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Journal Abstract Search

261 related items for PubMed ID: 22875491

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  • 3. Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
    Chen J, Yang L, Yang A, Zhu Y, Zhao J, Sun D, Tao Z, Tang X, Wang J, Wang X, Tsushima A, Lan J, Li W, Wu F, Yuan Q, Ji J, Feng J, Wu C, Liao Z, Li Z, Greinwald JH, Lu J, Guan MX.
    Gene; 2007 Oct 15; 401(1-2):4-11. PubMed ID: 17698299
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  • 5. Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
    Lu J, Qian Y, Li Z, Yang A, Zhu Y, Li R, Yang L, Tang X, Chen B, Ding Y, Li Y, You J, Zheng J, Tao Z, Zhao F, Wang J, Sun D, Zhao J, Meng Y, Guan MX.
    Mitochondrion; 2010 Jan 15; 10(1):69-81. PubMed ID: 19818876
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  • 7. [Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees].
    Peng GH, Zheng BJ, Fang F, Wu Y, Liang LZ, Zheng J, Nan BY, Yu X, Tang XW, Zhu Y, Lu JX, Chen BB, Guan MX.
    Yi Chuan; 2013 Jan 15; 35(1):62-72. PubMed ID: 23357266
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  • 8. Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
    Yuan H, Chen J, Liu X, Cheng J, Wang X, Yang L, Yang S, Cao J, Kang D, Dai P, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2007 Oct 12; 362(1):94-100. PubMed ID: 17698030
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  • 9. Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations.
    Ding Y, Xia BH, Liu Q, Li MY, Huang SX, Zhuo GC.
    Gene; 2016 Oct 10; 591(1):148-152. PubMed ID: 27397648
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  • 11. 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 10; 17(2):122-30. PubMed ID: 23256547
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  • 12. 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 04; 9():4. PubMed ID: 21205314
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  • 13. 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 04; 10(4):380-90. PubMed ID: 20100600
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  • 14. Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.
    Zhu Y, Li Q, Chen Z, Kun Y, Liu L, Liu X, Yuan H, Zhai S, Han D, Dai P.
    Mitochondrion; 2009 Nov 04; 9(6):418-28. PubMed ID: 19682603
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  • 15. 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 15; 146A(10):1248-58. PubMed ID: 18386806
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  • 20. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.
    Guan MX.
    Mitochondrion; 2011 Mar 15; 11(2):237-45. PubMed ID: 21047563
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