Determining the cause of patchwork HBA1 and HBA2 genes: Recurrent gene conversion or crossing over fixation events

by Law, H.-Y., Ng, I.S.L., Luo, H.-Y., Steinberg, M.H., Chui, D.H.K., Wang, W., Ho, J.F.V., Chong, S.S., Najmabadi, H.
Published 2011

p32 protein levels are integral to mitochondrial and endoplasmic reticulum morphology, cell metabolism and survival

by Hu, M, Crawford, S.A, Henstridge, D.C, Ng, I.H.W, Boey, E.J.H, Xu, Y, Febbraio, M.A, Jans, D.A, Bogoyevitch, M.A
Published 2020

Preleukemic and second-hit mutational events in an acute myeloid leukemia patient with a novel germline RUNX1 mutation

by Ng, I.K.S, Lee, J, Ng, C, Kosmo, B, Chiu, L, Seah, E, Mok, M.M.H, Tan, K, Osato, M, Chng, W.-J, Yan, B, Tan, L.K
Published 2020

Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease

by Lim S.W., Zhao Y., Chua E., Law H.Y., Yuen Y., Pavanni R., Wong M.C., Ng I.S., Yoon C.S., Puong K.Y., Lim S.H., Tan E.K.
Published 2018

Expanded FMR1 alleles are rare in idiopathic Parkinson's disease [3]

by Tan E.K., Zhao Y., Puong K.Y., Law H.Y., Chan L.L., Yew K., Shen H., Chandran V.R., Yuen Y., Pavanni R., Wong M.C., Ng I.S.
Published 2018

The C-terminal 18 Amino Acid Region of Dengue Virus NS5 Regulates its Subcellular Localization and Contains a Conserved Arginine Residue Essential for Infectious Virus Production

by Tay M.Y.F., Smith K., Ng I.H.W., Chan K.W.K., Zhao Y., Ooi E.E., Lescar J., Luo D., Jans D.A., Forwood J.K., Vasudevan S.G.
Published 2018

Spermine reduces infarction and neurological deficit following a rat model of middle cerebral artery occlusion: A magnetic resonance imaging study

by Shirhan, M.D., Moochhala, S.M., Ng, P.-Y., Lu, J., Ng, K.C., Teo, A.L., Yap, E., Ng, I., Hwang, P., Lim, T., Sitoh, Y.Y., Rumpel, H., Jose, R., Ling, E.
Published 2014

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort

by Tan E.K., Zhao Y., Puong K.Y., Law H.Y., Chan L.L., Yew K., Tan C., Shen H., Chandran V.R., Teoh M.L., Yih Y., Pavanni R., Wong M.C., Ng I.S.
Published 2018

Multi-center transferability of a breath-hold T2 technique for myocardial iron assessment

by He, T, Kirk, P, Firmin, D.N, Lam, W.M, Chu, W.C.W, Au, W.-Y, Chan, G.C.F, Tan, R.S, Ng, I, Biceroglu, S, Aydinok, Y, Fogel, M.A, Cohen, A.R, Pennell, D.J
Published 2020

Cryopreservation of neurospheres derived from human glioblastoma multiforme

by Chong, Y.-K., Toh, T.-B., Zaiden, N., Poonepalli, A., Siew, H.L., Ong, C.E.L., Yu, Y., Tan, P.B., See, S.-J., Ng, W.-H., Ng, I., Hande, M.P., Oi, L.K., Ang, B.-T., Tang, C.
Published 2014

Progenitor-like traits contribute to patient survival and prognosis in oligodendroglial tumors

by Ng, F.S.-L., Toh, T.B., Ting, E.H.-L., Koh, G.R.-H., Sandanaraj, E., Phong, M., Wong, S.S., Leong, S.H., Kon, O.L., Tucker-Kellogg, G., Ng, W.H., Ng, I., Tang, C., Ang, B.T.
Published 2014

