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Displacement of bacterial pathogens from mucus and Caco-2 cell surface by lactobacilli.
Lee YK, Puong KY, Ouwehand AC, Salminen S. Lee YK, et al. Among authors: puong ky. J Med Microbiol. 2003 Oct;52(Pt 10):925-930. doi: 10.1099/jmm.0.05009-0. J Med Microbiol. 2003. PMID: 12972590
Kinetics of adsorption and desorption of aflatoxin B1 by viable and nonviable bacteria.
Lee YK, El-Nezami H, Haskard CA, Gratz S, Puong KY, Salminen S, Mykkänen H. Lee YK, et al. Among authors: puong ky. J Food Prot. 2003 Mar;66(3):426-30. doi: 10.4315/0362-028x-66.3.426. J Food Prot. 2003. PMID: 12636295
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: puong ky. Neurology. 2005 Oct 25;65(8):1319-21. doi: 10.1212/01.wnl.0000180517.70572.37. Neurology. 2005. PMID: 16247070
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: puong ky. 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
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: puong ky. Neurology. 2004 Jul 27;63(2):362-3. doi: 10.1212/01.wnl.0000130199.57181.7b. Neurology. 2004. PMID: 15277639
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: puong ky. Neurosci Lett. 2005 Aug 26;384(3):327-9. doi: 10.1016/j.neulet.2005.04.103. Neurosci Lett. 2005. PMID: 15955629 Clinical Trial.
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: puong ky. 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
Case-control study of UCHL1 S18Y variant in Parkinson's disease.
Tan EK, Puong KY, Fook-Chong S, Chua E, Shen H, Yuen Y, Pavanni R, Wong MC, Puvan K, Zhao Y. Tan EK, et al. Among authors: puong ky. Mov Disord. 2006 Oct;21(10):1765-8. doi: 10.1002/mds.21064. Mov Disord. 2006. PMID: 16941465
Expanded FMR1 alleles are rare in idiopathic Parkinson's disease.
Tan EK, Zhao Y, Puong KY, Law HY, Chan LL, Yew K, Shen H, Chandran VR, Yuen Y, Pavanni R, Wong MC, Ng IS. Tan EK, et al. Among authors: puong ky. Neurogenetics. 2005 Feb;6(1):51-2. doi: 10.1007/s10048-004-0200-5. Neurogenetics. 2005. PMID: 15742217 No abstract available.
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: puong ky. Mov Disord. 2006 Jun;21(6):789-93. doi: 10.1002/mds.20810. Mov Disord. 2006. PMID: 16482571
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