Dai P - Search Results

1

[Using PGT to give birth to hereditary conductive deafness SYNS1 family a healthy offspring: a case report].

Fu Y, Huang SS, Wang QQ, Han MY, Wang GJ, Kang DY, Dai P, Yuan YY. Fu Y, et al. Among authors: dai p. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 Mar 7;59(3):243-248. doi: 10.3760/cma.j.cn115330-20230925-00116. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024. PMID: 38561263 Chinese.

2

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. Dai P, et al. Biochem Biophys Res Commun. 2006 Feb 3;340(1):194-9. doi: 10.1016/j.bbrc.2005.11.156. Biochem Biophys Res Commun. 2006. PMID: 16375862 Clinical Trial.

3

[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients].

Dai P, Yu F, Kang DY, Zhang X, Liu X, Mi WZ, Cao JY, Yuan HJ, Yang WY, Wu BL, Han DY. Dai P, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Oct;40(10):769-73. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005. PMID: 16408730 Chinese.

4

[Genotypic analysis of familial dilated vestibular aqueduct syndrome].

Dai P, Han D, Cao J, Zhai S, Kang D, Liu X, Yuan H, Zhang X, Li M, Liu L, Feng B, Yang W, Wu B. Dai P, et al. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006 Feb;20(4):147-50. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006. PMID: 16711435 Chinese.

5

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. Dai P, et al. Biochem Biophys Res Commun. 2006 Sep 15;348(1):200-5. doi: 10.1016/j.bbrc.2006.07.031. Epub 2006 Jul 17. Biochem Biophys Res Commun. 2006. PMID: 16875663

6

[Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening].

Dai P, Zhu XH, Yuan YY, Zhu QW, Teng GC, Zhang X, Liu LX, Wang JL, Feng B, Zhai SQ, Kang DY, Liu X, Huang DL. Dai P, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2006 Jul;41(7):497-500. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2006. PMID: 17007371 Chinese.

7

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. Han D, et al. Among authors: dai p. Biochem Biophys Res Commun. 2007 Jun 1;357(2):554-60. doi: 10.1016/j.bbrc.2007.03.199. Epub 2007 Apr 9. Biochem Biophys Res Commun. 2007. PMID: 17434445

8

[GJB6 gene mutation analysis in Chinese nonsyndromic deaf population].

Yuan Y, Huang D, Dai P, Zhu Q, Liu X, Wang G, Li Q, Wu B. Yuan Y, et al. Among authors: dai p. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jan;21(1):3-6. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17438853 Chinese.

9

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.

Dai P, Yu F, Han B, Yuan Y, Li Q, Wang G, Liu X, He J, Huang D, Kang D, Zhang X, Yuan H, Schmitt E, Han D, Wong LJ. Dai P, et al. Genet Med. 2007 May;9(5):283-9. doi: 10.1097/gim.0b013e31804d2371. Genet Med. 2007. PMID: 17505205 Free article.

10

[Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China].

Zhu Q, Liu X, Han D, Kang D, Zhang X, Jin Z, Li M, Dai P. Zhu Q, et al. Among authors: dai p. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 May;21(10):460-2. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17650818 Chinese.

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