Chen B - Search Results

1

[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. Yu X, et al. Among authors: chen b. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Nov;49(11):908-15. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014. PMID: 25598369 Chinese.

2

[Levels of serum IL-4, IFN-gamma, IL-32 in children with juvenile-onset recurrent respiratory papillomatosis].

Nan B, Chen B, Zhang C, Jiang M, Zhang Y, Xiang H, Yu X. Nan B, et al. Among authors: chen b. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Jun;27(12):651-3. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24015634 Chinese.

3

[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. Peng GH, et al. Yi Chuan. 2013 Jan;35(1):62-72. doi: 10.3724/sp.j.1005.2013.00062. Yi Chuan. 2013. PMID: 23357266 Chinese.

4

[Analysis of genotype-phenotype correlation for GJB2 in 221 non-syndromic deafness probands and their pedigrees].

Yu X, Chen BB, Xiang HJ, Nan BY, Zheng J, Zhang CQ, Gao JJ, Zheng BJ, Chen YY, Guan MX. Yu X, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Dec;48(12):991-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24506997 Chinese.

5

[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].

Zheng BJ, Peng GH, Chen BB, Fang F, Zheng J, Wu Y, Liang LZ, Nan BY, Tang XW, Zhu Y, Lu JX, Guan MX. Zheng BJ, et al. Yi Chuan. 2012 Jun;34(6):695-704. doi: 10.3724/sp.j.1005.2012.00695. Yi Chuan. 2012. PMID: 22698740 Chinese.

6

[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. Gong SS, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):382-7. doi: 10.3760/cma.j.issn.1003-9406.2012.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875491 Chinese.

7

[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. Peng GH, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Dec;47(12):996-1003. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23328039 Chinese.

8

A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.

Wang M, Liu H, Zheng J, Chen B, Zhou M, Fan W, Wang H, Liang X, Zhou X, Eriani G, Jiang P, Guan MX. Wang M, et al. Among authors: chen b. J Biol Chem. 2016 Sep 30;291(40):21029-21041. doi: 10.1074/jbc.M116.739482. Epub 2016 Aug 12. J Biol Chem. 2016. PMID: 27519417 Free PMC article.

9

Prognostic role of haematological indices in sudden sensorineural hearing loss: Review and meta-analysis.

Cao Z, Li Z, Xiang H, Huang S, Gao J, Zhan X, Zheng X, Li B, Wu J, Chen B. Cao Z, et al. Among authors: chen b. Clin Chim Acta. 2018 Aug;483:104-111. doi: 10.1016/j.cca.2018.04.025. Epub 2018 Apr 20. Clin Chim Acta. 2018. PMID: 29684383 Review.

10

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. Chen B, et al. Among authors: chen y. Am J Med Genet A. 2008 May 15;146A(10):1248-58. doi: 10.1002/ajmg.a.32285. Am J Med Genet A. 2008. PMID: 18386806

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