A distinct reactive oxygen species profile confers chemoresistance in glioma-propagating cells and associates with patient survival outcome

by Koh, L.W.-H., Koh, G.R.-H., Ng, F.S.-L., Toh, T.B., Sandanaraj, E., Chong, Y.K., Phong, M., Tucker-Kellogg, G., Kon, O.L., Ng, W.H., Ng, I.H.-B., Clement, M.-V., Pervaiz, S., Ang, B.T., Tang, C.S.-L.
Published 2014

ST3GAL1-Associated Transcriptomic Program in Glioblastoma Tumor Growth, Invasion, and Prognosis

by Chong Y.K., Sandanaraj E., Koh L.W.H., Thangaveloo M., Tan M.S.Y., Koh G.R.H., Toh T.B., Lim G.G.Y., Holbrook J.D., Kon O.L., Nadarajah M., Ng I., Ng W.H., Tan N.S., Lim K.L., Tang Soo Leng Carol, Ang B.T.
Published 2018

MS analysis of single-nucleotide differences in circulating nucleic acids: application to noninvasive prenatal diagnosis

by Ding, C.M., Chiu, R.W.K., Lau, T.K., Leung, T.N., Chan, L.C., Chan, A.Y.Y., Charoenkwan, P., Ng, I.S.L., Law, H.Y., Ma, E.S.K., Xu, X.M., Wanapirak, C., Sanguansermsri, T., Liao, C., Tan, J.A.M.A., Chui, D.H.K., Cantor, C.R., Lo, Y.M.D.
Published 2004

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis

by Ding C., Chiu R.W.K., Lau T.K., Leung T.N., Chan L.C., Chan A.Y.Y., Charoenkwan P., Ng I.S.L., Law H.-Y., Ma E.S.K., Xu X., Wanapirak C., Sanguansermsri T., Liao C., Tan Jin Ai M.A., Chui D.H.K., Cantor C.R., Lo Y.M.D.
Published 2014

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations

by Beaty, T.H., Hetmanski, J.B., Fallin, M.D., Park, J.W., Sull, J.W., Liang, K.Y., McIntosh, I., Boyadjiev, S.A., Jabs, E.W., Ingersoll, R., Scott, A.F., VanderKolk, C.A., Redett, R.J., Chong, S.S., Cheah, F.S.H., Wu-Chou, Y.H., Chen, P.K., Chiu, Y.F., Yeow, V., Ng, I.S.L., Cheng, J., Huang, S., Ye, X., Wang, H.
Published 2011

The Biomolecular Interaction Network Database and related tools 2005 update

by Alfarano, C., Andrade, C.E., Anthony, K., Bahroos, N., Bajec, M., Bantoft, K., Betel, D., Bobechko, B., Boutilier, K., Burgess, E., Buzadzija, K., Cavero, R., D'Abreo, C., Donaldson, I., Dorairajoo, D., Dumontier, M.J., Dumontier, M.R., Earles, V., Farrall, R., Feldman, H., Garderman, E., Gong, Y., Gonzaga, R., Grytsan, V., Gryz, E., Gu, V., Haldorsen, E., Halupa, A., Haw, R., Hrvojic, A., Hurrell, L., Isserlin, R., Jack, F., Juma, F., Khan, A., Kon, T., Konopinsky, S., Le, V., Lee, E., Ling, S., Magidin, M., Moniakis, J., Montojo, J., Moore, S., Muskat, B., Ng, I., Paraiso, J.P., Parker, B., Pintilie, G., Pirone, R., Salama, J.J., Sgro, S., Shan, T., Shu, Y., Siew, J., Skinner, D., Snyder, K., Stasiuk, R., Strumpf, D., Tuekam, B., Tao, S., Wang, Z., White, M., Willis, R., Wolting, C., Wong, S., Wrong, A., Xin, C., Yao, R., Yates, B., Zhang, S., Zheng, K., Pawson, T., Ouellette, B.F.F., Hogue, C.W.V.
Published 2014