BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 24401907)

  • 1. Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening.
    Yano T; Nishio SY; Usami S;
    J Hum Genet; 2014 Feb; 59(2):100-6. PubMed ID: 24401907
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation.
    Mutai H; Kouike H; Teruya E; Takahashi-Kodomari I; Kakishima H; Taiji H; Usami S; Okuyama T; Matsunaga T
    BMC Med Genet; 2011 Oct; 12():135. PubMed ID: 21989059
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.
    Subathra M; Selvakumari M; Ramesh A; Ramakrishnan R; Karan KR; Kaur M; Manikandan M; Srikumari Srisailapathy CR
    Ann Hum Genet; 2014 May; 78(3):217-34. PubMed ID: 24660976
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.
    Joo SY; Jang SH; Kim JA; Kim SJ; Kim B; Kim HY; Choi JY; Gee HY; Jung J
    J Korean Med Sci; 2023 Dec; 38(48):e355. PubMed ID: 38084023
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Mitochondrial mutations in maternally inherited hearing loss.
    Mutai H; Watabe T; Kosaki K; Ogawa K; Matsunaga T
    BMC Med Genet; 2017 Mar; 18(1):32. PubMed ID: 28320335
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial mutations in non-syndromic hearing loss at UAE.
    Mohamed WKE; Arnoux M; Cardoso THS; Almutery A; Tlili A
    Int J Pediatr Otorhinolaryngol; 2020 Nov; 138():110286. PubMed ID: 32871514
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.
    Bae JW; Kim DB; Choi JY; Park HJ; Lee JD; Hur DG; Bae SH; Jung DJ; Lee SH; Kim UK; Lee KY
    PLoS One; 2012; 7(8):e42463. PubMed ID: 22879993
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GJB2 and mitochondrial DNA 1555A>G mutations in students with hearing loss in the Hubei Province of China.
    Chen G; He F; Fu S; Dong J
    Int J Pediatr Otorhinolaryngol; 2011 Sep; 75(9):1156-9. PubMed ID: 21777984
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Application of next‑generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss.
    Lechowicz U; Pollak A; Frączak A; Rydzanicz M; Stawiński P; Lorens A; Skarżyński PH; Skarżyński H; Płoski R; Ołdak M
    Mol Med Rep; 2018 Jan; 17(1):1782-1790. PubMed ID: 29257206
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Heteroplasmy levels of mtDNA1555A>G mutation is positively associated with diverse phenotypes and mutation transmission in a Chinese family.
    Shen SS; Liu C; Xu ZY; Hu YH; Gao GF; Wang SY
    Biochem Biophys Res Commun; 2012 Apr; 420(4):907-12. PubMed ID: 22475488
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening of mitochondrial DNA mutations in subjects with non-syndromic familial hearing impairment in Taiwan.
    Chu SY; Chiang SC; Chien YH; Hwu WL
    Acta Paediatr Taiwan; 2002; 43(6):330-3. PubMed ID: 12632786
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss.
    Dowlati MA; Derakhshandeh-Peykar P; Houshmand M; Farhadi M; Shojaei A; Fallah M; Mohammadi E; Tajdini A; Arastoo S; Tavakkoly-Bazzaz J
    Mol Biol Rep; 2013 Mar; 40(3):2689-95. PubMed ID: 23242658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mitochondrial gene variants in Northwestern Chinese probands with non-syndromic hearing loss by whole mitochondrial genome screening.
    Chen X; Wang F; Maerhaba A; Li Q; Wang J; Liu X; Zheng J; Chen Y; Guo Y
    Gene; 2018 Apr; 652():59-65. PubMed ID: 29408584
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny.
    Zaragoza MV; Brandon MC; Diegoli M; Arbustini E; Wallace DC
    Eur J Hum Genet; 2011 Feb; 19(2):200-7. PubMed ID: 20978534
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.
    Yamamoto N; Mutai H; Namba K; Morita N; Masuda S; Nishi Y; Nakano A; Masuda S; Fujioka M; Kaga K; Ogawa K; Matsunaga T
    Orphanet J Rare Dis; 2017 Sep; 12(1):157. PubMed ID: 28946916
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.