A splicing LMNA mutation causing laminopathies accompanied by aortic valve malformation

by Duan, J., Li, S., Pi, X., Tao, J., Wang, H.
Published 2021

CRISPR-Cas9 Based Genome Editing in Wheat

by Clarke, M., Harwood, W.A, Hayta, S., Smedley, M.A
Published 2021

Association of circulating long non-coding RNA HULC expression with disease risk, inflammatory cytokines, biochemical index levels, severity-assessed scores, and mortality of sepsi...

by Feng, L., Feng, Q., Hou, L., Wang, C., Wang, H., Wang, J., Wei, P., Wu, Y., Yuan, H.
Published 2021

Constructing a 10-core genes panel for diagnosis of pediatric sepsis

by Chen, J., Pan, J., Wang, Y., Zhou, X.
Published 2021

A next generation sequencing-based protocol for screening of variants of concern in autism spectrum disorder

by Budjan, C., Fong, M., Huang, J., Jeong, M.-S, Kong, X.-J, Liu, J., Liu, K., Sherman, H.T, Tian, R., Zhuang, P.
Published 2022

Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome

by Alkhunaizi, E., Brandt, T., Chitayat, D.A, DeFilippo, C.P, Douglas, G.V, Dubbs, H.A, Elloumi, H.Z, Glassford, M.R, Graf, W.D, Hannibal, M.C, Héron, B., Kim, L.E, Marco, E.J, Mignot, C., Monaghan, K.G, Morrow, M.M, Myers, K.A, Parikh, S., Quinonez, S.C, Rajabi, F., Sarnat, H.B, Shankar, S.P, Shinawi, M.S, Steele, J.L, van de Kamp, J.J.P, Veerapandiyan, A., Waldman, A.T
Published 2022

An alternate method for DNA and RNA extraction from clotted blood

by Aziz, A.T.A, Hoh, B.P, Mokhtar, S.S, Mokhtar, U., Umi, S.H, Zaiharina, M.Z, Zakaria, Z.
Published 2013

Genetic analysis and identification of SSR markers associated with rice blast disease in a BC2F1 backcross population

by Abdullah, S., Hasan, N., Mazlan, N., Nusaibah, S.A, Rafii, M.Y, Rahim, H.A
Published 2017

Modulation of immune function in rats using oligosaccharides extracted from palm kernel cake

by Bashokouh, F., Ebrahimi, R., Idrus, Z., Jahromi, M.F, Liang, J.B, Shokryazdan, P.
Published 2017

Limited expression of non-integrating CpG-free plasmid is associated with increased nucleosome enrichment

by Abdullah, S., Chau, D.-M, Ghazalli, N., Habib, O., Ling, K.-H, Sakri, R.M
Published 2020

Genetic relatedness of indigenous ethnic groups in northern Borneo to neighboring populations from Southeast Asia, as inferred from genome-wide SNP data

by Hoh, B.-P, Hoque, M.Z, Kumar, S.V, Lau, S.T.Y, Minsong, A., Ong, R.T.-H, Phipps, M.E, Pugh-Kitingan, J., Ransangan, J., Saw, W.Y, Teo, Y.-Y, Voo, C.L.Y, Wang, X., Xu, S., Yew, C.W
Published 2018

Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene

by Ali, E.Z, Jusoh, S.A, Mohd Radzi, M.A, Ngu, L.H, Zakaria, Y.
Published 2018

Mutagenic study of benzimidazole derivatives with (+S9) and without (-S9) metabolic activation

by Ab dullah, S.S, Abdullah, R., Ahmat, N., Akim, A.M, Azahar, N.H, Hamid, H.A
Published 2019

CinA mediates multidrug tolerance in Mycobacterium tuberculosis

by Dartois, V., Ehrt, S., Gengenbacher, M., Gouzy, A., Hartman, T.E, Jansen, R.S, Kreutzfeldt, K.M, Krieger, I.V, Rhee, K.Y, Sacchettini, J.C, Sarathy, J.P, Schnappinger, D., Wang, R., Xie, M., Zimmerman, M.D
Published 2022

Genetic analysis of over half a million people characterises C-reactive protein loci

by Alizadeh, B.Z, Bodinier, B., Chadeau-Hyam, M., Chasman, D.I, Dehghan, A., Elliott, P., Evangelou, E., Jarvelin, M.-R, Karhunen, V., Koskeridis, F., Ligthart, S., Pazoki, R., Said, S., Sattar, N., Tzoulaki, I., Võsa, U., Welsh, P.
Published 2022

Experimental and computational investigation of enzyme functional annotations uncovers misannotation in the EC 1.1.3.15 enzyme class

by Engqvist, M.K.M, Rembeza, E.
Published 2021

Genetic dissection of complex traits using hierarchical biological knowledge

by Ideker, T., Kreisberg, J.F, Tanaka, H.
Published 2021