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Journal Abstract Search
332 related items for PubMed ID: 23605717
1. 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 [Abstract] [Full Text] [Related]
3. [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; 28(2):165-71. PubMed ID: 21462128 [Abstract] [Full Text] [Related]
5. 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]
8. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss]. Qu J, Wang J, Xu S. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov 10; 29(22):1936-40. PubMed ID: 26911053 [Abstract] [Full Text] [Related]
10. New polymorphic mtDNA restriction site in the 12S rRNA gene detected in Tunisian patients with non-syndromic hearing loss. Mkaouar-Rebai E, Tlili A, Masmoudi S, Charfeddine I, Fakhfakh F. Biochem Biophys Res Commun; 2008 May 09; 369(3):849-52. PubMed ID: 18325329 [Abstract] [Full Text] [Related]
11. 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 09; 18(12):1059-70. PubMed ID: 18820594 [Abstract] [Full Text] [Related]
12. Mitochondrial rRNA and tRNA and hearing function. Xing G, Chen Z, Cao X. Cell Res; 2007 Mar 09; 17(3):227-39. PubMed ID: 17199108 [Abstract] [Full Text] [Related]
14. 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]
16. Molecular pathogenetic mechanism of maternally inherited deafness. Guan MX. Ann N Y Acad Sci; 2004 Apr 01; 1011():259-71. PubMed ID: 15126302 [Abstract] [Full Text] [Related]
17. Mitochondrial tRNA mutations associated with deafness. Zheng J, Ji Y, Guan MX. Mitochondrion; 2012 May 01; 12(3):406-13. PubMed ID: 22538251 [Abstract] [Full Text] [Related]
18. [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 01; 30(6):728-34. PubMed ID: 18550495 [Abstract] [Full Text] [Related]
19. 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]
20. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss. Jin L, Yang A, Zhu Y, Zhao J, Wang X, Yang L, Sun D, Tao Z, Tsushima A, Wu G, Xu L, Chen C, Yi B, Cai J, Tang X, Wang J, Li D, Yuan Q, Liao Z, Chen J, Li Z, Lu J, Guan MX. Biochem Biophys Res Commun; 2007 Sep 14; 361(1):133-9. PubMed ID: 17659260 [Abstract] [Full Text] [Related] Page: [Next] [New Search]