Dai P - Search Results

1

[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.

2

Deletions are easy detectable in cochlear mitochondrial DNA of Cu/Zn superoxide dismutase gene knockout mice.

Zhang X, Han D, Ding D, Dai P, Yang W, Jiang S, Salvi RJ. Zhang X, et al. Among authors: dai p. Chin Med J (Engl). 2002 Feb;115(2):258-63. Chin Med J (Engl). 2002. PMID: 11940344

3

Cochlear mitochondrial DNA3867bp deletion in aged mice.

Zhang X, Han D, Ding D, Dai P, Yang W, Jiang S, Salvi RJ. Zhang X, et al. Among authors: dai p. Chin Med J (Engl). 2002 Sep;115(9):1390-3. Chin Med J (Engl). 2002. PMID: 12411120

4

Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis.

Dai P, Yang W, Jiang S, Gu R, Yuan H, Han D, Guo W, Cao J. Dai P, et al. Acta Otolaryngol. 2004 Mar;124(2):130-6. doi: 10.1080/00016480410016586. Acta Otolaryngol. 2004. PMID: 15072414

5

Stereo morphology of temporal bone and ear.

Dai P, Liu Y, Jiang SC, Fang YY, Wang JZ, Yang WY. Dai P, et al. Chin Med J (Engl). 2004 May;117(5):733-7. Chin Med J (Engl). 2004. PMID: 15161543

6

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.

7

[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.

8

[Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].

Liu X, Dai P, Huang DL, Yuan HJ, Li WM, Cao JY, Yu F, Zhang RN, Lin HY, Zhu XH, He Y, Yu YJ, Yao K. Liu X, et al. Among authors: dai p. Zhonghua Yi Xue Za Zhi. 2006 May 23;86(19):1318-22. Zhonghua Yi Xue Za Zhi. 2006. PMID: 16796900 Chinese.

9

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

10

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.

Young WY, Zhao L, Qian Y, Li R, Chen J, Yuan H, Dai P, Zhai S, Han D, Guan MX. Young WY, et al. Among authors: dai p. Am J Med Genet A. 2006 Oct 15;140(20):2188-97. doi: 10.1002/ajmg.a.31434. Am J Med Genet A. 2006. PMID: 16955413

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