Cao L - Search Results

1

Lysosomal degradation of GMPPB is associated with limb-girdle muscular dystrophy type 2T.

Tian WT, Zhou HY, Zhan FX, Zhu ZY, Yang J, Chen SD, Luan XH, Cao L. Tian WT, et al. Among authors: cao l. Ann Clin Transl Neurol. 2019 May 8;6(6):1062-1071. doi: 10.1002/acn3.787. eCollection 2019 Jun. Ann Clin Transl Neurol. 2019. PMID: 31211170 Free PMC article.

2

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

3

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

4

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

5

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

6

Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation.

Zhang Y, Deng YL, Ma JF, Zheng L, Hong Z, Wang ZQ, Sheng CY, Xiao Q, Cao L, Chen SD. Zhang Y, et al. Among authors: cao l. Neurodegener Dis. 2011;8(4):187-93. doi: 10.1159/000321679. Epub 2010 Dec 3. Neurodegener Dis. 2011. PMID: 21135536

7

Genetic polymorphisms in sigma-1 receptor and apolipoprotein E interact to influence the severity of Alzheimer's disease.

Huang Y, Zheng L, Halliday G, Dobson-Stone C, Wang Y, Tang HD, Cao L, Deng YL, Wang G, Zhang YM, Wang JH, Hallupp M, Kwok J, Chen SD. Huang Y, et al. Among authors: cao l. Curr Alzheimer Res. 2011 Nov;8(7):765-70. doi: 10.2174/156720511797633232. Curr Alzheimer Res. 2011. PMID: 21605063

8

DJ-1 modulates the expression of Cu/Zn-superoxide dismutase-1 through the Erk1/2-Elk1 pathway in neuroprotection.

Wang Z, Liu J, Chen S, Wang Y, Cao L, Zhang Y, Kang W, Li H, Gui Y, Chen S, Ding J. Wang Z, et al. Among authors: cao l. Ann Neurol. 2011 Oct;70(4):591-9. doi: 10.1002/ana.22514. Epub 2011 Jul 27. Ann Neurol. 2011. PMID: 21796667

9

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.

Wang JL, Cao L, Li XH, Hu ZM, Li JD, Zhang JG, Liang Y, San-A, Li N, Chen SQ, Guo JF, Jiang H, Shen L, Zheng L, Mao X, Yan WQ, Zhou Y, Shi YT, Ai SX, Dai MZ, Zhang P, Xia K, Chen SD, Tang BS. Wang JL, et al. Among authors: cao l. Brain. 2011 Dec;134(Pt 12):3493-3501. doi: 10.1093/brain/awr289. Epub 2011 Nov 26. Brain. 2011. PMID: 22120146 Free PMC article.

10

Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease.

Zhang Y, Chen S, Xiao Q, Cao L, Liu J, Rong TY, Ma JF, Wang G, Wang Y, Chen SD. Zhang Y, et al. Among authors: cao l. Parkinsonism Relat Disord. 2012 Jun;18(5):638-40. doi: 10.1016/j.parkreldis.2012.02.011. Epub 2012 Mar 10. Parkinsonism Relat Disord. 2012. PMID: 22410496

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