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Showing results 3 to 22 of 42
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Issue Date
Title
Author(s)
2016
Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2
Yoshimoto, S
;
Harahap, N.I.F
;
Hamamura, Y
;
Ar Rochmah, M
;
Shima, A
;
Morisada, N
;
Shinohara, M
;
Saito, T
;
Saito, K
;
Lai, P.S
;
Matsuo, M
;
Awano, H
;
Morioka, I
;
Iijima, K
;
Nishio, H
2009
Automated DNA mutation detection using universal conditions direct sequencing: Application to ten muscular dystrophy genes
Bennett, R.R.
;
Schneider, H.E.
;
Estrella, E.
;
Burgess, S.
;
Barrett, C.
;
Beggs, A.H.
;
Kunkel, L.M.
;
Cheng, A.S.
;
Lip, V.
;
Shen, Y.
;
Wu, B.-L.
;
Lai, P.S.
;
Darras, B.T.
Feb-2008
Characterization of a novel S13F desmin mutation associated with desmin myopathy and heart block in a Chinese family
Pica, E.C.
;
Kathirvel, P.
;
Pramono, Z.A.D.
;
Lai, P.-S.
;
Yee, W.-C.
2002
Comparative study on deletions of the dystrophin gene in three asian populations
Lai, P.-S.
;
Takeshima, Y.
;
Adachi, K.
;
Van Tran, K.
;
Nguyen, H.T.
;
Low, P.-S.
;
Matsuo, M.
1991
Consanguinity and health [19]
Tay, J.S.H.
;
Lai, P.-S.
2009
Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicing
Chen, H.Y.
;
Kathirvel, P.
;
Yee, W.C.
;
Lai, P.S.
28-Aug-2018
Data from: Association between the dopamine D4 receptor gene exon III variable number of tandem repeats and political attitudes in female Han Chinese
Ebstein, Richard P.
;
Monakhov, Mikhail V.
;
Lu, Yunfeng
;
Jiang, Yushi
;
Lai, Poh San
;
Chew, Soo Hong
1992
Deletion analysis of DMD/BMD children in Singapore using multiplex polymerase chain reaction (PCR) technique
Lai, P.S.
;
Tay, J.S.H.
;
Low, P.S.
;
Lee, W.L.
;
Koh, G.A.S.
;
Gan, G.C.
1992
Deletional types of alpha-thalassaemia in central Java
Tan, J.A.M.A.
;
Tay, J.S.H.
;
Soemantri, A.
;
Kham, S.K.Y.
;
Wong, H.B.
;
Lai, P.S.
;
Saha, N.
1997
Detection of Low Numbers of Neuroblastoma Cells in Vitro
Lai, P.S.
;
Chee, S.
;
Chiu, L.L.
;
Sano, K.
2006
Diagnostic strategy for the detection of dystrophin gene mutations in Asian patients and carriers using immortalized cell lines
Tay, S.K.H.
;
Khng, H.H.
;
Low, P.S.
;
Lai, P.S.
2010
Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy
Qin, W.J.
;
Yung, L.-Y.L.
;
Yim, O.S.
;
Lai, P.S.
2008
Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotides
Pramono, Z.A.D.
;
Wang, J.L.
;
Yee, W.C.
;
Wee, K.B.
;
MacDorman, K.F.
;
Lai, P.S.
1990
Dystrophin function: Calcium-related rather than mechanical
Tay, J.S.H.
;
Low, P.S.
;
Lee, W.L.
;
Lai, P.S.
;
Gan, G.C.
2007
ECTracker-an efficient algorithm for haplotype analysis and classification
Lin, L.
;
Wong, L.
;
Leong, T.-Y.
;
Lai, P.
2003
Ethnic variations of a retinoblastoma susceptibility gene (RB1) polymorphism in eight Asian populations
Kadam-Pai, P.
;
Su, X.-Y.
;
Heng, C.-K.
;
Lai, P.-S.
;
Miranda, J.J.
;
Soemantri, A.
;
Saha, N.
2018
Genetic Variation in the Maternal Oxytocin System Affects Cortisol Responsiveness to Breastfeeding in Infants and Mothers
Krol K.M.
;
Monakhov M.
;
Lai P.S.
;
Ebstein R.P.
;
Heinrichs M.
;
Grossmann T.
2009
High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma
Priya, K.
;
Jada, S.R.
;
Poh, S.L.
;
Boon, L.Q.
;
Thuan, C.Q.
2009
High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma
Priya, K.
;
Jada, S.R.
;
Poh, S.L.
;
Boon, L.Q.
;
Thuan, C.Q.
2009
Identification and characterisation of human dysferlin transcript variants: Implications for dysferlin mutational screening and isoforms
Pramono, Z.A.D.
;
Yee, W.C.
;
Tan, C.L.
;
Seah, I.A.L.
;
See, J.S.L.
;
Kam, S.Y.
;
Lai, P.S.