Zheng B - Search Results

1

Newborn screening for deafness genes with cord blood-based multicolour melting curve analysis.

Dai X, Xu K, Dai L, Chen X, Xie H, Zhang Y, Zheng H, Wang Q, Zheng B, Tong Y. Dai X, et al. Among authors: zheng b. Am J Otolaryngol. 2024 Dec 9;46(1):104530. doi: 10.1016/j.amjoto.2024.104530. Online ahead of print. Am J Otolaryngol. 2024. PMID: 39700758 Free article.

2

[Analysis of audiological characteristics and genetic background in patients with nonsyndromic deafness and mitochondrial DNA 1555A>G mutation].

Zhuo Y, Wu H, Jin H, Liu H, Zhang D, Huang J, Zheng B. Zhuo Y, et al. Among authors: zheng b. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Oct 10;35(5):625-629. doi: 10.3760/cma.j.issn.1003-9406.2018.05.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30298482 Chinese.

3

[Spectrum of GJB6 variants in 318 pedigrees with non-syndromic hearing loss:one deafness pedigree carrying both GJB6 and GJB2 deletion variant].

Zheng BJ, Zhang T, Wang H, Tang XW, Zheng J, Lv JX, Guan MX. Zheng BJ, et al. Among authors: zheng j. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Jun 20;30(12):933-937. doi: 10.13201/j.issn.1001-1781.2016.12.003. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016. PMID: 29771057 Chinese.

4

Development and external validation of a prognostic nomogram to predict survival in patients aged ≥60 years with pancreatic ductal adenocarcinoma.

Zheng B, Ding G, Lu G, Li L. Zheng B, et al. Transl Cancer Res. 2024 Jun 30;13(6):2751-2766. doi: 10.21037/tcr-24-5. Epub 2024 Jun 13. Transl Cancer Res. 2024. PMID: 38988930 Free PMC article.

5

[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.

6

[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.

7

[Modification factors associated with maternally inherited non-syndromic hearing loss].

Hong WJ, Zheng BJ, Qian JF, Wu H, Jin H, Zhu YT. Hong WJ, et al. Among authors: zheng bj. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Jun 7;52(6):472-477. doi: 10.3760/cma.j.issn.1673-0860.2017.06.017. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017. PMID: 28635225 Review. Chinese.

8

[Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family].

Wu Y, Liang LZ, Xiao HL, Yang YL, Yu X, Zheng J, Fang F, Zheng BJ, Tang XW, Jin LJ, Guan MX. Wu Y, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Dec;48(12):978-84. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24506995 Chinese.

9

[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.

10

[Mutation analysis of GJB2 gene in 1 822 patients with nonsyndromic hearing loss in Zhejiang Province].

Fan WL, Shi WW, Wang BB, Zheng BJ, Xue L, Tang XW, Guan MX. Fan WL, et al. Among authors: zheng bj. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Mar 5;31(5):352-355. doi: 10.13201/j.issn.1001-1781.2017.05.006. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017. PMID: 29871260 Chinese.

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