Qi Y - Search Results

1

[Molecular genetic analysis of mitochondrial DNA C1494T mutation in non-syndromic hearing loss of Chinese population].

Tian G, Liu YH, Ma YN, Li YJ, Zhang Y, Niu SL, Xu YE, Pei P, Wang ST, Bu DF, Du BR, Zhou X, Ke XM, Qi Y. Tian G, et al. Among authors: qi y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Aug;24(4):464-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17680545 Chinese.

2

Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.

Wang Z, Liu S, Yang Y, Yuan Y, Wu L, Qi Y, Chen Q. Wang Z, et al. Among authors: qi y. Chin Med J (Engl). 2002 Jul;115(7):995-7. Chin Med J (Engl). 2002. PMID: 12150728

3

[Apoptosis and re-expression of p16 gene in the myeloma cell line U266 induced by synergy of histone deacetylase inhibitor and demethylating agent].

Du HL, Qi Y, Shi YJ, Bu DF, Wu SL. Du HL, et al. Among authors: qi y. Ai Zheng. 2002 Oct;21(10):1057-61. Ai Zheng. 2002. PMID: 12508642 Chinese.

4

Connexin26 gene ( GJB2): prevalence of mutations in the Chinese population.

Liu Y, Ke X, Qi Y, Li W, Zhu P. Liu Y, et al. Among authors: qi y. J Hum Genet. 2002;47(12):688-90. doi: 10.1007/s100380200106. J Hum Genet. 2002. PMID: 12522692

5

[Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].

Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT. Wang ZX, et al. Among authors: qi y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Aug;20(4):273-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12903032 Chinese.

6

[Detection of mtDNA 11778 (G-->A) point mutation in a family with Leber's hereditary optic neuropathy by site-specific polymerase chain reaction].

Niu SL, Zhang Y, Xu YF, Bu DF, Ren ZQ, Wang SY, Liu GH, Qi Y. Niu SL, et al. Among authors: qi y. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2003 Apr;25(2):153-5. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2003. PMID: 12905709 Chinese.

7

Mutation analysis of potassium channel genes KCNQ1 and KCNH2 in patients with long QT syndrome.

Liu W, Hu D, Li C, Li P, Li Y, Li Z, Li L, Qin X, Dong W, Qi Y, Chen S, Wang Q. Liu W, et al. Among authors: qi y. Chin Med J (Engl). 2003 Sep;116(9):1333-5. Chin Med J (Engl). 2003. PMID: 14527360

8

[Five single nucleotide polymorphisms of casein kinase I gamma 2 gene in children with familial febrile convulsions].

Ma YN, Hao L, Niu SL, Xu YF, Zhang Y, Pei P, Bu DF, Qi Y. Ma YN, et al. Among authors: qi y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Aug;21(4):347-50. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15300631 Chinese.

9

[Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].

Zhang Y, Wang ZX, Niu SL, Xu YF, Pei P, Yuan Y, Yang YL, Qi Y. Zhang Y, et al. Among authors: qi y. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Feb;27(1):77-80. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005. PMID: 15782498 Chinese.

10

[Association between familial febrile convulsions and HCN2 gene].

Ma YN, Chen ZY, Zou LP, Zhang Y, Niu SL, Xu YF, Pei P, Bu DF, Qi Y. Ma YN, et al. Among authors: qi y. Zhonghua Yi Xue Za Zhi. 2005 Mar 16;85(10):663-6. Zhonghua Yi Xue Za Zhi. 2005. PMID: 15932727 Chinese.

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