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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
344 related items for PubMed ID: 14681830
1. 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 [Abstract] [Full Text] [Related]
2. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation. Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX. Biochem Biophys Res Commun; 2006 Feb 10; 340(2):583-8. PubMed ID: 16380089 [Abstract] [Full Text] [Related]
4. [Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations]. YANG AF, ZHENG J, LV JX, GUAN MX. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr 10; 28(2):165-71. PubMed ID: 21462128 [Abstract] [Full Text] [Related]
5. Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation. Qian Y, Guan MX. Antimicrob Agents Chemother; 2009 Nov 10; 53(11):4612-8. PubMed ID: 19687236 [Abstract] [Full Text] [Related]
6. 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 10; 5(7):963-71. PubMed ID: 8817331 [Abstract] [Full Text] [Related]
7. 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 10; 10(1):69-81. PubMed ID: 19818876 [Abstract] [Full Text] [Related]
8. 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 10; 18(12):1059-70. PubMed ID: 18820594 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
12. Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss. Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX. Am J Med Genet A; 2005 Oct 01; 138A(2):133-40. PubMed ID: 16152638 [Abstract] [Full Text] [Related]
13. 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 26; 362(3):670-6. PubMed ID: 17723226 [Abstract] [Full Text] [Related]
14. [Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation]. Gong SS, Chen BB, Peng GH, Zheng J, Zhang T, Zheng BJ, Fang F, Zhang CQ, Lv JX, Guan MX. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug 26; 29(4):382-7. PubMed ID: 22875491 [Abstract] [Full Text] [Related]
15. 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 01; 357(2):554-60. PubMed ID: 17434445 [Abstract] [Full Text] [Related]
16. 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 01; 9(6):418-28. PubMed ID: 19682603 [Abstract] [Full Text] [Related]
17. [Mitochondrial tRNA(Thr)T15943C mutation may be a new position that affects the phenotypic expression of deafness associated 12s rRNA A1555G mutation]. Xiao H, He Z, Gao Y, Yang Y, Zheng J, Cai Z, Zheng B, Tang X, Guan M. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 01; 32(2):163-8. PubMed ID: 25863077 [Abstract] [Full Text] [Related]
18. 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 01; 166(1):234-42. PubMed ID: 22068689 [Abstract] [Full Text] [Related]
19. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation. Tang X, Yang L, Zhu Y, Liao Z, Wang J, Qian Y, Tao Z, Hu L, Wu G, Lan J, Wang X, Ji J, Wu J, Ji Y, Feng J, Chen J, Li Z, Zhang X, Lu J, Guan MX. Gene; 2007 May 15; 393(1-2):11-9. PubMed ID: 17341440 [Abstract] [Full Text] [Related]
20. 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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]