Yew K - Search Results

1

Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association.

Tan EK, Puong KY, Chan DK, Yew K, Fook-Chong S, Shen H, Ng PW, Woo J, Yuen Y, Pavanni R, Wong MC, Puvan K, Zhao Y. Tan EK, et al. Among authors: yew k. Hum Genet. 2005 Dec;118(3-4):484-8. doi: 10.1007/s00439-005-0038-4. Epub 2005 Oct 22. Hum Genet. 2005. PMID: 16244875

2

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: yew k. Neurogenetics. 2005 Dec;6(4):179-84. doi: 10.1007/s10048-005-0001-5. Epub 2005 Aug 6. Neurogenetics. 2005. PMID: 16086186

3

Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity.

Tan EK, Tan C, Zhao Y, Yew K, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC. Tan EK, et al. Among authors: yew k. Neurosci Lett. 2004 Aug 26;367(1):109-12. doi: 10.1016/j.neulet.2004.05.090. Neurosci Lett. 2004. PMID: 15308309

4

Nurr1 mutational screen in Parkinson's disease.

Tan EK, Chung H, Chandran VR, Tan C, Shen H, Yew K, Pavanni R, Puvan KA, Wong MC, Teoh ML, Yih Y, Zhao Y. Tan EK, et al. Among authors: yew k. Mov Disord. 2004 Dec;19(12):1503-5. doi: 10.1002/mds.20246. Mov Disord. 2004. PMID: 15390059

5

Functional COMT variant predicts response to high dose pyridoxine in Parkinson's disease.

Tan EK, Cheah SY, Fook-Chong S, Yew K, Chandran VR, Lum SY, Yi Z. Tan EK, et al. Among authors: yew k. Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 5;137B(1):1-4. doi: 10.1002/ajmg.b.30198. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15965967 Clinical Trial.

6

PINK1 mutations in sporadic early-onset Parkinson's disease.

Tan EK, Yew K, Chua E, Puvan K, Shen H, Lee E, Puong KY, Zhao Y, Pavanni R, Wong MC, Jamora D, de Silva D, Moe KT, Woon FP, Yuen Y, Tan L. Tan EK, et al. Among authors: yew k. Mov Disord. 2006 Jun;21(6):789-93. doi: 10.1002/mds.20810. Mov Disord. 2006. PMID: 16482571

7

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.

Tan EK, Zhao Y, Puong KY, Law HY, Chan LL, Yew K, Tan C, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC, Ng IS. Tan EK, et al. Among authors: yew k. Neurology. 2004 Jul 27;63(2):362-3. doi: 10.1212/01.wnl.0000130199.57181.7b. Neurology. 2004. PMID: 15277639

8

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: yew k. Neurosci Lett. 2005 Aug 26;384(3):327-9. doi: 10.1016/j.neulet.2005.04.103. Neurosci Lett. 2005. PMID: 15955629 Clinical Trial.

9

Alpha-synuclein mRNA expression in sporadic Parkinson's disease.

Tan EK, Chandran VR, Fook-Chong S, Shen H, Yew K, Teoh ML, Yuen Y, Zhao Y. Tan EK, et al. Among authors: yew k. Mov Disord. 2005 May;20(5):620-3. doi: 10.1002/mds.20391. Mov Disord. 2005. PMID: 15719423

10

Analysis of MDR1 haplotypes in Parkinson's disease in a white population.

Tan EK, Drozdzik M, Bialecka M, Honczarenko K, Klodowska-Duda G, Teo YY, Tang K, Wong LP, Chong SS, Tan C, Yew K, Zhao Y, Lee CG. Tan EK, et al. Among authors: yew k. Neurosci Lett. 2004 Dec 6;372(3):240-4. doi: 10.1016/j.neulet.2004.09.046. Neurosci Lett. 2004. PMID: 15542248

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