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Issue Date
Title
Author(s)
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.
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.
2006
Identification and characterization of a novel human dysferlin transcript: Dysferlin_v1
Pramono, Z.A.D.
;
Tan, C.L.
;
Yee, W.C.
;
Lai, P.S.
;
Takeda, S.
Jun-2010
Identification of single nucleotide polymorphism (SNP) 153104 (A to G) of RB1 gene in Malaysian retinoblastoma children and its association with laterality and staging of the disease
Yusof, H.A.
;
Ramlee, N.
;
Ishak, S.R.
;
Ab Rajab, N.S.
;
Ghani, S.A.
;
Bachok, N.S.
;
Aziz, S.H.S.A.
;
Tajudin, L.-S.A.
;
Alagaratnam, J.V.
;
San, L.P.
;
Nishio, H.
;
Alwi, Z.B.
2003
IL-10 synergistically enhances GM-CSF-induced CCR1 expression in myelomonocytic cells
Li, H.
;
Choo, H.H.
;
Chan, J.H.P.
;
Fred, Wong W.S.
;
Cheung, W.
;
Lai, P.S.
2009
Mapping human genetic diversity in Asia
Abdulla, M.A.
;
Edo, J.
;
Jinam, T.A.
;
Phipps, M.E.
;
Ahmed, I.
;
Brahmachari, S.K.
;
Chaurasia, A.
;
Jha, P.
;
Mukerji, M.
;
Scaria, V.
;
Sinha, A.
;
Assawamakin, A.
;
Fuchareon, S.
;
Kulawonganunchai, S.
;
Ngamphiw, C.
;
Tongsima, S.
;
Bhak, J.
;
Ghang, H.
;
Kim, W.-Y.
;
Lee, S.
;
Oh, S.
;
Yang, J.O.
;
Yoo, H.-S.
;
Calacal, G.C.
;
De, Ungria M.C.A.
;
Delfin, F.C.
;
Perdigon, H.B.
;
Salvador, J.M.
;
Tabbada, K.A.
;
Villamor, L.P.
;
Chen, C.-H.
;
Chen, Y.-T.
;
Ho, S.-F.
;
Wu, J.-Y.
;
Chen, J.
;
Kumar, V.
;
Liu, E.T.
;
Ong, R.
;
Png, E.
;
Seielstad, M.
;
Tan, A.
;
Chu, J.
;
Cutiongco-de, La Paz E.M.C.
;
Padilla, C.D.
;
Gojobori, T.
;
Koike, T.
;
Suzuki, Y.
;
Han, J.
;
Xiao, H.
;
Hoh, B.P.
;
Sidek, M.R.
;
Zilfalil, B.A.
;
Huang, W.
;
Wang, Y.
;
Wang, H.
;
Yuan, W.
;
Zhao, G.
;
Inoko, H.
;
Oka, A.
;
Jin, L.
;
Jung, J.
;
Kim, H.-L.
;
Kim, K.
;
Lee, J.-Y.
;
Oh, B.
;
Kangwanpong, D.
;
Kampuansai, J.
;
Srikummool, M.
;
Kennedy, G.C.
;
Wang, E.
;
Khurana, P.
;
Mandapati, K.K.
;
Kim, S.
;
Kimm, K.
;
Kimura, R.
;
Nishida, N.
;
Ohashi, J.
;
Tokunaga, K.
;
Lai, P.S.
;
Majumder, P.P.
;
Marzuki, S.
;
Sandraling, Y.
;
Sudoyo, H.
;
Suryadi, H.
;
Mitchell, W.
;
Naritomi, K.
;
Palittapongarnpim, P.
;
Sakaki, Y.
;
Sugano, S.
;
Jin, L.
;
Xu, S.
;
Shugart, Y.Y.
;
Niikawa, N.
1993
Molecular characterization of β-thalassaemia in Singaporean Chinese: Application to prenatal diagnosis
Tan, J.A.M.A.
;
Tay, J.S.H.
;
Kham, S.
;
Chin, T.M.
;
Wong, H.B.
;
Lai, P.S.
1996
Molecular diagnosis of duchenne muscular dystrophy in Singapore
Low, P.S.
;
Lai, P.S.
;
Lee, W.L.
;
Chin, S.M.
;
Tay, J.S.H.
;
Ong, H.T.
2005
Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions
Tan, E.-C.
;
Poh, S.L.
1997
Molecular Studies of Loss of Heterozygosity in Retinoblastoma
Chiu, L.L.
;
Lai, P.S.
;
Low, P.S.
;
Chee, C.K.L.
;
Wong, P.K.
;
Ling, Y.L.F.
;
Cheong, P.Y.Y.
;
Lim, A.S.M.
2017
Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling
Tomar S.
;
Sethi R.
;
Sundar G.
;
Quah T.C.
;
Quah B.L.
;
Lai P.S.
1-Sep-2006
Overexpression of RB1 transcript is significantly correlated with 13q14 allelic imbalance in colorectal carcinomas
Lai, P.-S.
;
Cheah, P.Y.
;
Kadam, P.
;
Chua, C.L.-M.
;
Lie, D.K.H.
;
Li, H.-H.
;
Eu, K.-W.
;
Seow-Choen, F.
;
Lee, A.S.-G.
1992
Pathogenesis of Duchenne muscular dystrophy: The calcium hypothesis revisited
Tay, J.S.H.
;
Lai, P.S.
;
Low, P.S.
;
Lee, W.L.
;
Gan, G.C.
1990
Prenatal diagnosis of alpha-thalassaemia by analysis of enzymatically amplified DNA sequences.
Tan, J.A.
;
Tay, S.H.
;
Alain, K.
;
Wong, H.B.
;
Lai, P.S.
1991
Prenatal diagnosis of α- and β-thalassaemias in Singapore - Current status
Tan, J.A.M.A.
;
Tay, S.H.J.
;
Siang, O.K.
;
Lai, P.S.
;
Boon, W.H.
;
Kham, S.
2008
Screening of dystrophin gene deletions in Malaysian patients with Duchenne Muscular Dystrophy
Marini, M.
;
Watihayati, M.S.
;
Mardziah, M.D.S.
;
Zahri, M.K.
;
Hoh, B.P.
;
Ankathil, R.
;
Zilfalil, B.A.
;
Salmi, A.A.
;
Lai, P.S.
2003
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mapping
Weale, M.E.
;
Depondt, C.
;
Wood, N.W.
;
Macdonald, S.J.
;
Smith, A.
;
Goldstein, D.B.
;
Lai, P.S.
;
Shorvon, S.D.