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Journal Abstract Search

150 related items for PubMed ID: 12624722

  • 21. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
    Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ.
    Eur J Hum Genet; 1998; 6(6):563-9. PubMed ID: 9887373
    [Abstract] [Full Text] [Related]

  • 22. [An extensive matrilineal nonsyndromic sensorineural deafness family and mtDNA 12SrRNA gene mutation].
    Yan M, Liu N, Shan X, Xin G, Pu X, Wu J, Yang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):321-4. PubMed ID: 10514542
    [Abstract] [Full Text] [Related]

  • 23. Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.
    Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X.
    Biochem Biophys Res Commun; 2006 Aug 11; 346(4):1131-5. PubMed ID: 16782057
    [Abstract] [Full Text] [Related]

  • 24. Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation.
    Bykhovskaya Y, Mengesha E, Wang D, Yang H, Estivill X, Shohat M, Fischel-Ghodsian N.
    Mol Genet Metab; 2004 May 11; 82(1):27-32. PubMed ID: 15110318
    [Abstract] [Full Text] [Related]

  • 25. [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 11; 21(6):629-32. PubMed ID: 15583999
    [Abstract] [Full Text] [Related]

  • 26. [Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].
    Yang AF, Zhu Y, Lu JX, Yang L, Zhao JY, Sun DM.
    Yi Chuan; 2008 Jun 11; 30(6):728-34. PubMed ID: 18550495
    [Abstract] [Full Text] [Related]

  • 27. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.
    Chen T, Liu Q, Jiang L, Liu C, Ou Q.
    Genet Test Mol Biomarkers; 2013 Feb 11; 17(2):122-30. PubMed ID: 23256547
    [Abstract] [Full Text] [Related]

  • 28. [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 11; 19(1):64-7. PubMed ID: 11836692
    [Abstract] [Full Text] [Related]

  • 29. Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.
    Scrimshaw BJ, Faed JM, Tate WP, Yun K.
    J Hum Genet; 1999 Feb 11; 44(6):388-90. PubMed ID: 10570910
    [Abstract] [Full Text] [Related]

  • 30. 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 11; 15(11):1145-55. PubMed ID: 17637808
    [Abstract] [Full Text] [Related]

  • 31. Maternally inherited deafness associated with a T1095C mutation in the mDNA.
    Tessa A, Giannotti A, Tieri L, Vilarinho L, Marotta G, Santorelli FM.
    Eur J Hum Genet; 2001 Feb 11; 9(2):147-9. PubMed ID: 11313749
    [Abstract] [Full Text] [Related]

  • 32. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH, Reddy PP.
    Int J Audiol; 2008 Nov 11; 47(11):702-7. PubMed ID: 19031229
    [Abstract] [Full Text] [Related]

  • 33. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
    Ulubil SA, Furze AD, Angeli SI.
    J Laryngol Otol; 2006 Mar 11; 120(3):230-2. PubMed ID: 16359140
    [Abstract] [Full Text] [Related]

  • 34. Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.
    Mkaouar-Rebai E, Fendri-Kriaa N, Louhichi N, Tlili A, Triki C, Ghorbel A, Masmoudi S, Fakhfakh F.
    Biosci Rep; 2010 Dec 11; 30(6):405-11. PubMed ID: 20055758
    [Abstract] [Full Text] [Related]

  • 35. [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 11; 18(6):415-20. PubMed ID: 11774206
    [Abstract] [Full Text] [Related]

  • 36. Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12s rRNA gene: evidence of heteroplasmy.
    el-Schahawi M, López de Munain A, Sarrazin AM, Shanske AL, Basirico M, Shanske S, DiMauro S.
    Neurology; 1997 Feb 11; 48(2):453-6. PubMed ID: 9040738
    [Abstract] [Full Text] [Related]

  • 37. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness.
    Sevior KB, Hatamochi A, Stewart IA, Bykhovskaya Y, Allen-Powell DR, Fischel-Ghodsian N, Maw MA.
    Am J Med Genet; 1998 Jan 13; 75(2):179-85. PubMed ID: 9450881
    [Abstract] [Full Text] [Related]

  • 38. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
    Chapiro E, Feldmann D, Denoyelle F, Sternberg D, Jardel C, Eliot MM, Bouccara D, Weil D, Garabédian EN, Couderc R, Petit C, Marlin S.
    Eur J Hum Genet; 2002 Dec 13; 10(12):851-6. PubMed ID: 12461693
    [Abstract] [Full Text] [Related]

  • 39. Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.
    Nahili H, Charif M, Boulouiz R, Bounaceur S, Benrahma H, Abidi O, Chafik A, Rouba H, Kandil M, Barakat A.
    Int J Pediatr Otorhinolaryngol; 2010 Sep 13; 74(9):1071-4. PubMed ID: 20637512
    [Abstract] [Full Text] [Related]

  • 40. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2005 Oct 28; 336(3):967-73. PubMed ID: 16168391
    [Abstract] [Full Text] [Related]

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