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 *

300 related articles for article (PubMed ID: 16782057)

  • 41. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
    Chen B; Sun D; Yang L; Zhang C; Yang A; Zhu Y; Zhao J; Chen Y; Guan M; Wang X; Li R; Tang X; Wang J; Tao Z; Lu J; Guan MX
    Am J Med Genet A; 2008 May; 146A(10):1248-58. PubMed ID: 18386806
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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; 82(1):27-32. PubMed ID: 15110318
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [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; 30(6):728-34. PubMed ID: 18550495
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.
    Young WY; Zhao L; Qian Y; Li R; Chen J; Yuan H; Dai P; Zhai S; Han D; Guan MX
    Am J Med Genet A; 2006 Oct; 140(20):2188-97. PubMed ID: 16955413
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people.
    Zhu Y; Zhao J; Feng B; Su Y; Kang D; Yuan H; Zhai S; Dai P
    Acta Otolaryngol; 2015 Jan; 135(1):26-34. PubMed ID: 25376778
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Discrimination of A1555G and C1494T point mutations in the mitochondrial 12S rRNA gene by on/off switch.
    Guo ZF; Guo WS; Xiao L; Gao GQ; Lan F; Lu XG; Li K; Liao DF
    Appl Biochem Biotechnol; 2012 Jan; 166(1):234-42. PubMed ID: 22068689
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.
    Han D; Dai P; Zhu Q; Liu X; Huang D; Yuan Y; Yuan H; Wang X; Qian Y; Young WY; Guan MX
    Biochem Biophys Res Commun; 2007 Jun; 357(2):554-60. PubMed ID: 17434445
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family.
    Malik S; Sudoyo H; Sasmono T; Winata S; Arhya IN; Pramoonjago P; Sudana W; Marzuki S
    J Hum Genet; 2003; 48(3):119-24. PubMed ID: 12624722
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations.
    Yan Q; Bykhovskaya Y; Li R; Mengesha E; Shohat M; Estivill X; Fischel-Ghodsian N; Guan MX
    Biochem Biophys Res Commun; 2006 Apr; 342(4):1130-6. PubMed ID: 16513084
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [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; 26(6):610-4. PubMed ID: 19953480
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.
    Lu J; Li Z; Zhu Y; Yang A; Li R; Zheng J; Cai Q; Peng G; Zheng W; Tang X; Chen B; Chen J; Liao Z; Yang L; Li Y; You J; Ding Y; Yu H; Wang J; Sun D; Zhao J; Xue L; Wang J; Guan MX
    Mitochondrion; 2010 Jun; 10(4):380-90. PubMed ID: 20100600
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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; 15(11):1145-55. PubMed ID: 17637808
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.
    Liao Z; Zhao J; Zhu Y; Yang L; Yang A; Sun D; Zhao Z; Wang X; Tao Z; Tang X; Wang J; Guan M; Chen J; Li Z; Lu J; Guan MX
    Biochem Biophys Res Commun; 2007 Oct; 362(3):670-6. PubMed ID: 17723226
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
    Wang X; Lu J; Zhu Y; Yang A; Yang L; Li R; Chen B; Qian Y; Tang X; Wang J; Zhang X; Guan MX
    Pharmacogenet Genomics; 2008 Dec; 18(12):1059-70. PubMed ID: 18820594
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.
    Zhao L; Young WY; Li R; Wang Q; Qian Y; Guan MX
    Biochem Biophys Res Commun; 2004 Dec; 325(4):1503-8. PubMed ID: 15555598
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mitochondrial mutations associated with aminoglycoside ototoxicity and hearing loss susceptibility identified by meta-analysis.
    Jing W; Zongjie H; Denggang F; Na H; Bin Z; Aifen Z; Xijiang H; Cong Y; Yunping D; Ring HZ; Ring BZ
    J Med Genet; 2015 Feb; 52(2):95-103. PubMed ID: 25515069
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss.
    Li R; Xing G; Yan M; Cao X; Liu XZ; Bu X; Guan MX
    Am J Med Genet A; 2004 Jan; 124A(2):113-7. PubMed ID: 14699607
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
    Shen Z; Zheng J; Chen B; Peng G; Zhang T; Gong S; Zhu Y; Zhang C; Li R; Yang L; Zhou J; Cai T; Jin L; Lu J; Guan MX
    J Transl Med; 2011 Jan; 9():4. PubMed ID: 21205314
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.
    Zhu Y; Qian Y; Tang X; Wang J; Yang L; Liao Z; Li R; Ji J; Li Z; Chen J; Choo DI; Lu J; Guan MX
    Biochem Biophys Res Commun; 2006 Apr; 342(3):843-50. PubMed ID: 16500624
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.