Xia K - Search Results

1

A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.

Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K. Xia J, et al. Among authors: xia k. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

2

Han Chinese population data for ten STR loci in Changsha, China.

Ma Y, Gong B, Xia J, Deng H, Pan Q, Li Q, Dai H, Wen S, Xia K. Ma Y, et al. Among authors: xia j, xia k. J Forensic Sci. 2002 Mar;47(2):404-5. J Forensic Sci. 2002. PMID: 11908620 No abstract available.

3

[Molecular cloning of the human CX 58 gene].

Lu C, Zhang H, Deng H, Xia K, Pan Q, Xia J. Lu C, et al. Among authors: xia j, xia k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Apr;19(2):95-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11941580 Chinese.

4

[A simple and convenient method for construction of gene site-directed mutagenesis].

Zhang M, Wen J, Xia K, Zheng D, Zhang Z, Xia J. Zhang M, et al. Among authors: xia j, xia k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Apr;19(2):145-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11941593 Chinese.

5

[Translational frameshift may be occur in p11, an interaction protein of Cx31, in yeast].

Huang LQ, Shi XL, Tan ZP, Fang HY, Zheng D, Xia JH, Xia K. Huang LQ, et al. Among authors: xia jh, xia k. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2002 Mar;34(2):219-24. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2002. PMID: 12007000 Chinese.

6

[A new mutation in the connexin 32 gene of a Chinese family with Charcot-Marie-Tooth disease associated with central conduction slowing].

Luo W, Tang B, Zhao G, Xia K, Yang Y, Xiao J, Yan X, Xia J. Luo W, et al. Among authors: xia j, xia k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Oct;19(5):367-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12362307 Chinese.

7

Sodium chloride modified silica nanoparticles as a non-viral vector with a high efficiency of DNA transfer into cells.

Chen Y, Xue Z, Zheng D, Xia K, Zhao Y, Liu T, Long Z, Xia J. Chen Y, et al. Among authors: xia j, xia k. Curr Gene Ther. 2003 Jun;3(3):273-9. doi: 10.2174/1566523034578339. Curr Gene Ther. 2003. PMID: 12762484

8

[Spastin gene mutation in Chinese patients with hereditary spastic paraplegia].

Zhao GH, Tang BS, Luo W, Xia K, Zhuang MY, Kong FB, Yan XX, Deng HX, Xiao JF, Xia JH. Zhao GH, et al. Among authors: xia k, xia jh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Jun;20(3):177-80. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12778437 Chinese.

9

[In silicon cloning of the human TECTB gene].

Zhang HL, Deng H, Zhang RF, Xia K, Xia JH. Zhang HL, et al. Among authors: xia k, xia jh. Yi Chuan Xue Bao. 2003 Apr;30(4):317-20. Yi Chuan Xue Bao. 2003. PMID: 12812054 Chinese.

10

[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred].

Liu Z, Deng H, Xi XH, Xia JH, Pan Q, Dai HP, Yang YJ, Deng HX, Xia K, Zheng D. Liu Z, et al. Among authors: xia jh, xia k. Zhonghua Yan Ke Za Zhi. 2003 Apr;39(4):206-8. Zhonghua Yan Ke Za Zhi. 2003. PMID: 12882697 Chinese.

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