These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

92 related articles for article (PubMed ID: 19475720)

  • 1. Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation.
    Lu SY; Nishio S; Tsukada K; Oguchi T; Kobayashi K; Abe S; Usami S
    Clin Genet; 2009 May; 75(5):480-4. PubMed ID: 19475720
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation.
    Abe S; Kelley PM; Kimberling WJ; Usami SI
    Am J Med Genet; 2001 Nov; 103(4):334-8. PubMed ID: 11746015
    [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. [Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].
    Yuan YY; Dai P; Zhu XH; Kang DY; Zhang X; Huang DL
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Apr; 44(4):292-6. PubMed ID: 19558834
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. [Analysis of GJB2 gene and mitochondrial DNA A1555G mutations in 16 families with non-syndromic hearing loss].
    Wang W; Cheng HB; Yang N; Shi YC; Liu JZ; Li Q; Yang SM; Shen LY; Liu MJ; Chen Y; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):388-92. PubMed ID: 22875492
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutations affecting the secondary structure of MT-RNR1 gene: a causal relationship with profound nonsyndromic hearing impairment.
    Padma G; Ramchander PV; Nandur VU; Kumar KR; Padma T
    Genet Test Mol Biomarkers; 2012 Sep; 16(9):1092-7. PubMed ID: 22852811
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing loss.
    Chai Y; Sun L; Pang X; Wang X; Chen D; Chen Y; Wu H; Yang T
    Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):614-7. PubMed ID: 24507663
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].
    Wang G; Yuan Y; Li R; Han M; Huang S; Kang D; Zhang X; Dong M; Dai P; Han D
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 May; 25(10):445-8. PubMed ID: 21809555
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence of mitochondrial gene mutations among hearing impaired patients.
    Usami S; Abe S; Akita J; Namba A; Shinkawa H; Ishii M; Iwasaki S; Hoshino T; Ito J; Doi K; Kubo T; Nakagawa T; Komiyama S; Tono T; Komune S
    J Med Genet; 2000 Jan; 37(1):38-40. PubMed ID: 10633132
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.
    Mizutari K; Mutai H; Namba K; Miyanaga Y; Nakano A; Arimoto Y; Masuda S; Morimoto N; Sakamoto H; Kaga K; Matsunaga T
    Orphanet J Rare Dis; 2015 May; 10():60. PubMed ID: 25963016
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy.
    Matsushima K; Nakano A; Arimoto Y; Mutai H; Yamazawa K; Murayama K; Matsunaga T
    Int J Pediatr Otorhinolaryngol; 2018 May; 108():125-131. PubMed ID: 29605341
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated?
    Al-Malky G; Suri R; Sirimanna T; Dawson SJ
    Int J Pediatr Otorhinolaryngol; 2014 Jun; 78(6):969-73. PubMed ID: 24703164
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment.
    Loeza-Becerra F; Rivera-Vega Mdel R; Martínez-Saucedo M; Gonzalez-Huerta LM; Urueta-Cuellar H; Berrruecos-Villalobos P; Cuevas-Covarrubias S
    Int J Pediatr Otorhinolaryngol; 2014 Jul; 78(7):1057-60. PubMed ID: 24774219
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of mutations of 4 common genes among 216 patients with non-syndromic hearing impairment].
    Li C; Lu D; Chen X; Huang B; Chen K; Liu X; Hu A; Zhang Y; Xue X; Xing Y; Yan Z; Dong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct; 35(5):630-633. PubMed ID: 30298483
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The clinical and audiologic features of hearing loss due to mitochondrial mutations.
    Yelverton JC; Arnos K; Xia XJ; Nance WE; Pandya A; Dodson KM
    Otolaryngol Head Neck Surg; 2013 Jun; 148(6):1017-22. PubMed ID: 23525847
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Mitochondrial DNA mutations in matrilineal nonsyndromic deafness pedigrees of southwest China].
    Zhang N; Qiao X; Wang L; Liang C
    Hua Xi Yi Ke Da Xue Xue Bao; 2001 Dec; 32(4):596-8, 626. PubMed ID: 12528560
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Screening of the mitochondrial 12S rRNA (MTRNR1) gene in probands with sensorineural hearing loss].
    Cirçir YE; Incesulu A; Tekin M
    Kulak Burun Bogaz Ihtis Derg; 2007; 17(2):75-80. PubMed ID: 17527057
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.
    Duan SH; Zhu YM; Wang YL; Guo YF
    Acta Otolaryngol; 2015 Jun; 135(6):586-91. PubMed ID: 25761933
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.