Xia K - Search Results

1

Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients.

Long Z, Chen Z, Wang C, Huang F, Peng H, Hou X, Ding D, Ye W, Wang J, Pan Q, Li J, Xia K, Tang B, Ashizawa T, Jiang H. Long Z, et al. Among authors: xia k. PLoS One. 2015 Feb 17;10(2):e0117488. doi: 10.1371/journal.pone.0117488. eCollection 2015. PLoS One. 2015. PMID: 25689313 Free PMC article.

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 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.

5

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

6

[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.

7

[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.

8

[Silica nanoparticles modified as carriers for gene transfection].

Xue ZG, Zheng D, Ruan JM, Pan Q, Zhao DC, Liu XP, Chen YX, Xia JH, Xia K. Xue ZG, et al. Among authors: xia jh, xia k. Yi Chuan Xue Bao. 2003 Jul;30(7):606-10. Yi Chuan Xue Bao. 2003. PMID: 14579527 Chinese.

9

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

Tang B, Zhao G, Xia K, Pan Q, Luo W, Shen L, Long Z, Dai H, Zi X, Jiang H. Tang B, et al. Among authors: xia k. Arch Neurol. 2004 Jan;61(1):49-55. doi: 10.1001/archneur.61.1.49. Arch Neurol. 2004. PMID: 14732620

10

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.

Tang BS, Luo W, Xia K, Xiao JF, Jiang H, Shen L, Tang JG, Zhao GH, Cai F, Pan Q, Dai HP, Yang QD, Xia JH, Evgrafov OV. Tang BS, et al. Among authors: xia k, xia jh. Hum Genet. 2004 May;114(6):527-33. doi: 10.1007/s00439-004-1102-1. Epub 2004 Mar 12. Hum Genet. 2004. PMID: 15021985

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