Browsing by Author KOO SEOK HWEE

Showing results 1 to 17 of 17
Issue DateTitleAuthor(s)
2007Distribution of the FcγRIIIa 176 F/V polymorphism amongst healthy Chinese, Malays and Asian Indians in SingaporeChong, K.T. ; Ho, W.F.; Koo, S.H. ; Thompson, P.; Lee, E.J.D. 
2009Effect of dietary purines on the pharmacokinetics of orally administered ribavirinLi, L. ; Koo, S.H. ; Limenta, L.M.G.; Han, L.; Lee, E.J.D. ; Hashim, K.B.; Quek, H.H.
2006Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of SingaporeLee, E.J.D. ; Koo, S.H. ; Ho, W.F.
2009Genetic variability of RyR2 and CASQ2 genes in an Asian populationWong, C.H.; Koo, S.H. ; She, G.Q.; Lee, E.J.D. ; Chui, P.
2008Genetic variations of the ABCC2 gene in the Chinese, Malay, and Indian populations of SingaporeHo, W.F.; Koo, S.H. ; Yee, J.Y.; Lee, E.J.D. 
2009Genetic variations of the SLC22A4 gene in Chinese and Indian populations of SingaporeToh, D.S.L.; Koo, S.H. ; Limenta, L.M.G.; Yee, J.Y.; Lee, E.J.D. ; Murray, M.
2010Genetic variations of the SLC22A5 gene in the Chinese and Indian populations of SingaporeToh, D.S.L.; Yee, J.Y.; Koo, S.H. ; Murray, M.; Lee, E.J.D. 
2008Genetic variations of the SLCO1B1 gene in the Chinese, Malay and Indian populations of SingaporeHo, W.F.; Koo, S.H. ; Yee, J.Y.; Lee, E.J.D. 
2008Genetics of ion channels in sudden unexplained death syndrome: Moving beyond idiopathic reactions to personalized risk assessmentKoo, S.H. ; Lee, E.J.D. ; Chui, P.
2009Genomic imbalances in key ion channel genes and telomere shortening in sudden cardiac death victimsBanerjee, B. ; Peiris, D.N. ; Hande, M.P. ; Koo, S.H. ; Lee, E.J.D. ; Chui, P.
2007Identification and functional analysis of variants in the human concentrative nucleoside transporter 2, hCNT2 (SLC28A2) in Chinese, Malays and IndiansLi, L. ; Koo, S.H. ; Chong, K.T.; Lee, E.J.D. ; Tan, C.M.F.
2009Identification of functional promoter haplotypes of human concentrative nucleoside transporter 2, hCNT2 (SLC28A2)Li, L. ; Koo, S.H. ; Hong, I.H.K.; Lee, E.J.D. 
2007Multiplexed genotyping of ABC transporter polymorphisms with the Bioplex suspension arrayKoo, S.H. ; Chong, K.T. ; Lee, E.J.D. ; Ong, T.C. ; Chew, F.T. ; Lee, C.G.L.
Feb-2010Oral sulfasalazine as a clinical BCRP probe substrate: Pharmacokinetic effects of genetic variation (C421A) and pantoprazole coadministrationAdkison, K.K.; Vaidya, S.S.; Lee, D.Y.; Koo, S.H. ; Li, L.; Mehta, A.A.; Gross, A.S.; Polli, J.W.; Humphreys, J.E.; Lou, Y.; Lee, E.J.D.
2010Oral sulfasalazine as a clinical BCRP probe substrate: Pharmacokinetic effects of genetic variation (C421A) and pantoprazole coadministrationAdkison, K.K.; Vaidya, S.S.; Mehta, A.A.; Lee, D.Y.; Polli, J.W.; Humphreys, J.E.; Koo, S.H. ; Li, L. ; Lee, E.J.D. ; Gross, A.S.; Lou, Y.
2006Pharmacogenetics approach to therapeuticsKoo, S.H. ; Lee, E.J.D. 
2008The ABCG2 C421A polymorphism does not affect oral nitrofurantoin pharmacokinetics in healthy Chinese male subjectsAdkison, K.K.; Vaidya, S.S.; Mehta, A.A.; Lee, D.Y.; Polli, J.W.; Lou, Y.; Koo, S.H. ; Li, L. ; Lee, E.J.D. ; Gross, A.S.