BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 15694374)

  • 21. Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.
    Labay V; Garrido G; Madeo AC; Nance WE; Friedman TB; Friedman PL; Del Castillo I; Griffith AJ
    Clin Genet; 2008 Jan; 73(1):50-4. PubMed ID: 18028453
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 104(1-2):153-9. PubMed ID: 21621438
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.
    Chen J; Yuan H; Lu J; Liu X; Wang G; Zhu Y; Cheng J; Wang X; Han B; Yang L; Yang S; Yang A; Sun Q; Kang D; Zhang X; Dai P; Zhai S; Han D; Young WY; Guan MX
    Mitochondrion; 2008 Sep; 8(4):285-92. PubMed ID: 18639500
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 75(2):179-85. PubMed ID: 9450881
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.
    Giordano C; Pallotti F; Walker WF; Checcarelli N; Musumeci O; Santorelli F; d'Amati G; Schon EA; DiMauro S; Hirano M; Davidson MM
    Biochem Biophys Res Commun; 2002 Apr; 293(1):521-9. PubMed ID: 12054632
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao H; Young WY; Yan Q; Li R; Cao J; Wang Q; Li X; Peters JL; Han D; Guan MX
    Nucleic Acids Res; 2005; 33(3):1132-9. PubMed ID: 15722487
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment.
    Hutchin TP; Parker MJ; Young ID; Davis AC; Pulleyn LJ; Deeble J; Lench NJ; Markham AF; Mueller RF
    J Med Genet; 2000 Sep; 37(9):692-4. PubMed ID: 10978361
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.
    Müller T; Deschauer M; Neudecker S; Zierz S
    Acta Neuropathol; 2005 Oct; 110(4):426-30. PubMed ID: 16133542
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene.
    Bidooki S; Jackson MJ; Johnson MA; Chrzanowska-Lightowlers ZM; Taylor RW; Venables G; Lightowlers RN; Turnbull DM; Bindoff LA
    Neuromuscul Disord; 2004 Jul; 14(7):417-20. PubMed ID: 15210164
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagia.
    Souilem S; Kefi M; Mancuso M; Nesti C; Hentati F; Amouri R
    Diagn Mol Pathol; 2010 Mar; 19(1):28-32. PubMed ID: 20186009
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Loss of mutant mitochondrial DNA harboring the MELAS A3243G mutation in human cybrid cells after cell-cell fusion with normal tissue-derived fibroblast cells.
    Yano T; Tanaka M; Fukuda N; Ueda T; Nagase H
    Int J Mol Med; 2010 Jan; 25(1):153-8. PubMed ID: 19956914
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation.
    Maász A; Komlósi K; Hadzsiev K; Szabó Z; Willems PJ; Gerlinger I; Kosztolányi G; Méhes K; Melegh B
    Curr Med Chem; 2008; 15(13):1257-62. PubMed ID: 18537605
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mitochondrial tRNA mutations associated with deafness.
    Zheng J; Ji Y; Guan MX
    Mitochondrion; 2012 May; 12(3):406-13. PubMed ID: 22538251
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Mutations of mitochondrial tRNA
    Fan W; Tang X; Zheng B; Guan M; Xue L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):128-132. PubMed ID: 28186612
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.