BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 19835846)

  • 1. The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
    Kokotas H; Grigoriadou M; Korres GS; Ferekidou E; Papadopoulou E; Neou P; Giannoulia-Karantana A; Kandiloros D; Korres S; Petersen MB
    Biochem Biophys Res Commun; 2009 Dec; 390(3):755-7. PubMed ID: 19835846
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].
    Gallo-Terán J; Morales-Angulo C; del Castillo I; Villamar M; Moreno-Pelayo MA; García-Mantilla J; Moreno F
    Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome.
    Park MK; Sagong B; Lee JD; Bae SH; Lee B; Choi KS; Choo YS; Lee KY; Kim UK
    Int J Pediatr Otorhinolaryngol; 2014 Nov; 78(11):1996-9. PubMed ID: 25223473
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].
    Zhang CQ; Chen BB; Chen YY; Liu XJ; Zheng J; Gao JJ; Huang SY; Nan BY; Zhang YY; Yu X; Guan MX
    Yi Chuan; 2013 Mar; 35(3):352-8. PubMed ID: 23575541
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.
    Usami S; Abe S; Shinkawa H; Kimberling WJ
    J Commun Disord; 1998; 31(5):423-34; quiz 434-5. PubMed ID: 9777488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood onset].
    Gallo-Terán J; Morales-Angulo C; Rodríguez-Ballesteros M; Moreno-Pelayo MA; del Castillo I; Moreno F
    Acta Otorrinolaringol Esp; 2005 Dec; 56(10):463-8. PubMed ID: 16425640
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.
    Ji YB; Han DY; Lan L; Wang DY; Zong L; Zhao FF; Liu Q; Benedict-Alderfer C; Zheng QY; Wang QJ
    Acta Otolaryngol; 2011 Feb; 131(2):124-9. PubMed ID: 21162657
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence of GJB2 mutations in prelingual deafness in the Greek population.
    Pampanos A; Economides J; Iliadou V; Neou P; Leotsakos P; Voyiatzis N; Eleftheriades N; Tsakanikos M; Antoniadi T; Hatzaki A; Konstantopoulou I; Yannoukakos D; Gronskov K; Brondum-Nielsen K; Grigoriadou M; Gyftodimou J; Iliades T; Skevas A; Petersen MB
    Int J Pediatr Otorhinolaryngol; 2002 Sep; 65(2):101-8. PubMed ID: 12176179
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum of genetic changes in patients with non-syndromic hearing impairment and extremely high carrier frequency of 35delG GJB2 mutation in Belarus.
    Danilenko N; Merkulava E; Siniauskaya M; Olejnik O; Levaya-Smaliak A; Kushniarevich A; Shymkevich A; Davydenko O
    PLoS One; 2012; 7(5):e36354. PubMed ID: 22567152
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.
    Estivill X; Govea N; Barceló E; Badenas C; Romero E; Moral L; Scozzri R; D'Urbano L; Zeviani M; Torroni A
    Am J Hum Genet; 1998 Jan; 62(1):27-35. PubMed ID: 9490575
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.
    Moassass F; Al-Halabi B; Nweder MS; Al-Achkar W
    Int J Pediatr Otorhinolaryngol; 2018 Oct; 113():110-114. PubMed ID: 30173967
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.
    Iliades T; Eleftheriades N; Iliadou V; Pampanos A; Voyiatzis N; Economides J; Leotsakos P; Neou P; Tsakanikos M; Antoniadi T; Konstantopoulou I; Yannoukakos D; Grigoriadou M; Skevas A; Petersen MB
    ORL J Otorhinolaryngol Relat Spec; 2002; 64(5):321-3. PubMed ID: 12417772
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)].
    Morales Angulo C; Gallo Terán J; del Castillo I; Moreno Pelayo MA; García-Mantilla J; Moreno Herrero F
    Acta Otorrinolaringol Esp; 2002 Nov; 53(9):641-8. PubMed ID: 12584878
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of deafness-causing mutations in the Greek mitochondrial genome.
    Kokotas H; Grigoriadou M; Korres GS; Ferekidou E; Kandiloros D; Korres S; Petersen MB
    Dis Markers; 2011; 30(6):283-9. PubMed ID: 21725156
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.
    ØStergaard E; Montserrat-Sentis B; Grønskov K; Brøndum-Nielsen K
    Clin Genet; 2002 Oct; 62(4):303-5. PubMed ID: 12372057
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.
    Maniglia LP; Moreira BCL; da Silva MAOM; Piatto VB; Maniglia JV
    Braz J Otorhinolaryngol; 2008; 74(5):731-736. PubMed ID: 19082356
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Study of mitochondrial DNA A1555G and C1494T mutations in a large cohort of women individuals.
    Wang L; Wang X; Cai X; Qiang R
    Mitochondrial DNA A DNA Mapp Seq Anal; 2019 Mar; 30(2):222-225. PubMed ID: 29790807
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA].
    Gallo-Terán J; Morales-Angulo C; del Castillo I; Moreno-Pelayo MA; Mazón A; Moreno F
    Med Clin (Barc); 2003 Jul; 121(6):216-8. PubMed ID: 12882732
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition.
    Bai YH; Ren CC; Gong XR; Meng LP
    J Laryngol Otol; 2008 Oct; 122(10):1037-41. PubMed ID: 18282333
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.