1. ScholarBank@NUS

Poh San Lai

rp01459

Collaboration Map View Statistics Email Alert RSS Feed

Profile

Full Name
Poh San Lai
Variants
Lai, P.
Lai, P.-S.
Poh, S.L.
San, L.P.
Lai, P.S.
 
Main Affiliation
 
Faculty
 
Email
paelaips@nus.edu.sg
 

Publications

Refined By:
Date Issued:  [2000 TO 2009]

Results 1-19 of 19 (Search time: 0.015 seconds).

Issue DateTitleAuthor(s)
1Aug-2005A novel transthyretin mutation V32A in a Chinese man with late-onset amyloid polyneuropathyPica, E.C.; Pramono, Z.A.D.; Verma, K.K.; San, L.P. ; Chee, Y.W.
22009Automated DNA mutation detection using universal conditions direct sequencing: Application to ten muscular dystrophy genesBennett, 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.
3Feb-2008Characterization of a novel S13F desmin mutation associated with desmin myopathy and heart block in a Chinese familyPica, E.C.; Kathirvel, P.; Pramono, Z.A.D.; Lai, P.-S. ; Yee, W.-C.
42002Comparative study on deletions of the dystrophin gene in three asian populationsLai, P.-S. ; Takeshima, Y.; Adachi, K.; Van Tran, K.; Nguyen, H.T.; Low, P.-S. ; Matsuo, M.
52009Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicingChen, H.Y.; Kathirvel, P.; Yee, W.C.; Lai, P.S. 
62006Diagnostic strategy for the detection of dystrophin gene mutations in Asian patients and carriers using immortalized cell linesTay, S.K.H.; Khng, H.H.; Low, P.S. ; Lai, P.S. 
72008Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotidesPramono, Z.A.D.; Wang, J.L.; Yee, W.C.; Wee, K.B.; MacDorman, K.F.; Lai, P.S. 
82007ECTracker-an efficient algorithm for haplotype analysis and classificationLin, L. ; Wong, L. ; Leong, T.-Y. ; Lai, P. 
92003Ethnic variations of a retinoblastoma susceptibility gene (RB1) polymorphism in eight Asian populationsKadam-Pai, P.; Su, X.-Y.; Heng, C.-K. ; Lai, P.-S. ; Miranda, J.J.; Soemantri, A.; Saha, N.
102009High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastomaPriya, K.; Jada, S.R. ; Poh, S.L. ; Boon, L.Q.; Thuan, C.Q. 
112009High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastomaPriya, K. ; Jada, S.R. ; Poh, S.L. ; Boon, L.Q.; Thuan, C.Q.
122009Identification and characterisation of human dysferlin transcript variants: Implications for dysferlin mutational screening and isoformsPramono, Z.A.D.; Yee, W.C.; Tan, C.L.; Seah, I.A.L.; See, J.S.L.; Kam, S.Y.; Lai, P.S. 
132006Identification and characterization of a novel human dysferlin transcript: Dysferlin_v1Pramono, Z.A.D.; Tan, C.L.; Yee, W.C.; Lai, P.S. ; Takeda, S.
142003IL-10 synergistically enhances GM-CSF-induced CCR1 expression in myelomonocytic cellsLi, H.; Choo, H.H. ; Chan, J.H.P.; Fred, Wong W.S. ; Cheung, W.; Lai, P.S. 
152009Mapping human genetic diversity in AsiaAbdulla, 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.
162005Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansionsTan, E.-C.; Poh, S.L. 
171-Sep-2006Overexpression of RB1 transcript is significantly correlated with 13q14 allelic imbalance in colorectal carcinomasLai, 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.
182008Screening of dystrophin gene deletions in Malaysian patients with Duchenne Muscular DystrophyMarini, 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. 
192003Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mappingWeale, M.E.; Depondt, C.; Wood, N.W.; Macdonald, S.J.; Smith, A.; Goldstein, D.B.; Lai, P.S. ; Shorvon, S.D.