardel C; Eliot MM; Bouccara D; Weil D; Garabédian EN; Couderc R; Petit C; Marlin S
    Eur J Hum Genet; 2002 Dec; 10(12):851-6. PubMed ID: 12461693
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients.
    Rydzanicz M; Cywińska K; Wróbel M; Pollak A; Gawęcki W; Wojsyk-Banaszak I; Lechowicz U; Mueller-Malesińska M; Ołdak M; Płoski R; Skarżyński H; Szyfter K; Szyfter W
    Mol Genet Metab; 2011; 104(1-2):153-9. PubMed ID: 21621438
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [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]  

    [Next]    [New Search]
    of 10.