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Journal Abstract Search

175 related items for PubMed ID: 11836692

  • 1. [Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].
    Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb; 19(1):64-7. PubMed ID: 11836692
    [Abstract] [Full Text] [Related]

  • 2. [Sequence analysis of mtDNA 12S rRNA, tRNA(Leu(UUR)),tRNA(Ser(UCN))and 16S rRNA gene of 12 nonsyndromic inherited deafness pedigrees].
    Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):415-20. PubMed ID: 11774206
    [Abstract] [Full Text] [Related]

  • 3. [Nonsyndromic inherited hearing impairment caused by mtDNA double mutations of A1555G and 961 insC].
    Cao X, Xing GQ, Wei QJ, Bu XK, Wang DY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):629-32. PubMed ID: 15583999
    [Abstract] [Full Text] [Related]

  • 4. [Pedigree analysis and sequence analysis of mtDNA 12srRNA, tRNA(Leu(UUR)), tRNA(Ser(UCN)) gene in nonsyndromic inherited deafness pedigrees].
    Li W, Han D, Yuan H, Cao J.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2004 Oct; 18(10):582-5, 589. PubMed ID: 15620132
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. [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; 23(3):303-5. PubMed ID: 16767669
    [Abstract] [Full Text] [Related]

  • 7. [Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness].
    Yuan H, Jiang S, Yang W, Guo W, Cao J, Dai P.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):141-4. PubMed ID: 10359861
    [Abstract] [Full Text] [Related]

  • 8. [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; 45(7):982-91. PubMed ID: 19705751
    [Abstract] [Full Text] [Related]

  • 9. Sequence analysis of the mitochondrial genome from a large family with maternally inherited nonsyndromic deafness.
    Zhang HJ, Xu CH, Zhan YJ, Zhao SY, Shan YF, Geng XX, Shan XN.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):368-71. PubMed ID: 16086269
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. [Screening for the 1555G mutation in mitochondrial DNA in pedigrees with aminoglycoside antibiotic induced deafness].
    Yuan H, Jiang S, Yang W.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1998 Apr; 33(2):67-70. PubMed ID: 11498854
    [Abstract] [Full Text] [Related]

  • 12. A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss.
    Cardaioli E, Da Pozzo P, Gallus GN, Malandrini A, Gambelli S, Gaudiano C, Malfatti E, Viscomi C, Zicari E, Berti G, Serni G, Dotti MT, Federico A.
    Neuromuscul Disord; 2007 Oct; 17(9-10):681-3. PubMed ID: 17614276
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial tRNA(Leu(UUR)) gene mutation diabetes mellitus in Chinese.
    Xiang K, Wang Y, Wu S, Lu H, Zheng T, Sun D, Weng Q, Jia W, Shen W, Pu L, He J.
    Chin Med J (Engl); 1997 May; 110(5):372-8. PubMed ID: 9594306
    [Abstract] [Full Text] [Related]

  • 14. 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 May; 104(1-2):153-9. PubMed ID: 21621438
    [Abstract] [Full Text] [Related]

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  • 18. [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]

  • 19. A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome.
    Nakamura M, Nakano S, Goto Y, Ozawa M, Nagahama Y, Fukuyama H, Akiguchi I, Kaji R, Kimura J.
    Biochem Biophys Res Commun; 1995 Sep 05; 214(1):86-93. PubMed ID: 7669057
    [Abstract] [Full Text] [Related]

  • 20. [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 05; 37(5):338-42. PubMed ID: 12772452
    [Abstract] [Full Text] [Related]

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