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168 related items for PubMed ID: 26873147

  • 1. Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss.
    Jiang H, Chen J, Li Y, Lin PF, He JG, Yang BB.
    Braz J Otorhinolaryngol; 2016; 82(4):391-6. PubMed ID: 26873147
    [Abstract] [Full Text] [Related]

  • 2. [Mitochondrial 12S rRNA gene A827G in two pedigrees with nonsyndromic deafness].
    Chen ZB, Cao X, Xing GQ, Tian HQ, Zhou AD, Wei QU, Bu XK.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):415-8. PubMed ID: 16883529
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.
    Wei Q, Wang S, Yao J, Lu Y, Chen Z, Xing G, Cao X.
    J Transl Med; 2013 Jul 04; 11():163. PubMed ID: 23826813
    [Abstract] [Full Text] [Related]

  • 5. [Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang].
    Li YH, Jiang H, Yang LJ, Xu HX, Li H, Li HW, Luo YH, Wang CW, Zou GH.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Aug 04; 45(8):645-51. PubMed ID: 21055240
    [Abstract] [Full Text] [Related]

  • 6. [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 04; 45(7):982-91. PubMed ID: 19705751
    [Abstract] [Full Text] [Related]

  • 7. The role of mitochondrial DNA mutations in hearing loss.
    Ding Y, Leng J, Fan F, Xia B, Xu P.
    Biochem Genet; 2013 Aug 04; 51(7-8):588-602. PubMed ID: 23605717
    [Abstract] [Full Text] [Related]

  • 8. Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes.
    Rydzanicz M, Wróbel M, Cywińska K, Froehlich D, Gawecki W, Szyfter W, Szyfter K.
    Genet Test Mol Biomarkers; 2009 Apr 04; 13(2):167-72. PubMed ID: 19371214
    [Abstract] [Full Text] [Related]

  • 9. [Mutation analysis of mitochondrial 12S rRNA gene G709A in a maternally inherited pedigree with non-syndromic deafness].
    Wei Q, Lu Y, Zhang Y, Chen Z, Xing G, Cao X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 04; 26(6):610-4. PubMed ID: 19953480
    [Abstract] [Full Text] [Related]

  • 10. 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 04; 113():110-114. PubMed ID: 30173967
    [Abstract] [Full Text] [Related]

  • 11. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
    Qu J, Wang J, Xu S.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov 04; 29(22):1936-40. PubMed ID: 26911053
    [Abstract] [Full Text] [Related]

  • 12. Mutations in the mitochondrial tRNA Ser(UCN) and in the GJB2 (connexin 26) gene are not modifiers of the age at onset or severity of hearing loss in Spanish patients with the 12S rRNA A1555G mutation.
    López-Bigas N, Rabionet R, Martinez E, Bravo O, Girons J, Borragan A, Pellicer M, Arbonés ML, Estivill X.
    Am J Hum Genet; 2000 Apr 04; 66(4):1465-7. PubMed ID: 10739773
    [No Abstract] [Full Text] [Related]

  • 13. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
    Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1244-51. PubMed ID: 15708009
    [Abstract] [Full Text] [Related]

  • 14. [Mutations analysis in a pedigree with maternally inherited sensorineural hearing loss].
    Xu C, Zhang H, Zhang Y, Zhao S, Geng X, Shan Y, Shan X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 25; 22(2):125-8. PubMed ID: 15793769
    [Abstract] [Full Text] [Related]

  • 15. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients.
    Abreu-Silva RS, Lezirovitz K, Braga MC, Spinelli M, Pirana S, Della-Rosa VA, Otto PA, Mingroni-Netto RC.
    Braz J Med Biol Res; 2006 Feb 25; 39(2):219-26. PubMed ID: 16470309
    [Abstract] [Full Text] [Related]

  • 16. Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family.
    Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X.
    Biochem Biophys Res Commun; 2006 Jun 16; 344(4):1253-7. PubMed ID: 16650816
    [Abstract] [Full Text] [Related]

  • 17. Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
    Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX.
    Am J Med Genet A; 2005 Oct 01; 138A(2):133-40. PubMed ID: 16152638
    [Abstract] [Full Text] [Related]

  • 18. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec 01; (559):13-8. PubMed ID: 18340555
    [Abstract] [Full Text] [Related]

  • 19. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
    [Abstract] [Full Text] [Related]

  • 20. [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 02; 23(3):303-5. PubMed ID: 16767669
    [Abstract] [Full Text] [Related]

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