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204 related items for PubMed ID: 21504270
21. Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation. Bae JW, Kim DB, Choi JY, Park HJ, Lee JD, Hur DG, Bae SH, Jung DJ, Lee SH, Kim UK, Lee KY. PLoS One; 2012; 7(8):e42463. PubMed ID: 22879993 [Abstract] [Full Text] [Related]
22. [Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees]. Zhang T, Chen BB, Zheng J, Gong SS, Zhang CQ, Lv JX, Guan MX. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):367-73. PubMed ID: 21811972 [Abstract] [Full Text] [Related]
23. [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 [Abstract] [Full Text] [Related]
24. Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China. Wei Q, Wang S, Yao J, Lu Y, Chen Z, Xing G, Cao X. J Transl Med; 2013 Jul 04; 11():163. PubMed ID: 23826813 [Abstract] [Full Text] [Related]
25. 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 03; 340(1):194-9. PubMed ID: 16375862 [Abstract] [Full Text] [Related]
26. [Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis]. Lyu K, Xiong Y, Yu H, Zou L, Ran L, Liu D, Yin Q, Xu Y, Fang X, Song Z, Huang L, Tan D, Zhang Z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct 03; 31(5):547-52. PubMed ID: 25297577 [Abstract] [Full Text] [Related]
27. Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation. Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y, Ren X, Zhou M, Wang M, Gong S, Mo JQ, Shu Q, Guan MX. J Biol Chem; 2018 Mar 02; 293(9):3321-3334. PubMed ID: 29348176 [Abstract] [Full Text] [Related]
28. 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 02; 74(1):139-52. PubMed ID: 14681830 [Abstract] [Full Text] [Related]
29. [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 02; 23(4):415-8. PubMed ID: 16883529 [Abstract] [Full Text] [Related]
30. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China. Xiang YB, Tang SH, Li HZ, Xu CY, Chen C, Xu YZ, Ding LR, Xu XQ. Int J Pediatr Otorhinolaryngol; 2019 Jul 02; 122():185-190. PubMed ID: 31035178 [Abstract] [Full Text] [Related]
31. 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]
32. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation. Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH, Guan MX. Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1244-51. PubMed ID: 15708009 [Abstract] [Full Text] [Related]
33. Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation. Zhu Y, Huang S, Kang D, Han M, Wang G, Yuan Y, Su Y, Yuan H, Zhai S, Dai P. BMC Genet; 2014 Feb 17; 15():26. PubMed ID: 24533451 [Abstract] [Full Text] [Related]
34. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families. Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX. Biochem Biophys Res Commun; 2006 Sep 15; 348(1):200-5. PubMed ID: 16875663 [Abstract] [Full Text] [Related]
35. [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 [Abstract] [Full Text] [Related]
36. 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 15; 10(4):380-90. PubMed ID: 20100600 [Abstract] [Full Text] [Related]
37. [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 15; 32(2):163-8. PubMed ID: 25863077 [Abstract] [Full Text] [Related]
38. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated? Al-Malky G, Suri R, Sirimanna T, Dawson SJ. Int J Pediatr Otorhinolaryngol; 2014 Jun 15; 78(6):969-73. PubMed ID: 24703164 [Abstract] [Full Text] [Related]
39. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China. Duan SH, Zhu YM, Wang YL, Guo YF. Acta Otolaryngol; 2015 Jun 15; 135(6):586-91. PubMed ID: 25761933 [Abstract] [Full Text] [Related]
40. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China. Huang B, Han M, Wang G, Huang S, Zeng J, Yuan Y, Dai P. Int J Pediatr Otorhinolaryngol; 2018 May 15; 108():49-54. PubMed ID: 29605365 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]