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 *

137 related articles for article (PubMed ID: 8800928)

  • 1. Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree.
    Matthijs G; Claes S; Longo-Mbenza B; Cassiman JJ
    Eur J Hum Genet; 1996; 4(1):46-51. PubMed ID: 8800928
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.
    Guan MX; Fischel-Ghodsian N; Attardi G
    Hum Mol Genet; 1996 Jul; 5(7):963-71. PubMed ID: 8817331
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.
    Prezant TR; Agapian JV; Bohlman MC; Bu X; Oztas S; Qiu WQ; Arnos KS; Cortopassi GA; Jaber L; Rotter JI
    Nat Genet; 1993 Jul; 4(3):289-94. PubMed ID: 7689389
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.
    Pandya A; Xia X; Radnaabazar J; Batsuuri J; Dangaansuren B; Fischel-Ghodsian N; Nance WE
    J Med Genet; 1997 Feb; 34(2):169-72. PubMed ID: 9039999
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 48(2):453-6. PubMed ID: 9040738
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Nuclear gene involves in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation].
    Zhao SY; Zhang HJ; Xu CH; Shan XN
    Fen Zi Xi Bao Sheng Wu Xue Bao; 2006 Feb; 39(1):39-45. PubMed ID: 16944570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Mitochondrial 12S rRNA variants studies in 456 subjects with hearing loss in seven schools for deaf and mutes in Zhejiang province].
    Peng GH; Fang F; Zheng J; Zheng BJ; Yu X; Wu Y; Liang LZ; Zhang QM; Zhu Y; Tang XW; Chen BB
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Dec; 47(12):996-1003. PubMed ID: 23328039
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.
    Zhao H; Li R; Wang Q; Yan Q; Deng JH; Han D; Bai Y; Young WY; Guan MX
    Am J Hum Genet; 2004 Jan; 74(1):139-52. PubMed ID: 14681830
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Function study of non-syndromic deafness associated mitochondrial 12S rRNA A839G mutation].
    Yu X; He Z; Xiang H; Zheng J; Nan B; Zheng B; Gao J; Huang S; Guan M; Chen B
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2014 Nov; 49(11):908-15. PubMed ID: 25598369
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.
    Fischel-Ghodsian N; Prezant TR; Bu X; Oztas S
    Am J Otolaryngol; 1993; 14(6):399-403. PubMed ID: 8285309
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.
    Guan MX; Yan Q; Li X; Bykhovskaya Y; Gallo-Teran J; Hajek P; Umeda N; Zhao H; Garrido G; Mengesha E; Suzuki T; del Castillo I; Peters JL; Li R; Qian Y; Wang X; Ballana E; Shohat M; Lu J; Estivill X; Watanabe K; Fischel-Ghodsian N
    Am J Hum Genet; 2006 Aug; 79(2):291-302. PubMed ID: 16826519
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.
    Yamasoba T; Goto Yi; Oka Y; Nishino I; Tsukuda K; Nonaka I
    Neuromuscul Disord; 2002 Jun; 12(5):506-12. PubMed ID: 12031626
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.
    Men M; Jiang L; Wang H; Liu Y; Hu Z; He C; Feng Y
    Acta Otolaryngol; 2011 Sep; 131(9):970-5. PubMed ID: 21504270
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P; Liu X; Han D; Qian Y; Huang D; Yuan H; Li W; Yu F; Zhang R; Lin H; He Y; Yu Y; Sun Q; Qin H; Li R; Zhang X; Kang D; Cao J; Young WY; Guan MX
    Biochem Biophys Res Commun; 2006 Feb; 340(1):194-9. PubMed ID: 16375862
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness.
    Bacino C; Prezant TR; Bu X; Fournier P; Fischel-Ghodsian N
    Pharmacogenetics; 1995 Jun; 5(3):165-72. PubMed ID: 7550368
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3.
    Bykhovskaya Y; Mengesha E; Wang D; Yang H; Estivill X; Shohat M; Fischel-Ghodsian N
    Mol Genet Metab; 2004 Nov; 83(3):199-206. PubMed ID: 15542390
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 44(6):388-90. PubMed ID: 10570910
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.