Browsing by Author Chong, S.S.

Showing results 1 to 18 of 18
Issue DateTitleAuthor(s)
2006Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi traffickingBoyadjiev, S.A.; Hur, D.J.; Zhang, G.; Nauta, C.; Fromme, J.C.; Hamamoto, S.; Schekman, R.; Ben, J. ; Chong, S.S.; Ravazzola, M.; Orci, L.; Eyaid, W.
2006Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: A pilot studyNgiam, N.S.P. ; Chong, S.S.; Shek, L.P.C.; Goh, D.L.M.; Yeo, G.H. ; Goh, D.Y.T.; Chng, S.Y.; Ong, K.C.
2006Diagnostic pitfall in PCR-based α-thalassemia genotyping resulting from a (G→C) polymorphism at nucleotide 71 3′ to the α2-globin gene termination codon [2]Chan, A.Y.-Y.; Chan, L.-C.; Luo, H.-Y.; Chui, D.H.K.; Wang, W. ; Chong, S.S.; Ma, E.S.-K.
2004Genomic evidence for recent positive selection at the human MDR1 gene locusTang, K.; Wong, L.P.; Lee, C.G.L. ; See, E.J.D.; Chong, S.S.
2005Hypoxia up-regulated angiogenin and down-regulated vascular cell adhesion molecule-1 expression and secretion in human placental trophoblastsLoganath, A. ; Rajashekhar, G. ; Roy, A.C. ; Chong, S.S.; Wong, Y.C. 
Nov-2013Methylation-specific triplet-primed PCR and melting curve analysis as a rapid screening tool for identifying actionable FMR1 genotypesTeo, C.R.L.; Rajan-Babu, I.-S.; Law, H.-Y. ; Lee, C.G.; Chong, S.S.
Feb-2007Microsatellite markers within -SEA breakpoints for prenatal diagnosis of HbBarts hydrops fetalisHo, S.S.Y.; Chong, S.S.; Koay, E.S.C.; Yiong, H.C.; Sukumar, P. ; Chiu, L.-L.; Wang, W.; Roy, A.; Rauff, M.; Lin, L.S.; Biswas, A.; Choolani, M.
2007Novel CFTR gene mutation in a patient with CBAVDGoh, D.L.M. ; Zhou, Y.; Chong, S.S.; Ngiam, N.S.P. ; Goh, D.Y.T.
2006Nucleotide sequence analyses of the MRP1 gene in four populations suggest negative selection on its coding regionWang, Z.; Lee, C.G.L. ; Sew, P.-H.; Ambrose, H.; Ryan, S.; Chong, S.S.; Lee, E.J.D. 
2006Nucleotide sequence analyses of the MRP1 gene in four populations suggest negative selection on its coding regionWang, Z.; Lee, C.G.L. ; Sew, P.-H.; Ambrose, H.; Ryan, S.; Chong, S.S.; Lee, E.J.D. 
2004Pharmacogenetics of the human MDR1 multidrug transporterLee, C.G. ; Chong, S.S.; Lee, E.J.D.
2009Realtime exonuclease-mediated allelic discrimination (READ): A simple homogeneous genotyping assay for SNPs at the ABC gene lociWang, Z. ; Sew, P.-H.; Chong, S.S.; Lee, C.G.L. 
2003Simultaneous genotyping of seven single-nucleotide polymorphisms in the MDR1 gene by single-tube multiplex minisequencingGwee, P.-C.; Tang, K.; Chua, J.M.Z.; Lee, C.G.L. ; Lee, E.J.D.; Chong, S.S.
2005Strong linkage disequilibrium at the nucleotide analogue transporter ABCC5 gene locusGwee, P.C.; Tang, K.; Lee, C.G.L. ; Lee, E.J.D.; Chong, S.S.; Sew, P.H.
Jul-2010Tgfβ3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crestCheah, F.S.H.; Winkler, C. ; Jabs, E.W.; Chong, S.S.
Jan-2013The FGF and FGFR gene family and risk of cleft lip with or without cleft palateWang, H.; Zhang, T.; Wu, T.; Hetmanski, J.B.; Ruczinski, I.; Schwender, H.; Liang, K.Y.; Murray, T.; Daniele Fallin, M.; Redett, R.J.; Raymond, G.V.; Jin, S.-C.; Chou, Y.-H.W.; Chen, P.K.-T.; Yeow, V.; Chong, S.S.; Cheah, F.S.H. ; Jee, S.H.; Jabs, E.W.; Scott, A.F.; Beaty, T.H.
1988The identity of macrobrachiumlanchesteri (De man, 1911) (Decapoda, palaemonidae) from peninsular malaysia and singapore, and a description of its first zoeaChong, S.S.; Khoo, H.W. 
2006The promoter region of the MDR1 gene is largely invariant, but different single nucleotide polymorphism haplotypes affect MDR1 promoter activity differently in different cell linesWang, B.; Ngoi, S.; Lee, C.G.L. ; Wang, J. ; Chong, S.S.