Tan EK - Search Results

1

AMP kinase activation mitigates dopaminergic dysfunction and mitochondrial abnormalities in Drosophila models of Parkinson's disease.

Ng CH, Guan MS, Koh C, Ouyang X, Yu F, Tan EK, O'Neill SP, Zhang X, Chung J, Lim KL. Ng CH, et al. Among authors: tan ek. J Neurosci. 2012 Oct 10;32(41):14311-7. doi: 10.1523/JNEUROSCI.0499-12.2012. J Neurosci. 2012. PMID: 23055502 Free PMC article.

2

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

Tan EK, Shen H, Tan LC, Farrer M, Yew K, Chua E, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yih Y, Skipper L, Liu JJ. Tan EK, et al. Among authors: tan lc. Neurosci Lett. 2005 Aug 26;384(3):327-9. doi: 10.1016/j.neulet.2005.04.103. Neurosci Lett. 2005. PMID: 15955629 Clinical Trial.

3

Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease.

Tan EK, Shen H, Tan JM, Lim KL, Fook-Chong S, Hu WP, Paterson MC, Chandran VR, Yew K, Tan C, Yuen Y, Pavanni R, Wong MC, Puvan K, Zhao Y. Tan EK, et al. Among authors: tan c, tan jm. Neurogenetics. 2005 Dec;6(4):179-84. doi: 10.1007/s10048-005-0001-5. Epub 2005 Aug 6. Neurogenetics. 2005. PMID: 16086186

4

Analysis of LRRK2 functional domains in nondominant Parkinson disease.

Skipper L, Shen H, Chua E, Bonnard C, Kolatkar P, Tan LC, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yuen Y, Farrer M, Liu JJ, Tan EK. Skipper L, et al. Among authors: tan lc, tan ek. Neurology. 2005 Oct 25;65(8):1319-21. doi: 10.1212/01.wnl.0000180517.70572.37. Neurology. 2005. PMID: 16247070

5

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

Skipper L, Li Y, Bonnard C, Pavanni R, Yih Y, Chua E, Sung WK, Tan L, Wong MC, Tan EK, Liu J. Skipper L, et al. Among authors: tan l, tan ek. Hum Mol Genet. 2005 Dec 1;14(23):3549-56. doi: 10.1093/hmg/ddi376. Epub 2005 Nov 3. Hum Mol Genet. 2005. PMID: 16269443

6

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease.

Tan EK, Skipper L, Chua E, Wong MC, Pavanni R, Bonnard C, Kolatkar P, Liu JJ. Tan EK, et al. Mov Disord. 2006 Jul;21(7):997-1001. doi: 10.1002/mds.20875. Mov Disord. 2006. PMID: 16602113

7

Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease.

Lim SW, Zhao Y, Chua E, Law HY, Yuen Y, Pavanni R, Wong MC, Ng IS, Yoon CS, Puong KY, Lim SH, Tan EK. Lim SW, et al. Among authors: tan ek. Neurosci Lett. 2006 Jul 31;403(1-2):11-4. doi: 10.1016/j.neulet.2006.04.019. Epub 2006 May 9. Neurosci Lett. 2006. PMID: 16687213

8

The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.

Tan EK, Zhao Y, Skipper L, Tan MG, Di Fonzo A, Sun L, Fook-Chong S, Tang S, Chua E, Yuen Y, Tan L, Pavanni R, Wong MC, Kolatkar P, Lu CS, Bonifati V, Liu JJ. Tan EK, et al. Among authors: tan mg, tan l. Hum Genet. 2007 Feb;120(6):857-63. doi: 10.1007/s00439-006-0268-0. Epub 2006 Sep 30. Hum Genet. 2007. PMID: 17019612

9

LRRK2 G2019S founder haplotype in the Chinese population.

Tan EK, Skipper L, Tan L, Liu JJ. Tan EK, et al. Among authors: tan l. Mov Disord. 2007 Jan;22(1):105-7. doi: 10.1002/mds.21206. Mov Disord. 2007. PMID: 17083102

10

Identification of a common genetic risk variant (LRRK2 Gly2385Arg) in Parkinson's disease.

Tan EK. Tan EK. Ann Acad Med Singap. 2006 Nov;35(11):840-2. Ann Acad Med Singap. 2006. PMID: 17160203 Free article. Review.

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