Cao L - Search Results

1

Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease.

Chen Z, Wang C, Zheng C, Long Z, Cao L, Li X, Shang H, Yin X, Zhang B, Liu J, Ding D, Peng Y, Peng H, Ye W, Qiu R, Pan Q, Xia K, Chen S, Sequeiros J, Ashizawa T, Tang B, Jiang H; Chinese Clinical Research Cooperative Group for Spinocerebellar Ataxias (CCRCG-SCA). Chen Z, et al. Among authors: cao l. Brain. 2017 Apr 1;140(4):e25. doi: 10.1093/brain/awx028. Brain. 2017. PMID: 28334945 No abstract available.

2

[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6].

Zhang YH, Tang BS, Guo JF, Xia K, Xu B, Cai F, Deng HX, Yan XX, Chen T, Cao L, Pan Q, Long ZG. Zhang YH, et al. Among authors: cao l. Zhonghua Yi Xue Za Zhi. 2005 Jun 15;85(22):1538-41. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16179113 Chinese.

3

[Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].

Guo JF, Tang BS, Zhang YH, Xia K, Cai F, Pan Q, Shen L, Jiang H, Zhao GH, Yan XX, Cao L. Guo JF, et al. Among authors: cao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):641-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16331561 Chinese.

4

[The wild-type alpha-synuclein over-expression to induce the protein aberrant aggregation of alpha-synuclein in HEK293 cells in vitro].

Chen T, Tang BS, Liao XP, Yan XX, Zhang RX, Zhang YH, Tang JG, Cao L, Guo JF, Li J. Chen T, et al. Among authors: cao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Feb;23(1):19-22. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16456779 Chinese.

5

[Construction of the eukaryotic expression vector of MJD1 and its expression in SH-SY5Y cells].

Tang JG, Tang BS, Shen L, Jiang H, Hu ZP, Cao L, Xia K, Cai F. Tang JG, et al. Among authors: cao l. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2005 Dec;30(6):640-4. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 16708800 Chinese.

6

[Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR].

Guo JF, Tang BS, Li J, Zhang YH, Zhang XW, Chen T, Xia K, Yan XX, Cao L, Cai F, Pan Q, Shen L, Jiang H. Guo JF, et al. Among authors: cao l. Zhonghua Yi Xue Za Zhi. 2006 Jun 6;86(21):1447-9. Zhonghua Yi Xue Za Zhi. 2006. PMID: 16842693 Chinese.

7

GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients.

Zhang Y, Zheng L, Zhang T, Wang Y, Xiao Q, Fei QZ, Cui PJ, Cao L, Chen SD. Zhang Y, et al. Among authors: cao l. Neurosci Lett. 2009 Oct 9;463(3):172-5. doi: 10.1016/j.neulet.2009.07.067. Epub 2009 Jul 26. Neurosci Lett. 2009. PMID: 19638301

8

CALHM1 P86L polymorphism is a risk factor for Alzheimer's disease in the Chinese population.

Cui PJ, Zheng L, Cao L, Wang Y, Deng YL, Wang G, Xu W, Tang HD, Ma JF, Zhang T, Ding JQ, Cheng Q, Chen SD. Cui PJ, et al. Among authors: cao l. J Alzheimers Dis. 2010;19(1):31-5. doi: 10.3233/JAD-2010-1207. J Alzheimers Dis. 2010. PMID: 20061624

9

Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.

Fei QZ, Cao L, Xiao Q, Zhang T, Zheng L, Wang XJ, Wang G, Zhou HY, Wang Y, Chen SD. Fei QZ, et al. Among authors: cao l. Neurosci Lett. 2010 May 14;475(2):61-3. doi: 10.1016/j.neulet.2010.03.018. Epub 2010 Mar 19. Neurosci Lett. 2010. PMID: 20227461

10

Four novel mutations in the GCH1 gene of Chinese patients with dopa-responsive dystonia.

Cao L, Zheng L, Tang WG, Xiao Q, Zhang T, Tang HD, He SB, Wang XJ, Ding JQ, Chen SD. Cao L, et al. Mov Disord. 2010 Apr 30;25(6):755-60. doi: 10.1002/mds.22646. Mov Disord. 2010. PMID: 20437540

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